Section 3
Physical Constants of Organic Compounds
Organic
Physical Constants of Organic Compounds . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-1
Synonym Index of Organic Compounds . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-554
Diamagnetic Susceptibility of Selected Organic Compounds . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-576
3-i
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PHYSICAL CONSTANTS OF ORGANIC COMPOUNDS
• Laboratory reagent lists, e.g., the ACS Reagent Chemicals
volume (Ref. 1)
• The DIPPR list of industrially important compounds (Ref.
2) and the (much larger) TSCA Inventory of chemicals used
in commerce.
• The Hazardous Substance Data Bank (Ref. 3)
• The UNEP list of Persistent Organic Pollutants (Ref. 4)
• Chemicals on Reporting Rules (CORR), a database of about
7500 regulated compounds prepared by the Environmental
Protection Agency (Ref. 5)
• The EPA Integrated Risk Information System (IRIS), a database of human health effects of exposure to chemicals in
the environment (Ref. 6)
• Compendia of chemicals of biochemical or medical importance, such as The Merck Index (Ref. 10)
• Specialized tables in this Handbook
It should be noted that the above lists vary widely in their choice
of chemical names, and even in the use of Chemical Abstracts
Registry Numbers. To the extent possible, we have attempted to
systematize the names and registry numbers for this table.
Clearly, criteria of this type are somewhat subjective, and compounds considered important by some users have undoubtedly
been omitted. Suggestions for additional compounds or other
improvements are welcomed.
The data in the table have been derived from many sources,
including both the primary literature and evaluated compilations. The Handbook of Data on Organic Compounds, Third
Edition (Ref. 7) and the Combined Chemical Dictionary (Ref. 8)
were important sources. Other useful sources of physical property data on organic compounds are listed in Refs. 9-19. The values in the table for the normal boiling point and the melting point
that are accompanied with uncertainties (in parentheses) have
been critically evaluated using the NIST ThermoData Engine
(TDE, Ref. 20), designed to implement the dynamic data evaluation concept (Refs. 21-24). This concept requires large electronic
databases capable of storing essentially all relevant experimental
data known to date with detailed descriptions of metadata and
uncertainties. The combination of these electronic databases
with expert-system software, designed to automatically generate
recommended property values based on available experimental
and predicted data, leads to the ability to produce critically evaluated data dynamically or “to order.” The uncertainties listed are
combined expanded uncertainties (level of confidence, approximately 95 %) representing the most comprehensive measure of
the overall data reliability (Refs. 25-28).
The table is arranged alphabetically by substance name, which
generally is either an IUPAC systematic name or, in the case of
pesticides, pharmaceuticals, and other complex compounds,
a simple trivial name. Names in ubiquitous use, such as acetic
acid and formaldehyde, are adopted rather than their systematic
equivalents. Synonyms are given in the column following the primary name, and structure diagrams are given on the page facing
the data listing. The explanation of the data columns follows:
No.: An identification number used in the indexes.
Name: Primary name of the substance
Synonym: A synonym in common use. When the primary
name is non-systematic, a systematic name may appear
here.
Mol. Form.: The molecular formula written in the Hill
convention.
CAS RN.: The Chemical Abstracts Service Registry Number
for the compound.
Mol. Wt: Molecular weight (relative molar mass) as calculated
with the 2001 IUPAC Standard Atomic Weights.
Physical Form: A notation of the physical phase, color, crystal
type, or other features of the compound at ambient temperature. Abbreviations are given below.
mp: Normal melting point in °C. A value is sometimes followed by “dec”, indicating decomposition is observed at
the stated temperature (so that it is probably not a true
melting point). The notation “tp” indicates a triple point,
where solid, liquid, and gas are in equilibrium. A number in
parentheses following the melting point value is the combined expanded uncertainty (see above).
bp: Normal boiling point in °C, if it is available. This is the
temperature at which the liquid phase is in equilibrium
with the vapor at a pressure of 760 mmHg (101.325 kPa).
A number in parentheses following the boiling point value
is the combined expanded uncertainty (see above). A notation “sp” following the value indicates a sublimation point,
where the vapor pressure of the solid phase reaches 760
mmHg. When a notation such as “dec” (decomposes) or
“exp” (explodes) follows the value, the temperature may
not be a true boiling point. A simply entry “sub” indicates
the solid has a significant sublimation pressure at ambient
temperatures. When the normal boiling point is not available, a boiling point at reduced pressure may be listed with
a superscript indicating the pressure in mmHg.
den: Density (mass per unit volume) in g/cm3. The temperature in °C is indicated by a superscript. Values refer to the
liquid or solid phase, and all values are true densities, not
specific gravities. The number of decimal places gives a
rough estimate of the accuracy of the value.
nD: Refractive index, at the temperature in °C indicated by the
superscript. Unless otherwise indicated, all values refer to
a wavelength of 589 nm (sodium D line). Values are given
only for liquids and solids.
Solubility: Qualitative indication of solubility in common solvents. Abbreviations are:
i insoluble
sl slightly soluble
s soluble
vs very soluble
msc miscible
dec decomposes
Abbreviations for solvents are given below.
3-1
Organic
The basic physical constants and structure diagrams for about
10,900 organic compounds are presented in this table. An effort
has been made to include the compounds most frequently
encountered in the laboratory, the workplace, and the environment. Particular emphasis has been given to substances that are
considered environmental or human health hazards. In making the selection of compounds for the table, added weight was
assigned to the appearance of a compound in various lists or reference sources such as:
Physical Constants of Organic Compounds
3-2
In order to facilitate the location of compounds in the table, an
index to synonyms follows the main table. Indexes to Molecular
Formulas and CAS Registry Numbers are available in the electronic versions of the Handbook or as pdf files by request via
e-mail (fiona.macdonald@taylorandfrancis.com).
The assistance of members of the Thermodynamics Research
Center (TRC) of the National Institute of Standards and
Technology (Vladimir Diky, Rob Chirico, Andrei Kazakov) and
especially Chris Muzny and Michael Frenkel in the determination
of values of the normal-boiling-point and melting-point temperatures with uncertainties is greatly appreciated. The editors
of the Handbook are much indebted to Chris Muzny who spent
countless hours in producing these critically evaluated results.
The assistance of Fiona Macdonald in checking names and formulas is gratefully acknowledged, as well as the efforts of Janice
Shackleton, Trupti Desai, Nazila Kamaly, Matt Griffiths, and
Lawrence Braschi in preparing the structure diagrams.
List of Abbreviations
Organic
Ac
Ac2O
AcOEt
ac
ace
al
alk
amor
anh
aq
bipym
bl
blk
bp
br
bt
Bu
BuOH
bz
chl
col
con, conc
cry
ctc
cy, cyhex
dec
den
dil
diox
dk
DMF
DMSO
efflor
Et
EtOH
eth
exp
fl
acetyl
acetic anhydride
ethyl acetate
acid
acetone
alcohol (ethanol)
alkali
amorphous
anhydrous
aqueous
bipyramidal
blue
black
boiling point
brown
bright
butyl
1-butanol
benzene
chloroform
colorless
concentrated
crystals
carbon tetrachloride
cyclohexane
decomposes
density
dilute
dioxane
dark
dimethylformamide
dimethyl sulfoxide
efflorescent
ethyl
ethanol
diethyl ether
explodes
flakes
flr
fum
gl
gr
gran
grn
hex
HOAc
hp
hx
hyd
hyg
i
iiso
lf
lig
liq
lo
mcl
Me
MeCN
MeOH
misc
mp
n
nd
oct
oran
orth
os
pa
peth
Ph
PhCl
PhNH2
PhNO2
pl
fluorescent
fumes, fuming
glacial
gray
granular
green
hexagonal
acetic acid
heptane
hexane
hydrate
hygroscopic
insoluble
isoisooctane
leaves
ligroin
liquid
long
monoclinic
methyl
acetonitrile
methanol
miscible
melting point
refractive index
needles
octahedra, octahedral
orange
orthorhombic
organic solvents
pale
petroleum ether
phenyl
chlorobenzene
aniline
nitrobenzene
plates
pow
Pr
PrOH
pr
purp
py
pym
reac
rhom
s
sat
sc
sl
soln
sp
stab
sub
sulf
syr
tab
tcl
tetr
tfa
thf, THF
tol
tp
trg
unstab
vap
viol
visc
vol
vs
w
wh
xyl
ye
powder
propyl
1-propanol
prisms
purple
pyridine
pyramids, pyramidal
reacts
rhombic
soluble
saturated
scales
slightly soluble
solution
sublimation point
stable
sublimes
sulfuric acid
syrup
tablets
triclinic
tetragonal
trifluoroacetic acid
tetrahydrofuran
toluene
triple point
trigonal
unstable
vapor
violet
viscous
volatile
very soluble
water
white
xylene
yellow
References
1.American Chemical Society, Reagent Chemicals, Tenth Edition,
Oxford University Press, New York, 2005.
2.Design Institute for Physical Properties, American Institute of
Chemical Engineers, <http://www.aiche.org/dippr/>.
3. National Library of Medicine, Hazardous Substances Data Bank,
<http://toxnet.nlm.nih.gov/cgi-bin/sis/htmlgen?HSDB>.
4.United Nations Environmental Program, Persistent Organic
Pollutants, <http://www.chem.unep.ch/pops/>.
5. Environmental Protection Agency, Chemicals on Reporting Rules,
<http://www.epa.gov/opptintr/CORR>.
6.Environmental Protection Agency, Integrated Risk Information
System, <http://www.epa.gov/iris/index.html>.
7. Lide, D. R., and Milne, G. W. A., Editors, Handbook of Data on
Organic Compounds, Third Edition, CRC Press, Boca Raton, FL,
1993.
8. Combined Chemical Dictionary, <http://ccd.chemnetbase.com/>.
9.Linstrom, P. J., and Mallard, W. G., Editors, NIST Chemistry
WebBook, NIST Standard Reference Database No. 69, February 2010,
National Institute of Standards and Technology, Gaithersburg, MD
20899, <http://webbook.nist.gov>.
10. Thermodynamic Research Center, National Institute of Standards and
Technology, TRC Thermodynamic Tables, <http://trc.nist.gov>.
11. O’Neil, M. J., Editor, The Merck Index, Fourteenth Edition, Merck &
Co., Whitehouse Station, NJ, 2006.
12.Stevenson, R. M., and Malanowski, S., Handbook of the
Thermodynamics of Organic Compounds, Elsevier, New York, 1987.
13. Riddick, J. A., Bunger, W. B., and Sakano, T. K., Organic Solvents,
Fourth Edition, John Wiley & Sons, New York, 1986.
14. ChemSpider, <http://www.chemspider.com/>.
15. Crossfire Beilstein, <http://accelrys.com/products/>.
16. Springer Materials, The Landolt-Börnstein Database, <http://www.
springermaterials.com>.
3-3
17. Vargaftik, N.B., Vinogradov, Y. K., and Yargin, V. S., Handbook of
Physical Properties of Liquids and Gases, Third Edition, Begell House,
New York, 1996.
18. Lide, D. R., and Kehiaian, H. V., Handbook of Thermophysical and
Thermochemical Data, CRC Press, Boca Raton, FL, 1994.
19. Lide, D. R., Editor, Properties of Organic Compounds, <http://www.
chemnetbase.com/tours/poc/intro.jsf>.
20. Frenkel, M., Chirico, R. D., Diky, V. V., Kazakov, A., and Muzny, C.
D., ThermoData Engine, NIST Standard Reference Database 103b,
Version 5.0 (Pure Compounds, Binary Mixtures, and Chemical
Reactions, TDE-SOURCE Version 5.1), National Institute of
Standards and Technology, Gaithersburg, MD – Boulder, CO, 2010,
<http://www.nist.gov/srd/nist103b.cfm>.
21. Frenkel, M., Chirico, R. D., Diky, V., Yan, X., Dong, Q., and Muzny, C.,
J. Chem. Inf. Model. 45, 816, 2005.
22. Diky, V., Muzny, C. D., Lemmon, E. W., Chirico, R. D., and Frenkel,
M., J. Chem. Inf. Model. 47, 1713, 2007.
23. Diky, V., Chirico, R. D., Kazakov, A. F., Muzny, C., and Frenkel, M., J.
Chem. Inf. Model. 49, 503, 2009.
24. Diky, V., Chirico, R. D., Kazakov, A. F., Muzny, C., and Frenkel, M., J.
Chem. Inf. Model. 49, 2883, 2009.
25. Chirico, R. D., Frenkel, M., Diky, V. V., March, K. N., and Wilhoit, R.
C., J. Chem. Eng. Data 48, 1344, 2003.
26. Guide to the Expression of Uncertainty in Measurement, International
Organization for Standardization, Geneva, Switzerland, 1993.
27. U. S. Guide to the Expression of Uncertainty in Measurement, ANSI/
NCSL, Z540-2-1997, ISBN 1-58464-005-7, NCSL Int., Boulder, CO,
1997.
28. Taylor, B. N., and Kuyatt, C. E., Guidelines for the Evaluation and
Expression of Uncertainty in NIST Measurement Results, NIST Tech.
Note 1297, Natl. Inst. Stand. Technol., Gaithersburg, MD, 1994.
Organic
Physical Constants of Organic Compounds
Physical Constants of Organic Compounds
3-4
Organic
No.
Name
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
1
Abate
Temephos
C16H20O6P2S3
3383-96-8
466.469 cry
2
Abietic acid
C20H30O2
514-10-3
3
Abscisic acid
C15H20O4
4
Acacetin
5
6
Acebutolol, (±)Acedapsone
7
Acenaphthene
1,2-Dihydroacenaphthylene
8
Acenaphthylene
Acenaphthalene
9
1,2-Acenaphthylenedione
10
11
Acenocoumarol
Acephate
12
13
14
Acepromazine
Acesulfame
Acetaldehyde
15
16
Acetaldehyde phenylhydrazone
Acetaldoxime
17
5,7-Dihydroxy-2-(4methoxyphenyl)-4H-1benzopyran-4-one
C16H12O5
mp/˚C
bp/˚C
31.6(0.5)
302.451 mcl pl
173.5
(al-w)
21293-29-8 264.318 cry
160
(chl-peth)
480-44-4
284.263 ye nd (95% 263
al)
den
g cm –3
1.32
2509
120 sub
121
290
C12H10
93(2)
277.5(0.8)
1.22220
C12H8
208-96-8
89.4(0.3)
280
0.898716
C12H6O2
82-86-0
182.175 ye nd
259(9)
(HOAc)
152-72-7
353.325 cry (ace aq) 198
30560-19-1 183.166
92.0(0.5)
sub
1.480020
2300.5
123.2
-123.4(0.7)
20.8(0.6)
C8H10N2
61-00-7
326.455 oran oil
33665-90-6 163.153 nd (bz)
75-07-0
44.052 vol liq or
gas
935-07-9
134.178
99.5
15040
Acetaldehyde oxime
C2H5NO
107-29-9
59.067
nd
25(1)
115.24(0.1)
Acetamide
Ethanamide
C2H5NO
60-35-5
59.067
trg mcl
(al-eth)
80.16(0.04)
222.0
18
Acetanilide
N-Phenylacetamide
C8H9NO
103-84-4
135.163
114.35(0.04) 292(9)
19
Acetazolamide
N-[5-(Aminosulfonyl)-1,3,4thiadiazol-2-yl]acetamide
C4H6N4O3S2
59-66-5
222.246
260.5
20
21
Acethion
Acetic acid
C8H17O4PS2
C2H4O2
919-54-0
64-19-7
272.322 liq
60.052 col liq
17(3)
22
Acetic acid, 2-phenylhydrazide
C8H10N2O
114-83-0
150.177 hex pr (eth) 130.0
23
Acetic anhydride
C4H6O3
108-24-7
102.089 liq
24
Acetoacetanilide
C10H11NO2
102-01-2
177.200 pr or nd (bz 86
or lig)
25
Acetoacetic acid
C4H6O3
541-50-4
102.089 cry (eth)
26
C10H14O5
21282-97-3 214.215 liq
27
28
2-Acetoacetoxyethyl
methacrylate
Acetochlor
Acetohexamide
C14H20ClNO2
C15H20N2O4S
29
Acetohydrazide
C2H6N2O
34256-82-1 269.768 ye liq
968-81-0
324.396 cry (EtOH
aq)
1068-57-1 74.081
30
31
Acetohydroxamic acid
1-Acetonaphthone
C2H5NO2
C12H10O
546-88-3
941-98-0
32
2-Acetonaphthone
C12H10O
93-08-3
33
Acetone
C3H6O
34
Acetone cyanohydrin
35
Acetone (2,4-dinitrophenyl)­
hydrazone
Nicoumalone
Phosphoramidothioic acid,
acetyl-, O,S-dimethyl ester
Ethanal
Ethanoic acid
Acetyl acetate
2-(Methacryloyloxy)ethyl
acetoacetate
N-Hydroxyacetamide
2-Propanone
C19H15NO6
C4H10NO3PS
C19H22N2OS
C4H5NO4S
C2H4O
152.192
-73.4(0.8)
36.5
sl H2O, hx; s
ctc, eth, tol
vs ace, bz, eth,
EtOH
vs ace, eth, chl
1.604895 i H2O; sl EtOH,
chl; vs bz; s
HOAc
i H2O; vs EtOH,
eth, bz; sl chl
i H2O; sl EtOH,
bz, HOAc; s lig
i H2O
1.3520
1371.5
117.9(0.2)
139.5(0.3)
100 dec
1000.8
1340.4
188
13725
75.067 hyg cry
170.206
90
34
297
52(1)
302
67-64-1
170.206 nd (lig, dil
al)
58.079 liq
-94.9(0.4)
56.08(0.07)
C4H7NO
75-86-5
85.105
-19
180(21)
C9H10N4O4
1567-89-1
238.200 ye nd or pl
(al)
128
Solubility
sl H2O
67
liq
nD
vs EtOH
37517-30-9 336.426 cry
77-46-3
332.374 pa ye nd
(eth) lf (dil
al)
83-32-9
154.207
HCP_Section_03.indb 4
C18H28N2O4
C16H16N2O4S
Physical
Form
s bz, chl
0.783418 1.331620 msc H2O, EtOH,
eth, bz; sl chl
vs EtOH
0.965620 1.426420 s H2O, chl; msc
EtOH, eth
0.998685 1.4278
vs H2O, EtOH
1.219015
sl H2O; vs EtOH,
ace; s eth, s
bz, tol
sl H2O
1.1820
1.044625 1.372020 msc H2O, EtOH,
eth, ace, bz; s
chl, CS2
vs H2O, EtOH; sl
eth, chl, tfa; s
bz
1.08220 1.390120 vs H2O; s EtOH,
bz; msc eth; sl
ctc
sl H2O; s EtOH,
eth, bz, chl,
acid, lig
vs H2O, eth,
EtOH
1.122
1.456020
1.527220 sl H2O
i H2O, eth; sl
EtOH, chl; s py
s H2O, EtOH; sl
eth
1.117121 1.628022 i H2O; s EtOH,
eth, ace, chl
sl EtOH, ctc
0.784525 1.358820 msc H2O, EtOH,
eth, ace, bz,
chl
0.93219 1.399220 vs H2O, EtOH,
eth; s ace, bz,
chl; i peth
i H2O; s EtOH,
eth, bz, chl,
AcOEt
4/11/16 11:17 AM
Physical Constants of Organic Compounds
3-5
OH O
S
O
P O
O
S
O
O P
O
S
1
O
O
O
OH
3
4
Abscisic acid
Acacetin
O
O
O
OH
O
Abietic acid
H
N
N
H
O
2
Abate
HO
OH
H
COOH
HN
O
S
O
O
5
NH
O
6
8
7
Acedapsone
Acenaphthylene
Acenaphthene
9
1,2-Acenaphthylenedione
Organic
Acebutolol, (±)-
O
O
OH
N
O
O
O
N
O
O
O P
O
S
N
15
16
Acetaldehyde phenylhydrazone
OH
21
O
N
H
22
Acetic acid
Acetic acid, 2-phenylhydrazide
Acetaldehyde
N
H
S
19
O
O
O
23
24
O
O
OH
25
Acetoacetanilide
Acetic anhydride
O
Acethion
H
N
O
O
20
Acetazolamide
O
H
N
O
18
Acetanilide
Acetamide
H
14
S
O P S
O
O
N N
O
H2N S
O
O
17
Acetaldoxime
O
O
O
Acesulfame
H
N
NH2
OH
S
O
13
Acepromazine
O
N
N
H
12
Acephate
Acenocoumarol
O
S
11
10
H
N
O
N
H
N
Acetoacetic acid
O
Cl
O
N
O
H
N
O
O
O
O
O
26
27
2-Acetoacetoxyethyl methacrylate
O
H
N S
O
O
O
N
H
28
Acetochlor
O
NH2
29
Acetohexamide
30
Acetohydrazide
Acetohydroxamic acid
N
O
O
O
1-Acetonaphthone
32
2-Acetonaphthone
33
Acetone
NH O
N
O
OH
N
31
OH
N
H
34
Acetone cyanohydrin
O
N
35
O
Acetone (2,4-dinitrophenyl)hydrazone
Physical Constants of Organic Compounds
3-6
Mol. Form.
CAS RN
Mol.
Wt.
C6H12N2
627-70-3
C4H9N3S
C2H3N
Methyl phenyl ketone
Methylphenyl ketazine
Acetophos
No.
Name
36
37
38
Acetone (1-methylethylidene)­ Dimethyl ketazine
hydrazone
Acetone thiosemicarbazide
Acetonitrile
Methyl cyanide
39
Acetophenone
40
41
42
Acetophenone azine
Acetoxon
N-Acetylacetamide
43
44
Physical
Form
den
g cm –3
Organic
mp/˚C
bp/˚C
112.172 liq
-12.5
133
1752-30-3
75-05-8
131.199 ye cry
41.052 liq
176
-44(1)
81.6(0.2)
C8H8O
98-86-2
120.149 mcl pr or pl 19.4(0.4)
202.1(0.2)
C16H16N2
C8H17O5PS
C4H7NO2
729-43-1
2425-25-4
625-77-4
236.311
256.257 liq
101.105 nd (eth)
120
730.005
223.5
C5H9NO3
C8H8ClNO3S
97-69-8
121-60-8
C9H9NO3
89-52-1
131.130
233.673 nd (bz), pr
(bz-chl)
179.172 nd (HOAc)
125
149
45
N-Acetyl-L-alanine
4-(Acetylamino)benzenesulfo- Acetylsulfanilyl chloride
nyl chloride
2-(Acetylamino)benzoic acid
46
4-(Acetylamino)benzoic acid
C9H9NO3
556-08-1
179.172 nd (HOAc)
256.5
47
N-Acetyl-D-glucosamine
C8H15NO6
7512-17-6
221.208
205
N-Acetyl-D-mannosamine
C8H15NO6
3615-17-6
221.208 cry (ace aq) 128
dec alk
49
2-(Acetylamino)-2-deoxy-Dglucose
2-(Acetylamino)-2-deoxy-Dmannose
2-(Acetylamino)fluorene
C15H13NO
53-96-3
223.270 cry (dil al)
i H2O; s EtOH,
eth, HOAc
50
51
52
4-(Acetylamino)fluorene
6-(Acetylamino)hexanoic acid
4-Acetylanisole
ε-Acetamidocaproic acid
C15H13NO
C8H15NO3
C9H10O2
28322-02-3 223.270 br cry (bz)
57-08-9
173.210 cry (ace)
100-06-1
150.174 pl (peth)
200
104.5
38.2(0.6)
254(12)
53
2-Acetylbenzoic acid
C9H8O3
577-56-0
114.5
1112
54
3-Acetylbenzoic acid
C9H8O3
586-42-5
164.158 nd (w), pr
(bz)
164.158
172
1112
55
56
57
4-Acetylbenzoic acid
Acetyl benzoylperoxide
Acetyl bromide
Acetozone
Ethanoyl bromide
C9H8O3
C9H8O4
C2H3BrO
586-89-0
644-31-5
506-96-7
164.158 nd (w)
180.158 wh nd (lig)
122.948 liq
208
37
-96.5(0.5)
sub
13019
74(1)
1.662516 1.448620
58
Acetyl chloride
Ethanoyl chloride
C2H3ClO
75-36-5
78.497
-112.7(0.8)
51(2)
1.105120 1.388620
59
60
Acetylcholine bromide
Acetylcholine chloride
C7H16BrNO2
C7H16ClNO2
66-23-9
60-31-1
226.112 hyg cry
181.661
146
150
61
62
63
64
65
2260-50-6
874-23-7
1670-46-8
616-91-1
517-23-7
273.112 hyg
140.180
126.153
163.195 cry (w)
128.126
163
-11
11218
7320
1.078225 1.513820 s ctc
1.043125 1.490620
Acetylcysteine
α-Acetylbutyrolactone
C7H16INO2
C8H12O2
C7H10O2
C5H9NO3S
C6H8O3
1075
1.184620 1.458520 vs H2O
2,5-Dihydroxyacetophenone
C8H8O3
490-78-8
67
Acetylcholine iodide
2-Acetylcyclohexanone
2-Acetylcyclopentanone
N-Acetyl-L-cysteine
3-Acetyldihydro-2(3H)furanone
1-Acetyl-2,5-dihydroxy­
benzene
Acetylene
Ethyne
C2H2
74-86-2
152.148 ye grn nd
205.3
(dil al or w)
26.037 col gas
-81.5(0.9)
-84.7 sp
68
N-Acetylethanolamine
C4H9NO2
142-26-7
103.120
63.5
1668
0.37725
(p>1
atm)
1.107925 1.467420
69
Acetyl fluoride
Ethanoyl fluoride
C2H3FO
557-99-3
62.042
vol liq or
gas
-84
22(7)
1.03225
70
71
N-Acetylglutamic acid
N-Acetylglycine
Aceturic acid
C7H11NO5
C4H7NO3
1188-37-0
543-24-8
199
206
72
Oxaceprol
C7H11NO4
73
trans-1-Acetyl-4-hydroxy-Lproline
1-Acetyl-1H-imidazole
189.166 pr (w)
117.104 lo nd (w,
MeOH)
33996-33-7 173.167 cry (Ac)
C5H6N2O
2466-76-4
110.114
104.5
74
75
76
77
Acetyl iodide
Acetyl isothiocyanate
N6-Acetyl-L-lysine
N-Acetyl-DL-methionine
Ethanoyl iodide
C2H3IO
C3H3NOS
C8H16N2O3
C7H13NO3S
507-02-8
13250-46-9
692-04-6
1115-47-5
169.948
101.127
188.224
191.248
48
66
HCP_Section_03.indb 6
Synonym
liq
79
nD
Solubility
0.839020 1.453520 msc H2O, EtOH,
eth; s ace
s ace
0.785720 1.344230 msc H2O, EtOH,
eth, ace, bz,
ctc
1.028120 1.537220 sl H2O; s EtOH,
eth, ace, bz,
con sulf, chl
s H2O, EtOH,
eth, chl, lig
vs EtOH, eth; s
bz, chl
sl H2O; s EtOH;
vs eth, ace, bz,
HOAc
i H2O; s EtOH; sl
eth, tfa
187.5
193
1.081841 1.54741
sl H2O; s EtOH,
eth, ace, chl
vs H2O, eth,
EtOH
s H2O; msc
EtOH
vs H2O
vs eth
msc eth, bz,
chl; s ace
msc eth, ace,
bz, chl; s ctc
vs H2O
s H2O, EtOH; i
eth
109.5
132
109(5)
132.5
2.067320 1.549120
1.152313 1.523118
sl H2O, eth, bz;
s EtOH
sl H2O, EtOH,
CS2; s ace, bz,
chl
msc H2O; s ace;
sl bz, lig
msc EtOH, eth;
s bz, chl; sl
CS2
s H2O, EtOH
vs H2O, ace,
EtOH
vs H2O, MeOH
sl H2O; s EtOH,
eth, chl, THF
vs eth
s eth, CS2
265 dec
114.5
4/11/16 11:17 AM
Physical Constants of Organic Compounds
N
HN
N
N
N
N
N
37
Acetone (1-methylethylidene)hydrazone
O
O P S
O
O
S
NH2
36
3-7
38
Acetone thiosemicarbazide
39
Acetonitrile
40
Acetophenone
H
N
O
O
O
41
Acetophenone azine
Acetoxon
O
O S Cl
HO
O
O
42
N-Acetylacetamide
HO
O
HO
O
OH
N
H
H
N
NH
O
OH
O
O
NH
O
43
HN
O
44
N-Acetyl-L-alanine
OH
HO
47
4-(Acetylamino)benzoic acid
2-(Acetylamino)benzoic acid
2-(Acetylamino)-2-deoxy-D-glucose
Organic
4-(Acetylamino)benzenesulfonyl chloride
O
46
45
HO
O
O
HO
NH
HN
OH
HO
49
2-(Acetylamino)-2-deoxy-D-mannose
50
2-(Acetylamino)fluorene
HO
O
O
O
51
4-(Acetylamino)fluorene
HO
HO
OH
H
N
O
O
N
H
O
48
O
52
6-(Acetylamino)hexanoic acid
4-Acetylanisole
O
O
O
O
O
O
53
54
2-Acetylbenzoic acid
55
3-Acetylbenzoic acid
O
O
56
4-Acetylbenzoic acid
O
Br
O
O
Cl
57
Acetyl benzoylperoxide
58
Acetyl bromide
Acetyl chloride
O
O
O
Br
N
O
Cl
N
O
59
O
I
N
O
60
Acetylcholine bromide
O
O
OH
NH
O
O
61
Acetylcholine chloride
O
HS
62
Acetylcholine iodide
63
2-Acetylcyclohexanone
64
2-Acetylcyclopentanone
N-Acetyl-L-cysteine
O
O
O
O
O
OH
HO
65
H
66
3-Acetyldihydro-2(3H)-furanone
N
H
H
67
1-Acetyl-2,5-dihydroxybenzene
F
68
Acetylene
O
HO
O
OH
69
N-Acetylethanolamine
Acetyl fluoride
NH
OH
O
O
70
N-Acetylglutamic acid
O
HO
H
N
N
OH
COOH
N
O
N
O
O
71
N-Acetylglycine
O
I
O
72
trans-1-Acetyl-4-hydroxy-L-proline
73
O
O
1-Acetyl-1H-imidazole
74
Acetyl iodide
N
75
C
S
Acetyl isothiocyanate
S
O
HO
NH2
N
H
76
OH
N6-Acetyl-L-lysine
OH
HN
O
77
N-Acetyl-DL-methionine
Physical Constants of Organic Compounds
3-8
No.
Name
Synonym
Mol. Form.
CAS RN
78
79
Methionamine
Aspidospermine
C7H13NO3S
C22H30N2O2
65-82-7
466-49-9
Dehydroacetic acid
C5H9NO2
C8H15NO
C8H8O4
83
N-Acetyl-L-methionine
1-Acetyl-17-methoxyaspidospermidine
N-Acetyl-N-methylacetamide
1-Acetyl-3-methylpiperidine
3-Acetyl-6-methyl-2H-pyran2,4(3H)-dione
4-Acetylmorpholine
84
85
86
N-Acetylneuraminic acid
Acetyl nitrate
2-(Acetyloxy)benzoic acid
Aceneuramic acid
87
88
Mol.
Wt.
Physical
Form
den
g cm –3
mp/˚C
bp/˚C
105.5
208
2202
1113-68-4
4593-16-2
520-45-6
191.248
354.485 nd or pr (al)
nd (peth)
115.131 liq
141.211 liq
168.148
-25
-13.6
109
195
239
270
1.066325 1.450225
0.968425 1.473125
C6H11NO2
1696-20-4
129.157
14.5
15250
1.114520 1.482720
C11H19NO9
C2H3NO4
C9H8O4
131-48-6
591-09-3
50-78-2
186
60 exp
1.2415
4-(Acetyloxy)benzoic acid
2-(Acetyloxy)-5-bromobenzoic 5-Bromoacetylsalicylic acid
acid
4-(Acetyloxy)-3-methoxybenzaldehyde
2-(Acetyloxy)-1-phenylethanone
C9H8O4
C9H7BrO4
2345-34-8
1503-53-3
309.271
105.050
180.158 nd (w), mcl
tab (w)
180.158
259.054 nd (al)
C10H10O4
881-68-5
194.184
78
C10H10O3
2243-35-8
178.184 orth pl
49
91
1-(Acetyloxy)-2-propanone
Acetoxyacetone
C5H8O3
592-20-1
116.116
92
93
94
95
96
(Acetyloxy)tributylstannane
(Acetyloxy)triphenylstannane
4-Acetylphenyl acetate
N-Acetyl-L-phenylalanine
N-Acetyl-L-phenylalanine,
ethyl ester
N-Acetyl-L-phenylalanine,
methyl ester
Tributyltin acetate
Triphenyltin acetate
C14H30O2Sn
C20H18O2Sn
C10H10O3
C11H13NO3
C13H17NO3
56-36-0
900-95-8
13031-43-1
2018-61-3
2361-96-8
80
81
82
Organic
89
90
Acetylsalicylic acid
98
Acetyl phosphate
C2H5O5P
99
100
101
C7H13NO
C7H11NO2
C22H28N6O14P2
102
103
104
1-Acetylpiperidine
1-Acetyl-4-piperidinone
3-Acetylpyridine adenine
dinucleotide
4-Acetylthioanisole
Acetyl thiocholine iodide
N-Acetyl-L-tryptophan
349.097
409.066
178.184
207.226
235.279 cry (EtOH
aq)
3618-96-0 221.252 nd (peth) or
visc oil
(chl)
590-54-5
140.032 unstab in
soln
618-42-8
127.184 liq
32161-06-1 141.168
86-08-8
662.436 solid
C9H10OS
C7H16INOS
C13H14N2O3
1778-09-2
1866-15-5
1218-34-4
105
N-Acetyl-L-tyrosine
C11H13NO4
106
107
108
109
110
N-Acetyl-L-tyrosine ethyl ester
N-Acetyl-L-valine
Acid Fuchsin
Fuchsin, acid
Acifluorfen
5-[2-Chloro-4-(trifluoromethyl)­
phenoxy]-2-nitrobenzoic acid
Aconine
111
112
Aconitine
9-Acridinamine
113
97
C12H15NO3
3-Acetyl NAD
136(4)
Solubility
sl H2O, eth; s
EtOH, bz, chl
msc H2O; i eth
vs H2O
vs H2O, eth; sl
EtOH, chl
msc H2O; s
EtOH, ace, ctc
s H2O, eth, chl;
vs EtOH; sl bz
188.5
60
270
1.116965 1.503665
171
1.075720 1.414120
i H2O; vs EtOH,
eth
sl H2O; vs EtOH,
eth
i H2O; vs EtOH,
eth, chl; sl bz,
lig
vs H2O, eth,
EtOH
84.7
125.2(0.5)
s ctc, CS2
s EtOH
173.5
93
91
-13.4
226.5
218
81.5
205
189.5
C13H17NO4
C7H13NO3
C20H17N3Na2O9S3
C14H7ClF3NO5
166.239
289.177
246.261 nd (dil
MeOH)
537-55-3
223.226 cry (w); pl
(diox)
840-97-1
251.279
96-81-1
159.183
3244-88-0 585.539
50594-66-6 361.658
C25H41NO9
509-20-6
499.596 amor
132
Aminacrine
C34H47NO11
C13H10N2
302-27-2
90-45-9
645.737 orth lf
194.231 ye nd (ace
or al)
204
241
Acridine
Dibenzo[b,e]pyridine
C13H9N
260-94-6
110.06(0.05) 346.9(1)
114
3,6-Acridinediamine
Proflavine
C13H11N3
92-62-6
285
115
9(10H)-Acridinone
C13H9NO
578-95-0
179.217 orth nd or
pr (al)
209.246 ye nd (al or
w)
195.216 ye lf (al)
116
Acrolein
2-Propenal
C3H4O
107-02-8
56.063
liq
-87.8(0.9)
52.3(0.1)
117
Acrylamide
2-Propenamide
C3H5NO
79-06-1
71.078
lf (bz)
85(1)
192.6
118
Acrylic acid
2-Propenoic acid
C3H4O2
79-10-7
72.063
acrid liq
13.56(0.05)
142(2)
119
Acrylonitrile
Propenenitrile
C3H3N
107-13-1
53.063
liq
-83.51(0.05) 77.2(0.2)
120
Acyclovir
C8H11N5O3
59277-89-3 225.205 cry (EtOH)
HCP_Section_03.indb 8
nD
1.0119
1.14625
1.479025 vs H2O, EtOH
1.502620
s H2O, EtOH, alk
153
80.5
164
sl H2O, EtOH
164.3(0.5)
1.00520
>300
0.84020
1.401720
1.051120 1.422420
0.800725 1.391120
s H2O, EtOH,
chl; sl eth, lig
vs bz, EtOH, chl
s EtOH, ace; sl
DMSO; vs dil
HCl
i H2O; sl ctc; vs
EtOH, eth, bz
s H2O; vs EtOH;
sl eth, bz
i H2O, eth, bz; sl
EtOH; s HOAc,
alk
vs H2O; s EtOH,
eth, ace; sl chl
vs H2O, chl; s
EtOH, eth, ace
msc H2O, EtOH,
eth; s ace, bz,
ctc
s H2O; vs ace,
bz, eth, EtOH
225
4/11/16 11:17 AM
Physical Constants of Organic Compounds
3-9
N
O
S
OH
HN
N
N
H
O
O
O
78
O
79
N-Acetyl-L-methionine
O
OH O
H
O
O
O
80
1-Acetyl-17-methoxyaspidospermidine
N
N
81
N-Acetyl-N-methylacetamide
1-Acetyl-3-methylpiperidine
O
O
O
82
83
3-Acetyl-6-methyl-2H-pyran-2,4(3H )-dione
4-Acetylmorpholine
OH
O
O
O COOH
OH
OH
CH2OH
OH
HO
O
O
N
O
OH
84
O
O
O
O
Br
87
2-(Acetyloxy)benzoic acid
O
O
O
86
Acetyl nitrate
O
O
O
85
N-Acetylneuraminic acid
HO
O
O
88
4-(Acetyloxy)benzoic acid
89
2-(Acetyloxy)-5-bromobenzoic acid
4-(Acetyloxy)-3-methoxybenzaldehyde
Organic
NH
O
O
O
O
O
OH
O
O
O
O
Sn O
Sn O
O
O
90
O
91
2-(Acetyloxy)-1-phenylethanone
HN
92
1-(Acetyloxy)-2-propanone
(Acetyloxy)tributylstannane
O
94
93
95
4-Acetylphenyl acetate
(Acetyloxy)triphenylstannane
N-Acetyl-L-phenylalanine
NH2
N
O
CH2O P
O
O
O
O
HN
HN
O
O
96
97
N-Acetyl-L-phenylalanine, ethyl ester
N
N
O
P OCH2
O
OH
COCH3
O
O
O
O
O
P OH
O
OH
98
N-Acetyl-L-phenylalanine, methyl ester
Acetyl phosphate
102
4-Acetylthioanisole
O
N
O
O
99
OH OH
101
100
1-Acetylpiperidine
103
3-Acetylpyridine adenine dinucleotide
1-Acetyl-4-piperidinone
I
N
S
O
Acetyl thiocholine iodide
H2N
HN
O
OH
O
N
H
HO
HN
O
104
N-Acetyl-L-tyrosine
O
HO
F
O
F
O
O
N
O
H
N
HO
109
O
OH
H
Acid Fuchsin
O
O
H
H
N
OH
O
HO
O
H
O
O
OH
NH2
O
O
N
110
Acifluorfen
NH2
108
N-Acetyl-L-valine
OH
O
OH
H
O
107
N-Acetyl-L-tyrosine ethyl ester
OH
Cl
O
106
O
S
OH
O
O
S
NaO
O
HN
O
105
N-Acetyl-L-tryptophan
OH
O
HN
HO
NH
O
S
NaO
O
O
OH
O
F
O
OH OH
O N
N
S
N
N
112
111
Aconine
113
9-Acridinamine
Aconitine
Acridine
O
H
O
H 2N
O
H2N
N
114
3,6-Acridinediamine
NH2
N
H
115
9(10H )-Acridinone
O
116
Acrolein
N
N
N
N
O
O
NH2
117
Acrylamide
N
OH
118
Acrylic acid
119
Acrylonitrile
OH
120
Acyclovir
Physical Constants of Organic Compounds
3-10
No.
Name
Synonym
Mol. Form.
CAS RN
121
Adenine
1H-Purin-6-amine
C5H5N5
73-24-5
122
123
Adenosine
Adenosine cyclic
3’,5’-(hydrogen phosphate)
Adenosine 3’,5’-diphosphate
β-D-Ribofuranoside, adenine-9 C10H13N5O4
cAMP
C10H12N5O6P
124
3’-Adenylic acid, 5’-(dihydrogen phosphate)
Adenosine, 5’-[hydrogen
(phosphonomethyl)­
phosphonate]
3’-Adenylic acid
ATP
Mol.
Wt.
Physical
Form
mp/˚C
bp/˚C
360 dec
220 sub
Organic
58-61-7
60-92-4
135.128 orth nd
(+3w)
267.242 n(w+3/2)
329.206 cry
C10H15N5O10P2
1053-73-2
427.202 amor pow
C11H17N5O9P2
3768-14-7
425.229 cry (w)
204
C10H14N5O7P
C10H16N5O13P3
C14H20N6O5S
C10H14N5O7P
84-21-9
56-65-5
979-92-0
61-19-8
347.222 col nd
507.181
384.411
347.222
195 dec
144 dec
210 dec
195 dec
C6H11NO3
C20H26ClNO2
334-25-8
50-42-0
145.156 nd (w)
347.879 cry
161.5
113.5
den
g cm –3
nD
s H2O; sl EtOH; i
eth, chl
sl H2O; i EtOH
235.5
219
s H2O
125
Adenosine 5’-methylenediphosphonate
126
127
128
129
Adenosine 3’-phosphate
Adenosine 5’-triphosphate
S-Adenosyl-L-homocysteine
5’-Adenylic acid
130
131
Adipamic acid
Adiphenine hydrochloride
132
Adipic acid
1,6-Hexanedioic acid
C6H10O4
124-04-9
146.141 mcl pr (w,
ace, lig)
151.5(0.6)
337.5
1.36025
133
Adiponitrile
Hexanedinitrile
C6H8N2
111-69-3
108.141 nd (eth)
2.2(0.4)
295
0.967620 1.438020
134
Adrenalone
C9H11NO3
99-45-6
181.188 nd
235 dec
135
Affinin
C14H23NO
25394-57-4 221.339 ye oil
23
136
137
138
139
Aflatoxin B1
Aflatoxin B2
Aflatoxin G1
Agaritine
C17H12O6
C17H14O6
C17H12O7
C12H17N3O4
1162-65-8
7220-81-7
1165-39-5
2757-90-6
268
287.5
245
207 dec
C20H26N2O2
4360-12-7
Adenosine 5’-monophosphate
N-(2-Methylpropyl)-2,6,8decatrienamide
140
L-Glutamic acid,
5-[2-[4-(hydroxymethyl)­
phenyl]hydrazide]
Ajmalan-17,21-diol, (17R,21α) Ajmaline
141
142
Alachlor
DL-Alanine
DL-2-Aminopropanoic acid
C14H20ClNO2
C3H7NO2
143
D-Alanine
2-Aminopropanoic acid, (R)
144
L-Alanine
145
β-Alanine
146
312.273 cry
314.289
328.273 cry
267.281 cry (dil al)
206
C3H7NO2
326.432 pl (+3.5w)
(aq AcOEt)
15972-60-8 269.768
302-72-7
89.094 orth pr or
nd (w)
338-69-2
89.094 nd (w, al)
2-Aminopropanoic acid, (S)
C3H7NO2
56-41-7
89.094
3-Aminopropanoic acid
C3H7NO2
107-95-9
89.094
Alantolactone
C15H20O2
147
148
149
150
Aldicarb
Aldosterone
Aldoxycarb S,S-dioxide
Aldrin
151
Alizarin
152
153
orth (w)
297 dec
250 sub
C7H14N2O2S
C21H28O5
C7H14N2O4S
C12H8Cl6
116-06-3
52-39-1
1646-88-4
309-00-2
190.263
360.444 cry (HOAc)
222.262 cry
364.910
101.1(0.4)
166.5
141
103.8(0.3)
1,2-Dihydroxy-9,10-anthracenedione
C14H8O4
72-48-0
Alizarin Red S
Alizarin Yellow R
Sodium alizarinesulfonate
C14H7NaO7S
C13H9N3O5
130-22-3
2243-76-7
154
Alizurol purple
1-Hydroxy-4-[(4methylphenyl)­amino]-9,10anthracenedione
C21H15NO3
81-48-1
240.212 oran or red 289.5
tcl nd or pr
(al)
342.257
287.227 oran-br nd 253 dec
(dil HOAc)
329.349 flat viol nd
155
Alkannin
C16H16O5
149
156
Allantoic acid
C4H8N4O4
23444-65-7 288.295 br-red pr
(bz)
99-16-1
176.132 nd
157
Allantoin
C4H6N4O3
97-59-6
158.116 mcl pl or
239
158
Allene
C3H4
463-49-0
40.064
-136.4(0.5)
159
160
Allethrin
Allicin
C19H26O3
C6H10OS2
584-79-2
539-86-6
302.407
162.272
HCP_Section_03.indb 10
i H2O; s EtOH,
chl; sl eth, bz
sub
76
1.513425
vs H2O; sl EtOH,
eth
sl H2O; vs EtOH;
s eth; i HOAc,
lig
sl H2O, eth; s
chl, EtOH
sl H2O, EtOH,
eth
i H2O
vs H2O
314 dec
546-43-0
col gas
1620.5
1000.02
250 sub
200 dec
Bis[(aminocarbonyl)
amino]­acetic acid
vs H2O; s EtOH,
10% HCl
42(2)
300 dec
nd, orth pr
(al)
232.319 nd
Solubility
1.13325
1.42425
s H2O; vs EtOH
s H2O; sl EtOH; i
eth
s H2O; sl EtOH,
py; i eth, ace
s H2O; sl EtOH; i
eth, ace
vs bz, eth,
EtOH, chl
1.43222
1.43719
275
1.19525
sl H2O
i H2O; s EtOH,
eth, ace, bz
sl H2O; s EtOH,
eth, ace, bz; i
chl
vs H2O; s EtOH
vs H2O, EtOH
s H2SO4
140 sub
vs EtOH
-34.8(0.3)
1.4168
sl H2O, os, dil
acid
sl H2O; s EtOH,
NaOH; i eth,
MeOH
vs bz, peth
1.56120
vs H2O
170 dec
dec
0.58425
(p>1
atm)
1.01020
1.11220
4/11/16 11:17 AM
Physical Constants of Organic Compounds
3-11
NH2
NH2
N
N
NH2
HO
O
O
O
121
122
Adenine
HO P O
HO
O
O
O
OH
OH
OH
N
N
HO P O P O P O
124
O
O
HO
HO
127
N
Adipic acid
H
O
O
O
NH2
137
O
O
Aflatoxin B1
H
O
OH
140
Agaritine
O
NH2
NH2
143
H2N
145
Cl
O
N
O
148
O
N
O
OH O
O
OH
152
Alizarin
OH
COOH
O
O
H2N
OH O
155
Alkannin
N
H
N
H
156
Allantoic acid
O
O
NH2
H2N
N
H
157
Allantoin
O
N
N
H
O HN
OH
N
154
Alizurol purple
H
O
O
H
H
C
O
H
H
158
Allene
OH
HO
Alizarin Yellow R
N
N
H
149
153
Alizarin Red S
O
Aldoxycarb S,S-dioxide
O
OH
151
N
O O
Aldosterone
SO3Na
O
Aldrin
O
O
OH
Cl
Cl
OH
OH
O
Aldicarb
Cl
150
DL-Alanine
S
N
H
147
Alantolactone
OH
Cl
Cl
S
146
β-Alanine
L-Alanine
142
Alachlor
O
O
OH
144
D-Alanine
O
O
OH
O
141
Ajmalan-17,21-diol, (17R,21α)
O
OH
Cl
OH
O
O
N
NH2
139
Aflatoxin G1
O
N
N
H
Me
O
136
Affinin
N
H
O
138
Aflatoxin B2
H O
OH
H
N
HO
H O
O
O
135
Adrenalone
O
O
H
HO
O
H O
H
N
O
O
H
131
Adiphenine hydrochloride
O
H
N
134
Adiponitrile
O
130
Adipamic acid
O
133
N
O
OH
132
O
O
O
O
OH
HO
N
O
HCl
5’-Adenylic acid
O
OH
126
Adenosine 3’-phosphate
NH2
129
S-Adenosyl-L-homocysteine
O
OH
OH
125
O
HO
O
HO
OH
Adenosine 5’-methylenediphosphonate
HO
OH
128
Adenosine 5’-triphosphate
O
HO P
O
OH
OH
O
HO P O
N
N
O
NH2
OH
O
O
N
N
N
N
S
N
N
HO
N
N
NH2
N
N
N
N
HO
Adenosine 3’,5’-diphosphate
NH2
N
OH
OH
Adenosine cyclic 3’,5’-(hydrogen phosphate)
NH2
O
OH
123
Adenosine
O
O
HO P
P O
OH OH
N
N
N
O
OH
O
O P
OH OH
NH2
N
N
HO P O
N
N
O
N
H
N
N
N
N
N
N
N
NH2
N
N
Organic
NH2
159
Allethrin
O
O
S
S
160
Allicin
Physical Constants of Organic Compounds
3-12
No.
Name
161
Allopregnane-3β,21-diol11,20-dione
162
163
Allopregnan-20β-ol-3-one
Allopurinol
164
165
166
D-Allose
Alloxanic acid
Alloxantin
167
Allyl acetate
168
Synonym
Organic
Mol. Form.
CAS RN
C21H32O4
566-02-9
C21H34O2
C5H4N4O
516-58-5
315-30-0
C6H12O6
C4H4N2O5
C8H6N4O8
2595-97-3
470-44-0
76-24-4
C5H8O2
Allyl acetoacetate
169
Allyl acrylate
170
Allyl alcohol
171
Mol.
Wt.
Physical
Form
mp/˚C
348.477 cry (aq, ac,
+w) nd
(bz, ac)
318.494
136.112 cry
190
128
162 dec
254 dec
591-87-7
180.155 cry (w)
160.085 tcl pr (eth)
286.156 orth pr
(w+2)
100.117
C7H10O3
1118-84-9
142.152 liq
-85
C6H8O2
999-55-3
112.127
2-Propen-1-ol
C3H6O
107-18-6
58.079
liq
Allylamine
2-Propen-1-amine
C3H7N
107-11-9
57.095
liq
172
N-Allylaniline
Allylphenylamine
C9H11N
589-09-3
133.190
173
Allylbenzene
2-Propenylbenzene
C9H10
300-57-2
118.175 liq
174
175
α-Allylbenzenemethanol
Allyl benzoate
C10H12O
C10H10O2
936-58-3
583-04-0
176
Allyl butanoate
C7H12O2
177
178
179
180
Allyl carbamate
Allylchlorodimethylsilane
Allyl chloroformate
Allyl trans-cinnamate
C4H7NO2
C5H11ClSi
C4H5ClO2
C12H12O2
181
182
183
184
185
186
1-Allylcyclohexanol
1-Allylcyclohexene
Allylcyclopentane
Allyldiethoxymethylsilane
Allyldiethylamine
Allyldimethylamine
187
Allyl ethyl ether
188
Allyl formate
189
Allyl 2-furancarboxylate
190
191
192
Allyl glycidyl ether
Allyl hexanoate
Allyl (hydroxymethyl)­
carbamate
Allyl isocyanate
Allyl isothiocyanate
Allyl methacrylate
4-Allyl-2-methoxyphenol
193
194
195
196
197
5α-Pregnan-20β-ol-3-one
1,5-Dihydro-4H-pyrazolo[3,4d]pyrimidin-4-one
den
g cm –3
nD
Solubility
195(3)
350
vs H2O
vs H2O, EtOH
sl H2O, EtOH,
eth
sl H2O; s ace;
msc EtOH, eth
s H2O, lig; msc
EtOH, bz
sl H2O; s EtOH,
eth, acid
msc H2O, EtOH,
eth; s chl
msc H2O, EtOH,
eth; s chl
sl H2O; s EtOH,
ace; msc eth
i H2O; s EtOH,
eth, bz, ctc
104(2)
0.927520 1.404920
198(19)
1.036620 1.439820
121
0.944120 1.432020
-129
96.9(0.5)
0.854020 1.413520
-88.2
54(2)
0.75820
219
0.973625 1.56320
158(2)
0.892020 1.513120
148.201
162.185
228.5
2051-78-7
128.169
142
2114-11-6
4028-23-3
2937-50-0
1866-31-5
101.105
134.680
120.535 hyg liq
188.222
111
109.5
268 dec
1123-34-8
13511-13-2
3524-75-2
18388-45-9
5666-17-1
2155-94-4
140.222
122.207 liq
110.197 liq
174.314
113.201
85.148
190
159(9)
127(4)
155
110
62(4)
1.00418 1.528921
1.056915 1.517820 i H2O; s EtOH,
eth, ace,
MeOH
0.901720 1.415820 i H2O; msc
EtOH, eth; sl
ctc
sl ctc
0.896420 1.419520
1.136
1.422020
1.04823 1.53020 i H2O; vs EtOH;
msc eth; sl ctc
0.934122 1.475622
557-31-3
86.132
65(4)
C4H6O2
1838-59-1
86.090
83.6
C8H8O3
4208-49-5
152.148
207.5
C6H10O2
C9H16O2
C5H9NO3
106-92-3
114.142
123-68-2
156.222
24935-97-5 131.130 cry (tol)
Eugenol
C4H5NO
C4H5NS
C7H10O2
C10H12O2
1476-23-9
57-06-7
96-05-9
97-53-0
83.089
99.155 liq
126.153
164.201 liq
-7.5
88
160(6)
6750
254(7)
1,3,4-Eugenol acetate
C12H14O3
93-28-7
206.237 pr (al)
30.5
281
2835-39-4
1873-92-3
111-45-5
142.196
155.099
102.132
C9H10O
C9H10O
1745-81-9
501-92-8
134.174 liq
134.174
C9H10O
1746-13-0
134.174
3-Acetoxypropene
Allyl trans-3-phenyl-2-propenoate
C9H16O
C9H14
C8H14
C8H18O2Si
N,N-Diethyl-2-propen-1-amine C7H15N
N,N-Dimethyl-2-propen-1C5H11N
amine
C5H10O
1-(2-Propenyl)cyclohexene
Allyl 2-furanoate
198
199
200
4-Allyl-2-methoxyphenyl
acetate
Allyl 3-methylbutanoate
Allylmethyldichlorosilane
2-(Allyloxy)ethanol
C8H14O2
C4H8Cl2Si
Ethylene glycol monoallyl ether C5H10O2
201
202
2-Allylphenol
4-Allylphenol
Chavicol
203
Allyl phenyl ether
HCP_Section_03.indb 12
bp/˚C
-40(4)
-110.6(0.1)
154
186
0.79325
0.857225
0.747725
0.709425
1.420520
1.441220 s chl
1.410420
1.420920
1.401020
0.765120 1.388120 i H2O; msc
EtOH, eth; s
ace
0.946020
sl H2O; s EtOH;
msc eth
1.11525 1.494520 s eth, ace; sl
ctc
0.969820 1.433220
0.886920
57
-80
154
119.5
158.5
-6
15.8
220
238
190.5(0.8)
1.012620 1.530620 vs bz, eth, EtOH
0.933520 1.436020
1.065220 1.540520 i H2O; msc
EtOH, eth; s
chl, HOAc, oils
1.080620 1.520520 i H2O; s EtOH; sl
ctc
1.075820 1.441920
0.958020 1.435820 msc H2O; vs
EtOH; s bz,
ctc, MeOH
1.024615 1.518120 vs eth
1.020315 1.544118 vs eth, EtOH,
chl
0.981120 1.522320 i H2O; s EtOH;
msc eth; sl ctc
4/11/16 11:17 AM
Physical Constants of Organic Compounds
H
OH
O
OH
H
O
H
H
HN
HO
O
H
161
O
H
162
Allopregnane-3β,21-diol-11,20-dione
163
Allopregnan-20β-ol-3-one
O
N
N
H
N
CHO
OH
OH
OH
OH
CH2OH
H
H
H
H
Allopurinol
168
O
N
H
H
N
O O
OH
H
N
N
H
HO
O O
N
H
O
O
165
D-Allose
169
170
171
Allyl alcohol
Alloxanic acid
H2N
O
173
N-Allylaniline
Allylbenzene
Allyl butanoate
O
174
184
185
Allyldiethylamine
180
181
Allyl trans-cinnamate
O
186
187
Allyldimethylamine
O
O
188
Allyl ethyl ether
Allyl formate
O
191
Allyl hexanoate
H
N
1-Allylcyclohexene
O
O
N
182
1-Allylcyclohexanol
O
189
Allyl 2-furancarboxylate
O
O
190
Allyl glycidyl ether
O
O
HO
Allyl benzoate
HO
OH
O
175
α-Allylbenzenemethanol
O
Allyl chloroformate
N
Allyldiethoxymethylsilane
O
O
179
Allylchlorodimethylsilane
O
Si
O
183
Cl
178
Allyl carbamate
Allylcyclopentane
O
Si
Cl
177
Allyl acetate
O
O
176
167
Alloxantin
OH
172
Allylamine
O
O
O
NH2
OH
Allyl acrylate
O
166
H
N
O
Allyl acetoacetate
O OH
H
N
O
164
O
O
HO
O
O
O
O
O
N
192
Allyl (hydroxymethyl)carbamate
C
O
N
193
194
Allyl isocyanate
C
S
Allyl isothiocyanate
O
195
Allyl methacrylate
196
4-Allyl-2-methoxyphenol
197
4-Allyl-2-methoxyphenyl acetate
OH
OH
O
O
198
Allyl 3-methylbutanoate
Cl
Si
199
O
Cl
Allylmethyldichlorosilane
O
200
OH
2-(Allyloxy)ethanol
201
2-Allylphenol
202
4-Allylphenol
203
Allyl phenyl ether
Organic
O
3-13
Physical Constants of Organic Compounds
3-14
Mol.
Wt.
Physical
Form
Organic
Name
Synonym
Mol. Form.
CAS RN
204
205
206
207
208
Allyl propanoate
N-Allyl-2-propen-1-amine
Allyl propyl disulfide
3-(Allylsulfinyl)-L-alanine, (S)Allylthiourea
2-Propenyl propanoate
Diallylamine
C6H10O2
C6H11N
C6H12S2
C6H11NO3S
C4H8N2S
2408-20-0
124-02-7
2179-59-1
556-27-4
109-57-9
209
210
211
212
Allyltrichlorosilane
Allyltriethoxysilane
Allyltrimethylsilane
Allylurea
Trichloro-2-propenylsilane
C3H5Cl3Si
C9H20O3Si
C6H14Si
C4H8N2O
107-37-9
2550-04-1
762-72-1
557-11-9
114.142
97.158
148.289
177.221 nd (dil ac)
116.185 mcl or orth
pr (w)
175.517
204.339
114.261
100.119 nd (al)
213
Allyl vinyl ether
3-(Ethenyloxy)-1-propene
C5H8O
3917-15-5
84.117
214
Aloin A
C21H22O9
1415-73-2
418.395
215
216
217
218
Alphaprodine
Alstonidine
Alstonine
D-Altrose
C16H23NO2
C22H24N2O4
C21H20N2O3
C6H12O6
15867-21-7
25394-75-6
642-18-2
1990-29-0
261.360
380.437
348.395
180.155
219
220
221
222
Aluminum 2-butoxide
Aluminum distearate
Aluminum ethanolate
Aluminum isopropoxide
2-Butanol, aluminum salt
Hydroxyaluminum distearate
Aluminum ethoxide
C12H27AlO3
C36H71AlO5
C6H15AlO3
C9H21AlO3
2269-22-9
300-92-5
555-75-9
555-31-7
246.322
610.928 wh pow
145
162.163 liq/wh solid 140
204.243 hyg wh
119
solid
19720
223
Alverine
N-Ethyl-bis(3-phenylpropyl)­
amine
C20H27N
150-59-4
281.435 oil
1660.3
224
225
226
227
228
α-Amanitin
Amaranth dye
Ametryn
Amminetrimethylboron
19-Amino-8,11,13-abieta­
triene
2-Aminoacetamide
C39H54N10O14S
C20H11N2Na3O10S3
C9H17N5S
C3H12BN
C20H31N
23109-05-9
915-67-3
834-12-8
1830-95-1
1446-61-3
918.970 nd
604.472 dk red pow
227.330
72.945
285.467 cry
C2H6N2O
598-41-4
74.081
hyg nd (chl) 67.5
C2H4N2
C2H5ClN2
540-61-4
6011-14-9
56.066
92.527
hyg cry (al)
C8H10ClNO
5468-37-1
171.624
194 dec
C10H18ClN
665-66-7
187.710 cry (al-eth)
360 dec
vs H2O, EtOH
C6H11NO4
626-71-1
161.156 pl (w)
207.0
2,3-Diaminopropionic acid
1-Aminoanthraquinone
C3H8N2O2
C14H9NO2
515-94-6
82-45-1
104.108 hyg rosettes 110
223.227 red nd (al) 253.5
2-Aminoanthraquinone
C14H9NO2
117-79-3
223.227 red nd (al,
HOAc)
sl H2O, EtOH,
eth
vs H2O
vs ace, bz,
EtOH, chl
i H2O, eth; sl
EtOH; s ace,
bz, chl
sl H2O, lig; s
EtOH, eth, bz,
chl
sl H2O; vs EtOH,
eth; s bz, chl; i
lig
s eth, acid
s H2O, EtOH,
eth, acid
s H2O, EtOH; sl
eth, bz; vs
AcOEt
sl H2O; s EtOH,
eth
s alk; sl os
229
230
231
232
233
234
235
236
237
Aminoacetonitrile
Aminoacetonitrile
monohydrochloride
α-Aminoacetophenone
hydrochloride
1-Aminoadamantane
hydrochloride
2-Aminoadipic acid
3-Aminoalanine
1-Amino-9,10-anthracene­
dione
2-Amino-9,10-anthracene­
dione
Alliin
Thiosinamine
Adamantanamine
hydrochloride
mp/˚C
bp/˚C
den
g cm –3
No.
123(5)
112(3)
7913
165
77(3)
35
118(3)
10050
85
85
66
149.3
cry
cry (eth)
ye nd (ace)
pr
(MeOH,al)
103
189
207 dec
103.5
vs H2O
2007
13510
i H2O
dec H2O; sl xyl
reac H2O; s
EtOH, bz, peth,
chl
254 dec
s H2O
83.6(0.5)
73.5
44.5
5815
vs H2O, EtOH; sl
eth, bz; s ace,
chl
vs EtOH
165 dec
304.5
sub
sub
4-Aminoazobenzene
C12H11N3
60-09-3
197.235 oran mcl nd 125(1)
(al)
>360
239
2-Aminobenzaldehyde
C7H7NO
529-23-7
121.137 silv lf
40.5
802
240
241
3-Aminobenzaldehyde
4-Aminobenzaldehyde
C7H7NO
C7H7NO
1709-44-0
556-18-3
121.137 nd (AcOEt)
121.137 pl (w)
29
71.5
242
2-Aminobenzamide
C7H8N2O
88-68-6
136.151
110.5 dec
243
4-Aminobenzamide
C7H8N2O
2835-68-9
183
244
α-Aminobenzeneacetic acid,
(±)4-Aminobenzeneacetic acid
α-Phenylglycine
C8H9NO2
2835-06-5
136.151 ye cry
(+1/4w)
151.163 pl
292 dec
p-Aminophenylacetic acid
C8H9NO2
1197-55-3
151.163 pl (w)
195(1)
HCP_Section_03.indb 14
Solubility
vs ace, EtOH
238
245
nD
0.914020 1.410520 s EtOH, eth, ace
1.438720 s EtOH, eth
1.521920
vs H2O
1.21720 1.593678 s H2O, EtOH; sl
eth; i bz
1.201120 1.446020
0.903020 1.407220
0.715825 1.407420 i H2O
msc H2O, EtOH;
sl eth, chl; i
peth
0.790020 1.406220 i H2O; s eth,
ace, chl
s H2O, EtOH,
ace; sl eth, bz;
i chl
255 sub
i H2O; sl EtOH,
DMSO
4/11/16 11:17 AM
Physical Constants of Organic Compounds
3-15
O
O
O
N
H
204
205
Allyl propanoate
S
S
H2N
S
206
N-Allyl-2-propen-1-amine
S
HO
O
207
Allyl propyl disulfide
OH O
Allylthiourea
O
O
O
N
OH
213
212
214
Allyl vinyl ether
211
Allyltriethoxysilane
Allyltrimethylsilane
N
N
O
O
O
O
216
218
217
Alstonidine
Alphaprodine
H
CHO
H
OH
OH
OH
CH2OH
HO
H
H
H
H
O
215
Aloin A
OH
D-Altrose
Alstonine
Organic
Allylurea
N
H
O
HO
NH2
Si
210
Allyltrichlorosilane
N
O
OH
N
H
209
OH
O
O
O
O
Si
O
Cl
Cl
Si
Cl
NH2
208
3-(Allylsulfinyl)-L-alanine, (S)-
OH
HO
N
H
O
Al
O
OH
O
Al
O
H3C(CH2)16
O
219
O
O
(CH2)16CH3
O
220
Aluminum 2-butoxide
O
Al
O
N
O
O
221
Aluminum distearate
O
Al
222
Aluminum ethanolate
223
Aluminum isopropoxide
Alverine
OH
HN
H
HO
CONH
H
CO
OC
H
CONH
OC
S
NHCO
OH
N
H
O
S
ONa
S
O
O
CONH
O
N
O
NaO
CH2OH
OH
H
N
N
NH
HN
NHCO
N
H
O S O
ONa
CONH2
S
225
224
α-Amanitin
N
N
B NH3
N
H
226
Amaranth dye
227
Ametryn
Amminetrimethylboron
H 2N
NH2
229
2-Aminoacetamide
N
H2N
N
H2N
230
NH2
NH2
O
O
OH
NH2
232
233
α-Aminoacetophenone hydrochloride
Aminoacetonitrile monohydrochloride
O
OH
HCl
HCl
HCl
231
Aminoacetonitrile
228
19-Amino-8,11,13-abietatriene
NH2
O
O
H
H2N
234
1-Aminoadamantane hydrochloride
2-Aminoadipic acid
O
O
NH2
OH
O
H2N
NH2
NH2
O
235
236
3-Aminoalanine
O
237
1-Amino-9,10-anthracenedione
238
2-Amino-9,10-anthracenedione
O
O
O
O
NH2
NH2
3-Aminobenzaldehyde
4-Aminobenzaldehyde
2-Aminobenzamide
OH
OH
NH2
242
2-Aminobenzaldehyde
NH2
NH2
NH2
241
239
4-Aminoazobenzene
NH2
240
NH2
N
N
243
4-Aminobenzamide
O
244
α-Aminobenzeneacetic acid, (±)-
O
H2N
245
4-Aminobenzeneacetic acid
Physical Constants of Organic Compounds
3-16
Mol. Form.
CAS RN
Mol.
Wt.
C8H7NO4
99-31-0
C8H11NO
C7H10N2
C7H9NO
Sulfanilamide
2-Aminobenzenesulfonic acid
252
No.
Name
246
247
248
249
5-Amino-1,3-benzenedicarboxylic acid
4-Aminobenzeneethanol
2-Aminobenzenemethanamine
2-Aminobenzenemethanol
250
4-Aminobenzenesulfonamide
251
Physical
Form
den
g cm –3
Organic
mp/˚C
bp/˚C
181.147 pr(al), pl(w)
360
sub
i H2O; sl EtOH
104-10-9
4403-69-4
5344-90-1
137.179 nd (al)
122.167
123.152
108
61
83.5
269
273
C6H8N2O2S
63-74-1
172.205 lf (dil al)
162.2(0.4)
Orthanilic acid
C6H7NO3S
88-21-1
173.190 pr (+ 1/2w) >320 dec
3-Aminobenzenesulfonic acid
Metanilic acid
C6H7NO3S
121-47-1
253
4-Aminobenzenesulfonic acid
Sulfanilic acid
C6H7NO3S
121-57-3
254
p-Sulfanilyl fluoride
C6H6FNO2S
98-62-4
255
256
257
4-Aminobenzenesulfonyl
fluoride
2-Aminobenzenethiol
4-Aminobenzenethiol
2-Aminobenzonitrile
173.190 nd, pr (w
dec
+1)
173.190 orth pl or
288
mcl (w+2)
175.181
68.5
vs EtOH
s H2O, EtOH,
eth, HOAc; vs
bz, chl
s H2O, EtOH,
eth, ace; sl
chl, peth
sl H2O; i EtOH,
eth
sl H2O, EtOH; i
eth
sl H2O; i EtOH,
eth
C6H7NS
C6H7NS
C7H6N2
137-07-5
1193-02-8
1885-29-6
125.192
125.192
118.136 ye pr (CS2)
nd (peth)
26
46
51
234
14317
263
258
3-Aminobenzonitrile
C7H6N2
2237-30-1
53(2)
289
259
4-Aminobenzonitrile
C7H6N2
873-74-5
118.136 nd (dil al or
CCl4)
118.136 pr or pl (w)
86.2(0.5)
260
4-Aminobenzophenone
C13H11NO
1137-41-3
197.232 lf (dil al)
123(2)
261
C12H14N2O5
4271-30-1
266.249 cry (w)
173
262
263
N-(4-Aminobenzoyl)-Lglutamic acid
N-(4-Aminobenzoyl)glycine
2-Aminobiphenyl
C9H10N2O3
C12H11N
61-78-9
90-41-5
194.186 pr or nd (w) 198.5
169.222 lf (dil al)
49.13(0.04)
264
3-Aminobiphenyl
C12H11N
2243-47-2
169.222 nd
31.5
265
4-Aminobiphenyl
C12H11N
92-67-1
169.222 lf (dil al)
51.0(0.6)
266
267
C7H6BrNO2
C14H8BrNO5S
5794-88-7
116-81-4
216.033 nd
382.187 red nd (w)
219.5
268
2-Amino-5-bromobenzoic acid 5-Bromoanthranilic acid
1-Amino-4-bromo-9,101-Amino-4-bromoanthraquidihydro-9,10-dioxo-2none-2-sulfonic acid
anthracenesulfonic acid
DL-2-Aminobutanoic acid
C4H9NO2
2835-81-6
103.120 lf (w)
304 dec
269
L-2-Aminobutanoic acid
C4H9NO2
1492-24-6
270
DL-3-Aminobutanoic acid
C4H9NO2
2835-82-7
103.120 lf (dil al), cry 292 dec
(al)
103.120 nd (al)
194.3
271
4-Aminobutanoic acid
C4H9NO2
56-12-2
272
2-Amino-1-butanol, (±)-
273
4-Amino-1-butanol
274
275
4-Amino-N-[(butylamino)­
carbonyl]benzenesulfonamide
Aminocarb
276
N-(Aminocarbonyl)acetamide
277
[4-[(Aminocarbonyl)­amino]­
phenyl]arsonic acid
278
N-(Aminocarbonyl)-2-bromo2-ethylbutanamide
N-(Aminocarbonyl)-2-bromo3-methylbutanamide
279
HCP_Section_03.indb 16
Synonym
p-Aminohippuric acid
p-Biphenylamine
1.0825
1.48525
nD
Solubility
1.460620 s EtOH, eth
s H2O, EtOH
sl H2O; vs EtOH,
eth, ace, bz; i
peth
sl H2O; vs EtOH,
eth, ace, chl
sl H2O, ctc; vs
EtOH, eth, ace,
bz
sl H2O, tfa; s
EtOH, eth,
HOAc
24613
vs ace, bz, EtOH
i H2O; s EtOH,
eth, bz; sl
DMSO, peth
sl H2O; s EtOH,
eth, ace, bz
sl H2O; s EtOH,
eth, ace, chl
s DMSO
298.3(0.2)
302
sub
1.230020
C4H11NO
103.120 pr or nd (al) 203 dec
lf
(MeOHeth)
13054-87-0 89.136 liq
-1.0
178(9)
C4H11NO
13325-10-5 89.136
203(11)
0.916220 1.448925 msc H2O, EtOH,
eth; sl chl
0.96712 1.462520 s H2O, EtOH; i
eth
C11H17N3O3S
339-43-5
271.336
144.5
C11H16N2O2
2032-59-9
208.257 cry
95.0(0.3)
C3H6N2O2
591-07-1
102.092
218
Carbarsone
C7H9AsN2O4
121-59-5
260.079 nd (w)
174
Carbromal
C7H13BrN2O2
77-65-6
237.094 orth (dil al)
118
Bromisovalum
C6H11BrN2O2
496-67-3
223.067 nd or lf (to)
154
γ-Aminobutyric acid
Carbutamide
180 sub
1.54425
sub
1.5615
vs H2O; sl EtOH;
i eth, bz
s H2O; sl EtOH,
eth; i bz
vs H2O; i EtOH,
eth, bz
vs H2O; sl EtOH,
ace; i eth, bz
sl H2O, bz; s
ace
sl H2O, eth; s
EtOH
sl H2O, DMSO,
EtOH; i eth,
chl; s alk
sl H2O, chl; s
ace, bz
vs ace, bz, eth,
EtOH
4/11/16 11:18 AM
Physical Constants of Organic Compounds
O
3-17
NH2
O S O
OH
NH2
OH
OH
H2N
NH2
NH2
NH2
H2N
O
246
NH2
247
5-Amino-1,3-benzenedicarboxylic acid
248
4-Aminobenzeneethanol
249
2-Aminobenzenemethanamine
OH
O S O
OH
O S O
OH
O S O
OH
250
2-Aminobenzenemethanol
251
4-Aminobenzenesulfonamide
F
O S O
SH
2-Aminobenzenesulfonic acid
N
N
SH
NH2
NH2
252
3-Aminobenzenesulfonic acid
NH2
253
NH2
254
4-Aminobenzenesulfonic acid
255
4-Aminobenzenesulfonyl fluoride
2-Aminobenzenethiol
N
4-Aminobenzenethiol
O
O
N
H
NH2
H2N
NH2
260
259
HO
2-Aminobenzonitrile
3-Aminobenzonitrile
H2N
OH
O
NH2
NH2
262
N-(4-Aminobenzoyl)-L-glutamic acid
263
N-(4-Aminobenzoyl)glycine
O
O
258
O
OH
261
4-Aminobenzophenone
4-Aminobenzonitrile
257
OH
H
N
O
O
NH2
256
NH2
NH2
264
2-Aminobiphenyl
O
S OH
O
3-Aminobiphenyl
O
O
OH
OH
NH2
O
Br
265
266
4-Aminobiphenyl
267
2-Amino-5-bromobenzoic acid
NH2
NH2
Br
268
1-Amino-4-bromo-9,10-dihydro-9,10-dioxo-2-anthracenesulfonic acid
269
DL-2-Aminobutanoic acid
O H
N
L-2-Aminobutanoic acid
H
N
O S
O
OH
270
DL-3-Aminobutanoic acid
H2N
N
O
OH
NH2 O
OH
NH2
O
271
272
4-Aminobutanoic acid
2-Amino-1-butanol, (±)-
OH
H2N
N
H
NH2
273
O
274
4-Amino-1-butanol
275
4-Amino-N-[(butylamino)carbonyl]benzenesulfonamide
Aminocarb
OH
O As OH
O
H2N
O
N
H
276
N-(Aminocarbonyl)acetamide
Br
O
277
[4-[(Aminocarbonyl)amino]phenyl]arsonic acid
Br
H
N
NH2
HN
O
278
H
N
NH2
O
N-(Aminocarbonyl)-2-bromo-2-ethylbutanamide
O
279
NH2
O
N-(Aminocarbonyl)-2-bromo-3-methylbutanamide
Organic
NH2
NH2
Physical Constants of Organic Compounds
3-18
Mol.
Wt.
Physical
Form
No.
Name
Synonym
Mol. Form.
CAS RN
280
Salicylamide O-acetic acid
C9H9NO4
25395-22-6 195.172
221
C10H12N2O5S
C14H8ClNO2
957-68-6
117-11-3
272.277 cry
257.673
212
C6H8ClN3O4S2
121-30-2
285.729
254.5
6-Chlorometanilic acid
C6H6ClNO3S
88-43-7
207.635 nd (w)
280 dec
2-Benzoyl-4-chloroaniline
C7H6ClNO2
C7H6ClNO2
C13H10ClNO
635-21-2
89-54-3
719-59-5
171.582
171.582
231.677 ye nd
211
188
100.5
88-51-7
221.662 short nd (w)
95-85-2
52-52-8
143.571
129.157 cry (al-w)
297
[2-(Aminocarbonyl)­phenoxy]­
acetic acid
7-Aminocephalosporanic acid
1-Amino-5-chloro-9,10anthracenedione
4-Amino-6-chloro-1,3benzenedisulfonamide
5-Amino-2-chlorobenzenesulfonic acid
2-Amino-5-chlorobenzoic acid
5-Amino-2-chlorobenzoic acid
2-Amino-5-chlorobenzo­
phenone
2-Amino-4-chloro-5-methylbenzenesulfonic acid
2-Amino-4-chlorophenol
1-Aminocyclopentanecarboxylic acid
7-Aminodeacetoxycephalosporanic acid
1-Amino-1-deoxy-D-glucitol
2-Amino-2-deoxy-D-glucose
1-Amino-2,4-dibromo-9,10anthracenedione
3-Amino-2,5-dichlorobenzoic
acid
2-Amino-2’,5-dichlorobenzophenone
2-Amino-4,6-dichlorophenol
298
4-Amino-2,6-dichlorophenol
299
2-Amino-1,7-dihydro-7methyl-6H-purin-6-one
5-Amino-2,3-dihydro-1,4phthalazinedione
281
282
283
284
285
286
287
288
289
290
Organic
291
292
293
294
295
296
300
301
1-Amino-5-chloroanthraquinone
Chloraminophenamide
2-Chloro-p-toluidine-5-sulfonic C7H8ClNO3S
acid
2-Hydroxy-5-chloroaniline
C6H6ClNO
Cycloleucine
C6H11NO2
181.187 cry (MeOH)
179.171
381.020 red nd (xyl)
127
C7H5Cl2NO2
133-90-4
206.027
202(1)
C13H9Cl2NO
2958-36-3
266.122
≈80
C6H5Cl2NO
527-62-8
95.5
70 sub
C6H5Cl2NO
5930-28-9
178.016 long nd
(CS2)
178.016 nd or lf (w,
bz)
168
sub
7-Methylguanine
C6H7N5O
578-76-7
165.153
370
Luminol
C8H7N3O2
521-31-3
177.161 ye nd (al)
330.5
Thioguanine
C5H5N5S
154-42-7
167.193
>360
Isoguanine
C5H5N5O
3373-53-3
151.127
>360
Me-IQ
C12H12N4
77094-11-2 212.250 cry
297
Picramic acid
C6H5N3O5
96-91-3
168(1)
Taurine
Acetaldehyde ammonia
Diglycolamine
C2H7NO3S
C2H7NO
C4H11NO2
C4H10N2O
107-35-7
75-39-8
929-06-6
1001-53-2
C9H13N3O2
642-44-4
C5H14N2O
305
306
307
308
2-Aminoethanesulfonic acid
1-Aminoethanol
2-(2-Aminoethoxy)ethanol
N-(2-Aminoethyl)acetamide
309
314
6-Amino-3-ethyl-1-allylAminometradine
2,4(1H,3H)-pyrimidinedione
1-[(2-Aminoethyl)­amino]-2N-(2-Hydroxypropyl)­
propanol
ethylenediamine
4-(2-Aminoethyl)-1,2-benDopamine hydrochloride
zenediol, hydrochloride
α-(1-Aminoethyl)­
benzenemethanol,
[S-(R*,R*)]α-(1-Aminoethyl)­
benzenemethanol,
hydro­chloride
N-(2-Aminoethyl)ethanolamine
315
4-(2-Aminoethyl)phenol
316
N-(2-Aminoethyl)-1,3propanediamine
2-Amino-2-ethyl-1,3-propanediol
310
311
312
313
317
HCP_Section_03.indb 18
sl DMSO
488-43-7
3416-24-8
81-49-2
199.121 dk red nd
(al) pr (chl)
125.147 mcl pr (w)
61.083 orth (eth-al)
105.136
102.134
Solubility
vs EtOH
vs H2O, EtOH,
peth, chl
140
330 dec
C6H15NO5
C6H13NO5
C14H7Br2NO2
Chloramben
nD
1.51915
241 dec
Glucamine
D-Glucosamine
den
g cm –3
s alk
22252-43-3 214.241
304
303
bp/˚C
C8H10N2O3S
2-Amino-1,7-dihydro-6Hpurine-6-thione
6-Amino-1,3-dihydro-2Hpurin-2-one
2-Amino-3,4dimethylimidazo[4,5-f]­
quinoline
2-Amino-4,6-dinitrophenol
302
mp/˚C
vs H2O, EtOH
vs H2O
226
328
97
-12.5
51
sl DMSO
i H2O; vs EtOH,
eth; s ace; sl
bz, HOAc
i H2O; sl EtOH,
eth; vs alk; s
HOAc
i H2O
vs bz, EtOH
110 dec
223.1(0.1)
vs H2O
s H2O; sl eth
1.057220
s H2O, EtOH, bz;
i eth
143
123-84-2
195.218 cry (+1w,
w)
118.177
C8H12ClNO2
62-31-7
189.640 nd (w)
241 dec
vs H2O, MeOH
C9H13NO
492-39-7
151.205 pl(MeOH)
77.5
vs eth, EtOH,
chl
C9H14ClNO
53631-70-2 187.666
198.5
s H2O
C4H12N2O
111-41-1
104.150
242(5)
Tyramine
C8H11NO
51-67-2
137.179 pl or nd (bz, 164.5
w), cry (al)
20625
N-(3-Aminopropyl)­
ethylenediamine
C5H15N3
13531-52-7 117.193
C5H13NO2
115-70-8
119.163
943
37.5
0.983725 1.473820
873
1.028620 1.486320 msc H2O, EtOH;
s ace; sl bz, lig
sl H2O, bz,
DMSO; s EtOH,
xyl; i tol
1.480525
15210
1.09920
1.49020
msc H2O
4/11/16 11:18 AM
Physical Constants of Organic Compounds
O
H
H2N
OH
NH2
O
O
HO
O
O
Cl
281
[2-(Aminocarbonyl)phenoxy]acetic acid
7-Aminocephalosporanic acid
OH
O S O
HO
HO
H
H2N
O
290
NH2
O
Br
O
291
1-Aminocyclopentanecarboxylic acid
O
H
HO
H
H
N
O
Cl
288
O
2-Amino-4-chloro-5-methylbenzenesulfonic acid
CH2NH2
OH
H
OH
OH
CH2OH
H
HO
H
H
292
7-Aminodeacetoxycephalosporanic acid
OH
Cl
2-Amino-5-chlorobenzophenone
S
HO
289
OH
O S O
NH2
Cl
Cl
2-Amino-4-chlorophenol
4-Amino-6-chloro-1,3-benzenedisulfonamide
287
5-Amino-2-chlorobenzoic acid
OH
HO
H2N
NH2
NH2
286
2-Amino-5-chlorobenzoic acid
NH2
O
H2N
285
5-Amino-2-chlorobenzenesulfonic acid
283
O
S
Cl
Cl
284
282
O
NH2
H2N
O
NH2 O
1-Amino-5-chloro-9,10-anthracenedione
O
Cl
NH2
O S O
NH2
Cl
N
O
280
O
S
293
1-Amino-1-deoxy-D-glucitol
NH2
CHO
NH2
H
OH
OH
CH2OH
2-Amino-2-deoxy-D-glucose
OH
OH
Cl
Cl
NH2
Cl
Cl
O
NH2
Cl
Br
294
Cl
295
1-Amino-2,4-dibromo-9,10-anthracenedione
3-Amino-2,5-dichlorobenzoic acid
NH2
Cl
296
297
2-Amino-2’,5-dichlorobenzophenone
298
2-Amino-4,6-dichlorophenol
4-Amino-2,6-dichlorophenol
NH2
NH2 O
O
H
N
N
N
N
H2N
N
N
H
H
299
300
O
O
N
N
O
304
2-Amino-4,6-dinitrophenol
O
H2N
OH
305
306
2-Aminoethanesulfonic acid
O
2-(2-Aminoethoxy)ethanol
H2N
N
H
308
N-(2-Aminoethyl)acetamide
NH2
H2N
O
309
OH
HO
N
H
OH
NH2
HCl
OH
310
6-Amino-3-ethyl-1-allyl-2,4(1H,3H )-pyrimidinedione
311
1-[(2-Aminoethyl)amino]-2-propanol
312
α-(1-Aminoethyl)benzenemethanol, [S-(R *,R *)]-
4-(2-Aminoethyl)-1,2-benzenediol, hydrochloride
OH
HO
NH2
HCl
NH2
313
OH
307
1-Aminoethanol
N
N
302
6-Amino-1,3-dihydro-2H-purin-2-one
NH2
O
S
OH
O
O
H2N
N
N
H
O
H
N
NH2
O
2-Amino-3,4-dimethylimidazo[4,5-f]quinoline
N
2-Amino-1,7-dihydro-6H-purine-6-thione
H2N
303
N
N
OH
N
N
H
N
301
5-Amino-2,3-dihydro-1,4-phthalazinedione
NH2
S
N
H2N
O
2-Amino-1,7-dihydro-7-methyl-6H-purin-6-one
N
H
α-(1-Aminoethyl)benzenemethanol, hydrochloride
H2N
N
H
314
H2N
OH
N-(2-Aminoethyl)ethanolamine
HO
315
4-(2-Aminoethyl)phenol
N
H
316
NH2
N-(2-Aminoethyl)-1,3-propanediamine
HO
NH2
317
2-Amino-2-ethyl-1,3-propanediol
Organic
O
3-19
Physical Constants of Organic Compounds
3-20
No.
Name
Synonym
Mol. Form.
CAS RN
318
L-2-Aminohexanedioic acid
2-Aminoadipic acid
C6H11NO4
542-32-5
319
320
6-Aminohexanenitrile
6-Aminohexanoic acid
5-Cyano-1-pentylamine
ε-Aminocaproic acid
C6H12N2
C6H13NO2
321
322
6-Amino-1-hexanol
1-Amino-4-hydroxy-9,10anthracenedione
3-Amino-4-hydroxybenzenesulfonic acid
4-Amino-2-hydroxybenzo­
hydrazide
2-Amino-3-hydroxybenzoic
acid
4-Amino-2-hydroxybenzoic
acid
323
324
325
326
Organic
327
Mol.
Wt.
Physical
Form
mp/˚C
205 dec
2432-74-8
60-32-2
161.156 cry (EtOH,
w)
112.172 liq
131.173 lf (eth)
C6H15NO
C14H9NO3
4048-33-3
116-85-8
117.189
239.226
57
216.5
C6H7NO4S
98-37-3
189.190 orth (w+1)
>300
C7H9N3O2
6946-29-8
167.165 nd (al)
195
C7H7NO3
548-93-6
153.136 lf (w)
253.5
p-Aminosalicylic acid
C7H7NO3
65-49-6
153.136 nd, pl
(al-eth)
150 dec
Mesalamine
C7H7NO3
89-57-6
153.136
281.0(0.5)
γ-Hydroxy-β-aminobutyric acid C4H9NO3
589-44-6
119.119 pr
216
C4H9NO3
924-49-2
218
C8H11NO3
138-65-8
119.119 pr (w), cry
(dil al)
169.178
C15H11NO4
2379-90-0
269.253
5-Hydroxymethylcytosine
C5H7N3O2
1123-95-1
141.129
1-Naphthol-8-amino-3,6disulfonic acid
1-Amino-2-naphthol-4sulfonic acid
C10H9NO7S2
90-20-0
319.311
C10H9NO4S
116-63-2
239.248 gray nd
C6H5N5O
C4H6N4O
2236-60-4
360-97-4
163.137 ye cry
126.117 cry (EtOH)
>360
170
C5H12N4O3
543-38-4
176.174 cry (al)
172
C2H6N4O
141-83-3
102.095 pr
105
p-Aminosalicylic acid
hydrazide
bp/˚C
den
g cm –3
nD
Solubility
sl H2O, EtOH,
eth
11816
205
vs H2O; i EtOH;
sl MeOH
13730
s EtOH, ace
sl H2O; i EtOH,
eth
vs EtOH
sl H2O; s EtOH,
eth, chl
s H2O, EtOH,
eth, ace; i bz,
peth, chl
sl H2O; i EtOH
338
5-Amino-2-hydroxybenzoic
acid
3-Amino-4-hydroxybutanoic
acid
4-Amino-3-hydroxybutanoic
acid, (±)4-(2-Amino-1-hydroxyethyl)1,2-benzenediol, (±)1-Amino-4-hydroxy-2methoxy-9,10-anthracene­
dione
4-Amino-5-(hydroxymethyl)2(1H)-pyrimidinone
4-Amino-5-hydroxy-2,7naphthalenedisulfonic acid
4-Amino-3-hydroxy-1-naphthalenesulfonic acid
2-Amino-4-hydroxypteridine
5-Amino-1H-imidazole-4carboxamide
O-[(Aminoiminomethyl)
amino]-L-homoserine
(Aminoiminomethyl)urea
339
2-Amino-5-iodobenzoic acid
C7H6INO2
5326-47-6
263.033
220 dec
340
C8H6N2O2
2518-24-3
162.146
269.5
Cycloserine
C3H6N2O2
68-41-7
102.092
155 dec
s H2O; sl MeOH
1-Amino-2-methylanthraquinone
Phenylethanolamine
C15H11NO2
82-28-0
237.254
205.5
C8H11NO
7568-93-6
137.179
56.5
i H2O; s EtOH,
bz, chl; sl eth
vs H2O; s EtOH
4-Amino-3-phenylbutyric acid
C10H13NO2
1078-21-3
179.216
252 dec
C7H9NO3S
88-44-8
187.216 lt ye nd
132 dec
vs H2O
Tranexamic acid
C8H15NO2
1197-18-8
157.211
249(4)
vs H2O
Diacetonamine
C6H13NO
625-04-7
115.173
250.14
348
4-Amino-1H-isoindole1,3(2H)-dione
4-Amino-3-isoxazolidinone,
(R)1-Amino-2-methyl-9,10anthracenedione
α-(Aminomethyl)­
benzenemethanol
β-(Aminomethyl)­
benzenepropanoic acid
2-Amino-5-methylbenzenesulfonic acid
trans-4-(Aminomethyl)­
cyclohexanecarboxylic acid
4-Amino-4-methyl-2-pentanone
2-Amino-4-methylphenol
C7H9NO
95-84-1
sub
349
4-Amino-2-methylphenol
C7H9NO
2835-96-3
123.152 cry (w), orth 136
(bz), lf or
nd
123.152 nd or lf (bz) 176.5
350
4-Amino-3-methylphenol
C7H9NO
2835-99-6
351
352
(Aminomethyl)phosphonic acid
2-Amino-2-methyl-1,3propanediol
L-3-Amino-2-methylpropanoic
acid
2-Amino-2-methyl-1-propanol 2-Aminoisobutanol
CH6NO3P
C4H11NO2
328
329
330
331
332
333
334
335
336
337
341
342
343
344
345
346
347
353
354
HCP_Section_03.indb 20
Canavanine
vs H2O; sl EtOH,
chl, eth, AcOEt
vs H2O
189 dec
sl chl
>300 dec
sl H2O, EtOH,
eth
i H2O, EtOH, bz;
s alk
vs H2O
160 dec
s H2O, py; sl
EtOH; i eth, bz,
chl, CS2
sl H2O, tfa; vs
EtOH, eth, ace;
s bz
16017
s H2O; msc
EtOH, eth
sl H2O, bz; s
EtOH, eth, chl;
i lig
sl H2O, bz; s
EtOH, eth
sl H2O; vs EtOH,
eth; s DMSO
sub
1066-51-9
115-69-5
123.152 pr (dil al)
cry (bz)
111.038 cry
105.136
179
309
110.93(0.05) 15110
C4H9NO2
144-90-1
103.120 cry (w)
185
C4H11NO
124-68-5
89.136
25.5
163.8(0.8)
vs H2O; s EtOH
0.93420
1.44920
msc H2O; s ctc
4/11/16 11:18 AM
Physical Constants of Organic Compounds
OH
3-21
O
NH2
O
OH
NH2
O
O
OH
OH
NH2
N
318
H2N
319
L-2-Aminohexanedioic acid
320
6-Aminohexanenitrile
OH
O S O
OH
321
6-Aminohexanoic acid
H
N
O
H2N
O
322
6-Amino-1-hexanol
1-Amino-4-hydroxy-9,10-anthracenedione
HO
NH2
OH
O
O
OH
HO
OH
O
OH
NH2
NH2
325
4-Amino-2-hydroxybenzohydrazide
3-Amino-4-hydroxybenzenesulfonic acid
NH2
OH
324
323
H2N
326
2-Amino-3-hydroxybenzoic acid
327
4-Amino-2-hydroxybenzoic acid
5-Amino-2-hydroxybenzoic acid
OH
O
NH2
NH2
NH2 O
OH O
HO
328
OH
N
N
H
O
HO
S
S
OH
O S O
OH
OH
OH NH2
333
334
4-Amino-5-hydroxy-2,7-naphthalenedisulfonic acid
HO
336
5-Amino-1H-imidazole-4-carboxamide
O
HO
N
H
NH2
N
H
H
N
H2N
NH2
O-[(Aminoiminomethyl)amino]-L-homoserine
O
N H
NH2
339
(Aminoiminomethyl)urea
O
NH2
I
338
340
2-Amino-5-iodobenzoic acid
4-Amino-1H-isoindole-1,3(2H)-dione
NH2
H2N
OH
O
O
NH2
O
N H
NH2
2-Amino-4-hydroxypteridine
O
NH2
NH O
337
O
N
H
335
4-Amino-3-hydroxy-1-naphthalenesulfonic acid
NH
O
N
N
N
NH2
O
H2N
O
N
O
O
332
H2N
1-Amino-4-hydroxy-2-methoxy-9,10-anthracenedione
O
4-Amino-5-(hydroxymethyl)-2(1H )-pyrimidinone
H2N
331
4-(2-Amino-1-hydroxyethyl)-1,2-benzenediol, (±)-
O
OH
O
330
4-Amino-3-hydroxybutanoic acid, (±)-
NH2
HO
HO
329
3-Amino-4-hydroxybutanoic acid
O
HO
H2N
OH
Organic
NH2
OH
OH
O
341
342
4-Amino-3-isoxazolidinone, (R)-
343
344
α-(Aminomethyl)benzenemethanol
1-Amino-2-methyl-9,10-anthracenedione
β-(Aminomethyl)benzenepropanoic acid
OH
OH
OH
O S O
NH2
NH2
NH2 O
NH2
345
346
2-Amino-5-methylbenzenesulfonic acid
NH2
347
trans-4-(Aminomethyl)cyclohexanecarboxylic acid
348
4-Amino-4-methyl-2-pentanone
2-Amino-4-methylphenol
349
4-Amino-2-methylphenol
OH
NH2
350
4-Amino-3-methylphenol
H2N
O
OH
P
OH
351
(Aminomethyl)phosphonic acid
O
H2N
HO
352
OH
2-Amino-2-methyl-1,3-propanediol
H2N
OH
353
L-3-Amino-2-methylpropanoic acid
OH
NH2
354
2-Amino-2-methyl-1-propanol
Physical Constants of Organic Compounds
3-22
No.
Name
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
Physical
Form
mp/˚C
355
4-Amino-5-methyl-2(1H)pyrimidinone
3-(Aminomethyl)-3,5,5trimethylcyclohexanol
3-Amino-2-naphthalene­
carboxylic acid
2-Amino-1,4-naphthalenedione
5-Methylcytosine
C5H7N3O
554-01-8
125.129 pr (w+1/2)
270 dec
1-Hydroxy-3-aminomethyl3,5,5-trimethylcyclohexane
3-Amino-2-naphthoic acid
C10H21NO
15647-11-7 171.280
45.5
C11H9NO2
5959-52-4
187.195 ye lf (dil al)
216.5
s EtOH, eth
C10H7NO2
2348-81-4
173.169
207
7-Amino-1,3-naphthalenedisulfonic acid
2-Amino-1,5-naphthalenedisulfonic acid
4-Amino-1,6-naphthalenedisulfonic acid
4-Amino-1,7-naphthalenedisulfonic acid
2-Amino-1-naphthalenesulfonic acid
4-Amino-1-naphthalenesulfonic acid
Amido-G-Acid
C10H9NO6S2
86-65-7
2-Naphthylamine-1,5-disulfonic acid
1-Naphthylamine-4,7-disulfonic acid
1-Naphthylamine-4,6-disulfonic acid
2-Naphthylamine-1-sulfonic
acid
1-Naphthylamine-4-sulfonic
acid
C10H9NO6S2
117-62-4
303.311 mcl pr or nd 274
(w+4)
303.311
>300
i H2O, alk; s
EtOH, eth,
HOAc
vs H2O, EtOH
C10H9NO6S2
85-75-6
303.311
vs H2O
C10H9NO6S2
85-74-5
303.311
vs H2O, EtOH
C10H9NO3S
81-16-3
223.248 sc(hot w)
s DMSO
C10H9NO3S
84-86-6
C10H9NO3S
84-89-9
223.248 wh nd
(w+1/2)
red-br cry
223.248 wh cry
C10H9NO3S
81-05-0
223.248 nd(w)
i H2O, EtOH, eth
C10H9NO3S
86-60-2
vs HOAc
1-Naphthylamine-8-sulfonic
acid
Bronner acid
C10H9NO3S
82-75-7
223.248 nd (w+1), pl
(aq ace)
223.248 nd
C10H9NO3S
93-00-5
223.248 lf
1,7-Cleve’s acid
C10H9NO3S
119-28-8
223.248 nd or pr (w)
i cold H2O; sl
hot H2O
sl EtOH; s eth
1-Amino-6-hydroxynaphthalene
C10H9NO
83-55-6
159.184
170
sl DMSO
C10H9NO
2834-92-6
159.184 silvery lf
(bz, eth)
150 dec
C10H9NO
118-46-7
159.184 nd (w, al)
206
182.134 oran pr (dil 269
al)
182.134 lf (al), ye nd 278(5)
(w, dil al)
sl H2O, eth; s
EtOH; vs dil
alk, acid
s H2O, eth; vs
EtOH; sl bz, lig
i H2O; vs EtOH,
eth, ace; s xyl
i H2O, bz, chl,
xyl; s EtOH,
eth
sl DMSO
sl H2O
sl H2O, ace; vs
EtOH; s eth,
bz, HOAc
s H2O, EtOH, bz
s H2O, EtOH,
eth; sl DMSO
sl H2O, EtOH,
eth, bz; s
HOAc
sl H2O; i EtOH,
eth; vs alk,
acid
vs H2O, EtOH
356
357
358
359
360
361
362
Organic
363
364
365
den
g cm –3
nD
265
dec
0.96925
1.490420
1.670325
372
1-Amino-2-naphthol
373
8-Amino-2-naphthol
374
2-Amino-4-nitrobenzoic acid
C7H6N2O4
619-17-0
375
2-Amino-5-nitrobenzoic acid
C7H6N2O4
616-79-5
376
377
378
2-Amino-5-nitrobenzonitrile
3-Amino-1-nitroguanidine
2-Amino-4-nitrophenol
C7H5N3O2
CH5N5O2
C6H6N2O3
17420-30-3 163.134
18264-75-0 119.084
99-57-0
154.123 oran pr
(+w)
379
380
2-Amino-5-nitrophenol
4-Amino-2-nitrophenol
C6H6N2O3
C6H6N2O3
121-88-0
119-34-6
381
2-Aminooctanoic acid, (±)-
C8H17NO2
644-90-6
154.123
205.8
154.123 dk red pl or 131
nd (w, al)
159.227 lf (w)
270
382
Aminooxoacetohydrazide
C2H5N3O2
515-96-8
103.080
221 dec
383
C4H5NO3
557-24-4
115.088 cry (al)
172.5
C5H9NO3
C4H11ClN2O6
106-60-5
2921-14-4
131.130 cry (EtOH)
218.592
118
152.5
386
387
cis-4-Amino-4-oxo-2-butenoic Maleamic acid
acid
5-Amino-4-oxopentanoic acid 5-Aminolevulinic acid
(Aminooxy)acetic acid,
hydrochloride (2:1)
6-Aminopenicillanic acid
Penicin
5-Aminopentanoic acid
C8H12N2O3S
C5H11NO2
551-16-6
660-88-8
216.257 cry (w)
117.147 lf (dil al)
208
157 dec
dec
388
5-Amino-1-pentanol
C5H13NO
2508-29-4
103.163
38.5
221.5
0.948817 1.461817
389
2-Aminophenol
C6H7NO
95-55-6
109.126 wh orth
bipym nd
(bz)
173.5(0.3)
267(19)
1.32825
368
369
370
384
385
HCP_Section_03.indb 22
8-Amino-β-naphthol
Semioxamazide
i H2O; sl EtOH; s
MeOH, py
s H2O; i eth
371
367
Solubility
s H2O, acid; sl
EtOH; i eth
5-Amino-1-naphthalenesulfonic acid
6-Amino-1-naphthalenesulfonic acid
7-Amino-1-naphthalenesulfonic acid
8-Amino-1-naphthalenesulfonic acid
6-Amino-2-naphthalenesulfonic acid
8-Amino-2-naphthalenesulfonic acid
5-Amino-1-naphthol
366
1-Naphthylamine-5-sulfonic
acid
2-Naphthylamine-5-sulfonic
acid
Badische acid
bp/˚C
vs gl HOAc
sub
203.5
187.8
146
11012
sub
s H2O; sl EtOH; i
eth, bz, lig
msc H2O, EtOH,
ace
s H2O, eth; vs
EtOH; sl bz, tfa
4/11/16 11:18 AM
Physical Constants of Organic Compounds
OH
N
NH2
H2N
O
O
O
N
H
OH
O S O
O
OH
355
356
4-Amino-5-methyl-2(1H )-pyrimidinone
S
NH2
NH2
357
3-(Aminomethyl)-3,5,5-trimethylcyclohexanol
OH
O S O
358
3-Amino-2-naphthalenecarboxylic acid
OH
O S O
NH2
HO
OH
O S O
S
O
O
NH2
362
4-Amino-1,6-naphthalenedisulfonic acid
OH
O S O
NH2
NH2
361
360
2-Amino-1,5-naphthalenedisulfonic acid
7-Amino-1,3-naphthalenedisulfonic acid
OH
O S O
O
HO
OH
359
2-Amino-1,4-naphthalenedione
O
O S O
OH
O
O
363
4-Amino-1,7-naphthalenedisulfonic acid
OH
O S O
2-Amino-1-naphthalenesulfonic acid
OH
O S O
OH
O S O
H2N
NH2
NH2
364
H2N
365
4-Amino-1-naphthalenesulfonic acid
366
5-Amino-1-naphthalenesulfonic acid
O
S
OH
NH2
O
368
369
O
OH
O
373
O
374
8-Amino-2-naphthol
OH O
N
NH2
O
O
378
N
O
381
4-Amino-2-nitrophenol
O
5-Amino-4-oxopentanoic acid
O
O
0.5 HCl
NH2
385
(Aminooxy)acetic acid, hydrochloride (2:1)
O
H
N
H
O
O
NH2
383
cis-4-Amino-4-oxo-2-butenoic acid
OH
NH2
OH
H2N
6-Aminopenicillanic acid
O
HO
NH2
Aminooxoacetohydrazide
O
COOH
386
377
S
N
O
N
N
NH2 O
3-Amino-1-nitroguanidine
382
2-Aminooctanoic acid, (±)-
H2N
HO
H
N
O
H 2N
O
380
O
OH
376
NH2
NH2
2-Amino-5-nitrophenol
H2N
384
O
H2N
N
O
2-Amino-5-nitrobenzonitrile
OH
379
2-Amino-4-nitrophenol
N
O
2-Amino-5-nitrobenzoic acid
OH
NH2
O
375
2-Amino-4-nitrobenzoic acid
OH
NH2
NH2
NH2
372
1-Amino-2-naphthol
N
OH
NH2
O
371
5-Amino-1-naphthol
8-Amino-2-naphthalenesulfonic acid
OH
N
NH2
370
6-Amino-2-naphthalenesulfonic acid
O
OH
O
H 2N
8-Amino-1-naphthalenesulfonic acid
NH2
OH
S
O
O
7-Amino-1-naphthalenesulfonic acid
OH
OH
H2N O S O
N
367
6-Amino-1-naphthalenesulfonic acid
387
5-Aminopentanoic acid
OH
H2N
388
5-Amino-1-pentanol
389
2-Aminophenol
Organic
NH2
3-23
Physical Constants of Organic Compounds
3-24
Mol. Form.
CAS RN
Mol.
Wt.
3-Aminophenol
C6H7NO
591-27-5
391
4-Aminophenol
C6H7NO
392
N-(3-Aminophenyl)acetamide
393
N-(4-Aminophenyl)acetamide
394
395
No.
Name
390
Physical
Form
Organic
mp/˚C
bp/˚C
109.126 pr (to)
122.5(0.3)
16411
123-30-8
109.126 wh pl (w)
186(7)
1100.3
C8H10N2O
102-28-3
150.177 nd or pl (bz) 88
p-Aminoacetanilide
C8H10N2O
122-80-5
150.177 nd (w)
166.5
(4-Aminophenyl)arsonic acid
Arsanilic acid
C6H8AsNO3
98-50-0
217.055 mcl nd (w,
al)
232
4,4’-Diaminodiphenylamine
C12H13N3
537-65-5
199.251 lf (w)
158
dec
396
N-(4-Aminophenyl)-1,4benzenediamine
2-Amino-1-phenylethanone
Phenacylamine
C8H9NO
613-89-8
135.163 ye cry
20
251
397
1-(3-Aminophenyl)ethanone
m-Aminoacetophenone
C8H9NO
99-03-6
98.5
289.5
398
1-(4-Aminophenyl)ethanone
p-Aminoacetophenone
C8H9NO
399
1-(4-Aminophenyl)-1-pentanone
1-(4-Aminophenyl)-1-propanone
N-[(4-Aminophenyl)­sulfonyl]­
acetamide
400
401
402
5-[(4-Aminophenyl)
sulfonyl]-2-thiazolamine
4-Aminophthalimide
Synonym
p-Aminopropiophenone
C9H11NO
Sulfacetamide
C8H10N2O3S
135.163 pa ye pl (al),
lf (eth)
99-92-3
135.163 ye mcl pr
(al)
38237-74-0 177.243 cry
(bz-peth)
70-69-9
149.189 pl (al, w), nd
(w)
144-80-9
214.241
Thiazolsulfone
C9H9N3O2S2
473-30-3
255.316 nd (al)
3676-85-5
162.146
C11H15NO
404
5-Amino-1H-isoindole-1,3(2H)- C8H6N2O2
dione
3-Amino-1,2-propanediol, (±)C3H9NO2
405
406
3-Aminopropanenitrile
2-Amino-1-propanol, (±)-
3-Aminopropionitrile
407
408
3-Amino-1-propanol
1-Amino-2-propanol
Propanolamine
Isopropanolamine
409
α-(1-Aminopropyl)­
α-(α-Aminopropyl)benzyl
alcohol
benzenemethanol
N-(3-Aminopropyl)-N-methyl1,3-propanediamine
Aminopropylon
4-(2-Aminopropyl)phenol, (±)- Hydroxyamphetamine
403
410
411
412
413
414
415
416
417
418
419
420
421
422
423
424
Solubility
s H2O, tol; vs
EtOH, eth; sl
bz, DMSO
sl H2O, tfa; vs
EtOH; i bz, chl;
s alk
vs H2O, EtOH,
ace; sl eth, bz
s H2O; vs EtOH,
eth
s H2O, eth; sl
EtOH, DMSO; i
ace, bz
vs eth, EtOH
267
1.957110
1.616020 i H2O; s eth; sl
ctc
sl H2O; s EtOH
105(1)
294
vs eth, EtOH
74.5
1613
i H2O; s EtOH,
eth
s DMSO
220 dec
140
182.0(0.4)
sl H2O; s EtOH; i
eth; vs ace,
alk
vs ace, eth,
EtOH, diox
2240.5
265 dec
C3H6N2
C3H9NO
151-18-8
6168-72-5
70.093
75.109
185
174.5
C3H9NO
C3H9NO
156-87-6
1674-56-2
75.109
75.109
C10H15NO
5897-76-7
165.232 pl (bz-eth)
C7H19N3
105-83-9
145.246
C16H22N4O2
C9H13NO
3690-04-8
1518-86-1
302.372 pr (bz)
151.205 cry (bz)
181
125.5
C6H17N3
56-18-8
131.219
-5.1(0.3)
C19H20N8O5
C10H10N4O2S
54-62-6
116-44-9
440.413 ye cry
250.277 nd (PhNO2)
262 dec
251
C4H4N4
16617-46-2 108.102 cry (w)
173
C6H6N2O2
5345-47-1
138.124
296 dec
C6H6N2O2
3167-49-5
312
Sulfapyridine
C11H11N3O2S
144-83-2
138.124 cry (dil
HOAc,
+2w)
249.289 ye oran (al)
190(2)
5-Aminouracil
C4H5N3O2
932-52-5
127.102 nd (w)
dec
C4H5N3O2
873-83-6
127.102 cry (w)
dec
2-Thiocytosine
C4H5N3S
333-49-3
127.168
sl DMSO
Uramil
C4H5N3O3
118-78-5
143.101 nd or pl (w) >400
Sulfadiazine
C10H10N4O2S
68-35-9
250.277 cry (w), wh
pow
s H2O, chl; i eth,
bz
sl H2O, EtOH,
ace, DMSO
3-Amino-1H-pyrazole-43-Amino-4-cyanopyrazole
carbonitrile
2-Amino-3-pyridinecarboxylic
acid
6-Amino-3-pyridinecarboxylic 6-Aminonicotinic acid
acid
HCP_Section_03.indb 24
nD
13552-31-3 91.109
N-(3-Aminopropyl)-1,3Bis(3-aminopropyl)amine
propanediamine
Aminopterin
4-Amino-N-pyrazinylbenzene- Sulfapyrazine
sulfonamide
4-Amino-N-2-pyridinylbenzenesulfonamide
5-Amino-2,4(1H,3H)-pyrimidinedione
6-Amino-2,4(1H,3H)-pyrimidinedione
4-Amino-2(1H)-pyrimidinethione
5-Amino-2,4,6(1H,3H,5H)pyrimidinetrione
4-Amino-N-2-pyrimidinyl­
benzenesulfonamide
den
g cm –3
liq
12.1(1)
1.7(0.2)
185(4)
141(12)
1.175220 1.491025 s H2O, EtOH; i
eth, bz
0.958420 1.439620
1.450220 vs H2O, EtOH,
eth; sl chl
0.982426 1.461720 s H2O, EtOH, eth
0.961120 1.447920 msc H2O, EtOH,
eth, ace, bz,
ctc
79.5
232(3)
261(3)
15150
0.902320 1.470525
0.93825
1.481020
vs H2O
s H2O, EtOH, bz,
chl, AcOEt
s chl
i H2O, EtOH, eth,
bz, chl; s py; sl
ace
sl H2O
i H2O, bz, ctc; s
EtOH
i H2O; s alk,
acid
vs H2O
4/11/16 11:18 AM
Physical Constants of Organic Compounds
3-25
O
OH
O
OH
NH2
NH
NH2
NH2
390
391
3-Aminophenol
NH2
392
4-Aminophenol
OH
O As OH
NH
N-(3-Aminophenyl)acetamide
H2N
NH2
393
394
N-(4-Aminophenyl)acetamide
NH
NH2
395
(4-Aminophenyl)arsonic acid
N-(4-Aminophenyl)-1,4-benzenediamine
O
NH
O S O
O
O
O
O
O
NH2
397
2-Amino-1-phenylethanone
H2N
1-(3-Aminophenyl)ethanone
NH
NH2
402
1-(4-Aminophenyl)-1-pentanone
1-(4-Aminophenyl)-1-propanone
404
3-Amino-1,2-propanediol, (±)-
4-Aminophthalimide
H
N
H2N
409
NH2
NH2
N
H
H2N
H2N
N
H
N
N
N
H
413
417
2-Amino-3-pyridinecarboxylic acid
NH2
O
O
S NH
O
H2N
N
N
H
N
O
H2N
3-Amino-1H-pyrazole-4-carbonitrile
O
O
S NH
O
H2N
N
418
6-Amino-3-pyridinecarboxylic acid
O
6-Amino-2,4(1H,3H)-pyrimidinedione
N
H
422
H2N
NH
N
N
H
419
O
420
4-Amino-N-2-pyridinylbenzenesulfonamide
5-Amino-2,4(1H,3H )-pyrimidinedione
O
H2N
N
NH
N
416
415
4-Amino-N-pyrazinylbenzenesulfonamide
NH2
NH2
421
N
OH
OH
NH2
N
H
4-(2-Aminopropyl)phenol, (±)-
OH
414
O
O
412
Aminopropylon
Aminopterin
OH
NH2
HO
N
N-(3-Aminopropyl)-1,3-propanediamine
N
O
N
411
N-(3-Aminopropyl)-N-methyl-1,3-propanediamine
O
N
N
NH2
410
α-(1-Aminopropyl)benzenemethanol
1-Amino-2-propanol
N
3-Amino-1-propanol
O
O
NH2
OH
407
2-Amino-1-propanol, (±)-
3-Aminopropanenitrile
N
OH
H2N
406
405
OH
408
N-[(4-Aminophenyl)sulfonyl]acetamide
OH
N
OH
403
NH2
401
NH2
NH2
NH2
HO
O
5-[(4-Aminophenyl)sulfonyl]-2-thiazolamine
NH2
400
O
N
S
H2N
399
1-(4-Aminophenyl)ethanone
H2N
O
S
O
H2N
398
S
4-Amino-2(1H )-pyrimidinethione
O
NH
N
H
423
O
5-Amino-2,4,6(1H,3H,5H )-pyrimidinetrione
H2N
O
S NH
O
424
N
N
4-Amino-N-2-pyrimidinylbenzenesulfonamide
Organic
NH2
NH2
396
Physical Constants of Organic Compounds
3-26
No.
Name
425
426
427
428
429
430
431
432
433
Organic
434
435
436
437
438
439
440
Synonym
Mol. Form.
CAS RN
Aminopyrine
C13H17N3O
58-15-1
4-Amino-N-2-quinoxalinylben- Sulfaquinoxaline
zenesulfonamide
4-(Aminosulfonyl)benzoic acid Carzenide
C14H12N4O2S
Mol.
Wt.
Physical
Form
mp/˚C
59-40-5
231.293 pr or pl (lig
or AcOEt)
300.336
247.5
C7H7NO4S
138-41-0
201.201 pr or lf (w)
291 dec
C8H10N2O3S
121-61-9
214.241 nd (HOAc)
219.5
C2H3N3S2
2349-67-9
133.195
243.0
C3H4N2OS
556-90-1
116.141 pr or nd (w) 256 dec
101.5
den
g cm –3
Acetylsulfanilamide
N-(Aminothioxomethyl)­
acetamide
N-Amino-2-thioxo-4-thiazolidinone
1-Amino-2,2,2-trichloro­
ethanol
4-Amino-3,5,6-trichloro-2pyridinecarboxlic acid
11-Aminoundecanoic acid
Amiton
Amitraz
Acetylthiourea
C3H6N2OS
591-08-2
3-Aminorhodanine
C3H4N2OS2
1438-16-0
118.157 pr (w), orth
(al)
148.206
Chloral ammonia
C2H4Cl3NO
507-47-1
164.418 nd (al)
73
Picloram
C6H3Cl3N2O2
1918-02-1
241.459
218.5
C11H23NO2
C10H24NO3PS
C19H23N3
2432-99-7 201.307
78-53-5
269.342 liq
33089-61-1 293.406
189.0
86
1.12820
C20H23N
C6H12FeN3O12
C8H4F15NO2
50-48-6
277.404 cry
14221-47-7 374.017
3825-26-1 431.100 solid
196 (HCl)
165 dec
1.7817.5
C3H9NO2
C11H18N2O3
17496-08-1 91.109 hyg cry
57-43-2
226.272
45
153(1)
C20H23NO2
76-65-3
43.4
Amolanone
444
445
446
Amoxicillin
Amphecloral
Amphotericin B
C16H19N3O5S
C11H12Cl3N
C47H73NO17
26787-78-0 365.404 cry (w)
5581-35-1 264.579
1397-89-3 924.080 ye pr (DMF) 170 dec
447
448
Ampicillin
Ampyrone
C16H19N3O4S
C11H13N3O
69-53-4
83-07-8
449
Amygdalin
450
309.403 cry (peth)
200 dec
109
C20H27NO11
349.405 cry
203.240 pa ye cry
(bz)
29883-15-6 457.428
Anacardic acid
C22H32O3
11034-77-8 344.487 cry (ace)
35.5
451
Anagyrine
C15H20N2O
486-89-5
452
Androstane
C19H32
453
455
456
457
Androstane-17-carboxylic
acid, (5β,17β)
Androstane-3,17-diol,
(3α,5α,17β)
5α-Androstane-3,17-dione
5β-Androstane-3,17-dione
Androst-4-ene-3,17-dione
458
Androst-4-ene-3,11,17-trione Adrenosterone
459
Anemonin
460
461
Anhalamine
Anhalonidine
462
Anhalonine
463
2,5-Anhydro-3,4-dideoxyhexi- Tetrahydro-2,5-furandimethatol
nol
HCP_Section_03.indb 26
100 dec
vs bz, eth, EtOH
760.01
443
5-Ethyl-5-isopentyl2,4,6(1H,3H,5H)-pyrimidinetrione
3-[2-(Diethylamino)­ethyl]-3phenyl-2(3H)-benzofuranone
sl H2O; i EtOH,
eth
sl H2O, eth; s
DMSO, EtOH
s DMSO
165
441
442
1.465527
vs H2O; i EtOH
s H2O
vs bz, EtOH, chl
1932.0
1.561425
960.5
1.530
s H2O
i H2O; sl DMF; s
DMSO
sl H2O
s H2O, EtOH, bz,
chl; sl eth
vs H2O; sl EtOH;
i eth, chl
vs eth, EtOH,
peth
s H2O, eth, bz;
vs EtOH, chl; i
lig
vs ace, eth,
EtOH, peth
224.5
244.332 pe ye glass
Solubility
vs H2O, bz,
EtOH
sl H2O, EtOH,
ace; s aq alk
i H2O; vs EtOH;
sl eth; i bz
s H2O, EtOH,
ace
N-[4-(Aminosulfonyl)­phenyl]­
acetamide
5-Amino-1,3,4-thiadiazole2(3H)-thione
2-Amino-4(5H)-thiazolone
N-Methylbis(2,4-xylyliminomethyl)amine
nD
107.5
Amitriptyline
Ammonium ferric oxalate
Ammonium perfluorooctanoate
Ammonium propanoate
Amobarbital
454
bp/˚C
26512
Etiocholanic acid
C20H32O2
24887-75-0 260.457 lf
50
(aceMeOH)
438-08-4
304.467 nd (gl HOAc) 228.5
600.003
Epiandrostanediol
C19H32O2
1852-53-5
292.456 nd (ace aq)
4-Androstene-3,17-dione
C19H28O2
C19H28O2
C19H26O2
846-46-8
1229-12-5
63-05-8
C19H24O3
382-45-6
288.424 cry (MeOH) 130(3)
288.424 cry (ace-hx) 135
286.408
143(form a);
173(form b)
300.392 nd (al)
222
sub
160 sub
223
158
187.5
160.5
vs eth, EtOH
vs H2O, EtOH
C12H15NO3
192.169 orth pl (chl)
nd (al or
bz)
643-60-7
209.242 nd (al)
17627-77-9 223.268 oct cry (bz,
eth)
519-04-0
221.252 rhom nd
sl H2O; s EtOH,
eth, ace, chl
vs chl
86
1400.02
C6H12O3
104-80-3
<-50
265
trans-1,7C10H8O4
Dioxadispiro[4.0.4.2]­dodeca3,9-diene-2,8-dione
C11H15NO3
C12H17NO3
508-44-1
132.157
1.15420
vs EtOH, bz, chl,
eth, peth
vs H2O, ace, bz,
EtOH
4/11/16 11:18 AM
Physical Constants of Organic Compounds
3-27
NH2
O
N
O
N
O
O
S
HN
O
OH
HN
N
N
H
N
425
426
Aminopyrine
O S O
O S O
NH2
NH2
427
4-Amino-N-2-quinoxalinylbenzenesulfonamide
N N
S
428
4-(Aminosulfonyl)benzoic acid
NH2
S
429
N-[4-(Aminosulfonyl)phenyl]acetamide
5-Amino-1,3,4-thiadiazole-2(3H )-thione
NH2
O
S
N
H2N
NH2
S
N
430
O
N
H
431
2-Amino-4(5H)-thiazolone
Cl
Cl
S
S
432
N-(Aminothioxomethyl)acetamide
Cl
OH
NH2
NH2
Cl
OH
N
Cl
O
433
N-Amino-2-thioxo-4-thiazolidinone
Cl
434
1-Amino-2,2,2-trichloroethanol
4-Amino-3,5,6-trichloro-2-pyridinecarboxlic acid
3
O
O
N
H2N
O
N
N
N
435
O
O
O
O
436
O
437
Amiton
438
Amitraz
439
Amitriptyline
Ammonium ferric oxalate
HO
O
O
F
O
NH4
F F F F F F F F
O
440
O
NH4
Ammonium perfluorooctanoate
OH
OH
O
O
OH OH
Cl
Cl
OH
O
O
H
NH
O
NH2
O
N
Amoxicillin
OH
H
CH3
444
Amolanone
OH OH O
Cl
O
NH2 OH
445
H2N
S
N
OH
O
447
446
N
448
Ampicillin
Amphotericin B
O
N
HO
Amphecloral
OH
O
443
Amobarbital
Ammonium propanoate
HO
O
442
441
S
N
O
O
H
N
H
NH2
N
NH
O
H
NH
O
F F F F F F
3NH4
O
O
N
O
11-Aminoundecanoic acid
O
O
Fe
O
O P S
O
OH
Organic
O
Ampyrone
N
O
HO
OH
O
O
O
O
HO
OH
HO
HO HO
450
H
451
O
OH
HO
H
453
O
454
Androstane-17-carboxylic acid, (5β,17β)
O
H
O
H
455
Androstane-3,17-diol, (3α,5α,17β)
Androstane
O
H
H
H
452
Anagyrine
H
H
H
O
456
5α-Androstane-3,17-dione
457
5β-Androstane-3,17-dione
Androst-4-ene-3,17-dione
O
O
O
O
O
O
459
Anemonin
NH
O
O
O
458
H
H
H
Anacardic acid
COOH
Androst-4-ene-3,11,17-trione
N
O
449
H
N
OH
Amygdalin
O
OH
OH
460
Anhalamine
O
NH
O
OH
461
Anhalonidine
NH
O
O
462
Anhalonine
HO
O
463
OH
2,5-Anhydro-3,4-dideoxyhexitol
Physical Constants of Organic Compounds
3-28
Organic
No.
Name
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
464
Anilazine
2,4-Dichloro-6-(ochloroanilino)-s-triazine
C9H5Cl3N4
101-05-3
275.522
159.3(0.5)
465
466
Anileridine
Aniline
Benzenamine
C22H28N2O2
C6H7N
144-14-9
62-53-3
352.469 cry
93.127 oily liq
83
-6.0(0.1)
184.1(0.4)
467
Aniline-2-carboxylic acid
o-Anthranilic acid
C7H7NO2
118-92-3
137.137 lf (al)
144.6(0.5)
sub
468
Aniline-3-carboxylic acid
m-Anthranilic acid
C7H7NO2
99-05-8
137.137
179.7(0.6)
469
Aniline-4-carboxylic acid
p-Anthranilic acid
C7H7NO2
150-13-0
137.137 mcl pr (w)
188.2(0.6)
470
471
Aniline hydrobromide
Aniline hydrochloride
Benzenamine hydrochloride
C6H8BrN
C6H8ClN
542-11-0
142-04-1
174.039
129.588 lf or nd
286
198
1.22154
472
Aniline nitrate
C6H8N2O3
542-15-4
156.139 orth
190 dec
1.3564
473
Aniline sulfate (2:1)
C12H16N2O4S
542-16-5
284.331
474
Anisole
Methoxybenzene
C7H8O
100-66-3
108.138 liq
-37.3(0.2)
475
476
477
Anisotropine methylbromide
Antazoline
Anthra[9,1,2-cde]benzo[rst]
pentaphene-5,10-dione
Octatropine methylbromide
C17H32BrNO2
C17H19N3
C34H16O2
80-50-2
91-75-8
116-71-2
329
122
492 dec
478
2-Anthracenamine
C14H11N
613-13-8
362.346 cry (ace)
265.353 cry
456.490 viol-bl or
blk nd
(PhNO2)
193.244 ye lf (al)
479
Anthracene
C14H10
120-12-7
480
481
9-Anthracenecarbonitrile
9-Anthracenecarboxaldehyde
C15H9N
C15H10O
1210-12-4
642-31-9
482
1-Anthracenecarboxylic acid
1-Anthroic acid
C15H10O2
607-42-1
483
2-Anthracenecarboxylic acid
2-Anthroic acid
C15H10O2
613-08-1
484
485
486
487
9-Anthracenecarboxylic acid 9-Anthroic acid
9,10-Anthracenedicarbonitrile
9,10-Anthracenediol
9,10-Anthracenedione
Anthraquinone
C15H10O2
C16H8N2
C14H10O2
C14H8O2
723-62-6
1217-45-4
4981-66-2
84-65-1
488
489
490
9-Anthracenemethanol
1,4,9,10-Anthracenetetrol
1,2,10-Anthracenetriol
Anthrarobin
C15H12O
C14H10O4
C14H10O3
1468-95-7
476-60-8
577-33-3
491
1,8,9-Anthracenetriol
Anthralin
C14H10O3
1143-38-0
492
1-Anthracenol
C14H10O
610-50-4
493
9-Anthracenol
Anthranol
C14H10O
494
9(10H)-Anthracenone
Anthrone
C14H10O
495
Tartar emetic
C8H10K2O15Sb2
496
497
Antimony potassium tartrate
trihydrate
Apholate
Aphylline
194.228 cry (bz), br 158
nd or lf (al)
529-86-2
194.228 ye red lf (dil 152
al)
90-44-8
194.228 nd (bz-lig, 155(3)
HOAc)
28300-74-5 667.873 col cry
C12H24N9P3
C15H24N2O
52-46-0
577-37-7
387.300
248.364 cry
148
52.5
498
Apigenin
5,7-Dihydroxy-2-(4hydroxyphenyl)-4H-1-benzopyran-4-one
C15H10O5
520-36-5
270.237 ye nd (aq
py)
347.5
499
Apoatropine
C17H21NO2
500-55-0
271.355 pr (chl)
62
HCP_Section_03.indb 28
Physical
Form
mp/˚C
bp/˚C
den
g cm –3
nD
Solubility
1.820
s H2O
1.021720 1.586320 s H2O, ctc, lig;
msc EtOH, eth,
ace, bz
1.41220
s H2O, EtOH,
eth; sl bz, tfa;
vs chl, py
1.5125
sl H2O, EtOH; s
eth, tfa; vs
ace; i bz
1.37420
s H2O, EtOH,
eth; sl ace; i
bz, chl
1.3774
153.6(0.2)
238.8
sub
178.229 tab or mcl
pr (al)
216(2)
341.3(0.4)
203.239
206.239 oran nd (dil
HOAc)
222.239 ye nd
(HOAc) ye
pr (al)
222.239 ye lf (al) nd,
lf (sub)
222.239
228.248
210.228 br or ye nd
208.213 ye orth nd
(al, bz)
208.255
242.227
226.227 ye lf, nd
(al-w)
226.227 ye pl or nd
(lig)
177.5
107(1)
0.994020 1.517420
1.2825
vs H2O, EtOH; i
eth, chl; sl
DMSO
vs H2O, eth,
EtOH
s H2O; sl EtOH,
tfa; i eth
i H2O; s EtOH,
eth, chl; vs
ace, bz
i EtOH, bz,
HOAc; s xyl,
py, sulf
i H2O; s EtOH; i
con sulf
i H2O; sl EtOH,
eth, ace, bz,
chl, ctc
1.300020
i H2O; s bz,
HOAc
i H2O; s EtOH,
eth; sl bz, chl
251.5
sub
281
sub
vs HOAc
219(1)
337 dec
180
284.8(0.2)
sub
i H2O; s EtOH
377(2)
1.43820
160.5
148
208
sl H2O; vs EtOH,
eth, ace; s bz
i H2O; s EtOH,
ace, bz; sl eth;
vs py
i H2O; vs EtOH,
eth; s NaOH
179
23413
2.6
2004
vs eth, EtOH
i H2O; sl EtOH,
eth, bz, chl
s ace, bz, con
sulf, dil alk
sl H2O
vs ace, bz, eth,
EtOH
i H2O; s EtOH,
py; vs dil alk
sl H2O, lig; vs
EtOH, eth, ace,
bz
4/11/16 11:18 AM
Physical Constants of Organic Compounds
NH2
Cl
N
HO
O
N
N
Cl
3-29
N
O
HO
NH2
N
H
HO
O
O
O
NH2
HBr
NH2
NH2
Cl
464
465
Anilazine
466
Anileridine
467
Aniline
NH2
468
Aniline-2-carboxylic acid
470
469
Aniline-3-carboxylic acid
Aniline hydrobromide
Aniline-4-carboxylic acid
Br
N
NH2 0.5 H2SO4
NH2 HNO3
O
N
O
471
472
Aniline hydrochloride
473
Aniline nitrate
474
Aniline sulfate (2:1)
475
Anisole
N
N
H
O
476
Anisotropine methylbromide
Antazoline
N
O
NH2
O
O
477
478
Anthra[9,1,2-cde]benzo[rst]pentaphene-5,10-dione
479
2-Anthracenamine
480
Anthracene
481
9-Anthracenecarbonitrile
9-Anthracenecarboxaldehyde
N
OH
HO
O
OH
HO
O
O
O
N
482
483
1-Anthracenecarboxylic acid
2-Anthracenecarboxylic acid
484
9-Anthracenecarboxylic acid
9,10-Anthracenedicarbonitrile
OH
OH OH
489
9-Anthracenemethanol
1,4,9,10-Anthracenetetrol
O
486
487
9,10-Anthracenediol
9,10-Anthracenedione
OH
OH OH
OH
488
OH
485
OH OH OH
OH
OH
OH
490
491
1,2,10-Anthracenetriol
492
1,8,9-Anthracenetriol
493
1-Anthracenol
9-Anthracenol
N
O
O
O
O
O
494
9(10H )-Anthracenone
O
Sb
O O
O O
Sb
O
O
2
2K 3H2O
O
495
Antimony potassium tartrate trihydrate
N
N
N
P N
N P
N
N
P
N N
496
Apholate
OH O
H
N
N
H
HO
OH
O
497
Aphylline
O
O
498
Apigenin
O
499
Apoatropine
Organic
HCl
NH2
Physical Constants of Organic Compounds
3-30
Organic
Mol. Form.
CAS RN
Mol.
Wt.
Apocodeine
C18H19NO2
641-36-1
281.350 pr (MeOH)
123.5
501
Apomorphine
C17H17NO2
58-00-4
195 dec
502
Apomorphine, hydrochloride
C17H18ClNO2
314-19-2
503
Aprobarbital
C10H14N2O3
77-02-1
267.323 hex pl
(chl-peth)
rods (eth)
303.784 grn in air
mcl pr
210.229 cry
141
vs ace, eth,
EtOH, chl
504
L-Arabinitol
C5H12O5
7643-75-6
152.146
102.5
vs H2O; sl EtOH;
i eth
505
506
C5H10O5
C11H20O10
608-45-7
150.130 cry (MeOH)
14116-69-9 312.271 nd (dil al)
155.5
210 dec
1.58525
507
α-D-Arabinopyranose
6-O-α-L-Arabinopyranosyl-DGlucose
DL-Arabinose
C5H10O5
20235-19-2 150.130 pr, nd (al)
164.5
1.58520
508
α-D-Arabinose
C5H10O5
31178-68-4 150.130
156
1.58525
509
β-D-Arabinose
C5H10O5
31178-69-5 150.130
156
1.62525
510
Aramite
C15H23ClO4S
140-57-8
334.860
-37.3
511
Arecaidine
C7H11NO2
499-04-7
512
Arecoline
C8H13NO2
63-75-2
141.168 pl (dil al) tab 232 dec
(dil al
+1w)
155.195
513
D-Arginine
C6H14N4O2
7200-25-1
174.201
217 dec
514
L-Arginine
C6H14N4O2
74-79-3
174.201
260(3)
515
516
L-Arginine, monohydrochloride
Artemisin
8-Hydroxysantonin
C6H15ClN4O2
C15H18O4
1119-34-2
481-05-0
210.662
262.302 cry
219
203
2600.1
517
Ascaridole
1-Methyl-4-isopropyl-2,3dioxabicyclo[2.2.2]oct-5-ene
C10H16O2
512-85-6
168.233 liq
3.3
exp
518
L-Ascorbic acid
Vitamin C
C6H8O6
50-81-7
176.124
191(4)
1.6525
519
520
Ascorbyl palmitate
L-Asparagine
6-Hexadecanoylascorbic acid
α-Aminosuccinamic acid
C22H38O7
C4H8N2O3
137-66-6
70-47-3
414.533
132.118 orth (w+1)
112
235
1.54315
521
D-Asparagine, monohydrate
C4H10N2O4
5794-24-1
150.133
215
1.52315
522
L-Asparagine, monohydrate
C4H10N2O4
5794-13-8
150.133
234
1.54315
523
Aspartame
C14H18N2O5
22839-47-0 294.303 nd (w)
246.5
524
DL-Aspartic acid
C4H7NO4
617-45-8
133.104 mcl pr (w)
277.5
1.662213
525
L-Aspartic acid
C4H7NO4
56-84-8
133.104 orth lf (w)
270
1.660313
526
527
528
Aspergillic acid
Astemizole
Asulam
C12H20N2O2
C28H31FN4O
C8H10N2O4S
490-02-8
224.299 pa ye rods
68844-77-9 458.570 wh cry
3337-71-1 230.241
98
149.1
144.2(0.5)
529
Atenolol
C14H22N2O3
29122-68-7 266.336 cry (AcOEt)
147
530
Atisine
C22H33NO2
466-43-3
343.503 orth bipym
58.5
531
532
Atrazine
Atropine
C8H14ClN5
C17H23NO3
1912-24-9
51-55-8
177.0(0.5)
118.5
533
534
Auramine hydrochloride
Aureothin
C17H22ClN3
C22H23NO6
2465-27-2
2825-00-5
215.684
289.370 orth nd (dil
al)
303.83 ye nd (w)
397.421 ye pr
No.
Name
500
HCP_Section_03.indb 30
Synonym
5-Isopropyl-5-allyl2,4,6(1H,3H,5H)-pyrimidinetrione
Vicianose
1,2,5,6-Tetrahydro-1-methyl3-pyridinecarboxylic acid
L-α-Aspartyl-L-phenylalanine,
2-methyl ester
L-Aminosuccinic acid
Methyl [(4-aminophenyl)­
sulfonyl]carbamate
Anthorine
Physical
Form
mp/˚C
bp/˚C
den
g cm –3
nD
Solubility
sl EtOH; s eth,
ace, bz, lig
sl H2O; s EtOH,
eth, ace, bz,
alk
205 dec
267
158
vs H2O
1952
1.14320
209
1.048520 1.486-20
1.0103
20
1.510020
1.4769
20
vs H2O; sl EtOH;
i eth, bz
vs H2O; sl EtOH;
i eth, ace,
MeOH
vs H2O; sl EtOH;
i eth, ace,
MeOH
vs ace, bz, eth,
EtOH
vs H2O; i EtOH,
eth, bz, chl
msc H2O, EtOH,
eth; s chl
i H2O, EtOH, eth,
bz
s H2O; sl EtOH; i
eth
sl H2O, chl; s
AcOEt; i peth
i H2O; s EtOH,
ace, bz, tol; sl
chl
vs H2O; s EtOH;
i eth, bz, chl,
peth
s H2O; i EtOH,
eth, MeOH
sl H2O; i EtOH,
eth, bz, MeOH
sl H2O; i EtOH,
eth, bz, MeOH
sl H2O; i EtOH,
eth, bz, py
sl H2O; i EtOH,
eth, bz; s dil
HCl, py
vs bz, eth, EtOH
i H2O; s os
sl H2O, diox,
ace; i chl; s
MeOH, HOAc
vs eth, EtOH,
chl
95 sub
vs H2O, EtOH; i
eth; sl chl
sl H2O
vs ace, EtOH,
chl
4/11/16 11:18 AM
Physical Constants of Organic Compounds
HO
N
H
HO
O
N
H
HO
N
O
HCl
HO
O
500
501
Apocodeine
HO
O O
OH
502
Apomorphine
CH2
OH
O
N
H
HO
H
HO
HO
H
503
Apomorphine, hydrochloride
CH2OH
OH
H
H
CH2OH
O
HO
HO
504
Aprobarbital
505
α-D-Arabinopyranose
L-Arabinitol
O
O OH
OH
OH HO
HO
OH
OH
O
O
S
O
Cl
O
OH
509
508
510
β-D-Arabinose
α-D-Arabinose
DL-Arabinose
6-O-α-L-Arabinopyranosyl-D-Glucose
O
HO
OH
OH
507
506
O OH
HO
O
HO
OH
OH
OH
OH
Aramite
Organic
N
H
3-31
O
OH
NH
O
N
H2N
N
511
512
Arecaidine
O
O
NH
OH
N
H
H2N
N
H
NH2
513
Arecoline
NH
OH
H2N
NH2
514
D-Arginine
O
N
H
OH
HCl
NH2
515
L-Arginine
L-Arginine, monohydrochloride
O
CH2OH
OH
O
OH
O
O
O
OH
O
O
O
O
O
H2N
O
O
HO
516
517
Artemisin
OH
HO
518
Ascaridole
519
L-Ascorbic acid
H2N
NH2
O
H2N
H 2O
OH
521
L-Asparagine
O
H
N
O
O
O
O
H2O
O
HO
NH2
O
523
L-Asparagine, monohydrate
NH2 OH
524
Aspartame
O
HO
NH2 OH
522
D-Asparagine, monohydrate
NH2
HO
O
OH
520
Ascorbyl palmitate
O
O
OH
NH2
O
OH
525
DL-Aspartic acid
L-Aspartic acid
N
NH
N
N
O
O
O
S
N
O
O H
OH
O
N
N
527
Aspergillic acid
O
528
Astemizole
H
N
H2N
H2N
F
526
OH
O
529
Asulam
Atenolol
N
HN
O
H
N
N
OH
Cl
H
530
Atisine
NH
OH
N
N
531
O
O
O
N
H
Atrazine
O
532
Atropine
N
N
533
Auramine hydrochloride
ClH
N
O
O
O
O
534
Aureothin
Physical Constants of Organic Compounds
3-32
No.
Name
535
Aurin
536
Aurin tricarboxylic acid,
triammonium salt
Avermectin B1a
3-Azabicyclo[3.2.2]nonane
1-Azabicyclo[2.2.2]octane
537
538
539
Synonym
Mol.
Wt.
Physical
Form
Mol. Form.
CAS RN
C19H14O3
603-45-2
290.312 dk red lf or
orth
Aluminon
C22H23N3O9
569-58-4
473.433 red-br pow
Abamectin
C48H72O14
C8H15N
C7H13N
71751-41-2 873.078
283-24-9
125.212
100-76-5
111.185 cry (eth)
152
Quinuclidine
mp/˚C
127.184 cry (bz)
244.205 cry
221
229
542
543
544
C12H23NO
C4H4N6O
C5H7N3O4
947-04-6
134-58-7
115-02-6
152.5
300
150 dec
545
Azathioprine
C9H7N7O2S
446-86-6
197.317
152.114
173.128 ye-grn orth
cry
277.263 ye cry
546
6-Azauridine
C8H11N3O6
54-25-1
245.189
158
547
Azetidine
C3H7N
503-29-7
57.095
548
2-Azetidinecarboxylic acid
C4H7NO2
2517-04-6
217 dec
549
2-Azetidinone
C3H5NO
930-21-2
101.105 cry (95%
MeOH)
71.078
550
Azidobenzene
C6H5N3
622-37-7
551
552
553
554
1-Azido-4-chlorobenzene
2-Azidoethanol
1-Azido-4-methylbenzene
(Azidomethyl)benzene
C6H4ClN3
C2H5N3O
C7H7N3
C7H7N3
555
556
557
558
Azinphos ethyl
Azinphos-methyl
1-Aziridineethanol
trans-Azobenzene
559
cis-Azobenzene
560
563
564
565
566
3,3’-Azobenzenedisulfonyl
chloride
1,1’-Azobiscyclohexanecarbonitrile
2,2’-Azobis[isobutyronitrile]
2,2’-Azobis[2-methylpropionitrile]
Azobutane
Azopropane
cis-Azoxybenzene
Diphenyldiazene 1-oxide, (E)
trans-Azoxybenzene
Diphenyldiazene 1-oxide, (Z)
567
568
Azoxyethane
Azulene
Diethyldiazine 1-oxide
Bicyclo[5.3.0]decapentaene
569
Balan
570
571
Barban
Barbital
N-Butyl-N-ethyl-2,6-dinitro-4- C13H16F3N3O4
(trifluoromethyl)aniline
C11H9Cl2NO2
5,5-Diethylbarbituric acid
C8H12N2O3
572
Barbituric acid
573
574
Bayleton
Bebeerine
Triadimefon
575
576
Benactyzine
Benactyzine hydrochloride
2-(Diethylamino)ethyl benzilate C20H25NO3
2-Diethylaminoethyl benzilate C20H26ClNO3
hydrochloride
Organic
561
562
HCP_Section_03.indb 32
Solubility
i H2O, bz; s
EtOH, alk; sl
eth, chl
s H2O; sl EtOH; i
peth
166500
1619-34-7
320-67-2
vs H2O, ace,
eth, EtOH
s ace
120 sub
vs H2O; sl EtOH,
ace, MeOH
sl H2O, EtOH,
chl
s H2O
243 dec
58(7)
0.843620 1.428725 vs ace, bz, eth,
EtOH
73.5
10615
119.124 pa ye oil
-27.5
7011
1.086020 1.558925
3296-05-7
1517-05-1
2101-86-2
622-79-7
153.569
87.080
133.151
133.151
20
9620
7540
180 dec
10823
1.263425
1.14624
1.052723
1.073019 1.534125
2642-71-9
86-50-0
1072-52-2
17082-12-1
345.377 nd
317.324
87.120
182.220 oran-red
mcl lf (al)
51.3(0.5)
72(2)
1110.001
trans-Diphenyldiazene
C12H16N3O3PS2
C10H12N3O3PS2
C4H9NO
C12H10N2
1.28420
1.4420
1.08825
1.20320
vs eth, EtOH,
chl
i H2O; sl EtOH,
eth
i H2O; s eth
vs H2O
vs eth, EtOH
i H2O; msc
EtOH, eth
reac alk
cis-Diphenyldiazene
C12H10N2
1080-16-6
182.220 oran-red pl
(peth)
C12H8Cl2N2O4S2
379.239 red nd (eth) 166.5
C14H20N4
10411588-0
2094-98-6
C8H12N4
78-67-1
164.208
C8H18N2
C6H14N2
C12H10N2O
C12H10N2O
2159-75-3
821-67-0
21650-65-7
20972-43-4
142.242
114.188
198.219
198.219
C4H10N2O
C10H8
16301-26-1 102.134 liq
275-51-4
128.171 bl or gr-blk
lf (al)
99
46
249.0(0.5)
1861-40-1
335.279
65.6(0.5)
1210.5
101-27-9
57-44-3
258.101
184.192 nd (w)
72.4(0.5)
189(1)
C4H4N2O3
C14H16ClN3O2
C36H38N2O6
liq
nD
157(3)
C7H13NO
C8H12N4O5
1H-Purine, 6-[(1-methyl-4nitro-1H-imidazol-5-yl)thio]2-β-D-Ribofuranosyl-1,2,4triazine-3,5(2H,4H)-dione
den
g cm –3
309 dec
1-Azabicyclo[2.2.2]octan-3-ol 3-Quinuclidinol
Azacitidine
4-Amino-1-β-D-ribofuranosyl1,3,5-triazine-2(1H)-one
Azacyclotridecan-2-one
8-Azaguanine
Azaserine
540
541
bp/˚C
244.336
-70.0
-29.0
67.88(0.03)
71.6(0.4)
i H2O; s lig
i H2O; sl EtOH,
eth
60
114
18
87
34.6
128.086 orth pr (w
248
+2)
43121-43-3 293.749
77.0(0.5)
477-60-1
594.696 cry (bz, eth, 221
chl-MeOH)
327.418 cry
363.878
1.456020
1.626678 sl H2O; s EtOH,
eth, bz, chl; vs
py
sl H2O; s EtOH,
eth, bz, HOAc,
lig
vs eth
100
67-52-7
302-40-9
57-37-4
168
300.0(0.6)
51
177.5
1.16620 1.63320
1.159026
i H2O; s EtOH,
eth
i H2O; s EtOH,
eth, ace, acid;
sl chl
1.22025
260 dec
sl H2O; s EtOH,
eth, ace, chl,
lig, tfa
s H2O, eth; sl
EtOH
1.2220
s EtOH, MeOH,
eth; vs ace,
chl
s H2O; i eth
4/11/16 11:18 AM
Physical Constants of Organic Compounds
3-33
HO
HO
HO
OH
O
OH
O
O
O
O
H
O
O
O
O
O
OH H
O NH4
O NH4
O
H
536
535
N H
OH
538
537
Aurin tricarboxylic acid, triammonium salt
Aurin
H
O
O NH4
O
O
O
O
3-Azabicyclo[3.2.2]nonane
Avermectin B1a
NH2
N
N
N
N
HO
540
539
OH
541
1-Azabicyclo[2.2.2]octan-3-ol
1-Azabicyclo[2.2.2]octane
O
O
OH
H
H
O
H2N
542
Azacitidine
H
N
N
N
N
543
Azacyclotridecan-2-one
8-Azaguanine
O
N
O
O
HO
N
O
N
S
O N
O N
N
544
N
N
H
N
N
N
N
547
N
N
556
N
S
O
P
O
O
N
N
553
554
1-Azido-4-methylbenzene
N N
N N
558
559
N
N
S
555
(Azidomethyl)benzene
Azinphos ethyl
HO O
O S
O OH
S O
N N
OH
557
Azinphos-methyl
2-Azetidinone
2-Azetidinecarboxylic acid
N
2-Azidoethanol
H
549
548
Azetidine
N
N
H
N
S
O
P
S
O
N
N
N
H
OH
552
1-Azido-4-chlorobenzene
O
N
OH
N
N
O
O
6-Azauridine
551
Azidobenzene
HO
N
Cl
550
N
546
Azathioprine
N
N
O
HO
545
Azaserine
O
HO
N
N
NH2
N
HN
1-Aziridineethanol
trans-Azobenzene
560
cis-Azobenzene
3,3’-Azobenzenedisulfonyl chloride
N
N N
N
N
561
1,1’-Azobiscyclohexanecarbonitrile
O
N N
N
N
N
N
562
2,2’-Azobis[isobutyronitrile]
N
O
N
O
N
N
F
567
568
Azoxyethane
trans-Azoxybenzene
O
H
N
Cl
O
O
570
Balan
O
N
O
569
Azulene
566
cis-Azoxybenzene
O
F
F
565
Azopropane
Cl
O
N
N
564
Azobutane
O
N
N
563
N N
O
N
H
H
N
O
O
571
Barban
N
H
572
Barbital
O
Cl
N
N
N
573
Bayleton
N
H
O
OH
H
N
O
OH
574
O
Bebeerine
O
O
HCl
HO
HO
O
O
N
575
Benactyzine
O
Barbituric acid
O
O
H
N
576
Benactyzine hydrochloride
Organic
HO
N
N
O
Physical Constants of Organic Compounds
3-34
No.
Name
577
578
Benalaxyl
Bendiocarb
579
Mol.
Wt.
Physical
Form
Organic
CAS RN
C20H23NO3
C11H13NO4
71626-11-4 325.402
22781-23-3 223.226
79
129.6(0.5)
Bendroflumethiazide
C15H14F3N3O4S2
73-48-3
421.415 cry
225
580
581
582
583
584
585
Benomyl
Bensulfuron-methyl
Bensulide
Bentazon
Benz[c]acridine
Benzaldehyde
C14H18N4O3
C16H18N4O7S
C14H24NO4PS3
C10H12N2O3S
C17H11N
C7H6O
17804-35-2
83055-99-6
741-58-2
25057-89-0
225-51-4
100-52-7
290.318
410.402
397.514
240.278
229.276 nd (dil al)
106.122 liq
dec
187
38.4(0.5)
139.7(0.5)
132
-57.12(0.05) 178.7(0.4)
586
587
588
Benzaldehyde hydrazone
cis-Benzaldehyde oxime
trans-Benzaldehyde oxime
C7H8N2
C7H7NO
C7H7NO
5281-18-5
622-32-2
622-31-1
120.152 lf
121.137 pr
121.137 nd (eth)
16
36.5
35
589
Benzaldehyde, phenylhydrazone
C13H12N2
588-64-7
196.247 nd (lig), pr
157.0
590
Benzaldehyde, (phenylmethylene)hydrazone
C14H12N2
588-68-1
208.258 ye pr (al)
93(1)
591
Benzamide
C7H7NO
55-21-0
121.137 mcl pr or pl 128(1)
(w)
306(2)
592
593
Benz[a]anthracene
1,2-Benzanthracene
Benz[a]anthracene-7,12-dione
C18H12
C18H10O2
56-55-3
2498-66-0
228.288 lf (al)
258.271
438
594
595
Benzanthrone
Benzene
[6]Annulene
C17H10O
C6H6
82-05-3
71-43-2
230.260
173.0(0.3)
78.112 orth pr or liq 5.538(0.002) 80.08(0.07)
596
Benzeneacetaldehyde
Phenylacetaldehyde
C8H8O
122-78-1
120.149
33.5
597
Benzeneacetamide
α-Phenylacetamide
C8H9NO
103-81-1
135.163
157
598
Benzeneacetic acid
Phenylacetic acid
C8H8O2
103-82-2
136.149 lf, pl (peth)
76.7(0.2)
268(2)
599
600
Benzeneacetic acid, hydrazide
Benzeneacetic anhydride
C8H10N2O
C16H14O3
937-39-3
1555-80-2
115.5
73.3
19512
601
602
603
604
Benzeneacetonitrile
Benzeneacetyl chloride
Benzenearsonic acid
Benzeneboronic acid
Benzyl cyanide
Phenylacetyl chloride
C8H7N
C8H7ClO
C6H7AsO3
C6H7BO2
140-29-4
103-80-0
98-05-5
98-80-6
150.177
254.280 pr or nd
(eth)
117.149 liq
154.594
202.040 cry (w)
121.930
605
606
607
Benzenebutanoic acid
Benzenebutanol
Benzenecarboperoxoic acid
4-Phenylbutanoic acid
4-Phenyl-1-butanol
Perbenzoic acid
C10H12O2
C10H14O
C7H6O3
1821-12-1
3360-41-6
93-59-4
51(1)
608
609
Benzenecarbothioamide
Benzenecarbothioic acid
C7H7NS
C7H6OS
2227-79-4
98-91-9
164.201 lf (w)
150.217
138.121 mcl pl
(peth)
137.203
138.187 ye pl (HOAc)
610
C7H9ClN2
1670-14-0
611
Benzenecarboximidamide,
monohydrochloride
1,2-Benzenediamine
o-Phenylenediamine
C6H8N2
95-54-5
612
1,3-Benzenediamine
m-Phenylenediamine
C6H8N2
108-45-2
613
1,4-Benzenediamine
p-Phenylenediamine
C6H8N2
106-50-3
614
1,2-Benzenediamine,
dihydrochloride
1,3-Benzenediamine,
dihydrochloride
1,4-Benzenediamine,
dihydrochloride
1,2-Benzenedicarbonyl
dichloride
C6H10Cl2N2
615-28-1
108.141 wh pl (bz,
eth)
181.062
C6H10Cl2N2
541-69-5
181.062
s H2O
C6H10Cl2N2
624-18-0
181.062
s H2O
C8H4Cl2O2
88-95-9
203.023
616
617
HCP_Section_03.indb 34
1,3-Benzodioxol-4-ol,
2,2-dimethyl-, methylcarbamate
12-Azabenz[a]anthracene
Benzenecarboxaldehyde
Benzylidene hydrazine
Benzoic acid amide
Phthaloyl chloride
mp/˚C
160(2)
168(1)
-22.1(0.5)
bp/˚C
den
g cm –3
Mol. Form.
615
Synonym
14014
200
11910
202(5)
232(2)
170250
42
296(2)
14014
10014
117
24
8610
140.3(0.6)
Solubility
i H2O, bz, eth; s
EtOH, ace
158 dec
219
156.612 orth pr (w
169
+2)
108.141 brsh ye lf
103(1)
(w) pl (chl)
108.141 orth (al)
65.5(0.9)
nD
1.2725
1.2520
1.22420
vs bz, eth, EtOH
1.040125 1.546320 sl H2O; msc
EtOH, eth; vs
ace, bz
s EtOH
1.111120 1.590820 vs bz, eth, EtOH
1.14520
s H2O; vs EtOH,
eth
sl EtOH, eth; s
ace, bz, liq
NH3
i H2O; s EtOH,
eth, ace, bz,
chl; sl ctc
1.0792130
sl H2O, eth, bz;
vs EtOH, ctc,
CS2
i H2O; vs EtOH
sl EtOH, eth, lig;
s ace; vs bz,
chl
sl bz
0.876520 1.501120 sl H2O; msc
EtOH, eth, ace,
chl; s ctc
1.027220 1.525520 sl H2O; s ace;
msc EtOH, eth
sl H2O, eth, bz;
s EtOH
1.2286
sl H2O, chl; vs
EtOH, eth; s
ace; i lig
vs eth, chl
1.020515 1.521125
1.168220 1.532520 vs eth
vs H2O, EtOH
sl H2O; s EtOH,
eth, bz
s H2O, EtOH, eth
1.521420
vs ace, bz, eth,
EtOH
1.2820
257(9)
282(18)
267
1.009658
1.604020 vs ace, bz, eth,
EtOH
s H2O, EtOH; sl
tfa
s H2O, eth, bz,
chl; vs EtOH
1.633958 vs H2O; s EtOH,
eth, bz
sl H2O; s EtOH,
eth, bz, chl
250 dec
15.5
284(10)
1.408920 1.568420
4/11/16 11:18 AM
Physical Constants of Organic Compounds
O
O
O
N
O
3-35
F
F
F
O
S
H 2N
O
O
N
H
O
O
577
578
Benalaxyl
O
H
N
O
S
N
O
N
H
H
N
H
579
Bendiocarb
O
H
N
Benomyl
O
H
N
O O
O
O
580
Bendroflumethiazide
O
S
O
N
N
O
O O
S
N
H
N
S
O
581
N
S O
N
O
H
O
P
O
S
582
Bensulfuron-methyl
N
583
Bensulide
584
Bentazon
Benz[c]acridine
N
585
NH2
N
OH
586
Benzaldehyde
N
587
Benzaldehyde hydrazone
OH
H
N
N
588
cis-Benzaldehyde oxime
Organic
O
589
trans-Benzaldehyde oxime
Benzaldehyde, phenylhydrazone
O
O
N
N
NH2
O
O
590
591
Benzaldehyde, (phenylmethylene)hydrazone
592
Benzamide
593
Benz[a]anthracene
O
Benz[a]anthracene-7,12-dione
595
596
N
O
600
Benzeneacetic anhydride
602
Benzeneacetonitrile
Benzeneacetic acid, hydrazide
O
As OH
OH
O
601
599
Benzeneacetic acid
Cl
OH
B
OH
603
Benzeneacetyl chloride
604
Benzenearsonic acid
Benzeneboronic acid
OOH
O
NH2
O
598
Benzeneacetamide
O
O
H
N
O
597
Benzeneacetaldehyde
Benzanthrone
OH
NH2
O
Benzene
594
S
NH2
OH
OH
O
605
606
Benzenebutanoic acid
607
Benzenebutanol
608
Benzenecarboperoxoic acid
Benzenecarbothioamide
NH2
OH
O
NH2
S
SH
NH2
NH2
NH2
NH
NH2
HCl
609
Benzenecarbothioic acid
610
Benzenecarboximidamide, monohydrochloride
611
NH2
612
1,2-Benzenediamine
613
1,3-Benzenediamine
1,4-Benzenediamine
NH2
NH2
NH2
Cl
2HCl
614
1,2-Benzenediamine, dihydrochloride
O
2HCl
NH2
NH2
615
2HCl
1,3-Benzenediamine, dihydrochloride
O
Cl
NH2
616
1,4-Benzenediamine, dihydrochloride
617
1,2-Benzenedicarbonyl dichloride
Physical Constants of Organic Compounds
3-36
mp/˚C
bp/˚C
den
g cm –3
43.5
276
1.388017 1.57047
100-20-9
203.023 nd or pl (lig) 83.5
258
sl H2O, EtOH; s
eth
s eth
C8H6O2
643-79-8
830.8
vs eth, EtOH
1,3-Benzenedicarboxaldehyde
C8H6O2
626-19-7
134.133 ye cry or nd 55.8
(lig)
134.133 nd (dil al)
89(2)
246
622
1,4-Benzenedicarboxaldehyde
C8H6O2
623-27-8
134.133 nd (w)
117
246
623
1,2-Benzenedicarboxamide
C8H8N2O2
88-96-0
164.162 cry
222
dec
sl H2O, eth, chl;
vs EtOH; s
ace, bz
sl H2O; vs EtOH;
s eth, chl, alk
sl H2O, EtOH; i
eth
624
1,4-Benzenedicarboxamide
C8H8N2O2
3010-82-0
322.3
625
Bis(2-butoxyethyl) phthalate
C20H30O6
117-83-9
Bis(2-methoxyethyl) phthalate
C14H18O6
117-82-8
282.289
-60.0
Diallyl phthalate
C14H14O4
131-17-9
246.259
Dipropyl phthalate
C14H18O4
131-16-8
250.291 liq
629
1,2-Benzenedicarboxylic acid,
bis(2-butoxyethyl) ester
1,2-Benzenedicarboxylic acid,
bis(2-methoxyethyl) ester
1,2-Benzenedicarboxylic acid,
diallyl ester
1,2-Benzenedicarboxylic acid,
dipropyl ester
1,3-Benzenedimethanamine
164.162 nd (w), pl
(HOAc)
366.448
m-Xylene diamine
C8H12N2
1477-55-0
136.194
630
1,2-Benzenedimethanol
C8H10O2
612-14-6
66(3)
1453
631
1,3-Benzenedimethanol
C8H10O2
626-18-6
138.164 pl (eth,
peth)
138.164 nd (bz)
57
15613
632
1,4-Benzenedimethanol
C8H10O2
589-29-7
138.164 nd (w)
117.5
1401
633
1,2-Benzenediol, diacetate
C10H10O4
635-67-6
194.184 nd (al)
64.5
1429
634
1,4-Benzenediol, diacetate
C10H10O4
1205-91-0
194.184 pl (w, al)
123.5
635
C13H10O3
136-36-7
214.216
134.5
C6H6O6S2
C6H4Cl2O4S2
98-48-6
585-47-7
238.238 hyg cry
275.130
61.8
19510.5
638
1,3-Benzenediol,
monobenzoate
1,3-Benzenedisulfonic acid
1,3-Benzenedisulfonyl
dichloride
1,2-Benzenedithiol
C6H6S2
17534-15-5 142.242
28.5
238.5
639
640
1,3-Benzenedithiol
Benzeneethanamine
C6H6S2
C8H11N
626-04-0
64-04-0
142.242 lf
121.180 liq
27
<0
245
204(4)
641
C8H12ClN
156-28-5
157.641 pl or lf (al)
218.5
642
Benzeneethanamine,
hydrochloride
Benzeneethanol
Phenethyl alcohol
C8H10O
60-12-8
122.164 liq
-19(2)
643
Benzenehexacarboxylic acid
Mellitic acid
C12H6O12
517-60-2
342.169 nd (al)
287 dec
644
C7H10ClN
3287-99-8
143.614
258.3
C7H7ClO2S
1939-99-7
93
C7H7FO2S
329-98-6
190.648 pr (eth), nd
(bz)
174.193
92.0
647
Benzenemethanamine,
hydrochloride
Benzenemethanesulfonyl
chloride
Benzenemethanesulfonyl
fluoride
Benzenemethanethiol
Thiobenzyl alcohol
C7H8S
100-53-8
124.204 liq
-30
199(1)
648
Benzenepentanoic acid
5-Phenylvaleric acid
C11H14O2
2270-20-4
59(1)
19030
649
650
Benzenepentanol
Benzenepropanal
Hydrocinnamic aldehyde
C11H16O
C9H10O
178.228 pl (w), pr
(peth)
10521-91-2 164.244
104-53-0
134.174 mcl
47
15520
224
0.972520
1.019020
651
Benzenepropanenitrile
Hydrocinnamonitrile
C9H9N
645-59-0
-1
261
1.001620
652
653
Benzenepropanethiol
Benzenepropanoic acid
Hydrocinnamic acid
C9H12S
C9H10O2
24734-68-7 152.256
501-52-0
150.174 nd (w)
48.4(0.3)
12123
284(2)
1.0125
1.071249
654
Benzenepropanol
Hydrocinnamyl alcohol
C9H12O
122-97-4
<-18
241(4)
0.99525
No.
Name
618
620
1,3-Benzenedicarbonyl
dichloride
1,4-Benzenedicarbonyl
dichloride
1,2-Benzenedicarboxaldehyde
621
619
Organic
626
627
628
636
637
645
646
HCP_Section_03.indb 36
Synonym
Phthalamide
1-Amino-2-phenylethane
Mol. Form.
CAS RN
Mol.
Wt.
Physical
Form
C8H4Cl2O2
99-63-8
203.023 pr(eth)
C8H4Cl2O2
131.174 liq
136.190
nD
Solubility
409(18)
23010
1.159620
1614
-31.0
319(2)
1.076720
247
1.05220
i H2O; s EtOH,
eth
vs H2O, eth,
EtOH
s H2O, EtOH; vs
eth; sl bz
vs H2O, eth,
EtOH
vs H2O, ace,
eth, EtOH
i H2O; vs EtOH,
eth, chl; s peth
s H2O; vs EtOH,
eth, chl, lig
1.161018
0.873125
220(3)
0.964025 1.529025
vs EtOH, eth,
bz; s AcOEt
vs bz, eth, EtOH
s H2O, ctc; vs
EtOH, eth
vs H2O, EtOH
1.020220 1.532520 sl H2O; msc
EtOH, eth
vs H2O; s EtOH,
sulf
vs H2O, EtOH
vs eth, bz
1.05820
1.515120 i H2O; vs EtOH,
eth; sl ctc; s
CS2
sl H2O; vs EtOH;
s os
1.515620 vs eth, EtOH
i H2O; vs EtOH;
msc eth
1.526628 s EtOH, eth; sl
chl
1.549420
s H2O, EtOH,
eth, ctc, CS2;
vs bz
1.535725 s H2O, ctc; msc
EtOH, eth
4/11/16 11:18 AM
Physical Constants of Organic Compounds
Cl
Cl
O
3-37
O
O
O
O
Cl
O
Cl
618
1,3-Benzenedicarbonyl dichloride
O
621
620
1,4-Benzenedicarbonyl dichloride
H2N
O
O
619
1,3-Benzenedicarboxaldehyde
1,2-Benzenedicarboxaldehyde
O
O
O
623
O
O
O
O
NH2
1,2-Benzenedicarboxamide
1,4-Benzenedicarboxaldehyde
O
O
H 2N
622
NH2
O
O
624
626
1,2-Benzenedicarboxylic acid, bis(2-butoxyethyl) ester
1,2-Benzenedicarboxylic acid, bis(2-methoxyethyl) ester
NH2
O
O
O
O
625
1,4-Benzenedicarboxamide
O
O
O
OH
O
O
O
O
O
OH
NH2
O
627
628
1,2-Benzenedicarboxylic acid, diallyl ester
Organic
O
629
1,2-Benzenedicarboxylic acid, dipropyl ester
630
1,3-Benzenedimethanamine
1,2-Benzenedimethanol
O
O
OH
O
O
OH
O
O
O
OH
O
O
HO
631
1,3-Benzenedimethanol
633
1,4-Benzenedimethanol
634
1,2-Benzenediol, diacetate
1,4-Benzenediol, diacetate
635
1,3-Benzenediol, monobenzoate
O
Cl S O
O
HO S O
SH
SH
O
OH
O
632
S
O
OH
S
O
Cl
636
1,3-Benzenedisulfonic acid
O
SH
637
638
1,3-Benzenedisulfonyl dichloride
OH
HOOC
HCl
641
Benzeneethanamine, hydrochloride
639
1,2-Benzenedithiol
HOOC
NH2
NH2
SH
642
640
Benzeneethanamine
COOH
COOH
Benzenehexacarboxylic acid
O
S
O
Cl
NH2
COOH
COOH
643
Benzeneethanol
1,3-Benzenedithiol
HCl
644
Benzenemethanamine, hydrochloride
645
Benzenemethanesulfonyl chloride
O
O
S
O
F
647
646
Benzenemethanesulfonyl fluoride
OH
OH
SH
649
648
Benzenemethanethiol
Benzenepentanol
Benzenepentanoic acid
O
N
650
Benzenepropanal
OH
SH
O
651
Benzenepropanenitrile
652
Benzenepropanethiol
653
Benzenepropanoic acid
OH
654
Benzenepropanol
Physical Constants of Organic Compounds
3-38
Organic
No.
Name
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
655
Benzenepropanol carbamate
Phenprobamate
C10H13NO2
673-31-4
179.216
103.4(0.5)
656
657
Benzenepropanoyl chloride
Benzeneseleninic acid
Phenylseleninic acid
C9H9ClO
C6H6O2Se
645-45-4
6996-92-5
168.619
189.07
124.5
658
Benzeneselenol
C6H6Se
645-96-5
157.07
659
Benzenesulfinic acid
C6H6O2S
618-41-7
142.176 pr (w)
84
dec
660
661
Benzenesulfinyl chloride
Benzenesulfonamide
C6H5ClOS
C6H7NO2S
4972-29-6
98-10-2
160.621 pl (peth)
157.191 lf, nd (w)
38
156(1)
711.5
1.346925 1.347025
662
Benzenesulfonic acid
Besylic acid
C6H6O3S
98-11-3
158.175 nd (bz)
65
663
Benzenesulfonyl chloride
Phenylsulfonyl chloride
C6H5ClO2S
98-09-9
176.621 liq
14.5
252(7)
1.347015
664
665
Benzenesulfonyl fluoride
1,2,4,5-Benzenetetracarboxylic acid
Benzenethiol
Phenylsulfonyl fluoride
Pyromellitic acid
C6H5FO2S
C10H6O8
368-43-4
89-05-4
160.166
254.150 tcl pr (w+2) 271(2)
203.5
1.328620 1.493218
Phenyl mercaptan
C6H6S
108-98-5
110.177 liq
-14.87(0.05) 169.1(0.2)
C9H3Cl3O3
4422-95-1
265.477
36.3
Hemimellitic acid
C9H6O6
569-51-7
210.140 pr (al)
209(2)
Trimellitic acid
C9H6O6
528-44-9
219
vs H2O, eth,
EtOH
C9H6O6
554-95-0
380
sl H2O; vs EtOH,
eth
C9H3ClO4
1204-28-0
210.140 nd (w) cry
(al) cry
(HOAc)
210.140 pr or nd
(w+1)
210.571
C18H18O6
2694-54-4
330.332
<-30
666
667
668
669
670
1,3,5-Benzenetricarbonyl
trichloride
1,2,3-Benzenetricarboxylic
acid
1,2,4-Benzenetricarboxylic
acid
Physical
Form
mp/˚C
bp/˚C
225 dec
1.13521
1.9320
183.6
1.486515
18016
673
Pyrogallol
C6H6O3
87-66-1
126.110 lf or nd (bz) 125.5(0.5)
674
1,2,4-Benzenetriol
Hydroxyhydroquinone
C6H6O3
533-73-3
675
1,3,5-Benzenetriol
Phloroglucinol
C6H6O3
108-73-6
126.110 pl (eth), lf or 140.5
pl (w)
126.110 lf or pl (w
216(1)
+2)
676
1,2,4-Benzenetriol triacetate
C12H12O6
613-03-6
252.219
99
677
Benzestrol
C20H26O2
85-95-0
298.419 cry (al)
164
678
Benzethonium chloride
C27H42ClNO2
121-54-0
448.081 pl (chl/eth)
165 (hyd)
679
3,3’-Dicarboxybenzidine
C14H12N2O4
2130-56-5
272.256 nd
300 dec
680
Benzidene-3,3’-dicarboxylic
acid
p-Benzidine
[1,1’-Biphenyl]-4,4’-diamine
C12H12N2
92-87-5
184.236 nd (w)
127.0(0.5)
401
681
Benzil
Diphenylethanedione
C14H10O2
134-81-6
210.228 ye pr (al)
94.84(0.03)
332(13)
682
1H-Benzimidazol-2-amine
C7H7N3
934-32-7
133.151 pl (w)
231.9(0.3)
683
1H-Benzimidazole
51-17-2
118.136 orth bipym
pl (w)
172.2(0.9)
684
1H-Benzimidazole-2-aceto­
nitrile
1H-Benz[de]isoquinoline1,3(2H)-dione
Benzo[c]chrysene
Benzo[g]chrysene
1H,3H-Benzo[1,2-c:4,5-c’]
difuran-1,3,5,7-tetrone
1,3,2-Benzodioxaborole
1,3-Benzodioxol-5-amine
1,3-Benzodioxole
C9H7N3
4414-88-4
157.172
208.4
C12H7NO2
81-83-4
197.190 nd (chl-al)
300
C22H14
C22H14
C10H2O6
194-69-4
196-78-1
89-32-7
278.346 nd (AcOH)
278.346 nd (AcOH)
218.119
125.4(0.5)
114.5
286(2)
C6H5BO2
C7H7NO2
C7H6O2
274-07-7
119.914
14268-66-7 137.137
274-09-9
122.122
672
685
686
687
688
689
690
691
HCP_Section_03.indb 38
4-(Chloroformyl)phthalic
anhydride
N,N’-Methenyl-o-phenylenedi- C7H6N2
amine
Benzo[a]triphenylene
nD
Solubility
i H2O; s EtOH,
chl
s eth, CS2
sl H2O; i bz; vs
alk
i H2O; s EtOH;
vs eth, ctc
sl H2O; s EtOH,
eth, bz; i peth
s eth, chl
sl H2O, tfa; s
EtOH, eth
vs H2O, EtOH; i
eth; sl bz; s
HOAc
i H2O; vs EtOH;
s eth, ctc
s EtOH, eth
sl H2O; s EtOH
1.077520 1.589320 i H2O; s EtOH,
eth, bz; sl ctc
s chl
1.54620
1,3,5-Benzenetricarboxylic
acid
1,2,4-Benzenetricarboxylic
acid 1,2-anhydride,
4-chloride
1,2,4-Benzenetricarboxylic
acid, triallyl ester
1,2,3-Benzenetriol
671
den
g cm –3
vs eth, EtOH
66
12
42
1.16420
307(4)
1.4534
sub
1.4625
1.561134
300
sl H2O, eth,
DMSO; s EtOH
i H2O; vs EtOH,
eth; s ace; sl
ctc
s H2O, EtOH,
ace; sl eth, bz,
DMSO
sl H2O, eth; vs
EtOH; i bz; s
dil alk
1.084102
>360
88156
14416
169(1)
vs H2O, EtOH,
eth, NH3; s
ace; i bz
vs H2O, EtOH,
eth; i bz, chl
sl H2O; vs EtOH,
eth, bz, py; s
ace
s EtOH, chl,
MeOH
vs ace, eth,
EtOH, HOAc
vs H2O; s ace,
chl, EtOH
1.270020 1.507020
1.06425
1.539820
4/11/16 11:18 AM
Physical Constants of Organic Compounds
O
655
656
660
661
662
666
1,2,4,5-Benzenetetracarboxylic acid
O
O
OH
O
O
O
669
1,2,3-Benzenetricarboxylic acid
1,2,4-Benzenetricarboxylic acid
O
OH
OH
O
O
OH
OH
OH
O
O
O
HO
668
1,3,5-Benzenetricarbonyl trichloride
Cl
OH
O
O
OH
OH
O
OH
OH
O
O
664
Benzenesulfonyl fluoride
O
Cl
667
Benzenethiol
O
1,3,5-Benzenetricarboxylic acid
663
Cl
O
COOH
665
F
O S O
Benzenesulfonyl chloride
SH
HOOC
670
OH
Benzenesulfinic acid
Cl
O S O
Benzenesulfonic acid
Cl
O
S
659
658
Benzeneselenol
OH
O S O
Benzenesulfonamide
COOH
COOH
HO
O
SeH
Benzeneseleninic acid
NH2
O S O
Benzenesulfinyl chloride
HO
OH
657
Benzenepropanoyl chloride
Cl
S
Se
Cl
NH2
Benzenepropanol carbamate
O
O
O
Organic
O
3-39
O
671
O
OH
672
1,2,4-Benzenetricarboxylic acid 1,2-anhydride, 4-chloride
1,2,4-Benzenetricarboxylic acid, triallyl ester
HO
OH
673
674
1,2,3-Benzenetriol
1,2,4-Benzenetriol
OH
675
1,3,5-Benzenetriol
HO
O
O
O
O
Cl
O
O
O
O
N
676
1,2,4-Benzenetriol triacetate
OH
H 2N
HO
O
O
HO
677
Benzestrol
H2N
NH2
679
678
Benzidene-3,3’-dicarboxylic acid
Benzethonium chloride
NH2
680
p-Benzidine
O
O
O
N
N
H
681
Benzil
NH2
682
N
N
N
H
N
H
683
1H-Benzimidazol-2-amine
1H-Benzimidazole
O
NH
O
N
684
1H-Benzimidazole-2-acetonitrile
685
1H-Benz[de]isoquinoline-1,3(2H )-dione
686
Benzo[c]chrysene
O
O
O
H2N
O
O
O
B H
O
O
687
Benzo[g]chrysene
688
1H,3H-Benzo[1,2-c:4,5-c’]difuran-1,3,5,7-tetrone
O
689
1,3,2-Benzodioxaborole
O
O
690
1,3-Benzodioxol-5-amine
691
1,3-Benzodioxole
Physical Constants of Organic Compounds
3-40
No.
Name
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
692
1,3-Benzodioxole-5-carbox­
aldehyde
Piperonal
C8H6O3
120-57-0
693
1,3-Benzodioxole-5-carboxylic Piperonylic acid
acid
1,3-Benzodioxole-5-ethanamine
1,3-Benzodioxole-5-methanamine
1,3-Benzodioxole-5-methanol
C8H6O4
694
695
696
697
698
Physical
Form
den
g cm –3
Organic
mp/˚C
bp/˚C
150.132
37(1)
263
nD
94-53-1
166.132
229
C9H11NO2
1484-85-1
165.189
16620
1.22520
1.562020
C8H9NO2
2620-50-0
151.163
13913
1.21425
1.563520
C8H8O3
495-76-1
152.148 nd (peth)
58
15716
sl H2O; s EtOH,
eth, bz, chl; i
lig
C7H6O3
C12H10O4
533-31-3
136-72-1
138.121
218.205 nd (al), ye
nd (sub)
64.9
215.8
sub
vs EtOH
C19H12O2
604-59-1
272.297 ye pl (al)
157
C20H12
C20H12
205-99-2
205-82-3
168.4(0.7)
165.2(0.7)
C20H12
207-08-9
C17H12
238-84-6
C17H12
C8H6O
243-17-4
271-89-6
252.309 nd (bz)
252.309 ye pl (al) nd
(HOAc)
252.309 pa ye nd
(bz)
216.277 pl (ace or
HOAc)
216.277
118.133
496-41-3
553-86-6
7169-34-8
1646-26-0
480-96-6
613-94-5
162.142 nd (w)
134.133
134.133 red nd (al)
160.170
136.108
136.151 pl (w)
sl H2O; vs EtOH;
msc eth; s
ace, chl
699
1,3-Benzodioxol-5-ol
trans,trans-5-(1,3-Benzodioxol-5-yl)-2,4-pentadienoic
acid
7,8-Benzoflavone
700
701
Benzo[b]fluoranthene
Benzo[j]fluoranthene
2-Phenyl-4H-naphtho[1,2-b]­
pyran-4-one
Benz[e]acephenanthrylene
Dibenzo[a,jk]fluorene
702
Benzo[k]fluoranthene
2,3,1’,8’-Binaphthylene
703
11H-Benzo[a]fluorene
704
705
11H-Benzo[b]fluorene
Benzofuran
706
707
708
709
710
711
2-Benzofurancarboxylic acid
2(3H)-Benzofuranone
3(2H)-Benzofuranone
1-(2-Benzofuranyl)ethanone
Benzofurazan, 1-oxide
Benzohydrazide
Benzoic acid, hydrazide
C9H6O3
C8H6O2
C8H6O2
C10H8O2
C6H4N2O2
C7H8N2O
712
Benzoic acid
Benzenecarboxylic acid
C7H6O2
65-85-0
122.122 mcl lf or nd 122.340​
(0.005)
250.2(0.6)
1.265915 1.504132
713
Benzoic anhydride
C14H10O3
93-97-0
226.227 pr (eth)
42.6(0.8)
360
1.98915
714
Benzoin
343(13)
1.31020
715
Piperinic acid
Coumarone
Coumarilic acid
217(1)
480
189.6(0.5)
405
215(5)
<-18
401
172(6)
192.5
50
102.5
76
72(1)
115
312.5
249
15215
12611
1.091325 1.561517
sl EtOH, chl; s
sulf
i H2O; msc bz
i H2O; sl EtOH,
HOAc
i H2O; s EtOH,
bz, HOAc
i H2O; sl EtOH; s
eth, bz, chl
i H2O
i H2O; s EtOH,
eth
vs EtOH
1.223614
vs bz
s H2O
1.28080
267 dec
C14H12O2
579-44-2
212.244
137(2)
Benzonitrile
2-Hydroxy-1,2-diphenylethanone, (±)
Phenyl cyanide
C7H5N
100-47-0
103.122 liq
-12.82(0.02) 191(1)
716
Benzo[ghi]perylene
1,12-Benzperylene
C22H12
191-24-2
280(1)
717
Benzo[c]phenanthrene
Tetrahelicene
C18H12
195-19-7
276.330 ye-grn lf
(bz)
228.288
718
Benzophenone
Diphenyl ketone
C13H10O
119-61-9
719
720
Benzophenone hydrazone
Benzophenone, oxime
Diphenyl ketoxime
C13H12N2
C13H11NO
5350-57-2
574-66-3
182.217 (α) orth pr
48.0(0.2)
(al); (β) mcl
pr
196.247
97.3
197.232 nd (al)
144
721
C17H6O7
2421-28-5
322.226
216
722
3,3’,4,4’-Benzophenonetetra- 4,4’-Carbonyldiphthalic
carboxylic acid dianhydride
anhydride
Benzo-2-phenylhydrazide
C13H12N2O
532-96-7
168
314
723
Benzopurpurine 4B
C.I. Direct Red 2, disodium salt C34H26N6Na2O6S2
992-59-6
212.246 pr (al), nd
(w)
724.716 br pow
724
725
1,2-Chromene
1,4,5,8-Naphthalenetetracarboxylic acid anhydride
Isocoumarin
C9H8O
C14H4O6
254-04-6
81-30-1
132.159
268.178 nd (al)
450
132102
320 sub
726
2H-1-Benzopyran
[2]Benzopyrano[6,5,4-def]­[2]­
benzopyran-1,3,6,8-tetrone
1H-2-Benzopyran-1-one
C9H6O2
491-31-6
146.143 pl (bz)
47
286
727
2H-1-Benzopyran-2-one
Coumarin
C9H6O2
91-64-5
146.143 orth pym
(eth)
68(3)
301.7
0.93520
728
4H-1-Benzopyran-4-one
C9H6O2
491-38-3
146.143 nd (peth w) 57.11(0.04)
sub
1.290020
HCP_Section_03.indb 40
Solubility
1.576715
1.009315 1.528920 sl H2O; msc
EtOH; vs ace,
bz; s ctc
i H2O
67(2)
305.9(0.2)
s H2O, EtOH; sl
eth, ace, chl
sl H2O; vs EtOH,
eth; s ace, bz,
chl
i H2O, lig; s
EtOH, eth; sl
chl
vs EtOH, chl
1.11118
1.607719
i H2O; sl EtOH,
lig
i H2O; vs EtOH,
eth, chl, ace; s
bz
22755
i H2O; vs EtOH,
eth, chl, ace; s
bz
1.099316 1.586924
sl H2O, eth; s
EtOH, bz, chl
s H2O, EtOH, ac,
H2SO4
i H2O
i H2O; s Na2CO3,
HOAc
i H2O; vs EtOH,
eth, bz, CS2
s H2O, EtOH,
alk; vs eth,
chl, py
sl H2O; s EtOH,
eth, bz, chl
4/11/16 11:18 AM
Physical Constants of Organic Compounds
3-41
O
O
O
H2N
O
HO
O
O
693
1,3-Benzodioxole-5-carboxaldehyde
694
1,3-Benzodioxole-5-carboxylic acid
O
HO
O
O
O
O
692
O
H2N
695
1,3-Benzodioxole-5-ethanamine
696
1,3-Benzodioxole-5-methanamine
1,3-Benzodioxole-5-methanol
O
O
HO
O
O
HO
O
697
698
700
699
trans,trans-5-(1,3-Benzodioxol-5-yl)-2,4-pentadienoic acid
701
Benzo[b]fluoranthene
7,8-Benzoflavone
Benzo[j]fluoranthene
Organic
1,3-Benzodioxol-5-ol
O
O
O
O
702
Benzo[k]fluoranthene
703
704
11H-Benzo[a]fluorene
O
O
709
710
1-(2-Benzofuranyl)ethanone
OH
N
H
N
O
711
Benzofurazan, 1-oxide
O
706
707
2-Benzofurancarboxylic acid
O
O
O
O
3(2H )-Benzofuranone
Benzofuran
N
O
708
705
11H-Benzo[b]fluorene
O
OH
O
2(3H )-Benzofuranone
OH
O
NH2
Benzohydrazide
712
713
Benzoic acid
Benzoic anhydride
NH2
N
O
N
O
O
O
714
Benzoin
OH
N
715
716
Benzonitrile
O
Benzo[ghi]perylene
O
O
Benzophenone, oxime
O
H
N
O
724
2H-1-Benzopyran
721
3,3’,4,4’-Benzophenonetetracarboxylic acid dianhydride
O
O
O
O
O
O
725
718
719
Benzophenone
Benzophenone hydrazone
NH2
NH2
O
O
O
720
717
Benzo[c]phenanthrene
[2]Benzopyrano[6,5,4-def][2]benzopyran-1,3,6,8-tetrone
N
O
N
H
N
N
SO3Na
N
SO3Na
722
723
Benzo-2-phenylhydrazide
Benzopurpurine 4B
O
O
O
726
1H-2-Benzopyran-1-one
O
727
O
2H-1-Benzopyran-2-one
O
728
4H-1-Benzopyran-4-one
Physical Constants of Organic Compounds
3-42
Mol.
Wt.
Physical
Form
Organic
No.
Name
Synonym
Mol. Form.
CAS RN
729
730
Benzo[a]pyrene
Benzo[e]pyrene
2,3-Benzopyrene
1,2-Benzpyrene
C20H12
C20H12
50-32-8
192-97-2
731
Benzo[f]quinoline
β-Naphthoquinoline
C13H9N
85-02-9
732
Benzo[h]quinoline
C13H9N
230-27-3
733
p-Benzoquinone
2,5-Cyclohexadiene-1,4-dione C6H4O2
106-51-4
734
735
2,1,3-Benzothiadiazole
2-Benzothiazolamine
2-Aminobenzothiazole
C6H4N2S
C7H6N2S
273-13-2
136-95-8
108.095 ye mcl pr
113(2)
(w)
136.174
43.7(0.4)
150.201 pl (w), lf (w) 132
736
6-Benzothiazolamine
6-Aminobenzothiazole
C7H6N2S
533-30-2
150.201 pr (w)
87
737
Benzothiazole
Benzosulfonazole
C7H5NS
95-16-9
135.187
2.5(0.1)
738
2(3H)-Benzothiazolethione
2-Mercaptobenzothiazole
C7H5NS2
149-30-4
182(1)
739
2(3H)-Benzothiazolethione,
sodium salt
2(3H)-Benzothiazolone
C7H4NNaS2
2492-26-4
167.252 pa ye mcl
nd(al,
MeOH)
189.234
C7H5NOS
934-34-9
139
C7H7N3S
615-21-4
151.186 pr (dil al),
nd
165.216
202.8
C13H9NOS
C8H6S
3411-95-8
95-15-8
227.281 nd or lf (al)
134.199 lf
131
31.33(0.03)
C9H6O2S
6314-28-9
178.208 nd (w)
240.5
C6H5N3
95-14-7
119.124 nd (chl or
bz)
100
278.346 nd (al,
205
HOAc)
184.170 nd or pr (bz) 129.5
740
741
2(3H)-Benzothiazolone,
hydrazone
2-(2-Benzothiazolyl)phenol
Benzo[b]thiophene
Thianaphthene
745
Benzo[b]thiophene-2-carboxylic acid
1H-Benzotriazole
Thionaphthene-2-carboxylic
acid
1,2,3-Triaza-1H-indene
746
Benzo[b]triphenylene
C22H14
215-58-7
747
3H-2,1-Benzoxathiol-3-one
1,1-dioxide
2H-3,1-Benzoxazine-2,4(1H)dione
C7H4O4S
81-08-3
C8H5NO3
118-48-9
C7H5NO
742
743
744
748
1-Oxa-3-azaindene
252.309
252.309 pa ye nd
(bz-MeOH)
179.217 lf (peth or
w)
179.217 lf (eth), pl
(peth)
bp/˚C
179(2)
180(3)
311
92(2)
352
50.94(0.05)
341.3(0.3)
1.234020
sub
1.31820
234.6(0.6)
Solubility
i H2O; vs chl
i H2O
1.246020 1.637920
1.4220
sl H2O; vs EtOH,
bz, eth; s ace
sl H2O; s EtOH,
eth, ace, bz,
ctc
sl H2O, peth; s
EtOH, eth, chl
sl H2O; s EtOH,
eth, chl, con
HCl
i H2O, eth; s
EtOH
sl H2O; vs EtOH,
eth, CS2; s ace
i H2O; s EtOH; sl
eth, bz, DMSO
sl H2O
243 dec
273-53-0
163.131 pr (al, gl
HOAc) cry
(al)
119.121 pr (dil al)
29.36(0.02)
360
1793
220.9(0.4)
i H2O; vs EtOH,
eth
s EtOH
1.148432 1.637437 i H2O; vs EtOH;
s eth, ace, bz;
sl chl
vs eth
20415
sl H2O; s EtOH,
bz, chl, tol,
DMF
i H2O; vs bz
18418
vs bz, chl
185.3(0.5)
Benzoxazole
750
2(3H)-Benzoxazolethione
C7H5NOS
2382-96-9
151.186 nd (w)
195.1(0.5)
751
2(3H)-Benzoxazolone
C7H5NO2
59-49-4
135.121
140.0(0.4)
335
752
2-(2-Benzoxazolyl)phenol
C13H9NO2
835-64-3
123.5
338
753
N-Benzoyl-DL-alanine
C10H11NO3
165.5
dec
754
755
756
4-(Benzoylamino)-2-hydroxybenzoic acid
Benzoyl azide
2-Benzoylbenzoic acid
757
Benzoylpas
C14H11NO4
211.216 pink nd (al,
HOAc)
1205-02-3 193.199 pl, pr or lf
(eth)
13898-58-3 257.242
Benzazide
C7H5N3O
C14H10O3
582-61-6
85-52-9
147.134 pl (ace)
32
226.227 tcl nd (w+1) 129.0(0.4)
exp
4-Benzoylbenzoic acid
C14H10O3
611-95-0
199
sub
758
2-Benzoylbenzoic acid,
hydrazide
C14H12N2O2
787-84-8
226.227 nd (HOAc),
pl (al) mcl
lf (w)
240.257 nd (al)
759
760
761
4-Benzoylbiphenyl
Benzoyl bromide
Benzoyl chloride
4-Phenylbenzophenone
Benzoic acid, bromide
Benzenecarbonyl chloride
C19H14O
C7H5BrO
C7H5ClO
2128-93-0
618-32-6
98-88-4
258.313
185.018 liq
140.567 liq
101.5
-24
-0.5(0.2)
420
220(10)
201(8)
762
763
764
765
Benzoyl cyclohexane
Benzoylecgonine
Benzoylferrocene
Benzoyl fluoride
Cyclohexyl phenyl ketone
C13H16O
C16H19NO4
C17H14FeO
C7H5FO
712-50-5
519-09-5
1272-44-2
455-32-3
188.265 nd (peth)
289.327 nd (w)
290.137
124.112 liq
59.5
195
108(1)
-28
16418
HCP_Section_03.indb 42
nD
206
749
Benzoic acid, fluoride
den
g cm –3
mp/˚C
1.175420 1.559420
sl H2O, EtOH,
ace; i eth, bz,
chl
i H2O; s EtOH,
sulf
sl H2O, ace,
EtOH; vs eth,
HOAc
sl H2O; s EtOH,
eth, tfa
sl H2O; vs EtOH;
s eth, ace, bz
s H2O, EtOH; sl
eth, DMSO
260.5
1.168035
238(3)
vs eth, EtOH
vs EtOH, eth; s
bz; sl chl
sl H2O, tfa, bz; s
EtOH, eth,
HOAc
sl H2O; i EtOH,
eth, chl; s
MeOH
1.57015 1.586825 msc eth
1.212020 1.553720 msc eth; s bz,
ctc, CS2
vs bz, EtOH
154.5
1.140020
vs EtOH, eth; s
ctc
4/11/16 11:18 AM
Physical Constants of Organic Compounds
3-43
O
N
N
S
N
730
H
N
N
NH2
S
NH
735
H
N
S
S
S
737
S
NH
NH2
739
2(3H )-Benzothiazolethione, sodium salt
2-(2-Benzothiazolyl)phenol
N
743
O
O
S
O O
N
H
OH
744
Benzo[b]thiophene
O
Benzo[b]thiophene-2-carboxylic acid
O
747
Benzo[b]triphenylene
S
S
742
N
H
746
O
S
N
745
SH
S
N
2(3H )-Benzothiazolone, hydrazone
1H-Benzotriazole
S
S
N Na
N
S
2(3H )-Benzothiazolethione
741
2(3H )-Benzothiazolone
2,1,3-Benzothiadiazole
HO
S
740
734
p-Benzoquinone
738
Benzothiazole
N
OH
S
N
736
733
Benzo[h]quinoline
N
6-Benzothiazolamine
N
O
732
Benzo[f]quinoline
H 2N
S
2-Benzothiazolamine
H
N
731
Benzo[e]pyrene
Organic
729
Benzo[a]pyrene
N
O
N
O
O
748
3H-2,1-Benzoxathiol-3-one 1,1-dioxide
749
2H-3,1-Benzoxazine-2,4(1H )-dione
Benzoxazole
HO
H
N
N
OH
O
O
H
N
N
SH
S
O
750
O
752
2(3H )-Benzoxazolone
O
O
N
H
O
751
2(3H )-Benzoxazolethione
O
HO
N
O
2-(2-Benzoxazolyl)phenol
O
OH
O
753
OH
N
H
754
N-Benzoyl-DL-alanine
4-(Benzoylamino)-2-hydroxybenzoic acid
OH
O
HO
O
N
755
N
Benzoyl azide
O
O
O
O
N
H
N
756
2-Benzoylbenzoic acid
757
O
H
N
Br
O
758
4-Benzoylbenzoic acid
759
2-Benzoylbenzoic acid, hydrazide
4-Benzoylbiphenyl
760
Benzoyl bromide
O
OH
O
O
N
Cl
O
Fe
O
O
F
O
761
Benzoyl chloride
762
Benzoyl cyclohexane
763
Benzoylecgonine
764
Benzoylferrocene
765
Benzoyl fluoride
Physical Constants of Organic Compounds
3-44
No.
Name
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
766
N-Benzoylglycine
Hippuric acid
C9H9NO3
495-69-2
179.172 pr (w or al)
767
768
C7H5IO
C22H28ClNO2
618-38-2
232.018 nd
63990-84-1 373.916
3(2)
183.5
C18H23NO4
529-38-4
317.381 pr (eth)
109
770
Benzoyl iodide
Benzoic acid, iodide
2-Benzoylmethyl-6(2-hydroxy2-phenylethyl)-1-methylpiperidine, hydrochloride
3-(Benzoyloxy)-8-methyl-8Cocaethylene
azabicyclo[3.2.1]
octane-2-carboxylic acid,
ethyl ester, [1R-(exo,exo)]
Benzoyl peroxide
C14H10O4
94-36-0
242.227 orth (eth), pr 104.5(0.9)
exp
771
1-Benzoylpiperidine
C12H15NO
776-75-0
189.253 tcl
49
320.5
772
C18H19NO4
3483-82-7
313.349
119.5
773
N-Benzoyl-L-tyrosine ethyl
ester
Benzphetamine
C17H21N
156-08-1
239.356
774
775
776
777
778
Benzpiperylon
Benzquinamide
Benzthiazide
N-Benzylacetamide
Benzyl acetate
C22H25N3O
C22H32N2O5
C15H14ClN3O4S3
C9H11NO
C9H10O2
53-89-4
63-12-7
91-33-8
588-46-5
140-11-4
347.453
404.499
431.938
149.189
150.174
779
Benzyl acrylate
C10H10O2
2495-35-4
162.185
780
Benzyl alcohol
Benzenemethanol
C7H8O
100-51-6
108.138 liq
781
Benzylamine
Benzenemethanamine
C7H9N
100-46-9
107.153 liq
782
4-(Benzylamino)benzenesulfonamide
2-[Benzylamino]ethanol
4-Benzylaniline
N-Benzylaniline
α-Benzylbenzenepropanoic
acid
N4-Benzylsulfanilamide
C13H14N2O2S
104-22-3
262.327
104-63-2
1135-12-2
103-32-2
618-68-8
769
Organic
(Acetoxymethyl)benzene
mp/˚C
bp/˚C
191.5
den
g cm –3
12820
liq
182 dec
131
236
61
-51.5(0.4)
-15.5(0.2)
vs eth, EtOH
1.543
1.055020 1.523220
228
1.057320 1.514320
205.3(0.2)
1.041924 1.539620
185(3)
0.981320 1.540120
280
300
306.5
23518
1.06525 1.543020
1.03825
vs eth, EtOH, lig
1.029865 1.611825 vs eth, EtOH
vs bz, eth, EtOH
171
Bendazol
C14H12N2
621-72-7
788
Benzyl benzoate
Benzyl benzenecarboxylate
C14H12O2
120-51-4
212.244 nd or lf
19(1)
321.3(0.9)
1.112125 1.568020
789
4-Benzyl-1,1’-biphenyl
C19H16
613-42-3
244.330 lf
85
285110
1.1710
790
Benzyl butanoate
C11H14O2
103-37-7
178.228
239
1.011120 1.492020
791
792
793
794
Benzyl butyl phthalate
Benzyl chloroacetate
Benzyl chloroformate
Benzyl trans-cinnamate
85-68-7
140-18-1
501-53-1
78277-23-3
312.360 liq
184.619
170.594 oily liq
238.281 pr
39
370
1479
10320
350 dec
1.11925
1.22234
1.19525
1.10915
795
Benzyl dodecanoate
Carbobenzoxy chloride
Benzyl trans-3-phenyl-2propenoate
Benzyl laurate
C19H20O4
C9H9ClO2
C8H7ClO2
C16H14O2
C19H30O2
140-25-0
290.440
8.5
21012
0.942925 1.481224
796
Benzylethylamine
N-Ethylbenzenemethanamine
C9H13N
14321-27-8 135.206
194
0.934217 1.511720
797
N-Benzyl-N-ethylaniline
Ethylbenzylaniline
C15H17N
92-59-1
211.303 pa ye oil
288
1.00155
798
Benzyl ethyl ether
(Ethoxymethyl)benzene
C9H12O
539-30-0
136.190
188(4)
0.947820 1.495520
799
Benzyl formate
C8H8O2
104-57-4
136.149
203(8)
1.08120
800
Benzyl fumarate
C18H16O4
538-64-7
296.318 cry pow
59
2105
801
802
Benzylidene diacetate
Benzylimidobis(p-methoxyphenyl)methane
C11H12O4
C22H21NO2
581-55-5
524-96-9
208.211 pl (eth)
331.408 pa ye cry
45.1(0.5)
90
220
HCP_Section_03.indb 44
i H2O; s alk
vs EtOH, eth
sl H2O; msc
EtOH; s eth,
ace, chl
i H2O; s EtOH,
eth, ace, ctc
s H2O, EtOH,
eth, ace, bz,
MeOH, chl
msc H2O, EtOH,
eth; vs ace; s
bz; sl chl
1572
215(1)
2-Benzyl-1H-benzimidazole
Toluene-α,α-diol, diacetate
sl H2O; s EtOH,
eth, ace, bz,
CS2
i H2O; s EtOH,
eth; sl ctc
1.551519 vs eth, EtOH,
MeOH, chl
787
Butyl benzyl phthalate
Solubility
s H2O, EtOH; sl
eth, bz, chl; i
peth
vs eth, EtOH
sl H2O; s EtOH;
vs chl
1.74618
1270.02
cry (al)
cry
cry (EtOH)
nD
1.37120
151.205
183.249 mcl (lig)
183.249 pr
240.297 pl (peth
HOAc) nd
(w)
208.258 nd (bz)
783
784
785
786
C9H13NO
C13H13N
N-Phenylbenzenemethanamine C13H13N
C16H16O2
Physical
Form
34.5
33(4)
90
187
35
1.1120
1.542618
1.519020
1.594323
1.515420
vs bz, EtOH, gl
HOAc
i H2O; s EtOH,
eth, ace, bz,
MeOH, chl
i H2O; s EtOH,
ctc; vs eth, bz
i H2O; vs EtOH,
eth; s ctc
i H2O
vs eth, EtOH
s eth, ace, bz
i H2O; s EtOH,
eth; sl bz
vs bz, eth,
EtOH, peth
sl H2O, ctc; s
EtOH, eth, bz,
chl
i H2O; s EtOH,
eth, chl
i H2O; msc
EtOH, eth
i H2O; s EtOH,
ace; msc eth;
sl ctc
vs eth, EtOH,
chl
vs bz, eth, EtOH
vs eth, chl
4/11/16 11:18 AM
Physical Constants of Organic Compounds
3-45
O
O
O
OH
O
OH
N
H
O
N
N
I
O
766
767
N-Benzoylglycine
O
768
Benzoyl iodide
O
ClH
2-Benzoylmethyl-6(2-hydroxy-2-phenylethyl)-1-methylpiperidine, hydrochloride
769
3-(Benzoyloxy)-8-methyl-8-azabicyclo[3.2.1]octane-2-carboxylic acid, ethyl ester, [1R-(exo,exo)]
O
O
HN
HO
N
O
O
O
O
O
O
O
771
770
772
1-Benzoylpiperidine
N-Benzoyl-L-tyrosine ethyl ester
N
H
773
774
Benzphetamine
N
Benzpiperylon
Organic
Benzoyl peroxide
N
N
CH3
O
O
O
N
O
Cl
N
N
H2N
S
O O
O
775
777
776
O
778
N-Benzylacetamide
Benzthiazide
O
O
N
H
S
O O
Benzquinamide
O
O
S
NH
OH
779
Benzyl acetate
780
Benzyl acrylate
Benzyl alcohol
NH2
O S O
NH2
HN
782
781
NH2
O
784
783
4-(Benzylamino)benzenesulfonamide
Benzylamine
H
N
OH
N
H
785
4-Benzylaniline
2-[Benzylamino]ethanol
OH
786
α-Benzylbenzenepropanoic acid
N-Benzylaniline
O
N
O
N
H
O
O
O
O
O
O
787
788
2-Benzyl-1H-benzimidazole
Benzyl benzoate
792
Benzyl chloroacetate
Cl
O
790
4-Benzyl-1,1’-biphenyl
O
O
O
789
O
O
794
793
N
H
795
Benzyl trans-cinnamate
Benzyl chloroformate
O
O
O
O
O
O
O
N-Benzyl-N-ethylaniline
798
Benzyl ethyl ether
799
Benzyl formate
800
Benzyl fumarate
Benzylethylamine
O
N
O
O
797
796
Benzyl dodecanoate
O
N
Benzyl butyl phthalate
O
O
Cl
791
Benzyl butanoate
O
801
Benzylidene diacetate
O
802
Benzylimidobis(p-methoxyphenyl)methane
Physical Constants of Organic Compounds
3-46
Mol. Form.
CAS RN
Mol.
Wt.
C15H11NO2
2142-01-0
237.254 ye nd (al)
102-97-6
149.233
200
0.89225
622-78-6
149.214 ye oil
243
1.124616 1.604915 i H2O; msc
EtOH; s eth
C11H12O2
C12H16O2
C8H10O
2495-37-6
103-38-8
538-86-3
176.212
192.254
122.164 liq
14450
245
175(3)
C8H12N2
10309-79-2 136.194 liq
11720
C11H14O2
C7H7NO2
C22H24N2O7
103-28-6
178.228
935-05-7
137.137 oil
33605-72-0 428.435 cry
228
8135
122
C13H16N2O5
2650-64-8
280.276
134.5
s DMSO
C10H11NO4
C16H22N2O5
1138-80-3
1421-69-8
209.199
322.356
121
100
s ace
C19H20N2O5
1170-76-9
356.372
126
C9H12O2
622-08-2
152.190 oil
<-75
C16H17N2NaO4S
69-57-8
356.372 nd (BuOH
aq)
215
C13H12O
C13H12O
28994-41-4 184.233
101-53-1
184.233
21
84
312
322
Benzyl phenyl ether
1-Benzylpiperazine
C13H12O
C11H16N2
946-80-5
2759-28-6
39(3)
285(13)
14612
823
824
1-Benzylpiperidine
4-Benzylpiperidine
C12H17N
C12H17N
2905-56-8 175.270
31252-42-3 175.270
16.8
245
270
0.962516
0.997020
825
826
Benzyl propanoate
2-Benzylpyridine
C10H12O2
C12H11N
122-63-4
101-82-6
164.201
169.222 nd
12.5
224(20)
277
827
4-Benzylpyridine
C12H11N
2116-65-6
169.222
12.4
288
1.033520
1.0670
1.578520 i H2O; s EtOH,
eth, chl
1.061220 1.581820 i H2O; s EtOH,
ctc; vs eth
828
829
Benzyl 3-pyridinecarboxylate
1-Benzyl-1H-pyrrole
Benzyl nicotinate
C13H11NO2
C11H11N
94-44-0
2051-97-0
213.232
157.212
14(2)
1703
247
830
Benzyl 1,2-pyrrolidinedicarboxylate, (S)Benzyl salicylate
N-(Benzyloxycarbonyl)-Lproline
C13H15NO4
1148-11-4
249.263
78.5
C14H12O3
118-58-1
228.243
3-(Benzyloxy)-L-alanine
C10H13NO3
C7H8O3S
C14H13NO4S
4726-96-9
100-87-8
536-95-8
195.215
172.202 hyg cry
291.323
218 dec
835
O-Benzyl-L-serine
Benzylsulfonic acid
4-[(Benzylsulfonyl)­amino]­
benzoic acid
(Benzylsulfonyl)benzene
C13H12O2S
3112-88-7
232.298 nd (al)
146(3)
836
(Benzylthio)benzene
C13H12S
831-91-4
200.299 lf (al)
43.5
19727
837
Benzyl thiocyanate
C8H7NS
3012-37-1
149.214 pr (al)
43
232
838
C10H16ClN
56-93-9
185.694
243
839
840
841
Benzyltrimethylammonium
chloride
Benzylurea
Bephenium chloride
Berberine
C8H10N2O
C17H22ClNO
C20H19NO5
148
135
145
842
843
844
Berberine chloride dihydrate
Bergenin
Beryllium 2,4-pentanedioate
C20H22ClNO6
C14H16O9
C10H14BeO4
538-32-9
150.177 nd (al)
13928-81-9 291.816 cry (ace)
2086-83-1 353.369 red-ye nd
(w+6) cry
(chl)
5956-60-5 407.845 ye cry
477-90-7
328.272 cry (MeOH)
10210-64-7 207.228
No.
Name
803
804
2-Benzyl-1H-isoindole1,3(2H)-dione
Benzylisopropylamine
805
Benzyl isothiocyanate
806
807
808
Benzyl methacrylate
Benzyl 3-methylbutanoate
Benzyl methyl ether
809
1-Benzyl-2-methylhydrazine
810
811
812
817
Benzyl 2-methylpropanoate
Benzyl nitrite
N-Benzyloxycarbonylaspartame
Benzyloxycarbonyl-L-glutamine
Benzyloxycarbonylglycine
Benzyloxycarbonylglycyl-Lleucine
Benzyloxycarbonylglycyl-Lphenylalanine
2-(Benzyloxy)ethanol
818
Benzylpenicillin sodium
819
820
2-Benzylphenol
4-Benzylphenol
821
822
813
Organic
814
815
816
831
832
833
834
HCP_Section_03.indb 46
Synonym
N-Isopropylbenzenemethana- C10H15N
mine
(Isothiocyanatomethyl)benzene C8H7NS
1-Methyl-2-phenylmethylhydrazine
Benzyl isobutyrate
Ethylene glycol monobenzyl
ether
o-Benzylphenol
p-Benzylphenol
p-(Benzylsulfonamido)benzoic
acid
α-Thiocyanatotoluene
Beryllium acetylacetonate
Physical
Form
184.233 lf (al)
176.258
mp/˚C
bp/˚C
116
-52.6(0.4)
den
g cm –3
256
320
Solubility
s EtOH, HOAc;
sl DMSO
1.502520
0.998315 1.488420
0.963420 1.500820 i H2O, lig; vs
EtOH, eth; s bz
1.015918 1.488320
1.07525 1.498925
1.064020 1.523320 vs H2O, eth,
EtOH
1.41
vs H2O; s
MeOH; i ace,
eth, chl
1.599420 vs ace, bz, EtOH
s H2O, EtOH,
eth, bz, ctc,
HOAc, chl
1.543028 s H2O, EtOH,
eth; sl chl
1.522720
1.533725 i H2O; s EtOH,
eth
1.018320 1.565524 i H2O; vs EtOH,
eth
1.531020 sl chl
1.179920 1.580520 sl H2O; s EtOH,
eth, ctc
229.5
238
108(1)
nD
1.34318
vs EtOH
1.1261153
200 dec
i H2O; sl EtOH,
eth, bz
i H2O; s EtOH,
eth, con sulf
i H2O; s EtOH,
eth, chl, CS2
vs H2O; s ace
vs ace, EtOH
vs eth, EtOH
vs H2O, EtOH
270
1.16820
4/11/16 11:18 AM
Physical Constants of Organic Compounds
3-47
O
O
N
N
N
H
O
803
2-Benzyl-1H-isoindole-1,3(2H )-dione
804
C
O
O
S
805
Benzylisopropylamine
O
O
806
Benzyl isothiocyanate
807
Benzyl methacrylate
808
Benzyl 3-methylbutanoate
Benzyl methyl ether
O
O
O
HN
O
O
O
809
810
1-Benzyl-2-methylhydrazine
O
O
O
H
N
N
H
O
O
OH
O
O
812
Benzyl nitrite
O
N
H
O
811
Benzyl 2-methylpropanoate
O
O
N
O
O
OH
814
O
OH
O
O
815
816
Benzyloxycarbonylglycyl-L-leucine
817
Benzyloxycarbonylglycyl-L-phenylalanine
2-(Benzyloxy)ethanol
O
N
H
N
824
825
4-Benzylpiperidine
N
826
Benzyl propanoate
N
827
2-Benzylpyridine
828
4-Benzylpyridine
829
Benzyl 3-pyridinecarboxylate
1-Benzyl-1H-pyrrole
H
N
H
S
OH
N
O
N
O Na
HO
819
Benzylpenicillin sodium
820
2-Benzylphenol
OH
821
4-Benzylphenol
O
Benzyl 1,2-pyrrolidinedicarboxylate, (S)-
O
S
O
O
834
Benzylsulfonic acid
O-Benzyl-L-serine
4-[(Benzylsulfonyl)amino]benzoic acid
O
N
S
835
O
O
HO
833
832
Benzyl salicylate
O O
S
S
NH2
831
1-Benzylpiperidine
H
N
OH
OH
OH
830
823
1-Benzylpiperazine
O
O
O
822
Benzyl phenyl ether
O
O
(Benzylsulfonyl)benzene
N
O
818
O
N
O
O
N
OH
O
O
O
O
HO
Benzyloxycarbonylglycine
O
NH2
N
H
Benzyloxycarbonyl-L-glutamine
H
N
N
H
OH
813
N-Benzyloxycarbonylaspartame
O
O
Organic
H
N
N
H
H
N
S
836
N
837
(Benzylthio)benzene
N
H
Cl
838
Benzyl thiocyanate
NH2
839
Benzyltrimethylammonium chloride
Benzylurea
O
O
N
O
N
O
Cl
O
840
Bephenium chloride
Cl
N
O
O
O
HO
O
O
2H2O
O
841
Berberine
O
HO
H
O
HO
842
Berberine chloride dihydrate
843
Bergenin
H
OH
OH
O O
Be
O O
844
Beryllium 2,4-pentanedioate
Physical Constants of Organic Compounds
3-48
Organic
No.
Name
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
Physical
Form
mp/˚C
845
Betaine
1-Carboxy-N,N,N-trimethylmethanaminium, inner salt
C5H11NO2
107-43-7
117.147 pr or lf (al)
293 dec
846
847
848
Betaine, hydrochloride
Betamethasone
Bethanidine
C5H12ClNO2
C22H29FO5
C10H15N3
590-46-5
378-44-9
55-73-2
849
Betonicine
C7H13NO3
850
851
852
Betulaprenol 9
9,9’-Bianthracene
Δ2,2’(3H,3’H)-Bibenzo[b]­
thiophene-3,3’-dione
853
Bicyclo[2.2.1]heptane
854
855
856
857
860
861
862
863
864
Bicyclo[4.1.0]heptane
Bicyclo[2.2.1]heptan-2-one
Bicyclo[2.2.1]hept-2-ene
Bicyclo[2.2.1]hept-5-ene-2carbonitrile
Bicyclo[2.2.1]hept-5-ene-2carboxaldehyde
Bicyclo[2.2.1]hept-5-ene-2methanol
[1,1’-Bicyclohexyl]-2-one
1,1’-Bicyclopentyl
[1,1’-Bicyclopentyl]-2-ol
[1,1’-Bicyclopentyl]-2-one
Bifenox
865
866
Bifenthrin
Biguanide
867
Bikhaconitine
868
Bilirubin
869
Biliverdine
870
871
Binapacryl
1,1’-Binaphthalene
872
Nonaisoprenol
Durindone Red
C7H12
153.608 mcl cry (al) 227.5
392.460 cry (AcOMe) 232 dec
177.246 cry (aq
196
MeOH)
515-25-3
159.183 pr (dil al,
252 dec
+1w)
13190-97-1 631.069 oil or cry
41
1055-23-8 354.443
321.3
522-75-8
296.364 br nd (xyl) 359
red mcl nd
(bz)
279-23-2
96.170
87.3(0.6)
C7H12
C7H10O
C7H10
C8H9N
286-08-8
497-38-1
498-66-8
95-11-4
96.170
110.153
94.154
119.164
C8H10O
5453-80-5
C8H12O
C45H74O
C28H18
C16H8O2S2
bp/˚C
den
g cm –3
nD
vs H2O, MeOH;
s EtOH; sl eth,
chl
vs H2O
vs EtOH
s chl
sub
i H2O, EtOH; sl
chl, CS2; s bz,
xyl
vs ace, bz, eth,
EtOH
107(6)
113.8(0.3)
170
95.69(0.08)
8410
0.85325
1.456420
0.99925
1.488520
122.164
7120
1.01825
1.489320
95-12-5
124.180
10320
C12H20O
C10H18
C10H18O
C10H16O
C14H9Cl2NO5
90-42-6
1636-39-1
4884-25-7
4884-24-6
42576-02-3
180.286 liq
138.250
154.249
152.233 liq
342.131
Imidodicarbonimidic diamide
C23H22ClF3O2
C2H7N5
82657-04-3 422.868
69
56-03-1
101.111 pr or nd (al) 136
3-Deoxypseudaconitine
C36H51NO11
6078-26-8
673.790
C33H36N4O6
635-65-4
Dehydrobilirubin
C33H34N4O6
114-25-0
584.662 red mcl pr
or pl (chl)
582.646 dk grn pl or >300
pr (MeOH)
1,1’-Binaphthyl
C15H18N2O6
C20H14
485-31-4
604-53-5
2,2’-Binaphthalene
C20H14
612-78-2
873
[1,1’-Binaphthalene]-2,2’-diol
C20H14O2
602-09-5
874
Biotin
Coenzyme R
C10H16N2O3S
875
876
2,2’-Bioxirane
Biphenyl
Diepoxybutane
Diphenyl
877
878
[1,1’-Biphenyl]-4-acetic acid
[1,1’-Biphenyl]-4-carbonitrile
Felbinac
879
[1,1’-Biphenyl]-4-carbonyl
chloride
[1,1’-Biphenyl]-2,2’-diamine
[1,1’-Biphenyl]-2,4’-diamine
858
859
880
881
882
Norcarane
2-Cyclohexylcyclohexanone
2-Hydroxybicyclopentyl
Methyl
5-(2,4-dichlorophenoxy)-2nitrobenzoate
2,4’-Biphenyldiamine
[1,1’-Biphenyl]-4,4’-diamine,
dihydrochloride
[1,1’-Biphenyl]-2,2’-dicarbox- o,o’-Diphenic acid
ylic acid
20
-13
86.1(0.5)
264
0.969625 1.487725
190.46(0.03)
s ctc, CS2
233(11)
0.978515 1.488417
232.5
0.974521 1.4763
1.2125
142 dec
>360
188.1(1)
452(26)
220
58-85-5
286.324 nd (al), cry
(w)
244.310 nd (w)
232 dec
C4H6O2
C12H10
1464-53-5
92-52-4
86.090 liq
154.207 lf (dil al)
2.0
68.93(0.02)
144
255.2(0.3)
C14H12O2
C13H9N
5728-52-9
2920-38-9
212.244
179.217
160.5
88
19020
C13H9ClO
14002-51-8 216.662
111
1602
C12H12N2
C12H12N2
1454-80-4
492-17-1
184.236 pr or nd (al) 81
184.236 nd (dil al)
54.5
1624
363
C12H14Cl2N2
531-85-1
257.158
>300
C14H10O4
482-05-3
233.5
sub
113.6(0.5)
320
97.5
[1,1’-Biphenyl]-2,2’-diol
C12H10O2
1806-29-7
885
[1,1’-Biphenyl]-2,5-diol
C12H10O2
1079-21-6
186.206 nd (dil al)
vs H2O; s EtOH;
i bz, chl
vs eth, EtOH,
chl
i H2O; sl EtOH,
eth; s bz, chl
i H2O; s EtOH,
bz; sl eth, chl,
CS2
164
70.6(0.5)
159(12)
884
HCP_Section_03.indb 48
-32
322.313
254.325 (i) pl(HOAc)
(ii) orth
(peth)
254.325 bl flr pl (al)
242.227 mcl pr or lf
(w) cry
(HOAc)
186.206
883
98.0(0.5)
46.2(0.7)
13
Solubility
1.2720
1.300020
1.11320
1.0420
1.43520
1.58877
i H2O; sl EtOH; s
eth, ace, bz,
CS2
i H2O; sl EtOH; s
eth, bz, CS2
i H2O; s EtOH,
eth, alk; sl chl
s H2O, EtOH; sl
eth, chl
vs H2O, EtOH
i H2O; s EtOH,
eth; vs bz, ctc,
MeOH
i H2O; vs EtOH,
eth
1.309020
s H2O, ace, bz
i H2O; s EtOH,
eth
i H2O; s EtOH,
eth
1.342020
s H2O, EtOH,
eth, ace, bz; sl
peth, chl
vs EtOH
4/11/16 11:19 AM
Physical Constants of Organic Compounds
3-49
O
OH
OH
HO
O
O
N
O
845
O
846
Betaine
N
H
F
HCl
N
O
847
Betaine, hydrochloride
HO
N
H
N
H
OH
H
O
848
Betamethasone
O
N
9
849
Bethanidine
850
Betonicine
Betulaprenol 9
O
S
O
S
O
853
Δ2,2’(3H,3’H )-Bibenzo[b]thiophene-3,3’-dione
854
Bicyclo[2.2.1]heptane
855
Bicyclo[4.1.0]heptane
856
Bicyclo[2.2.1]heptan-2-one
Bicyclo[2.2.1]hept-2-ene
Organic
852
851
9,9’-Bianthracene
O
O
OH
H
N
857
858
Bicyclo[2.2.1]hept-5-ene-2-carbonitrile
859
Bicyclo[2.2.1]hept-5-ene-2-carboxaldehyde
860
Bicyclo[2.2.1]hept-5-ene-2-methanol
861
[1,1’-Bicyclohexyl]-2-one
1,1’-Bicyclopentyl
O
OH
H
Cl
O
Cl
862
O
H
O
O
H
H2N
O
N
H
865
Bifenthrin
OO
OO
NH HN
NH HN
NH HN
NH N
NH2
866
Biguanide
O
O
O N
O
N
H
NO2
Bifenox
[1,1’-Bicyclopentyl]-2-one
OH
O
O
NH NH
O
F3C
864
863
[1,1’-Bicyclopentyl]-2-ol
O
Cl
O
H
O
O
O
O
O
O
HO
OH
867
O
HO
N
O O
O
869
868
Bikhaconitine
HO
O
870
Biliverdine
Bilirubin
OH
OH
Binapacryl
H H
N
O
N
H H
S
O
O
OH
871
872
1,1’-Binaphthalene
873
2,2’-Binaphthalene
N
O
877
[1,1’-Biphenyl]-4-acetic acid
879
[1,1’-Biphenyl]-4-carbonitrile
[1,1’-Biphenyl]-4-carbonyl chloride
HO
H2N
NH2
882
Biphenyl
H2N NH2
H2N
H2N
880
[1,1’-Biphenyl]-2,2’-diamine
881
[1,1’-Biphenyl]-2,4’-diamine
HO
OH
OO
876
2,2’-Bioxirane
O
878
O
875
Biotin
Cl
OH
H
874
[1,1’-Binaphthalene]-2,2’-diol
H
HO OH
2HCl
[1,1’-Biphenyl]-4,4’-diamine, dihydrochloride
OH
883
[1,1’-Biphenyl]-2,2’-dicarboxylic acid
884
[1,1’-Biphenyl]-2,2’-diol
885
[1,1’-Biphenyl]-2,5-diol
Physical Constants of Organic Compounds
3-50
Mol. Form.
CAS RN
Mol.
Wt.
[1,1’-Biphenyl]-4,4’-diol
C12H10O2
92-88-6
186.206
287.6(0.5)
[1,1’-Biphenyl]-4,4’-disulfonic
acid
[1,1’-Biphenyl]-3,3’,4,4’tetramine, tetrahydrochloride
[1,1’-Biphenyl]-3,3’,5,5’-tetrol Diresorcinol
C12H10O6S2
5314-37-4
314.333 pr
72.5
C12H18Cl4N4
7411-49-6
360.110
245 dec
C12H10O4
531-02-2
310
C14H13NO
4075-79-0
C14H12O
92-91-1
C20H14N2O
852-38-0
218.205 pl or nd
(w+2)
211.259 cry (dil
MeOH)
196.244 pr (ace), cry
(al)
298.337
No.
Name
886
887
888
889
890
Synonym
Physical
Form
mp/˚C
bp/˚C
den
g cm –3
nD
Solubility
sl H2O, bz,
DMSO; s EtOH,
eth
vs H2O
>200
vs H2O, eth,
EtOH
i H2O; vs EtOH,
ace, MeOH
i H2O; vs EtOH,
ace; sl chl
172.8
893
N-[1,1’-Biphenyl]-4-ylacetamide
1-[1,1’-Biphenyl]-4-ylethanone
2-[1,1’-Biphenyl]-4-yl-5phenyl-1,3,4-oxadiazole
2,2’-Bipyridine
α,α’-Dipyridyl
C10H8N2
366-18-7
156.184 pr (peth)
894
2,3’-Bipyridine
2,3’-Bipyridyl
C10H8N2
581-50-0
156.184
895
2,4’-Bipyridine
2,4’-Bipyridyl
C10H8N2
581-47-5
156.184
59.7(0.5)
283(11)
896
3,3’-Bipyridine
3,3’-Bipyridyl
C10H8N2
581-46-4
156.184
68
291.5
897
4,4’-Bipyridine
γ,γ’-Dipyridyl
C10H8N2
553-26-4
156.184 nd (w+2)
104.4(0.5)
305
898
2,2’-Biquinoline
C18H12N2
119-91-5
256.301 pl or lf (al)
196
899
4,4’-Bis(acetoacetamido)N,N’-Bis(acetoacetyl)-3,3’3,3’-dimethyl-1,1’-biphenyl
dimethylbenzidine
Bisacodyl
Bis(4-amino-3-chlorophenyl)­ 4,4-Methylene bis(2-chloroaniline)
methane
Bis(4-aminocyclohexyl)­
methane
Bis(2-aminoethyl)amine
Diethylenetriamine
C22H24N2O4
91-96-3
380.437
212
C22H19NO4
C13H12Cl2N2
603-50-9
101-14-4
361.391
267.153
134(1)
C13H26N2
1761-71-3
210.358
15
320
0.9275
C4H13N3
111-40-0
103.166 ye hyg liq
-39
206.5(0.3)
C6H18N4
112-24-3
146.234 oil
12
266.5
C12H12N2S2
1141-88-4
248.366
93
85
0.956920 1.481025 msc H2O, EtOH;
i eth; s lig
1.497120 s H2O, EtOH,
acid
i H2O; vs EtOH,
eth
s H2O; vs EtOH,
eth, chl; sl bz,
lig
i H2O; vs EtOH
s EtOH; sl
DMSO
s H2O, EtOH
0.9620
1.461920
891
892
Organic
900
901
902
903
904
326
69.9(0.2)
273(10)
295.5
906
Bis(4-aminophenyl) disulfide
C12H12N2S2
722-27-0
248.366
907
908
1,2-Bis(4-aminophenyl)ethane
Bis(4-aminophenyl) sulfone
Dapsone
C14H16N2
C12H12N2O2S
621-95-4
80-08-0
212.290 pl (w)
137
248.300 cry (95% al) 178(1)
909
910
C12H12N2OS
C10H24N2O2
119-59-5
7300-34-7
232.300 pr (w, al)
204.310 liq
175 dec
C10H26N4
71-44-3
202.340
29
C10H30Cl4N4
306-67-2
348.184
301.5
913
914
Bis(4-aminophenyl) sulfoxide
1,4-Bis(3-aminopropoxy)­
butane
N,N’-Bis(3-aminopropyl)-1,4butanediamine
N,N’-Bis(3-aminopropyl)-1,4butanediamine,
tetrahydrochloride
Bis(2-bromoethyl) ether
1,2-Bis(bromomethyl)benzene
C4H8Br2O
C8H8Br2
5414-19-7
91-13-4
231.914
263.958 orth (chl)
95(1)
11532
1294.5
915
1,3-Bis(bromomethyl)benzene
C8H8Br2
626-15-3
77(1)
13720
916
1,4-Bis(bromomethyl)benzene
C8H8Br2
623-24-5
144.5
245
917
2,2-Bis(bromomethyl)-1,3propanediol
1,3-Bis(bromomethyl)­
tetramethyldisiloxane
Bis(4-bromophenyl) ether
C5H10Br2O2
3296-90-0
263.958 nd (chl), pr
(ace)
263.958 mcl pr (al),
cry (chl,
bz)
261.940 nd (bz)
C6H16Br2OSi2
2351-13-5
320.169
C12H8Br2O
2050-47-7
327.999 lf (al)
C22H42O8
141-17-3
434.563 liq
912
918
919
920
Bis(2-(2-butoxyethoxy)ethyl)
adipate
HCP_Section_03.indb 50
Bromex
Pentaerythritol dibromide
1.14020
1.622320
1.161420
sl H2O; vs EtOH,
eth, bz, chl
i H2O; vs EtOH,
eth, bz, chl; sl
peth
sl H2O; vs EtOH,
eth, chl
vs H2O, EtOH; sl
eth
sl H2O; vs EtOH,
bz, chl; s eth
i H2O; vs EtOH;
s eth, ace, bz
sl DMSO
s ctc
905
4,4’-Sulfinyldianiline
1,4-Butanediol bis(3-aminopropyl) ether
Spermine
1.25100
168
N,N’-Bis(2-aminoethyl)-1,2ethanediamine
Bis(2-aminophenyl) disulfide
911
Triethylenetetramine
121
sub
1353
1505
s H2O
1.845220 1.513127
1.98825
i H2O; s EtOH,
eth, ctc, chl,
peth, lig
1.95925
i H2O; s EtOH,
eth, chl, lig
2.01225
i H2O; vs EtOH,
chl; sl eth; s
bz
113
54(1)
233
1.391825 1.471925
339
1.825
i H2O; s EtOH,
bz; vs eth; sl
chl
1.125
4/11/16 11:19 AM
Physical Constants of Organic Compounds
3-51
OH
HO
HO
O
HO S
O
OH
886
H2N
O
S OH
O
H 2N
887
[1,1’-Biphenyl]-4,4’-diol
NH2
NH2
4HCl
[1,1’-Biphenyl]-4,4’-disulfonic acid
OH
HO
888
889
[1,1’-Biphenyl]-3,3’,4,4’-tetramine, tetrahydrochloride
[1,1’-Biphenyl]-3,3’,5,5’-tetrol
N N
O
N
N
O
O
890
891
N-[1,1’-Biphenyl]-4-ylacetamide
892
1-[1,1’-Biphenyl]-4-ylethanone
N
N
893
2-[1,1’-Biphenyl]-4-yl-5-phenyl-1,3,4-oxadiazole
N
N
894
2,2’-Bipyridine
895
2,3’-Bipyridine
2,4’-Bipyridine
O
O
N
HN
N
N
N
896
O
N
N
O
H2N
S S
910
905
Bis(2-aminophenyl) disulfide
O
S
O
S
O
NH2
H2N
H
N
N
H
Bis(4-aminophenyl) sulfoxide
H
N
H 2N
NH2
911
NH2
909
Bis(4-aminophenyl) sulfone
NH2
H2N
S S
908
1,2-Bis(4-aminophenyl)ethane
1,4-Bis(3-aminopropoxy)butane
NH2
904
907
H2N
O
NH2
H
N
N
H
Bisacodyl
N,N’-Bis(2-aminoethyl)-1,2-ethanediamine
H2N
NH2
Bis(4-aminophenyl) disulfide
O
NH2
Bis(2-aminoethyl)amine
H2N
906
H2N
H2N
903
Bis(4-aminocyclohexyl)methane
NH2
H
N
H 2N
902
Bis(4-amino-3-chlorophenyl)methane
H2N
NH2
H2N
NH2
901
900
4,4’-Bis(acetoacetamido)-3,3’-dimethyl-1,1’-biphenyl
Cl
Cl
O
899
2,2’-Biquinoline
4,4’-Bipyridine
O
O
O
N
898
897
3,3’-Bipyridine
NH
NH2
N
H
4HCl
912
N,N’-Bis(3-aminopropyl)-1,4-butanediamine
N,N’-Bis(3-aminopropyl)-1,4-butanediamine, tetrahydrochloride
Br
Br
Br
Br
913
914
Bis(2-bromoethyl) ether
915
1,2-Bis(bromomethyl)benzene
1,3-Bis(bromomethyl)benzene
Si
O
918
Si
Br
1,3-Bis(bromomethyl)tetramethyldisiloxane
Br
919
OH
OH
916
917
1,4-Bis(bromomethyl)benzene
O
Br
Bis(4-bromophenyl) ether
Br
2,2-Bis(bromomethyl)-1,3-propanediol
O
O
Br
Br
Br
Br
Br
O
Br
O
O
O
O
920
Bis(2-(2-butoxyethoxy)ethyl) adipate
O
O
Organic
NH
Physical Constants of Organic Compounds
3-52
No.
Name
921
1,4-Bis(α-(tert-butyldioxy)­
isopropyl)benzene
Bis(3-tert-butyl-5-ethyl-2hydroxyphenyl)methane
Bis(4-chlorobenzoyl) peroxide
1,2-Bis(2-chloroethoxy)ethane
Bis(2-chloroethoxy)methane
N,N-Bis(2-chloroethyl)aniline Aniline mustard
922
923
924
925
926
927
928
929
930
Bis(2-chloroethyl) carbonate
Bis(2-chloroethyl)
2-chloroethylphosphonate
Bis(2-chloroethyl) ether
Synonym
Dichloroethyl ether
Mol. Form.
CAS RN
Mol.
Wt.
Physical
Form
Organic
den
g cm –3
C20H34O4
2781-00-2
338.482 cry
79
nD
C25H36O2
88-24-4
368.553 cry
123
C14H8Cl2O4
C6H12Cl2O2
C5H10Cl2O2
C10H13Cl2N
94-17-7
112-26-5
111-91-1
553-27-5
311.118 pr cry (bz)
187.064
173.037
218.123 pr
141
214(18)
216(3)
16414
1.19520
1.459225 s ctc
C5H8Cl2O3
C6H12Cl3O3P
623-97-2
6294-34-4
187.021
269.490
8
241
170.25
1.350620 1.46120
1.48825
C4H8Cl2O
111-44-4
143.012 liq
-46.9(0.5)
178(2)
1.2220
C5H12Cl3N
55-86-7
192.515 hyg nd
111.5
C5H9Cl2N3O2
154-93-8
214.049 lt ye pow
31
C4H8Cl2S
C6H12Cl2O4S2
505-60-2
3944-87-4
13.5
205
198(9)
1.274120 1.531320
C8H8Cl2
612-12-4
159.078 liq
283.193 cry (MeOH/
HOAc)
175.056 mcl (lig)
55(1)
239.5
1.39325
mp/˚C
45
bp/˚C
1.45120
934
Bis(2-chloroethyl)methylamine Nitrogen mustard
hydrochloride
hydrochloride
N,N’-Bis(2-chloroethyl)-NCarmustine
nitrosourea
Bis(2-chloroethyl) sulfide
Mustard gas
1,2-Bis(2-chloroethylsulfonyl)­
ethane
1,2-Bis(chloromethyl)benzene
935
1,3-Bis(chloromethyl)benzene
C8H8Cl2
626-16-4
175.056 cry
34(1)
251.5
1.30220
936
1,4-Bis(chloromethyl)benzene
C8H8Cl2
623-25-6
175.056 pl (al)
100
257(18)
1.41725
937
938
939
Bis(chloromethyl) ether
3,3-Bis(chloromethyl)oxetane
2,2-Bis(chloromethyl)-1,3Pentaerythritol dichlorohydrin
propanediol
1,3-Bis(chloromethyl)­
tetramethyldisiloxane
Bis(4-chlorophenoxy)methane Di(4-chlorophenoxy)methane
Bis(4-chlorophenyl) disulfide
Bis(4-chlorophenyl)­
ethanedione
1,1-Bis(4-chlorophenyl)­
ethanol
1,2-Bis(2-chlorophenyl)2,2’-Dichlorohydrazobenzene
hydrazine
Bis(4-chlorophenyl)methane
Bis(4-chlorophenyl) sulfone
C2H4Cl2O
C5H8Cl2O
C5H10Cl2O2
542-88-1
78-71-7
2209-86-1
114.958 liq
155.022 liq
173.037 cry
-41.5
19.0(0.1)
83
104(4)
10127
15912
1.32315
1.29525
1.43521
C6H16Cl2OSi2
2362-10-9
231.267 liq
-90
205(3)
1.04520
1.439820
C13H10Cl2O2
C12H8Cl2S2
C14H8Cl2O2
555-89-5
1142-19-4
3457-46-3
269.123 cry (peth)
287.228
279.119
70.5
72.8
197.8
1916
C14H12Cl2O
80-06-8
267.150
70
C12H10Cl2N2
782-74-1
253.126
87
C13H10Cl2
C12H8Cl2O2S
101-76-8
80-07-9
237.124
287.162
55.5
148.8(1)
C13H10Cl2N2S
1220-00-4
297.202 nd
176
C14H9Cl5O
115-32-2
370.485 cry (petr)
75.1(0.3)
1800.1
C6H12Cl2O
C6H8N2O
C6H8N2S
C10H10Cl2Ti
629-36-7
1656-48-0
111-97-7
1271-19-8
171.064
124.140
140.206
248.959 red cry
289
205(7)
1615
1631.5
25810
C10H10Cl2Zr
1291-32-3
292.316 col cry
248
1800.5
C8H6Br4
13209-15-9 421.750 mcl
116.5
C14H6Cl4O4
133-14-2
380.008
106
C6H14Cl4OSi2
2943-70-6
300.157
C12H6Cl4O
28076-73-5 307.987 cry (eth)
71
C21H28N2O
90-93-7
95.3
C10H20N2NiS4
14267-17-5 355.232
2020.02
C10H20N2S4Zn
14324-55-1 361.948
1780.05
C2H2F4O
1691-17-4
5.5(0.4)
931
932
933
940
941
942
943
944
945
946
947
948
949
950
951
952
953
954
955
956
957
958
959
960
961
962
N,N’-Bis(4-chlorophenyl)­
Di(p-chlorophenyl)thiourea
thiourea
1,1-Bis(4-chlorophenyl)-2,2,2trichloroethanol
Bis(3-chloropropyl) ether
3-Chloropropyl ether
Bis(2-cyanoethyl) ether
Bis(2-cyanoethyl) sulfide
Bis(η-cyclopentadienyl)­
titanium chloride
Bis(η-cyclopentadienyl)­
zirconium chloride
1,2-Bis(dibromomethyl)­
benzene
Bis(2,4-dichlorobenzoyl)
peroxide
1,3-Bis(dichloromethyl)­
tetramethyldisiloxane
Bis(2,4-dichlorophenyl)ether 2,2’,4,4’-Tetrachlorodiphenyl
ether
4,4’-Bis(diethylamino)­
Michler’s ethyl ketone
benzophenone
Bis(diethyldithiocarbamate)­
nickel
Bis(diethyldithiocarbamate)­
zinc
Bis(difluoromethyl) ether
Difluoromethyl ether
HCP_Section_03.indb 52
324.459 lf (al)
118.030 col gas
Solubility
sl eth; s EtOH,
MeOH
i H2O
i H2O; s EtOH,
eth, ace; msc
bz
vs H2O, EtOH
i H2O; vs EtOH,
eth, chl; s ctc
i H2O; vs EtOH,
eth; sl chl
i H2O; vs EtOH,
eth, ace, chl;
sl HOAc
msc EtOH, eth
vs ace, bz
s chl
i H2O, EtOH; s
eth, bz
18818
25010
1.36517
s EtOH
sl H2O; s EtOH,
chl
i H2O, os
1.13620 1.415820 s EtOH, eth
1.050420 1.440520
1.504720
1.60
sl H2O, bz; s
chl, EtOH, tol
sl H2O; vs chl; i
lig
14950
1.221320 1.466020
1.4320
4/11/16 11:19 AM
Physical Constants of Organic Compounds
O
3-53
O
OH
OH
O O
Cl
Cl
921
922
1,4-Bis(α-(tert-butyldioxy)isopropyl)benzene
923
Bis(3-tert-butyl-5-ethyl-2-hydroxyphenyl)methane
N
O
O
925
O
Cl
Cl
926
Bis(2-chloroethoxy)methane
O
Cl
Cl
O
927
N,N-Bis(2-chloroethyl)aniline
930
Bis(2-chloroethyl) 2-chloroethylphosphonate
N
N
Cl
Cl
Cl
O
931
Bis(2-chloroethyl)methylamine hydrochloride
Cl
O
929
Bis(2-chloroethyl) ether
Cl
N
H
HCl
Cl
N
Cl
Cl
O
Cl
Cl
Cl
928
Bis(2-chloroethyl) carbonate
Cl
1,2-Bis(2-chloroethoxy)ethane
O
O P O
Cl
O
O
924
Bis(4-chlorobenzoyl) peroxide
Cl
Cl
Cl
O O
Organic
O
O
932
N,N’-Bis(2-chloroethyl)-N-nitrosourea
S
O O
Cl
S
O O
S
Cl
Cl
933
Bis(2-chloroethyl) sulfide
934
1,2-Bis(2-chloroethylsulfonyl)ethane
1,2-Bis(chloromethyl)benzene
Cl
Cl
Cl
Cl
Cl
Cl
Cl
Cl
935
936
1,3-Bis(chloromethyl)benzene
O
Cl
Cl
937
1,4-Bis(chloromethyl)benzene
938
Bis(chloromethyl) ether
OH
OH
O
939
3,3-Bis(chloromethyl)oxetane
2,2-Bis(chloromethyl)-1,3-propanediol
O
Cl
Si
Si
O
Cl
O
940
OH
Cl3C
S S
942
943
Cl
946
Bis(4-chlorophenyl)ethanedione
H
N
O
S
O
Cl
1,2-Bis(2-chlorophenyl)-hydrazine
O
Bis(4-chlorophenyl) disulfide
Cl
945
Cl
Cl
Cl
H H
N N
Cl
1,1-Bis(4-chlorophenyl)ethanol
Cl
Bis(4-chlorophenoxy)methane
Cl
944
Cl
941
1,3-Bis(chloromethyl)tetramethyldisiloxane
Cl
Cl
O
Cl
Cl
S
Cl
Cl
948
947
Bis(4-chlorophenyl)methane
H
N
N,N’-Bis(4-chlorophenyl)thiourea
Bis(4-chlorophenyl) sulfone
OH
O
Cl
Cl
Cl
949
1,1-Bis(4-chlorophenyl)-2,2,2-trichloroethanol
Br
Cl
N
N
953
Bis(2-cyanoethyl) sulfide
Cl
Br
Bis(η-cyclopentadienyl)titanium chloride
Cl
O O
Br
Cl
952
Bis(2-cyanoethyl) ether
Cl
954
955
O
Si
Cl
Cl
Cl
956
1,2-Bis(dibromomethyl)benzene
Si
Cl
Cl
O O
Bis(η-cyclopentadienyl)zirconium chloride
Cl
N
N
951
Bis(3-chloropropyl) ether
Br
Zr
Cl
O
950
Cl
Ti
S
957
Bis(2,4-dichlorobenzoyl) peroxide
1,3-Bis(dichloromethyl)tetramethyldisiloxane
O
Cl
Cl
Cl
O
958
Bis(2,4-dichlorophenyl)ether
S
Cl
N
N
S
Ni
N
S
959
4,4’-Bis(diethylamino)benzophenone
S
N
S
960
Bis(diethyldithiocarbamate)nickel
S
Zn
N
S
N
S
961
Bis(diethyldithiocarbamate)zinc
F
O
F
F
F
962
Bis(difluoromethyl) ether
Physical Constants of Organic Compounds
3-54
CAS RN
Mol.
Wt.
Bis(2-dimethylaminoethyl)
2,2’-Oxybis[N,N-dimethyletha- C8H20N2O
ether
namine]
Bis[4-(dimethylamino)­phenyl]­ Michler’s Base
C17H22N2
methane
3033-62-3
160.257 liq
8015
101-61-1
254.370 pl or tab (al, 91.5
lig)
390 dec
No.
Name
963
964
Synonym
Mol. Form.
Physical
Form
mp/˚C
965
Bis[4-(dimethylamino)­phenyl]­ 4,4’-Bis(dimethylamino)­
methanethione
thiobenzophenone
C17H20N2S
1226-46-6
284.419 pl
204
966
Bis(4-dimethylaminophenyl)­
methanol
C17H22N2O
119-58-4
270.369
102.0
967
C7H18N2O
5966-51-8
146.230
C23H26N2
129-73-7
C6H12CuN2S4
137-29-1
330.465 nd or lf (al,
bz)
303.978
C6H12N2NiS4
15521-65-0 299.125
979
1,3-Bis(dimethylamino)-2propanol
4,4’-Bis(dimethylamino)­
triphenylmethane
Bis(dimethyldithiocarbamate)­
copper
Bis(dimethyldithiocarbamate)­
nickel
2,5-Bis(1,1-dimethylpropyl)1,4-benzenediol
2,4-Bis(1,1-dimethylpropyl)­
phenol
1,2-Bis(diphenylphosphino)­
ethane
1,3-Bis(2,3-epoxypropoxy)­
benzene
Bis(2-ethoxyethyl) phthalate
Bis(ethoxymethyl) ether
N,N’-Bis(4-ethoxyphenyl)­
ethanimidamide
monohydrochloride
Bis(ethylenediamine)copper
dichloride
Bis(2-ethylhexyl) adipate
980
981
Bis(2-ethylhexyl)amine
Bis(2-ethylhexyl) azelate
982
983
984
985
Bis(2-ethylhexyl) ether
Bis(2-ethylhexyl) phosphate
Bis(2-ethylhexyl) phosphonate
Bis(2-ethylhexyl)
phosphorodithioate
Bis(2-ethylhexyl) phthalate
Bis(2-ethylhexyl) sebacate
Bis(2-ethylhexyl) sodium
sulfosuccinate
Bis(2-ethylhexyl) terephthalate
2,2-Bis(ethylsulfonyl)butane
Bis[4-(hexyloxy)phenyl]­
diazene, 1-oxide
N,N’-Bis(2hydroxybenzylidene)-1,2ethylenediamine
Bis(2-hydroxy-3-tert-butyl-5methylphenyl)methane
Bis(2-hydroxy-5-chlorophenyl)
sulfide
2-[Bis(2-hydroxyethyl)­amino]­
ethanol hydrochloride
N,N-Bis(2-hydroxyethyl)­
butylamine
Bis(2-hydroxyethyl) disulfide
N,N-Bis(2-hydroxyethyl)­
dodecanamide
N,N-Bis(2-hydroxyethyl)­
ethylamine
N,N’-Bis(2-hydroxyethyl)­
ethylenediamine
N,N-Bis(2-hydroxyethyl)­
glycine
968
969
Organic
970
971
972
973
974
975
976
977
978
986
987
988
989
990
991
992
993
994
995
996
997
998
999
1000
1001
HCP_Section_03.indb 54
4,4’-Bis(dimethylamino)­
benzhydrol
2,5-Di-tert-pentylhydroquinone C16H26O2
bp/˚C
181.5
den
g cm –3
nD
0.878820 1.441820
102
2060.01
2080.002
250.376
180
C16H26O
120-95-6
234.376
26.0
Diphos
C26H24P2
1663-45-2
398.417
143.5
Diglycidyl resorcinol ether
C12H14O4
101-90-6
222.237
42.5
1470.4
1.218330 1.540820
605-54-9
5648-29-3
620-99-5
310.342
134.173
334.841 cry (w+1)
34
345
136(10)
1.122921
Phenacaine hydrochloride
C16H22O6
C6H14O3
C18H23ClN2O2
2,2’-Diethyldihexyl ether
Bis(2-ethylhexyl) phosphite
i H2O; sl EtOH;
vs eth, bz; s
acid
i H2O, EtOH, lig;
sl eth; s bz,
chl, HOAc
i H2O; vs EtOH;
s eth, bz,
HOAc
vs H2O
vs bz, eth
79-74-3
Cupriethylenediamine
C4H16Cl2CuN4
dichloride
Bis(2-ethylhexyl) hexanedioate C22H42O4
Solubility
16922
191
vs H2O, EtOH,
chl
15243-01-3 254.649 dk bl cry
s EtOH
103-23-1
370.566
-67.8
2145
0.92225
1.447420 vs ace, eth,
EtOH
C16H35N
C25H48O4
106-20-7
103-24-2
241.456
412.647
-78
16121
2375
0.91525
1.44625
C16H34O
C16H35O4P
C16H35O3P
C16H35O2PS2
10143-60-9
298-07-7
3658-48-8
5810-88-8
242.440
322.420 visc liq
306.421 liq
354.552 cry
279(8)
1550.015
1501
0.97525
0.9325
C24H38O4
C26H50O4
C20H37NaO7S
117-81-7
122-62-3
577-11-7
390.557 liq
426.673
444.559 waxy solid
C24H38O4
C8H18O4S2
C24H34N2O3
6422-86-2
76-20-0
2587-42-0
C16H16N2O2
1.432520
i H2O; s EtOH,
ace, bz; sl ctc
sl ctc
sl H2O; s bz, hx
1.442020
s bz, hp, chl
-55
-55(1)
384
2565
0.98125
0.91225
1.485320 sl ctc
1.45125 vs ace, bz, EtOH
s peth, ctc, eth,
ace
390.557
242.357 pl (w)
398.538
76
383
dec
1.19985
s chl
s chl
94-93-9
268.310
125.5
C23H32O2
119-47-1
340.499 nd (peth)
131
Fenticlor
C12H8Cl2O2S
97-24-5
287.162
174
Triethanolamine hydrochloride
C6H16ClNO3
637-39-8
185.649 cry (al)
179.5
102-79-4
161.243
C4H10O2S2
C16H33NO3
1892-29-1
120-40-1
154.251
287.438 waxy solid
26
38.7
1603.5
C6H15NO2
139-87-7
133.189 ye liq
-50
248(19)
C6H16N2O2
4439-20-7
148.203
100.1(0.5)
1361
C6H13NO4
150-25-4
163.172 nd (al)
194 dec
Di-sec-octyl phthalate
Docusate sodium
Sulfonethylmethane
Disalicylidene-1,2-ethanediamine
Butylbis(2-hydroxyethyl)amine C8H19NO2
N-Ethyldiethanolamine
Bicine
sl EtOH, eth; s
bz, chl
i H2O; s EtOH,
eth, gl HOAc
vs H2O
279(19)
0.968120 1.462520 s chl
1.013520 1.466320 vs H2O, EtOH; sl
eth
s H2O
vs H2O; i EtOH
4/11/16 11:19 AM
Physical Constants of Organic Compounds
3-55
S
N
N
N
O
963
N
N
964
Bis(2-dimethylaminoethyl) ether
OH
N
N
965
Bis[4-(dimethylamino)phenyl]methane
OH
N
N
966
Bis[4-(dimethylamino)phenyl]methanethione
N
967
Bis(4-dimethylaminophenyl)methanol
1,3-Bis(dimethylamino)-2-propanol
OH
OH
N
N
Cu
S
968
S
S
N
S
N
S
969
4,4’-Bis(dimethylamino)triphenylmethane
S
Ni
N
OH
S
970
Bis(dimethyldithiocarbamate)copper
971
Bis(dimethyldithiocarbamate)nickel
O
P
H
N
974
Bis(2-ethoxyethyl) phthalate
N
O
Bis(ethoxymethyl) ether
O
2Cl
O
979
Bis(ethylenediamine)copper dichloride
O
O
O
978
N,N’-Bis(4-ethoxyphenyl)ethanimidamide monohydrochloride
O
O
976
2
H H
N
N
Cu
N
N
H H
977
O
975
1,3-Bis(2,3-epoxypropoxy)benzene
O
O
O
O
1,2-Bis(diphenylphosphino)ethane
O
O
O
O
973
2,4-Bis(1,1-dimethylpropyl)phenol
O
O
P
972
2,5-Bis(1,1-dimethylpropyl)-1,4-benzenediol
Organic
S
N
Bis(2-ethylhexyl) adipate
O
O
O
O
O
P
O
O
H
N
980
981
Bis(2-ethylhexyl)amine
982
Bis(2-ethylhexyl) azelate
OH
983
Bis(2-ethylhexyl) ether
Bis(2-ethylhexyl) phosphate
O
O
O
P
O
O
H
O
P
S
O
O
SH
O
O
O
984
985
Bis(2-ethylhexyl) phosphonate
986
Bis(2-ethylhexyl) phosphorodithioate
987
Bis(2-ethylhexyl) phthalate
O Na
OO S O
O
O
O
988
Bis(2-ethylhexyl) sebacate
O
O
O
O
O S
O
989
Bis(2-ethylhexyl) sodium sulfosuccinate
O
O
S O
O
990
Bis(2-ethylhexyl) terephthalate
2,2-Bis(ethylsulfonyl)butane
O
O
OH
N
N
HO
N
N
OH
OH
OH
S
OH
O
Cl
991
Bis[4-(hexyloxy)phenyl]diazene, 1-oxide
992
993
N,N’-Bis(2-hydroxybenzylidene)-1,2-ethylenediamine
Bis(2-hydroxy-3-tert-butyl-5-methylphenyl)methane
Cl
994
Bis(2-hydroxy-5-chlorophenyl) sulfide
O
OH
N
HO
OH
995
N
HCl
2-[Bis(2-hydroxyethyl)amino]ethanol hydrochloride
OH
HO
N
HO
OH
996
S
S
997
N,N-Bis(2-hydroxyethyl)butylamine
OH
Bis(2-hydroxyethyl) disulfide
OH
998
N,N-Bis(2-hydroxyethyl)dodecanamide
O
HO
N
999
HO
OH
N,N-Bis(2-hydroxyethyl)ethylamine
H
N
N
H
1000
OH
OH
N,N’-Bis(2-hydroxyethyl)ethylenediamine
HO
N
1001
OH
N,N-Bis(2-hydroxyethyl)glycine
Physical Constants of Organic Compounds
3-56
No.
Name
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
1002
Bis(2-hydroxyethyl)­
methylamine
N,N-Bis(2-hydroxyethyl)-3methylaniline
N,N-Bis(2-hydroxyethyl)-1,3propanediamine
Bis(2-hydroxyethyl) sulfide
Methyldiethanolamine
C5H13NO2
105-59-9
Diethanol-m-toluidine
C11H17NO2
3-(Aminopropyl)diethanolamine
2,2’-Thiodiethanol
Bis(2-hydroxyethyl)
1,4-benzenedicarboxylate
1003
1004
1005
1006
1007
1008
1009
Organic
1010
1011
1012
1013
1014
Bis(2-hydroxyethyl)
terephthalate
1,2-Bis(2-hydroxyethylthio)­
ethane
Bis(2-hydroxy-4-methoxyphenyl)methanone
1,3-Bis(hydroxymethyl)-2imidazolidone
2,2-Bis(4-hydroxy-3-methylphenyl)propane
2,2-Bis(hydroxymethyl)-1,3propanediol, tetra(2-propenoyl) ester
2,2-Bis(hydroxymethyl)-1,3propanediol, tri(2-propenoyl)
ester
2,2-Bis(4-hydroxyphenyl)­
butane
Bis(4-hydroxyphenyl)methane
Physical
Form
mp/˚C
bp/˚C
den
g cm –3
nD
119.163 liq
-21
245(1)
1.04325
1.468520 vs H2O
91-99-6
195.259
64.5
1601
C7H18N2O2
4985-85-7
162.230
C4H10O2S
111-48-8
122.186 liq
-10.2
C12H14O6
959-26-2
254.235 cry (w)
109.5
C6H14O2S2
5244-34-8
182.304
64.8
131-54-4
274.269
139.1(0.5)
C5H10N2O3
136-84-5
146.144 cry (MeOH)
101
Bisphenol C
C17H20O2
79-97-0
256.340 nd (xyl)
140
Pentaerythritol tetraacrylate
C17H20O8
4986-89-4
352.336
17.3
Pentaerythritol triacrylate
C14H18O7
3524-68-3
298.289
Bisphenol B
C16H18O2
77-40-7
242.313
120.5
Bisphenol AD
C13H12O2
620-92-8
200.233
162.5
sub
2204
80-05-7
228.287 cry or fl
160(2)
1016
2,2-Bis(4-hydroxyphenyl)­
propane dimethacrylate
Bis(4-hydroxyphenyl) sulfone
Bisphenol A dimethacrylate
C23H24O4
3253-39-2
364.435
73
Bisphenol S
C12H10O4S
80-09-1
250.270 nd (w), orth 240.5
bipym
1022
1023
1024
1025
1026
1027
2,2’-Dimercaptodiethyl sulfide C4H10S3
C9H14O3
2-Methoxy-N-(2C6H15NO2
methoxyethyl)­ethanamine
Bis(4-methoxyphenyl)diazene,
C14H14N2O3
1-oxide
Bis(4-methoxyphenyl)­
C16H14O4
ethanedione
1,4-Bis(methylamino)-9,10C16H14N2O2
anthracenedione
1,3-Bis(1-methylethenyl)­
1,3-Diisopropenylbenzene
C12H14
benzene
Bis(4-methylphenyl) disulfide Di-p-Tolyl disulfide
C14H14S2
p-Tolyl ether
Dicumyl peroxide
1030
Bis(4-methylphenyl) ether
Bis(1-methyl-1-phenylethyl)
peroxide
Bis(4-methylphenyl)mercury
1,4-Bis(4-methyl-5-phenyloxazol-2-yl)benzene
Bis(4-methylphenyl) sulfide
1031
Bis(4-methylphenyl) sulfone
Di-p-tolyl sulfone
1032
1034
1035
N,N’-Bis(2-methylphenyl)­
thiourea
1,3-Bis(1-methyl-4-piperidyl)­
propane
Bis(methylthio)methane
1,2-Bis(N-morpholino)ethane
1036
1037
Bismuth acetate
Bismuth subsalicylate
1028
1029
1033
HCP_Section_03.indb 56
3570-55-6 154.317
64057-79-0 170.205
111-95-5
133.189
1562-94-3
258.272 ye nd (al)
1226-42-2
270.280
2475-44-7
266.294
3748-13-8
158.239 liq
103-19-5
246.391 nd or lf (al)
1579-40-4
80-43-3
s H2O, EtOH, bz,
peth
1.18525
1.18020
C15H16O2
Bis(2-mercaptoethyl) sulfide
Bis(2-methallyl) carbonate
Bis(2-methoxyethyl)amine
1.179325 1.521120 msc H2O, EtOH,
chl, AcOEt; s
eth; sl bz
1700.5
C15H14O5
Bisphenol A
1021
282
2,2’-Dihydroxy-4,4’-dimethoxybenzophenone
1,3-Dimethylolethyleneurea
2,2-Bis(4-hydroxyphenyl)­
propane
1018
1019
1020
sl chl
1601
1015
1017
-11
201.3
vs ace, MeOH
s EtOH, eth, chl,
alk; sl DMSO; i
CS2
i H2O; vs EtOH,
eth, bz, alk; s
HOAc
1.366315
13518
663
1.18325
0.94325
sl chl
21220
1.11451
198.260
270.367 cry (EtOH)
51
40
285
1000.2
537-64-4
3073-87-8
382.85
392.449
245.7
232
620-94-0
214.326 nd (al)
57.3
>300
C14H14O2S
599-66-6
246.325 pr(bz),
nd(w,al)
150(8)
406
C15H16N2S
137-97-3
256.366 nd (al, sub)
C15H30N2
64168-11-2 238.412
13.7
21550
C3H8S2
C10H20N2O2
1618-26-4
1723-94-0
75
148
285
C6H9BiO6
C7H5BiO4
s EtOH, ace, bz;
sl chl
sl EtOH, chl
133
47.5
108.226
200.278 wh-ye
(eth,lig)
22306-37-2 386.111 col tablets
14882-18-9 362.093 pr
1.598220
1.437120
1.171111
0.925
Di-p-tolylmercury
C14H14Hg
2,2’-p-Phenylenebis(4-methyl- C26H20N2O2
5-phenyloxazole)
Di-p-tolyl sulfide
C14H14S
i H2O; s EtOH,
eth; sl bz,
DMSO
s ctc
231
C14H14O
C18H22O2
Solubility
250
1.557020
i H2O; s EtOH,
ace; vs eth
vs bz, eth, EtOH
sl chl
i H2O; s EtOH,
ace, bz, HOAc;
sl chl
sl H2O, eth; s
EtOH, bz, chl,
CS2
vs bz, EtOH, chl
0.896225 1.480425
vs H2O, ace, bz,
EtOH
i H2O
i H2O, EtOH;
reac alk
4/11/16 11:19 AM
Physical Constants of Organic Compounds
HO
N
3-57
OH
OH
N
HO
H2N
OH
1002
1003
Bis(2-hydroxyethyl)methylamine
N
HO
OH
1004
N,N-Bis(2-hydroxyethyl)-3-methylaniline
S
OH
O
1007
Bis(2-hydroxyethyl) terephthalate
O
HO
OH
O
1008
1009
Bis(2-hydroxy-4-methoxyphenyl)methanone
OH
1010
1,3-Bis(hydroxymethyl)-2-imidazolidone
2,2-Bis(4-hydroxy-3-methylphenyl)propane
O
O
O
O
O
O
O
O
O
O
O
O
OH
O
O
HO
1012
1011
O
HO
OH
1014
HO
1015
Bis(4-hydroxyphenyl)methane
2,2-Bis(4-hydroxyphenyl)butane
O O
S
O
O
OH
O
HO
1016
2,2-Bis(4-hydroxyphenyl)propane
OH
1017
2,2-Bis(4-hydroxyphenyl)propane dimethacrylate
Bis(4-hydroxyphenyl) sulfone
O
O
O
O
1019
O
O
N
H
Bis(2-methallyl) carbonate
N
N
O HN
1024
Bis(4-methoxyphenyl)ethanedione
O
1025
O
1026
Bis(4-methylphenyl) disulfide
N
N
O
O
Bis(1-methyl-1-phenylethyl)peroxide
O O
S
H
N
1023
1,4-Bis(methylamino)-9,10-anthracenedione
O
1027
Bis(4-methylphenyl) ether
S
O HN
O
1022
S
1,3-Bis(1-methylethenyl)benzene
1018
Bis(2-mercaptoethyl) sulfide
O
Bis(4-methoxyphenyl)diazene, 1-oxide
S
SH
S
O
1021
Bis(2-methoxyethyl)amine
HS
O
O
1020
OH
1013
2,2-Bis(hydroxymethyl)-1,3-propanediol, tri(2-propenoyl) ester
2,2-Bis(hydroxymethyl)-1,3-propanediol, tetra(2-propenoyl) ester
O
OH
Organic
S
1,2-Bis(2-hydroxyethylthio)ethane
O
OH
N
N
HO
O
1006
Bis(2-hydroxyethyl) sulfide
OH
O
HO
1005
N,N-Bis(2-hydroxyethyl)-1,3-propanediamine
OH O
OH
S
O
H
N
Hg
1028
Bis(4-methylphenyl)mercury
N
N
S
1029
1,4-Bis(4-methyl-5-phenyloxazol-2-yl)benzene
1030
1031
Bis(4-methylphenyl) sulfide
O
N
N
S
S
1034
Bis(methylthio)methane
1032
Bis(4-methylphenyl) sulfone
O
N,N’-Bis(2-methylphenyl)thiourea
O
O
O
Bi
O
O
O
O
1035
1,2-Bis(N-morpholino)ethane
1033
1,3-Bis(1-methyl-4-piperidyl)propane
1036
Bismuth acetate
O
O
Bi
1037
OH
Bismuth subsalicylate
Physical Constants of Organic Compounds
3-58
CAS RN
Mol.
Wt.
C12H8N2O4S2
1155-00-6
308.333
198.5
Nitrophenide
C12H8N2O4S2
537-91-7
308.333
84
4,4’-Dinitrobibenzyl
C12H8N2O4S2
C14H12N2O4
100-32-3
736-30-1
308.333
182
272.256 ye nd (al,bz) 181.8
C13H10N4O5
C10H14CoO4
C16H19N
C14H8Br6O2
587-90-6
14024-48-7
10024-74-5
37853-59-1
C5H6Cl6N2O3
116-52-9
302.242
257.149 bl-viol cry
225.329
687.637 nd (bz/
EtOH)
354.831
C8H4Cl6
68-36-0
312.836 cry (bz, eth) 109
C3Cl6O3
C32H62O4S
C8H5F6N
C8H4F6
32315-10-9 296.748 cry (eth,
peth)
10595-72-9 542.897
328-74-5
229.123
402-31-3
214.108
C8H4F6
433-19-2
Name
1038
Bis(2-nitrophenyl) disulfide
1039
Bis(3-nitrophenyl) disulfide
1040
1041
Bis(4-nitrophenyl) disulfide
1,2-Bis(4-nitrophenyl)ethane
1042
1043
1044
1045
N,N’-Bis(4-nitrophenyl)urea
4,4’-Dinitrocarbanilide
Bis(2,4-pentanedionato)cobalt Cobalt(II) bis(acetylacetonate)
Bis(1-phenylethyl)amine
1,2-Bis(2,4,6-tribromophenoxy)ethane
N,N’-Bis(2,2,2-trichloro-1hydroxyethyl)urea
1,4-Bis(trichloromethyl)­
benzene
Bis(trichloromethyl) carbonate Triphosgene
1046
1047
Organic
Mol. Form.
No.
1048
1049
1050
1051
Synonym
Physical
Form
mp/˚C
bp/˚C
den
g cm –3
2550.1
312 dec
167
296.5
1.01815
196
79
vs ace, EtOH
s chl
203
1.629080
2650.25
8515
116
vs EtOH
1.48725 1.433520
1.379025 1.391625 i H2O
372-64-5
202.141
14630-40-1 170.400
2217-06-3 456.258 ye cry
26
230
1056
1057
1058
C8H14O3
C12H6Cl4O2S
C8H6S2
764-99-8
97-18-7
492-97-7
158.195
356.052
166.264
188
31.1(0.4)
1059
Bixin
C25H30O4
6983-79-5
394.504 viol pr (ace) 198
1060
1061
1062
Boldenone
Boldine
Bomyl
Dehydrotestosterone
C19H26O2
C19H21NO4
C9H15O8P
846-48-0
476-70-0
122-10-1
286.408
327.375 cry (eth)
282.184 ye oil
1063
1064
Borane carbonyl
Borneol, (±)-
Borine carbonyl
CH3BO
C10H18O
13205-44-2 41.845 col gas
6627-72-1 154.249 lf (lig)
-137
206(7)
-64
213(7)
1.01120
1065
l-Bornyl acetate
C12H20O2
5655-61-8
27
223.5
0.98225
1066
Bornylamine
C10H19N
32511-34-5 153.265
163
1067
Bornyl chloride
C10H17Cl
464-41-5
128(6)
1068
C15H26O2
53022-14-3 238.366
C2H6BF3O
353-42-4
113.874
1070
Bornyl 3-methylbutanoate,
(1R)Boron trifluoride - dimethyl
ether complex
Boron trifluoride etherate
C4H10BF3O
109-63-7
141.927 liq
1071
Brilliant Green
C27H34N2O4S
633-03-4
1072
Brilliant Yellow
C26H20N4Na2O8S2
3051-11-4
482.635 small gold
cry
626.569 ye cry (w)
1073
Brodifacoum
C31H23BrO3
56073-10-0 523.417 off-wh pow 230
1074
Bromacil
C9H13BrN2O2
314-40-9
1075
Bromadiolone
C30H23BrO4
28772-56-7 527.406 ye-wh pow
205
1076
Bromal hydrate
C2H3Br3O2
507-42-6
46.0(0.7)
1077
Bromdian
C15H12Br4O2
79-94-7
298.756 mcl pr
(w+1)
543.871
1078
N-Bromoacetamide
C2H4BrNO
79-15-2
137.963 nd (chl-hx)
103.5
1069
HCP_Section_03.indb 58
2-Chloro-1,7,7-trimethylbicyclo[2.2.1]heptane, endo
d-Bornyl isovalerate
Trifluoroboron etherate
5-Bromo-3-sec-butyl-6methyluracil
Tetrabromobisphenol A
214.108 liq
196.286
172.695 nd
261.115
1.573
222
C2F6S2
C8H18Si2
C12H4N6O12S
1053
1054
1055
Solubility
i H2O, eth; sl
EtOH, ace, bz,
HOAc
sl EtOH, chl; s
eth
sl EtOH, HOAc
i EtOH; sl eth,
bz, chl, HOAc
Bis(tridecyl) thiodipropanoate Ditridecyl thiodipropionate
3,5-Bis(trifluoromethyl)aniline
1,3-Bis(trifluoromethyl)­
benzene
1,4-Bis(trifluoromethyl)­
benzene
Bis(trifluoromethyl) disulfide
1,2-Bis(trimethylsilyl)acetylene
Bis(2,4,6-trinitrophenyl)
Dipicryl sulfide
sulfide
Bis[2-(vinyloxy)ethyl] ether
Diethylene glycol divinyl ether
Bithionol
2,2’-Bithiophene
1052
nD
115
34.6
134
vs EtOH, peth
0.77020
1.41320
8110
1.7325
vs ace
i H2O; vs EtOH;
s eth, ctc,
HOAc
i H2O; s EtOH,
ace; sl eth, bz,
HOAc
260
165
163
16017
1.462620
207.5
257.5
0.95525
-14
127 dec
1.241020 1.30220
-60.4
125.5
1.12525
dec H2O; vs eth,
EtOH
vs H2O, EtOH
s H2O, EtOH; sl
ace
i H2O; sl EtOH,
bz; s ace, chl
157.8(0.5)
179
1.34820
vs EtOH, chl
sl H2O; vs ace,
EtOH, xyl
dec H2O
i H2O; vs EtOH,
eth, bz
sl H2O; s EtOH,
eth
vs ace, bz, eth,
EtOH
vs bz, eth,
EtOH, peth
vs eth, EtOH
1.5525
dec
2.566140
vs DMF; sl ace,
chl, EtOH, eth;
i hx
vs eth, EtOH
s EtOH, eth, bz,
chl
vs eth
4/11/16 11:19 AM
Physical Constants of Organic Compounds
O
O N
O
N O
O
O N
S
S
O
N
O
S
1038
S
1039
O
N
O
O
N
O
S
O
N
O
1040
Bis(3-nitrophenyl) disulfide
1041
Bis(4-nitrophenyl) disulfide
1,2-Bis(4-nitrophenyl)ethane
H
N
Br
O
N
O
O
O
Co
O
1042
O
N
H
O
1043
N,N’-Bis(4-nitrophenyl)urea
Cl
Cl
O
1045
Bis(1-phenylethyl)amine
1,2-Bis(2,4,6-tribromophenoxy)ethane
O
Cl
NH2
O
Cl
Cl
Cl
H
N
Cl
H
N
OH O
S
Cl
Cl
Cl
OH
1046
F
Cl
F
O
O
Cl
O
O
Cl
Cl
F
F
O
1048
1,4-Bis(trichloromethyl)benzene
F
Cl
Cl
Cl
Cl
1047
N,N’-Bis(2,2,2-trichloro-1-hydroxyethyl)urea
F
1049
Bis(trichloromethyl) carbonate
F
1051
F
O
O
N OO N
F
F
F
S
S
O
N
O
F
F
Si
F
1053
1052
1,3-Bis(trifluoromethyl)benzene
F
F
F
3,5-Bis(trifluoromethyl)aniline
F
F
F
F
F
1050
Bis(tridecyl) thiodipropanoate
F
F
Br
Br
Br
1044
Bis(2,4-pentanedionato)cobalt
Br
O
Br
N OO N
O
O
Si
1054
Bis(trifluoromethyl) disulfide
1,4-Bis(trifluoromethyl)benzene
O
N
O
S
1055
1,2-Bis(trimethylsilyl)acetylene
Bis(2,4,6-trinitrophenyl) sulfide
OH HO
Cl
O
O
O
Cl
1056
O
Cl
S
O
Cl
1057
Bis[2-(vinyloxy)ethyl] ether
S
S
OH
O
1058
Bithionol
1059
2,2’-Bithiophene
Bixin
HO
OH
N
H
O
H
O
O
O
O
1060
P
O
O
H 3B
O
OH
1061
Boldenone
O
1062
Boldine
O
1063
Bomyl
1064
Borane carbonyl
1065
Borneol, (±)-
l-Bornyl acetate
Cl
NH2
O
OH
1066
1067
Bornylamine
Bornyl chloride
N
O
1068
1069
Bornyl 3-methylbutanoate, (1R)-
HO
F
O B F
F
F
O B F
F
O
N
HSO4
1070
Boron trifluoride - dimethyl ether complex
1071
Boron trifluoride etherate
Brilliant Green
N
N
N
N
S O
O O O S
Na
O O
Na
O
Br
O
1072
N
N
H
O
1073
Brilliant Yellow
O
1074
Brodifacoum
Bromacil
OH
OH
Br
O
Br
OH
OH
HO
O
Br
1075
Bromadiolone
Br
Br
OH
1076
Bromal hydrate
Br
Br
HO
OH
O
Br
Br
1077
Bromdian
N
H
1078
Br
N-Bromoacetamide
Organic
H
N
N
O
O
N O
S
Bis(2-nitrophenyl) disulfide
O
3-59
Physical Constants of Organic Compounds
3-60
No.
Name
1079
Synonym
Mol. Form.
CAS RN
Bromoacetic acid
C2H3BrO2
79-08-3
1080
Bromoacetone
C3H5BrO
1081
α-Bromoacetophenone
ω-Bromoacetophenone
1082
4-(Bromoacetyl)biphenyl
2-Bromo-4’-phenylacetophenone
1083
1084
1085
Bromoacetyl bromide
Bromoacetylene
5-(2-Bromoallyl)-5-secbutylbarbituric acid
5-(2-Bromoallyl)-5-isopropylbarbituric acid
Mol.
Wt.
Physical
Form
den
g cm –3
bp/˚C
138.948 hex or orth
cry
50
208
598-31-2
136.975 liq
-36.5
138
C8H7BrO
70-11-1
13518
C14H11BrO
135-73-9
199.045 nd (al) orth 51(1)
pr (al)
pl(peth)
275.140 nd (95% al) 127
598-21-0
593-61-3
1142-70-7
201.844
104.933 col gas
303.152
148.5
4.7
Butallylonal
C2H2Br2O
C2HBr
C11H15BrN2O3
Propallylonal
C10H13BrN2O3
545-93-7
181
30.9(0.5)
229
1.57820
nD
Solubility
1.933550 1.480450 msc H2O, EtOH,
eth; s ace, bz;
sl chl
1.63423 1.469715 sl H2O; s EtOH,
eth, ace
1.64720
i H2O; s EtOH,
peth; vs eth,
bz, chl
2.31222
131.5
1.544920 s ace, ctc
vs eth
vs eth, EtOH
1087
2-Bromoaniline
C6H6BrN
615-36-1
289.125 cry (dil
HOAc, dil
al)
172.023
1088
3-Bromoaniline
C6H6BrN
591-19-5
172.023
18.5
250(3)
1.579320 1.626020
1089
4-Bromoaniline
C6H6BrN
106-40-1
78.2(0.5)
220(6)
1.4970100
1090
2-Bromoanisole
C7H7BrO
578-57-4
172.023 orth bipym
nd (60%
al)
187.034
1.3
216
1091
3-Bromoanisole
C7H7BrO
2398-37-0
187.034
1092
4-Bromoanisole
C7H7BrO
104-92-7
187.034
13.5
215
1093
2-Bromobenzaldehyde
C7H5BrO
6630-33-7
185.018
21.5
230
1094
3-Bromobenzaldehyde
C7H5BrO
3132-99-8
185.018
1095
4-Bromobenzaldehyde
C7H5BrO
1122-91-4
185.018 lf (dil al)
61.1(0.4)
1096
Bromobenzene
C6H5Br
108-86-1
157.008 liq
-30.74(0.03) 155.9(0.2)
1097
4-Bromobenzeneacetic acid
C8H7BrO2
1878-68-8
215.045 nd (w)
116
1098
4-Bromobenzeneacetonitrile
C8H6BrN
48.0
1099
α-Bromobenzeneacetonitrile
16532-79-9 196.045 pa ye cry
(al)
5798-79-8 196.045 ye cry (dil
al)
1.501820 1.572720 i H2O; vs EtOH,
eth
1.563520 i H2O; s EtOH,
eth, bz, CS2
1.456420 1.564220 sl H2O; vs EtOH,
eth, chl; s ctc
1.592520 i H2O; vs EtOH,
bz; sl ctc
1.593520 i H2O; vs EtOH,
eth; sl ctc
i H2O; vs EtOH,
bz; sl chl
1.495020 1.559720 i H2O; vs EtOH,
eth, bz; s ctc
sl H2O; vs EtOH,
eth, CS2
vs bz, EtOH
29
255(9)
1100
2-Bromo-1,4-benzenediol
C6H5BrO2
583-69-7
189.007 lf (lig), cry
(chl)
111.5
sub
1101
C6H4BrClO2S
98-58-8
C6H5BrS
106-53-6
255.517 tcl or mcl pl 76
(eth)
189.073 lf (al)
73
15315
1102
4-Bromobenzenesulfonyl
chloride
4-Bromobenzenethiol
230.5
1.526083
1103
2-Bromobenzoic acid
C7H5BrO2
88-65-3
201.018 mcl pr (w),
nd
149.0(0.9)
295(18)
1.92925
1104
3-Bromobenzoic acid
C7H5BrO2
585-76-2
285(15)
1.84520
1105
4-Bromobenzoic acid
C7H5BrO2
586-76-5
1106
2-Bromobenzonitrile
C7H4BrN
2042-37-7
201.018 mcl nd (dil 156.7(0.5)
al)
201.018 nd (eth), lf 254(1)
(w), mcl pr
182.018 nd (w)
55.5
1107
3-Bromobenzonitrile
C7H4BrN
6952-59-6
182.018
39.5
225
1108
4-Bromobenzonitrile
C7H4BrN
623-00-7
182.018 nd (w, al)
114
236
1109
6-Bromobenzo[a]pyrene
C20H11Br
223
1110
1111
2-Bromobenzoyl chloride
4-Bromobenzoyl chloride
C7H4BrClO
C7H4BrClO
21248-00-0 331.205 cry (ace/
MeOH)
7154-66-7 219.463 nd
586-75-4
219.463 nd (peth)
11
37(1)
238(14)
245(11)
1112
1113
2-Bromobiphenyl
3-Bromobiphenyl
C12H9Br
C12H9Br
2052-07-5
2113-57-7
0.8
297
300
1086
Organic
mp/˚C
HCP_Section_03.indb 60
Phenyl bromide
α-Bromobenzyl cyanide
p-Brosyl chloride
C8H6BrN
233.103
233.103
211
234
672
sub
1.53929
1.89420
252
1.217526
1.611320
sl H2O, eth, bz;
vs EtOH, ace,
HOAc
i H2O; s EtOH,
eth
sl H2O; s EtOH,
eth
i H2O; s EtOH,
eth; sl chl
i H2O; vs EtOH,
eth, ace, bz,
chl
vs H2O, EtOH,
eth, bz; sl chl,
lig; s HOAc
i H2O; vs eth; s
chl
sl H2O, EtOH; vs
eth, ctc, chl
sl H2O, DMSO; s
EtOH, eth, ace,
chl
i H2O; s EtOH,
eth
sl H2O, DMSO; s
EtOH, eth
s H2O; vs EtOH;
sl chl
vs EtOH, eth; sl
chl
s H2O, EtOH,
eth, chl
1.596320 sl ctc
vs EtOH, eth,
bz, lig
1.624825 vs eth, EtOH
1.641120 i H2O
4/11/16 11:19 AM
Physical Constants of Organic Compounds
3-61
O
O
O
Br
O
Br
OH
1079
Br
1080
Bromoacetic acid
1081
1082
α-Bromoacetophenone
Bromoacetone
N
H
Br
Bromoacetylene
5-(2-Bromoallyl)-5-sec-butylbarbituric acid
O
O
Br
O
Br
1087
1088
2-Bromoaniline
Br
Br
Br
1089
3-Bromoaniline
1090
4-Bromoaniline
Br
1091
2-Bromoanisole
1092
3-Bromoanisole
4-Bromoanisole
O
Br
1094
3-Bromobenzaldehyde
1095
4-Bromobenzaldehyde
1096
N
O
Br
1098
4-Bromobenzeneacetic acid
HO
HO
O
1099
α-Bromobenzeneacetonitrile
4-Bromobenzeneacetonitrile
HO
SH
N
Br
1097
Bromobenzene
Br
Br
OH
Br
Cl
O S O
O
Br
Br
1101
1102
4-Bromobenzenethiol
Br
Br
1104
1105
3-Bromobenzoic acid
2-Bromobenzoic acid
N
4-Bromobenzoic acid
Cl
Br
1108
2-Bromobenzonitrile
1107
3-Bromobenzonitrile
O
Br
Br
Br
Br
1109
6-Bromobenzo[a]pyrene
Br
1106
O
Br
4-Bromobenzonitrile
1100
2-Bromo-1,4-benzenediol
Br
1103
Cl
OH
N
N
O
Br
4-Bromobenzenesulfonyl chloride
1093
2-Bromobenzaldehyde
OH
O
Br
O
O
O
Br
1086
N
H
1085
NH2
5-(2-Bromoallyl)-5-isopropylbarbituric acid
NH
O
1084
Bromoacetyl bromide
NH2
NH2
NH
O
Br
1083
4-(Bromoacetyl)biphenyl
O
Br
Br
O
Br
Organic
O
Br
1110
2-Bromobenzoyl chloride
1111
4-Bromobenzoyl chloride
1112
2-Bromobiphenyl
1113
3-Bromobiphenyl
Physical Constants of Organic Compounds
3-62
Mol. Form.
CAS RN
Mol.
Wt.
4-Bromobiphenyl
C12H9Br
92-66-0
1-Bromo-2-(bromomethyl)­
benzene
1-Bromo-3-(bromomethyl)­
benzene
1-Bromo-4-(bromomethyl)­
benzene
C7H6Br2
No.
Name
1114
1115
1116
1117
1118
mp/˚C
bp/˚C
den
g cm –3
233.103 pl (al)
87.0(0.2)
309(3)
0.932725
3433-80-5
249.931 cry (al, lig)
31
12919
C7H6Br2
823-78-9
249.931 nd or lf
42
12212
p-Bromobenzyl bromide
C7H6Br2
589-15-1
249.931 nd (al)
63
1,2-Dibromo-2,4-dicyanobutane
p-Bromophenacyl bromide
C6H6Br2N2
35691-65-7 265.933
52
C8H6Br2O
99-73-0
277.941 nd (al)
111
Synonym
Physical
Form
1120
1121
2-Bromo-2-(bromomethyl)­
pentanedinitrile
2-Bromo-1-(4-bromophenyl)­
ethanone
2-Bromo-1,3-butadiene
1-Bromobutane
Butyl bromide
C4H5Br
C4H9Br
1822-86-2
109-65-9
132.987
137.018 liq
-112.5(0.3)
1122
1123
2-Bromobutane, (±)Bromobutanedioic acid, (±)-
(±)-sec-Butyl bromide
Bromosuccinic acid
C4H9Br
C4H5BrO4
5787-31-5
584-98-5
137.018 liq
196.985
-112.6(0.2)
161
1124
1125
1126
1127
1128
4-Bromobutanenitrile
2-Bromobutanoic acid, (±)4-Bromobutanoic acid
3-Bromo-2-butanone
cis-1-Bromo-1-butene
C4H6BrN
C4H7BrO2
C4H7BrO2
C4H7BrO
C4H7Br
5332-06-9
2385-70-8
2623-87-2
814-75-5
31849-78-2
148.002
167.002
167.002
151.002
135.003
1129
trans-1-Bromo-1-butene
C4H7Br
32620-08-9 135.003 liq
-100.3
95(3)
1130
2-Bromo-1-butene
C4H7Br
23074-36-4 135.003 liq
-133.4
81(3)
1131
4-Bromo-1-butene
C4H7Br
5162-44-7
135.003
98.5
1132
1-Bromo-2-butene
C4H7Br
4784-77-4
135.003
98(4)
1133
cis-2-Bromo-2-butene
C4H7Br
3017-68-3
135.003 liq
-111.2(0.5)
89(3)
1134
trans-2-Bromo-2-butene
C4H7Br
3017-71-8
135.003 liq
-115.4(0.5)
86(3)
1135
1136
(4-Bromobutoxy)benzene
1-Bromo-4-tert-butylbenzene
C10H13BrO
C10H13Br
1200-03-9
3972-65-4
229.113 cry (al)
213.114
41
19
15418
231(10)
1137
C8H6BrClO
41011-01-2 233.490 nd
40
397.5
1138
2-Bromo-3’-chloroacetophenone
1-Bromo-2-chlorobenzene
C6H4BrCl
694-80-4
191.453 liq
-12.6(0.3)
204
1139
1-Bromo-3-chlorobenzene
C6H4BrCl
108-37-2
191.453 liq
-21.4(0.3)
196(6)
1140
1-Bromo-4-chlorobenzene
C6H4BrCl
106-39-8
191.453 nd or pl (al, 64.78(0.05)
eth)
197(3)
1141
1-Bromo-4-chlorobutane
C4H8BrCl
6940-78-9
171.464
161(11)
1142
1143
CBrClF2
C5H6BrClN2O2
353-59-3
126-06-7
165.365 col gas
241.471
-159.5
162
1144
1145
Bromochlorodifluoromethane
3-Bromo-1-chloro-5,5dimethylhydantoin
1-Bromo-1-chloroethane
1-Bromo-2-chloroethane
C2H4BrCl
C2H4BrCl
593-96-4
107-04-0
143.410
143.410 liq
-16.7(0.3)
101(12)
106(2)
1146
Bromochlorofluoromethane
CHBrClF
593-98-6
147.374 liq
-115
39(15)
1147
Bromochloromethane
Halon 1011
CH2BrCl
74-97-5
129.384 liq
-87.9(0.2)
67.9(0.4)
1148
1-Bromo-4-(chloromethyl)­
benzene
2-Bromo-1-(4-chlorophenyl)­
ethanone
p-Bromobenzyl chloride
C7H6BrCl
589-17-3
205.480 nd (al, peth) 42(4)
4-Chlorophenacyl bromide
C8H6BrClO
536-38-9
233.490 nd
1119
Organic
1149
HCP_Section_03.indb 62
DL-α-Bromobutyric acid
3-Chlorophenacyl bromide
Halon 1211
2-Chloro-1-bromoethane
-2.0
33
nD
42165
101.4(0.7)
1.39720 1.498820
1.275820 1.440120
91(4)
1.258520 1.436620
2.07325
198(7)
217 dec
14225
3611
86(5)
1.496720 1.481820
1.564120
Solubility
i H2O; s EtOH,
eth, bz, HOAc;
sl chl
vs eth, EtOH,
HOAc
s chl
sl H2O; s EtOH,
bz, chl; vs eth,
CS2
i H2O; vs ace,
bz, DMF
i H2O; s EtOH,
eth, chl
vs eth, EtOH
i H2O; msc
EtOH, eth, ace;
sl ctc; s chl
vs ace, eth, chl
s H2O, EtOH; sl
HOAc
s EtOH, eth, chl
s H2O, EtOH, eth
1.326515 1.453620 i H2O; s eth,
ace, bz, chl; sl
ctc
1.320915 1.452720 i H2O; s eth,
ace, bz, chl; sl
ctc
1.320915 1.452720 i H2O; s eth,
ace, bz, chl; sl
ctc
1.323020 1.462220 sl H2O; vs bz,
eth, EtOH
1.337125 1.482220 i H2O; s EtOH,
eth, ctc; vs
chl, bz
1.341615 1.463119 i H2O; s EtOH,
eth, ctc; vs
chl, bz
1.332315 1.460216 i H2O; s EtOH,
eth, ctc; vs
chl, bz
sl EtOH, ctc
1.228620 1.543620 i H2O; s eth, bz,
chl
vs EtOH
1.638725 1.580920 i H2O; vs bz; sl
ctc
1.630220 1.577120 i H2O; vs EtOH,
eth
1.57671 1.553170 i H2O; sl EtOH; s
eth, bz, ctc,
chl
1.48920 1.488520 i H2O; s EtOH,
eth, chl; sl ctc
-3.9(0.7)
236
1.66710 1.466020
1.739220 1.490820 sl H2O; s EtOH,
eth, chl
1.97710 1.414425 i H2O; s eth,
ace, chl
1.934420 1.483820 i H2O; s EtOH,
eth, ace, bz
i H2O; vs EtOH,
eth; s peth
96.5
4/11/16 11:19 AM
Physical Constants of Organic Compounds
3-63
Br
Br
Br
Br
Br
1115
1114
Br
1116
1-Bromo-2-(bromomethyl)benzene
4-Bromobiphenyl
O
N
N
Br
Br
Br
1118
1117
1-Bromo-3-(bromomethyl)benzene
2-Bromo-2-(bromomethyl)pentanedinitrile
1-Bromo-4-(bromomethyl)benzene
Br
OH
Br
OH
O
Br
Br
1120
1119
2-Bromo-1,3-butadiene
2-Bromo-1-(4-bromophenyl)ethanone
Br
1121
1122
1-Bromobutane
Br
Br
O
1123
2-Bromobutane, (±)-
N
1124
Bromobutanedioic acid, (±)-
4-Bromobutanenitrile
O
O
OH
1125
2-Bromobutanoic acid, (±)-
O
Br
Br
Br
OH
1126
1127
4-Bromobutanoic acid
Br
Br
3-Bromo-2-butanone
1128
Br
1129
cis-1-Bromo-1-butene
1130
trans-1-Bromo-1-butene
Br
1131
2-Bromo-1-butene
1132
4-Bromo-1-butene
1-Bromo-2-butene
Br
O
Br
O
Br
Br
Br
Cl
Br
Cl
1133
cis-2-Bromo-2-butene
1134
1135
trans-2-Bromo-2-butene
1136
(4-Bromobutoxy)benzene
1137
1-Bromo-4-tert-butylbenzene
2-Bromo-3’-chloroacetophenone
Br
O
Br
1139
1-Bromo-3-chlorobenzene
F
Cl
Cl
1140
Br
N
Cl
Br
F
1141
1-Bromo-4-chlorobenzene
1142
1-Bromo-4-chlorobutane
Br
Cl
Br
1145
1-Bromo-2-chloroethane
Br
1144
3-Bromo-1-chloro-5,5-dimethylhydantoin
1-Bromo-1-chloroethane
O
Br
Cl
H
F
1146
Cl
O
1143
Bromochlorodifluoromethane
Br
Cl
Br
N
Cl
Cl
1138
1-Bromo-2-chlorobenzene
Bromochlorofluoromethane
H
H
Br
1147
Bromochloromethane
Cl
1148
1-Bromo-4-(chloromethyl)benzene
Cl
1149
2-Bromo-1-(4-chlorophenyl)ethanone
Organic
Br
Physical Constants of Organic Compounds
3-64
Mol. Form.
CAS RN
Mol.
Wt.
bp/˚C
den
g cm –3
1-Bromo-2-chloropropane
C3H6BrCl
3017-96-7
157.437
118
1.53120
1151
1-Bromo-3-chloropropane
C3H6BrCl
109-70-6
157.437 liq
143(6)
1.596920
1152
2-Bromo-1-chloropropane
C3H6BrCl
3017-95-6
157.437
117
1.53720
1153
2-Bromo-2-chloropropane
C3H6BrCl
2310-98-7
157.437
95
1.49520
1154
1156
1-Bromo-2-chloro-1,1,2-trifluoroethane
2-Bromo-2-chloro-1,1,1-triflu- Halothane
oroethane
Bromocresol Green
Bromcresol Green
C2HBrClF3
354-06-3
197.381
52.4(0.2)
1.857425
C2HBrClF3
151-67-7
197.381
50(1)
1.856325 1.36970
C21H14Br4O5S
76-60-8
218.5
Bromcresol Purple
Cycloheptyl bromide
C21H16Br2O5S
C7H13Br
115-40-2
2404-35-5
698.014 wh or red
(+7w) ye
(HOAc)
540.222
177.082
1157
1158
Bromocresol Purple
Bromocycloheptane
1159
Bromocyclohexane
Cyclohexyl bromide
C6H11Br
108-85-0
163.055 liq
-56.28(0.07) 165.9(0.8)
1160
1161
1162
trans-4-Bromocyclohexanol
2-Bromocyclohexanone
3-Bromocyclohexene
C6H11BrO
C6H9BrO
C6H9Br
32388-22-0 179.054 pl (hx)
822-85-5
177.038
1521-51-3 161.039
1163
1164
Bromocyclopentane
1-Bromodecane
C5H9Br
C10H21Br
137-43-9
112-29-8
1165
1166
2-Bromodecanoic acid
1-Bromo-3,5-dichlorobenzene
C10H19BrO2
C6H3BrCl2
1167
4-Bromo-1,2-dichlorobenzene
1168
1169
Bromodichlorofluoromethane
Bromodichloromethane
1170
1171
1172
1173
1174
No.
Name
1150
1155
Organic
1175
1176
1177
1178
1179
1180
Synonym
11432
8140
18282-59-2 225.898 pr
25
237
CBrCl2F
CHBrCl2
353-58-2
75-27-4
181.819 liq
163.829 liq
-56.0(0.4)
52.8
90(2)
4-Bromo-2,5-dichlorophenol
2-Bromo-1,1-diethoxyethane
4-Bromo-N,N-diethylaniline
C6H3BrCl2O
C6H13BrO2
C10H14BrN
1940-42-7
2032-35-1
2052-06-4
241.897 nd
197.070
228.129 nd or pr
Bromodifluoromethane
3-Bromo-4,5-dihydro-2(3H)- α-Bromo-γ-butyrolactone
furanone
5-Bromo-N,2-dihydroxybenza- 5-Bromosalicylhydroxamic
mide
acid
2-Bromo-1,4-dimethoxybenzene
4-Bromo-1,2-dimethoxybenzene
2-Bromo-1,1-dimethoxyethane
4-Bromo-N,N-dimethylaniline
CHBrF2
C4H5BrO2
1511-62-2
5061-21-2
130.920
164.986
-145(4)
C7H6BrNO3
5798-94-7
232.032 cry (al)
232 dec
C8H9BrO2
1.308020 1.499620 i H2O; vs eth,
chl
1.335920 1.495720 i H2O; msc
EtOH, eth, ace,
bz, lig, ctc
1.34025 1.508525
1.389020 1.532020 i H2O; s eth, bz,
chl
1.387320 1.488620 sl ctc
1.070220 1.455720 i H2O; vs eth,
chl; s ctc
1.191224 1.459524 vs eth
i H2O; s EtOH,
eth, chl; vs bz
i H2O; sl EtOH;
vs eth, bz, chl
1.9522
1.98020 1.496420 i H2O; vs EtOH,
eth, ace, bz; sl
ctc
70.8(0.5)
170
270
1.28320
-15.6(0.5)
13020
1.5516
1.820
1.438720 s EtOH, eth
i H2O; vs EtOH,
eth
s H2O; vs EtOH
1.505920
25245-34-5 217.060 oil
262
1.445
1.570020
C8H9BrO2
2859-78-1
217.060
254.5
1.70225
1.574320
C4H9BrO2
7252-83-7
169.017
149
1.43020
1.445020 s eth, ace, chl
C8H10BrN
586-77-6
200.076
55
264
1.3220100
C8H9Br
583-70-0
185.061 liq
-17
204(8)
1.341920 1.550120
C8H9Br
556-96-7
185.061
203(8)
1.36220
C8H9Br
576-22-7
185.061
204(6)
1.555220
C8H9Br
553-94-6
185.061 lf or pl
9
207(6)
1.358218 1.551418
C8H9Br
583-71-1
185.061 liq
-0.2
215(7)
1.370820 1.553020
C10H17Br
6138-90-5
217.146
10112
1.094022 1.502720
C5H11Br
630-17-1
151.045
108(11)
262.018 ye nd (al or
HOAc)
247.003 ye nd (al)
1.199720 1.437020 i H2O; s EtOH,
eth, ace, bz;
vs chl
vs EtOH, ace; s
HOAc
vs EtOH
1817-73-8
1188
1-Bromo-2,4-dinitrobenzene
C6H3BrN2O4
584-48-5
HCP_Section_03.indb 64
sl H2O; s peth
81.5
C6H3BrCl2
C6H4BrN3O4
1185
10140
1402
232
2-Bromo-4,6-dinitroaniline
1184
Solubility
1.474520 vs ace, bz, eth,
EtOH
1.486420 i H2O; vs EtOH,
eth, chl
1.479520 i H2O; vs EtOH,
eth; s ace, bz
1.457520 vs ace, bz, eth,
EtOH
1.373820
241.5
2.0
83
1187
1183
nD
sl H2O; vs EtOH,
eth, AcOEt; s
bz
2623-95-2 251.161
19752-55-7 225.898 pr (al)
1186
1182
-58.8(0.2)
137.5
240.6
Halon 1121
149.029
221.178 liq
mp/˚C
-29.3(0.5)
Cyclopentyl bromide
Decyl bromide
1-Bromo-2,4-dimethylbenzene
1-Bromo-3,5-dimethylbenzene
2-Bromo-1,3-dimethylbenzene
2-Bromo-1,4-dimethylbenzene
4-Bromo-1,2-dimethylbenzene
trans-1-Bromo-3,7-dimethyl- trans-Geranyl bromide
2,6-octadiene
1-Bromo-2,2-dimethylpropane
1181
Physical
Form
38
153.5
75
sub
1.546222
i H2O; s EtOH;
vs eth
i H2O; vs EtOH,
eth, ace
vs eth; s ace,
bz
vs eth; s ace,
bz
i H2O; vs EtOH;
s bz
i H2O; vs EtOH,
eth
4/11/16 11:19 AM
Physical Constants of Organic Compounds
3-65
Cl
Cl
Br
Br
Cl
1150
Br
OH
Br
Br
Br Cl
1152
1-Bromo-3-chloropropane
Br
HO
Cl
Br
1151
1-Bromo-2-chloropropane
F
1153
2-Bromo-1-chloropropane
HO
Br
Br
F
F
F
1154
2-Bromo-2-chloropropane
1-Bromo-2-chloro-1,1,2-trifluoroethane
OH
Br
1155
2-Bromo-2-chloro-1,1,1-trifluoroethane
OH
Br
Br
O
F
F
Cl
O
Br
O
S
O O
Br
S
O O
1156
Br
1158
1157
1159
Bromocycloheptane
Bromocresol Purple
1160
Bromocyclohexane
trans-4-Bromocyclohexanol
1161
2-Bromocyclohexanone
Organic
Bromocresol Green
Br
O
Br
OH
Br
Br
1162
3-Bromocyclohexene
1163
Br
1164
Bromocyclopentane
1-Bromodecane
Cl
1166
2-Bromodecanoic acid
Cl
1-Bromo-3,5-dichlorobenzene
N
OH
Cl
Cl
Br
Cl
1167
4-Bromo-1,2-dichlorobenzene
Br
F
Br
Cl
H
Cl
Cl
Cl
Br
1168
1169
1170
Br
Bromodichlorofluoromethane
Bromodichloromethane
H
N
Br
Br
H
F
O
1173
Bromodifluoromethane
O
1172
4-Bromo-N,N-diethylaniline
O
Br
O
O
Br
1176
5-Bromo-N,2-dihydroxybenzamide
N
2-Bromo-1,1-diethoxyethane
O
1175
3-Bromo-4,5-dihydro-2(3H)-furanone
Br
O
1171
OH
OH
Br
1174
O
4-Bromo-2,5-dichlorophenol
O
F
Cl
1165
2-Bromo-1,4-dimethoxybenzene
1177
4-Bromo-1,2-dimethoxybenzene
Br
Br
Br
Br
Br
O
O
1178
2-Bromo-1,1-dimethoxyethane
Br
1179
4-Bromo-N,N-dimethylaniline
1180
1-Bromo-2,4-dimethylbenzene
1181
1-Bromo-3,5-dimethylbenzene
1182
2-Bromo-1,3-dimethylbenzene
O
Br
1184
4-Bromo-1,2-dimethylbenzene
Br
Br
1185
trans-1-Bromo-3,7-dimethyl-2,6-octadiene
1186
1-Bromo-2,2-dimethylpropane
O
N
1183
2-Bromo-1,4-dimethylbenzene
O
N
Br
NH2
Br
O
N
1187
O
2-Bromo-4,6-dinitroaniline
O
N
O
O
1188
1-Bromo-2,4-dinitrobenzene
Physical Constants of Organic Compounds
3-66
No.
Name
1189
α-Bromodiphenylmethane
1190
1-Bromododecane
1191
2-Bromododecanoic acid
1192
Bromoethane
1193
Mol. Form.
CAS RN
Mol.
Wt.
C13H11Br
776-74-9
C12H25Br
Physical
Form
den
g cm –3
Organic
mp/˚C
bp/˚C
247.130
45
18420
143-15-7
249.231 liq
-9.6(0.4)
275(20)
1.039920 1.458320
C12H23BrO2
111-56-8
279.214 pl
32
1582
1.147474 1.458524
Ethyl bromide
C2H5Br
74-96-4
108.965 liq
-118.4(1)
38.2(0.6)
1.460420 1.423920
2-Bromoethanol
Ethylene bromohydrin
C2H5BrO
540-51-2
124.964
142(4)
1.762920 1.491520
1194
Bromoethene
Vinyl bromide
C2H3Br
593-60-2
106.949 vol liq or
gas
-139.5(0.2)
16(16)
1.493320 1.438020
1195
1196
1-Bromo-2-ethoxybenzene
1-Bromo-4-ethoxybenzene
C8H9BrO
C8H9BrO
583-19-7
588-96-5
201.060
201.060
2.0
223
231
1.422320
1.407125 1.551720
1197
(2-Bromoethoxy)benzene
C8H9BrO
589-10-6
201.060
39
240 dec
1.355520
1198
1-Bromo-2-ethoxyethane
C4H9BrO
592-55-2
153.017
127(4)
1.38520
1.444720
1199
2-Bromoethyl acetate
C4H7BrO2
927-68-4
167.002 liq
-13.8
159(5)
1.51420
1.45723
1200
C2H7Br2N
2576-47-8
204.892
174.0
1201
1202
2-Bromoethylamine
hydrobromide
(1-Bromoethyl)benzene
(2-Bromoethyl)benzene
C8H9Br
C8H9Br
585-71-7
103-63-9
185.061
185.061 liq
-55.9(0.2)
201(8)
216(4)
1203
1-Bromo-2-ethylbenzene
C8H9Br
1973-22-4
185.061 liq
-67.5(0.2)
202(4)
1204
1205
1-Bromo-3-ethylbenzene
1-Bromo-4-ethylbenzene
C8H9Br
C8H9Br
2725-82-8
1585-07-5
185.061
185.061 liq
-43.4(0.2)
203(11)
204(4)
1206
1207
1208
1209
1210
1211
(2-Bromoethyl)cyclohexane
N-(2-Bromoethyl)phthalimide
1-Bromo-4-ethynylbenzene
1-Bromo-2-fluorobenzene
1-Bromo-3-fluorobenzene
1-Bromo-4-fluorobenzene
C8H15Br
C10H8BrNO2
C8H5Br
C6H4BrF
C6H4BrF
C6H4BrF
1647-26-3
574-98-1
766-96-1
1072-85-1
1073-06-9
460-00-4
191.109 liq
254.081 nd (w)
181.030
174.998
174.998
174.998 liq
1212
1213
1-Bromo-2-fluoroethane
Bromofluoromethane
C2H4BrF
CH2BrF
762-49-2
373-52-4
1214
2-Bromofuran
C4H3BrO
584-12-3
126.955
112.929 vol liq or
gas
146.970
1.353525 1.554325
1.364320 1.537220 i H2O; s eth, bz;
sl ctc
1.354820 1.547220 vs ace, bz, eth,
EtOH
1.349320 1.546520
1.342320 1.544520 vs ace, bz, eth,
EtOH
1.235720 1.489920
vs eth; sl chl
s chl
1.073821 1.533720
1.708120 1.525720 s ctc
1.59315 1.531015 i H2O; s EtOH,
eth, chl
1.704425 1.423620 vs eth, EtOH
s EtOH; vs chl
1215
3-Bromofuran
C4H3BrO
22037-28-1 146.970
106(6)
1216
C5H3BrO2
1899-24-7
174.981 cry (50% al) 83.5
201
1217
1218
5-Bromo-2-furancarboxaldehyde
1-Bromoheptadecane
1-Bromoheptane
Heptyl bromide
C17H35Br
C7H15Br
3508-00-7
629-04-9
319.364
179.098 liq
28.4(0.4)
-56.1(0.3)
345(13)
179(5)
1219
2-Bromoheptane
2-Heptyl bromide
C7H15Br
1974-04-5
179.098
47
166(6)
1220
4-Bromoheptane
4-Heptyl bromide
C7H15Br
998-93-6
179.098
1221
1222
1223
1-Bromohexadecane
2-Bromohexadecanoic acid
1-Bromohexane
Hexyl bromide
C16H33Br
C16H31BrO2
C6H13Br
112-82-3
305.337
18263-25-7 335.320
111-25-1
165.071 liq
1224
2-Bromohexane
C6H13Br
3377-86-4
165.071
139(9)
1225
3-Bromohexane
C6H13Br
3377-87-5
165.071
143(4)
1226
1227
1228
1229
1230
2-Bromohexanoic acid, (±)6-Bromohexanoic acid
6-Bromohexanoyl chloride
1-Bromo-4-(hexyloxy)benzene
5-Bromo-2-hydroxybenzaldehyde
C6H11BrO2
C6H11BrO2
C6H10BrClO
C12H17BrO
C7H5BrO2
2681-83-6
4224-70-8
22809-37-6
30752-19-3
1761-61-1
195.054
195.054 cry (peth)
213.499
257.166
201.018 nd (al), lf
(eth)
HCP_Section_03.indb 66
Synonym
Lauryl bromide
2-Bromoethyl ethyl ether
2-Bromoethanamine
hydrobromide
-57
81.5(0.5)
64.5
-17.4
212(3)
8916
154
150
150(2)
58(12)
23(12)
103(6)
163(9)
17.5(0.4)
52.8
-84.9(0.4)
2.0
35
105.5
336
156(4)
242(11)
16720
1016
15613
nD
Solubility
s EtOH, chl; vs
bz
i H2O; s EtOH,
eth, ctc; msc
ace
vs bz, eth,
EtOH, lig
sl H2O; msc
EtOH, eth, chl
msc H2O, EtOH,
eth; sl lig
i H2O; s EtOH,
eth, ace, bz,
chl
vs eth, EtOH
i H2O; vs EtOH,
eth; s chl
i H2O; vs EtOH,
eth
sl H2O; msc
EtOH, eth
vs H2O, chl;
msc EtOH, eth
1.650020 1.498020 sl H2O; s EtOH,
eth, ace, bz
1.660620 1.495820 vs ace, bz, eth,
EtOH
vs eth, EtOH
0.991620 1.462520 i H2O; vs chl
1.140020 1.450220 i H2O; vs EtOH,
eth; sl ctc; s
chl
1.127720 1.450320 i H2O; vs bz; s
ctc, chl
1.135120 1.449520 i H2O; s bz, ctc,
chl
0.999120 1.461825 i H2O; s eth
1.174420 1.447820 i H2O; msc
EtOH, eth; s
ace; vs chl
1.165820 1.483225 i H2O; vs EtOH;
s eth, ace; sl
ctc
1.179920 1.447220 vs ace, eth,
EtOH, chl
1.281033
s EtOH, eth
vs peth
1.230620 1.526220
i H2O; s EtOH,
eth; sl chl
4/11/16 11:19 AM
Physical Constants of Organic Compounds
3-67
Br
O
OH
Br
1189
1190
α-Bromodiphenylmethane
1191
1-Bromododecane
Br
1193
1192
2-Bromododecanoic acid
OH
Br
Br
Br
1194
2-Bromoethanol
Bromoethane
Bromoethene
Br
Br
O
O
O
Br
O
1195
1196
1197
1-Bromo-4-ethoxybenzene
1198
(2-Bromoethoxy)benzene
Br
O
1199
1-Bromo-2-ethoxyethane
Br
HBr H2N
1200
2-Bromoethyl acetate
2-Bromoethylamine hydrobromide
Organic
1-Bromo-2-ethoxybenzene
Br
O
Br
Br
Br
O
Br
N
Br
Br
Br
O
1202
1201
(2-Bromoethyl)benzene
(1-Bromoethyl)benzene
1203
1204
1-Bromo-2-ethylbenzene
1205
1-Bromo-3-ethylbenzene
Br
1207
1206
1-Bromo-4-ethylbenzene
N-(2-Bromoethyl)phthalimide
(2-Bromoethyl)cyclohexane
Br
Br
Br
F
1208
1209
1-Bromo-4-ethynylbenzene
Br
F
F
1-Bromo-2-fluorobenzene
F
F
1210
1211
1-Bromo-3-fluorobenzene
H
Br
1212
1-Bromo-4-fluorobenzene
1-Bromo-2-fluoroethane
H
Br
Br
O
1213
O
1214
Bromofluoromethane
1215
2-Bromofuran
3-Bromofuran
O
Br
Br
O
1216
Br
1217
5-Bromo-2-furancarboxaldehyde
Br
1218
1-Bromoheptadecane
Br
1219
1-Bromoheptane
1220
2-Bromoheptane
4-Bromoheptane
Br
O
Br
Br
OH
1221
1222
1-Bromohexadecane
Br
1223
2-Bromohexadecanoic acid
1224
1-Bromohexane
2-Bromohexane
Br
O
Br
O
OH
Br
1225
3-Bromohexane
OH
Br
1226
2-Bromohexanoic acid, (±)-
Br
O
1227
6-Bromohexanoic acid
OH
Cl
O
1228
6-Bromohexanoyl chloride
O
Br
1229
1-Bromo-4-(hexyloxy)benzene
1230
5-Bromo-2-hydroxybenzaldehyde
Physical Constants of Organic Compounds
3-68
No.
Name
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
1231
4-Bromo-αhydroxybenzeneacetic acid,
(±)5-Bromo-2-hydroxybenzenemethanol
5-Bromo-2-hydroxybenzoic
acid
3-Bromo-4-hydroxy-5methoxybenzaldehyde
p-Bromomandelic acid
C8H7BrO3
7021-04-7
231.044
119
vs H2O, EtOH,
eth, bz, chl
Bromosaligenin
C7H7BrO2
2316-64-5
203.034 lf (bz)
113
C7H5BrO3
89-55-4
217.017 nd (w, dil al) 169.8
C8H7BrO3
2973-76-4
231.044 pl (HOAc),
nd, pl (al)
167.0
vs bz, eth,
EtOH, chl
sl H2O, ace; vs
EtOH, eth
i H2O; s EtOH,
DMSO; sl eth,
bz
i H2O; sl EtOH,
HOAc; s ace
i H2O; sl EtOH,
HOAc
i H2O; sl EtOH,
chl; s eth
vs chl
vs eth
1232
1233
1234
Physical
Form
mp/˚C
bp/˚C
Organic
1-Bromo-2-iodobenzene
C6H4BrI
583-55-1
282.904
2.1(0.5)
257
1236
1-Bromo-3-iodobenzene
C6H4BrI
591-18-4
282.904 liq
-9.3(0.6)
252
1237
1-Bromo-4-iodobenzene
C6H4BrI
589-87-7
90.37(0.05)
252
1238
1239
CH2BrI
C7H4BrNO
557-68-6
2493-02-9
1240
Bromoiodomethane
1-Bromo-4-isocyanatobenzene
1-Bromo-4-isopropylbenzene
282.904 pr or pl
(eth-al)
220.835
198.017 nd
C9H11Br
586-61-8
199.087 liq
1241
1242
4-Bromoisoquinoline
Bromomethane
C9H6BrN
CH3Br
1532-97-4
74-83-9
208.055 cry (peth)
94.939 col gas
1243
1244
1245
1-Bromo-2-methoxyethane
Bromomethoxymethane
2-Bromo-4-methylaniline
C3H7BrO
C2H5BrO
C7H8BrN
1246
4-Bromo-2-methylaniline
1247
(Bromomethyl)benzene
1248
1249
1250
1251
4-(Bromomethyl)benzoic acid
3-(Bromomethyl)benzonitrile
4-(Bromomethyl)benzonitrile
1-Bromo-2-methylbutane, DL
1252
1-Bromo-3-methylbutane
1253
1254
2-Bromo-2-methylbutane
3-Bromo-3-methylbutanoic
acid
1-Bromo-3-methyl-2-butene
1256
2.92617
-22.4(0.2)
219(3)
41.5
-93.7(0.4)
282.5
3.4(0.1)
6482-24-2 138.991
13057-17-5 124.964
583-68-6
186.050 lf
26
112(4)
87
240
C7H8BrN
583-75-5
186.050 cry (al)
59.5
240
C7H7Br
100-39-0
171.035 liq
-1.5
191(4)
1.314520 1.556920 i H2O; s eth, bz,
chl; sl ctc
vs eth
1.675520 1.421820 sl H2O; msc
EtOH, eth, chl,
CS2
1.462320 1.4475320
1.597620 1.456220
1.51020 1.599920 i H2O; s EtOH,
eth
sl H2O, chl; s
EtOH; vs eth,
HOAc
1.438025 1.575220 i H2O; msc
EtOH, eth; s
ctc
C8H7BrO2
C8H6BrN
C8H6BrN
C5H11Br
6232-88-8
28188-41-2
17201-43-3
5973-11-5
215.045
196.045
196.045
151.045
226.3
96.5
114
1304
Isopentyl bromide
C5H11Br
107-82-4
151.045 liq
-112
tert-Pentyl bromide
β-Bromoisovaleric acid
C5H11Br
C5H9BrO2
507-36-8
5798-88-9
151.045
181.028 nd (lig)
74
C5H9Br
870-63-3
149.029
121(18)
C7H6BrCl
611-17-6
205.480
10910
C3H8BrClSi
16532-02-8 187.539
131
1.37525
C7H13Br
13905-48-1 177.082
181
C7H13Br
C7H6BrF
2550-36-9
456-41-7
7626
8820
1.267615 1.497920 i H2O; vs eth; s
bz
1.28320 1.490730 vs bz, eth, chl
1.547420
C8H17Br
C8H9Br
18908-66-2 193.125
89-92-9
185.061 pr
C8H9Br
620-13-3
185.061
C8H9Br
104-81-4
185.061 nd (al)
34(2)
220
C11H9Br
3163-27-7
56(2)
18318
56
213100
Methyl bromide
Benzyl bromide
119
1266
2-(Bromomethyl)naphthalene
C11H9Br
939-26-4
221.093 cry (peth,
al)
221.093 lf (al)
1267
1-(Bromomethyl)-3-nitrobenzene
1-(Bromomethyl)-4-nitrobenzene
C7H6BrNO2
3958-57-4
216.033 nd or pl (al) 59.3
C7H6BrNO2
100-11-8
216.033 nd (al)
1259
1260
1261
1262
1263
1264
1268
HCP_Section_03.indb 68
121(1)
105(8)
1265
1258
2.257025 1.661825
177.082
189.025
21
6710
217
212.5
99(2)
16213
1.641020
Solubility
136(14)
226
p-Bromophenyl isocyanate
1-(Bromomethyl)-2-chlorobenzene
(Bromomethyl)chlorodimethylsilane
1-Bromo-3-methylcyclohex- 3-Methylcyclohexyl bromide
ane
(Bromomethyl)cyclohexane
1-(Bromomethyl)-3-fluorobenzene
3-(Bromomethyl)heptane
1-(Bromomethyl)-2-methylbenzene
1-(Bromomethyl)-3-methylbenzene
1-(Bromomethyl)-4-methylbenzene
1-(Bromomethyl)naphthalene
1257
nD
100 sub
1235
1255
den
g cm –3
1.220520 1.445220 i H2O; s EtOH,
eth; vs chl
1.207120 1.442020 i H2O; s EtOH,
eth; sl ctc; vs
chl
1.19718 1.4421
vs bz, eth, EtOH
1.293015 1.493015 vs ace, bz, eth,
EtOH
1.463025
1.381123 1.573020 i H2O; s EtOH,
eth, ace, bz
1.371123 1.566020 i H2O; vs EtOH,
eth
1.32425
i H2O; s EtOH;
vs eth, chl
vs ace, bz, eth,
EtOH
s EtOH, eth, chl,
HOAc
i H2O; s EtOH
sl H2O, chl; vs
EtOH, eth; s
HOAc
4/11/16 11:19 AM
Physical Constants of Organic Compounds
3-69
O
OH
OH
O
OH
OH
OH
O
O
Br
HO
Br
1231
1232
4-Bromo-α-hydroxybenzeneacetic acid, (±)-
1234
1233
5-Bromo-2-hydroxybenzenemethanol
Br
OH
Br
3-Bromo-4-hydroxy-5-methoxybenzaldehyde
5-Bromo-2-hydroxybenzoic acid
Br
Br
Br
Br
Br
Br
Br
I
I
I
1235
1236
1-Bromo-3-iodobenzene
O
I
H
1237
1238
1-Bromo-4-iodobenzene
C
N
N
1239
Bromoiodomethane
1240
1-Bromo-4-isocyanatobenzene
1241
1-Bromo-4-isopropylbenzene
4-Bromoisoquinoline
Organic
1-Bromo-2-iodobenzene
H
O
Br
Br
H
H
Br
Br
O
H
Br
1243
1242
O
Br
1245
1244
1-Bromo-2-methoxyethane
Bromomethane
OH
NH2
NH2
2-Bromo-4-methylaniline
Bromomethoxymethane
Br
1246
1247
4-Bromo-2-methylaniline
(Bromomethyl)benzene
1248
4-(Bromomethyl)benzoic acid
N
N
3-(Bromomethyl)benzonitrile
OH
Br
Br
1249
Br
Br
Br
Br
1250
O
1251
4-(Bromomethyl)benzonitrile
1252
1-Bromo-2-methylbutane, DL
1253
1-Bromo-3-methylbutane
2-Bromo-2-methylbutane
Br
1254
3-Bromo-3-methylbutanoic acid
Br
Br
Cl
1255
1-Bromo-3-methyl-2-butene
Si
Br
Br
1256
Cl
1257
1-(Bromomethyl)-2-chlorobenzene
1258
(Bromomethyl)chlorodimethylsilane
1-Bromo-3-methylcyclohexane
1259
(Bromomethyl)cyclohexane
Br
Br
Br
Br
Br
F
1260
1-(Bromomethyl)-3-fluorobenzene
1261
1262
3-(Bromomethyl)heptane
1-(Bromomethyl)-2-methylbenzene
1263
1-(Bromomethyl)-3-methylbenzene
1264
1-(Bromomethyl)-4-methylbenzene
Br
Br
Br
Br
1265
1-(Bromomethyl)naphthalene
1266
2-(Bromomethyl)naphthalene
N
O
1267
O
1-(Bromomethyl)-3-nitrobenzene
O
N
O
1268
1-(Bromomethyl)-4-nitrobenzene
Physical Constants of Organic Compounds
3-70
No.
Name
1269
1270
2-(Bromomethyl)-4-nitrophenol
(Bromomethyl)oxirane, (±)-
1271
1272
1273
1274
1275
1-Bromo-2-methylpentane
1-Bromo-4-methylpentane
2-Bromo-2-methylpentane
3-Bromo-3-methylpentane
2-Bromo-4-methylphenol
1276
1-(Bromomethyl)-3-phenoxy- 3-Phenoxybenzyl bromide
benzene
2-Bromo-1-(4-methylphenyl)­
ethanone
N-(Bromomethyl)phthalimide 2-(Bromomethyl)-1H-isoindole1,3(2H)-dione
1-Bromo-2-methylpropane
Isobutyl bromide
1277
1278
1279
Organic
1280
1281
Synonym
2-Methylpentyl bromide
CAS RN
Mol.
Wt.
Physical
Form
bp/˚C
den
g cm –3
C7H6BrNO3
772-33-8
232.032
C3H5BrO
82584-73-4 136.975 liq
-40
138(3)
1.61514
C6H13Br
C6H13Br
C6H13Br
C6H13Br
C7H7BrO
25346-33-2
626-88-0
4283-80-1
25346-31-0
6627-55-0
1.162420
1.168320
55.3(0.5)
139(8)
145
142.5
130
213.5
C13H11BrO
51632-16-7 263.129 oil
C9H9BrO
619-41-0
213.070 nd or lf (al)
51
15714
C9H6BrNO2
5332-26-3
240.054 pr (chl, bz)
151.5
C4H9Br
78-77-3
137.018 liq
-117.8(0.7)
91.3(0.5)
1.27215
C4H9Br
C4H7BrO2
507-19-7
2052-01-9
137.018 liq
167.002 cry (peth)
-16.8(0.9)
48.5
73.3
199
1.427820 1.427820
1.496960
C4H6Br2O
20769-85-1 229.898
163
1.406714
C4H7Br
C4H7Br
C5H9BrO
3017-69-4
1458-98-6
1192-30-9
91(7)
92(18)
170
1.33620
1.31320
1.467920 1.485020 s EtOH, eth
C4H11BrSi
C10H7Br
18243-41-9 167.120
90-11-9
207.067 oily liq
6.1(0.1)
116.5
280(2)
281(9)
1.17025 1.446020
1.478520 1.65820 s H2O, ace; msc
EtOH, eth, bz;
sl ctc
1.60525 1.638260 i H2O; s EtOH,
eth, bz, CS2; sl
ctc
165.071
165.071
165.071
165.071
187.034 nd (peth)
mp/˚C
1286
1287
1288
2-Bromonaphthalene
C10H7Br
580-13-2
207.067 pl or orth lf
(al)
58(2)
1289
C12H5BrO3
81-86-7
277.070
222
1290
4-Bromo-1,8-naphthalenedicarboxylic anhydride
1-Bromo-2-naphthol
C10H7BrO
573-97-7
1291
4-Bromo-2-nitroaniline
C6H5BrN2O2
875-51-4
1292
1-Bromo-2-nitrobenzene
C6H4BrNO2
577-19-5
223.066 orth pr
84
(bz-lig) nd
(HOAc)
217.020 oran-ye nd 111.5
(w)
202.006 pa ye (al)
38.5(0.2)
1293
1-Bromo-3-nitrobenzene
C6H4BrNO2
585-79-5
202.006 orth
1294
1-Bromo-4-nitrobenzene
C6H4BrNO2
586-78-7
1295
1296
CH2BrNO2
C3H6BrNO4
1297
1298
Bromonitromethane
2-Bromo-2-nitro-1,3-propane- Bronopol
diol
1-Bromononane
1-Bromooctadecane
1299
1-Bromooctane
1300
1283
1284
1285
1-Naphthyl bromide
1-Bromo-β-naphthol
nD
135.003
135.003
165.028
1.183520
1.542225
1.484120 i H2O; s EtOH,
eth, bz, chl
1.449520 vs eth, chl
1.4490
vs eth, chl
1.44223 vs eth, chl
1.452520 vs eth, chl
1.577220 sl H2O; s EtOH,
bz, chl
vs eth, EtOH
1.434820
130
i H2O; s EtOH,
eth, bz; sl chl;
vs HOAc
vs EtOH
sub
1.624580
54(3)
265
1.703620 1.597920
133.0(0.2)
252(5)
1.94825
563-70-2
52-51-7
202.006 orth or mcl
pr (al)
139.937
199.989
C9H19Br
C18H37Br
693-58-3
112-89-0
207.151 liq
333.391 cry (al)
-29.0(0.2)
27.6(0.4)
221.4
357(17)
C8H17Br
111-83-1
193.125 liq
-55.0(0.3)
199(6)
2-Bromooctane, (±)-
C8H17Br
60251-57-2 193.125
1301
1302
8-Bromooctanoic acid
1-Bromopentadecane
C8H15BrO2
C15H31Br
17696-11-6 223.108 nd (peth)
629-72-1
291.311
38.5
18.6(0.3)
1472
322
1303
1304
1305
Bromopentafluorobenzene
Bromopentafluoroethane
1-Bromopentane
C6BrF5
C2BrF5
C5H11Br
344-04-7
354-55-2
110-53-2
246.960 liq
198.917 col gas
151.045 liq
-31
-88.0(0.2)
133(2)
-21
126(3)
1306
2-Bromopentane
C5H11Br
107-81-3
151.045 liq
-95.5
117(5)
1307
3-Bromopentane
C5H11Br
1809-10-5
151.045 liq
-126.2
118(5)
1308
5-Bromopentanenitrile
C5H8BrN
5414-21-1
162.029
HCP_Section_03.indb 70
Octyl bromide
Pentyl bromide
149
s ace; sl bz, chl;
vs AcOEt
i H2O; vs EtOH,
eth, ace, chl,
bz; s ctc
i H2O; sl ctc
vs ace, CS2
253(6)
p-Nitrobromobenzene
Solubility
148
2-Bromo-2-methylpropane
2-Bromo-2-methylpropanoic
acid
2-Bromo-2-methylpropanoyl
bromide
1-Bromo-2-methylpropene
3-Bromo-2-methylpropene
2-(Bromomethyl)­
tetrahydrofuran
(Bromomethyl)trimethylsilane
1-Bromonaphthalene
1282
tert-Butyl bromide
α-Bromoisobutyric acid
Mol. Form.
1.488020
i H2O; vs EtOH;
s eth, ace, bz;
sl chl
sl H2O; s EtOH,
eth, bz
i H2O; s EtOH,
eth, bz; sl chl
vs EtOH
131.5
188.5
11112
1.084525 1.452225
0.984820 1.463120 i H2O; s EtOH,
eth; sl ctc
1.107225 1.450325 i H2O; msc
EtOH, eth; sl
ctc
1.087825 1.444225 i H2O; msc
EtOH, eth
vs bz, eth, EtOH
1.067520 1.461120 i H2O; s ace; vs
chl
1.98125 1.449020
1.809825
1.218220 1.444720 i H2O; s EtOH,
bz, chl; sl ctc;
msc eth
1.207520 1.441320 vs bz, eth,
EtOH, chl
1.21420 1.444120 i H2O; s EtOH,
eth, bz, chl
1.398920 1.478020
4/11/16 11:19 AM
Physical Constants of Organic Compounds
3-71
OH
Br
Br
N
O
O
1269
2-(Bromomethyl)-4-nitrophenol
1270
1271
(Bromomethyl)oxirane, (±)-
OH
Br
Br
Br
O
1272
1-Bromo-2-methylpentane
1273
1-Bromo-4-methylpentane
O
O
Br
1274
2-Bromo-2-methylpentane
Br
3-Bromo-3-methylpentane
O
Br
N
Br
1276
2-Bromo-4-methylphenol
1277
1-(Bromomethyl)-3-phenoxybenzene
Br
2-Bromo-1-(4-methylphenyl)ethanone
Br
OH
Br
1280
N-(Bromomethyl)phthalimide
1282
1281
1-Bromo-2-methylpropane
Br
O
Br
1283
2-Bromo-2-methylpropanoyl bromide
2-Bromo-2-methylpropanoic acid
1279
Br
O
2-Bromo-2-methylpropane
1278
Organic
1275
Br
O
Br
1284
1-Bromo-2-methylpropene
3-Bromo-2-methylpropene
O
O
O
Br
Br
Si
Br
O
1285
Br
1286
2-(Bromomethyl)tetrahydrofuran
1287
(Bromomethyl)trimethylsilane
NH2 O
N
Br
Br
1288
1-Bromonaphthalene
Br
O
O
N
O
HO
Br
Br
N
O
Br
1291
1-Bromo-2-naphthol
4-Bromo-1,8-naphthalenedicarboxylic anhydride
Br
OH
1290
1289
2-Bromonaphthalene
1292
4-Bromo-2-nitroaniline
O
O
1293
1-Bromo-2-nitrobenzene
1-Bromo-3-nitrobenzene
NO2
OH
N
O
N
Br
O
1294
1-Bromo-4-nitrobenzene
Bromonitromethane
Br
1296
Br
1297
2-Bromo-2-nitro-1,3-propanediol
O
1295
1298
1-Bromononane
1-Bromooctadecane
OH
Br
Br
Br
1299
1300
1-Bromooctane
O
Br
1301
2-Bromooctane, (±)-
1302
8-Bromooctanoic acid
1-Bromopentadecane
F
F
Br
F
F
F
1303
Bromopentafluorobenzene
F
F
F
Br
1304
F
F
Bromopentafluoroethane
Br
Br
Br
Br
1305
1-Bromopentane
N
1306
2-Bromopentane
1307
3-Bromopentane
1308
5-Bromopentanenitrile
Physical Constants of Organic Compounds
3-72
Organic
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
9-Phenanthryl bromide
C5H9BrO2
C5H9Br
C14H9Br
2067-33-6
1119-51-3
573-17-1
2-Bromophenol
C6H5BrO
1313
3-Bromophenol
1314
4-Bromophenol
1315
Bromophenol Blue
1316
1317
1318
1-Bromo-4-phenoxybenzene
(4-Bromophenoxy)­
trimethylsilane
N-(4-Bromophenyl)acetamide
1319
1320
No.
Name
1309
1310
1311
5-Bromopentanoic acid
5-Bromo-1-pentene
9-Bromophenanthrene
1312
Physical
Form
mp/˚C
bp/˚C
181.028
149.029
257.125 pr (al)
40.0
64.5
14213
125.5
>360
95-56-7
173.007
5.6
194.5
C6H5BrO
591-20-8
173.007
33
236.5
C6H5BrO
106-41-2
173.007
63(1)
238
Bromphenol Blue
C19H10Br4O5S
115-39-9
4-Bromophenyl phenyl ether
C12H9BrO
C9H13BrOSi
669.960 hex pr
(HOAcace)
101-55-3
249.102
17878-44-3 245.188
p-Bromoacetanilide
C8H8BrNO
103-88-8
214.060 nd (60% al) 168
1-(3-Bromophenyl)ethanone
1-(4-Bromophenyl)ethanone
p-Bromoacetophenone
C8H7BrO
C8H7BrO
2142-63-4
99-90-1
199.045
199.045 lf (al)
7.5
50.5
1321
(4-Bromophenyl)hydrazine
(p-Bromophenyl)hydrazine
C6H7BrN2
589-21-9
108
1322
2-(4-Bromophenyl)-1Hindene-1,3(2H)-dione
(4-Bromophenyl)­
phenylmethanone
2-Bromo-1-phenyl-1-propanone
Bromindione
C15H9BrO2
1146-98-1
187.037 nd (w), lf
(lig), cry
(al)
301.135 cry (lig)
C13H9BrO
90-90-4
261.113 lf (al)
82.5
C9H9BrO
2114-00-3
213.070
C8H8BrCl2PS
2104-96-3
317.999 ye cry
56.3(0.3)
1410.01
1323
1324
279 dec
18.7(0.2)
1263.5
12625
13319
257
247.5
Bromophos-ethyl
1-Bromopropane
Propyl bromide
C10H12BrCl2O3PS
C3H7Br
4824-78-6
106-94-5
394.049 pale-ye liq
122.992 liq
-110.1(0.3)
1220.004
70.8(0.2)
1328
2-Bromopropane
Isopropyl bromide
C3H7Br
75-26-3
122.992 liq
-88.9(0.5)
59.34(0.09)
1329
3-Bromopropanenitrile
C3H4BrN
2417-90-5
133.975
1330
2-Bromopropanoic acid, (±)-
C3H5BrO2
10327-08-9 152.975 pr
25.7
203.5
1331
3-Bromopropanoic acid
C3H5BrO2
590-92-1
152.975 pl (CCl4)
62.5
14145
1332
3-Bromo-1-propanol
C3H7BrO
627-18-9
138.991
105185
1333
1-Bromo-2-propanol
C3H7BrO
19686-73-8 138.991
146.5
1334
1335
1336
2-Bromopropanoyl bromide
2-Bromopropanoyl chloride
cis-1-Bromopropene
C3H4Br2O
C3H4BrClO
C3H5Br
563-76-8
7148-74-5
590-13-6
215.871
171.420
120.976 liq
-113
153
132
58(3)
1337
1338
trans-1-Bromopropene
2-Bromopropene
C3H5Br
C3H5Br
590-15-8
557-93-7
120.976
120.976 liq
-126
61(5)
49(4)
1339
3-Bromopropene
C3H5Br
106-95-6
120.976 liq
-119.3(0.5)
70.1(0.5)
1340
1341
1342
C9H9Br
C9H11BrO
C3H9Br2N
4392-24-9
588-63-6
5003-71-4
197.071 nd (al, eth)
215.086
218.918
34
10.7
171.5
13010
12718
C17H16Br2O3
18181-80-1 428.115
1344
1345
(3-Bromo-1-propenyl)benzene
(3-Bromopropoxy)benzene
3-Bromopropylamine
3-Bromo-1-propanamine
hydrobromide
hydrobromide
Bromopropylate
4,4’-Dibromobenzilic acid
isopropyl ester
(3-Bromopropyl)benzene
3-Bromo-1-propyne
Propargyl bromide
C9H11Br
C3H3Br
637-59-2
106-96-7
199.087
118.960
1346
2-Bromopyridine
C5H4BrN
109-04-6
157.997 liq
HCP_Section_03.indb 72
s chl
1.258120 1.464020
1.409310
i H2O; s EtOH,
eth, CS2; sl chl
1.492420 1.58920 sl H2O, chl; s
EtOH, eth, alk
sl H2O, ctc; vs
EtOH, eth; s
chl, alk
1.84015
s H2O, chl; vs
EtOH, eth
sl H2O; s EtOH,
bz, HOAc
1.608820 1.608420 i H2O; s eth, ctc
1.261920 1.514520
1.64725
1.575520
1.647
350
1326
1327
1343
Solubility
i H2O; s EtOH,
chl; sl eth, bz
i H2O; s ace, bz
i H2O; s EtOH,
eth, bz, ctc,
HOAc
vs eth, EtOH, lig
138
Bromophos
Allyl bromide
nD
1.71725
1325
β-Bromopropionic acid
den
g cm –3
9225
76.0(0.5)
1.353720 1.434320 sl H2O; s EtOH,
eth, ace, bz,
chl, ctc
1.314020 1.425120 sl H2O; s ace,
bz, chl; msc
EtOH, eth
1.615220 1.480020 vs EtOH, eth; sl
ctc
1.700020 1.475320 vs H2O, EtOH,
eth; sl chl
1.4825
s H2O, EtOH,
eth, bz, chl
1.537420 1.483425 s H2O; msc
EtOH, eth
1.558530 1.480120 s H2O; vs EtOH,
eth
2.061116
1.69711 1.478020 s eth, chl; sl ctc
1.429120 1.456020 i H2O; s eth,
ace, chl
1.396516 1.446716 i H2O; s eth,
ace, chl
1.39820 1.469720 i H2O; msc
EtOH, eth; s
ctc, chl, CS2
1.342830 1.61320 vs EtOH
1.36416
vs eth
1.5920
219.5
73(14)
-40.1
1.429820 1.572020
i H2O; sl EtOH,
eth, bz, peth
i H2O; s EtOH,
eth, ace, bz,
ctc
sl H2O; s eth,
ctc, tol
193
1.310625 1.544025 i H2O; vs eth
1.57919 1.492220 s EtOH, eth, bz,
ctc, chl
1.633720 1.573420 sl H2O; s EtOH,
eth, ctc
4/11/16 11:19 AM
Physical Constants of Organic Compounds
3-73
OH
Br
Br
Br
OH
Br
Br
OH
OH
OH
O
Br
O
Br
OH
1309
Br
1310
5-Bromopentanoic acid
1311
5-Bromo-1-pentene
1312
9-Bromophenanthrene
1313
2-Bromophenol
3-Bromophenol
Br
S
O
O
Br
1314
1315
4-Bromophenol
Bromophenol Blue
O
O
Si
O
HN
HN
O
NH2
Br
1316
1-Bromo-4-phenoxybenzene
Br
Br
Br
1317
1318
N-(4-Bromophenyl)acetamide
(4-Bromophenoxy)trimethylsilane
Br
1319
O
O
O
O
Br
1-(4-Bromophenyl)ethanone
S
O
P
O
Cl
O
Cl
O
1322
1323
2-(4-Bromophenyl)-1H-indene-1,3(2H )-dione
Br
1324
(4-Bromophenyl)phenylmethanone
(4-Bromophenyl)hydrazine
S
O
P
O
Cl
Br
Br
1325
2-Bromo-1-phenyl-1-propanone
1321
Cl
Br
Br
Br
1320
1-(3-Bromophenyl)ethanone
1326
Bromophos
1327
Bromophos-ethyl
1-Bromopropane
Br
O
N
1329
2-Bromopropane
3-Bromopropanenitrile
2-Bromopropanoic acid, (±)-
Br
1331
3-Bromopropanoic acid
Br
OH
1332
3-Bromo-1-propanol
1333
1-Bromo-2-propanol
Br
O
1335
1336
2-Bromopropanoyl chloride
Br
Br
Br
Br
O
1334
2-Bromopropanoyl bromide
O
Br
Br
1337
cis-1-Bromopropene
Br
OH
OH
1330
Cl
Br
O
OH
Br
Br
1328
Br
Organic
O
trans-1-Bromopropene
1338
1339
2-Bromopropene
3-Bromopropene
1340
(3-Bromo-1-propenyl)benzene
1341
(3-Bromopropoxy)benzene
O
HO
O
Br
H2N
Br
1342
HBr
3-Bromopropylamine hydrobromide
Br
Br
1343
Bromopropylate
1344
(3-Bromopropyl)benzene
Br
N
1345
3-Bromo-1-propyne
Br
1346
2-Bromopyridine
Physical Constants of Organic Compounds
3-74
Organic
mp/˚C
bp/˚C
den
g cm –3
157.997 liq
-27.3
172(3)
1.6450
1120-87-2
51-20-7
157.997
190.983
0.5
310
290.4
1.64500
C9H6BrN
C9H6BrN
5332-24-1
5332-25-2
208.055 ye oil
208.055
13.3
24
275
281
N-Bromosuccinimide
C4H4BrNO2
128-08-5
177.985 cry (bz)
174
C14H29Br
C3H2BrNS
C6H5BrOS
112-71-0
3034-53-5
5370-25-2
277.284
164.024
205.072 nd (al)
5.7(0.4)
1356
1-Bromotetradecane
2-Bromothiazole
1-(5-Bromo-2-thienyl)­
ethanone
2-Bromothiophene
C4H3BrS
1003-09-4
1357
3-Bromothiophene
C4H3BrS
1358
1359
Bromothymol Blue
2-Bromotoluene
1360
No.
Name
1347
3-Bromopyridine
1348
1349
1350
1351
4-Bromopyridine
5-Bromo-2,4(1H,3H)-pyrimidinedione
3-Bromoquinoline
6-Bromoquinoline
1352
1353
1354
1355
Synonym
5-Bromouracil
Mol. Form.
CAS RN
Mol.
Wt.
C5H4BrN
626-55-1
C5H4BrN
C4H3BrN2O2
Physical
Form
2.09825
nD
Solubility
1.569420 s H2O; vs EtOH,
eth
1.569420 s ace, bz
1.664120 s chl; vs HOAc
s EtOH, eth,
acid
sl H2O, AcOEt,
eth; vs ace; i
hx
1.460320 vs ace, bz, EtOH
1.592720
sl EtOH; s ctc
307
171
1034
1.017020
1.8225
163.036
141(6)
1.68420
872-31-1
163.036
149(7)
1.73520
C27H28Br2O5S
C7H7Br
76-59-5
95-46-5
624.381
171.035 liq
201
-27.5(0.8)
182(2)
1.423220
3-Bromotoluene
C7H7Br
591-17-3
171.035 liq
-38.1(0.2)
184(2)
1.409920
1361
4-Bromotoluene
C7H7Br
106-38-7
171.035 cry (al)
26.2(0.7)
184(4)
1.395935
1362
1363
1364
1365
Bromotrichloromethane
1-Bromotridecane
Bromotriethylsilane
2-Bromo-1,1,1-trifluoroethane
CBrCl3
C13H27Br
C6H15BrSi
C2H2BrF3
75-62-7
765-09-3
1112-48-7
421-06-7
-5.6(0.2)
5.9(0.3)
-49.3
-93.9
103(5)
292
163
26
2.01225
1.023425
1.14320
1.788120
1366
1367
1368
C2BrF3
CBrF3
C7H4BrF3
598-73-2
75-63-8
392-83-6
-174.4(0.2)
-2.5
-57.8(0.4)
167.5
1.580020
i H2O; vs chl
1.65225 1.481720
C7H4BrF3
401-78-5
225.006
1
151.5
1.61325
1.471620
C7H4BrF3
402-43-7
225.006
160
1.60725
1.470525
C9H11Br
576-83-0
199.087 liq
-1
225
1372
1373
1374
1375
Bromotrifluoroethene
Bromotrifluoromethane
1-Bromo-2-(trifluoromethyl)­
benzene
1-Bromo-3-(trifluoromethyl)­
benzene
1-Bromo-4-(trifluoromethyl)­
benzene
2-Bromo-1,3,5-trimethylbenzene
Bromotrinitromethane
Bromotriphenylmethane
1-Bromoundecane
11-Bromoundecanoic acid
198.274 liq
263.257
195.173 liq
162.936 vol liq or
gas
160.920 col gas
148.910 col gas
225.006
CBrN3O6
C19H15Br
C11H23Br
C11H21BrO2
560-95-2
596-43-0
693-67-4
2834-05-1
229.931
323.226
235.205 liq
265.188 nd (liq)
18(1)
153
-9.9(0.4)
57
5610
23015
258.8
18818
1376
1377
1378
(1-Bromovinyl)benzene
(cis-2-Bromovinyl)benzene
(trans-2-Bromovinyl)benzene
C8H7Br
C8H7Br
C8H7Br
98-81-7
588-73-8
588-72-7
183.046
183.046
183.046
-44
-7
7
8614
552
219 dec
1379
1380
1381
1-Bromo-2-vinylbenzene
1-Bromo-3-vinylbenzene
1-Bromo-4-vinylbenzene
C8H7Br
C8H7Br
C8H7Br
2039-88-5
2039-86-3
2039-82-9
183.046 liq
183.046
183.046
-52.7(0.2)
215(2)
9220
213(1)
1382
1383
Brompheniramine
Brucine
C16H19BrN2
C23H26N2O4
86-22-6
357-57-3
1384
Brucine hydrochloride
319.239 ye oily liq
394.463 mcl pr (w
+4)
430.924 pr
1.319110 1.551020 i H2O; vs eth; s
bz; sl ctc
2.031220 1.480820 vs EtOH, chl
1.550020
1.049425 1.455225 sl ctc
vs ace, bz, eth,
EtOH
1.402523 1.588120
1.432210 1.599022
1.426916 1.609320 i H2O; msc
EtOH, eth; s
chl
1.416020 1.592720
1.405920 1.593320
1.398420 1.594720 i H2O; vs chl; s
HOAc
s dil acid
sl H2O, eth, bz;
vs EtOH, chl
vs H2O, EtOH
1385
Brucine sulfate heptahydrate
1386
Bucolome
1387
1388
1369
1370
1371
2-Thienyl bromide
Bromthymol Blue
Halon-1301
Triphenylmethyl bromide
2,3-Dimethoxystrychnidin-10- C23H27ClN2O4
one, monohydrochloride
2,3-Dimethoxystrychnidin-10- C46H68N4O19S
one, sulfate, heptahydrate
5786-96-9
94.5
5(2)
1500.5
178
60583-39-3 1013.113 nd (w)
s H2O; sl EtOH,
chl, tfa; vs
MeOH; i bz
C14H22N2O3
841-73-6
266.336 nd (MeOH)
84
Bufotalin
C26H36O6
471-95-4
444.560 cry (+1 al)
223 dec
Bulbocapnine
C19H19NO4
298-45-3
325.359 pr (al)
199.5
HCP_Section_03.indb 74
5-Butyl-1-cyclohexyl2,4,6(1H,3H,5H)-pyrimidinetrione
1.586820 i H2O; vs eth,
ace; s ctc
1.591920 i H2O; s ace, bz;
sl chl
vs eth, EtOH
1.556520 i H2O; vs EtOH,
eth, bz; msc
ctc
1.551020 i H2O; s EtOH,
ace, chl; msc
eth; sl ctc
1.547720 i H2O; s EtOH,
eth, ace, bz,
chl; sl ctc
1.506520 vs eth, EtOH
1.457425 i H2O; vs chl
1.456120
1.333120
1860.8
i H2O; s EtOH,
chl
i H2O; s EtOH;
vs chl
4/11/16 11:19 AM
Physical Constants of Organic Compounds
3-75
O
Br
Br
N
Br
N
N
H
N
1347
1348
3-Bromopyridine
H
Br
O
N
1349
4-Bromopyridine
Br
O
1351
1350
5-Bromo-2,4(1H,3H )-pyrimidinedione
1352
6-Bromoquinoline
3-Bromoquinoline
O
N
Br
N
N-Bromosuccinimide
Br
N
1354
1-Bromotetradecane
HO
OH
Br
Br
Br
S
S
O
2-Bromothiazole
Br
S
1355
S
1356
1-(5-Bromo-2-thienyl)ethanone
1357
2-Bromothiophene
3-Bromothiophene
Organic
Br
1353
Br
Br
Br
O
S O
O
Br
Br
Cl
Cl
Br
Cl
1358
1359
Bromothymol Blue
1360
2-Bromotoluene
1361
3-Bromotoluene
1362
4-Bromotoluene
1363
Bromotrichloromethane
1-Bromotridecane
Br
Br
Si
Br
F
1364
F
F
1365
Bromotriethylsilane
Br
F
F
F
Br
F
F
F
F
F
F
F
1366
2-Bromo-1,1,1-trifluoroethane
Br
1367
Bromotrifluoroethene
1368
Bromotrifluoromethane
F
F
1369
1-Bromo-2-(trifluoromethyl)benzene
1-Bromo-3-(trifluoromethyl)benzene
Br
Br
Br
Br
F
F
O2N
F
1370
1371
1-Bromo-4-(trifluoromethyl)benzene
NO2
NO2
Br
1372
2-Bromo-1,3,5-trimethylbenzene
1374
1373
Bromotrinitromethane
1-Bromoundecane
Bromotriphenylmethane
Br
Br
Br
O
Br
Br
OH
1375
1376
11-Bromoundecanoic acid
1377
(1-Bromovinyl)benzene
1378
(cis-2-Bromovinyl)benzene
N
Br
N
O
1381
1-Bromo-3-vinylbenzene
N
H
O
Br
1380
H
O
N
1382
1-Bromo-4-vinylbenzene
O
N
HCl
H
O
O
1383
Brompheniramine
NH
H
H
H
1-Bromo-2-vinylbenzene
O
H
Br
1379
(trans-2-Bromovinyl)benzene
H
O
1384
Brucine
Brucine hydrochloride
O
O
O
NH
O
H
O
N
O
N
H2SO4.7H2O
O
N
O
H
H
O
H
O
OH
H
HO
O
1385
Brucine sulfate heptahydrate
1386
Bucolome
H
O
N
H
O
HO
O
1387
Bufotalin
1388
Bulbocapnine
Physical Constants of Organic Compounds
3-76
Mol.
Wt.
Physical
Form
Organic
No.
Name
Synonym
Mol. Form.
CAS RN
1389
sec-Bumeton
C10H19N5O
26259-45-0 225.291
1390
BUSAN 72A
N2-sec-Butyl-N4-ethyl-6methoxy-1,3,5-triazine-2,4diamine
(2-Benzothiazolylthio)methyl
thiocyanate
C9H6N2S3
21564-17-0 238.352 liq
1391
1392
Butachlor
1,2-Butadiene
Methylallene
C17H26ClNO2
C4H6
23184-66-9 311.847
590-19-2
54.091 vol liq or
gas
<-5
156.5
-136.20(0.05) 11.0(0.2)
1393
1,3-Butadiene
Divinyl
C4H6
106-99-0
-108.9(0.1)
1394
1395
1,3-Butadien-1-ol acetate
trans-1,3-Butadienylbenzene
C6H8O2
C10H10
1515-76-0 112.127
16939-57-4 130.186
1396
1,3-Butadiyne
Diacetylene
C4H2
460-12-8
50.059
1397
Butalbital
C11H16N2O3
77-26-9
224.256 pr
1398
Butanal
5-Isobutyl-5-allyl2,4,6(1H,3H,5H)-pyrimidinetrione
Butyraldehyde
C4H8O
123-72-8
72.106
liq
1399
Butanal oxime
C4H9NO
110-69-0
87.120
liq
1400
Butanamide
C4H9NO
541-35-5
87.120
lf (bz)
1401
Butane
C4H10
106-97-8
58.122
col gas
1402
Butanedial
C4H6O2
638-37-9
86.090
1403
1404
Putrescine
C4H12N2
C4H14Cl2N2
110-60-1
333-93-7
1405
1,4-Butanediamine
1,4-Butanediamine
dihydrochloride
1,2-Butanediol, (±)-
1406
1407
1,3-Butanediol
1,4-Butanediol
1,3-Butylene glycol
Tetramethylene glycol
1408
1409
1410
1411
Butyramide
54.091
mp/˚C
col gas
vol liq or
gas
C4H10O2
C4H10O2
107-88-0
110-63-4
90.121
90.121
visc liq
2,3-Butanediol
C4H10O2
6982-25-8
90.121
cry (eth)
1,4-Butanediol diacetate
1,4-Butanediol diacrylate
1,4-Butanediol diglycidyl ether 1,4-Bis(2,3-epoxypropoxy)­
butane
1,3-Butanediol dimethacrylate
C8H14O4
C10H14O4
C10H18O4
628-67-1
1070-70-8
2425-79-8
174.195
198.216
202.248
C12H18O4
1189-08-8
226.269
C12H18O4
C6H14O6S2
2082-81-7
55-98-1
226.269 liq
246.301 cry
116
1415
1,4-Butanediol dimethacrylate
1,4-Butanediol dimethylsulfo- Busulfan
nate
2,3-Butanedione
Diacetyl
C4H6O2
431-03-8
86.090
1416
2,3-Butanedione monooxime
C4H7NO2
57-71-6
1417
1418
Butanedioyl dichloride
1,4-Butanedithiol
Succinyl chloride
Tetramethylenedithiol
C4H4Cl2O2
C4H10S2
1419
Butanenitrile
Propyl cyanide
1420
1421
1422
1423
1424
1425
nD
Solubility
1.07025
0.6760
1.42051
i H2O; msc
EtOH, eth; vs
bz
i H2O; s EtOH,
eth, bz; vs ace
0.614925 1.4292-25
(p>1
atm
5840
0.94525 1.469020
2.3
7611
0.928620 1.608925 i H2O; s EtOH,
eth, ace, bz
-35(3)
10(2)
0.73640 1.41895 vs H2O, eth,
ace; s chl,
EtOH
138.5
sl H2O; s EtOH,
eth, ace, chl; i
lig
-96.86(0.02) 74.8(0.2)
0.801620 1.384320 s H2O; msc
EtOH; vs ace,
bz; sl chl
-29.5
152(9)
0.92320
vs H2O, ace, bz;
msc EtOH, eth;
s chl
116(1)
231.8(1)
0.8850120 1.4087130 sl H2O, eth; i bz;
s EtOH
-138.3(0.1) -0.5(0.5)
0.57325 1.332620 i H2O; vs EtOH,
(p>1
eth, chl
atm)
170 dec
1.06520 1.426218 vs H2O, ace,
eth, EtOH
21.9(0.4)
156(10)
0.87725 1.496920 s H2O
280 dec
sub
vs H2O, EtOH; i
eth, bz, MeOH
196.42(0.06) 1.002420 1.437820 s H2O, EtOH,
ace
-77
208.2(0.1) 1.005320 1.440120
20.43(0.02) 229.5(0.4) 1.017120 1.446020 msc H2O; s
EtOH, DMSO;
sl eth
7(2)
178(3)
1.003320 1.431025 msc H2O, EtOH;
s eth, ace, chl
12
233(6)
1.047915 1.425115
830.3
1.10525
266
1.125
1.461120
C4H10O2
1413
1414
den
g cm –3
87
88.151 lf
161.073 nd or lf (al,
w)
26171-83-5 90.121
1412
bp/˚C
-4.6(0.2)
290
1334
1.02520
-1.2
87.5(0.8)
0.980818
76.8
185.5
543-20-4
1191-08-8
101.105 pr (chl), lf
(w)
154.980 pl or lf
122.252 liq
16.7(0.6)
-53.9
190(5)
195.5
C4H7N
109-74-0
69.106
-111.76(0.05) 117.6(0.4)
1-Butanesulfonyl chloride
1,4-Butane sultone
1,2-Oxathiane 2,2-dioxide
1,2,3,4-Butanetetracarboxylic
acid
1,2,3,4-Butanetetrol
Erythritol
C4H9ClO2S
C4H8O3S
C8H10O8
2386-60-9
1633-83-6
1703-58-8
C4H10O4
149-32-6
1,2,3,4-Butanetetrol
tetranitrate, (R*,S*)1-Butanethiol
Erythrityl tetranitrate
C4H6N4O12
7297-25-8
156.631
136.170 liq
234.160 lf (w) cry
(ace)
122.120 bipym tetr
pr
302.111
Butyl mercaptan
C4H10S
109-79-5
90.187
HCP_Section_03.indb 76
liq
liq
liq
13.5
236.5
118.1(0.7)
1.374820
1.00210
0.793620
7510
1354
1.33120
330.5
1.45120
61
-115.66(0.06) 98.4(0.5)
1.449525 vs ace, eth,
EtOH, lig
1.456020 sl H2O
i H2O; sl EtOH,
ace
1.395120 vs H2O; msc
EtOH, eth; s
bz, ctc
sl H2O; vs EtOH,
eth, chl; s alk
1.468320 s eth, ace, bz
1.529020 i H2O; vs EtOH;
sl ctc
1.384220 sl H2O, ctc; msc
EtOH, eth; s bz
1.455920
1.464020
vs H2O, EtOH
s H2O; i eth, bz
vs EtOH
0.841620 1.444020 sl H2O, chl; vs
EtOH, eth
4/11/16 11:20 AM
Physical Constants of Organic Compounds
3-77
O
HN
N
N
N
O
Cl
N
O
N
N
O
S
N
H
S
1389
C
S
1390
sec-Bumeton
1391
BUSAN 72A
O
1392
Butachlor
1393
1,2-Butadiene
1394
1,3-Butadiene
1395
1,3-Butadien-1-ol acetate
trans-1,3-Butadienylbenzene
O
O
1396
N
H
H
O
O
1397
1,3-Butadiyne
N
O
1398
Butalbital
1399
Butanal
O
NH2
OH
1400
Butanal oxime
1401
Butanamide
1402
Butane
NH2
H2N
O
Organic
N
1403
Butanedial
1,4-Butanediamine
OH
NH2 2HCl
H2N
1404
O
O
OH
OH
1405
1,4-Butanediamine dihydrochloride
O
OH
OH
1406
1,2-Butanediol, (±)-
O
O
O
1410
S
1411
1414
O
O
1415
O
S
O O
1421
1,4-Butane sultone
1417
2,3-Butanedione monooxime
COOH
COOH
COOH
1422
1,2,3,4-Butanetetracarboxylic acid
Cl
Cl
N OH
1416
2,3-Butanedione
HOOC
O
O
O
O
O
1413
1,4-Butanediol dimethacrylate
O
O
O
1,4-Butanediol dimethylsulfonate
1409
1,3-Butanediol dimethacrylate
O
O O
O
1,4-Butanediol diacetate
1412
1,4-Butanediol diglycidyl ether
O O
S
O
O
O
O
O
O
1,4-Butanediol diacrylate
1408
2,3-Butanediol
1,4-Butanediol
O
O
OH
1407
1,3-Butanediol
O
OH
HO
Butanedioyl dichloride
H
H
CH2OH
OH
OH
CH2OH
1423
1,2,3,4-Butanetetrol
HS
SH
1418
1419
1,4-Butanedithiol
H
H
Cl
O
S
O
N
Butanenitrile
1420
1-Butanesulfonyl chloride
CH2ONO2
ONO2
ONO2
CH2ONO2
1424
1,2,3,4-Butanetetrol tetranitrate, (R*,S*)-
SH
1425
1-Butanethiol
Physical Constants of Organic Compounds
3-78
Mol.
Wt.
Organic
No.
Name
Synonym
Mol. Form.
CAS RN
1426
2-Butanethiol
sec-Butyl mercaptan
C4H10S
91840-99-2 90.187
1427
1428
1,2,4-Butanetriol
Butanilicaine
1429
Butanoic acid
C4H10O3
2-(Butylamino)-N-(2-chloro-6- C13H19ClN2O
methylphenyl)acetamide
Butyric acid
C4H8O2
1430
1431
Butanoic anhydride
1-Butanol
Butyric anhydride
Butyl alcohol
1432
2-Butanol
1433
2-Butanone
1434
1435
2-Butanone (1-methylpropylidene)hydrazone
2-Butanone oxime
1436
1437
1438
1439
2-Butanone peroxide
Butanoyl chloride
Butaperazine
Butazolamide
1440
Physical
Form
mp/˚C
bp/˚C
liq
-165
85.0(0.7)
den
g cm –3
3068-00-6
3785-21-5
106.120
254.755 cry
46
19018
1450.001
107-92-6
88.106
-5.12(0.09)
163.7(0.1)
C8H14O3
C4H10O
106-31-0
71-36-3
158.195 liq
74.121 liq
-75.0(0.6)
195(1)
-88.60(0.02) 117.6(0.2)
sec-Butyl alcohol
C4H10O
78-92-2
74.121
liq
-88.44(0.07) 99.4(0.2)
Methyl ethyl ketone
C4H8O
78-93-3
72.106
liq
-86.67(0.01) 79.6(0.2)
C8H16N2
5921-54-0
140.226
C4H9NO
96-29-7
87.120
1338-23-4
141-75-3
653-03-2
16790-49-1
176.211 col liq
106.551 liq
409.587
250.298 cry
261 dec
trans-2-Butenal
N-[5-(Aminosulfonyl)-1,3,4thiadiazol-2-yl]butanamide
trans-Crotonaldehyde
C8H16O4
C4H7ClO
C24H31N3OS
C6H10N4O3S2
C4H6O
123-73-9
70.090
liq
-76.6(0.3)
1441
1-Butene
1-Butylene
C4H8
106-98-9
56.107
col gas
-185.33(0.02) -6.3(0.2)
1442
cis-2-Butene
C4H8
590-18-1
56.107
col gas
-138.89(0.02) 3.72(0.08)
1443
trans-2-Butene
C4H8
624-64-6
56.107
col gas
-105.52(0.02) 0.88(0.09)
1444
trans-2-Butenedinitrile
C4H2N2
764-42-1
78.072
nd (bz-peth) 96.0(0.8)
1445
1446
1447
1448
1449
1450
cis-2-Butene-1,4-diol
trans-2-Butene-1,4-diol
trans-2-Butenedioyl dichloride
cis-2-Butenenitrile
trans-2-Butenenitrile
3-Butenenitrile
Fumaric acid dichloride
Isocrotononitrile
Crotononitrile
Allyl cyanide
C4H8O2
C4H8O2
C4H2Cl2O2
C4H5N
C4H5N
C4H5N
6117-80-2
821-11-4
627-63-4
1190-76-7
627-26-9
109-75-1
88.106
88.106
152.964
67.090
67.090
67.090
1451
cis-2-Butenoic acid
Isocrotonic acid
C4H6O2
503-64-0
86.090
1452
trans-2-Butenoic acid
Crotonic acid
C4H6O2
107-93-7
86.090
1453
3-Butenoic acid
C4H6O2
625-38-7
86.090
1454
1455
1456
2-Butenoic anhydride
cis-2-Buten-1-ol
trans-2-Buten-1-ol
C8H10O3
C4H8O
C4H8O
623-68-7
4088-60-2
504-61-0
154.163
72.106
72.106
1457
3-Buten-1-ol
C4H8O
627-27-0
72.106
112(5)
1458
1459
3-Buten-2-ol
3-Buten-2-one
C4H8O
C4H6O
598-32-3
78-94-4
72.106
70.090
97(4)
81(4)
0.86420
1460
1461
2-Butenoyl chloride
trans-1-Butenylbenzene
C4H5ClO
C10H12
10487-71-5 104.535
1005-64-7 132.202 liq
121(8)
201(4)
1.090520
0.901920
1462
1463
1464
2-Butenylbenzene
3-Butenylbenzene
1-Buten-3-yne
C10H12
C10H12
C4H4
1560-06-1
768-56-9
689-97-4
182(6)
183(4)
6.0(0.9)
0.883120
0.883120
0.70940
HCP_Section_03.indb 78
Methyl ethyl ketone peroxide
n-Butyryl chloride
Crotonic acid anhydride
cis-Crotyl alcohol
trans-Crotyl alcohol
Methyl vinyl ketone
Vinylacetylene
liq
170(7)
liq
-29.5(0.5)
151.5(0.6)
-89.0(0.5)
exp
101(3)
2750.05
11.0(0.5)
27(1)
pa ye lig
liq
liq
liq
-51.5
-87
nd or pr
15
(peth)
mcl pr or nd 71.3(0.2)
(w, lig)
liq
-35
132.202
132.202 liq
52.075 col gas
<-30
-43.1(0.4)
-70
102.2(0.3)
186
235
13113
159
106(6)
120
117(5)
169
184.7
169
247
123
121.2
nD
Solubility
0.829520 1.436620 s EtOH, eth, bz,
peth; sl ctc
1.1820
1.468820 vs H2O, EtOH
0.952825 1.398020 msc H2O, EtOH,
eth; sl ctc
0.966820 1.407020 s eth; sl ctc
0.809520 1.398820 s H2O, bz; msc
EtOH, eth; vs
ace
0.806320 1.397820 vs H2O; msc
EtOH, eth; s
bz, ctc
25
20
0.7999
1.3788
vs H2O; msc
EtOH, eth, ace,
bz; s chl
0.840420 1.451120
0.923220 1.441020 s H2O, chl; msc
EtOH, eth
sl H2O; misc os
1.027720 1.412120 msc eth
0.851620 1.436620 s H2O, chl; vs
EtOH, eth, ace;
msc bz
0.58825 1.396220 i H2O; vs EtOH,
(p>1
eth; s bz
atm)
0.61625 1.3931-25 i H2O; vs EtOH,
(p>1
eth; s bz
atm)
0.59925 1.3848-25 s bz
(p>1
atm)
0.9416111 1.4349111 s H2O, EtOH,
eth, ace, bz,
chl; sl peth
1.069820 1.478220 s H2O; vs EtOH
1.070020 1.475520 vs H2O, EtOH
1.40820 1.500418
0.823920 1.422520 s eth, ace
0.834120 1.406020 sl H2O; msc
EtOH, eth
1.026720 1.445020 vs H2O; s EtOH
0.960477 1.424977 vs H2O, EtOH; s
eth, ace, lig
1.009120 1.423920 s H2O; msc
EtOH, eth
1.039720 1.474520 vs eth
0.866220 1.434225 s H2O
0.852120 1.428820 vs H2O; msc
EtOH, eth; s
chl
0.842420 1.422420 s H2O, ace; msc
EtOH, eth; sl
chl
1.408120 s H2O, EtOH, bz;
vs eth, ace; sl
ctc
1.46018 vs ace
1.542020 i H2O; s EtOH,
eth, bz, ctc
1.510120
1.505920 i H2O; s eth, bz
1.41611 i H2O; s bz
4/11/16 11:20 AM
Physical Constants of Organic Compounds
Cl
HO
H
N
OH
SH
1427
2-Butanethiol
1433
1431
Butanoic anhydride
1-Butanol
O O
N
N
1434
2-Butanone
OH
1435
2-Butanone (1-methylpropylidene)hydrazone
Cl
O
O O
1436
2-Butanone oxime
1437
2-Butanone peroxide
Butanoyl chloride
Organic
2-Butanol
OH
1430
Butanoic acid
O
1432
O
O
1429
Butanilicaine
N
O
O
1428
1,2,4-Butanetriol
OH
OH
N
H
O
OH
1426
3-79
N
O
H
N
N
O
S
1438
S
O
O
NH2
S
N N
O
1439
Butaperazine
1440
Butazolamide
1441
trans-2-Butenal
1-Butene
1442
cis-2-Butene
1443
trans-2-Butene
Cl
O
N
HO
N
1444
1445
trans-2-Butenedinitrile
N
1450
3-Butenenitrile
HO
OH
OH
1446
cis-2-Butene-1,4-diol
O
O
1451
O
cis-2-Butenoic acid
O
OH
1452
trans-2-Butenenitrile
O
OH
1454
3-Butenoic acid
1449
cis-2-Butenenitrile
O
1453
trans-2-Butenoic acid
1448
trans-2-Butenedioyl dichloride
OH
N
N
1447
trans-2-Butene-1,4-diol
HO
O
Cl
2-Butenoic anhydride
1455
cis-2-Buten-1-ol
OH
1456
trans-2-Buten-1-ol
O
OH
1457
3-Buten-1-ol
OH
1458
3-Buten-2-ol
Cl
O
1459
3-Buten-2-one
1460
2-Butenoyl chloride
1461
trans-1-Butenylbenzene
1462
2-Butenylbenzene
1463
3-Butenylbenzene
1464
1-Buten-3-yne
Physical Constants of Organic Compounds
3-80
No.
Name
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
1465
Butethamine hydrochloride
2-Isobutylaminoethyl
4-aminobenzoate
C13H21ClN2O2
553-68-4
272.771 cry
1466
Buthalital sodium
C11H15N2NaO2S
510-90-7
262.304
1467
1468
1469
1470
1471
1472
1473
Buthiazide
Buthiobate
Butonate
Butoxyacetylene
4-Butoxyaniline
4-Butoxybenzaldehyde
2-Butoxyethanol
C11H16ClN3O4S2
C21H28N2S2
C8H14Cl3O5P
C6H10O
C10H15NO
C11H14O2
C6H14O2
2043-38-1
51308-54-4
126-22-7
3329-56-4
4344-55-2
5736-88-9
111-76-2
353.846
372.590 ye oil
327.527
98.142
165.232
178.228
118.174 liq
1474
2-[2-(2-Butoxyethoxy)­ethoxy]­
ethanol
2-(2-Butoxyethoxy)ethyl
Lethane 384
thiocyanate
1-(2-Butoxyethoxy)-2-propanol
2-Butoxyethyl acetate
Ethylene glycol monobutyl
ether acetate
2-Butoxyethyl (2,4-dichloro2,4-D 2-Butoxyethyl ester
phenoxy)acetate
2-Butoxyethyl (2,4,5-trichloro- 2,4,5-T Butoxyethyl ester
phenoxy)acetate
4-Butoxy-N-hydroxybenzeBufexamac
neacetamide
1-Butoxy-4-methylbenzene
4-Butoxyphenol
C10H22O4
143-22-6
206.280
278
C9H17NO2S
112-56-1
203.302 liq
1220.25
C9H20O3
124-16-3
176.253 col liq
C8H16O3
112-07-2
160.211 liq
191.1(0.9)
C14H18Cl2O4
1929-73-3
321.197
1591
1.23220
C14H17Cl3O4
2545-59-7
355.642
1641
1.28020
C12H17NO3
2438-72-4
223.268 nd (ace)
C11H16O
C10H14O2
10519-06-9 164.244
122-94-1
166.217
229.5
1254
0.920525 1.497020 s eth
vs ace, bz, eth,
EtOH
C17H27NO3
140-65-8
293.401
1966
1484
4-[3-(4-Butoxyphenoxy)propyl] Pramoxine
morpholine
1-Butoxy-2-propanol
C7H16O2
5131-66-8
132.201
172(3)
1485
Butralin
C14H21N3O4
33629-47-9 295.335
59.3(0.5)
1350.5
1486
1487
N-Butylacetamide
Butyl acetate
C6H13NO
C6H12O2
1119-49-9
123-86-4
115.173
116.158 liq
-77.0(0.1)
229
126.0(0.1)
1488
sec-Butyl acetate
C6H12O2
105-46-4
116.158 liq
-98.9
108(4)
1489
tert-Butyl acetate
C6H12O2
540-88-5
116.158 liq
1490
1491
tert-Butylacetic acid
Butyl acetoacetate
C6H12O2
C8H14O3
1070-83-3
591-60-6
116.158
158.195
6(2)
-35.6
184(2)
12750
1492
Butyl acrylate
C7H12O2
141-32-2
128.169 liq
-63.6(0.5)
146.6(0.6)
1493
1494
tert-Butyl acrylate
Butylamine
1-Butanamine
C7H12O2
C4H11N
1663-39-4
109-73-9
128.169 liq
73.137 liq
-49(1)
120
77.0(0.2)
1495
sec-Butylamine
2-Butanamine, (±)-
C4H11N
33966-50-6 73.137
liq
-104.5(0.6)
62.71(0.08)
1496
tert-Butylamine
2-Methyl-2-propanamine
C4H11N
75-64-9
73.137
liq
-66.92(0.06) 44.02(0.07)
1497
1498
Butylamine hydrochloride
Butyl 4-aminobenzoate
1-Butanamine hydrochloride
Butamben
C4H12ClN
C11H15NO2
3858-78-4
94-25-7
213
57(2)
1499
2-(Butylamino)ethanol
C6H15NO
111-75-1
109.598
193.243 cry (al or
bz)
117.189
1500
1501
C6H15NO
C10H19NO2
4620-70-6
3775-90-4
117.189
185.264
44
C11H14N2S2
95-31-8
238.372
108
1503
2-(tert-Butylamino)ethanol
N-tert-Butylaminoethyl
methacrylate
2-(tert-Butylaminothio)­
benzothiazole
2-sec-Butylaniline
C10H15N
1504
1505
1506
4-Butylaniline
4-sec-Butylaniline
4-tert-Butylaniline
C10H15N
C10H15N
C10H15N
1475
Organic
1476
1477
1478
1479
1480
1481
1482
1483
1502
HCP_Section_03.indb 80
Denmert
Ethylene glycol monobutyl
ether
4-tert-Butyl-N-sec-butyl-2,6dinitroaniline
1-Methylpropyl acetate
N-tert-Butyl-2-benzothiazolesulfenamide
Physical
Form
mp/˚C
bp/˚C
den
g cm –3
nD
194
s H2O; sl EtOH,
bz, chl; i eth
vs H2O; sl EtOH;
i eth, bz
221.5
32
-74.8
-90
Solubility
1290.5
104
1324
14810
171(2)
234(14)
1.086525 1.59626
i H2O; s os
0.820020 1.4067
vs eth, EtOH
0.901520 1.419820 msc H2O, EtOH,
eth; sl ctc
0.989020 1.438920 vs EtOH, MeOH
i H2O; vs os
0.93120
s H2O
s ctc
154
65.5
0.88220
1.416820 s EtOH, eth, bz,
ctc, MeOH
180(16)
10212
0.896025 1.438825
0.882520 1.394120 sl H2O; msc
EtOH, eth; s
ace, chl
0.874820 1.388820 sl H2O, ctc; s
EtOH, eth
0.866520 1.385520 s EtOH, eth, chl,
HOAc
0.912420 1.409620 s EtOH, eth
0.967125 1.413720 sl H2O; msc
EtOH, bz, lig
0.889820 1.418520 i H2O; s EtOH,
eth, ace; sl ctc
0.87925 1.411020
0.741420 1.403120 msc H2O; s
EtOH, eth
0.724620 1.393220 s H2O, chl; msc
EtOH, eth; vs
ace
0.695820 1.378420 msc H2O, EtOH,
eth; s chl
0.98220
sl H2O, EtOH
i H2O; s EtOH,
eth, bz, chl
0.890720 1.443720 vs H2O, EtOH,
eth
0.881820
s chl
55751-54-7 149.233
12016
0.957420
104-13-2
149.233 pa ye
30273-11-1 149.233
769-92-6
149.233 ye rd (peth) 17
261
238
241
0.94520
0.94915 1.536029
0.952515 1.538020
97.9(1)
1738
199
s EtOH, ace, bz;
sl ctc
sl ctc
vs bz, eth
sl H2O; msc
EtOH, eth; vs
bz; s ctc
4/11/16 11:20 AM
Physical Constants of Organic Compounds
3-81
N
N
O
H2N
O
N
H
O
NH
HCl
O
1465
S
NH
O
1467
Buthalital sodium
1468
Buthiazide
Buthiobate
O
O
1469
O
1470
Butonate
1471
Butoxyacetylene
O
O
O
1474
O
O
O
O
O
2-Butoxyethyl acetate
1-(2-Butoxyethoxy)-2-propanol
O
O
Cl
H
N
Cl
1479
2-Butoxyethyl (2,4-dichlorophenoxy)acetate
N
1481
4-Butoxy-N-hydroxybenzeneacetamide
O
O
O
1480
2-Butoxyethyl (2,4,5-trichlorophenoxy)acetate
O
OH
O
O
Cl
1478
O
N
NH O
N
H
N
O
OH
1484
4-[3-(4-Butoxyphenoxy)propyl]morpholine
O
1-Butoxy-2-propanol
O
O
O
O
1489
1490
tert-Butyl acetate
tert-Butylacetic acid
1491
Butyl acetoacetate
O
NH2
1497
tert-Butylamine
Butylamine hydrochloride
1485
1486
Butralin
O
1487
N-Butylacetamide
1488
Butyl acetate
sec-Butyl acetate
O
O
1493
Butyl acrylate
NH2
NH2
O
1492
1498
Butyl 4-aminobenzoate
H
N
1499
1494
tert-Butyl acrylate
1495
Butylamine
H
N
OH
OH
2-(Butylamino)ethanol
NH2
sec-Butylamine
1500
2-(tert-Butylamino)ethanol
NH2
H
N
O
O
1501
N-tert-Butylaminoethyl methacrylate
NH2
NH2
N
S
O
O
O
NH2
NH2 HCl
1496
4-Butoxyphenol
O
O
O
O
OH
1482
1-Butoxy-4-methylbenzene
O
O
1483
OH
O
Cl
Cl
O
1477
1476
2-(2-Butoxyethoxy)ethyl thiocyanate
O
2-Butoxyethanol
O
O
N
1475
2-[2-(2-Butoxyethoxy)ethoxy]ethanol
1473
4-Butoxybenzaldehyde
S
O
OH
O
1472
4-Butoxyaniline
OH
O
O
S
HN
1502
2-(tert-Butylaminothio)benzothiazole
1503
2-sec-Butylaniline
1504
4-Butylaniline
1505
4-sec-Butylaniline
1506
4-tert-Butylaniline
Organic
P
O
O
O
O
O
Cl
Cl
O
O
S
NH2
Cl
O
H2N
1466
Butethamine hydrochloride
O
O
S
N
H
H
N
Cl
Na+
S
S
Physical Constants of Organic Compounds
3-82
Organic
Mol. Form.
CAS RN
Mol.
Wt.
N-Butylaniline
N-tert-Butylaniline
C10H15N
C10H15N
1126-78-9
937-33-7
C18H16O2
1510
1511
1512
1513
2-tert-Butyl-9,10-anthracenedione
tert-Butyl azidoformate
tert-Butyl carbonazidate
4-Butylbenzaldehyde
4-tert-Butylbenzaldehyde
Butylbenzene
1-Phenylbutane
1514
sec-Butylbenzene, (±)-
1515
tert-Butylbenzene
1516
1517
1518
No.
Name
1507
1508
1509
Physical
Form
mp/˚C
bp/˚C
149.233 liq
149.233
-14.4
254(9)
215
84-47-9
264.319
99
C5H9N3O2
C11H14O
C11H14O
C10H14
1070-19-5
1200-14-2
939-97-9
104-51-8
143.144 unstab >80
162.228
162.228 liq
134.218 liq
-87.81(0.05)
2-Phenylbutane
C10H14
36383-15-0 134.218 liq
-75.5(0.3)
(1,1-Dimethylethyl)benzene
C10H14
98-06-6
134.218 liq
-57.84(0.04) 169.1(0.3)
C10H14O2
C10H14O2
C11H17N
98-29-3
1948-33-0
3378-72-1
166.217
166.217
163.260
54(2)
128
1519
1520
4-tert-Butyl-1,2-benzenediol
2-tert-Butyl-1,4-benzenediol
N-tert-Butylbenzenemethanamine
4-tert-Butylbenzenemethanol
Butyl benzoate
C11H16O
C11H14O2
877-65-6
136-60-7
164.244
178.228 liq
-22.4(0.4)
1521
1522
1523
2-tert-Butylbenzoic acid
3-tert-Butylbenzoic acid
4-tert-Butylbenzoic acid
C11H14O2
C11H14O2
C11H14O2
1077-58-3
7498-54-6
98-73-7
178.228 pl (dil al)
178.228 nd (peth)
178.228 nd (dil al)
80.5(0.3)
127.3(0.5)
164(2)
1524
1525
1526
1527
1528
4-Butylbenzoyl chloride
4-tert-Butylbenzoyl chloride
2-Butyl-1,1’-biphenyl
tert-Butyl bromoacetate
Butyl butanoate
C11H13ClO
C11H13ClO
C16H18
C6H11BrO2
C8H16O2
28788-62-7
1710-98-1
54532-97-7
5292-43-3
109-21-7
196.673
196.673
210.314 liq
195.054
144.212 liq
1529
1530
1531
1532
1533
1534
Butyl cis-2-butenedioate
Butyl carbamate
Butyl chloroacetate
tert-Butyl chloroacetate
Butylchlorodimethylsilane
Butyl chloroformate
Monobutyl maleate
C8H12O4
C5H11NO2
C6H11ClO2
C6H11ClO2
C6H15ClSi
C5H9ClO2
925-21-3
592-35-8
590-02-3
107-59-5
1000-50-6
592-34-7
172.179 oil
117.147 pr
150.603
150.603
150.722
136.577
1535
Buclosamide
C11H14ClNO2
575-74-6
227.688
1536
1537
1538
N-Butyl-4-chloro-2-hydroxybenzamide
Butyl 2-chloropropanoate
Butyl 3-chloropropanoate
tert-Butyl chromate
C7H13ClO2
C7H13ClO2
C8H18CrO4
1539
1540
1541
1542
1543
1544
1545
1546
1547
1548
Butyl citrate
Butyl cyanoacetate
Butylcyclohexane
sec-Butylcyclohexane
tert-Butylcyclohexane
2-tert-Butylcyclohexanol
cis-4-tert-Butylcyclohexanol
trans-4-tert-Butylcyclohexanol
4-tert-Butylcyclohexanone
Butylcyclohexylamine
N-Butylcyclohexanamine
C18H32O7
C7H11NO2
C10H20
C10H20
C10H20
C10H20O
C10H20O
C10H20O
C10H18O
C10H21N
54819-86-2 164.630
27387-79-7 164.630
1189-85-1 230.223 red cry
(peth)
77-94-1
360.443
5459-58-5 141.168
1678-93-9 140.266 liq
7058-01-7 140.266
3178-22-1 140.266 liq
13491-79-7 156.265
937-05-3
156.265
21862-63-5 156.265
98-53-3
154.249
10108-56-2 155.281
23322
231
-74.68(0.05) 180.9(0.6)
179.3(0.5)
-41.2(0.3)
171.6(0.4)
45
13995
82(3)
11215
83
11215
48(3)
909
208.3
1549
1550
Butyl cyclohexyl phthalate
Butylcyclopentane
C18H24O4
C9H18
84-64-0
2040-95-1
-107.95(0.05) 156(1)
1551
1552
Butyl dichloroacetate
Butyl (2,4-dichlorophenoxy)
2,4-D Butyl ester
acetate
5-Butyldihydro-2(3H)-furanone
Butyldimethylamine
N,N-Dimethyl-1-butanamine
C6H10Cl2O2
C12H14Cl2O3
29003-73-4 185.048
94-80-4
277.143
C8H14O2
C6H15N
104-50-7
927-62-8
142.196
101.190
1-tert-Butyl-3,5-dimethylbenzene
C12H18
98-19-1
162.271 liq
1553
1554
1555
HCP_Section_03.indb 82
Synonym
p-tert-Butylbenzoic acid
304.382 col liq
126.239 liq
7370
1237
10711
183.3(0.3)
173.3(0.4)
286(1)
den
g cm –3
-91.5(0.1)
Solubility
1.5265
0.970
1.527020
0.860120 1.489820 i H2O; msc
EtOH, eth, ace,
bz, peth, ctc
0.862120 1.490220 i H2O; msc
EtOH, eth, ace,
bz, peth, ctc
0.866520 1.492720 i H2O; vs EtOH,
eth; msc ace,
bz
s tfa
755
-9.6(0.2)
nD
0.932320 1.534120 vs eth, EtOH
1.527020 s EtOH; vs ace,
bz, chl
s ctc, CS2
1.495125
236
249(3)
0.92825
1.00020
15526
266
292(3)
7325
164.95(0.1)
1.05125
1.00725
0.967620
0.870020
1.517920
1.494025 i H2O; msc
EtOH, eth; s
ace; sl ctc
vs EtOH
vs EtOH, peth
i H2O; vs EtOH,
bz; s chl
1.535120
1.536420
1.560420
1.443020 vs eth, EtOH
1.407520 i H2O; msc
EtOH, eth; s
ctc
1.0925
53
204 dec
181(3)
150
139
142
vs EtOH; sl chl
1.070420 1.429720 vs eth, EtOH
1.426020 dec H2O
0.87620 1.514520
1.07425 1.411420 msc eth; s ace;
sl ctc
184
10422
1.025320 1.426320 vs eth
1.037020 1.432120 vs H2O, eth
reac H2O
91.5
-5
-20
9
-18(2)
1.04320
1.001020
0.790220
0.813120
0.812720
0.90225
1.446020
1.420020
1.440820 i H2O
1.446720 i H2O; s ace
1.446920 i H2O
1.07625
0.784620 1.431620
sl H2O, ctc; vs
EtOH, eth
sl H2O; misc os
vs ace, bz, eth,
EtOH
vs eth, EtOH
193.5
1331
1.182020 1.442020
13220
92.2(0.7)
0.979619 1.445119 s EtOH; sl ctc
0.720620 1.397020 msc H2O, EtOH,
eth, ace, bz
0.866820
s ctc
207(1)
4/11/16 11:20 AM
Physical Constants of Organic Compounds
3-83
H
N
O
O
1507
1508
N-Butylaniline
N-tert-Butylaniline
O
1509
N
N
N
1510
2-tert-Butyl-9,10-anthracenedione
1511
tert-Butyl azidoformate
1512
4-Butylbenzaldehyde
OH
OH
N
H
OH
1514
1515
tert-Butylbenzene
1517
1516
HO
HO
O
1518
2-tert-Butyl-1,4-benzenediol
4-tert-Butyl-1,2-benzenediol
HO
Butylbenzene
OH
OH
sec-Butylbenzene, (±)-
1513
4-tert-Butylbenzaldehyde
1519
N-tert-Butylbenzenemethanamine
O
O
O
O
Cl
4-tert-Butylbenzenemethanol
Organic
H
N
O
O
O
Cl
O
O
1520
1521
Butyl benzoate
2-tert-Butylbenzoic acid
O
O
Br
1522
1527
O
O
O
O
Cl
Butyl chloroformate
O
N-Butyl-4-chloro-2-hydroxybenzamide
OH
N
O
O
O Cr O
O
O
Cl
Cl
1535
O
tert-Butyl chloroacetate
O
O
1534
Butylchlorodimethylsilane
Butyl chloroacetate
O
1532
H
N
OH
Cl
O
Cl
O
1531
Butyl carbamate
O
1533
1526
2-Butyl-1,1’-biphenyl
O
Cl
O
1530
Butyl cis-2-butenedioate
O
Cl
Si
4-tert-Butylbenzoyl chloride
O
H2N
1529
Butyl butanoate
1525
4-Butylbenzoyl chloride
O
O O
1528
tert-Butyl bromoacetate
1524
4-tert-Butylbenzoic acid
HO
O
O
1523
3-tert-Butylbenzoic acid
1536
O
1537
Butyl 2-chloropropanoate
Butyl 3-chloropropanoate
1538
tert-Butyl chromate
O
O
1539
1540
Butyl citrate
1541
Butyl cyanoacetate
OH
1542
Butylcyclohexane
OH
sec-Butylcyclohexane
O
1543
tert-Butylcyclohexane
O
OH
O
O
H
N
O
1544
1545
2-tert-Butylcyclohexanol
1546
cis-4-tert-Butylcyclohexanol
trans-4-tert-Butylcyclohexanol
O
O
Cl
Cl
1550
Butylcyclopentane
1548
4-tert-Butylcyclohexanone
Butylcyclohexylamine
1549
Butyl cyclohexyl phthalate
O
O
Cl
1547
1551
Butyl dichloroacetate
O
O
Cl
1552
Butyl (2,4-dichlorophenoxy)acetate
1553
O
5-Butyldihydro-2(3H)-furanone
N
1554
Butyldimethylamine
1555
1-tert-Butyl-3,5-dimethylbenzene
Physical Constants of Organic Compounds
3-84
Mol. Form.
CAS RN
Mol.
Wt.
C14H18N2O5
81-14-1
294.303 ye cry
135.5
C12H18O
1879-09-0
178.270
22.3
247(9)
0.91780
1.518320 i alk
C12H18O
17696-37-6 178.270
71.2
262(27)
0.93980
1.531120 s alk
C12H18O
879-97-0
178.270
82.4
248
0.91680
s alk
C12H15N3O6
81-15-2
297.263 pl, nd (al)
111.5(0.2)
C10H12N2O5
C26H54
C26H54
C16H32O2
C6H15N
1420-07-1
55282-16-1
13475-76-8
106-18-3
13360-63-9
240.212 ye solid
366.707
366.707
256.424
101.190
126
208
C12H18
C6H14O
7364-19-4
628-81-9
162.271 liq
102.174 liq
-38.4
-124
C6H14O
2679-87-0
102.174
C6H14O
637-92-3
102.174 liq
-94.0(0.3)
72.7(0.1)
C12H18O
C9H20O2
96-70-8
115-84-4
178.270
160.254 wh cry
23
43(2)
250
269.0(0.2)
C10H16N2O3
77-28-1
212.245
123(1)
C6H14S
C6H14S
C5H11NO
C5H10O2
638-46-0
14290-92-7
2425-74-3
592-84-7
118.240
118.240
101.147
102.132
C5H10O2
589-40-2
102.132
93.6(0.3)
Butyl enanthate
C5H10O2
C7H14O2
C11H22O2
762-75-4
2426-08-6
5454-28-4
102.132 liq
130.185
186.292 liq
-68(1)
83(6)
171(18)
225(4)
Butyl caproate
C10H20O2
626-82-4
172.265 liq
-50.0(0.5)
204(3)
C4H13ClN2
7400-27-3
124.612
192.5
Monobutyl succinate
C8H14O4
C4H10O2
5150-93-6
75-91-2
174.195
90.121 liq
8.6
6
136.53
89 dec
tert-Butyl-4-hydroxyanisole
Butylated hydroxyanisole
C11H16O2
25013-16-5 180.244 wax
51
268
1586
1587
Butyl 2-hydroxybenzoate
Butyl 4-hydroxybenzoate
C11H14O3
C11H14O3
2052-14-4
94-26-8
194.227 liq
194.227
-5.9
68.5
271
Butylparaben
1588
Butyl ricinoleate
C22H42O3
151-13-3
354.566
27513
1589
Butyl cis-12-hydroxy-9octadecenoate, (R)tert-Butyl hypochlorite
1.073220 1.436020
0.896020 1.401520 s H2O, EtOH,
eth, ctc, chl
i H2O; s peth,
EtOH
1.072820 1.511520 sl ctc
sl H2O, ctc; s
EtOH
0.905822 1.456622 vs eth
C4H9ClO
507-40-4
108.566 ye liq
77.5
0.958318 1.40320
1590
Butyl isobutyl ether
C8H18O
17071-47-5 130.228 liq
135(8)
0.76315
1591
1592
1593
1594
1595
1596
tert-Butyl isobutyl ether
Butyl isocyanate
Butyl isocyanide
tert-Butyl isopropyl ether
Butyl isothiocyanate
sec-Butyl isothiocyanate, (±)-
C8H18O
C5H9NO
C5H9N
C7H16O
C5H9NS
C5H9NS
112.9(0.3)
125(3)
120
87.3(0.3)
167(7)
159.5
0.88020 1.406020
0.7820
0.736525
0.954620 1.50120
0.94412
1597
tert-Butyl isothiocyanate
33021-02-2
111-36-4
2769-64-4
17348-59-3
592-82-5
11672411-9
590-42-1
140
0.918710
1598
1599
1600
Butyl lactate
Butyl methacrylate
tert-Butyl methacrylate
7710
163.7(0.8)
135.2
0.974427
vs eth, EtOH
0.893620 1.424020 vs eth, EtOH
No.
Name
1556
1561
1562
1563
1564
1565
4-tert-Butyl-2,6-dimethyl-3,5- Musk ketone
dinitroacetophenone
2-tert-Butyl-4,6-dimethylphenol
4-tert-Butyl-2,5-dimethylphenol
4-tert-Butyl-2,6-dimethylphenol
1-tert-Butyl-3,5-dimethyl2,4,6-trinitrobenzene
2-tert-Butyl-4,6-dinitrophenol
5-Butyldocosane
11-Butyldocosane
Butyl dodecanoate
Butylethylamine
N-Ethyl-1-butanamine
1566
1567
1-tert-Butyl-4-ethylbenzene
Butyl ethyl ether
1568
sec-Butyl ethyl ether
1569
tert-Butyl ethyl ether
1570
1571
1573
1574
1575
1576
2-tert-Butyl-4-ethylphenol
2-Butyl-2-ethyl-1,3-propanediol
5-Butyl-5-ethyl2,4,6(1H,3H,5H)-pyrimidinetrione
Butyl ethyl sulfide
tert-Butyl ethyl sulfide
N-tert-Butylformamide
Butyl formate
1577
sec-Butyl formate
1578
1579
1580
tert-Butyl formate
Butyl glycidyl ether
Butyl heptanoate
1581
Butyl hexanoate
1582
1583
1584
tert-Butylhydrazine
hydrochloride
Butyl hydrogen succinate
tert-Butyl hydroperoxide
1585
1557
1558
1559
1560
Organic
1572
HCP_Section_03.indb 84
Synonym
Ethyl butyl ether
Ethyl tert-butyl ether
Butethal
2-Methyl-2-propanethiol
1,1-Dimethylethyl formate
1-Isothiocyanatobutane
2-Isothiocyanatobutane, (±)
2-Isothiocyanato-2-methylpro- C5H9NS
pane
C7H14O3
C8H14O2
C8H14O2
Physical
Form
34451-18-8 146.184
97-88-1
142.196
585-07-9
142.196
bp/˚C
liq
liq
liq
liq
-95.1(0.2)
-85.9(0.3)
16
-90.0(0.4)
-88.3(0.4)
10.5
den
g cm –3
nD
Solubility
vs chl
i H2O; sl EtOH; s
eth, chl
24410
242.510
18018
104.8(0.8)
211
89(2)
81(4)
130.228 liq
99.131
83.132
116.201 liq
115.197
115.197
115.197
mp/˚C
144.2(0.8)
120.4(0.6)
202
106.1(0.1)
0.805820 1.450320
0.804120 1.449920
0.739820 1.404020 msc EtOH, eth,
ace, bz
0.864120
0.749520 1.381820 i H2O; msc
EtOH, eth; vs
ace
0.750320 1.380220 i H2O; vs EtOH,
eth
0.73625 1.375620 i H2O; vs EtOH,
eth
0.92750
1.458725 sl H2O, ace; s
EtOH
0.837620 1.449210 vs EtOH; s chl
0.903
1.433020
0.895820 1.388720 sl H2O; s ace;
msc EtOH, eth
0.884620 1.386520 sl H2O; s ace;
msc EtOH, eth
0.872
1.379020
0.91820
0.863820 1.420420 vs ace, bz, eth,
EtOH
0.865320 1.415220 i H2O; s EtOH;
msc eth
1.407721
i H2O; vs eth,
bz; s ace
vs ace, eth,
EtOH
vs eth, EtOH
s chl
vs eth, EtOH
vs eth, EtOH
4/11/16 11:20 AM
Physical Constants of Organic Compounds
3-85
O
OH
OH
OH
O
N
O
N
O
O
1556
1557
4-tert-Butyl-2,6-dimethyl-3,5-dinitroacetophenone
O
O
N
O
N
N
O
1558
2-tert-Butyl-4,6-dimethylphenol
O
O
O
N
O
N
O
1561
1562
2-tert-Butyl-4,6-dinitrophenol
1563
5-Butyldocosane
11-Butyldocosane
Organic
1-tert-Butyl-3,5-dimethyl-2,4,6-trinitrobenzene
4-tert-Butyl-2,6-dimethylphenol
OH
O
1560
1559
4-tert-Butyl-2,5-dimethylphenol
OH
O
O
H
N
O
1564
O
1565
Butyl dodecanoate
1566
Butylethylamine
O
1567
1-tert-Butyl-4-ethylbenzene
1568
Butyl ethyl ether
1569
sec-Butyl ethyl ether
tert-Butyl ethyl ether
1570
2-tert-Butyl-4-ethylphenol
O
N
OH HO
O
1571
2-Butyl-2-ethyl-1,3-propanediol
H
S
H
N
1574
1575
O
N
H
O
S
1572
5-Butyl-5-ethyl-2,4,6(1H,3H,5H )-pyrimidinetrione
O
O
1573
Butyl ethyl sulfide
tert-Butyl ethyl sulfide
N-tert-Butylformamide
O
O
1576
1577
Butyl formate
sec-Butyl formate
O
O
O
O
O
O
1578
O
1579
tert-Butyl formate
O
1580
Butyl glycidyl ether
1581
Butyl heptanoate
O
O
NH2 HCl
O
1583
tert-Butylhydrazine hydrochloride
Butyl hydrogen succinate
O
O
O
O
OH
OH
O
1584
tert-Butyl hydroperoxide
O
OH
O
1582
Butyl hexanoate
OH
O
H
N
O
OH
1585
1586
tert-Butyl-4-hydroxyanisole
N
O
1589
1590
tert-Butyl hypochlorite
1591
Butyl isobutyl ether
tert-Butyl isobutyl ether
C
1592
Butyl isocyanate
O
N
1596
C
N
S
sec-Butyl isothiocyanate, (±)-
C
1597
S
tert-Butyl isothiocyanate
1588
Butyl 4-hydroxybenzoate
O
Cl
OH
1587
Butyl 2-hydroxybenzoate
Butyl cis-12-hydroxy-9-octadecenoate, (R)-
N
O
O
N
C
1593
1594
Butyl isocyanide
tert-Butyl isopropyl ether
O
O
OH
1598
Butyl lactate
C
S
1595
Butyl isothiocyanate
O
O
1599
Butyl methacrylate
O
1600
tert-Butyl methacrylate
Physical Constants of Organic Compounds
3-86
mp/˚C
bp/˚C
den
g cm –3
164.244
19.1(0.3)
223(5)
0.938320 1.503920
83-66-9
268.265 pa ye lf (al)
85
18516
C11H16O2
C11H16O2
C5H13N
C11H16
121-00-6
88-32-4
110-68-9
1074-92-6
180.244
180.244
87.164
148.245 liq
1-tert-Butyl-3-methylbenzene 3-tert-Butyltoluene
C11H16
1075-38-3
148.245 liq
-41.36(0.08) 204(5)
1608
1-tert-Butyl-4-methylbenzene 4-tert-Butyltoluene
C11H16
98-51-1
148.245 liq
-52.49(0.08) 193(3)
1609
1610
1611
Butyl 2-methylbutanoate
Butyl 3-methylbutanoate
Butyl methyl ether
C9H18O2
C9H18O2
C5H12O
15706-73-7 158.238
109-19-3
158.238
628-28-4
88.148 liq
179(7)
1612
sec-Butyl methyl ether
C5H12O
1613
2-tert-Butyl-4-methylphenol
C11H16O
11678323-4
2409-55-4
164.244
52.3(0.9)
236(7)
1614
2-tert-Butyl-5-methylphenol
C11H16O
88-60-8
164.244
46.5
12711
1615
1616
2-tert-Butyl-6-methylphenol
4-tert-Butyl-2-methylphenol
C11H16O
C11H16O
2219-82-1
98-27-1
164.244
164.244
29(1)
27.5
233(7)
256(4)
1617
1618
1619
Butyl methyl sulfide
tert-Butyl methyl sulfide
4-Butylmorpholine
C5H12S
C5H12S
C8H17NO
628-29-5
6163-64-0
1005-67-0
104.214 liq
104.214 liq
143.227 liq
-97.81(0.05) 123.4(0.5)
98.9(0.3)
-57.1
213.5
1620
1-Butylnaphthalene
C14H16
1634-09-9
184.277 liq
-19.7(0.2)
288(5)
1621
1622
2-Butylnaphthalene
Butyl nitrate
C14H16
C4H9NO3
1134-62-9
928-45-0
184.277 liq
119.119
-7(4)
286(5)
133
1623
1624
Butyl nitrite
tert-Butyl nitrite
C4H9NO2
C4H9NO2
544-16-1
540-80-7
103.120
103.120 pa ye liq
78
64(2)
1625
sec-Butyl nitrite
C4H9NO2
924-43-6
103.120
65(2)
1626
C8H18N2O2
3817-11-6
174.241
1150.01
1627
1628
1629
4-(Butylnitrosoamino)-1butanol
5-Butylnonane
Butyl nonanoate
Butyl octanoate
C13H28
C13H26O2
C12H24O2
17312-63-9 184.361
50623-57-9 214.344
589-75-3
200.318 liq
1630
1631
1632
1633
1634
2-Butyl-1-octanol
Butyl oleate
tert-Butyl 3-oxobutanoate
Butyl 4-oxopentanoate
Butyl palmitate
C12H26O
C22H42O2
C8H14O3
C9H16O3
C20H40O2
3913-02-8
142-77-8
1694-31-1
2052-15-5
111-06-8
186.333
338.567 ye cry
158.195
172.221
312.531 cry (dil al)
1635
Butyl pentanoate
C9H18O2
591-68-4
158.238 liq
1636
sec-Butyl pentanoate
C9H18O2
158.238
174.5
1637
1638
1639
4-(1-Butylpentyl)pyridine
tert-Butyl peroxybenzoate
2-Butylphenol
C14H23N
C11H14O3
C10H14O
11683632-9
2961-47-9
614-45-9
3180-09-4
205.340
194.227
150.217 liq
-20(2)
265
750.2
234(5)
1640
1641
2-sec-Butylphenol
2-tert-Butylphenol
C10H14O
C10H14O
89-72-5
88-18-6
150.217
150.217 liq
18(3)
-5.6(0.2)
229(3)
224.3(0.6)
1642
1643
3-Butylphenol
3-tert-Butylphenol
C10H14O
C10H14O
4074-43-5
585-34-2
150.217
150.217 nd (peth)
47(1)
249(4)
240
1644
4-Butylphenol
C10H14O
1638-22-8
150.217
22
251(4)
1645
4-sec-Butylphenol
C10H14O
99-71-8
150.217
60(1)
243(3)
No.
Name
1601
1603
1604
1605
1606
1-tert-Butyl-4-methoxybenzene
1-tert-Butyl-2-methoxy-4methyl-3,5-dinitrobenzene
2-tert-Butyl-4-methoxyphenol
3-tert-Butyl-4-methoxyphenol
Butylmethylamine
N-Methyl-1-butanamine
1-tert-Butyl-2-methylbenzene 2-tert-Butyltoluene
1607
1602
Organic
HCP_Section_03.indb 86
Synonym
Butyl o-toluate
Butyl p-toluate
N-Butyl-N-(4-hydroxybutyl)­
nitrosamine
Butyl pelargonate
Butyl cis-9-octadecenoate
Butyl levulinate
Butyl hexadecanoate
Benzoyl tert-butyl peroxide
4-(1-Methylpropyl)phenol
Mol. Form.
CAS RN
Mol.
Wt.
C11H16O
5396-38-3
C12H16N2O5
Physical
Form
nD
Solubility
i H2O; sl EtOH; s
eth, chl
18450
65
-50.3(0.2)
-115.7(0.1)
88.148
91(2)
200(4)
70.1(0.3)
59.1
-38.0(0.7)
-42.9(0.5)
-26.4
219(5)
12320
240(4)
248(23)
22715
71.511
237.5
16(2)
-83.77(0.02) 186(5)
0.763715
0.889720 1.507620 vs ace, bz, eth,
EtOH
0.865720 1.494420 vs ace, bz, eth,
EtOH
0.861220 1.491820 i H2O; sl EtOH;
vs eth, chl; s
ace, bz
0.862020 1.413520
1.405825
0.739225 1.373620 i H2O; msc
EtOH, eth; s
ace
0.741520 1.368025 vs ace, eth,
EtOH
0.924775 1.496975 sl H2O; s ace,
bz, chl
0.92280 1.525020 i H2O; s EtOH,
eth, ace
0.924080 1.519520
0.96520 1.523020 i H2O; s eth,
ace, bz
0.842620 1.447720 vs EtOH, MeOH
0.906820 1.445120 vs H2O, ace, bz,
EtOH
0.973820 1.581920 i H2O; s EtOH,
eth, ace, bz
0.967320 1.577720 vs ace, bz, EtOH
1.022830 1.401323 i H2O; s EtOH,
eth; sl ctc
0.911425 1.376220 msc EtOH, eth
0.867020 1.36820 sl H2O; s EtOH,
eth, chl, CS2
0.872620 1.371020 vs eth, EtOH,
chl
0.763518 1.427318
0.852025 1.426225
0.862820 1.423225 vs ace, eth,
EtOH
0.89120
0.870415 1.448025 vs EtOH
0.975620 1.418020
0.973520 1.429020 sl chl
1.431250 i H2O; s EtOH,
eth
0.871015 1.412820 sl H2O; s EtOH,
eth
0.860520 1.407020 vs bz, eth, py,
EtOH
0.887825 1.484625
1.02125 1.499020
0.97520 1.518025 i H2O; s EtOH,
eth, alk
0.980425 1.520025
0.978320 1.516020 s EtOH, ctc, alk;
vs eth
0.97420
vs eth, EtOH
s EtOH, alk; vs
eth
0.97622 1.516525 i H2O; s EtOH,
eth, alk; sl ctc
0.98620 1.518221 i H2O; s EtOH,
alk; vs eth
4/11/16 11:20 AM
Physical Constants of Organic Compounds
3-87
OH
OH
O
O
O
O
O
1601
N
O
N
O
O
1602
1-tert-Butyl-4-methoxybenzene
1603
1-tert-Butyl-2-methoxy-4-methyl-3,5-dinitrobenzene
H
N
1604
2-tert-Butyl-4-methoxyphenol
1605
3-tert-Butyl-4-methoxyphenol
Butylmethylamine
O
O
O
1606
1607
1-tert-Butyl-2-methylbenzene
1608
1-tert-Butyl-3-methylbenzene
O
1609
1-tert-Butyl-4-methylbenzene
Butyl 2-methylbutanoate
1610
Butyl 3-methylbutanoate
Organic
OH
OH
OH
OH
O
O
1611
1612
Butyl methyl ether
1613
sec-Butyl methyl ether
1614
2-tert-Butyl-4-methylphenol
1615
2-tert-Butyl-5-methylphenol
2-tert-Butyl-6-methylphenol
1616
4-tert-Butyl-2-methylphenol
N
O
S
S
O
1617
1618
Butyl methyl sulfide
N
O
1619
tert-Butyl methyl sulfide
O
O
N
N
N
N
O
Butyl nitrate
O
OH
1627
1626
sec-Butyl nitrite
O
1622
2-Butylnaphthalene
1625
tert-Butyl nitrite
Butyl nitrite
1621
1-Butylnaphthalene
O
O
1624
1623
1620
4-Butylmorpholine
N
O
5-Butylnonane
4-(Butylnitrosoamino)-1-butanol
O
O
O
O
OH
O
O
1628
1629
Butyl nonanoate
1630
Butyl octanoate
1631
2-Butyl-1-octanol
Butyl oleate
O
O
O
O
O
O
1632
tert-Butyl 3-oxobutanoate
O
O
O
O
1633
1634
Butyl 4-oxopentanoate
Butyl palmitate
1636
sec-Butyl pentanoate
Butyl pentanoate
OH
O
O
O
O
1635
HO
O
N
1637
4-(1-Butylpentyl)pyridine
1638
tert-Butyl peroxybenzoate
1639
2-Butylphenol
1640
2-sec-Butylphenol
OH
OH
OH
OH
1641
2-tert-Butylphenol
OH
1642
3-Butylphenol
1643
3-tert-Butylphenol
1644
4-Butylphenol
1645
4-sec-Butylphenol
Physical Constants of Organic Compounds
3-88
Mol. Form.
CAS RN
Mol.
Wt.
mp/˚C
bp/˚C
den
g cm –3
4-tert-Butylphenol
C10H14O
98-54-4
150.217 nd (lig)
100(2)
244(5)
0.90880
C30H39O4P
78-33-1
494.602
C13H18O2
3101-60-8
206.281
C12H17NO
C12H16O
91-49-6
943-27-1
191.269
176.254
1651
1652
1653
4-tert-Butylphenol, phosphate
(3:1)
[(4-tert-Butylphenoxy)­methyl]­
oxirane
N-Butyl-N-phenylacetamide
1-(4-tert-Butylphenyl)­
ethanone
Butyl phenyl ether
Butoxybenzene
N-Butylpiperidine
Butylpropanedioic acid
n-Butylmalonic acid
16714
1.03625
24.5(0.2)
17.7
281
263
0.991220 1.514620 sl chl
0.963520 1.51815
C10H14O
C9H19N
C7H12O4
1126-79-0
4945-48-6
534-59-8
150.217 liq
141.254
160.168 pr (w)
-19.4
210(1)
174(3)
590-01-2
130.185 liq
-89.5(0.5)
C7H14O2
C7H13NO
C7H16O
591-34-4
107-58-4
3073-92-5
130.185
127.184 cry (bz)
116.201
128
C9H13N
C10H13NO2
3978-81-2
536-69-6
135.206 liq
179.216
-39.7(0.5)
97
197(5)
0.935120 1.496920 s eth, ace
0.824520 1.446720
vs H2O; s EtOH,
eth
0.875420 1.401420 sl H2O, ctc; msc
EtOH, eth
0.865720 1.395220 s EtOH, eth
sl H2O; i peth
0.77720
i H2O; vs EtOH,
eth
0.91525 1.495820 s ctc, CS2
1654
Butyl propanoate
Butyl propionate
C7H14O2
1655
1656
1657
sec-Butyl propanoate
N-tert-Butyl-2-propenamide
Butyl propyl ether
N-tert-Butylacrylamide
1658
1659
1660
4-tert-Butylpyridine
5-Butyl-2-pyridinecarboxylic
acid
Butyl stearate
C22H44O2
123-95-5
340.583
26.56(0.02)
343
0.85425
1661
Butyl thiocyanate
C5H9NS
628-83-1
115.197
186
0.956315
1662
1663
1664
2-Butylthiophene
Butyl thiophene-2-carboxylate Butyl 2-thiophenecarboxylate
Butyl 4-toluenesulfonate
C8H12S
C9H12O2S
C11H16O3S
1455-20-5 140.246
56053-84-0 184.255
778-28-9
228.308
179(17)
580.15
1656
0.953720
1665
1666
C6H9Cl3O2
C12H13Cl3O3
3657-07-6
93-79-8
219.493
311.588
1667
Butyl trichloroacetate
Butyl (2,4,5-trichlorophenoxy)­ 2,4,5-T Butyl ester
acetate
Butyltrichlorosilane
Trichlorobutylsilane
C4H9Cl3Si
7521-80-4
191.559
1668
1669
Butyl trifluoroacetate
Butylurea
C6H9F3O2
C5H12N2O
367-64-6
592-31-4
1670
1671
sec-Butylurea
tert-Butylurea
(1-Methylpropyl)urea
C5H12N2O
C5H12N2O
689-11-2
1118-12-3
170.129
116.161 tab (w), nd
(bz)
116.161 pr (w)
116.161
169
176.6(0.7)
1672
1673
1-tert-Butyl-4-vinylbenzene
Butyl vinyl ether
p-tert-Butylstyrene
1-(Ethenyloxy)butane
C12H16
C6H12O
1746-23-2
111-34-2
160.255 liq
100.158 liq
-36.9
-92
9914
94(1)
1674
tert-Butyl vinyl ether
C6H12O
926-02-3
100.158 liq
-112
75
1675
1-Butyne
2-(Ethenyloxy)-2-methylpropane
Ethylacetylene
0.8920
0.788820 1.402620 i H2O; vs EtOH,
ace; msc eth;
s bz
0.769120 1.392220
C4H6
107-00-6
54.091
-125.7(0.2)
8.1(0.3)
0.67830
1676
2-Butyne
Dimethylacetylene
C4H6
503-17-3
54.091
-32.2(0.1)
27.1(0.5)
0.691020
1677
2-Butynediamide
Cellocidin
C4H4N2O2
543-21-5
vol liq or
gas
112.087 cry (dil
MeOH)
1678
1679
2-Butynedinitrile
2-Butynedioic acid
C4N2
C4H2O4
1071-98-3
142-45-0
76.056
114.057
20(1)
166(3)
76.5
0.970825
1680
2-Butyne-1,4-diol
Bis(hydroxymethyl)acetylene
C4H6O2
110-65-6
86.090
57(1)
238(8)
1681
1682
2-Butyne-1,4-diol diacetate
2-Butynoic acid
1,4-Diacetoxy-2-butyne
C8H10O4
C4H4O2
1573-17-7
590-93-2
78
12210
203
0.964120
1683
1684
1685
2-Butyn-1-ol
3-Butyn-1-ol
3-Butyn-2-ol
C4H6O
C4H6O
C4H6O
764-01-2
927-74-2
2028-63-9
170.163
84.074 pl (eth,
peth)
70.090 liq
70.090 liq
70.090 liq
-1.1
-63.5(0.4)
-1.5
140(5)
129(5)
106.5
0.937020
0.925720
0.861820
1686
1687
1688
3-Butyn-2-one
3-Butynylbenzene
γ-Butyrolactone
C4H4O
C10H10
C4H6O2
1423-60-5 68.074
16520-62-0 130.186
96-48-0
86.090 liq
84
177(8)
-43.36(0.08) 204.6(0.4)
1689
Cacotheline
C21H21N3O7
561-20-6
>300
No.
Name
1646
1647
1648
1649
1650
Organic
HCP_Section_03.indb 88
Synonym
Fusaric acid
1-Thiocyanatobutane
Ethynyl methyl ketone
Oxolan-2-one
Physical
Form
104.5
145.1(0.1)
133
117(4)
28.5
204
337
148.5
col gas
pl (bz,
AcOEt)
427.408 ye cry
104.5(0.4)
96.3(0.9)
nD
Solubility
1.4787114 s H2O, EtOH,
eth, chl, alk
i EtOH; sl eth,
bz
1.514520
1.432850 i H2O; s EtOH;
vs ace
1.436020 i H2O; s EtOH,
eth
1.509020
1.131920 1.505020 i H2O; s eth; sl
ctc
1.277820 1.452525 s ctc
1.160620 1.436320 s eth, bz, tol,
AcOEt
1.026822 1.35322 s chl
vs H2O, EtOH; sl
chl
s H2O; vs EtOH;
sl bz
217 dec
0.879320
0.925820
1.129620
1.396220 i H2O; s EtOH,
eth
1.392120 i H2O; s EtOH,
eth, ctc
sl H2O, chl,
EtOH, eth, gl
HOAc
1.464725
vs H2O, EtOH,
eth
1.480420 vs H2O, EtOH,
ace; sl eth; i
bz, peth
1.461120 s ctc
vs H2O, eth,
EtOH, chl
1.453020 vs eth, EtOH
1.440920 vs H2O, EtOH
1.420720 vs H2O, eth,
EtOH
1.407020
1.520820
1.434120 vs ace, bz, eth,
EtOH
sl H2O
4/11/16 11:20 AM
Physical Constants of Organic Compounds
3-89
O
O P O
O
OH
O
O
O
O
N
1647
O
OH
O
O
1655
Butyl propanoate
sec-Butyl propanoate
1660
Butyl propyl ether
C
Cl
Cl
O
1663
1664
Butyl thiophene-2-carboxylate
H
N
O
O
F
1676
NH2
1677
2-Butyne
1667
Butyltrichlorosilane
O
O
1672
N
OH
O
tert-Butyl vinyl ether
Butyl vinyl ether
HO
O
OH
O
1679
2-Butynedinitrile
1674
1673
1-tert-Butyl-4-vinylbenzene
HO
N
Cl
Cl
Si
Cl
1666
1671
1678
2-Butynediamide
Cl
NH2
O
H2N
O
Butyl (2,4,5-trichlorophenoxy)acetate
tert-Butylurea
sec-Butylurea
O
Cl
O
1670
Butylurea
1662
2-Butylthiophene
O
H
N
NH2
O
1669
1668
Butyl trifluoroacetate
O
Cl
Butyl trichloroacetate
H
N
NH2
S
N
Cl
O
1665
Butyl 4-toluenesulfonate
O
4-tert-Butylpyridine
Butyl thiocyanate
O
O O
S
O
N
1658
1661
Butyl stearate
O
1675
N-tert-Butyl-2-propenamide
S
5-Butyl-2-pyridinecarboxylic acid
1-Butyne
O
1657
O
1659
F
F
O
1656
O
OH
O
S
Butyl phenyl ether
1-(4-tert-Butylphenyl)ethanone
H
N
O
1654
Butylpropanedioic acid
N
O
O
1653
N-Butylpiperidine
1651
1650
N-Butyl-N-phenylacetamide
[(4-tert-Butylphenoxy)methyl]oxirane
OH
N
1652
1649
1648
4-tert-Butylphenol, phosphate (3:1)
Organic
1646
4-tert-Butylphenol
O
1680
2-Butynedioic acid
O
O
O
1681
2-Butyne-1,4-diol
2-Butyne-1,4-diol diacetate
H
O
N
H
O
OH
OH
O
1682
2-Butynoic acid
2-Butyn-1-ol
O
OH
OH
1683
O
1684
3-Butyn-1-ol
O
1685
3-Butyn-2-ol
1686
3-Butyn-2-one
1687
3-Butynylbenzene
1688
O
γ-Butyrolactone
N
N
H H
H
O
O
O
1689
OH
Cacotheline
Physical Constants of Organic Compounds
3-90
Physical
Form
Mol. Form.
CAS RN
C15H24
C10H20CdN2S4
39029-41-9 204.352
14239-68-0 408.950 wh cry
3,7-Dihydro-1,3,7-trimethyl1H-purine-2,6-dione
C8H10N4O2
58-08-2
19-Oxogomphoside
C29H40O9
mp/˚C
bp/˚C
den
g cm –3
12612
0.918215 1.316620
90 sub
1.2319
Organic
Name
1690
1691
1692
γ-Cadinene
Cadmium
bis(diethyldithiocarbamate)
Caffeine
1693
Calactin
1694
Calcium ascorbate
1695
Calcium citrate
1696
1697
1698
1699
Calcium cyanamide
Calcium cyclamate
Calcium gluconate
Calcium iodobehenate
1700
1701
Calcium lactate
Calcium 2,4-pentanedioate
1702
Calcium thioglycollate
1703
Calotoxin
1704
Calotropin
1705
1706
Calusterone
Camphene, (+)
1707
Camphene, (-)
1708
d-Camphocarboxylic acid
1709
Camphor, (±)-
1,7,7-Trimethylbicyclo[2.2.1]­
heptan-2-one, (±)
C10H16O
1710
Camphor, (+)
C10H16O
464-49-3
152.233 pl
178.7(0.5)
1711
Camphor, (-)
1,7,7-Trimethylbicyclo[2.2.1]­
heptan-2-one, (1R)
1,7,7-Trimethylbicyclo[2.2.1]­
heptan-2-one, (1S)
C10H16O
464-48-2
152.233
180(2)
0.985318
1712
(±)-Camphoric acid
5394-83-2
200.232 pr, lf
202
1.186
1713
d-Camphorsulfonic acid
3144-16-9
232.297 pr (HOAc)
195 dec
1714
1715
Canadine, (±)Cannabidiol
DL-Tetrahydroberberine
1716
Cannabinol
6,6,9-Trimethyl-3-pentyl-6Hdibenzo[b,d]pyran-1-ol
1717
1718
Canrenone
Cantharidin
1719
Caprolactam
1720
Capsaicin
1721
Capsanthin
1722
1723
1724
Captafol
Captan
Captopril
1725
Carbachol
1726
1727
1728
Carbamic chloride
Carbamodithioic acid
Carbamoyl dihydrogen
phosphate
HCP_Section_03.indb 90
Synonym
Mol.
Wt.
No.
nD
Solubility
255
C12H14CaO12
194.191 wh nd
236.1(0.2)
(w+1), hex
pr (sub)
20304-47-6 532.623 small pr
271
(ace)
5743-27-1 390.310 tricl cry (w)
Tricalcium citrate
C12H10Ca3O14
813-94-5
498.433 cry (w)
Calcium carbimide
CCaN2
C12H24CaN2O6S2
C12H22CaO14
C44H84CaI2O4
156-62-7
139-06-0
299-28-5
1319-91-1
80.102
396.536
430.373
971.023
C6H10CaO6
C10H14CaO4
C4H6CaO4S2
814-80-2
218.217 wh pow (w)
19372-44-2 238.294 col cry
dec
(MeOH)
814-71-1
222.297 pr (w)
220 dec
C29H40O10
20304-49-8 548.622 cry (EtOH)
268
C29H40O9
1986-70-5
221
C21H32O2
C10H16
17021-26-0 316.483 cry (ace)
5794-03-6 136.234 nd
157.5
52
161
0.895050 1.457025 vs eth
C10H16
5794-04-7
52
158
0.844650 1.456454 vs eth
C11H16O3
18530-30-8 196.243 pr (eth, 50% 127.5
al)
21368-68-3 152.233 wh rhom
177.7(0.2)
cry (EtOH)
Iododocosanoic acid, calcium
salt
Calcium acetylacetonate
4’β-Hydroxy-19oxogomphoside
2,2-Dimethyl-3-methylenebicyclo[2.2.1]heptane, (1R)2,2-Dimethyl-3-methylenebicyclo[2.2.1]heptane, (1S)-
1,2,2-Trimethyl-1,3-cyclopen- C10H16O4
tanedicarboxylic acid
C10H16O4S
6-Hexanelactam
532.623 pl (EtOH)
136.234
s H2O; i MeOH,
EtOH
sl H2O; i EtOH
sub
dec H2O
vs H2O
i EtOH, os
i H2O, EtOH,
eth; s chl
s H2O; i EtOH
s H2O, EtOH; i
eth
vs bz, eth, EtOH
sub
209(31)
29074-38-2 339.386 mcl nd (al)
13956-29-1 314.462 rods (peth)
134
67
1882
C21H26O2
521-35-7
310.430 pl, lf (peth)
77
1850.05
C22H28O3
C10H12O4
976-71-6
56-25-7
340.455 cry (AcOEt)
196.200 orth pl
150
218
84 sub
C6H11NO
105-60-2
113.157 lf (lig)
69.16(0.01)
270.8(0.1)
C18H27NO3
404-86-4
305.412 mcl pl or sc 65
(peth)
465-42-9
584.871
CH2ClNO
CH3NS2
CH4NO5P
2.29
s H2O, chl; sl
EtOH; i eth, bz
C20H21NO4
C21H30O2
3,3’-Dihydroxy-β,κ-caroten-6’- C40H56O3
one, (3R,3’S,5’R)
C10H9Cl4NO2S
C9H8Cl3NO2S
1-(3-Mercapto-2-methyl-1C9H15NO3S
oxypropyl)proline
C6H15ClN2O2
Carbamyl chloride
col hex cry
cry
cry
wh-ye pow
≈100 dec
(hyd)
≈1340
sl H2O, EtOH; i
eth, ctc; s chl,
py
0.99025
1.04040
1.5462
1.540420
i H2O; vs EtOH,
eth; s ace, bz,
ctc
i H2O; vs EtOH,
eth; s ace, bz
i H2O; vs EtOH,
eth, HOAc; s
ace, bz
sl H2O; s chl,
eth, EtOH
vs H2O; i eth; sl
HOAc
vs EtOH, chl
i H2O; s EtOH,
eth, bz, chl
i H2O; s EtOH,
eth, ace, bz,
peth, alk
i H2O; sl EtOH,
eth, ace, bz; s
HOAc
vs H2O, bz,
EtOH, chl
i H2O; vs EtOH;
s eth, bz, peth;
sl con HCl
2150.01
176
2425-06-1 349.061 cry
133-06-2
300.590 cry (CCl4)
62571-86-2 217.285 cry (AcOEt)
159.0(0.9)
173.9(0.3)
105
51-83-2
182.648
208(6)
463-72-9
594-07-0
590-55-6
79.486
93.172
141.021 unstab in
soln
1.7425
vs chl
s H2O, EtOH, chl
vs H2O, MeOH;
sl EtOH; i eth,
chl
62 dec
vs EtOH, eth
4/11/16 11:20 AM
Physical Constants of Organic Compounds
3-91
O
O
CH2O
H
S
H
N
O
O
O
N
Ca
2
N
S
2
Calcium gluconate
O
HO
2
Ca
O
Ca
O
O
2
1700
Calcium iodobehenate
Calcium 2,4-pentanedioate
O
O
O
O
O
HS
O
Ca
O
HO
H
OH H
O
O
O
2
H
1702
O
OH
O
H
H
O
1703
Calcium thioglycollate
OH
H
OH
2
H
O
1704
Calotoxin
1705
Calotropin
Calusterone
O
COOH
1707
Camphene, (+)
1708
Camphene, (-)
1710
Camphor, (±)-
O
O
O
1709
d-Camphocarboxylic acid
OH
HO
O
O
1706
O
1701
Calcium lactate
OH H
O
O
Ca
O
2
2
1699
HO
2
Ca
1698
Calcium cyclamate
O
HO
COO
OH
H
OH
OH
CH2OH
2
1697
Calcium cyanamide
I
H
HO
H
H
Ca2
O
2
1696
Calcium citrate
Calcium ascorbate
O
O
2
2
1694
Calactin
2
Ca2
O
HO HO
H
Caffeine
3Ca
1695
O
H
1693
H
N
O
OH
O
1692
Cadmium bis(diethyldithiocarbamate)
OH
O
H
OH
N
N
O
1691
γ-Cadinene
O
N
S
O
OH H
O
N
N
Cd
S
1690
O
S
HO
Organic
O
1711
Camphor, (+)
1712
Camphor, (-)
(±)-Camphoric acid
O
N
O
OH
OH
O
O
O S O
OH
O
1713
HO
O
1714
d-Camphorsulfonic acid
1715
Canadine, (±)-
1716
Cannabidiol
Cannabinol
O
O
O
O
O
O
O
N
H
O
O
1717
1718
Canrenone
O
HO
1719
Cantharidin
1720
Caprolactam
Capsaicin
O
O
H
N S
OH
HO
1721
OH
O
O
SH
1724
Captopril
N S
H
1722
N
O
1725
O
NH2
O
Carbachol
H2N
Captan
S
Cl
1726
Carbamic chloride
H2N
Cl
O Cl Cl
1723
Captafol
Cl
O
Cl
O Cl Cl Cl
Capsanthin
N
N
H
O
SH
1727
Carbamodithioic acid
H2N
O
O
OH
P
OH
1728
Carbamoyl dihydrogen phosphate
Physical Constants of Organic Compounds
3-92
Organic
No.
Name
1729
1730
Carbaryl
Carbazole
1731
9H-Carbazole-9-acetic acid
1732
Carbendazim
1733
1734
1735
Carbetapentane
N-Carbethoxyphthalimide
Carbic anhydride
1736
1737
1738
1739
1740
Carbimazole
Carbobenzoxyhydrazine
Carbofuran
Carboimidic difluoride
γ-Carboline
1741
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
Dibenzopyrolle
C12H11NO2
C12H9N
63-25-2
86-74-8
201.221
167.206 pl or lf
142.7(0.7)
245(2)
C14H11NO2
524-80-1
225.243 lf (AcOEt)
215
Carbamic acid, 1H-benzimid- C9H9N3O2
azol-2-yl-, methyl ester
Pentoxyverine
C20H31NO3
N-(Ethoxycarbonyl)phthalimide C11H9NO4
C9H8O3
Physical
Form
10605-21-7 191.186
mp/˚C
bp/˚C
den
g cm –3
354.6(0.2)
1.22825
1.29725
300 dec
5H-Pyrido[4,3-b]indole
C7H10N2O2S
C8H10N2O2
C12H15NO3
CHF2N
C11H8N2
Carbon dioxide
Carbonic anhydride
CO2
124-38-9
44.010
col gas
-56.561 tp​
(0.008)
-78.464 sp
1742
1743
Carbon diselenide
Carbon disulfide
Carbon selenide
Carbon bisulfide
CSe2
CS2
506-80-9
75-15-0
169.93
76.141
ye liq
col liq
-43.6(0.3)
-111.7(0.3)
125.5
46.2(0.1)
1744
1745
1746
Carbonic acid
Carbonic dihydrazide
Carbon monoxide
Carbohydrazide
Carbon oxide
CH2O3
CH6N4O
CO
463-79-6
497-18-7
630-08-0
62.025
90.085
28.010
nd (dil al)
col gas
154
-205.1(0.1)
1747
C7H4ClNO4
7693-46-1
201.565
80
C8H6ClNO4
4457-32-3
215.592
32.8
C3H2Cl4O2
17341-93-4 211.859
6311
1750
Carbonochloridic acid,
4-nitrophenyl ester
Carbonochloridic acid,
(4-nitrophenyl)methyl ester
Carbonochloridic acid,
2,2,2-trichloroethyl ester
Carbonothioic dichloride
Thiophosgene
CCl2S
463-71-8
114.982 red liq
73
1751
Carbonothioic dihydrazide
1,3-Diamino-2-thiourea
CH6N4S
2231-57-4
1752
Carbon oxyselenide
Carbonyl selenide
COSe
1603-84-5
1753
Carbon oxysulfide
Carbonyl sulfide
COS
463-58-1
106.151 nd, pl (w)
nd, pl (w)
106.97 col gas;
unstab
60.075 col gas
1754
1755
1756
Carbon suboxide
Carbonyl bromide
Carbonyl chloride
1,2-Propadiene-1,3-dione
Bromophosgene
Phosgene
C3O2
CBr2O
CCl2O
504-64-3
593-95-3
75-44-5
68.031 col gas
187.818
98.916 col gas
6.8
64(4)
-127.77(0.02) 7.5(0.4)
1757
1758
Carbonyl chloride fluoride
Carbonyl dicyanide
Carbonic chloride fluoride
CClFO
C3N2O
353-49-1
1115-12-4
82.461
80.044
-148
-36
1759
1760
1761
1762
1763
1764
N,N’-Carbonyldiimidazole
Carbonyl fluoride
Carbophenothion
Carbosulfan
Carboxin
2-Carboxybenzeneacetic acid
C7H6N4O
CF2O
C11H16ClO2PS3
C20H32N2O3S
C12H13NO2S
C9H8O4
530-62-1
353-50-4
786-19-6
55285-14-8
5234-68-4
89-51-0
162.149 cry (bz)
66.007 col gas
342.866
380.544
235.302
180.158
1765
C9H18N4O4
34522-32-2 246.264 nd (w)
281
C6H9NO6
C5H9NO4S
C14H10O5
53861-57-7 191.138 cry
638-23-3
179.195 nd
552-94-3
258.226
167
206
147
1769
1770
1771
N-(D-1-Carboxyethyl)-LOctopine
arginine
L-γ-Carboxyglutamic acid
S-(Carboxymethyl)-L-cysteine Carbocysteine
2-Carboxyphenyl
Salsalate
2-hydroxybenzoate
3-Carene, (+)
Carisoprodol
Carminic acid
C10H16
C12H24N2O4
C22H20O13
498-15-7
78-44-4
1260-17-9
92
136 dec
1772
Carnitine
C7H15NO3
541-15-1
1773
Carnosine
C9H14N4O3
305-84-0
1748
1749
1766
1767
1768
HCP_Section_03.indb 92
4-Amino-3-hydroxybutanoic
acid trimethylbetaine
N-β-Alanyl-L-histidine
col gas
liq
136.234
260.330 cry
492.386 red mcl pr
(aq, MeOH)
161.199 cry (al-ace),
hyg
226.232
Solubility
vs ace, DMF
i H2O; sl EtOH,
eth, bz, chl; s
ace
vs eth, EtOH,
chl, HOAc
1.45
77-23-6
333.465
22509-74-6 219.194
129-64-6
164.158 orth cry
(peth)
22232-54-8 186.231 cry, pow
5331-43-1 166.177
1563-66-2 221.252
2712-98-3 65.023 gas
244-69-9
168.195 nd
Benzyl carbazate
nD
1650.01
91
163(3)
123.5
69.5
153.2(0.5)
-90
225
1.41725
1.18
-13 dec
1.352
-191.51​
(0.09)
16019
-124.4
-21.7
-138.8(0.1)
-50.2(0.3)
-112.5
1.50815
1.544220 dec H2O, EtOH;
s eth
vs H2O
dec H2O
1.02817
1.24-87
1.1140
1.45380
2.5215
1.371925
(p>1
atm
-47.2
65.5
1.12420
-84.5
820.01
126
1.27120
1.05620
96(7)
184.5
sl H2O, bz; vs
MeOH; s EtOH
sl H2O
0.72025
(p>1
atm)
2.682320 1.845420 i H2O; vs ctc, tol
1.263220 1.631920 s H2O, chl; msc
EtOH, eth
Aq. soln. of CO2
1.61620
vs H2O, EtOH
sl H2O; s bz,
0.7909-19
HOAc
170 dec
119
-111.2
vs ace, bz,
EtOH, chl
vs ace, chl
1.391920
sl H2O; s EtOH;
vs KOH
s eth, bz, CS2
reac H2O
sl H2O; s bz,
ctc, chl, tol,
HOAc
reac H2O
s eth, ace, ctc,
chl
reac H2O
1.410020
s H2O, EtOH; sl
eth; i bz, chl
sl ace
171
0.854930 1.4693
197 dec
vs ace, bz, eth
s os
s H2O, EtOH; sl
eth; i bz, chl
vs H2O, EtOH
260
vs H2O
4/11/16 11:20 AM
Physical Constants of Organic Compounds
3-93
O
O
N
H
NH
OH
N
H
1729
1731
Carbazole
O
N
N
O
O
O
O
1734
O
1733
Carbetapentane
O
H
N
NH2
O
F
F
O
1737
Carbimazole
Carbic anhydride
N
H
O
1736
1735
N-Carbethoxyphthalimide
O
N
O
Carbendazim
O
S
N
O
O
O
1732
9H-Carbazole-9-acetic acid
O
O
N
H
O
1730
Carbaryl
O
N
N
1738
Carbobenzoxyhydrazine
N
F
N
H
NH
1739
Carbofuran
1740
γ-Carboline
Carboimidic difluoride
Se C Se
S C S
1741
1742
1743
Carbon dioxide
Carbon diselenide
O
HO
H2N
OH
1744
Carbon disulfide
O
O
O
O C O
Organic
Cl
O
N
H
N
H
NH2
C O
1745
Carbonic acid
O
1746
Carbonic dihydrazide
N
O
1747
Carbon monoxide
Carbonochloridic acid, 4-nitrophenyl ester
Cl
O
O
O
N
Cl
Cl
O
1748
O
Cl
Cl
1749
Carbonochloridic acid, (4-nitrophenyl)methyl ester
O C C C O
1753
1754
Carbon oxysulfide
Br
Cl
Cl
Br
N
H
Cl
F
O C Se
1752
Carbon oxyselenide
O
O
Cl
N
1757
Carbonyl chloride
NH2
Carbonothioic dihydrazide
O
1756
Carbonyl bromide
N
H
1751
Carbonothioic dichloride
O
1755
Carbon suboxide
H2N
1750
Carbonochloridic acid, 2,2,2-trichloroethyl ester
O
O C S
S
S
Cl
N
N
1758
Carbonyl chloride fluoride
N
N
N
1759
Carbonyl dicyanide
N,N’-Carbonyldiimidazole
OH
S
S
O
Cl
F
F
1760
O
S
O
P
O
O
S
N
S
O
O
1762
Carbophenothion
OH
O
H
N
O
N
1761
Carbonyl fluoride
O
1763
Carbosulfan
1764
Carboxin
2-Carboxybenzeneacetic acid
HO
O
OH
NH2
H
N
O
HO
N
H
NH
OH
OH
O
O
H 2N
O
1765
N-(D-1-Carboxyethyl)-L-arginine
OH
O
OH O
S
O
NH2
OH
1766
O
O
OH
1767
L-γ-Carboxyglutamic acid
1768
S-(Carboxymethyl)-L-cysteine
1769
2-Carboxyphenyl 2-hydroxybenzoate
3-Carene, (+)
HO
O
OH
OH O
OH
H2N
O
H
N
O
O
O
1770
Carisoprodol
OH
OH
O
O
OH
HO
O
OH
OH O
1771
Carminic acid
N
O
1772
Carnitine
N
H2N
OH
NH
O
1773
Carnosine
N
H
Physical Constants of Organic Compounds
3-94
No.
Name
1774
Synonym
Organic
Mol. Form.
CAS RN
α-Carotene
C40H56
7488-99-5
1775
β-Carotene
C40H56
7235-40-7
1776
β,ψ-Carotene
γ-Carotene
C40H56
472-93-5
1777
ψ,ψ-Carotene
trans-Lycopene
C40H56
502-65-8
1778
β,β-Carotene-3,3’-diol,
(3R,3’R)-
Zeaxanthin
C40H56O2
144-68-3
1779
β,ε-Carotene-3,3’-diol,
(3R,3’R,6’R)-
Xanthophyll
C40H56O2
1780
β,β-Caroten-3-ol, (3R)-
Cryptoxanthin
C40H56O
1781
β,ψ-Caroten-3-ol, (3R)-
Rubixanthin
C40H56O
1782
ψ,ψ-Caroten-16-ol
Lycoxanthin
C40H56O
1783
1784
Caroverine
Carpaine
C22H27N3O2
C28H50N2O4
1785
Cartap hydrochloride
1786
1787
Carvenone, (S)(R)-Carvone
1788
Mol.
Wt.
Physical
Form
mp/˚C
bp/˚C
den
g cm –3
nD
Solubility
536.873 red pl or pr
(peth,
bz-MeOH)
536.873 red br hex
pr
(bz-MeOH)
536.873 red pr
(bz-MeOH),
viol pr
(eth)
536.873 red pr or nd
(peth)
187.5
1.0020
vs bz, eth, chl
183(2)
1.0020
i H2O; sl EtOH,
chl; s eth, ace,
bz
i H2O, EtOH; sl
eth, peth; s bz,
chl
215.5
C7H16ClN3O2S2
568.872 ye pr
(MeOH)
orth
(chl-eth)
127-40-2
568.872 ye or viol pr
(ethMeOH)
472-70-8
552.872 garnet red
pr
(bz-MeOH)
3763-55-1 552.872 dk red nd
(bz-MeOH)
oran-red
(bz-peth)
19891-74-8 552.872 red pl
(bz-MeOH)
23465-76-1 365.468 cry
3463-92-1 478.708 mcl pr (al,
ace)
22042-59-7 273.804 cry
p-Mentha-1,8-dien-6-one, (R)
C10H16O
C10H14O
10395-45-6 152.233
6485-40-1 150.217
25.2
233
231
0.928920 1.480520
0.959320 1.498820
(S)-Carvone
p-Mentha-1,8-dien-6-one, (S)
C10H14O
2244-16-8
150.217
<15
231
0.96520
1789
1790
Caryophyllene
Casimiroin
87-44-5
477-89-4
204.352
233.220
12213.5
0.907520 1.498620
1791
Cassaine
C15H24
6-Methoxy-9-methyl-1,3C12H11NO4
dioxolo[4,5-h]quinolin-8(9H)one
C24H39NO4
468-76-8
405.572 fl (eth)
1792
Caulophylline
C12H16N2O
486-86-2
1793
1794
1795
α-Cedrene
Cedrol
Cefazolin
1796
153
177(2)
vs bz, eth,
EtOH, peth
160
vs bz, chl
160
sl EtOH, peth; s
bz, chl
168
i H2O; sl EtOH; s
bz, CS2
sl i-PrOH
vs ace, bz, eth,
EtOH
s H2O; sl EtOH,
MeOH
i H2O; s ace
sl H2O; vs EtOH;
s eth, ctc, chl
sl H2O; vs EtOH;
s eth, chl
vs bz
sl chl
69
121
β-Cellobiose
C12H22O11
13360-52-6 342.296 cry (dil al)
225 dec
1797
1798
1799
1800
1801
1802
1803
Cellotriose
Cephalexin
Cephaloglycin
Cephaloridine
Cephalothin
Cephapirin
Cepharanthine
C18H32O16
C16H17N3O4S
C18H19N3O6S
C19H17N3O4S2
C16H16N2O6S2
C17H17N3O6S2
C37H38N2O6
33404-34-1
15686-71-2
3577-01-3
50-59-9
153-61-7
21593-23-7
481-49-2
208
1804
1805
Cephradine
Cerulenin
1806
1807
1808
1809
262.5
0.947990 1.482490
s DMF, py; sl
MeOH; i chl,
bz, eth
s H2O; i EtOH,
eth, ace, bz
≈220 dec
s H2O
C16H19N3O4S
C12H17NO3
Cevadine
Chavicine
C32H49NO9
C17H19NO3
62-59-9
495-91-0
Cheirolin
Chelerythrine
C5H9NO2S2
C21H19NO5
505-34-0
179.261 cry (eth)
34316-15-9 365.380 cry
(chlMeOH)
HCP_Section_03.indb 94
s EtOH, ace,
chl, eth, bz,
MeOH
vs H2O, ace, bz,
EtOH
137
160
cry (ace aq) 155
ye amor
150
pow
38821-53-3 349.405 col cry (w) 141 dec
17397-89-6 223.268 wh nd
94
2,3-Epoxy-4-oxo-7,10dodecadienamide, (2R,3S)-
1.498920
142.5
86
200 dec
Kafocin
2020.01
180
C15H24
C15H26O
C14H14N8O4S3
cry
cry (w)
cry
2270.06
196
204.267 cry (w+2),
nd (al, bz)
469-61-4
204.352 oil
77-53-2
222.366
25953-19-9 454.508 nd (ace aq)
504.437
347.389
405.425
415.486
396.437
423.463
606.707
sl EtOH, peth; s
eth; vs bz, chl,
CS2
i H2O; sl EtOH; s
eth, ace, bz,
py, chl
sl H2O; s bz,
EtOH, ace; i
peth
591.733 flat nd (eth) 213 dec
285.338
47.5
2003
207
vs eth, EtOH,
peth
vs EtOH, chl
vs chl
4/11/16 11:20 AM
Physical Constants of Organic Compounds
3-95
1775
1774
β-Carotene
α-Carotene
1776
1777
β,ψ-Carotene
ψ,ψ-Carotene
OH
OH
H
HO
HO
1778
1779
β,ε-Carotene-3,3’-diol, (3R,3’R,6’R)-
Organic
β,β-Carotene-3,3’-diol, (3R,3’R)-
HO
HO
1781
1780
β,ψ-Caroten-3-ol, (3R)-
β,β-Caroten-3-ol, (3R)-
N
H
N
O
N
O
O
O
O
HO
N
H
N
1782
1783
ψ,ψ-Caroten-16-ol
1784
Caroverine
Carpaine
O
O
N
S
NH2
S
NH2
O
H
O
O
1786
Cartap hydrochloride
Carvenone, (S)-
1787
1788
(R)-Carvone
N
O
O
HO
O
H
1790
Caryophyllene
N
N
H
O
1789
(S)-Carvone
N
H
H
O
O
O
HCl
1785
O
O
1791
Casimiroin
1792
Cassaine
Caulophylline
HO
HO
N N
N
N
NH H
O
OH
H
O
1794
HN
NH
S
NH2
O
N
O
O
O
N
H
N
O
OH
N
O
HO
N
O
O
1801
H
NH2
S
O
N
O
NH2
O
1803
OH
O
O
1804
1805
Cephradine
Cerulenin
H
OH
H
O
O
O
H
OH
1806
Cevadine
H
OH
O
OH
Cephalothin
NH
N
H
O
Cepharanthine
N
O
O
O
1802
S
N
O
O
Cephapirin
H
HN
N
O
O
O
O
O
S
S
1800
N
H
O
NH
Cephaloridine
O
S
Cellotriose
O
H
O
O
1799
H
1797
β-Cellobiose
Cephaloglycin
H
OH
1796
S
OH
OH
OH
OH
S
O
1798
S
H
OH
HO
OH
N
OH
Cephalexin
O
O
O
O
O
OH
OH
OH
Cefazolin
O
NH2
S
1795
Cedrol
H
S
O
O
OH
O
HO
HO
H
α-Cedrene
N N
N
O
1793
S
OH
HO
O
HO
O OH
OH
OH
OH
O
O
O
O
O
N
1807
Chavicine
O
S
O
N
1808
Cheirolin
C
N
O
S
O
1809
Chelerythrine
Physical Constants of Organic Compounds
3-96
Organic
No.
Name
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
1810
Chelidonine
Stylophorine
C20H19NO5
476-32-4
1811
1812
Chinomethionat
Chloral hydrate
C10H6N2OS2
C2H3Cl3O2
1813
1814
Chlorambucil
Chloramine B
1815
Chloramine T
1816
Chloramphenicol
1817
1818
Chloramphenicol palmitate
Chloranilic acid
1819
Chlorbenside
1820
1821
1822
Chlorbicyclen
Chlorbromuron
Chlorbufam
1823
1824
1825
1826
1827
1828
Chlorcyclizine
Chlordane
Chlordantoin
Chlordene
Chlordimeform
Chlorendic acid
1829
1830
1831
Chlorendic anhydride
Chlorfenvinphos
Chlorflurecol
1832
Chloridazon
1833
1834
Chlorimuron-ethyl
Chlormephos
1835
1836
1837
Chlormequat chloride
Chlormezanone
Chlornaphazine
1838
1839
Chloroacetaldehyde
2-Chloroacetamide
1840
Chloroacetic acid
1841
1842
1843
Chloroacetic anhydride
4-Chloroacetoacetanilide
Chloroacetone
N-Acetoacetyl-4-chloroaniline
1844
1845
Chloroacetonitrile
α-Chloroacetophenone
Chloromethyl cyanide
ω-Chloroacetophenone
1846
1847
Physical
Form
mp/˚C
bp/˚C
353.369 mcl pr (al)
135.5
2200.002
2439-01-2
302-17-0
234.297
165.403
170.5(0.5)
52(2)
96 dec
C14H19Cl2NO2
N-Chlorobenzenesulfonamide C6H5ClNNaO2S
sodium
N-Chloro-4-methylbenzenesul- C7H7ClNNaO2S
fonamide sodium
C11H12Cl2N2O5
305-03-3
127-52-6
304.213
213.618 pr (w)
66.9(0.5)
190
127-65-1
227.645 pr (hyd)
180 (hyd)
56-75-7
C27H42Cl2N2O6
2,5-Dichloro-3,6-dihydroxyC6H2Cl2O4
2,5-cyclohexadiene-1,4-dione
1-Chloro-4-[[(4-chlorophenyl)­ C13H10Cl2S
methyl]thio]benzene
C9H6Cl8
C9H10BrClN2O2
1-Methyl-2-propynyl(3-chloro- C11H10ClNO2
phenyl)carbamate
C18H21ClN2
C10H6Cl8
C11H17Cl3N2O2S
C10H6Cl6
C10H13ClN2
1,4,5,6,7,7-Hexachloro-5C9H4Cl6O4
norbornene-2,3-dicarboxylic
acid
C9H2Cl6O3
C12H14Cl3O4P
9H-Fluorene-9-carboxylic acid, C14H9ClO3
2-chloro-9-hydroxy3(2H)-Pyridazinone,
C10H8ClN3O
5-amino-4-chloro-2-phenylC15H15ClN4O6S
Chloromethyl O,O-diethyl
C5H12ClO2PS2
dithiophosphate
C5H13Cl2N
C11H12ClNO3S
C14H15Cl2N
530-43-8
87-88-7
323.129 pa ye pl or 150(1)
nd (w)
561.537 cry (bz)
90
208.984 red lf (w+2) 283.5
103-17-3
269.189
105
97.2(0.5)
45.5
82-93-9
57-74-9
5588-20-5
3734-48-3
6164-98-3
115-28-6
300.826 oil
409.779
347.689
338.873 cry (EtOH)
196.676
388.844 cry (w)
115-27-5
470-90-6
2464-37-1
370.828
359.569
260.672
235
1698-60-8
221.643
206.8(0.9)
101.1(0.3)
nD
Solubility
i H2O; s EtOH,
eth, chl
1.908120
vs H2O, bz, eth,
EtOH
sl EtOH; i chl,
eth
s H2O; i bz, chl,
eth
vs ace, EtOH,
chl
vs bz, eth, EtOH
s H2O
sub
71.0(0.7)
2550-75-6 397.768 pow
13360-45-7 293.544
1967-16-4 223.656 cry
den
g cm –3
1.421020
1742
1.6920
sl H2O; s MeOH,
EtOH, ace
1400.12
1751
1.6025
s CS2
155
32.6(0.5)
232
1560.4
1.10525
1.588525 vs bz, eth, EtOH
1700.05
1.49620
90982-32-4 414.821
24934-91-6 234.705 oil
186
999-81-5
80-77-3
494-03-1
158.069
273.736 cry
268.182 pl (peth)
239 dec
117
55
2105
C2H3ClO
C2H4ClNO
107-20-0
79-07-2
78.497
93.512
liq
-16.3
121
87(13)
225
C2H3ClO2
79-11-8
94.497
mcl pl
62.0(0.7)
189.11(0.03) 1.404340 1.435155
C4H4Cl2O3
C10H10ClNO2
C3H5ClO
541-88-8
101-92-8
78-95-5
170.979 pr (bz)
211.645
92.524 liq
46
132
-44.5
203
1.549720
116(13)
1.1520
C2H2ClN
C8H7ClO
107-14-2
532-27-4
56.5
108(5)
247
1.193020 1.420225
1.32415
4-(2-Chloroacetyl)acetanilide
Chloroacetyl chloride
C10H10ClNO2
C2H2Cl2O
140-49-8
79-04-9
75.497
154.594 pl(dil al),
rhom, lf
(peth)
211.645
112.942 liq
218
-21.7(0.2)
106.0(0.4)
1848
1849
1850
Chloroacetylene
9-Chloroacridine
2-Chloroaniline
C2HCl
C13H8ClN
C6H6ClN
593-63-5
1207-69-8
95-51-2
60.482 col gas
213.663 nd (al)
127.572 liq
-126
121
-2.3(0.9)
-30
sub
209(1)
1851
3-Chloroaniline
C6H6ClN
108-42-9
127.572 liq
-10.3(0.2)
230(1)
1852
4-Chloroaniline
C6H6ClN
106-47-8
127.572 orth pr
70.4(0.7)
231(4)
1853
1854
2-Chloroaniline hydrochloride
3-Chloroaniline hydrochloride
C6H7Cl2N
C6H7Cl2N
137-04-2
141-85-5
164.033 pl (w, aq al) 235
164.033 pl
222
1.420220 1.453020 msc eth; s ace,
ctc
sl EtOH
vs H2O, EtOH
1.589520 i H2O; msc
EtOH; s eth,
ace
1.216120 1.594120 i H2O; msc
EtOH, eth, ace,
bz; s chl
1.42919 1.554687 s H2O, EtOH,
eth, chl
1.50518
vs H2O
vs H2O, EtOH
HCP_Section_03.indb 96
830.1
1.5244
1.19
sl H2O; misc os
sl EtOH
vs ace, bz, eth,
EtOH
s eth
s H2O; vs EtOH;
sl eth
vs H2O; s EtOH,
eth, bz, chl; sl
ctc
s H2O, EtOH,
eth, chl
vs eth, EtOH
i H2O; vs EtOH,
eth, bz; s ace,
peth
4/11/16 11:20 AM
Physical Constants of Organic Compounds
3-97
OH
HO
O
O
H
O
N
O
N
S
N
S
Cl
Cl
O
O
1810
1811
Chelidonine
O
OH
OH
1812
Chinomethionat
O
N
S
Cl
Na
OH
Chloral hydrate
O
N
O
O
Cl
O
HO
1814
Chlorambucil
Chloramine B
Cl
H
N
Cl
H
N
Cl
1813
OH
O
N
Cl
Cl
Na
O
N
S
Cl
O
Cl
HO
O
N
O
Cl
O
Cl
OH
O
1815
1816
Chloramine T
O
1817
Chloramphenicol
1818
Chloramphenicol palmitate
Chloranilic acid
Organic
H
Cl
Cl
Cl
Cl
Cl
H
N
Cl
Cl
Cl
S
Cl
Cl
Cl
1819
H
N
O
O
O
Br
1822
Chlorbromuron
Cl
O
Cl
Cl H
Cl
O
N
S
Cl
1824
Cl Cl
Cl H
Cl
Cl
Cl
1825
Chlordane
Cl
1827
Chlordene
OH
OH
Cl
Cl
1826
Chlordantoin
Chlorcyclizine
Cl Cl
O
Cl
Cl
N
N
Cl H
Cl
1823
Chlorbufam
H
N
Cl Cl
Cl
Cl H
N
Cl
1821
Chlorbicyclen
N
O
Cl
1820
Chlorbenside
N
Cl
O
O
O
Cl
Cl
1828
Chlordimeform
Cl Cl
O
Cl
1829
Chlorendic acid
Chlorendic anhydride
O
Cl
Cl
Cl
O
H
N
Cl
O
O
O P O
O
HO
H2N
OH
Cl
O
N
O
N
S
H
N
O O
N
Cl
S
O
P
O
S
N
Cl
O
1830
1831
Chlorfenvinphos
1832
Chlorflurecol
1833
Chloridazon
1834
Chlorimuron-ethyl
Chlormephos
O
N
Cl
N
S
Cl
O O
Cl
N
1835
1837
Chlormezanone
Chlornaphazine
Cl
O
Cl
1836
Chlormequat chloride
O
Cl
Cl
1838
1839
Chloroacetaldehyde
O
O
Cl
1842
O
4-Chloroacetoacetanilide
Cl
O
Cl
1843
Chloroacetone
Cl
N
1845
α-Chloroacetophenone
Chloroacetonitrile
O
Cl
O
1841
Chloroacetic acid
Chloroacetic anhydride
O
O
O
Cl
Cl
1844
Cl
OH
1840
2-Chloroacetamide
H
N
H
N
O
O
Cl
NH2
1846
4-(2-Chloroacetyl)acetanilide
Cl
Cl
1847
Chloroacetyl chloride
1848
Chloroacetylene
NH2
Cl
NH2
NH2
Cl
N
1849
9-Chloroacridine
Cl
1850
2-Chloroaniline
NH2 HCl
NH2
Cl
1851
3-Chloroaniline
HCl
Cl
1852
4-Chloroaniline
Cl
1853
2-Chloroaniline hydrochloride
1854
3-Chloroaniline hydrochloride
Physical Constants of Organic Compounds
3-98
Organic
No.
Name
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
1855
2-Chloroanisole
1-Chloro-2-methoxybenzene
C7H7ClO
766-51-8
142.583 liq
1856
3-Chloroanisole
1-Chloro-3-methoxybenzene
C7H7ClO
2845-89-8
142.583
1857
4-Chloroanisole
1-Chloro-4-methoxybenzene
C7H7ClO
623-12-1
142.583
<-18
1858
1-Chloroanthracene
C14H9Cl
4985-70-0
212.674 lf (HOAc)
83.5
1859
1-Chloro-9,10-anthracenedione
C14H7ClO2
82-44-0
242.658 ye nd (to or 163
al)
sub
1860
2-Chloro-9,10-anthracenedione
C14H7ClO2
131-09-9
242.658 pa ye nd (al, 209.9(0.4)
HOAc)
sub
1861
2-Chlorobenzaldehyde
C7H5ClO
89-98-5
140.567 nd
11.9(0.6)
212.1(1)
1862
3-Chlorobenzaldehyde
C7H5ClO
587-04-2
140.567 pr
17.5
213.5
1863
4-Chlorobenzaldehyde
C7H5ClO
104-88-1
140.567 pl
47(1)
213.5
1864
1865
2-Chlorobenzamide
Chlorobenzene
C7H6ClNO
C6H5Cl
609-66-5
108-90-7
155.582 orth nd (w)
112.557 liq
141.8
-45.2(0.1)
131.6(0.2)
1866
1867
2-Chlorobenzeneacetic acid
3-Chlorobenzeneacetic acid
C8H7ClO2
C8H7ClO2
2444-36-2
1878-65-5
1868
4-Chlorobenzeneacetic acid
C8H7ClO2
1878-66-6
170.594 nd (w)
94.2(0.4)
170.594 pl (dil al), nd 76.6(0.4)
(lig)
170.594 nd (w)
104.8(0.4)
1869
1870
1871
1872
C8H6ClN
C8H6ClN
C8H6ClN
C8H6Cl2O
2856-63-5
1529-41-5
140-53-4
2912-62-1
151.594
151.594
151.594
189.039
24
11.5
29
C7H5ClO3
937-14-4
172.566
92 dec
1874
2-Chlorobenzeneacetonitrile
3-Chlorobenzeneacetonitrile
4-Chlorobenzeneacetonitrile
α-Chlorobenzeneacetyl
chloride
3-Chlorobenzenecarboperoxoic acid
4-Chloro-1,2-benzenediamine 4-Chloro-o-phenylenediamine
C6H7ClN2
95-83-0
76
1875
1876
1877
1878
4-Chloro-1,3-benzenediamine
2-Chloro-1,4-benzenediamine 2-Chloro-p-phenylenediamine
3-Chloro-1,2-benzenediol
4-Chloro-1,2-benzenediol
C6H7ClN2
C6H7ClN2
C6H5ClO2
C6H5ClO2
5131-60-2
615-66-7
4018-65-9
2138-22-9
142.586 pl (bz-lig) lf
(w)
142.586 pl or nd
142.586 nd
144.556 cry (lig)
144.556 lf (bz-peth)
1879
4-Chloro-1,3-benzenediol
C6H5ClO2
95-88-5
144.556
1880
2-Chloro-1,4-benzenediol
C6H5ClO2
615-67-8
144.556 red lf (chl),
nd (bz)
1881
1882
1883
1884
1885
2-Chlorobenzenemethanamine
3-Chlorobenzenemethanamine
4-Chlorobenzenemethanamine
4-Chlorobenzenemethanethiol
2-Chlorobenzenemethanol
C7H8ClN
C7H8ClN
C7H8ClN
C7H7ClS
C7H7ClO
89-97-4
4152-90-3
104-86-9
6258-66-8
17849-38-6
1886
4-Chlorobenzenemethanol
C7H7ClO
873-76-7
1887
1888
1889
2-Chlorobenzenesulfonamide
4-Chlorobenzenesulfonamide
4-Chlorobenzenesulfonic acid
C6H6ClNO2S
C6H6ClNO2S
C6H5ClO3S
6961-82-6
98-64-6
98-66-8
141.599
141.599
141.599
158.649
142.583 lf or nd (dil
al)
142.583 nd (w), pl
(bz or
bz-lig)
191.636 lf (al)
191.636 pr or pl (eth)
192.620 nd (w+1)
188.3(0.5)
146
67
14725
1890
C6H4Cl2O2S
98-60-2
211.066
51
14115
1891
1892
4-Chlorobenzenesulfonyl
chloride
2-Chlorobenzenethiol
3-Chlorobenzenethiol
C6H5ClS
C6H5ClS
6320-03-2
2037-31-2
144.622
144.622
1893
4-Chlorobenzenethiol
C6H5ClS
106-54-7
144.622
1894
Chlorobenzilate
C16H14Cl2O3
510-15-6
325.186
1873
HCP_Section_03.indb 98
Phenyl chloride
p-Chlorobenzenesulfonic acid
Physical
Form
mp/˚C
bp/˚C
-26.5(0.2)
201.8(0.4)
193.5
91
64
48.5
90.5
197.5
251
261
265.0
12023
den
g cm –3
nD
Solubility
1.191120 1.548020 i H2O; s EtOH,
eth; sl chl
1.175912 1.536520 i H2O; s EtOH,
eth
1.20120 1.539020 i H2O; vs EtOH,
eth, chl; s ctc
1.1707100 1.6959100 i H2O; s EtOH,
eth, bz, ctc
i H2O; sl EtOH,
ctc; msc eth; s
bz
i H2O, eth; sl
EtOH, bz; vs
tol; s PhNO2
1.248320 1.566220 sl H2O; s EtOH,
eth, ace, bz,
ctc
1.241020 1.565020 sl H2O, chl; s
EtOH, eth, ace,
bz
1.19661 1.55561 s H2O, ace, chl;
vs EtOH, eth,
bz
s H2O, EtOH, eth
1.105820 1.524120 i H2O; msc
EtOH, eth; vs
bz, ctc
sl H2O; vs EtOH
sl H2O, bz, ctc,
EtOH; msc eth
s H2O, EtOH,
eth, bz
1.173718
1.180630 1.543720
1.177830
s ctc
1.19625 1.544020
sl H2O; vs EtOH,
eth; s bz, lig
vs EtOH
11011
13910.5
vs lig
vs H2O, ace,
eth, EtOH
vs H2O, EtOH,
eth, ace, bz,
CS2
vs H2O, chl; s
EtOH, eth; vs
bz
257
108
263
19.5
73
722
892
10913
11317
230
75
235
1.20225
1.559425
1.557025
1.556625
1.589320
sl H2O; vs EtOH,
eth, lig
vs bz, eth, EtOH
vs EtOH
vs bz, eth
s H2O, EtOH; i
eth, bz
vs eth, bz
205.5
206
1.275210
1.263713
61
206
1.191120 1.548020
39.0(0.5)
1570.07
1.281620
sl H2O, EtOH
i H2O; s EtOH,
eth, chl, peth
i H2O; vs EtOH,
eth, bz; sl chl
4/11/16 11:20 AM
Physical Constants of Organic Compounds
3-99
O
O
O
O
Cl
O
O
Cl
Cl
Cl
Cl
1856
2-Chloroanisole
O
Cl
Cl
1855
1857
3-Chloroanisole
1858
4-Chloroanisole
O
1859
1-Chloroanthracene
1860
1-Chloro-9,10-anthracenedione
1861
2-Chloro-9,10-anthracenedione
2-Chlorobenzaldehyde
O
O
O
NH2
OH
Cl
OH
Cl
Cl
Cl
Cl
1862
1865
1864
4-Chlorobenzaldehyde
1867
2-Chlorobenzeneacetic acid
O
Cl
Cl
1866
Chlorobenzene
2-Chlorobenzamide
O
1868
3-Chlorobenzeneacetic acid
4-Chlorobenzeneacetic acid
Organic
3-Chlorobenzaldehyde
1863
OH
O
O
N
2-Chlorobenzeneacetonitrile
NH2
Cl
Cl
Cl
1869
OH
O
N
Cl
O
Cl
N
1870
3-Chlorobenzeneacetonitrile
1871
Cl
1872
α-Chlorobenzeneacetyl chloride
4-Chlorobenzeneacetonitrile
NH2
NH2
3-Chlorobenzenecarboperoxoic acid
OH
Cl
NH2
1873
OH
OH
OH
OH
NH2
OH
NH2
Cl
Cl
1874
4-Chloro-1,2-benzenediamine
1875
Cl
1876
4-Chloro-1,3-benzenediamine
Cl
1878
1877
2-Chloro-1,4-benzenediamine
Cl
1879
4-Chloro-1,2-benzenediol
3-Chloro-1,2-benzenediol
4-Chloro-1,3-benzenediol
OH
Cl
NH2
NH2
Cl
OH
1880
2-Chloro-1,4-benzenediol
1885
2-Chlorobenzenemethanol
OH
Cl
Cl
Cl
1881
2-Chlorobenzenemethanamine
OH
Cl
SH
NH2
1882
3-Chlorobenzenemethanamine
O
O S NH2
Cl
Cl
1883
1884
4-Chlorobenzenemethanamine
4-Chlorobenzenemethanethiol
O
O S NH2
O
O S OH
Cl
1886
4-Chlorobenzenemethanol
1887
2-Chlorobenzenesulfonamide
O
O S Cl
Cl
1888
1889
4-Chlorobenzenesulfonamide
4-Chlorobenzenesulfonic acid
SH
SH
SH
HO
O
O
Cl
Cl
Cl
1890
4-Chlorobenzenesulfonyl chloride
1891
2-Chlorobenzenethiol
1892
3-Chlorobenzenethiol
Cl
1893
4-Chlorobenzenethiol
Cl
Cl
1894
Chlorobenzilate
Physical Constants of Organic Compounds
3-100
Mol. Form.
CAS RN
Mol.
Wt.
Organic
mp/˚C
bp/˚C
den
g cm –3
C6H4ClO2P
1641-40-3
1896
2-Chloro-1,3,2-benzodioxaphosphole
2-Chlorobenzoic acid
174.522
30
8020
1.465020 1.571220
C7H5ClO2
118-91-2
156.567 mcl pr (w)
140.4(0.7)
274(14)
1.54420
1897
3-Chlorobenzoic acid
C7H5ClO2
535-80-8
156.567 pr (w)
154.2(0.2)
283(17)
1.49625
1898
4-Chlorobenzoic acid
C7H5ClO2
74-11-3
156.567 tcl pr
(al-eth)
239.5(0.6)
1899
2-Chlorobenzonitrile
C7H4ClN
873-32-5
137.567 nd
43.5(0.4)
235.1(0.5)
1900
3-Chlorobenzonitrile
C7H4ClN
766-84-7
137.567
41
10015
1901
4-Chlorobenzonitrile
C7H4ClN
623-03-0
137.567 nd (al)
91.6(0.4)
223.0(0.4)
1902
1903
1904
1905
2-Chlorobenzophenone
2-Chlorophenyl phenyl ketone
4-Chloro-2-benzothiazolamine
6-Chloro-2-benzothiazolamine
2-Chlorobenzothiazole
C13H9ClO
C7H5ClN2S
C7H5ClN2S
C7H4ClNS
5162-03-8
19952-47-7
95-24-9
615-20-3
216.662 pl (chl-lig)
184.646
184.646
169.632
54
204
200
24
330
1906
1907
5-Chloro-1H-benzotriazole
6-Chloro-2H-3,1-benzoxazine- 5-Chloroisatoic anhydride
2,4(1H)-dione
5-Chloro-2-benzoxazolamine Zoxazolamine
2-Chlorobenzoxazole
5-Chloro-2(3H)-benzoxazolone Chlorzoxazone
2-Chlorobenzoyl chloride
3-Chlorobenzoyl chloride
4-Chlorobenzoyl chloride
1-Chloro-4-benzylbenzene
o-Chlorobenzylidene
malononitrile
C6H4ClN3
C8H4ClNO3
94-97-3
4743-17-3
153.569
197.576
158
280 dec
C7H5ClN2O
C7H4ClNO
C7H4ClNO2
C7H4Cl2O
C7H4Cl2O
C7H4Cl2O
C13H11Cl
C10H5ClN2
61-80-3
615-18-9
95-25-0
609-65-4
618-46-2
122-01-0
831-81-2
2698-41-1
168.580
153.566
169.566
175.012
175.012
175.012
202.679
188.613
No.
Name
1895
1908
1909
1910
1911
1912
1913
1914
1915
Synonym
Physical
Form
pl (bz)
248
1.371510 1.633810 vs ace, eth,
EtOH
201.5
1.345318 1.567820
cry (ace)
liq
184.5
7
191.5
-4
wh cry
16
7.5
96
241(12)
225
222
299
312
vs EtOH
1.377020
1.124720
2-Chlorobiphenyl
C12H9Cl
2051-60-7
188.652 mcl (dil al)
31.78(0.08)
273(7)
1.149932
1917
3-Chlorobiphenyl
C12H9Cl
2051-61-8
188.652
16
284.5
1.157925
1918
4-Chlorobiphenyl
C12H9Cl
2051-62-9
188.652 lf (lig or al)
75.4(0.2)
293(3)
1919
4-Amino-4’-chlorodiphenyl
C12H10ClN
135-68-2
203.667 cry (peth)
134
1920
4’-Chloro-[1,1’-biphenyl]-4amine
3-Chloro-[1,1’-biphenyl]-2-ol
2-Phenyl-6-chlorophenol
C12H9ClO
85-97-2
204.651
6
1921
1922
4-Chloro-1,2-butadiene
1-Chloro-1,3-butadiene
C4H5Cl
C4H5Cl
25790-55-0 88.536
627-22-5
88.536
1923
2-Chloro-1,3-butadiene
C4H5Cl
126-99-8
88.536
1924
4-Chlorobutanal
C4H7ClO
6139-84-0
106.551
1925
1-Chlorobutane
Butyl chloride
C4H9Cl
109-69-3
92.567
liq
1926
2-Chlorobutane
(±)-sec-Butyl chloride
C4H9Cl
53178-20-4 92.567
liq
1927
4-Chlorobutanenitrile
C4H6ClN
628-20-6
1928
2-Chlorobutanoic acid
C4H7ClO2
1929
3-Chlorobutanoic acid
1930
1931
1932
1933
1934
1935
4-Chlorobutanoic acid
4-Chloro-1-butanol
1-Chloro-2-butanol
3-Chloro-2-butanone
4-Chlorobutanoyl chloride
2-Chloro-1-butene
1936
3-Chloro-1-butene
HCP_Section_03.indb 100
α-Butylene chlorohydrin
319(4)
1.2425
88
67(6)
0.989120
0.960620
59(3)
0.95620
5113
1.1068
-123.1(0.2)
78.4(0.2)
0.885720
-131.3
71(8)
0.873220
103.551
175(12)
1.093415
4170-24-5
122.551
189627
1.179620
C4H7ClO2
625-68-3
122.551 cry (eth)
16
11622
1.189820
C4H7ClO2
C4H9ClO
C4H9ClO
C4H7ClO
C4H6Cl2O
C4H7Cl
627-00-9
928-51-8
1873-25-2
4091-39-8
4635-59-0
2211-70-3
122.551
108.566
108.566
106.551
140.996
90.552
16
19622
8416
141
129(13)
173.5
58(3)
1.223620
1.088320
1.06825
1.055425
1.258120
0.910715
C4H7Cl
563-52-0
90.552
64(3)
0.897820
liq
-130
Solubility
s H2O, bz; vs
EtOH, eth, ace;
sl CS2
sl H2O, bz, ctc,
CS2; s EtOH,
eth
i H2O, bz, ctc;
vs EtOH; sl
eth, ace
sl H2O; s EtOH,
eth, chl
i H2O; s EtOH,
eth
sl H2O, lig; s
EtOH, eth, bz,
chl
1.113317
1916
Chloroprene
nD
vs EtOH, MeOH
1.572616 s ctc
1.567720
1.575620 sl chl
vs ace
sl H2O; s bz,
diox, EtOAc,
ace
i H2O; vs eth,
EtOH, lig
1.618125 vs ace, eth,
EtOH
i H2O; s EtOH,
eth, lig
vs ace, bz, eth
1.623730 i H2O; s EtOH,
eth, ace, bz
1.477520 vs ace, bz, eth
1.471220 vs eth, EtOH,
chl
1.458320 sl H2O; msc eth,
ace, bz
1.44668 vs ace, eth,
EtOH
1.402320 i H2O; msc
EtOH, eth; sl
ctc
1.397120 vs bz, eth,
EtOH, chl
1.441320 i H2O; s EtOH,
eth; sl ctc
1.44120 sl H2O; vs EtOH,
eth
1.422120 s EtOH; vs eth;
sl ctc
1.464220 vs EtOH
1.451820 vs eth, EtOH
1.440020 s EtOH, eth
1.421920
1.461620 s eth
1.416521 vs ace, bz, eth,
EtOH
1.414920 vs eth, ace; s
chl
4/11/16 11:20 AM
Physical Constants of Organic Compounds
3-101
O
O
O
OH
O
N
N
Cl
P Cl
Cl
O
Cl
Cl
1895
1896
2-Chloro-1,3,2-benzodioxaphosphole
1897
2-Chlorobenzoic acid
3-Chlorobenzoic acid
1899
4-Chlorobenzoic acid
1900
2-Chlorobenzonitrile
S
1902
1901
3-Chlorobenzonitrile
4-Chlorobenzonitrile
Cl
N
N
NH2
N
N
H
Cl
S
1904
1905
6-Chloro-2-benzothiazolamine
1906
2-Chlorobenzothiazole
5-Chloro-1H-benzotriazole
Organic
4-Chloro-2-benzothiazolamine
N
N
NH2
S
Cl
1903
2-Chlorobenzophenone
Cl
Cl
1898
Cl
Cl
O
N
OH
OH
O
Cl
O
N
H
Cl
O
1907
Cl
O
Cl
O
1909
5-Chloro-2-benzoxazolamine
Cl
O
O
1908
6-Chloro-2H-3,1-benzoxazine-2,4(1H )-dione
O
NH2
O
O
H
N
Cl
N
N
1910
2-Chlorobenzoxazole
1911
5-Chloro-2(3H )-benzoxazolone
2-Chlorobenzoyl chloride
Cl
Cl
N
Cl
Cl
Cl
Cl
Cl
1912
Cl
1913
3-Chlorobenzoyl chloride
1914
4-Chlorobenzoyl chloride
1915
1-Chloro-4-benzylbenzene
o-Chlorobenzylidene malononitrile
HO
Cl
1918
4-Chlorobiphenyl
N
Cl
Cl
1920
4’-Chloro-[1,1’-biphenyl]-4-amine
1917
3-Chlorobiphenyl
Cl
NH2
1919
1916
2-Chlorobiphenyl
C
1921
3-Chloro-[1,1’-biphenyl]-2-ol
4-Chloro-1,2-butadiene
Cl
1922
1-Chloro-1,3-butadiene
Cl
1923
2-Chloro-1,3-butadiene
O
Cl
Cl
O
1924
1925
4-Chlorobutanal
O
O
OH
1928
4-Chlorobutanenitrile
2-Chlorobutane
Cl
Cl
N
1927
1926
1-Chlorobutane
OH
Cl
Cl
2-Chlorobutanoic acid
1929
3-Chlorobutanoic acid
Cl
OH
1930
4-Chlorobutanoic acid
Cl
OH
1931
4-Chloro-1-butanol
OH
1932
1-Chloro-2-butanol
O
Cl
Cl
Cl
O
1933
3-Chloro-2-butanone
Cl
1934
4-Chlorobutanoyl chloride
Cl
Cl
1935
2-Chloro-1-butene
1936
3-Chloro-1-butene
Physical Constants of Organic Compounds
3-102
Mol. Form.
CAS RN
Mol.
Wt.
4-Chloro-1-butene
cis-1-Chloro-2-butene
C4H7Cl
C4H7Cl
927-73-1
4628-21-1
90.552
90.552
1939
1940
trans-1-Chloro-2-butene
cis-2-Chloro-2-butene
C4H7Cl
C4H7Cl
4894-61-5
2211-69-0
90.552
90.552
liq
-117.3
85(4)
65(5)
1941
trans-2-Chloro-2-butene
C4H7Cl
2211-68-9
90.552
liq
-105.8
63(3)
1942
1943
C10H13Cl
C6H15ClSi
3972-56-3 168.663
18162-48-6 150.722
89.5
214(10)
125
C16H19ClSi
58479-61-1 274.861
1200.06
1.0720
C10H13ClO
C4H5Cl
C4H10Cl3N
98-28-2
184.662
21020-24-6 88.536
821-48-7
178.488
1148
68.5
1.421825 1.421825
215.0
HN1
C6H13Cl2N
538-07-8
170.080 col liq
-34
6612
1.086123 1.465325 i H2O
Mechlorethamine
C5H11Cl2N
51-75-2
156.053
-60
8718
2-Chlorobenzyl chloride
C7H6Cl2
611-19-8
161.029 liq
-17
217
1.26990
3-Chlorobenzyl chloride
C7H6Cl2
620-20-2
161.029
216
1.269515 1.555420
4-Chlorobenzyl chloride
C7H6Cl2
104-83-6
161.029 nd (dil al)
C3H8Cl2Si
1719-57-9
143.088
C4H6Cl2
1871-57-4
124.997 liq
C7H6Cl2S
7205-90-5
C8H6Cl2O
1957
1-Chloro-4-tert-butylbenzene
Chloro-(tert-butyl)­
dimethylsilane
Chloro(tert-butyl)­
diphenylsilane
2-Chloro-4-tert-butylphenol
3-Chloro-1-butyne
2-Chloro-N-(2-chloroethyl)­
ethanamine, hydrochloride
2-Chloro-N-(2-chloroethyl)-Nethylethanamine
2-Chloro-N-(2-chloroethyl)-Nmethylethanamine
1-Chloro-2-(chloromethyl)­
benzene
1-Chloro-3-(chloromethyl)­
benzene
1-Chloro-4-(chloromethyl)­
benzene
Chloro(chloromethyl)­
dimethylsilane
3-Chloro-2-(chloromethyl)-1propene
1-Chloro-4-[(chloromethyl)­
thio]benzene
2-Chloro-1-(4-chlorophenyl)­
ethanone
3-Chlorocholest-5-ene, (3β)
1958
1959
1960
trans-o-Chlorocinnamic acid
trans-m-Chlorocinnamic acid
trans-p-Chlorocinnamic acid
1961
Chlorocyclohexane
1962
No.
Name
1937
1938
1944
Organic
1945
1946
1947
1948
1949
1950
1951
1952
Synonym
Physical
Form
mp/˚C
bp/˚C
74(5)
84(4)
31
den
g cm –3
nD
Solubility
0.921120 1.423320 vs ace, eth, chl
0.942620 1.439020 i H2O; s EtOH,
ace, chl
0.929520 1.435020 i H2O; s ace, chl
0.923920 1.424020 i H2O; msc
EtOH; s ace,
chl
0.913820 1.419020 i H2O; msc
EtOH; s ace,
chl
1.007518 1.512320
1.567520
1.553020
223
sl H2O; msc ctc,
DMF
i H2O; sl EtOH,
ctc; vs eth, bz
vs EtOH
sl ctc
115.5
1.086520 1.436020
-14
138
1.178220 1.4753
193.094
21.5
12812
1.34625
937-20-2
189.039 nd (al)
101.5
270
C27H45Cl
910-31-6
405.099 nd (al, ace)
96
C9H7ClO2
C9H7ClO2
C9H7ClO2
939-58-2
182.604
14473-90-6 182.604
940-62-5
182.604
212
165
249.5
C6H11Cl
542-18-7
118.604 liq
-45(1)
142.6(0.5)
1.00020
1.462620
2-Chlorocyclohexanone
C6H9ClO
822-87-7
132.587
23
8215
1.16020
1.482520
1963
1-Chlorocyclohexene
C6H9Cl
930-66-5
116.588
140(4)
1.036119 1.479720
1964
Chlorocyclopentane
C5H9Cl
930-28-9
104.578
113.1(0.6)
1.005120 1.451020
1965
1966
2-Chlorocyclopentanone
3-Chlorocyclopentene
C5H7ClO
C5H7Cl
694-28-0
96-40-2
118.562
102.563
8719
4040
1.18525 1.475020
1.038825 1.470826 vs eth, EtOH,
chl
1967
1968
4-Chloro-2-cyclopentylphenol Dowicide 9
1-Chlorodecane
C11H13ClO
C10H21Cl
13347-42-7 196.673
1002-69-3 176.727 liq
1969
1970
1971
1972
10-Chloro-1-decanol
2-Chloro-N,N-diallylacetamide Allidochlor
Chlorodiazepoxide
Chlorodibromomethane
C10H21ClO
C8H12ClNO
C16H14ClN3O
CHBr2Cl
51309-10-5
93-71-0
58-25-3
124-48-1
1973
C3H7Cl3Si
1975
Chloro(dichloromethyl)­
dimethylsilane
5-Chloro-N-(3,4dichlorophenyl)-2-hydroxybenzamide
2-Chloro-1,1-diethoxyethane
1976
3-Chloro-1,1-diethoxypropane
1953
1954
1955
1956
1974
HCP_Section_03.indb 102
Cyclohexyl chloride
Cyclopentyl chloride
(Dichloromethyl)dimethylchlorosilane
3’,4’,5-Trichlorosalicylanilide
18318
225(3)
1.605520
s EtOH, bz,
MeOH
i H2O; s EtOH,
ace, bz, chl; vs
CS2
vs eth, EtOH
s EtOH, eth
vs ace, eth,
EtOH
i H2O; msc
EtOH, eth, ace,
bz; vs chl
s eth, bz, diox;
sl ctc
s eth, ace, ctc,
chl
i H2O; s eth,
ace, bz, ctc
18715
1161
0.869620 1.438020 i H2O; vs eth,
chl; s ctc
0.963025 1.457820 vs eth, EtOH
1.08825 1.493225 sl H2O; s EtOH
236.2
-20
120
2.45120
18171-59-0 177.533 liq
-48
149
1.236920
C13H8Cl3NO2
642-84-2
316.568
247
C6H13ClO2
621-62-5
152.619
157(4)
C7H15ClO2
35573-93-4 166.646
1.018020 1.417020 sl H2O, ctc; msc
EtOH, eth
0.995119 1.426820 vs ace, bz
192.726
173.640 liq
299.754
208.280 liq
-31.3
vs EtOH, chl
12.5
8425
1.548220 i H2O; s EtOH,
eth, ace, bz
1.46120
4/11/16 11:21 AM
Physical Constants of Organic Compounds
Cl
Cl
1937
Cl
1938
4-Chloro-1-butene
3-103
cis-1-Chloro-2-butene
1940
trans-1-Chloro-2-butene
cis-2-Chloro-2-butene
Si Cl
Cl
Cl
1941
1942
Cl
1939
trans-2-Chloro-2-butene
1943
1-Chloro-4-tert-butylbenzene
Chloro-(tert-butyl)dimethylsilane
OH
Cl
Cl
Cl
1944
1946
1945
Chloro(tert-butyl)diphenylsilane
Cl
HCl
N
Cl
1947
3-Chloro-1-butyne
2-Chloro-4-tert-butylphenol
H
N
Cl
Cl
1948
2-Chloro-N-(2-chloroethyl)ethanamine, hydrochloride
2-Chloro-N-(2-chloroethyl)-N-ethylethanamine
Organic
Si
Cl
Cl
Cl
N
Cl
Cl
Cl
Cl
1949
1950
2-Chloro-N-(2-chloroethyl)-N-methylethanamine
Cl
1951
1-Chloro-2-(chloromethyl)benzene
1952
1-Chloro-3-(chloromethyl)benzene
1-Chloro-4-(chloromethyl)benzene
Cl
O
Cl
Cl
Si
Cl
Cl
1953
S
Cl
Chloro(chloromethyl)dimethylsilane
Cl
Cl
1955
1954
1956
1-Chloro-4-[(chloromethyl)thio]benzene
3-Chloro-2-(chloromethyl)-1-propene
2-Chloro-1-(4-chlorophenyl)ethanone
O
O
O
OH
OH
Cl
Cl
1957
1959
trans-o-Chlorocinnamic acid
Cl
O
Cl
Cl
1958
3-Chlorocholest-5-ene, (3β)
1960
trans-m-Chlorocinnamic acid
Cl
Cl
Cl
OH
1961
trans-p-Chlorocinnamic acid
O
Chlorocyclohexane
HO
Cl
Cl
1962
1963
2-Chlorocyclohexanone
1964
1-Chlorocyclohexene
1965
Chlorocyclopentane
Cl
1966
2-Chlorocyclopentanone
1967
3-Chlorocyclopentene
4-Chloro-2-cyclopentylphenol
H
N
N
Cl
N
Cl
O
Cl
1968
1-Chlorodecane
Cl
OH
1969
Cl
Si
Cl
1973
Chloro(dichloromethyl)dimethylsilane
Cl
Br
1971
Chlorodiazepoxide
2-Chloro-N,N-diallylacetamide
1972
Chlorodibromomethane
Cl
OH O
Cl
H
1970
10-Chloro-1-decanol
Br
O
N
N
H
Cl
Cl
Cl
O
1974
5-Chloro-N-(3,4-dichlorophenyl)-2-hydroxybenzamide
O
1975
2-Chloro-1,1-diethoxyethane
Cl
O
O
1976
3-Chloro-1,1-diethoxypropane
Physical Constants of Organic Compounds
3-104
No.
Name
1977
2-Chloro-N,N-diethylacetamide
2-Chloro-N,N-diethylethanamine, hydrochloride
Chlorodifluoroacetic acid
1-Chloro-1,1-difluoroethane
1-Chloro-2,2-difluoroethane
1-Chloro-2,2-difluoroethene
Chlorodifluoromethane
1978
1979
1980
1981
1982
1983
1984
CAS RN
Mol.
Wt.
C6H12ClNO
2315-36-8
149.618
C6H15Cl2N
869-24-9
172.096
1-Chloro-2,2-difluoroethylene
Refrigerant 22
C2HClF2O2
C2H3ClF2
C2H3ClF2
C2HClF2
CHClF2
76-04-0
75-68-3
338-65-8
359-10-4
75-45-6
130.478
100.495
100.495
98.479
86.469
Chlorindanol
C9H9ClO
145-94-8
168.619 nd (peth)
92
Phenarsazine chloride
C12H9AsClN
578-94-9
277.581 ye cry
195
C8H10ClNO2
C4H9ClO2
97-50-7
97-97-2
187.624
124.566
91
C12H14ClNO4
4433-79-8
271.697
107
C2H6AlCl
C17H20Cl2N2S
1184-58-3
69-09-0
92.504 hyg liq
355.325
-45
198(2)
C8H10ClN
C8H10ClN
698-01-1
6848-13-1
155.625
155.625
Refrigerant 142b
Physical
Form
mp/˚C
bp/˚C
hyg
col gas
col gas
col gas
25
122
-130.43(0.02) -9.12(0.07)
35(7)
-138.5
-18.8(0.5)
-157.41(0.03) -40.8(0.5)
4-Chloro-N,N-dimethylaniline
2-Chloro-1,4-dimethylbenzene
C8H10ClN
C8H9Cl
698-69-1
95-72-7
155.625 nd (al)
140.610
35.5
0.8
231
185(8)
1995
4-Chloro-1,2-dimethylbenzene
C8H9Cl
615-60-1
140.610 liq
-6
190(13)
1996
C4H11Cl2N
4584-46-7
144.043
201.0
C10H13Cl
515-40-2
168.663
1998
2-Chloro-N,N-dimethylethanamine, hydrochloride
(2-Chloro-1,1-dimethylethyl)­ Neophyl chloride
benzene
4-Chloro-2,5-dimethylphenol
C8H9ClO
1124-06-7
74.5
1999
4-Chloro-2,6-dimethylphenol
C8H9ClO
1123-63-3
156.609 silv-grn nd
(lig)
156.609 nd (w)
2000
4-Chloro-3,5-dimethylphenol
C8H9ClO
88-04-0
156.609
115
2001
2002
Chlorodimethylphenylsilane
1-Chloro-N,N-dimethyl-2propanamine, hydrochloride
1-Chloro-2,2-dimethylpropane
C8H11ClSi
C5H13Cl2N
768-33-2
170.712
17256-39-2 158.069
C5H11Cl
753-89-9
1989
1990
1997
Dimethylaluminum chloride
Aminazin hydrochloride
Chloroxylenol
Solubility
sl H2O
1993
1994
1988
nD
200
1991
1992
1986
1987
den
g cm –3
19225
7-Chloro-2,3-dihydro-1Hinden-4-ol
10-Chloro-5,10-dihydrophenarsazine
5-Chloro-2,4-dimethoxyaniline
2-Chloro-1,1-dimethoxyethane
N-(4-Chloro-2,5dimethoxyphenyl)-3-oxobutanamide
Chlorodimethylaluminum
2-Chloro-10-(3-dimethylaminopropyl)phenothiazine
monohydrochloride
2-Chloro-N,N-dimethylaniline
3-Chloro-N,N-dimethylaniline
1985
Organic
Mol. Form.
Synonym
1.355920 s chl
i H2O; s bz
1.4909-69
sl H2O; s eth,
ace, chl
1.65
i H2O; sl ctc, bz,
xyl
127.5
1.06820
126
0.996
205
232
1.106720 1.557820 vs bz, EtOH
sl H2O; s EtOH,
ace, bz
1.0480100
s EtOH
1.058915
i H2O; s ace,
ctc; vs bz
1.068215
i H2O; s ace,
ctc; vs bz
sl H2O
227(12)
1.04720
83
246
194(3)
1.03220
-20(4)
84(1)
1.415020 sl EtOH, eth, bz,
ctc
s chl
reac H2O; s hx
s H2O; i eth, bz;
vs chl, EtOH
1.524720 vs ace, bz, eth,
EtOH
sl H2O; vs bz,
EtOH, peth
sl H2O; vs bz,
EtOH, HOAc
sl H2O, bz, peth;
s EtOH, eth
1.508220
s chl
C5H9ClO2
13511-38-1 136.577
41(4)
11010
2005
2006
3-Chloro-2,2-dimethylpropanoic acid
Chlorodimethylsilane
2-Chloro-4,6-dinitroaniline
0.866020 1.404420 vs bz, eth,
EtOH, chl
vs ctc
C2H7ClSi
C6H4ClN3O4
1066-35-9
3531-19-9
-111
157
34.7
0.852
2007
4-Chloro-2,6-dinitroaniline
C6H4ClN3O4
5388-62-5
2008
1-Chloro-2,4-dinitrobenzene
C6H3ClN2O4
97-00-7
2009
2-Chloro-1,3-dinitrobenzene
C6H3ClN2O4
606-21-3
2010
1-Chloro-2,4-dinitronaphthalene
4-Chloro-2,6-dinitrophenol
C10H5ClN2O4
2401-85-6
94.616 liq
217.567 ye cry (DMF
aq)
217.567 oran-ye nd
(al)
202.552 ye orth (eth)
nd (al) ye
cry
202.552 ye nd (al,
HOAc)
252.611 ye nd (bz)
C6H3ClN2O5
88-87-9
218.551 pa ye cry
81
C5H2ClN3O4
C7H2ClF3N2O4
2578-45-2
393-75-9
203.541
270.550
66.5
57
C3H3ClO3
C14H11ClO
3967-54-2
447-31-4
122.507 liq
230.689 nd (al)
110
68.5
213
dec
1.504
C13H11Cl
C12H25Cl
90-99-3
112-52-7
202.679
204.780 liq
17.0(0.4)
-9.3
1403
263(4)
1.14025 1.595120
0.867320 1.443420
2003
2004
2011
2012
2013
2014
2015
2016
2017
2-Chloro-3,5-dinitropyridine
2-Chloro-1,3-dinitro-5(trifluoromethyl)benzene
4-Chloro-1,3-dioxolan-2-one
2-Chloro-1,2-diphenylethanone
Chlorodiphenylmethane
1-Chlorododecane
HCP_Section_03.indb 104
Chloroethylene carbonate
Lauryl chloride
106.594 liq
1.10725
1.383020
147
s EtOH
50.2(0.9)
315
1.498275 1.585760 i H2O; sl EtOH; s
eth, bz, CS2
88
315
1.686716
i H2O; s EtOH,
eth, tol; sl chl
1.7422
vs eth, EtOH,
chl
146.5
1.454020
s EtOH; sl chl; i
alk
s chl
i H2O; vs EtOH;
msc ace, ctc;
s bz
4/11/16 11:21 AM
Physical Constants of Organic Compounds
O
Cl
Cl
N
N
1977
3-105
F
F
1978
2-Chloro-N,N-diethylacetamide
OH
O
1980
Chlorodifluoroacetic acid
Cl
F
Cl
F
F F
1979
2-Chloro-N,N-diethylethanamine, hydrochloride
F
Cl
Cl
HCl
1981
1-Chloro-1,1-difluoroethane
Cl
F
1982
1-Chloro-2,2-difluoroethane
1-Chloro-2,2-difluoroethene
NH2
H
N
O
Cl
H
Cl
As
Cl
OH
F
1983
1984
Chlorodifluoromethane
Cl
O
1985
1986
10-Chloro-5,10-dihydrophenarsazine
7-Chloro-2,3-dihydro-1H-inden-4-ol
Cl
O
O
1987
5-Chloro-2,4-dimethoxyaniline
2-Chloro-1,1-dimethoxyethane
N
H
N
O
O
N
O
Cl
Al
O
1988
N
HCl
Cl
S
1989
N-(4-Chloro-2,5-dimethoxyphenyl)-3-oxobutanamide
Cl
Organic
F
1990
Chlorodimethylaluminum
1991
2-Chloro-10-(3-dimethylaminopropyl)phenothiazine monohydrochloride
2-Chloro-N,N-dimethylaniline
N
N
Cl
Cl
Cl
1992
Cl
1993
3-Chloro-N,N-dimethylaniline
1994
4-Chloro-N,N-dimethylaniline
2-Chloro-1,4-dimethylbenzene
OH
N
Cl
1995
HCl
1996
4-Chloro-1,2-dimethylbenzene
2-Chloro-N,N-dimethylethanamine, hydrochloride
OH
OH
Si
Cl
Cl
1997
1998
(2-Chloro-1,1-dimethylethyl)benzene
1999
4-Chloro-2,5-dimethylphenol
2000
4-Chloro-2,6-dimethylphenol
2001
4-Chloro-3,5-dimethylphenol
Chlorodimethylphenylsilane
O
Cl
HCl
2002
2003
1-Chloro-N,N-dimethyl-2-propanamine, hydrochloride
O
O
N
NH2 O
N
O
Cl
O
N
N
O
3-Chloro-2,2-dimethylpropanoic acid
O
O
N
Cl
Cl
N
O
O
2009
1-Chloro-2,4-dinitrobenzene
O
O
2005
O
OH O
N
O
O
2-Chloro-1,3-dinitrobenzene
N
O
2010
1-Chloro-2,4-dinitronaphthalene
Cl
2011
O
2-Chloro-4,6-dinitroaniline
O
O
N
2006
Chlorodimethylsilane
O
N
Cl
4-Chloro-2,6-dinitrophenol
O
N
O
N
N
O
Cl
2012
2-Chloro-3,5-dinitropyridine
O
Cl
F
F
N
O
2008
2007
O
O
N
H
Si Cl
OH
2004
1-Chloro-2,2-dimethylpropane
Cl
4-Chloro-2,6-dinitroaniline
Cl
Cl
NH2
O
N
O
N
Cl
Cl
Cl
N
O
F
2013
2-Chloro-1,3-dinitro-5-(trifluoromethyl)benzene
Cl
O
Cl
O
O
O
2014
Cl
O
4-Chloro-1,3-dioxolan-2-one
Cl
2015
2-Chloro-1,2-diphenylethanone
2016
Chlorodiphenylmethane
2017
1-Chlorododecane
Physical Constants of Organic Compounds
3-106
No.
Name
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
Physical
Form
2018
Chloroethane
Ethyl chloride
C2H5Cl
75-00-3
64.514
vol liq or
gas
2019
2-Chloroethanesulfonyl
chloride
2-Chloroethanol
C2H4Cl2O2S
1622-32-8
163.023
C2H5ClO
107-07-3
80.513
C9H11ClO3S
80-41-1
234.699
C2H3Cl
75-01-4
62.498
2020
2021
Ethylene chlorohydrin
liq
mp/˚C
bp/˚C
den
g cm –3
-138(2)
12.3(0.2)
0.92390
201.5
1.55520
126(2)
1.201920 1.441920 msc H2O, EtOH;
sl eth; s chl
i H2O; s ctc
-68(2)
21021
Organic
2022
2-Chloroethanol,
4-methylbenzenesulfonate
Chloroethene
2023
1-Chloro-4-ethoxybenzene
C8H9ClO
622-61-7
156.609
17.1(0.2)
212(1)
2024
(2-Chloroethoxy)benzene
C8H9ClO
622-86-6
156.609
28
218.5
2025
2026
1-Chloro-1-ethoxyethane
2-(2-Chloroethoxy)ethanol
C4H9ClO
C4H9ClO2
7081-78-9
628-89-7
108.566
124.566
93.5
194(3)
2027
2-Chloroethyl acetate
C4H7ClO2
542-58-5
122.551
129(11)
2028
2029
C6H9ClO3
C2H7Cl2N
54527-68-3 164.586
870-24-6
115.990
2030
2031
2-Chloroethyl acetoacetate
2-Chloroethylamine
hydrochloride
(1-Chloroethyl)benzene
(2-Chloroethyl)benzene
C8H9Cl
C8H9Cl
672-65-1
622-24-2
140.610
140.610
2032
1-Chloro-2-ethylbenzene
C8H9Cl
89-96-3
140.610 liq
2033
1-Chloro-3-ethylbenzene
C8H9Cl
620-16-6
2034
1-Chloro-4-ethylbenzene
C8H9Cl
2035
2-Chloroethyl chloroformate
2036
1-(2-Chloroethyl)-3-cycloLomustine
hexyl-1-nitrosourea
N-(2-Chloroethyl)­
Dibenamine
dibenzylamine
Dibenamine hydrochloride
N-(2-Chloroethyl)­
dibenzylamine hydrochloride
Chloroethyldimethylsilane
2-Chloroethyl ethyl ether
2037
2038
2039
2040
2041
2042
Vinyl chloride
β-Chloroethyl acetate
2-Chloroethanamine
hydrochloride
col gas
-153.84(0.02) -13.8(0.3)
198
146.3
1.06925
-83.3(0.2)
177(3)
1.056920
140.610 liq
-55.0(0.2)
180(3)
1.052920
622-98-0
140.610 liq
-62.5(0.1)
184.4(0.9)
1.045520
C3H4Cl2O2
627-11-2
142.969
155
1.384720
C9H16ClN3O2
13010-47-4 233.695 ye pow
C16H18ClN
51-50-3
259.774 oily liq
C16H19Cl2N
55-43-6
296.235 cry
C4H11ClSi
C4H9ClO
6917-76-6
628-34-2
122.669
108.566
C3H4ClNO
C10H18ClN3O2
1943-83-5 105.523
13909-09-6 247.722 cry
C6H8ClNS
533-45-9
161.653 oil
90
194
i H2O; s EtOH,
dil acid
89.5
98(4)
149.618
186.079
185
2046
2047
C4H9ClS
C4H7ClO
693-07-2
110-75-8
124.632
106.551 liq
-70
2048
2049
2050
2051
3-Chloro-4-fluoroaniline
1-Chloro-2-fluorobenzene
1-Chloro-3-fluorobenzene
1-Chloro-4-fluorobenzene
C6H5ClFN
C6H4ClF
C6H4ClF
C6H4ClF
367-21-5
348-51-6
625-98-9
352-33-0
145.562
130.547 liq
130.547
130.547 liq
2052
1-Chloro-1-fluoroethane
C2H4ClF
1615-75-4
82.504
2053
2054
2055
1-Chloro-2-fluoroethane
Chlorofluoromethane
1-Chloro-3-fluoro-2-methylbenzene
2-Chloro-1-fluoro-4-nitroben- 3-Chloro-4-fluoronitrobenzene
zene
C2H4ClF
CH2ClF
C7H6ClF
762-50-5
593-70-4
443-83-4
82.504
68.478 col gas
144.574
-135.1
53.1(0.2)
-9.1
154
C6H3ClFNO2
350-30-1
175.545
41.5
229.5
HCP_Section_03.indb 106
0.867520 1.410520
0.989520 1.411320 sl H2O; msc eth;
s chl
4417
3240-94-6
3647-69-6
2056
1.527620 i H2O; s EtOH,
eth, ace, bz,
CS2
1.521820 i H2O; s ace, bz,
ctc, chl
1.519520 vs ace, bz, eth,
EtOH
1.517520 i H2O; msc
EtOH, eth, ace,
peth; s HOAc
1.448320 i H2O; s EtOH,
eth, ace, bz; sl
ctc
i H2O; s EtOH
1693
C6H12ClNO
C6H13Cl2NO
2044
2045
Solubility
1.367620 sl H2O, chl; vs
EtOH; msc eth
1.492020
0.910620 1.370020 sl H2O; s EtOH;
vs eth
1.125420 1.525220 s EtOH, eth,
HOAc; vs bz;
sl ctc
i H2O; vs EtOH,
eth, ace, bz; sl
ctc
0.965520 1.405320
1.1825
1.452920 vs H2O; msc
EtOH, eth
1.17820 1.423420 i H2O; msc
EtOH, eth; s
ctc
1.205521 1.443020 vs bz, eth, EtOH
vs H2O, ace,
EtOH
10550
198(15)
2-Chloroethyl isocyanate
1-(2-Chloroethyl)-3-(4Semustine
methylcyclohexyl)-1-nitrosourea
5-(2-Chloroethyl)-4-methylthi- Clomethiazole
azole
N-(2-Chloroethyl)morpholine
4-(2-Chloroethyl)morpholine,
hydrochloride
1-Chloro-2-(ethylthio)ethane
2-Chloroethyl vinyl ether
2043
nD
64 dec
927
1.23325
421
45.0
-43
-26.8
vol liq or
gas
157
108
227.0
137.6
128(25)
130
1.066325
1.049520 1.437820 vs EtOH, eth; sl
chl
1.223330 1.491830 i H2O; s ace, bz
1.22125 1.4911
1.499015 1.499015 i H2O; s EtOH,
eth, bz
16(5)
1.174720 1.377520 vs eth, EtOH
sl H2O; vs chl
1.19125 1.502620
4/11/16 11:21 AM
Physical Constants of Organic Compounds
3-107
Cl
Cl
2018
S
O
Cl
Cl
2019
Chloroethane
O
OH
2021
2-Chloroethanol
2024
2025
(2-Chloroethoxy)benzene
O
Cl
2026
1-Chloro-1-ethoxyethane
2-(2-Chloroethoxy)ethanol
2028
2-Chloroethyl acetate
1-Chloro-4-ethoxybenzene
Cl
Cl
O
2027
2023
O
Cl
O
OH
Chloroethene
O
O
O
2022
2-Chloroethanol, 4-methylbenzenesulfonate
Cl
Cl
O
Cl
2020
2-Chloroethanesulfonyl chloride
Cl
NH2 HCl
2029
2-Chloroethyl acetoacetate
2-Chloroethylamine hydrochloride
Organic
O
Cl
O
O S O
Cl
Cl
Cl
Cl
Cl
O
Cl
2030
2031
(1-Chloroethyl)benzene
(2-Chloroethyl)benzene
N
N
H
N
2032
2033
1-Chloro-2-ethylbenzene
O
2034
1-Chloro-3-ethylbenzene
1-Chloro-4-ethylbenzene
Cl
Cl
2037
2036
HCl
2038
N-(2-Chloroethyl)dibenzylamine
1-(2-Chloroethyl)-3-cyclohexyl-1-nitrosourea
2-Chloroethyl chloroformate
N
N
Cl
O
Cl
O
2035
N-(2-Chloroethyl)dibenzylamine hydrochloride
Cl
Si
O
2039
2040
Chloroethyldimethylsilane
Cl
2-Chloroethyl ethyl ether
Cl
O
C
N
N
H
N
N
O
Cl
O
Cl
2041
2042
2-Chloroethyl isocyanate
S
O
2043
1-(2-Chloroethyl)-3-(4-methylcyclohexyl)-1-nitrosourea
2044
5-(2-Chloroethyl)-4-methylthiazole
Cl
N
N
N
Cl
N-(2-Chloroethyl)morpholine
NH2
Cl
Cl
HCl
S
O
2045
Cl
Cl
2046
4-(2-Chloroethyl)morpholine, hydrochloride
Cl
O
F
2047
1-Chloro-2-(ethylthio)ethane
F
F
2048
2-Chloroethyl vinyl ether
2049
3-Chloro-4-fluoroaniline
1-Chloro-2-fluorobenzene
2050
1-Chloro-3-fluorobenzene
F
Cl
Cl
Cl
H
Cl
F
2051
1-Chloro-4-fluorobenzene
F
2052
1-Chloro-1-fluoroethane
Cl
F
2053
1-Chloro-2-fluoroethane
Cl
F
H
2054
Chlorofluoromethane
F
2055
1-Chloro-3-fluoro-2-methylbenzene
O
N
O
2056
2-Chloro-1-fluoro-4-nitrobenzene
Physical Constants of Organic Compounds
3-108
Mol. Form.
CAS RN
Mol.
Wt.
C10H10ClFO
3874-54-2
200.636
Refrigerant C317
C4HClO3
C4ClF7
96-02-6
377-41-3
132.502
216.485 liq or gas
Heptyl chloride
C7H15Cl
629-06-1
134.647 liq
2-Chloroheptane
C7H15Cl
1001-89-4
134.647
2062
2063
2064
3-Chloroheptane
4-Chloroheptane
7-Chloro-1-heptanol
Heptamethylene chlorohydrin
C7H15Cl
C7H15Cl
C7H15ClO
2065
2066
1-Chlorohexadecane
1-Chlorohexane
Hexyl chloride
C16H33Cl
C6H13Cl
999-52-0
134.647
998-95-8
134.647
55944-70-2 150.646 cry (peth,
bz)
4860-03-1 260.886
544-10-5
120.620 liq
2067
2-Chlorohexane
2-Hexyl chloride
C6H13Cl
638-28-8
120.620
124(5)
2068
3-Chlorohexane
3-Hexyl chloride
C6H13Cl
2346-81-8
120.620
121(5)
2069
6-Chloro-1-hexanol
C6H13ClO
2009-83-8
136.619
10712
2070
4-Chloro-17-hydroxyandrost4-en-3-one, (17β)
5-Chloro-2-hydroxybenzaldehyde
4-Chloro-αhydroxybenzeneacetic acid
3-Chloro-4-hydroxybenzoic
acid
C19H27ClO2
1093-58-9
322.869
189
C7H5ClO2
635-93-8
156.567 pl (al)
100.3
C8H7ClO3
492-86-4
186.593
120.3
C7H5ClO3
3964-58-7
172.566 nd (w)
171
No.
Name
2057
2060
4-Chloro-1-(4-fluorophenyl)1-butanone
3-Chloro-2,5-furandione
1-Chloro-1,2,2,3,3,4,4heptafluorocyclobutane
1-Chloroheptane
2061
2058
2059
Organic
2071
2072
2073
Synonym
Clostebol
Physical
Form
bp/˚C
den
g cm –3
nD
1366
1.2225
1.525520
33
-39.1
196
25
1.537525 1.498020
1.60215
-69.4(0.4)
159(2)
0.876220 1.426420 i H2O; msc
EtOH, eth; sl
ctc; s chl
0.867220 1.422120 i H2O; vs eth; s
bz, chl, HOAc
0.869020 1.422820 vs bz, eth
0.871020 1.423720 vs bz, eth
0.999815 1.453725 vs EtOH, peth
mp/˚C
6132
11
156(9)
156(9)
15020
17.9
-94(1)
326(4)
135.0(0.5)
Solubility
0.863520 1.450320 i H2O
0.873825 1.420020 i H2O; s EtOH,
eth, ace, bz;
vs chl; sl ctc
0.869421 1.414222 vs ace, bz, eth,
EtOH
0.868420 1.416320 vs ace, bz, eth,
EtOH
1.024120 1.455020 sl H2O; vs EtOH,
eth
10512
i H2O; vs EtOH;
s eth, alk
vs bz, EtOH
sub
sl H2O, bz, chl;
vs EtOH, eth,
ace
s H2O, eth; vs
EtOH, bz; sl
ace
i H2O
2074
5-Chloro-2-hydroxybenzoic
acid
C7H5ClO3
321-14-2
172.566 nd (w, al)
174.8
2075
C13H9ClO2
85-19-8
232.662
95.3
C8H7ClO3
19463-48-0 186.593 tetr
169.4(0.6)
2077
2-Chloro-5-hydroxybenzophenone
3-Chloro-4-hydroxy-5methoxybenzaldehyde
1-Chloro-2-iodobenzene
C6H4ClI
615-41-8
238.453
0.7
234.5
1.951525 1.633125
2078
2079
1-Chloro-3-iodobenzene
1-Chloro-4-iodobenzene
C6H4ClI
C6H4ClI
625-99-0
637-87-6
238.453
238.453 lf (ace, al)
53.57(0.05)
230
226(19)
1.925520
1.88627
2080
2081
1-Chloro-4-iodobutane
Chloroiodomethane
C4H8ClI
CH2ClI
10297-05-9 218.464 liq
593-71-5
176.384
116
114(14)
1.785
2.42220
2082
1-Chloro-3-iodopropane
C3H6ClI
6940-76-7
204.437
163(6)
1.90420
2083
2084
C9H5ClINO
C7H4ClNO
130-26-7
3320-83-0
305.499 ye br nd (al) 178.5
153.566
30.5
200.9(0.2)
C7H4ClNO
2909-38-8
153.566
11343
2086
5-Chloro-7-iodo-8-quinolinol
1-Chloro-2-isocyanatobenzene
1-Chloro-3-isocyanatobenzene
1-Chloro-2-isopropylbenzene
C9H11Cl
2077-13-6
154.636 liq
-74.4
191(7)
2087
1-Chloro-4-isopropylbenzene
C9H11Cl
2621-46-7
154.636 liq
-12.3
193(6)
2088
C7H4ClNS
2131-55-7
169.632 nd (al)
46
249.5
2089
1-Chloro-4-isothiocyanatobenzene
Chloromethane
Methyl chloride
CH3Cl
74-87-3
50.488
-97.6(0.2)
-24.1(0.3)
2090
4-Chloro-2-methoxyaniline
4-Chloro-2-anisidine
C7H8ClNO
93-50-5
260
2091
2092
2093
2094
5-Chloro-2-methoxyaniline
(Chloromethoxy)ethane
1-Chloro-2-methoxyethane
[(Chloromethoxy)­methyl]­
benzene
1-(Chloromethoxy)propane
C7H8ClNO
C3H7ClO
C3H7ClO
C8H9ClO
95-03-4
3188-13-4
627-42-9
3587-60-8
157.598 nd or pr (dil 52
al)
157.598 nd (dil al)
84
94.540
94.540
156.609
83
79(13)
10313
1.018815
1.034520
1.135020
C4H9ClO
3587-57-3
108.566
109
0.988420 1.412520 vs eth, EtOH
2076
2085
2095
HCP_Section_03.indb 108
Iodochlorhydroxyquin
Chloromethyl ethyl ether
col gas
i H2O; s EtOH,
HOAc
i H2O; s ace; sl
ctc
i H2O; s ace
i H2O; s EtOH,
PhNO2; sl chl
1.540020
1.582220 vs ace, bz, eth,
EtOH
1.547220 i H2O; s eth, bz,
chl; sl ctc
sl EtOH; s HOAc
sl ctc
sl chl
1.034120 1.516820 vs ace, bz, eth,
EtOH
1.020820 1.511720 i H2O; msc
EtOH, eth, ace,
ctc; vs bz
i H2O; s EtOH
0.91125
(p>1
atm)
1.338920 sl H2O; s EtOH;
msc eth, ace,
bz, chl
s EtOH, eth, bz,
chl
s EtOH; sl lig
1.404020
1.411120 vs H2O, eth
1.519220
4/11/16 11:21 AM
Physical Constants of Organic Compounds
O
3-109
F F
Cl
Cl
O
F
2057
Cl
F
O
O
Cl
Cl
F F
2058
4-Chloro-1-(4-fluorophenyl)-1-butanone
F
F
2059
3-Chloro-2,5-furandione
Cl
2060
1-Chloro-1,2,2,3,3,4,4-heptafluorocyclobutane
2061
1-Chloroheptane
2-Chloroheptane
Cl
Cl
Cl
Cl
OH
2063
Cl
2064
7-Chloro-1-heptanol
1-Chlorohexadecane
Cl
Cl
2066
2067
1-Chlorohexane
3-Chloroheptane
2068
2-Chlorohexane
OH
2069
3-Chlorohexane
6-Chloro-1-hexanol
Organic
4-Chloroheptane
2065
2062
OH
O
H
O
O
2071
4-Chloro-17-hydroxyandrost-4-en-3-one, (17β)
4-Chloro-α-hydroxybenzeneacetic acid
2075
H
I
Cl
I
2076
2-Chloro-5-hydroxybenzophenone
Cl
N
I
1-Chloro-3-iodopropane
2077
3-Chloro-4-hydroxy-5-methoxybenzaldehyde
O
C
N
C
5-Chloro-7-iodo-8-quinolinol
2080
1-Chloro-4-iodobenzene
1-Chloro-4-iodobutane
Cl
O
I
Cl
H
2081
Chloroiodomethane
C
N
S
Cl
Cl
N
2083
2079
1-Chloro-3-iodobenzene
Cl
I
I
2078
1-Chloro-2-iodobenzene
OH
Cl
5-Chloro-2-hydroxybenzoic acid
Cl
OH
Cl
2074
3-Chloro-4-hydroxybenzoic acid
Cl
Cl
2082
2073
O
O
Cl
OH
2072
5-Chloro-2-hydroxybenzaldehyde
OH O
I
OH
Cl
O
Cl
Cl
2070
OH
OH
OH
O
Cl
OH
OH
Cl
2084
1-Chloro-2-isocyanatobenzene
2085
1-Chloro-3-isocyanatobenzene
Cl
2086
1-Chloro-2-isopropylbenzene
2087
1-Chloro-4-isopropylbenzene
2088
1-Chloro-4-isothiocyanatobenzene
NH2
O
NH2
H
H
O
Cl
H
2089
Chloromethane
Cl
2090
4-Chloro-2-methoxyaniline
Cl
Cl
2091
5-Chloro-2-methoxyaniline
O
2092
(Chloromethoxy)ethane
O
O
Cl
O
Cl
2093
1-Chloro-2-methoxyethane
2094
[(Chloromethoxy)methyl]benzene
2095
Cl
1-(Chloromethoxy)propane
Physical Constants of Organic Compounds
3-110
No.
Name
2096
2097
Chloromethyl acetate
5-Chloro-2-(methylamino)­
benzophenone
4-Chloro-N-methylaniline
2-Chloro-4-methylaniline
2-Chloro-6-methylaniline
3-Chloro-2-methylaniline
2098
2099
2100
2101
2102
2103
2104
2105
2106
Organic
2107
3-Chloro-4-methylaniline
4-Chloro-2-methylaniline
5-Chloro-2-methylaniline
1-Chloro-2-methyl-9,10anthracenedione
(Chloromethyl)benzene
Synonym
N-Methyl-2-amino-5-chlorobenzophenone
p-Chloro-o-toluidine
Benzyl chloride
Mol. Form.
CAS RN
Mol.
Wt.
Physical
Form
C3H5ClO2
C14H12ClNO
625-56-9
1022-13-5
108.524
245.704
C7H8ClN
C7H8ClN
C7H8ClN
C7H8ClN
932-96-7
615-65-6
87-63-8
87-60-5
141.599
141.599
141.599
141.599
C7H8ClN
C7H8ClN
C7H8ClN
C15H9ClO2
95-74-9
95-69-2
95-79-4
129-35-1
141.599
141.599 lf (al)
141.599
256.684
26
30.3
26
170.5
233(3)
244
239
C7H7Cl
100-44-7
126.584 liq
-39.4(0.6)
174(7)
C8H10ClN
39191-07-6 155.625
884
C8H9ClO
1674-30-2
156.609
12817
C8H9ClO
3391-10-4
156.609
12115
C8H7ClO2
20850-43-5 170.594
20.5
13414
1.31225
C5H11Cl
107-84-6
106.594 liq
-104.4
99(2)
-72.6(0.5)
85(1)
76
87(6)
233(18)
0.875020 1.408420 sl H2O; msc
EtOH, eth; vs
chl
0.865320 1.405520 sl H2O; s EtOH,
eth, ctc
0.87820
0.927320 1.448520 vs ace, eth,
EtOH, chl
0.906120
0.9825
1.435020
1.058019
vs bz, eth, EtOH
mp/˚C
bp/˚C
den
g cm –3
nD
Solubility
116
1.19420
1.40920
vs eth, EtOH
240
220
215
245
1.16911
1.15120
1.583520 s EtOH, ace, bz
1.574822 sl EtOH, bz
92
7
1
1.100420
1.588020 s H2O, EtOH; i
eth, bz
s EtOH; sl ctc
s EtOH; sl ctc
vs EtOH
i EtOH, eth; sl
py
1.539120 i H2O; msc
EtOH, eth, chl;
sl ctc
1.535025 s chl
2111
3-Chloro-N-methylbenzenemethanamine
α-(Chloromethyl)­
benzenemethanol
4-Chloro-αmethylbenzenemethanol
5-(Chloromethyl)-1,3-benzodioxole
1-Chloro-3-methylbutane
Isopentyl chloride
2112
2-Chloro-2-methylbutane
C5H11Cl
594-36-5
106.594 liq
2113
2114
2-Chloro-3-methylbutane
1-Chloro-3-methyl-2-butene
C5H11Cl
C5H9Cl
631-65-2
503-60-6
106.594
104.578
2115
2116
2117
3-Chloro-3-methyl-1-butyne
(Chloromethyl)cyclopropane
1-(Chloromethyl)-2,4-dimethylbenzene
(Chloromethyl)dimethylphenylsilane
Chloromethyldiphenylsilane
1-Chloro-3-(1-methylethoxy)2-propanol
1-(Chloromethyl)-4-ethylbenzene
(1-Chloro-1-methylethyl)­
benzene
1-(Chloromethyl)-2-fluorobenzene
1-(Chloromethyl)-4-fluorobenzene
2-(Chloromethyl)furan
3-(Chloromethyl)heptane
2-Ethylhexyl chloride
C5H7Cl
C4H7Cl
C9H11Cl
1111-97-3
5911-08-0
824-55-5
102.563 liq
90.552 liq
154.636
C9H13ClSi
1833-51-8
184.738
225
1.024025
C13H13ClSi
C6H13ClO2
144-79-6
4288-84-0
232.781
152.619
296(3)
182
1.127720 1.574220
1.091020 1.437025 s EtOH, eth
C9H11Cl
1467-05-6
154.636
9515
C9H11Cl
934-53-2
154.636
981
1.19225
1.529025
C7H6ClF
345-35-7
144.574
172
1.21625
1.515020
C7H6ClF
352-11-4
144.574
8226
1.214320 1.5130
C5H5ClO
C8H17Cl
617-88-9
123-04-6
116.546
148.674
4926
171(3)
C10H13ClO
89-68-9
184.662
63
258.5
C8H9ClO
824-94-2
156.609 nd
24.5
262.5
1.178320 1.494120 vs bz, eth, EtOH
0.876920 1.431920 i H2O; s EtOH,
eth, ace, bz; sl
ctc
vs H2O; s EtOH,
eth, bz, ctc,
peth, alk
1.26120 1.58020 vs ace, bz, eth
C8H9Cl
552-45-4
140.610
202(13)
1.06325
1.541025 vs eth, EtOH
C8H9Cl
620-19-9
140.610
195.5
1.06420
C8H9Cl
104-82-5
140.610
201
1.051220
C2H5ClO
107-30-2
80.513
59(3)
1.06310
C4H7ClO
598-09-4
106.551
122
1.101120
2134
2-(Chloromethyl)-2-methyloxirane
1-(Chloromethyl)naphthalene
1.534520 i H2O; s EtOH,
eth
1.5380
i H2O; s EtOH;
msc eth
1.39720 s EtOH, eth,
ace, chl
1.431020 vs H2O, eth
C11H9Cl
86-52-2
176.642 pr
32
291(21)
2135
2-(Chloromethyl)naphthalene
C11H9Cl
2506-41-4
176.642 lf (al)
48.5
16920
1.181320 1.638020 i H2O; s EtOH,
ctc, peth
i H2O; s EtOH,
peth
2108
2109
2110
2118
2119
2120
2121
2122
2123
2124
2125
2126
2127
4-Chloro-5-methyl-2-isopropylphenol
2128
1-(Chloromethyl)-4-methoxybenzene
1-(Chloromethyl)-2-methylbenzene
1-(Chloromethyl)-3-methylbenzene
1-(Chloromethyl)-4-methylbenzene
Chloromethyl methyl ether
2129
2130
2131
2132
2133
HCP_Section_03.indb 110
Chlorothymol
92(2)
109
liq
-61
-90.9
-103.5
1.192620 1.552320 s EtOH; vs eth
1.550520 s ctc
1.566020
s ctc, CS2
1.529025 vs bz, EtOH, chl
4/11/16 11:21 AM
Physical Constants of Organic Compounds
NH O
3-111
HN
NH2
NH2
NH2
NH2
Cl
Cl
O
O
Cl
Cl
Cl
2096
2097
Chloromethyl acetate
2098
5-Chloro-2-(methylamino)benzophenone
2099
4-Chloro-N-methylaniline
NH2
O
Cl
2101
2-Chloro-6-methylaniline
3-Chloro-2-methylaniline
Cl
Cl
2106
1-Chloro-2-methyl-9,10-anthracenedione
2107
(Chloromethyl)benzene
3-Chloro-N-methylbenzenemethanamine
2108
α-(Chloromethyl)benzenemethanol
Organic
5-Chloro-2-methylaniline
OH
N
H
O
2105
2104
2102
3-Chloro-4-methylaniline
Cl
Cl
Cl
4-Chloro-2-methylaniline
2100
2-Chloro-4-methylaniline
NH2
2103
Cl
Cl
OH
O
Cl
O
Cl
2109
Cl
Cl
2110
4-Chloro-α-methylbenzenemethanol
2111
5-(Chloromethyl)-1,3-benzodioxole
2112
1-Chloro-3-methylbutane
Cl
2-Chloro-2-methylbutane
2113
2-Chloro-3-methylbutane
Cl
2114
1-Chloro-3-methyl-2-butene
Cl
Si Cl
Cl
Cl
2115
Si
2116
3-Chloro-3-methyl-1-butyne
2117
(Chloromethyl)cyclopropane
Cl
2118
1-(Chloromethyl)-2,4-dimethylbenzene
(Chloromethyl)dimethylphenylsilane
2119
Chloromethyldiphenylsilane
Cl
Cl
Cl
OH
O
Cl
F
Cl
F
2120
2121
1-Chloro-3-(1-methylethoxy)-2-propanol
1-(Chloromethyl)-4-ethylbenzene
2122
(1-Chloro-1-methylethyl)benzene
2123
1-(Chloromethyl)-2-fluorobenzene
Cl
Cl
2125
2-(Chloromethyl)furan
Cl
2127
3-(Chloromethyl)heptane
4-Chloro-5-methyl-2-isopropylphenol
Cl
O
Cl
2126
1-(Chloromethyl)-4-fluorobenzene
Cl
OH
O
2124
2128
1-(Chloromethyl)-4-methoxybenzene
2129
1-(Chloromethyl)-2-methylbenzene
2130
1-(Chloromethyl)-3-methylbenzene
Cl
Cl
O
Cl
2131
1-(Chloromethyl)-4-methylbenzene
Cl
Cl
O
2132
Chloromethyl methyl ether
2133
2-(Chloromethyl)-2-methyloxirane
2134
1-(Chloromethyl)naphthalene
2135
2-(Chloromethyl)naphthalene
Physical Constants of Organic Compounds
3-112
CAS RN
Mol.
Wt.
1-(Chloromethyl)-2-nitrobenzene
C7H6ClNO2
612-23-7
171.582 cry (lig)
1-(Chloromethyl)-3-nitrobenzene
1-(Chloromethyl)-4-nitrobenzene
C7H6ClNO2
619-23-8
17334
C7H6ClNO2
100-14-1
171.582 pa ye nd
46
(lig)
171.582 pl or nd (al) 71
C7H6ClNO2
83-42-1
171.582 nd (dil al)
37.8
238
C7H6ClNO2
13290-74-9 171.582 ye cry
42.5
249
C7H6ClNO2
89-60-1
171.582
7.2(0.2)
261
1.557220 i H2O; s ctc
C7H6ClNO2
121-86-8
171.582 nd (al)
66.5
260
C7H6ClNO2
89-59-8
171.582 mcl nd
36.5(1)
242
1.255980
C6H13Cl
C6H13Cl
C7H7ClO
C7H7ClO
C7H7ClO
C7H7ClO
C7H7ClO
C7H7ClO
25346-32-1
4737-41-1
6640-27-3
615-74-7
87-64-9
615-62-3
1570-64-5
59-50-7
120.620
120.620
142.583
142.583
142.583
142.583
142.583
142.583
116(10)
126(5)
195.5
198(8)
189
228
223
232(9)
0.861020
0.891420
1.178527
1.21515
C9H9ClO3
94-74-6
200.618 pl (bz, to)
119.7(0.9)
1.547069 sl H2O, chl; s
EtOH, eth,
HOAc
i H2O; s EtOH,
eth; sl chl
1.411320 vs eth
1.422220 vs bz, eth, chl
1.520027 vs bz, eth, EtOH
vs H2O, EtOH
1.544920 sl H2O; s eth
vs bz, eth, EtOH
sl H2O; s peth
sl H2O, chl; s
EtOH, eth,
peth
sl H2O; vs EtOH,
eth; s bz, ctc
228.672
100.4(0.5)
113100
1.04320
90
69(1)
1.05315 1.416016 vs eth, EtOH
0.877320 1.398420 sl H2O, ctc; s
eth, ace, chl
0.842020 1.385720 sl H2O; msc
EtOH, eth; s
bz, ctc, chl
0.918620 1.422120 sl H2O; s chl
0.916520 1.429120 msc EtOH, eth;
s ace; vs chl
Name
2136
2137
2138
2139
2140
2141
2142
Organic
Mol. Form.
No.
2143
2144
2145
2146
2147
2148
2149
2150
2151
1-Chloro-2-methyl-3-nitrobenzene
1-Chloro-2-methyl-4-nitrobenzene
1-Chloro-4-methyl-2-nitrobenzene
2-Chloro-1-methyl-4-nitrobenzene
4-Chloro-1-methyl-2-nitrobenzene
2-Chloro-4-methylpentane
3-(Chloromethyl)pentane
2-Chloro-4-methylphenol
2-Chloro-5-methylphenol
2-Chloro-6-methylphenol
3-Chloro-4-methylphenol
4-Chloro-2-methylphenol
4-Chloro-3-methylphenol
Synonym
4-Nitrobenzyl chloride
4-Chloro-3-nitrotoluene
2-Chloro-p-cresol
6-Chloro-m-cresol
6-Chloro-o-cresol
3-Chloro-p-cresol
4-Chloro-o-cresol
4-Chloro-m-cresol
Physical
Form
mp/˚C
bp/˚C
47.7(0.2)
1254
pr (peth)
46(3)
nd (al)
nd (peth)
nd (peth)
55.5
51
55(2)
den
g cm –3
vs eth
C11H13ClO3
94-81-5
2154
2155
C7H9ClSi
CH4ClO3P
1631-82-9
2565-58-4
2156
2157
2158
N-Chloromethylphthalimide
2-Chloro-2-methylpropanal
1-Chloro-2-methylpropane
Isobutyl chloride
C9H6ClNO2
C4H7ClO
C4H9Cl
156.685
130.468 nd (bz/
MeNO2)
17564-64-6 195.603
917-93-1
106.551
513-36-0
92.567 liq
2159
2-Chloro-2-methylpropane
tert-Butyl chloride
C4H9Cl
507-20-0
92.567
2160
2161
1-Chloro-2-methylpropene
3-Chloro-2-methylpropene
Dimethylvinyl chloride
C4H7Cl
C4H7Cl
513-37-1
563-47-3
90.552
90.552
2162
C6H7Cl2N
6959-48-4
164.033 hyg
143.8
CH5ClSi
C7H7ClO2S
993-00-0
98-57-7
80.590 col gas
190.648
-135
98
C7H7ClS
123-09-1
158.649
10510
2166
2167
2168
2169
3-(Chloromethyl)pyridine,
hydrochloride
Chloromethylsilane
1-Chloro-4-(methylsulfonyl)­ 4-Chlorobenzenethiol,
benzene
S-methyl, S,S-dioxide
1-Chloro-4-(methylthio)­
benzene
1-Chloro-2-(methylthio)ethane
Chloro(methylthio)methane
(Chloromethyl)trimethylsilane
1-Chloronaphthalene
1-Naphthyl chloride
C3H7ClS
C2H5ClS
C4H11ClSi
C10H7Cl
542-81-4
2373-51-5
2344-80-1
90-13-1
110.606
96.579
122.669
162.616 oily liq
-6.0(0.2)
140
105
98.5
259(2)
1.12320
1.15325
0.87925
1.188025
2170
2-Chloronaphthalene
C10H7Cl
91-58-7
162.616 pl (dil al), lf
58.02(0.05)
257(21)
1.137771
2171
4-Chloro-1-naphthol
C10H7ClO
604-44-4
120.5
2172
Chloroneb
C8H8Cl2O2
2675-77-6
178.615 nd (chl, aq
al)
207.055
131.2(0.3)
2173
2-Chloro-4-nitroaniline
C6H5ClN2O2
121-87-9
172.569 ye nd (w)
108.4(0.5)
2174
2-Chloro-5-nitroaniline
C6H5ClN2O2
6283-25-6
172.569 ye nd (lig)
120.8(0.5)
2175
4-Chloro-2-nitroaniline
C6H5ClN2O2
89-63-4
172.569 dk oran-ye
pr (dil al)
116.5
2153
2163
2164
2165
HCP_Section_03.indb 112
Benzene, 1,4-dichloro-2,5dimethoxy-
liq
Solubility
1.555762 i H2O; s EtOH,
eth, HOAc; vs
ace, bz
1.557762 vs ace, bz, eth,
EtOH
1.564762 i H2O; s EtOH,
eth; vs ace,
bz, AcOEt
1.537769 i H2O; s EtOH
(4-Chloro-2-methylphenoxy)­ MCPA
acetic acid
4-(4-Chloro-2methylphenoxy)­butanoic acid
Chloromethylphenylsilane
(Chloromethyl)phosphonic acid
2152
nD
1.517120
90
133.5(0.5)
-130.3
-25.60(0.02) 50.9(0.5)
68(4)
72(2)
7
1.490220 s EtOH, eth, ace
1.496320
1.417520
1.632620 i H2O; s EtOH,
eth, bz, CS2; sl
ctc
1.607913 i H2O; s EtOH,
eth, bz, chl,
CS2
s EtOH, eth,
ace, bz, chl
268
vs eth, EtOH,
HOAc
vs eth, EtOH,
HOAc
vs EtOH, eth,
HOAc; sl ace,
lig
4/11/16 11:21 AM
Physical Constants of Organic Compounds
3-113
Cl
Cl
Cl
O
N
O
N
O
2136
Cl
O
N
O
O
2137
1-(Chloromethyl)-2-nitrobenzene
O
N
O
N
O
2139
N
O
2140
1-Chloro-2-methyl-3-nitrobenzene
1-Chloro-2-methyl-4-nitrobenzene
OH
Cl
O
Cl
Cl
O
Cl
2143
2142
1-Chloro-4-methyl-2-nitrobenzene
O
N
O
O
1-(Chloromethyl)-4-nitrobenzene
Cl
O
N
2138
1-(Chloromethyl)-3-nitrobenzene
2141
Cl
Cl
2144
4-Chloro-1-methyl-2-nitrobenzene
2-Chloro-4-methylpentane
2146
3-(Chloromethyl)pentane
2-Chloro-4-methylphenol
Organic
2-Chloro-1-methyl-4-nitrobenzene
2145
OH
OH
OH
O
OH
OH
O
Cl
Cl
Cl
2147
2148
2-Chloro-5-methylphenol
Cl
SiH
Cl
Cl
2154
Cl
2158
1-Chloro-2-methylpropane
(4-Chloro-2-methylphenoxy)acetic acid
Cl
O
P OH
OH
N
Cl
O
O
2156
2155
Chloromethylphenylsilane
4-(4-Chloro-2-methylphenoxy)butanoic acid
2152
4-Chloro-3-methylphenol
O
OH
2153
OH
Cl
2151
4-Chloro-2-methylphenol
3-Chloro-4-methylphenol
O
O
2150
2149
2-Chloro-6-methylphenol
Cl
Cl
2157
N-Chloromethylphthalimide
(Chloromethyl)phosphonic acid
2-Chloro-2-methylpropanal
H
Si Cl
H
Cl
Cl
Cl
Cl
2159
2-Chloro-2-methylpropane
Cl
2160
1-Chloro-2-methylpropene
HCl
N
2161
2162
3-Chloro-2-methylpropene
3-(Chloromethyl)pyridine, hydrochloride
2163
Chloromethylsilane
Cl
Cl
O S O
2164
1-Chloro-4-(methylsulfonyl)benzene
S
Cl
S
2165
Si
1-Chloro-4-(methylthio)benzene
2170
2-Chloronaphthalene
2171
4-Chloro-1-naphthol
(Chloromethyl)trimethylsilane
NH2
O
NH2
Cl
Cl
O
Cl
Cl
2168
Chloro(methylthio)methane
Cl
Cl
Cl
2167
1-Chloro-2-(methylthio)ethane
OH
S
Cl
2166
O
2172
Chloroneb
O
N
O
2173
2-Chloro-4-nitroaniline
N
O
2169
1-Chloronaphthalene
NH2 O
N
O
Cl
2174
2-Chloro-5-nitroaniline
2175
4-Chloro-2-nitroaniline
Physical Constants of Organic Compounds
3-114
No.
Name
2176
Mol.
Wt.
Physical
Form
Organic
CAS RN
4-Chloro-3-nitroaniline
C6H5ClN2O2
635-22-3
2177
5-Chloro-2-nitroaniline
C6H5ClN2O2
1635-61-6
2178
C14H6ClNO4
129-40-8
2179
2180
2181
1-Chloro-5-nitro-9,10-anthracenedione
2-Chloro-5-nitrobenzaldehyde
4-Chloro-3-nitrobenzaldehyde
1-Chloro-2-nitrobenzene
o-Chloronitrobenzene
C7H4ClNO3
C7H4ClNO3
C6H4ClNO2
6361-21-3 185.565 cry (al)
16588-34-4 185.565
88-73-3
157.555 mcl nd
81.3
64.5
32.1(0.3)
246.2(0.7)
1.368242
2182
1-Chloro-3-nitrobenzene
m-Chloronitrobenzene
C6H4ClNO2
121-73-3
157.555 pa ye orth
pr (al)
43.6(0.2)
236.5(0.6)
1.34350
2183
1-Chloro-4-nitrobenzene
p-Chloronitrobenzene
C6H4ClNO2
100-00-5
157.555 mcl pr
82.2(0.7)
238(3)
1.297990 1.5376100
2184
C6H6ClN3O2
42389-30-0 187.584
167
C6H5ClN2O4S
97-09-6
175
C6H3Cl2NO4S
97-08-5
236.633 ye cry
(EtOH)
256.064
2187
5-Chloro-3-nitro-1,2-benzenediamine
4-Chloro-3-nitrobenzenesulfonamide
4-Chloro-3-nitrobenzenesulfonyl chloride
2-Chloro-4-nitrobenzoic acid
C7H4ClNO4
99-60-5
201.565 nd (w)
141.8
2188
2-Chloro-5-nitrobenzoic acid
C7H4ClNO4
2516-96-3
201.565 nd or pr (w) 166.5
1.60818
2189
4-Chloro-3-nitrobenzoic acid
C7H4ClNO4
96-99-1
201.565 nd or pl (w) 182.8
1.64518
2190
1-Chloro-1-nitroethane
C2H4ClNO2
598-92-5
109.512
2191
2-Chloro-4-nitrophenol
C6H4ClNO3
619-08-9
2192
4-Chloro-2-nitrophenol
C6H4ClNO3
89-64-5
2193
5-Chloro-2-nitrophenol
C6H4ClNO3
611-07-4
2194
1-Chloro-1-nitropropane
C3H6ClNO2
600-25-9
173.554 wh nd (50% 107.5(0.4)
al)
173.554 ye mcl pr
87.2(0.4)
(al)
173.554 ye pr or nd 39(3)
(w)
123.539
2195
2-Chloro-2-nitropropane
C3H6ClNO2
594-71-8
123.539
2196
2197
C5H3ClN2O2
C7H3ClF3NO2
5470-18-8
121-17-5
C7H3ClF3NO2
2199
2200
2201
2202
2-Chloro-3-nitropyridine
1-Chloro-2-nitro-4(trifluoromethyl)benzene
1-Chloro-4-nitro-2(trifluoromethyl)benzene
1-Chlorononane
9-Chloro-1-nonanol
1-Chlorooctadecane
1-Chlorooctane
2203
2186
172.569 ye nd or pr
(w) nd
(peth)
172.569 ye nd (CS2)
ye lf (al,
bz)
287.656
mp/˚C
bp/˚C
den
g cm –3
Mol. Form.
2185
Synonym
nD
103
125.8(0.5)
s H2O, eth, chl;
vs EtOH; sl lig
sub
vs eth, EtOH
315.3
1.537480
124.5
1.283720 1.422420
sub
1.20720
1.425120
-21.5(0.2)
142(6)
1.220
1.437819
158.543 nd (w)
225.553 liq
104.0
-1.3
222
1.51125
1.489320
777-37-7
225.553
22
232
1.52725
1.508326
C9H19Cl
C9H19ClO
C18H37Cl
C8H17Cl
2473-01-0
51308-99-7
3386-33-2
111-85-3
162.700 liq
178.699
288.940
148.674 liq
-39.4
28
28.6
-57.8
204(3)
14714
337(15)
183(3)
0.867425 1.434320
1.457520
0.861620 1.452420
0.873420 1.430920
2-Chlorooctane
C8H17Cl
628-61-5
148.674
172(7)
0.865817 1.427321
2204
2205
2206
2207
8-Chloro-1-octanol
Chloropentafluoroacetone
Chloropentafluorobenzene
Chloropentafluoroethane
Refrigerant 115
C8H17ClO
C3ClF5O
C6ClF5
C2ClF5
23144-52-7
79-53-8
344-07-0
76-15-3
164.673
182.476 col gas
202.509
154.466 col gas
-99.4(0.1)
13919
7.8(0.9)
117.96
-39.2(0.2)
2208
1-Chloropentane
Pentyl chloride
C5H11Cl
543-59-9
106.594 liq
-99.0
107.9(0.3)
2209
2-Chloropentane, (+)
sec-Amyl chloride
C5H11Cl
29882-57-3 106.594 liq
-137
96.3(0.9)
2210
3-Chloropentane
C5H11Cl
616-20-6
106.594 liq
-105(2)
95(3)
2211
2212
2213
5-Chloropentanoic acid
5-Chloro-1-pentanol
5-Chloro-2-pentanone
C5H9ClO2
C5H11ClO
C5H9ClO
1119-46-6
5259-98-3
5891-21-4
136.577
122.593
120.577
18
234(10)
11212
106110
2214
2215
1-Chloro-3-pentanone
5-Chloropentanoyl chloride
C5H9ClO
C5H8Cl2O
32830-97-0 120.577
1575-61-7 155.022
HCP_Section_03.indb 114
Octyl chloride
i H2O, EtOH, eth,
lig; sl bz; s py
vs EtOH, chl
sl H2O; s chl
i H2O; s EtOH,
eth, bz; vs
ace, tol, py
i H2O; s EtOH,
eth, bz, chl,
CS2
i H2O; sl EtOH; s
eth, chl, CS2
60.8
142
2198
Solubility
-133
6820
8312
1.456325
s H2O, EtOH,
eth, bz
sl H2O, ace; s
EtOH, eth, bz
i H2O; sl EtOH,
ace
i H2O; s EtOH,
ctc, alk
s H2O, EtOH,
eth, chl; sl bz
i H2O; s EtOH,
eth, chl; sl ace
sl H2O; s EtOH,
eth, HOAc
sl H2O, chl; s
EtOH, eth, oils
sl H2O; s EtOH,
eth, ctc, oils; i
KOH
i H2O; s eth, chl
vs eth, EtOH
i H2O; sl ctc
i H2O; vs EtOH,
eth; sl ctc
i H2O; vs EtOH,
eth
vs eth, EtOH
1.56825 1.425620
1.5678-42 1.2678-42 i H2O; s EtOH,
eth
0.882020 1.412620 i H2O; msc
EtOH, eth; s
bz, ctc; vs chl
0.869820 1.406920 i H2O; s EtOH,
eth, bz; vs chl
0.873120 1.408220 i H2O; s EtOH,
eth, bz; sl ace
1.341625 1.455520 vs eth, EtOH
1.451820 vs eth, EtOH
1.052320 1.437520 s eth, ace; sl
ctc
1.436120 vs eth, EtOH
1.21018 1.463920 vs eth
4/11/16 11:21 AM
Physical Constants of Organic Compounds
3-115
O
NH2
Cl
N
O
NH2 O
N
O
2176
O
O
O
2177
N
O
O
N
O
Cl
O
2181
4-Chloro-3-nitrobenzaldehyde
1-Chloro-2-nitrobenzene
Cl
O S O
NH2
O S O
NH2
O
N
O
2180
2-Chloro-5-nitrobenzaldehyde
1-Chloro-5-nitro-9,10-anthracenedione
Cl
Cl
N
O
2179
2178
5-Chloro-2-nitroaniline
Cl
O
O
Cl
Cl
4-Chloro-3-nitroaniline
Cl
NH2
O
N
O
O
2182
N
Cl
2183
O
2184
1-Chloro-4-nitrobenzene
N
O
Cl
O
2185
5-Chloro-3-nitro-1,2-benzenediamine
N
O
Cl
O
2186
4-Chloro-3-nitrobenzenesulfonamide
4-Chloro-3-nitrobenzenesulfonyl chloride
Organic
1-Chloro-3-nitrobenzene
N
O
O
OH
O
O
N
OH
O
2187
N
O
N
O
Cl
2188
2-Chloro-4-nitrobenzoic acid
O
N
O
2189
2-Chloro-5-nitrobenzoic acid
O
Cl
2190
4-Chloro-3-nitrobenzoic acid
O
N
O
Cl N O
O
N
Cl
2194
2195
1-Chloro-1-nitropropane
O
O
Cl
2192
2-Chloro-4-nitrophenol
O
N
OH O
N
O
Cl
2191
1-Chloro-1-nitroethane
2193
4-Chloro-2-nitrophenol
5-Chloro-2-nitrophenol
F
Cl
O
F
F
O
F
Cl
2196
2-Chloro-2-nitropropane
N
O
Cl
O
N
OH O
N
Cl
Cl
O
O
OH
O
OH
Cl
F
F
O
2197
2-Chloro-3-nitropyridine
N
O
2198
1-Chloro-2-nitro-4-(trifluoromethyl)benzene
1-Chloro-4-nitro-2-(trifluoromethyl)benzene
Cl
Cl
Cl
OH
2199
1-Chlorononane
Cl
Cl
2200
2201
9-Chloro-1-nonanol
2203
2202
1-Chlorooctadecane
2-Chlorooctane
1-Chlorooctane
Cl
F
Cl
OH
2204
8-Chloro-1-octanol
O
F
Cl
F
F
F
F
F
F
F
F F
F
2205
2206
Chloropentafluoroacetone
2207
Chloropentafluorobenzene
Chloropentafluoroethane
O
Cl
Cl
5-Chloropentanoic acid
Cl
OH
2212
5-Chloro-1-pentanol
Cl
Cl
2208
2209
1-Chloropentane
2-Chloropentane, (+)
O
2213
5-Chloro-2-pentanone
2210
3-Chloropentane
Cl
O
OH
2211
Cl
Cl
F F
F
2214
1-Chloro-3-pentanone
O
Cl
Cl
2215
5-Chloropentanoyl chloride
Physical Constants of Organic Compounds
3-116
Organic
Mol. Form.
CAS RN
Mol.
Wt.
4-Chloro-2-pentene
2-Chlorophenol
C5H9Cl
C6H5ClO
1458-99-7
95-57-8
2218
3-Chlorophenol
C6H5ClO
2219
4-Chlorophenol
2220
2221
2222
2223
2224
2225
2226
Chlorophenol Red
2-Chloro-10H-phenothiazine
2-Chlorophenoxyacetic acid
3-Chlorophenoxyacetic acid
(4-Chlorophenoxy)acetic acid
1-Chloro-4-phenoxybenzene
3-(4-Chlorophenoxy)-1,2propanediol
2227
2228
2-(3-Chlorophenoxy)propanoic Cloprop
acid
2-Chloro-N-phenylacetamide
2229
No.
Name
2216
2217
Physical
Form
mp/˚C
bp/˚C
104.578
128.556 liq
8(1)
97(5)
173.4(0.6)
108-43-0
128.556
32.5(0.3)
210(3)
C6H5ClO
106-48-9
128.556
43.1(0.7)
219(4)
C19H12Cl2O5S
C12H8ClNS
C8H7ClO3
C8H7ClO3
C8H7ClO3
C12H9ClO
C9H11ClO3
4430-20-0
92-39-7
614-61-9
588-32-9
122-88-3
7005-72-3
104-29-0
423.266
233.717
186.593
186.593
186.593
204.651
202.634
C9H9ClO3
101-10-0
200.618 cry
C8H8ClNO
587-65-5
N-(2-Chlorophenyl)acetamide
C8H8ClNO
533-17-5
169.609 nd (dil
HOAc)
169.609
86.7(0.5)
2230
N-(3-Chlorophenyl)acetamide
C8H8ClNO
588-07-8
169.609 nd
76.6(0.5)
333
2231
N-(4-Chlorophenyl)acetamide
C8H8ClNO
539-03-7
169.609
178.4(0.5)
332(27)
2232
4-Chloro-αphenylbenzenemethanol
4-Chlorophenyl benzenesulfonate
4-Chloro-1-phenyl-1-butanone
4-Chlorophenyl 4-chlorobenzenesulfonate
(2-Chlorophenyl)­(4chlorophenyl)methanone
N’-(4-Chlorophenyl)-N,Ndimethylurea
1-(3-Chlorophenyl)ethanone
1-(4-Chlorophenyl)ethanone
C13H11ClO
119-56-2
218.678
59
C12H9ClO3S
80-38-6
268.715 col cry
59.3(0.5)
C10H11ClO
939-52-6
182.646
19.5
Ovex
C12H8Cl2O3S
80-33-1
303.161
88(1)
2,4’-Dichlorodiphenyl ketone
C13H8Cl2O
85-29-0
251.108 pr (al)
65.7(0.5)
Monuron
C9H11ClN2O
150-68-5
168.3(0.3)
m-Chloroacetophenone
p-Chloroacetophenone
C8H7ClO
C8H7ClO
99-02-5
99-91-2
198.648 wh pl
(MeOH)
154.594
154.594
Pyrimethamine
C12H13ClN4
58-14-0
248.711
233.5
Clorindione
C15H9ClO2
1146-99-2
Clortermine
2233
2234
2235
2236
2237
2238
2239
2240
2241
2242
2243
2244
2245
2246
2247
2248
2249
2250
2251
2252
2253
2254
2255
5-(4-Chlorophenyl)-6-ethyl2,4-pyrimidinediamine
2-(4-Chlorophenyl)-1Hindene-1,3(2H)-dione
4-Chlorophenyl isocyanate
1-(2-Chlorophenyl)-2-methyl2-propylamine
N-(2-Chlorophenyl)-3-oxobutanamide
(4-Chlorophenyl)­
phenylmethanone
3-(2-Chlorophenyl)propanoic
acid
3-(3-Chlorophenyl)propanoic
acid
3-(4-Chlorophenyl)propanoic
acid
3-Chloro-1-phenyl-1-propanone
1-(4-Chlorophenyl)-1-propanone
3-(3-Chlorophenyl)-2-propynoic acid
Chlorophenylsilane
1-Chloro-4-(phenylsulfonyl)­
benzene
5-Chloro-1-phenyltetrazole
(2-Chlorophenyl)thiourea
HCP_Section_03.indb 116
Synonym
4-Chlorophenyl phenyl ether
Chlorphenesin
2-Chloroethyl phenyl ketone
Phenylchlorosilane
Sulphenone
grn-br cry
261
198.5
nd (w, al)
148.5
cry (w)
110
pr or nd (w) 158.3(0.5)
cry
den
g cm –3
nD
s H2O, EtOH
i H2O
vs H2O; sl chl
78
284.5
21419
113
1001.5
1.202615 1.599
i H2O; vs EtOH,
eth; s bz, con
sulf
sub
18.4(0.2)
1314
21422
244
237(1)
145.5
C7H4ClNO
C10H14ClN
C10H10ClNO2
93-70-9
211.645
106.5
C13H9ClO
134-85-0
216.662 nd (al)
77.5
C9H9ClO2
1643-28-3
184.619 nd or lf (w)
102
C9H9ClO2
21640-48-2 184.619 lf (peth)
77
C9H9ClO2
2019-34-3
184.619
126
C9H9ClO
936-59-4
49.5
1134
C9H9ClO
6285-05-8
168.619 lf (eth), cry
(al, peth)
168.619
37.3
13531
C9H5ClO2
7396-28-3
144.5
C6H7ClSi
C12H9ClO2S
4206-75-1
80-00-2
180.588 cry (HOAc,
bz-peth)
142.659
252.716
C7H5ClN4
C7H7ClN2S
14210-25-4 180.595
5344-82-1 186.662 nd or pl
123
143.3(0.5)
i H2O; s EtOH,
bz, chl; vs eth
sl H2O; vs EtOH,
eth, bz, CS2; s
chl
i H2O; s EtOH;
vs eth; sl ctc
sl chl
1.38522
1.13725
sl H2O
1.545920
1.39314
1.213040 1.549420
1.192220 1.555020
i H2O; sl EtOH; s
ace
s EtOH; sl chl
i H2O; sl EtOH,
ace
s EtOH, eth, ace
i H2O; msc
EtOH, eth; s
chl
vs bz, eth, EtOH
11645
11716
s EtOH; i eth, lig
332
162.5
94
vs bz, eth, EtOH
1.33
256.684 dk red nd
(al)
104-12-1
153.566
10389-73-8 183.678 liq
31.3
Solubility
0.898820 1.432220 vs ace, eth, chl
1.263420 1.552420 sl H2O, chl; s
EtOH, eth; vs
bz
1.24545 1.556540 sl H2O, chl; s
EtOH, eth; vs
bz
1.265140 1.557940 sl H2O; vs EtOH,
eth, bz; s alk
sl H2O; s EtOH
s EtOH, eth,
ace; sl ctc
i H2O; s EtOH,
CS2; sl chl
vs HOAc
1.068320 1.534020
i H2O; sl EtOH; s
eth; vs ace, bz
vs bz, EtOH
4/11/16 11:21 AM
Physical Constants of Organic Compounds
3-117
HO
Cl
Cl
OH
OH
OH
2216
2217
2219
2218
2-Chlorophenol
S
O
O
Cl
Cl
Cl
O
S
2220
4-Chlorophenol
3-Chlorophenol
Cl
2222
2-Chloro-10H-phenothiazine
OH
OH
Cl
2221
Chlorophenol Red
O
O
H
N
O
Cl
Cl
4-Chloro-2-pentene
O
OH
2-Chlorophenoxyacetic acid
2223
3-Chlorophenoxyacetic acid
O
O
O
O
OH
O
O
OH
Cl
Cl
Cl
2224
2225
Cl
O
Cl
2228
2229
Cl
2226
1-Chloro-4-phenoxybenzene
H
N
H
N
2227
3-(4-Chlorophenoxy)-1,2-propanediol
2-(3-Chlorophenoxy)propanoic acid
2-Chloro-N-phenylacetamide
O
N-(2-Chlorophenyl)acetamide
Organic
(4-Chlorophenoxy)acetic acid
OH
OH
H
N
OH
H
N
O
O
Cl
Cl
2230
Cl
2231
N-(3-Chlorophenyl)acetamide
2232
N-(4-Chlorophenyl)acetamide
O
O
S O
O
Cl
Cl
2233
4-Chloro-α-phenylbenzenemethanol
2234
4-Chlorophenyl benzenesulfonate
4-Chloro-1-phenyl-1-butanone
O
Cl
O
S O
O
Cl
O
Cl
2236
4-Chlorophenyl 4-chlorobenzenesulfonate
N
O
Cl
Cl
2235
O
H
N
Cl
2237
(2-Chlorophenyl)(4-chlorophenyl)methanone
N’-(4-Chlorophenyl)-N,N-dimethylurea
N
O
1-(3-Chlorophenyl)ethanone
N
NH2
Cl
O
2240
2241
5-(4-Chlorophenyl)-6-ethyl-2,4-pyrimidinediamine
H
N
NH2
Cl
H2N
2239
1-(4-Chlorophenyl)ethanone
O
C
N
Cl
Cl
2238
Cl
2242
2-(4-Chlorophenyl)-1H-indene-1,3(2H )-dione
Cl
2243
4-Chlorophenyl isocyanate
O
O
2244
1-(2-Chlorophenyl)-2-methyl-2-propylamine
N-(2-Chlorophenyl)-3-oxo-butanamide
O
O
O
O
OH
Cl
Cl
Cl
2245
(4-Chlorophenyl)phenylmethanone
2246
3-(2-Chlorophenyl)propanoic acid
Cl
Cl
OH
SiH2
O
2251
3-(3-Chlorophenyl)-2-propynoic acid
2252
Chlorophenylsilane
O
O
OH
OH
Cl
Cl
Cl
2247
2248
3-(3-Chlorophenyl)propanoic acid
3-(4-Chlorophenyl)propanoic acid
2249
3-Chloro-1-phenyl-1-propanone
Cl
O
S
O
2253
N N
N
N
Cl
1-Chloro-4-(phenylsulfonyl)benzene
2250
1-(4-Chlorophenyl)-1-propanone
Cl
H
N
NH2
S
2254
5-Chloro-1-phenyltetrazole
2255
(2-Chlorophenyl)thiourea
Physical Constants of Organic Compounds
3-118
Organic
Mol. Form.
CAS RN
Mol.
Wt.
α-Chlorophyll
C55H72MgN4O5
479-61-8
893.490 bl blk hex pl 152.3
2257
β-Chlorophyll
C55H70MgN4O6
519-62-0
907.473 bl-blk or grn 125
pow
2258
Chloropropamide
94-20-2
276.739 cry (EtOH)
128
2259
2260
2-Chloropropanal
1-Chloropropane
4-Chloro-N-[(propylamino)­
C10H13ClN2O3S
carbonyl]benzenesulfonamide
C3H5ClO
Propyl chloride
C3H7Cl
683-50-1
540-54-5
92.524
78.541
liq
-122.9(0.7)
86
46.2(0.5)
1.18215 1.43117
0.889920 1.387920
2261
2-Chloropropane
Isopropyl chloride
C3H7Cl
75-29-6
78.541
liq
-117.1(0.2)
35.0(0.6)
0.861720 1.377720
2262
2263
3-Chloro-1,2-propanediol
2-Chloro-1,3-propanediol
α-Chlorohydrin
Glycerol β-chlorohydrin
C3H7ClO2
C3H7ClO2
96-24-2
497-04-1
110.540 ye liq
110.540
221(18)
14618
1.32518 1.480920
1.321920 1.483120
2264
Clonitrate
C3H5ClN2O6
2612-33-1
200.534 sl ye liq
192.5
1.51129
2265
2266
3-Chloro-1,2-propanediol
dinitrate
3-Chloropropanenitrile
2-Chloropropanoic acid
β-Chloropropionitrile
2-Chloropropionic acid
C3H4ClN
C3H5ClO2
542-76-7
598-78-7
89.524 liq
108.524
-51.4(0.2)
175.5
185
1.157320 1.436020
1.258520 1.438020
2267
3-Chloropropanoic acid
3-Chloropropionic acid
C3H5ClO2
107-94-8
41(4)
204 dec
2268
2-Chloro-1-propanol
Propylene chlorohydrin
C3H7ClO
78-89-7
108.524 lf (w), hyg
cry (lig)
94.540
2269
3-Chloro-1-propanol
C3H7ClO
627-30-5
2270
1-Chloro-2-propanol
C3H7ClO
2271
3-Chloropropanoyl chloride
2272
No.
Name
2256
Synonym
Physical
Form
mp/˚C
bp/˚C
den
g cm –3
nD
i H2O; vs EtOH,
eth; s lig
i H2O; vs EtOH,
eth, py; s
MeOH
i H2O; s EtOH; sl
eth, bz
vs bz, eth
sl H2O, ctc; msc
EtOH, eth; s
bz, chl
sl H2O; msc
EtOH, eth; s
bz, ctc, chl
s H2O, EtOH, eth
vs H2O, ace,
EtOH
vs ace, EtOH,
chl
sl ctc
msc H2O, EtOH,
eth; s ace
s H2O, EtOH,
chl; msc eth
vs H2O, eth,
EtOH
vs H2O; s EtOH,
eth; sl ctc
msc H2O, EtOH,
eth; sl ctc
sl H2O; vs EtOH,
eth, chl
i H2O; s eth,
ace, bz, chl
i H2O; s eth,
ace, bz, chl
i H2O; s eth,
ace, bz, chl
i H2O; msc
EtOH, eth, ace,
bz, lig; sl ctc
133.5
1.10320
94.540
149(8)
1.130920 1.445920
127-00-4
94.540
124.4(0.2)
1.11320
C3H4Cl2O
625-36-5
126.969
144
1.330713 1.454920
cis-1-Chloropropene
C3H5Cl
16136-84-8 76.525
liq
-134.8
32(2)
0.934720 1.405520
2273
trans-1-Chloropropene
C3H5Cl
16136-85-9 76.525
liq
-99
37(2)
0.934920 1.405420
2274
2-Chloropropene
Isopropenyl chloride
C3H5Cl
557-98-2
76.525
-137.4(0.4)
23(2)
0.901720 1.397320
2275
3-Chloropropene
Allyl chloride
C3H5Cl
107-05-1
76.525
vol liq or
gas
liq
-136(2)
44.8(0.4)
0.937620 1.415720
2276
2277
2278
C3H2ClN
C3H3ClO2
C9H9Cl
920-37-6
87.508 liq
598-79-8
106.508
21087-29-6 152.620
-65
66
8.5
88.5
sub
10613
1.09625
C10H12ClNO2
C17H16Cl2O3
C9H11Cl
C4H6Cl2O2
C6H15ClO3Si
101-21-3
5836-10-2
104-52-9
628-11-5
2530-87-2
213.661
339.213 pow
154.636
156.996
198.720
42.5(0.3)
72.3(0.3)
1492
2284
2285
2-Chloro-2-propenenitrile
2-Chloropropenoic acid
2-Chloroacrylic acid
trans-(3-Chloro-1-propenyl)­
benzene
Chloropropham
Chloropropylate
(3-Chloropropyl)benzene
3-Chloropropyl chloroformate
(3-Chloropropyl)trimethoxysilane
(3-Chloropropyl)trimethylsilane
3-Chloro-1-propyne
Propargyl chloride
C6H15ClSi
C3H3Cl
2344-83-4
624-65-7
150.722
74.509
-78
151
56(4)
0.878920 1.431920
1.03025 1.434920 i H2O; msc
EtOH, eth, bz;
s ctc
2286
2287
2288
6-Chloro-1H-purine
6-Chloro-3-pyridazinamine
5-Chloro-2-pyridinamine
C5H3ClN4
C4H4ClN3
C5H5ClN2
87-42-3
5469-69-2
1072-98-6
154.558 nd (w)
129.548
128.560 pl
176 dec
220
137
12711
2289
2-Chloropyridine
C5H4ClN
109-09-1
113.546 oil
2290
2291
3-Chloropyridine
4-Chloropyridine
C5H4ClN
C5H4ClN
626-60-8
626-61-9
113.546
113.546 liq
-43.5
s H2O, EtOH; sl
DMSO; i peth,
lig
sl H2O; s EtOH,
eth
sl H2O
s H2O; msc
EtOH
2292
2-Chloro-3-pyridinecarboxylic
acid
6-Chloro-3-pyridinecarboxylic
acid
4-Chloropyridine,
hydrochloride
Chloroquine
C6H4ClNO2
2942-59-8
157.555
>175 dec
C6H4ClNO2
5326-23-8
157.555
198 dec
C5H5Cl2N
7379-35-3
150.006
C18H26ClN3
54-05-7
319.872
2279
2280
2281
2282
2283
2293
2294
2295
HCP_Section_03.indb 118
sec-Propylene chlorohydrin
6-Chloropurine
216(14)
177
91
1.439020
Solubility
1.439220
1.429020
1.092620 1.585120 vs ace, bz, eth,
EtOH
1.1830
1.538820
sl H2O; s os
1.05621 1.516025 sl ctc
1.292625 1.445620 i H2O
1.07725 1.418325
170(2)
1.20515
151(20)
151(20)
1.200025
1.532020
1.530420
210 sub
90
4/11/16 11:21 AM
Physical Constants of Organic Compounds
3-119
O
N
Mg
N
N
N
N
N
N
Mg
O
N
HN
N
H
O S O
O
O
O
O
O
O
O
Cl
2256
2257
α-Chlorophyll
Cl
1-Chloropropane
2261
2-Chloropropane
HO
OH
Cl
2260
OH
2262
2263
2268
Cl
2269
2-Chloro-1-propanol
2270
3-Chloro-1-propanol
O
N
3-Chloro-1,2-propanediol dinitrate
1-Chloro-2-propanol
Cl
2271
3-Chloropropanenitrile
2272
2273
cis-1-Chloropropene
Cl
H
N
2278
2-Chloropropenoic acid
2-Chloropropene
Cl
2275
N
2276
3-Chloropropene
2-Chloro-2-propenenitrile
O
O
O
Cl
Cl
Cl
2279
trans-(3-Chloro-1-propenyl)benzene
3-Chloropropanoic acid
O
O
OH
2277
2-Chloropropanoic acid
2274
trans-1-Chloropropene
OH
2267
Cl
HO
Cl
2266
Cl
Cl
3-Chloropropanoyl chloride
Cl
Cl
Cl
Cl
Cl
O
O
O
2265
O
OH
OH
Cl
OH
Cl
2264
2-Chloro-1,3-propanediol
2-Chloropropanal
Cl
NO2
O
O2N
2259
Chloropropamide
Cl
Cl
OH
3-Chloro-1,2-propanediol
Cl
OH
2258
β-Chlorophyll
Cl
O
Cl
O
2280
Chloropropham
2281
Chloropropylate
O
Cl
2282
(3-Chloropropyl)benzene
3-Chloropropyl chloroformate
Cl
O
O Si
O
Cl
2283
(3-Chloropropyl)trimethoxysilane
Si
Cl
2284
(3-Chloropropyl)trimethylsilane
Cl
6-Chloro-1H-purine
3-Chloro-1-propyne
O
Cl
OH
OH
N
2291
4-Chloropyridine
N
Cl
2292
N
N
2286
2285
2-Chloro-3-pyridinecarboxylic acid
Cl
NH2
N
HN
Cl
N
N
N
2287
2288
6-Chloro-3-pyridazinamine
N
2293
6-Chloro-3-pyridinecarboxylic acid
NH2
5-Chloro-2-pyridinamine
N
Cl
N
2289
2290
3-Chloropyridine
2-Chloropyridine
HN
Cl
O
Cl
Cl
HCl
N
Cl
2294
4-Chloropyridine, hydrochloride
N
2295
Chloroquine
N
Organic
O
O
Physical Constants of Organic Compounds
3-120
Mol. Form.
CAS RN
Mol.
Wt.
2-Chloroquinoline
C9H6ClN
612-62-4
2297
4-Chloroquinoline
C9H6ClN
2298
6-Chloroquinoline
2299
8-Chloroquinoline
2300
2301
5-Chloro-8-quinolinol
2-Chlorostyrene
2302
No.
Name
2296
Physical
Form
den
g cm –3
Organic
mp/˚C
bp/˚C
163.604 nd (aq al)
38.4(0.5)
266
611-35-8
163.604 cry
34.9(0.5)
262
C9H6ClN
612-57-7
45.9(0.5)
262(22)
C9H6ClN
611-33-6
163.604 pr (eth), nd
(al)
163.604 liq
-20
288.5
1.283414 1.640814 s H2O; vs EtOH,
eth, ace, bz,
chl
C9H6ClNO
C8H7Cl
130-16-5
2039-87-4
179.603 cry (al)
138.595 liq
130
-63.1
188.6(1)
3-Chlorostyrene
C8H7Cl
2039-85-2
138.595
2303
4-Chlorostyrene
C8H7Cl
1073-67-2
138.595
15.9
2304
N-Chlorosuccinimide
C4H4ClNO2
128-09-6
133.534 pl (CCl4)
150
2305
1-Chlorotetradecane
C14H29Cl
2425-54-9
232.833
4.9
296(4)
2306
C11H20ClN5
580-48-3
257.764 oily liq
27
1559
C2HClF4
354-25-6
136.476 col gas
-117
-13(6)
C2HClF4
2837-89-0
136.476 col gas
-199.15
-11.96(0.09)
2309
6-Chloro-N,N,N’,N’-tetraethyl1,3,5-triazine-2,4-diamine
1-Chloro-1,1,2,2-tetrafluoroethane
1-Chloro-1,2,2,2-tetrafluoro- HCFC-124
ethane
Chlorothalonil
1.100020 1.564920 s EtOH, eth,
ace, ctc,
HOAc; msc
peth
1.103320 1.562520 i H2O; s EtOH,
eth
1.086820 1.566020 i H2O; s EtOH,
eth; msc ace,
bz, ctc
1.6525
sl H2O, EtOH,
bz, lig; s ace,
HOAc
0.865420 1.447420 i H2O; s EtOH,
chl; vs ace, bz;
sl ctc
1.095620 1.532020 vs bz, chl, EtOH,
lig
C8Cl4N2
1897-45-6
265.911
253.1(0.7)
350
2310
2311
2312
Chlorothen
Chlorothiazide
2-Chlorothiophene
C14H18ClN3S
C7H6ClN3O4S2
C4H3ClS
148-65-2
58-94-6
96-43-5
295.831
295.724
118.585 liq
15510
350 dec
-71.85(0.05) 126(2)
2313
C5H3ClOS
7283-96-7
146.595
C13H7ClOS
86-39-5
246.712
153.5
2315
5-Chloro-2-thiophenecarboxaldehyde
2-Chloro-9H-thioxanthen-9one
2-Chlorotoluene
1-Chloro-2-methylbenzene
C7H7Cl
95-49-8
126.584 liq
-35.9(0.7)
158.8(0.4)
2316
3-Chlorotoluene
1-Chloro-3-methylbenzene
C7H7Cl
108-41-8
126.584 liq
-47.8
162.1(0.4)
2317
4-Chlorotoluene
1-Chloro-4-methylbenzene
C7H7Cl
106-43-4
126.584 liq
7.4(0.2)
161.8(0.2)
2318
C3H4ClN5
3397-62-4
145.551
>330
C7H4Cl4
2136-89-2
229.919
29.4(0.2)
C7H4Cl4
5216-25-1
229.919
2321
2322
2323
2324
6-Chloro-1,3,5-triazine-2,4diamine
1-Chloro-2-(trichloromethyl)­
benzene
1-Chloro-4-(trichloromethyl)­
benzene
Chlorotriethoxysilane
Chlorotriethylplumbane
Lead triethyl chloride
Chlorotriethylsilane
1-Chloro-1,1,2-trifluoroethane
C6H15ClO3Si
C6H15ClPb
C6H15ClSi
C2H2ClF3
4667-99-6
1067-14-7
994-30-9
421-04-5
-51
123 dec
2325
1-Chloro-1,2,2-trifluoroethane
C2H2ClF3
431-07-2
2326
2327
2328
2329
2-Chloro-1,1,1-trifluoroethane
Chlorotrifluoroethene
Chlorotrifluoroethylene
Chlorotrifluoromethane
Refrigerant 13
2-Chloro-5-(trifluoromethyl)­
aniline
4-Chloro-3-(trifluoromethyl)­
aniline
1-Chloro-2-(trifluoromethyl)­ o-Chlorobenzotrifluoride
benzene
C2H2ClF3
C2ClF3
CClF3
C7H5ClF3N
75-88-7
79-38-9
75-72-9
121-50-6
198.720 liq
329.8
150.722
118.485 vol liq or
gas
118.485 vol liq or
gas
118.485 col gas
116.469 col gas
104.459 col gas
195.570
C7H5ClF3N
320-51-4
195.570
36.5
13227
C7H4ClF3
88-16-4
180.555 liq
-6(2)
153(3)
2307
2308
2314
2319
2320
2330
2331
HCP_Section_03.indb 120
Synonym
Cloxyquin
Chloromethapyrilene
2-Thienyl chloride
636
191(2)
77.55
263(3)
nD
Solubility
1.246425 1.634225 i H2O; vs EtOH,
eth; s bz, chl
1.25125
sl H2O; vs EtOH,
eth; s dil HCl
1.611056
1.725
i H2O; sl ace,
cyhex
1.175125
1.286320 1.548720 i H2O; msc
EtOH, eth; sl
chl
1.603625 sl chl
1.082520 1.526820 i H2O; s EtOH,
bz; msc eth,
ace, chl
1.07520 1.521419 i H2O; s EtOH,
bz, ctc, chl;
msc eth
1.069720 1.515020 i H2O; s EtOH,
ctc, chl; msc
eth
245
1.518720 1.583620 i H2O; s eth,
ace; sl ctc
1.446320
vs ace, eth
156
1.03020
146(3)
16(19)
0.896720
1.399920 vs EtOH
s H2O
1.431420
1.3890
1.54-60
1.30900
1.380
1.42825
1.497520
17.3
-105.5
6.0(0.6)
-158.14(0.05) -28.3(0.3)
-181.2
-81.37
10325
s bz, chl
i H2O
1.254030 1.451325 s chl
4/11/16 11:21 AM
Physical Constants of Organic Compounds
3-121
Cl
Cl
Cl
Cl
Cl
N
Cl
2296
N
2297
2-Chloroquinoline
2299
6-Chloroquinoline
2300
8-Chloroquinoline
2301
5-Chloro-8-quinolinol
2-Chlorostyrene
2302
2303
3-Chlorostyrene
O
N
Cl
OH
Cl
2298
4-Chloroquinoline
O
N
N
N
Cl
2304
4-Chlorostyrene
N-Chlorosuccinimide
Cl
N
2305
N
N
H2N
Cl
N
S
S
F
Cl
Cl
2312
S
O
F
F
Cl
Cl
N
Cl
2309
1-Chloro-1,2,2,2-tetrafluoroethane
Chlorothalonil
Cl
Cl
Cl
S
2313
2-Chlorothiophene
Chlorothiazide
F
2308
Cl
S
Cl
F
1-Chloro-1,1,2,2-tetrafluoroethane
NH
2311
Chlorothen
F
O
O O
O O
2310
Cl
2307
6-Chloro-N,N,N’,N’-tetraethyl-1,3,5-triazine-2,4-diamine
N
F
F
2306
1-Chlorotetradecane
S
Cl
N
N
Cl
Cl
N
N
2314
5-Chloro-2-thiophenecarboxaldehyde
2-Chloro-9H-thioxanthen-9-one
2315
2-Chlorotoluene
2317
2316
4-Chlorotoluene
3-Chlorotoluene
Cl
NH2
N
N
Cl
Cl
Cl
N
Cl
Cl
Cl
NH2
2318
6-Chloro-1,3,5-triazine-2,4-diamine
2319
Cl
O
O Si Cl
O
Cl
2320
1-Chloro-2-(trichloromethyl)benzene
1-Chloro-4-(trichloromethyl)benzene
Si Cl
Pb Cl
2321
2322
Chlorotriethoxysilane
2323
Chlorotriethylplumbane
NH2
Chlorotriethylsilane
Cl
F
F
2325
1-Chloro-1,2,2-trifluoroethane
Cl
F
2326
F
F
2-Chloro-1,1,1-trifluoroethane
F
F
Cl
F
2327
Chlorotrifluoroethene
Cl
F
F
F
2328
Chlorotrifluoromethane
F
F
2324
1-Chloro-1,1,2-trifluoroethane
Cl
Cl
F
2329
Cl
F
NH2
Cl
F
F
F
2-Chloro-5-(trifluoromethyl)aniline
F
2330
F
F
F
4-Chloro-3-(trifluoromethyl)aniline
2331
F
F
1-Chloro-2-(trifluoromethyl)benzene
Organic
N
Physical Constants of Organic Compounds
3-122
mp/˚C
bp/˚C
den
g cm –3
180.555 liq
-56
126(10)
1.331125 1.443825
98-56-6
180.555 liq
-33
138.5
1.334025 1.443130
C3H4ClF3
460-35-5
132.512 liq
-93.73(0.06) 45.1
1.325320 1.335020 i H2O
C8H17Cl
6111-88-2
148.674
-26
0.874620 1.430820 vs EtOH
C3H9ClSn
C6H2ClN3O6
1066-45-1
88-88-0
199.266
38.5
247.549 wh nd or pl 82(1)
(chl, al-lig)
148
Chlorotrinitromethane
CClN3O6
1943-16-4
185.480
5.8(0.2)
156(18)
2339
Chlorotriphenylmethane
C19H15Cl
76-83-5
278.775 nd or pr
(bz-peth)
109.2(0.5)
310
2340
2341
2342
2343
2344
2345
2346
Chlorotriphenylsilane
Chlorotriphenylstannane
Chlorotripropylstannane
Chlorovinyldimethylsilane
Chloroxuron
Chlorozotocin
Chlorphenesin carbamate
C18H15ClSi
C18H15ClSn
C9H21ClSn
C4H9ClSi
C15H15ClN2O2
C9H16ClN3O7
C10H12ClNO4
76-86-8
639-58-7
2279-76-7
1719-58-0
1982-47-4
54749-90-5
886-74-8
294.851
385.475
283.426
120.653
290.745
313.692 cry
245.660 cry (bz)
2347
2348
2349
Chlorpheniramine
Chlorpheniramine maleate
Chlorphentermine
C16H19ClN2
C20H23ClN2O4
C10H14ClN
132-22-9
113-92-8
461-78-9
274.788 oily liq
390.861
183.678 liq
2350
Chlorpromazine
C17H19ClN2S
50-53-3
318.864
2351
Chlorprothixene
C18H18ClNS
113-59-7
315.861 pale ye cry
97.1(0.3)
2352
2353
2354
2355
Chlorpyrifos
Chlorpyrifos-methyl
Chlorsulfuron
Chlortetracycline
C9H11Cl3NO3PS
C7H7Cl3NO3PS
C12H12ClN5O4S
C22H23ClN2O8
2921-88-2
5598-13-0
64902-72-3
57-62-5
350.586
322.534
357.773
478.879 gold-ye
43(1)
46.0(0.5)
176
168.5
2356
Chlorthalidone
C14H11ClN2O4S
77-36-1
225 dec
2357
Chlorthion
C8H9ClNO5PS
500-28-7
338.766 wh pow or
cry
297.653 ye cry
2358
2359
Chlorthiophos
Chlortoluron
2360
2361
Cholane
Cholan-24-oic acid
2362
Cholesta-3,5-diene
2363
Cholesta-5,7-dien-3-ol, (3β)
2364
2365
Cholesta-8,24-dien-3-ol,
(3β,5α)
Cholestane, (5α)
2366
No.
Name
2332
2336
2337
1-Chloro-3-(trifluoromethyl)­ m-Chlorobenzotrifluoride
benzene
1-Chloro-4-(trifluoromethyl)­ p-Chlorobenzotrifluoride
benzene
3-Chloro-1,1,1-trifluoropropane
2-Chloro-2,4,4-trimethylpentane
Chlorotrimethylstannane
2-Chloro-1,3,5-trinitrobenzene Picryl chloride
2338
2333
2334
2335
Synonym
Organic
Triphenyltin chloride
Chloroprophenpyridamine
2-(4-Chlorobenzyl)-2-propylamine
2-Chloro-N,N-dimethyl-10Hphenothiazine-10-propanamine
Mol. Form.
CAS RN
Mol.
Wt.
C7H4ClF3
98-15-7
C7H4ClF3
C11H15Cl2O3PS2
N’-(3-Chloro-4-methylphenyl)- C10H13ClN2O
N,N-dimethylurea
C24H42
Cholanic acid
C24H40O2
Physical
Form
21923-23-9 361.245
15545-48-9 212.675 cry
150(8)
1.79720
12313
82.3(0.4)
s H2O
vs ace, EtOH,
diox
1421
132.5
231
2020.8
21
1250.1
i H2O; vs EtOH,
eth, bz, chl; s
dil HCl
i H2O, EtOH, eth,
chl
1.43720
1.566120
i H2O, eth; sl
EtOH, ace, bz;
s diox
s alk, EtOH; sl
eth
i H2O; vs bz,
eth, EtOH
1500.001
147
sl H2O; s os
1900.001
C27H44
80
26013
C27H44O
434-16-2
150.5
C27H44O
128-33-6
28,29,30-Trinorlanostane
C27H48
481-21-0
Cholestane, (5β)
Coprostane
C27H48
481-20-9
2367
2368
2369
Cholestanol
Cholestan-3-ol, (3α,5α)
Cholest-4-en-3-ol, (3β)
Dihydrocholesterol
Epicholestanol
Allocholesterol
C27H48O
C27H48O
C27H46O
80-97-7
516-95-0
517-10-2
2370
Cholest-5-en-3-ol, (3α)
Epicholesterol
C27H46O
474-77-1
2371
Cholest-5-en-3-ol (3β),
acetate
C29H48O2
604-35-3
HCP_Section_03.indb 122
s H2O, chl, os
i H2O; s EtOH,
bz; sl eth; vs
ace, tol
vs eth, EtOH,
chl
i H2O; sl EtOH;
vs eth, bz, chl;
s ace
s chl
1.267828 1.4910228 s ctc, os
0.874420 1.414120
152.0(0.9)
147 dec
90
90
163.5
384.637 pl (+1w),
(ethMeOH)
384.637 pl
(MeOH),nd
372.670 sc or pl
(eth-al,
ace)
372.670 orth nd (al,
ace)
388.669 sc (al,+1w)
388.669 nd (al)
386.653 nd
(ethMeOH)
386.653 cry (al,
chl-MeOH)
428.690 wh nd (ace,
al)
1.676920 1.450020
Solubility
24135
103.5
-23.5
548-98-1
330.590 pr (al)
25312-65-6 360.574 nd (al), cry
(HOAc)
747-90-0
368.638 wh nd (al)
7-Dehydrocholesterol
nD
110
1600.001
78.6(0.5)
2501
72
141.5
185.5
132
0.925100
0.909088 1.488788
s EtOH, chl,
HOAc
i H2O; s EtOH;
msc eth, bz,
chl; vs lig
i H2O; sl EtOH; s
eth, ace
s ace, chl,
MeOH
i H2O; sl EtOH;
vs eth, bz, chl
0.911987 1.488488 vs eth, chl
141.5
vs eth, chl
s chl
i H2O; s EtOH;
vs eth, ace, bz,
chl
sl EtOH
114.6(0.5)
vs bz, eth, chl
4/11/16 11:21 AM
Physical Constants of Organic Compounds
3-123
Cl
Cl
F
F
F
F
F
2332
F
F
2333
1-Chloro-3-(trifluoromethyl)benzene
Cl
F
F
Cl
2334
1-Chloro-4-(trifluoromethyl)benzene
O O
N
O N
O
2336
Cl
Si
NO2
NO2
Cl
NO2
N O
O
2337
Chlorotrimethylstannane
2-Chloro-2,4,4-trimethylpentane
Cl
Cl
Sn Cl
2335
3-Chloro-1,1,1-trifluoropropane
2338
2-Chloro-1,3,5-trinitrobenzene
2339
Chlorotrinitromethane
2340
Chlorotriphenylmethane
Chlorotriphenylsilane
HO
O
2341
2342
Chlorotriphenylstannane
Chlorozotocin
HO
N
Cl
OH
O O
2349
Chlorphentermine
Chlorpheniramine maleate
O
N
Cl
Cl
Cl
Cl
S
S
2350
2351
Chlorpromazine
N
Cl
S
O
P
O
O
N
Cl
Cl
N
S
O
P
O
O
HO
OH
S
NH
O
O O O
S
N
H
O O
O
Chlorsulfuron
O N
O
S
Cl
2358
Chlorthion
2359
Chlorthiophos
Chlortoluron
O
OH
H
HO
2361
2360
Cholane
HO
2362
H
2365
Cholesta-8,24-dien-3-ol, (3β,5α)
Cholesta-5,7-dien-3-ol, (3β)
HO
H
H
2364
2363
Cholesta-3,5-diene
Cholan-24-oic acid
2366
Cholestane, (5α)
H
2367
Cholestane, (5β)
Cholestanol
H
H
O
HO
HO
HO
H
2368
Cholestan-3-ol, (3α,5α)
2369
Cholest-4-en-3-ol, (3β)
O
2370
Cholest-5-en-3-ol, (3α)
N
O
Cl
Cl
2357
Chlorthalidone
H
N
Cl
O
P
O
S
Cl
2354
Chlorpyrifos-methyl
NH2
2356
Chlortetracycline
N
H
O
O P S
O
O
2355
N
N
2353
Chlorpyrifos
Cl
NH2
HO
OH O HO
O
Cl
2352
Chlorprothixene
N
NH2
Cl
2348
Chlorpheniramine
N
H
Chloroxuron
2347
Chlorphenesin carbamate
OH
H
Cl
2345
N
N
Cl
2346
N
ON
N
NH2
O
Cl
O
HN
2344
N
O
N
O
O
Chlorovinyldimethylsilane
OH
O
Cl
2343
Chlorotripropylstannane
OH
H
N
Cl
Organic
Sn Cl
Si
Cl
OH
OH
Cl
Sn
2371
Cholest-5-en-3-ol (3β), acetate
Physical Constants of Organic Compounds
3-124
Mol. Form.
CAS RN
Mol.
Wt.
C34H50O2
604-32-0
490.760 wh nd
150(1)
C43H76O2
601-34-3
79.7(0.5)
C45H78O2
303-43-5
625.062 wh nd (eth
al)
651.100
i EtOH; s eth,
chl
vs bz, chl
47.9(0.5)
s chl
C27H44O
C27H46O
601-57-0
57-88-5
C24H40O5
81-25-4
384.637 nd or pl (al) 81.5
386.653 orth or tcl lf 148.2(0.8)
(al), nd
(eth)
408.572
198
C5H14ClNO
C5H15ClNO4P
67-48-1
107-73-3
139.624 hyg cry
219.604 visc liq
C10H10O6
C6CrO6
617-12-9
226.182 cry
148
13007-92-6 220.056 col orth cry dec 130
Chromium(II) oxalate
C2CrO4
814-90-4
2386
2387
Chromium(III) 2,4-pentanedio- Chromium acetylacetonate
ate
Chromotrope 2B
Chrysamminic acid
1,8-Dihydroxy-2,4,5,7-tetranitro-9,10-anthracenedione
6-Chrysenamine
6-Aminochrysene
Chrysene
Benzo[a]phenanthrene
2388
Ciafos
2389
2391
2392
8,10,12-Heptadecatriene-4,6- C17H22O2
diyne-1,14-diol
C.I. Direct Blue 6, tetrasodium Direct Blue 6
C32H20N6Na4O14S4
salt
Cimetidine
C10H16N6S
Cinchonamine
C19H24N2O
2393
Cinchonidine
C19H22N2O
2394
Cinchonine
C19H22N2O
118-10-5
2395
Cinchotoxine
C19H22N2O
69-24-9
2396
trans-Cinnamaldehyde
3-Phenyl-2-propenal, (E)-
C9H8O
14371-10-9 132.159 ye liq
-7.5
2397
Cinnamedrine
90-86-8
281.392
75
2398
cis-Cinnamic acid
C19H23NO
α-[1-[Methyl(3-phenylallyl)­
amino]ethyl]benzenemethanol
3-Phenyl-2-propenoic acid, (Z) C9H8O2
102-94-3
148.159 mcl pr (w)
42
2399
trans-Cinnamic acid
3-Phenyl-2-propenoic acid, (E) C9H8O2
140-10-3
148.159 mcl pr (dil
al)
134(2)
2400
2401
trans-Cinnamyl anthranilate
Cinnamyl cinnamate
C16H15NO2
C18H16O2
87-29-6
122-69-0
253.296 cry
264.319 nd (al)
64
44
2402
Cinnamyl formate
C10H10O2
104-65-4
162.185
0
252
2403
Cinnoline
C8H6N2
253-66-7
38
1140.3
2404
Cinoxate
104-28-9
130.147 pa ye cry
(lig)
250.291 col liq
-25
1852
1.10225
2405
2406
2407
2408
2409
Cinquasia Red
Ciodrin
C.I. Pigment Red 170
C.I. Pigment Yellow 1
C.I. Pigment Yellow 12
1047-16-1
7700-17-6
2786-76-7
2512-29-0
6358-85-6
312.321
314.271
454.478
340.334
629.492
1350.03
1.1925
No.
Name
2372
2375
2376
Cholest-5-en-3-ol (3β),
benzoate
Cholest-5-en-3-ol (3β)-,
hexadecanoate
Cholest-5-en-3-ol (3β)-,
cis-9-octadecenoate
Cholest-4-en-3-one
Cholesterol
2377
Cholic acid
2378
2379
2380
2381
Choline chloride
Choline chloride dihydrogen
phosphate
Chorismic acid
Chromium carbonyl
2382
2383
2373
2374
Organic
2384
2385
2390
Synonym
3,7,12-Trihydroxycholan-24oic acid, (3α,5β,7α,12α)
Phosphorylcholine
HCP_Section_03.indb 124
mp/˚C
bp/˚C
den
g cm –3
1.06720
sub
1.77
C15H21CrO6
140.015 ye-grn pow
(hyd)
21679-31-2 349.320 red mcl cry 208.7(0.5)
345
1.34
C16H9N3Na2O10S2
C14H4N4O12
548-80-1
517-92-0
513.366 red-br pow
420.202 ye pl or lf
dec
C18H13N
C18H12
2642-98-0
218-01-9
C9H10NO3PS
2636-26-2
243.303 lf (al)
210.5
228.288 red bl fl or 255.0(0.1)
orth pl (bz,
HOAc)
243.219 ye to red-ye 15
liq
3-(4-Methoxyphenyl)-2C14H18O4
propenoic acid, 2-ethoxyethyl
ester
Quinacridone
C20H12N2O2
C14H19O6P
C26H22N4O4
C17H16N4O4
C32H26Cl2N6O4
505-75-9
nD
0.9413200
2450.03
459(20)
Cicutoxin
3-Phenyl-2-propen-1-ol,
formate
1,2-Benzodiazine
Physical
Form
i H2O; sl EtOH,
ace; s bz,
HOAc; vs diox
sl H2O; s EtOH,
ace, alk; vs
eth, chl
vs H2O, EtOH
305 dec
300
exp
448
s H2O
i H2O, EtOH; s
eth, chl
i H2O, EtOH; s
dil acid
i H2O; s bz
s H2O; i EtOH
vs eth, EtOH
1.27420
1200.09 dec
1.540432
258.356 pr (eth/peth) 54
932.752 dk bronze
pow
51481-61-9 252.339 cry
482-28-0
296.406 orth nd (al)
orth pr
(MeOH)
485-71-2
294.390 or pl or pr
(al)
Solubility
i H2O; sl EtOH,
eth, ace, bz,
CS2; s tol
sl H2O; vs chl,
EtOH, ace,
MeOH
s hot H2O, EtOH,
eth, chl
2602-46-2
294.390 pr nd (al,
eth)
294.390 nd or pr
(eth)
142
186
210.5
i H2O; vs EtOH,
eth; s bz, chl
sub
i H2O, bz; s
EtOH, chl, py;
sl eth
265
59
246
300
1.049720 1.619520
vs EtOH, HOAc,
lig
i H2O, lig; vs
EtOH; s eth,
ace, bz
1.24754
1.15654
i H2O; s EtOH,
chl; vs eth
1.08625
vs eth, EtOH
red-viol cry 390
red solid
ye cry
ye cry
i H2O; vs EtOH,
eth, ace, bz,
chl
sl H2O; s EtOH,
eth, chl; i lig
1.56720
i H2O; msc EtOH
i H2O, os
256
317
4/11/16 11:21 AM
Physical Constants of Organic Compounds
3-125
H
H
H
O
O
O
O
H
O
O
O
2372
2373
Cholest-5-en-3-ol (3β), benzoate
2374
Cholest-5-en-3-ol (3β)-, hexadecanoate
2375
Cholest-5-en-3-ol (3β)-, cis-9-octadecenoate
Cholest-4-en-3-one
O
HO
OH
O
H
H
HO
HO
OH
H
2376
HO
2377
Cl
2378
Cholic acid
Cl
N
OH
Choline chloride
O
CO
CO
CO
2381
Chorismic acid
Choline chloride dihydrogen phosphate
Cr
OC
2380
2379
CO
OC
OH
O
Chromium carbonyl
Organic
Cholesterol
N
O
O P OH
OH
OH
O
O
O
O
O
O
Cr
O
Cr
2
O
N
O
OH OH
O
N
O
2383
Chromium(II) oxalate
O
P
OH O
O
N
OH O
N
O
N
O
2384
Chromium(III) 2,4-pentanedioate
O
O
SO3 Na
Na O3S
2382
O
N
O
O
O
N
NH2
O
2385
Chromotrope 2B
2386
Chrysamminic acid
S
NH2
O
O S
O
OH
S
O
OH
2388
HO
N
N O
N
O N
H2N
S
O
S O
O
O
O
O
2389
Ciafos
Chrysene
4 Na
OH
O
N
2387
6-Chrysenamine
2390
Cicutoxin
C.I. Direct Blue 6, tetrasodium salt
NH
N
H
N
H
N
S
N
N
H
N
2391
HO
OH
H
H
O
N
2393
Cinchonamine
N
N
2394
Cinchonidine
2395
Cinchonine
OH
O
2397
2399
cis-Cinnamic acid
N
2402
O
N
O
O
O
N
H
O
2404
Cinnoline
2401
Cinnamyl cinnamate
O
O
2403
Cinnamyl formate
O
trans-Cinnamyl anthranilate
H
N
O
O
O
2400
trans-Cinnamic acid
O
O
NH2
OH
2398
Cinnamedrine
trans-Cinnamaldehyde
O
OH
O
2396
Cinchotoxine
O
N
2405
Cinoxate
O
O
P
O
O
2406
Cinquasia Red
Ciodrin
NH2
O
N
O
N
N
N
H H
2392
Cimetidine
HO
N
N
O
N
OH
H
N
O
O
N
H
N
O
N
O
N
O
N
H
NH O
N
Cl
Cl
O
O
N
N
O
N
N
HN
NH
O
O
O
2407
C.I. Pigment Red 170
2408
C.I. Pigment Yellow 1
2409
C.I. Pigment Yellow 12
Physical Constants of Organic Compounds
3-126
No.
Name
2410
2411
Cisapride
Citral
2412
β-Citraurin
2413
Citrazinic acid
2414
Citric acid
2415
Citric acid monohydrate
2416
Mol.
Wt.
Physical
Form
Organic
Synonym
Mol. Form.
CAS RN
3,7-Dimethyl-2,6-octadienal
C23H29ClFN3O4
C10H16O
81098-60-4 465.945 cry (hp)
141-27-5
152.233
C30H40O2
650-69-1
432.638 pl (bz-peth), 147
cry (al)
1,2-Dihydro-6-hydroxy-2-oxo- C6H5NO4
4-pyridinecarboxylic acid
2-Hydroxy-1,2,3-propanetriC6H8O7
carboxylic acid
99-11-6
155.109 ye pow
>300 dec
77-92-9
192.124 orth (w+1)
153
5949-29-1
210.138 cry (w)
135
Citrinin
2-Hydroxy-1,2,3-propanetriC6H10O8
carboxylic acid, monohydrate
Antimycin
C13H14O5
518-75-2
178 dec
2417
Citrulline
N5-(Aminocarbonyl)-L-ornithine C6H13N3O3
372-75-8
2418
2419
Citrus Red 2
C.I. Vat Blue 6
2420
2421
C.I. Vat Yellow 4
Clayton Yellow
2422
2423
Clemastine fumarate
Clindamycin
2424
2425
Cloconazole
Clofentezine
2426
2427
2428
Clofibrate
Cloforex
Clomazone
2429
2430
Clomiphene
Clonazepam
2431
2432
2433
Clonidine
Clopidol
Clopyralid
2434
2435
Clorophene
Clotrimazole
C9H9Cl2N3
C7H7Cl2NO
3,6-Dichloro-2-pyridinecarbox- C6H3Cl2NO2
ylic acid
C13H11ClO
C22H17ClN2
2436
2437
Clozapine
Cobalt carbonyl
Clozaril
Dicobalt octacarbonyl
2438
2439
2440
Cobalt hydrocarbonyl
Cobalt(III) 2,4-pentanedioate
Cocaine
Tetracarbonylhydrocobalt
Cobalt(III) acetylacetonate
2441
2442
7,16-Dichloro-6,15-dihydro5,9,14,18-anthrazinetetrone
Anthanthrone
Thiazol Yellow G
3,6-Bis(2-chlorophenyl)1,2,4,5-tetrazine
2-(2-Chlorobenzyl)-4,4dimethyl-1,2-oxazolidin-3one
mp/˚C
229
C18H16N2O3
C28H12Cl2N2O4
6358-53-8
130-20-1
250.247 ye nd
(MeOH)
175.185 pr (aq
MeOH)
308.331 cry
511.312 viol-bl pow
C24H12O2
C28H19N5Na2O6S4
128-66-5
1829-00-1
332.351 ye cry
695.721 ye-br pow
C25H30ClNO5
C18H33ClN2O5S
C18H15ClN2O
C14H8Cl2N4
14976-57-9 459.963
18323-44-9 424.983 ye amorp
solid
77175-51-0 310.777
74115-24-5 303.147
C12H15ClO3
C13H18ClNO2
C12H14ClNO2
637-07-0
242.698
14261-75-7 255.741 cry
81777-89-1 239.698
52.8
C26H28ClNO
C15H10ClN3O3
911-45-5
1622-61-3
405.959
315.711 wh cry
117
237.5
4205-90-7
2971-90-6
1702-17-6
230.093 cry
192.043 pow
192.000
137
>320
151
dec
222
156
nD
Solubility
0.888820 1.489820 i H2O; msc
EtOH, eth
i H2O; vs EtOH,
eth, ace, bz; sl
lig
s H2O, alk; sl
HCl
1.66520
vs H2O, EtOH; s
eth, AcOEt; i
bz, chl
1.542
vs H2O; vs
EtOH, eth
i H2O; sl EtOH,
eth; s ace, bz
s H2O; i EtOH,
MeOH
sl H2O; s EtOH
s H2O, EtOH,
H2SO4
181
73
182
s EtOAc
14920
890.005
1.19220
48.5
148
C18H19ClN4
C8Co2O8
5786-21-0 326.824 ye cry
10210-68-1 341.947 oran cry
183(1)
51 dec
C4HCoO4
C15H21CoO6
C17H21NO4
16842-03-8 171.982 ye liq or gas ≈-30
21679-46-9 356.257 dark grn cry 213
50-36-2
303.354 mcl pr (al) 98
Coclaurine
Codamine
C17H19NO3
C20H25NO4
486-39-5
285.338 pl (al)
21040-59-5 343.418 pr (bz, eth)
2443
Codeine
C18H21NO3
76-57-3
299.365 orth cry (w, 157.5
dil al, eth)
2444
Codeine phosphate
C18H24NO7P
52-28-8
2445
Coenzyme A
C21H36N7O16P3S
85-61-0
2446
Coenzyme I
C21H27N7O14P2
53-84-9
397.361 lf or pr (dil 227 dec
al)
767.535 pow; unstab
in air
663.425 hyg pow
2447
Coenzyme II
C21H28N7O17P3
53-59-8
2448
Colchiceine
C21H23NO6
477-27-0
2449
Colchicine
C22H25NO6
64-86-8
HCP_Section_03.indb 126
den
g cm –3
132
120-32-1
218.678
23593-75-1 344.836 cry
Nicotinamide adenine
dinucleotide
Nicotinamide adenine
dinucleotide phosphate
bp/˚C
i H2O, bz; sl
ace, MeOH,
chl
i H2O
1613.5
1.18558
s ctc, CS2
sl H2O, bz; s
ace, chl,
AcOEt, DMF
1.78
i H2O; s EtOH,
eth, CS2
s os
s bz, ace
sl H2O; vs EtOH,
eth, bz, py; s
CS2
10
1870.1
1.502298
220.5
127
743.405 gray-wh
pow
385.411 pa ye nd
178.5
(diox)
399.437 ye pl (w + 156
1/2) ye cry
(bz)
25022
1.3225
vs eth, EtOH,
chl
s H2O, eth, bz,
chl, tol; vs
EtOH; i peth
vs EtOH, chl
s H2O
s H2O
s H2O
1.2425
sl H2O; vs EtOH,
chl; i eth, bz
vs H2O, EtOH
4/11/16 11:21 AM
Physical Constants of Organic Compounds
3-127
O
Cl
HN
H2N
O
N
O
O
O
O
F
O
HO
HO
2410
2412
2411
Cisapride
OH
β-Citraurin
Citral
N
OH
2413
Citrazinic acid
O
O
Cl
O
O
COOH
OH
COOH
HOOC
HOOC
OH
2414
COOH
COOH
O
HO
H 2O
O
O
2415
Citric acid
HO
2416
Citric acid monohydrate
N
H
NH2
OH
N
O
NH O
OH
NH2
Cl
O
2417
Citrinin
O HN
N
2418
Citrulline
2419
Citrus Red 2
C.I. Vat Blue 6
N
N N
HN
S
N
OH
SO3 Na
O
2420
2422
Clemastine fumarate
Clayton Yellow
Cl
Cl
NH
N
O
HO
O
O
O
Cl
2421
C.I. Vat Yellow 4
N
HO
O
N
S
SO3 Na
N
OH
Cl
O
N
N
O
S
OH
O
N
N
Cl
2423
2424
Clindamycin
Cloconazole
H
N
Cl
O
O
N
Cl
2430
N
H
Cl
Cl
Cl
N
H
Clopidol
OC
Co
OC
CO
N
H
2436
H
CO
CO
CO
OC Co
Co
CO
Clozapine
CO
Clorophene
O
O
O
O
O
N
O
N
H
H
HO
O
O
OH
2439
Cobalt hydrocarbonyl
Cobalt carbonyl
2434
Clopyralid
CO
2438
2437
Co
O
Cl
2433
O
O O
C C
OH
N
O
2432
O
N
Clotrimazole
OH
Cl
N
Clonidine
Cl
2435
Cl
Clomazone
O
Cl
N
Cl
N
2428
Cloforex
OH
Cl
N
N
2427
Clofibrate
2431
Clonazepam
N
2426
H
N
Cl
Cl
Clomiphene
O
O
N
2429
O
O
Cl
Clofentezine
N
N
O
Cl
2425
O
H
N
O
2440
Cobalt(III) 2,4-pentanedioate
2441
Cocaine
Coclaurine
NH2
O
O
N
H
HO
H
O
N
HO
2442
HO
2443
Codamine
O
Codeine
O
O
O
O
P
P
OH
O
O
NH2
N
H
O
OH
O
O
O
O
P
P
OH OH
HO
2445
Codeine phosphate
Coenzyme A
N
O
O
P
OH
N
O
O
O
O
O
P
P
O
OH
O
OH
NH2
O
HO
O
O P OH
OH
O
O
NH
O
O
O
NH
O
O
O
O
O
HO
OH
2446
Coenzyme I
OH
N
N
O N
O N
HO
N
O
N
N
O
HO
O
N
NH2
N
N
N
H
N
2444
NH2
N
H
O
HS
H2PO4
O
O
O
N
O
OH
O
OH
2447
Coenzyme II
2448
Colchiceine
2449
Colchicine
Organic
O
Physical Constants of Organic Compounds
3-128
Organic
Mol. Form.
CAS RN
Mol.
Wt.
C53H100N16O13
7722-44-3
1169.47 amor pow
C27H20O12
C20H22O6
27267-69-2 536.441 oran pr (chl- 281
MeOH)
546-97-4
358.385 nd (MeOH) 195.5
Conessine
C24H40N2
546-06-5
356.588 lf or pl (ace) 125.5
2454
Congo Red
C32H22N6Na2O6S2
573-58-0
696.663 pow
>360
2455
Conhydrine
C8H17NO
495-20-5
143.227 lf (eth)
121
226
2456
Conhydrine, (+)
C8H17NO
495-20-5
143.227 lf (eth)
121
226
2457
Coniferin
C16H22O8
531-29-3
342.341 nd (w+2)
186
2458
Conquinamine
C19H24N2O2
464-86-8
312.406 ye tetr
123
2459
Convallatoxin
C29H42O10
508-75-8
238
2460
Copaene
C15H24
3856-25-5
550.637 pr (eth/
MeOH)
204.352
2461
Copper(II) ethylacetoacetate
Bis(ethylacetoacetato)copper
C12H18CuO6
192
2462
2463
2464
Copper(II) gluconate
Copper(II) 2,4-pentanedioate
Copper(II) phthalocyanine
Cupric gluconate
Copper(II) acetylacetonate
Pigment Blue 15
C12H22CuO14
C10H14CuO4
C32H16CuN8
14284-06-1 321.813 grn cry
(EtOH)
527-09-3
453.841 bl-grn cry
13395-16-9 261.762 bl pow
147-14-8
576.069 bl-purp cry
156
284 dec
sub
2465
Coronene
C24H12
191-07-1
300.352 ye nd (bz)
437.3(0.3)
525
2466
Corticosterone
C21H30O4
50-22-6
181
2467
Corybulbine
C21H25NO4
518-77-4
346.461 nd (al, pl)
(ace)
355.429 nd (al)
2468
2469
Corycavamine
Corydaline
C21H21NO5
C22H27NO4
521-85-7
518-69-4
367.396 pr (eth, al)
369.454 pr (al)
149
136
2470
Corydine
C20H23NO4
476-69-7
341.402 tetr pr (eth)
149
2471
2472
Corynantheine
Cotarnine
C22H26N2O3
C12H15NO4
18904-54-6 366.452
82-54-2
237.252 nd (bz), cry
(eth)
165.5
132 dec
2473
2474
Coumaphos
Coumestrol
C14H16ClO5PS
C15H8O5
56-72-4
479-13-0
362.766
268.222 cry rods
95.2(0.2)
385 dec
1.474
2475
Creatine
C4H9N3O2
57-00-1
303 dec
1.3325
2476
Creatinine
C4H7N3O
60-27-5
2477
o-Cresol
2-Methylphenol
C7H8O
95-48-7
131.133 mcl pr
(w+1)
113.118 orth pr
(w+2) lf
(w)
108.138
31.0(0.6)
191.0(0.1)
2478
m-Cresol
3-Methylphenol
C7H8O
108-39-4
108.138 liq
12.2(0.3)
202.2(0.1)
2479
p-Cresol
4-Methylphenol
C7H8O
106-44-5
108.138 pr
34.77(0.05)
201.9(0.1)
2480
2481
o-Cresolphthalein
o-Cresolphthalein complexone Metalphthalein
C22H18O4
C32H32N2O12
596-27-0
2411-89-4
346.376 cry (al)
636.602 ye cry pow
223
186
2482
Cresol Red
C21H18O5S
1733-12-6
2483
2484
2485
2486
p-Cresyl diphenyl phosphate
Crimidine
Cromolyn
Crufomate
No.
Name
2450
Colistin A
2451
Collinomycin
2452
Columbin
2453
HCP_Section_03.indb 128
Synonym
α-Rubromycin
2-(α-Hydroxypropyl)piperidine
3,9-Dihydroxy-6Hbenzofuro[3,2-c][1]
benzopyran-6-one
o-Cresolsulfonphthalein
Cromoglicic acid
C19H17O4P
C7H10ClN3
C23H16O11
C12H19ClNO3P
Physical
Form
382.430 red-br cry
pow
78-31-9
340.309 col liq
535-89-7
171.627 br wax
16110-51-3 468.366 col cry
299-86-5
291.711
mp/˚C
bp/˚C
den
g cm –3
Solubility
sl H2O, EtOH,
hx; s acids,
MeOH
vs ace, diox, chl
1660.1
248.5
0.899620 1.489420
1.37125
237.5
i H2O; sl ace,
AcOEt, MeOH;
s chl
sl H2O; s chl,
HOAc
sl H2O; s EtOH; i
eth
sl H2O; vs eth,
EtOH, chl
sl H2O; vs eth,
EtOH, chl
s H2O, py; sl
EtOH; i eth
sl H2O; s EtOH,
eth, chl
s EtOH, ace; sl
chl; i eth
i H2O; s eth,
ace, HOAc, lig
s EtOH, chl
sl EtOH; i os
sl H2O; s chl
i H2O, EtOH; s
conc H2SO4
i H2O, con sulf;
sl bz
i H2O; s EtOH,
eth, ace
i H2O; sl EtOH,
eth; s ace, bz,
HCl
vs EtOH, chl
vs bz, eth,
EtOH, chl
vs eth, EtOH,
chl
vs EtOH
sl H2O; s EtOH,
eth, bz, chl,
NH4OH
i H2O; sl EtOH,
ace; i eth
300 dec
>300
-40
87
241 dec
60.1(0.5)
nD
1.032735 1.538635 s H2O; vs EtOH,
eth; msc ace,
bz, ctc
1.033920 1.540120 sl H2O; msc
EtOH, eth, ace,
bz, ctc
1.018540 1.531220 sl H2O; msc
EtOH, eth, ace,
bz, ctc
vs EtOH
i H2O; s EtOH,
ace, alk
vs H2O, EtOH
1.20825
1434
s H2O; sl EtOH; i
eth
s H2O; sl EtOH; i
eth, ace, chl
i H2O; s os
vs EtOH
1180.01
4/11/16 11:22 AM
Physical Constants of Organic Compounds
3-129
O
O
H
O
O
HO
H
O
H
OH
N
N
N
H
SO3Na
2452
Collinomycin
NH2
N
N
O
2451
NH2
H
O
O
HO
O
N
O
O
O
O HO
O
H
SO3Na
2453
Columbin
2454
Conessine
Congo Red
O
O
OH
OH
O
O
O O
H
N
H
N
H
OH
2455
HO
HO
OH
2456
Conhydrine
H
HO
H
H
O
H
O
O
O
Cu
O
H
O
2460
2461
Copaene
COO
OH
H
OH
OH
CH2OH
N
2
Cu
N
O
2463
N
N
2464
Coronene
O
O
N
O
N
O
O
O
H
O
O
2467
2468
Corybulbine
O
HO
O
O
O
2469
Corycavamine
N
H
2470
Corydaline
Corydine
OH
O
H
O
O
2471
O
O
HN
O
HO
2473
Cotarnine
NH2
O
OH
2472
Corynantheine
Cl
S
O
P
O
O
N
O
O
O
2474
Coumaphos
2475
Coumestrol
Creatine
HO
OH
O
H
OH
NH2
N
2476
Creatinine
OH
NH
O
O
2477
2478
2479
m-Cresol
2480
p-Cresol
OH
O
O
O
o-Cresol
HO
OH
OH
N
N
N
O
OH
O
OH
N
O
O
N
2465
Copper(II) phthalocyanine
N
N
H
H
N
N
O
Copper(II) 2,4-pentanedioate
O
2466
Corticosterone
Cu
N
O
O
O
O
Cu
O
2
N
H
Convallatoxin
N
Copper(II) gluconate
O
2459
Conquinamine
HO
OH
HO
OH
OH
2458
2462
Copper(II) ethylacetoacetate
O
HO
HO
Coniferin
H
OH
O O
OH
2457
Conhydrine, (+)
O
H
N
Organic
HO
N
H
N
O
OH
OH
2481
o-Cresolphthalein
o-Cresolphthalein complexone
HO
OH
O
O P O
O
O
O
2482
Cresol Red
HO
N
S
O O
N
2483
p-Cresyl diphenyl phosphate
O
O
O
HO
N
2484
Crimidine
Cl
O
Cl
OH
O
O
O
2485
Cromolyn
2486
O
O P O
NH
Crufomate
Physical Constants of Organic Compounds
3-130
Mol.
Wt.
Physical
Form
Organic
No.
Name
Synonym
Mol. Form.
CAS RN
2487
Cryptopine
Cryptocavine
C21H23NO5
482-74-6
2488
2489
Crystal Violet
Cubebin
Gentian violet
C25H30ClN3
C20H20O6
369.412 pr or pl (bz) 223
nd
(chlMeOH)
548-62-9
407.979 grn pow
215 dec
18423-69-3 356.369 nd (al, bz)
131.5
2490
2491
2492
2493
2494
Cucurbitacin B
Cucurbitacin C
Cupferron
Cupreine
Curan-17-ol, (16α)
Geissoschizoline
C32H46O8
C32H48O8
C6H9N3O2
C19H22N2O2
C19H26N2O
6199-67-3
5988-76-1
135-20-6
524-63-0
18397-07-4
2495
Curcumin
Turmeric
C21H20O6
458-37-7
2496
Curine
C36H38N2O6
436-05-5
2497
Cuscohygrine
C13H24N2O
454-14-8
2498
Cusparine
C19H17NO3
529-92-0
2499
2500
Cyamemazine
Cyanamide
Cyanogenamide
C19H21N3S
CH2N2
3546-03-0
420-04-2
2501
2502
Cyanazine
Cyanic acid
Hydrogen cyanate
C9H13ClN6
CHNO
2503
2504
2-Cyanoacetamide
Cyanoacetic acid
C3H4N2O
C3H3NO2
21725-46-2 240.692
420-05-3
43.025 unstab liq
or gas
107-91-5
84.076 pl (w)
372-09-8
85.062
2505
2506
2507
Cyanoacetohydrazide
Cyanoacetylene
3-Cyanobenzoic acid
C3H5N3O
C3HN
C8H5NO2
140-87-4
1070-71-9
1877-72-1
2508
4-Cyanobenzoic acid
C8H5NO2
619-65-8
2509
4-Cyanobutanoic acid
C5H7NO2
39201-33-7 113.116 hyg cry
45
2510
2511
2512
2513
2514
2-Cyanoethyl acrylate
Cyanofenphos
Cyanogen
Cyanogen bromide
Cyanogen chloride
Bromine cyanide
Chlorine cyanide
C6H7NO2
C15H14NO2PS
C2N2
CBrN
CClN
106-71-8
13067-93-1
460-19-5
506-68-3
506-77-4
83
-27.83
52
-6.55
2515
2516
2517
Cyanogen fluoride
Cyanogen iodide
Cyanoguanidine
Fluorine cyanide
Iodine cyanide
Dicyanodiamide
CFN
CIN
C2H4N4
2518
Cyanomethylmercury
Methylmercurynitrile
2519
2520
2521
2522
(4-Cyanophenoxy)acetic acid
2-Cyano-N-phenylacetamide
4-Cyanothiazole
Cyanuric acid
2523
2524
2525
2526
Cyanuric fluoride
Cycasin
Cyclandelate
Cyclizine
2,4,6-Trifluoro-1,3,5-triazine
2527
Cycloate
Carbamothioic acid,
C11H21NOS
cyclohexylethyl-, S-ethyl ester
HCP_Section_03.indb 130
2-[2-(1,3-Benzodioxol-5-yl)­
ethyl]-4-methoxyquinoline
Cyacetacide
1,3,5-Triazine2,4,6(1H,3H,5H)-trione
558.702
560.718
155.154
310.390
298.421
cry (EtOH)
cry (AcOEt)
pr (eth)
pa ye amor
pow
368.380 oran ye pr,
orth pr
(MeOH)
594.696 pr, nd
(chlMeOH)
224.342 oil
mp/˚C
bp/˚C
den
g cm –3
nD
1.31520
Solubility
i H2O; sl EtOH,
eth, bz; s chl,
HOAc
vs H2O, chl
vs eth, EtOH,
chl
181
207.5
163.5
202
135 dec
183
sl DMSO
vs EtOH
i H2O; vs EtOH,
eth, chl
vs EtOH, HOAc
221
vs ace, bz, py
16923
307.343 (α) wh or ye 92(α; 111(β)
nd (peth);
(β) amber
pr
323.455 ye pow
92
42.040 nd
45.55(0.04)
0.973320 1.483220 vs H2O, bz, eth,
EtOH
i H2O; vs ace,
bz, eth, EtOH
2120.25
14019
1.28220
165.6(0.5)
-86
23
1.14020
114.1(0.3)
66
160 dec
99.091 pr (al)
51.047
147.132 nd (w)
114.5
5
223(1)
61(18)
sub
0.816717 1.386825
147.132
220(1)
10812
1.06220
-21.1
61.5
13
0.9537-21
2.01520
1.18620
1495-50-7
506-78-5
461-58-5
125.126
303.317
52.034 col gas
105.922 nd
61.471 col vol liq or
gas
45.016 col gas
152.922 nd (al, eth)
84.080
-82
146.7
207(2)
C2H3HgN
2597-97-9
241.64
cry (chl)
92
C9H7NO3
C9H8N2O
C4H2N2S
C3H3N3O3
1878-82-6
621-03-4
1452-15-9
108-80-5
177.157
160.172
110.137
129.074
cry (w)
nd (al)
nd
wh cry
178
199.5
58
>330
C3F3N3
C8H16N2O7
C17H24O3
C18H22N2
675-14-9
14901-08-7
456-59-7
82-92-8
135.047
252.222 nd (ace aq)
276.371
266.381 cry (peth)
154 dec
52
106
19314
1134-23-2
215.356
11.5
14510
-46
sub
i H2O; s EtOH
1.441848 vs H2O, EtOH; s
eth, ace, bz; sl
CS2
vs H2O, bz, eth,
chl
vs H2O
s H2O, EtOH,
eth; sl chl,
HOAc
vs H2O, EtOH
sl H2O; s EtOH
sl H2O; s EtOH,
eth
s H2O, EtOH,
eth, HOAc; sl
tfa
s H2O, EtOH,
eth, bz
1.583925 sl H2O
s H2O, EtOH, eth
s H2O, EtOH, eth
s H2O, EtOH; vs
eth
2.8418
1.40414
vs eth, EtOH
s H2O, EtOH,
ace; i eth, bz,
chl
vs H2O, EtOH,
bz; s eth
1.7525
sl hot H2O, ace,
bz, EtOH; s
conc HCl
72.8
i H2O
i H2O; s chl; sl
EtOH
1.015630
4/11/16 11:22 AM
Physical Constants of Organic Compounds
3-131
N
N
O
HO
O
O
O
N
O
O
O
H
O
H
HO
O
OH
O
N
O
2487
Cl
Cryptopine
2489
Crystal Violet
2490
Cubebin
Cucurbitacin B
O
HO
O
N
O
H
O
H
OH
HO
O
OH
O
2488
N
N
HO
O
N
H
HO
N
H
H
NH4
O
OH
N
2492
2491
2494
2493
Cupferron
Cucurbitacin C
H
OH
Organic
O
O
Curan-17-ol, (16α)
Cupreine
O
O
O
O
OH
OH
OH
2495
O
N
N
N
O
2498
2497
Curine
Cusparine
Cuscohygrine
Cl
N
N
N
H2N
S
2499
N
H
N
2500
Cyamemazine
N
N
NH2
N
H
HO
N
2501
Cyanamide
O
O
O
O
2496
Curcumin
N
H
N
O
O
HO
O
O
N
H
N
N
2502
Cyanazine
O
2503
Cyanic acid
H
N
OH
N
N
O
2504
2-Cyanoacetamide
NH2
O
N
2505
Cyanoacetic acid
Cyanoacetohydrazide
2506
Cyanoacetylene
OH
OH
O
O
N
N
N
2507
2509
2508
3-Cyanobenzoic acid
O
N
OH
N
N
2510
4-Cyanobutanoic acid
4-Cyanobenzoic acid
O
S
P
O
2-Cyanoethyl acrylate
Br
N
2511
2512
Cyanofenphos
N
2513
Cyanogen
Cyanogen bromide
O
O
H 2N
Cl
N
2514
Cyanogen chloride
F
N
I
2515
2516
Cyanogen fluoride
Cyanogen iodide
O
N
H 2N
Hg
2517
N
N
N
N
H
2522
F
H
N
O
Cyanuric acid
F
(4-Cyanophenoxy)acetic acid
OH
2523
Cyanuric fluoride
2-Cyano-N-phenylacetamide
S
2521
4-Cyanothiazole
N
O
OH
O
N
N
S
O
HO
F
2520
N
O
O O
N
N
2519
Cyanomethylmercury
N
O
N
2518
Cyanoguanidine
HO
O
H
N
N
H
N
OH
N
N
N
OH
2524
Cycasin
2525
Cyclandelate
2526
Cyclizine
2527
Cycloate
Physical Constants of Organic Compounds
3-132
Organic
Mol. Form.
CAS RN
Mol.
Wt.
C12H16N2O3
52-31-3
236.266 lf (w)
173
Aminocyclobutane
Tetramethylene
C4H9N
C4H8
2516-34-9
287-23-0
71.121
56.107
-90.7(0.3)
83(20)
12.5(0.2)
Cyanocyclobutane
C5H7N
C5H8O2
4426-11-3
3721-95-7
81.117
100.117 liq
-7(1)
148(1)
192(4)
C6H8O4
5445-51-2
144.126 pr (w, eth)
158.0
C4H8O
C4H6O
2919-23-5
1191-95-3
72.106
70.090
liq
-50.9
Cyclobutene
C4H6
822-35-5
54.091
col gas
2537
2538
2539
2540
2541
2542
Cyclochlorotine
Cyclodecane
1,2-Cyclodecanedione
Cyclodecanol
Cyclodecanone
α-Cyclodextrin
Cyclomaltohexaose
C24H31Cl2N5O7
C10H20
C10H16O2
C10H20O
C10H18O
C36H60O30
12663-46-6
293-96-9
96-01-5
1502-05-2
1502-06-3
10016-20-3
572.439 nd (MeOH)
140.266
168.233
156.265
154.249 amor pow
972.843 hx pl or nd
2543
2544
β-Cyclodextrin
γ-Cyclodextrin
Cyclomaltoheptaose
Cyclomaltooctaose
C42H70O35
C48H80O40
2545
2546
2547
2548
2549
2550
2551
2552
2553
2554
Cyclododecane
Cyclododecanol
Cyclododecanone
1,5,9-Cyclododecatriene
CDT
cis-Cyclododecene
trans-Cyclododecene
cis-9-Cycloheptadecen-1-one Civetone
1,3-Cycloheptadiene
Cycloheptanamine
Cycloheptane
C12H24
C12H24O
C12H22O
C12H18
C12H22
C12H22
C17H30O
C7H10
C7H15N
C7H14
7585-39-9 1134.984 mcl cry (w)
17465-86-0 1297.125 sq pl or
rods
294-62-2
168.319 nd (al)
1724-39-6 184.318
830-13-7
182.302
4904-61-4 162.271 liq
1129-89-1 166.303
1486-75-5 166.303
542-46-1
250.419
4054-38-0 94.154 liq
5452-35-7 113.201
291-64-5
98.186 liq
2555
2556
1,2-Cycloheptanedione
Cycloheptanol
C7H10O2
C7H14O
3008-39-7
502-41-0
126.153
114.185
2557
Cycloheptanone
Suberone
C7H12O
502-42-1
112.169
2558
1,3,5-Cycloheptatriene
Tropilidene
C7H8
544-25-2
92.139
2559
2560
2,4,6-Cycloheptatrien-1-one
Cycloheptene
C7H6O
C7H12
539-80-0
628-92-2
2561
1,3-Cyclohexadiene
C6H8
2562
1,4-Cyclohexadiene
2563
2564
No.
Name
2528
Cyclobarbital
2529
2530
Cyclobutanamine
Cyclobutane
2531
2532
Cyclobutanecarbonitrile
Cyclobutanecarboxylic acid
2533
2534
2535
1,1-Cyclobutanedicarboxylic
acid
Cyclobutanol
Cyclobutanone
2536
Synonym
Hydroxycyclobutane
Physical
Form
vol liq or
gas
mp/˚C
bp/˚C
nD
Solubility
i H2O; vs EtOH;
s eth, dil alk;
sl HOAc
124(8)
98.8(0.6)
2.5(0.4)
255 dec
10.4(0.9)
41(3)
42(3)
23(2)
den
g cm –3
0.832820 1.436319
0.70380 1.37520 i H2O; vs EtOH,
ace; msc eth;
s bz
1.059920 1.440020 sl H2O; msc
EtOH, eth
vs H2O; s EtOH,
eth, bz; sl lig
0.921815 1.437120
0.95470 1.421520 s H2O, eth, bz,
chl, tol; vs
EtOH; i peth
0.7330
vs ace; s bz,
peth
202.3(0.3)
10410
12512
10613
0.853825 1.471620
0.8280
-8.0(0.2)
244.0(0.5)
286
12712
240
13335
11317
343
120.5
5411
118.8(0.2)
-40
7.15(0.05)
10817
185
1.058322
0.955420
180.4(0.9)
0.950820
-75.18(0.06) 116.3(0.7)
0.887519
106.122
96.170 liq
-5(2)
-55.3(0.2)
11315
115(3)
1.09522
0.822820
592-57-4
80.128
liq
-89
80.3(0.3)
0.840520
C6H8
628-41-1
80.128
liq
-49(1)
89.5(0.2)
0.847120
3,5-Cyclohexadiene-1,2-dione
C6H4O2
583-63-1
108.095 red pl or pr
C6H6N2O2
105-11-3
138.124 pa ye nd (w) 240 dec
2565
2,5-Cyclohexadiene-1,4dione, dioxime
Cyclohexane
C6H12
110-82-7
84.159
6.7(0.2)
80.7(0.7)
2566
Cyclohexaneacetic acid
C8H14O2
5292-21-7
142.196 nd (HCO2H)
28.9(1)
245
2567
2568
2569
2570
Cyclohexanecarbonitrile
Cyclohexyl cyanide
Cyclohexanecarbonyl chloride
Cyclohexanecarboxaldehyde
Cyclohexanecarboxylic acid
Hexahydrobenzoic acid
C7H11N
C7H11ClO
C7H12O
C7H12O2
766-05-2
2719-27-9
2043-61-0
98-89-5
109.169 liq
146.614
112.169
128.169 mcl pr
12.0(0.3)
28(3)
188(3)
183(6)
155(12)
233(6)
2571
2572
cis-1,2-Cyclohexanediamine cis-1,2-Diaminocyclohexane
C6H14N2
trans-1,2-Cyclohexanediamine trans-1,2-Diaminocyclohexane C6H14N2
1436-59-5
1121-22-8
114.188 liq
114.188
14.8
402
8015
0.773925 1.423525 i H2O; msc
EtOH, eth, ace,
bz, lig, ctc
1.042318 1.477520 sl H2O; s eth,
ace
0.919
1.450520
1.096215 1.471129
0.903520 1.449620 s H2O, eth
1.033422 1.453020 sl H2O, ctc; vs
EtOH, bz, chl
0.95220 1.495120
0.95120
HCP_Section_03.indb 132
Sebacil
1,4-Dihydrobenzene
Hexahydrobenzene
liq; cub cry
(-80¯C)
liq
0.960620 1.492620 s EtOH
0.965420 1.480620 vs bz, eth, chl
vs cold H2O; i
hot H2O
260 dec
60.8(0.4)
62.4(0.3)
-17
32.5
-110.4
≈65 dec
0.905966 1.457160
0.84100
1.484020 vs bz, chl
1.485020 vs bz, chl
0.86825
0.809820
1.497820
1.472420
1.443620 i H2O; vs EtOH,
eth; s bz, chl
1.468922 s EtOH
1.4070520 sl H2O; vs EtOH,
eth
1.460820 i H2O; vs EtOH,
eth
1.534320 i H2O; s EtOH,
eth; vs bz, chl
1.617222 vs bz, chl
1.455220 i H2O; s EtOH,
eth, bz, chl; sl
ctc
1.475520 i H2O; s EtOH,
bz, chl, peth;
vs eth
1.472520 i H2O; msc
EtOH, eth; s
bz, chl, peth
s eth, ace, bz; i
peth
s H2O
4/11/16 11:22 AM
Physical Constants of Organic Compounds
3-133
O
O
H
2528
HO
2531
Cyclobutane
N
2533
Cyclobutanecarboxylic acid
2534
1,1-Cyclobutanedicarboxylic acid
Cl
2535
Cyclobutanol
O
OH
2538
2539
Cyclodecane
OH
OH
OH
O
O
OH
OH
O
O
2542
2543
α-Cyclodextrin
HO
O
O
OH
OH
4
OH
OH
O
O
O
Cyclodecanone
OH
OH
OH
2541
Cyclodecanol
O
O
OH
O
2540
1,2-Cyclodecanedione
OH
OH
O
OH
5
β-Cyclodextrin
HO
O
O
OH
Cyclobutene
OH
Cl
O
2537
HO
2536
Cyclobutanone
O
Cyclochlorotine
OH
O
OH
O
2532
Cyclobutanecarbonitrile
OH
OH
NH O
O
O
H
N
N
H
O
2530
Cyclobutanamine
H
N
O
OH
2529
Cyclobarbital
HO
O
N
NH2
O
N
H
O
OH
O
O
OH
OH
O
OH
OH
OH
6
O
2544
2545
γ-Cyclodextrin
2546
Cyclododecane
Cyclododecanol
2547
2548
Cyclododecanone
O
NH2
2549
1,5,9-Cyclododecatriene
cis-Cyclododecene
O
OH
O
2550
trans-Cyclododecene
O
2551
cis-9-Cycloheptadecen-1-one
2552
2553
1,3-Cycloheptadiene
2554
Cycloheptanamine
2555
Cycloheptane
1,2-Cycloheptanedione
2556
N
O
2,4,6-Cycloheptatrien-1-one
N
Cycloheptanone
OH
OH
O
2560
2561
Cycloheptene
1,3-Cyclohexadiene
O
Cl
2562
N
1,4-Cyclohexadiene
O
2563
3,5-Cyclohexadiene-1,2-dione
O
OH
2564
2,5-Cyclohexadiene-1,4-dione, dioxime
OH
NH2
2567
2568
Cyclohexanecarbonyl chloride
2569
Cyclohexanecarboxaldehyde
2570
Cyclohexanecarboxylic acid
2565
Cyclohexane
2566
Cyclohexaneacetic acid
NH2
NH2
Cyclohexanecarbonitrile
2558
1,3,5-Cycloheptatriene
O
O
2559
2557
Cycloheptanol
2571
cis-1,2-Cyclohexanediamine
NH2
2572
trans-1,2-Cyclohexanediamine
Organic
N
Physical Constants of Organic Compounds
3-134
Mol. Form.
CAS RN
Mol.
Wt.
trans-1,4-Cyclohexanedicarboxylic acid
C8H12O4
619-82-9
C8H18N2
2575
2576
1,3-Cyclohexanedimethanamine
1,4-Cyclohexanedimethanol
cis-1,2-Cyclohexanediol
2577
trans-1,4-Cyclohexanediol
2578
1,2-Cyclohexanedione
2579
No.
Name
2573
2574
Physical
Form
den
g cm –3
Organic
mp/˚C
bp/˚C
172.179 pr (w)
312.5
300 sub
2579-20-6
142.242
<-70
220
0.94520
C8H16O2
C6H12O2
105-08-8
1792-81-0
144.212
116.158
43
95(4)
283
12015
1.0297101
C6H12O2
6995-79-5
116.158 mcl pr (ace) 143
1,2-Dioxocyclohexane
C6H8O2
765-87-7
112.127 cry (peth)
40
1,3-Cyclohexanedione
Dihydroresorcinol
C6H8O2
504-02-9
112.127 pr (bz)
105(2)
2580
1,4-Cyclohexanedione
Tetrahydroquinone
C6H8O2
637-88-7
78.4(0.1)
2581
1,2-Cyclohexanedione dioxime Nioxime
C6H10N2O2
492-99-9
2582
2583
2584
2585
Cyclohexaneethanol
Cyclohexanemethanamine
Cyclohexanemethanol
Cyclohexanepropanoic acid
C8H16O
C7H15N
C7H14O
C9H16O2
4442-79-9
3218-02-8
100-49-2
701-97-3
112.127 mcl pl
(w),nd
(peth)
142.155 nd (w,
HOAc)
128.212
113.201
114.185 liq
156.222
2586
Cyclohexanethiol
Cyclohexyl mercaptan
C6H12S
1569-69-3
116.224
2587
Cyclohexanol
Cyclohexyl alcohol
C6H12O
108-93-0
100.158 hyg nd
26(1)
2588
Cyclohexanone
Pimelic ketone
C6H10O
108-94-1
98.142
2589
Cyclohexanone oxime
C6H11NO
100-64-1
113.157 hex pr (lig)
89.05(0.09)
2590
Cyclohexanone peroxide
C12H22O5
78-18-2
79
2591
Cyclohexene
C6H10
110-83-8
246.300 cry or long
nd
82.143 liq
2592
2593
C7H9N
C7H10O
1855-63-6
1192-88-7
107.153
110.153
C7H10O
100-50-5
110.153
1.0
164(9)
C7H10O2
636-82-8
126.153
38
241
C7H10O2
4771-80-6
126.153
17
237(13)
C8H10O4
88-98-2
170.163 pr (w)
173.0
C6H10O
C6H8O
C12H14
C12H18O
822-67-3
930-68-7
771-98-2
1502-22-3
98.142
96.127 liq
158.239 liq
178.270
-53
-11
176(10)
172.3(0.7)
268(15)
1163
0.992315 1.479025 s EtOH, ace
0.962025 1.488320 vs EtOH; s ace
0.993920 1.571820 vs MeOH
1.507020
C8H12O
932-66-1
124.180
73
202(12)
0.965520 1.488120 s EtOH, eth
C14H20O2
2611-00-9
220.308 liq
2604
2605
2606
2607
1-Cyclohexenecarbonitrile
1-Cyanocyclohexene
1-Cyclohexene-1-carboxaldehyde
3-Cyclohexene-1-carboxaldehyde
1-Cyclohexene-1-carboxylic
acid
3-Cyclohexene-1-carboxylic
acid
4-Cyclohexene-1,2-dicarboxylic acid
2-Cyclohexen-1-ol
2-Cyclohexen-1-one
1-Cyclohexen-1-ylbenzene
2-(1-Cyclohexen-1-yl)­
cyclohexanone
1-(1-Cyclohexen-1-yl)­
ethanone
3-Cyclohexenylmethyl
3-cyclohexenecarboxylate
4-(3-Cyclohexen-1-yl)pyridine
Cycloheximide
Cyclohexyl acetate
Cyclohexyl acrylate
C11H13N
C15H23NO4
C8H14O2
C9H14O2
70644-46-1
66-81-9
622-45-7
3066-71-5
159.228
281.349 pl (al)
142.196
154.206
22.1
119
2608
Cyclohexylamine
Cyclohexanamine
C6H13N
108-91-8
99.174
-17.7(0.7)
2609
Cyclohexylamine
hydrochloride
Cyclohexanamine
hydrochloride
C6H14ClN
4998-76-9
135.635 nd (w,
al-eth)
2594
2595
2596
2597
2598
2599
2600
2601
2602
2603
HCP_Section_03.indb 134
Synonym
Cyclohexylcarbinol
Tetrahydrobenzene
liq
194
1.118721 1.499520
1.086191 1.4576102
13220
1.086191
208(3)
162(7)
183
276.5
0.922920
0.8725
0.929720
0.91225
158.8(0.4)
0.978220
160.9(0.2)
0.962420
-27.93(0.05) 155.4(0.1)
0.947820
192
-43
16
-103.5(0.4)
208(2)
82.9(0.2)
Solubility
sl H2O, eth; vs
EtOH; s ace; i
chl
vs H2O, eth,
EtOH
1.1820
8112
6918
liq
nD
s EtOH, ace, bz;
sl chl
s H2O, EtOH,
MeOH; i eth; sl
ace
s H2O, EtOH,
eth, bz
s H2O, EtOH,
ace, chl; sl
eth, bz
s H2O, EtOH,
eth, ace, bz,
chl
s H2O, ace, chl;
sl tfa
s EtOH, eth, bz
1.464120
1.463020
1.464420 vs eth, EtOH
1.463820 s H2O, eth; sl
ctc
1.492120 vs ace, bz, eth,
EtOH
1.464120 s H2O, EtOH,
eth, ace; msc
bz; sl chl
1.450720 s H2O, EtOH,
eth, ace, bz,
chl, ctc
s H2O, EtOH,
eth, MeOH; sl
chl
0.811020 1.446520 i H2O; msc
EtOH, eth, ace,
bz, lig, ctc
0.969420 1.500520 s EtOH, eth
0.969220 1.474520 s ace, MeOH; sl
ctc
1.10920 1.490220 sl H2O; s EtOH,
ace
1.082020 1.481420 vs H2O; s EtOH,
ace
1537
226
174(4)
183
206.5
133.6(0.5)
1.022225 1.546625
vs EtOH
0.96820 1.44220 vs eth, EtOH
1.027520 1.467320 i H2O; msc
EtOH, eth; s
chl
0.819120 1.462515 s H2O, ctc; vs
EtOH; msc eth,
ace, bz
vs H2O, EtOH
4/11/16 11:22 AM
Physical Constants of Organic Compounds
O
3-135
OH
OH
OH
NH2
OH
O
OH
O
NH2
OH
2573
2574
trans-1,4-Cyclohexanedicarboxylic acid
O
OH
OH
2575
1,3-Cyclohexanedimethanamine
2577
2576
1,4-Cyclohexanedimethanol
2578
trans-1,4-Cyclohexanediol
cis-1,2-Cyclohexanediol
1,2-Cyclohexanedione
O
O
N
OH
O
N
O
OH
OH
NH2
OH
OH
2579
2580
1,3-Cyclohexanedione
OH
SH
2586
2587
Cyclohexanethiol
2581
1,4-Cyclohexanedione
Cyclohexanol
N
O
2588
2584
Cyclohexanemethanamine
Cyclohexanemethanol
2585
Cyclohexanepropanoic acid
N
OH
HO
O O
2590
Cyclohexanone oxime
O
2583
Cyclohexaneethanol
2589
Cyclohexanone
HO
O
2582
1,2-Cyclohexanedione dioxime
O
Cyclohexanone peroxide
HO
O
O
OH
2591
2592
Cyclohexene
O
1-Cyclohexenecarbonitrile
OH
OH
2593
1-Cyclohexene-1-carboxaldehyde
OH
O
O
2594
3-Cyclohexene-1-carboxaldehyde
2595
1-Cyclohexene-1-carboxylic acid
2596
3-Cyclohexene-1-carboxylic acid
O
O
2597
4-Cyclohexene-1,2-dicarboxylic acid
1-Cyclohexen-1-ylbenzene
O
2601
2-(1-Cyclohexen-1-yl)cyclohexanone
2-Cyclohexen-1-one
O
O
2600
2599
2598
2-Cyclohexen-1-ol
2602
1-(1-Cyclohexen-1-yl)ethanone
2603
3-Cyclohexenylmethyl 3-cyclohexenecarboxylate
N
2604
4-(3-Cyclohexen-1-yl)pyridine
OH
H
NH2
O
N
H
2605
Cycloheximide
O
O
2606
NH2
HCl
O
O
Cyclohexyl acetate
O
2607
Cyclohexyl acrylate
2608
Cyclohexylamine
2609
Cyclohexylamine hydrochloride
Organic
O
Physical Constants of Organic Compounds
3-136
Organic
Mol. Form.
CAS RN
Mol.
Wt.
C13H16N2S2
95-33-0
264.409
103
C12H17N
1821-36-9
175.270 mcl pr
16
279
C12H16
827-52-1
160.255 pl
7.02(0.1)
239(2)
Cyclohexyl benzoate
C13H16O2
2412-73-9
204.265
<-10
285
2614
Cyclohexyl butanoate
C10H18O2
1551-44-6
170.249
2615
3-Cyclohexyl-2-butenoic acid
C10H16O2
2616
2617
Cyclohexyl chloroformate
Cyclohexylcyclohexane
25229-42-9 168.233 pr
85.5
(aq-MeOH)
13248-54-9 162.614
87.527
92-51-3
166.303
3.684(0.002) 239(2)
2618
2619
2620
Cyclohexyldiethylamine
Cyclohexyldimethylamine
2-Cyclohexyl-4,6-dinitrophenol
(1,2-Cyclohexylenedinitrilo)­
tetraacetic acid monohydrate
1-Cyclohexylethanone
Cyclohexylethylamine
N,N-Diethylcyclohexanamine
C10H21N
N,N-Dimethylcyclohexanamine C8H17N
C12H14N2O5
2625
4-Cyclohexyl-3-ethyl-4H1,2,4-triazole
Cyclohexyl formate
2626
2627
2628
No.
Name
2610
2611
2-(Cyclohexylaminothio)­
benzothiazole
N-Cyclohexylaniline
2612
Cyclohexylbenzene
2613
2621
2622
2623
2624
2629
2630
2631
2632
2633
2634
2635
2636
2637
2638
Synonym
Phenylcyclohexane
Cicrotoic acid
C7H11ClO2
C12H22
91-65-6
98-94-2
131-89-5
Physical
Form
155.281
127.228
266.249 cry
CDTA
C14H24N2O9
13291-61-7 364.349 cry (w)
N-Ethylcyclohexanamine
C8H14O
C8H17N
823-76-7
5459-93-8
126.196
127.228
Hexazole
C10H17N3
4671-03-8
179.262 pr (eth)
C7H12O2
4351-54-6
128.169
Cyclohexyl hydroperoxide
C6H12O2
766-07-4
116.158
Cyclohexylideneacetonitrile
2-Cyclohexylidenecyclohexanone
Cyclohexyl isocyanate
Cyclohexylisopropylamine
Cyclohexyl isothiocyanate
C8H11N
C12H18O
4435-18-1
1011-12-7
C7H11NO
C9H19N
C7H11NS
3173-53-3
1195-42-2
1122-82-3
121.180
178.270 cry (MeOH
aq)
125.168
141.254
141.234
C6H11ClMg
931-51-1
142.909 hyg liq
C10H16O2
C7H15N
101-43-9
100-60-7
C10H18O2
Cyclohexylmagnesium
chloride
Cyclohexyl methacrylate
Cyclohexylmethylamine
Isocyanatocyclohexane
N-Isopropylcyclohexanamine
Isothiocyanatocyclohexane
N-Methylcyclohexanamine
Cyclohexyl 2-methylpropanoate
2-Cyclohexylphenol
4-Cyclohexylphenol
Trihexphenidyl
2639
α-Cyclohexyl-α-phenyl-1piperidinepropanol
Cyclohexyl propanoate
2640
2641
2642
2643
2644
2645
2646
2647
2648
Cyclohexylsulfamic acid
Cyclononane
Cyclononanone
1,4-Cyclooctadiene
cis,cis-1,5-Cyclooctadiene
Cyclooctanamine
Cyclooctane
Cyclooctanol
Cyclooctanone
Cyclamic acid
2649
1,3,5,7-Cyclooctatetraene
2650
2651
2652
1,3,5-Cyclooctatriene
cis-Cyclooctene
trans-Cyclooctene
2653
2654
2655
Cyclooctyne
Cyclopamine
Cyclopentadecane
HCP_Section_03.indb 136
Aminocyclooctane
[8]Annulene
11-Deoxojervine
mp/˚C
bp/˚C
213(8)
192
161(21)
den
g cm –3
nD
Solubility
1.015520 1.561020 i H2O; s EtOH,
eth, bz
0.942720 1.532920 i H2O; vs EtOH;
s eth; sl ctc
1.042920 1.520020 i H2O; s EtOH,
eth
0.95720
i H2O; s EtOH; sl
ctc
vs eth
sl H2O; s EtOH,
eth
s EtOH; sl ctc
0.844325
105.5(0.3)
sl H2O; s bz,
DMF
215
180.5
164
22710
0.917620 1.456516 i H2O; s eth
0.8680
sl H2O, ctc; msc
EtOH, eth
vs H2O, bz, chl
162
1.00570
420.1
1.01920
10722
0.948315
172
6212
221
0.9825
1.455120
0.85925 1.448020
1.033920 1.537520 i H2O; s EtOH,
eth; sl ctc
s eth
168.233
113.201
209(25)
147
1129-47-1
170.249
204
0.962620 1.457820
0.866023 1.456020 sl H2O; vs EtOH;
msc eth; s chl
0.94890
vs eth, EtOH
C12H16O
C12H16O
119-42-6
1131-60-8
176.254 nd (lig)
176.254 nd (bz)
54.7(0.7)
130.6(0.5)
C20H31NO
144-11-6
301.466
114
C9H16O2
6222-35-1
156.222
C6H13NO3S
C9H18
C9H16O
C8H12
C8H12
C8H17N
C8H16
C8H16O
C8H14O
100-88-9
293-55-0
3350-30-9
1073-07-0
111-78-4
5452-37-9
292-64-8
696-71-9
502-49-8
179.237
126.239
140.222
108.181 liq
108.181 liq
127.228 liq
112.213
128.212
126.196
169.5
10.7(0.3)
31.9(0.3)
-53(4)
-69.2(0.2)
-48
14.82(0.04)
25.1
44.2(0.3)
173(5)
14824
144(5)
149(3)
190
151.1(0.1)
9916
201.4(0.2)
C8H8
629-20-9
104.150 liq
-4.7(0.1)
140(3)
C8H10
C8H14
C8H14
1871-52-9
931-87-3
931-89-5
106.165 liq
110.197 liq
110.197 liq
-86(8)
-13(4)
-59(5)
144(11)
145(3)
146(5)
C8H12
C27H41NO2
C15H30
1781-78-8
4449-51-8
295-48-7
108.181
411.621 nd (EtOH)
210.399 nd (MeOH)
237
64.0(0.6)
89.5
-20
1.443020 i H2O; s EtOH,
HOAc, HCOOH;
vs eth
1.464525 vs eth, EtOH,
HOAc
1.438225 vs eth, EtOH
56.5
vs EtOH, HOAc
i H2O; vs EtOH,
eth; s bz; sl lig
294(26)
194(6)
158
0.935920 1.440320 i H2O; s EtOH,
eth, ace, ctc
vs alk
0.846325 1.466620
0.956020 1.472920 s EtOH
0.875420
0.88320 1.490525 vs bz
0.92825 1.480420
0.834920 1.458620 i H2O; s bz, lig
0.974020 1.487120 s EtOH
0.958120 1.469420 i H2O; s EtOH,
ace, bz; sl ctc
0.920620 1.538120 s EtOH, eth,
ace, bz
0.897125 1.503525
0.847220 1.469820 s EtOH, eth, ctc
0.848320 1.474125 s EtOH, chl; sl
ctc
0.86820 1.485020
0.836461 1.459261
4/11/16 11:22 AM
Physical Constants of Organic Compounds
O
H
N
N
S
HN
S
3-137
O
O
2610
2611
2-(Cyclohexylaminothio)benzothiazole
O
N
N
2619
2618
O
H
N
COOH
O
2620
Cyclohexyldimethylamine
Cyclohexyldiethylamine
Cyclohexyl chloroformate
2621
2-Cyclohexyl-4,6-dinitrophenol
2622
(1,2-Cyclohexylenedinitrilo)tetraacetic acid monohydrate
2623
1-Cyclohexylethanone
Cyclohexylethylamine
Organic
Cyclohexylcyclohexane
2616
3-Cyclohexyl-2-butenoic acid
COOH
COOH
N
O
2617
HOOC
N
N
2615
Cyclohexyl butanoate
OH
Cl
O
2614
Cyclohexyl benzoate
Cyclohexylbenzene
O
N
2613
2612
N-Cyclohexylaniline
O
OH
O
O
N
N
N
N
2624
4-Cyclohexyl-3-ethyl-4H-1,2,4-triazole
S
C
O
O
2625
Cyclohexyl formate
O
2626
Cyclohexyl hydroperoxide
2627
2628
Cyclohexylideneacetonitrile
2-Cyclohexylidenecyclohexanone
H
N
O
Cl
2632
Cyclohexyl isothiocyanate
Cyclohexylmagnesium chloride
N
H
N
2633
Cyclohexyl methacrylate
2629
Cyclohexyl isocyanate
HO
O
2634
2635
Cyclohexylmethylamine
2630
Cyclohexylisopropylamine
OH
O
O
2631
C
OH
N
Mg
O
O
Cyclohexyl 2-methylpropanoate
2636
2637
2-Cyclohexylphenol
4-Cyclohexylphenol
N
OH
H
N
O
O
2638
α-Cyclohexyl-α-phenyl-1-piperidinepropanol
OH
2639
Cyclohexyl propanoate
NH2
O
O
S
OH
O
2640
Cyclohexylsulfamic acid
2641
Cyclononane
2642
Cyclononanone
2643
1,4-Cyclooctadiene
2644
cis,cis-1,5-Cyclooctadiene
2645
Cyclooctanamine
2646
Cyclooctane
H H
N
O
O
H
HO
2647
Cyclooctanol
2648
Cyclooctanone
2649
1,3,5,7-Cyclooctatetraene
2650
1,3,5-Cyclooctatriene
2651
cis-Cyclooctene
2652
trans-Cyclooctene
2653
Cyclooctyne
2654
Cyclopamine
2655
Cyclopentadecane
Physical Constants of Organic Compounds
3-138
Organic
No.
Name
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
2656
2657
Cyclopentadecanol
Cyclopentadecanone
Exaltol
C15H30O
C15H28O
4727-17-7
502-72-7
2658
1,3-Cyclopentadiene
Pyropentylene
C5H6
2659
Cyclopentane
Pentamethylene
2660
2661
2662
Cyclopentaneacetic acid
Cyclopentanecarbonitrile
Cyclopentanecarboxaldehyde
2663
Cyclopentanecarboxylic acid
2664
2665
2666
2667
2668
2669
Physical
Form
mp/˚C
bp/˚C
226.398 cry (MeOH)
224.382
80.5
65.2(0.5)
17711
1200.3
542-92-7
66.102
liq
-96.54(0.05) 41(1)
C5H10
287-92-3
70.133
liq
-93.4(0.3)
49.2(0.1)
Cyanocyclopentane
C7H12O2
C6H9N
C6H10O
1123-00-8
4254-02-8
872-53-7
128.169 pl
95.142 liq
98.142
13.5
-76
228
169(2)
133.5
Cyclopentanoic acid
C6H10O2
3400-45-1
114.142 liq
-7
212
cis-1,2-Cyclopentanediol
trans-1,2-Cyclopentanediol
Cyclopentanemethanol
Cyclopentanepropanoic acid
Cyclopentanethiol
Cyclopentanol
5057-98-7
5057-99-8
3637-61-4
140-77-2
1679-07-8
96-41-3
102.132
102.132
100.158
142.196
102.198
86.132 liq
30
46(4)
Cyclopentyl mercaptan
Cyclopentyl alcohol
C5H10O2
C5H10O2
C6H12O
C8H14O2
C5H10S
C5H10O
12429
226
163
15826
132.2(0.6)
140.4(0.2)
2670
Cyclopentanone
Adipic ketone
C5H8O
120-92-3
84.117
liq
-51.70(0.02) 130.5(0.2)
2671
2672
Cyclopentanone oxime
Cyclopentene
C5H9NO
C5H8
1192-28-5
142-29-0
99.131
68.118
liq
57.8
196
-135.02(0.09) 44.2(0.2)
2673
2674
1-Cyclopentenecarbonitrile
1-Cyclopentene-1-carboxaldehyde
2-Cyclopentene-1-tridecanoic
acid, (S)2-Cyclopentene-1-undecanoic
acid, (R)2-Cyclopenten-1-one
3-Cyclopenten-1-one
N-(1-Cyclopenten-1-yl)­
pyrrolidine
Cyclopenthiazide
Cyclopentobarbital
C6H7N
C6H8O
3047-38-9
6140-65-4
93.127
96.127
liq
liq
-32
8130
146
Chaulmoogric acid
C18H32O2
68(2)
24720
Hydnocarpic acid
C16H28O2
29106-32-9 280.446 pl or lf (al,
HOAc)
459-67-6
252.392
1-Pyrrolidinylcyclopentene
C5H6O
C5H6O
C9H15N
930-30-3
82.101
14320-37-7 82.101 liq
7148-07-4 137.222
C13H18ClN3O4S2
C12H14N2O3
742-20-1
76-68-6
C5H11N
C11H14
C10H14O
1003-03-8
700-88-9
825-25-2
2685
2686
Cyclopentylamine
Cyclopentanamine
Cyclopentylbenzene
2-Cyclopentylidenecyclopentanone
Cyclopentyl methyl sulfide
Cyclophosphamide
Cyclophosphane
379.883
234.250 cry (w, dil
al)
85.148 liq
146.229
150.217
C6H12S
C7H15Cl2N2O2P
7133-36-0
50-18-0
116.224
261.086
2687
2688
Cycloposine
Cyclopropane
C33H51NO7
C3H6
23185-94-6 573.761
75-19-4
42.080 col gas
2689
2690
2691
2692
Cyclopropanecarbonitrile
Cyclopropyl cyanide
Cyclopropanecarbonyl chloride
Cyclopropanecarboxaldehyde Formylcyclopropane
Cyclopropanecarboxylic acid
C4H5N
C4H5ClO
C4H6O
C4H6O2
5500-21-0
4023-34-1
1489-69-6
1759-53-1
67.090
104.535
70.090 liq
86.090
2693
1,1-Cyclopropanedicarboxylic
acid
C5H6O4
598-10-7
140.5
2694
2695
Cyclopropanemethanol
Cyclopropanone
C4H8O
C3H4O
2516-33-8
5009-27-8
130.100 pr or nd
(chl) pr (w
+1)
72.106
56.063
2696
2697
Cyclopropene
Cyclopropylamine
C3H4
C3H7N
2781-85-3
765-30-0
40.064
57.095
-36(6)
-35.38(0.05) 49.2(0.1)
2698
Cyclopropylbenzene
C9H10
873-49-4
118.175 liq
-31
172(3)
2699
Cyclopropyl methyl ether
C4H8O
540-47-6
72.106
-110.0(0.5)
45(5)
2675
2676
2677
2678
2679
2680
2681
2682
2683
2684
HCP_Section_03.indb 138
1-Cyanocyclopentene
Trimethylene
Cyclopropanamine
-17(2)
den
g cm –3
nD
0.933220 1.457920
1.010017 1.457020
0.955020
0.948820 1.453020 sl H2O, ctc; s
EtOH, eth, ace
0.948720 1.436620 i H2O; s EtOH,
ace, ctc, hx;
msc eth
vs H2O, bz
0.772020 1.422520 i H2O; s EtOH,
eth, bz, ctc,
peth
0.97021
1.487217
vs eth, chl
60.5
136
2817
10515
Solubility
0.93020 1.455598
0.889525 1.463760 sl H2O; s EtOH,
ace
0.802120 1.444020 i H2O; msc
EtOH, eth, bz;
s ace
0.745720 1.406520 i H2O; msc
EtOH, eth, ace,
bz, peth, ctc
1.021618 1.452318
0.912
1.441020
0.937120 1.443220 vs H2O, eth,
EtOH
1.052720 1.453220 sl H2O, ctc; s
MeOH
0.98915
1.462915
vs EtOH, chl,
peth
vs eth, EtOH
1.512820
238
139.5
sl H2O; vs EtOH
-82.69(0.05) 108.5(0.1)
223(4)
13525
0.868920 1.472825 s ace, bz, chl
0.946220 1.528020 vs eth
1.017918 1.521518
156.2(0.8)
50.4(0.5)
gas
liq
liq
268
-127.6(0.2)
18.5
vs H2O; sl bz,
chl, diox, EtOH
-31(2)
0.61725
(p>1
atm)
135(1)
0.894620
119
1.151620
100
0.938
182.20(0.02) 1.088520
124
0.91125
1.3799-42 s H2O, bz, peth;
vs EtOH, eth
1.422920 s eth, hx; sl ctc
1.429820
1.439020 s H2O, EtOH,
eth; sl ctc
vs H2O, eth
sl ctc
stable only at
low temp.
0.824020 1.421020 msc H2O; s
EtOH, eth, chl
0.931720 1.528520 i H2O; s eth,
ace, chl
0.810020 1.380220 vs H2O, bz, eth,
EtOH
4/11/16 11:22 AM
Physical Constants of Organic Compounds
OH
3-139
O
N
O
HO
O
OH
O
2656
2657
Cyclopentadecanol
2658
Cyclopentadecanone
OH
2659
1,3-Cyclopentadiene
Cyclopentane
2664
2666
trans-1,2-Cyclopentanediol
O
OH
N
OH
O
OH
2665
Cyclopentanecarboxylic acid
Cyclopentanecarboxaldehyde
2668
2667
Cyclopentanemethanol
2670
2669
Cyclopentanethiol
Cyclopentanepropanoic acid
2671
Cyclopentanone
Cyclopentanol
Cyclopentanone oxime
2672
Cyclopentene
Organic
cis-1,2-Cyclopentanediol
SH
OH
OH
2663
2662
Cyclopentanecarbonitrile
Cyclopentaneacetic acid
OH
OH
2661
2660
N
OH
O
OH
O
2673
1-Cyclopentenecarbonitrile
2674
2675
1-Cyclopentene-1-carboxaldehyde
O
H2N
S
O
O
2679
S
O
2677
2-Cyclopentene-1-undecanoic acid, (R)-
2-Cyclopenten-1-one
2678
3-Cyclopenten-1-one
O
NH2
NH
NH
N
H
O
2680
N-(1-Cyclopenten-1-yl)pyrrolidine
2676
2-Cyclopentene-1-tridecanoic acid, (S)-
H
N
Cl
N
O
O
S
O
O
2681
Cyclopenthiazide
2682
Cyclopentobarbital
Cyclopentylamine
2683
2684
Cyclopentylbenzene
2-Cyclopentylidenecyclopentanone
2685
Cyclopentyl methyl sulfide
H H
N
O
H
HO
O
NH
P
O N
O
Cl
Cl
HO
HO
O
N
2687
Cyclophosphamide
O
Cyclopropane
OH
O
HO
2692
2688
Cycloposine
OH
Cyclopropanecarboxylic acid
Cl
O
OH
2686
O
O
2689
Cyclopropanecarbonitrile
2690
Cyclopropanecarbonyl chloride
NH2
O
2691
Cyclopropanecarboxaldehyde
O
OH
2693
1,1-Cyclopropanedicarboxylic acid
2694
Cyclopropanemethanol
2695
Cyclopropanone
2696
Cyclopropene
2697
Cyclopropylamine
2698
Cyclopropylbenzene
2699
Cyclopropyl methyl ether
Physical Constants of Organic Compounds
3-140
Mol. Form.
CAS RN
Mol.
Wt.
Physical
Form
mp/˚C
bp/˚C
Cyclopropyl methyl ketone
C5H8O
765-43-5
84.117
liq
-68.2(0.4)
111(5)
C4H8N8O8
2691-41-0
296.156 cry
278(3)
C14H16ClN3O4S2
C11H22N2O
2259-96-3
2163-69-1
389.878
198.305 cry
234
138
C22H18Cl2FNO3
C5H12NO3PS2
C23H19ClF3NO3
68359-37-5 434.287
60-51-5
229.258
91465-08-6 449.850
60
51.4(0.2)
49.2
C18H34OSn
13121-70-5 385.172
196
2708
2709
2710
Cyclotetramethylenetetranitra- HMX
mine
Cyclothiazide
Cycluron
N’-Cyclooctyl-N,N-dimethylurea
Cyfluthrin
Cygon
Cyhalothrin
2,2-Dimethylcyclopropanecarboxylate
Cyhexatin
Stannane, tricyclohexylhydroxyCypermethrin
Cyprazine
Cyproheptadine
C22H19Cl2NO3
C9H14ClN5
C21H21N
70
170.4(0.5)
113
2711
Cyromazine
C6H10N6
52315-07-8 416.297
22936-86-3 227.694
129-03-3
287.399 cry (EtOH
aq)
66215-27-8 166.183 cry
2712
2713
2714
2715
Cystamine dihydrochloride
Cysteamine
L-Cysteic acid
L-Cysteine
C4H14Cl2N2S2
C2H7NS
C3H7NO5S
C3H7NO2S
56-17-7
60-23-1
13100-82-8
52-90-4
225.203
77.149
169.157
121.159
218 dec
99.5
260 dec
240 dec
2716
C5H12ClNO2S
868-59-7
185.673
2717
2718
L-Cysteine, ethyl ester,
hydrochloride
L-Cysteine, hydrochloride
L-Cystine
C3H8ClNO2S
C6H12N2O4S2
52-89-1
56-89-3
157.620 cry
175 dec
240.300 hex pl or pr 260 dec
(w)
2719
2720
Cytarabine
Cytidine
2721
2722
2723
2724
No.
Name
2700
2701
2702
2703
2704
2705
2706
2707
Synonym
Organic
N-Cyclopropyl-1,3,5-triazine2,4,6-triamine
Propanoic acid, 2-amino-3mercapto-, (R)-
3,3’-Dithiobis(2-aminopropanoic acid)
nd (MeOH)
cry (sub)
cry
cry (w)
147-94-4
65-46-3
243.216 pr (EtOH aq) 212
243.216 nd (dil al)
230 dec
2’-Cytidylic acid
3’-Cytidylic acid
5’-Cytidylic acid
Cytisine
C9H14N3O8P
C9H14N3O8P
C9H14N3O8P
C11H14N2O
85-94-9
84-52-6
63-37-6
485-35-8
323.196
323.196
323.196 orth nd
190.241 pr
2725
2726
Cytochalasin B
Cytochalasin D
Zygosporin A
C29H37NO5
C30H37NO6
2727
2728
Cytochalasin E
Cytosine
2729
Dacarbazine
14930-96-2 479.608 nd (ace)
22144-77-0 507.618 nd (ace/
peth)
36011-19-5 495.565
71-30-7
111.102 mcl or tcl pl
(w+1)
4342-03-4 182.182 cry
205
2730
2731
Dactinomycin
Daidzein
50-76-0
486-66-8
1255.416
254.238 pa ye pr
(50% al)
245 dec
323 dec
2732
Daminozide
1596-84-5
160.170
152.7(0.3)
2733
Dantrolene
2734
Datiscetin
C15H10O6
2735
2736
2737
Daucol
Daunorubicin
Dazomet
2738
2739
2740
2741
2742
Decabromobiphenyl ether
Decachlorobiphenyl
1,3-Decadiene
1,9-Decadiene
2,2’,3,3’,4,4’,5,5’,6,6’-Decafluoro-1,1’-biphenyl
cis-Decahydronaphthalene
2743
HCP_Section_03.indb 140
Bis(pentabromophenyl) ether
1-Hexyl-1,3-butadiene
cis-Decalin
7261-97-4
Solubility
sl H2O; s bz,
ace; vs MeOH
1170.1
1.27765
1.2520
vs H2O, EtOH
vs H2O, EtOH
s H2O; i EtOH
vs H2O, ace,
EtOH
vs H2O
dec
125.8
C9H13N3O5
C9H13N3O5
5-(3,3-Dimethyl-1-triazenyl)- C6H10N6O
1H-imidazole-4-carboxamide
C62H86N12O16
7-Hydroxy-3-(4C15H10O4
hydroxyphenyl)-4H-1-benzopyran-4-one
Butanedioic acid,
C6H12N2O3
mono(2,2-dimethylhydrazide)
C14H10N4O5
nD
0.898420 1.425120 vs H2O, eth,
EtOH
220
Cytosine arabinoside
4-Amino-1-β-D-ribofuranosyl2(1H)-pyrimidinone
Cytidine 2’-monophosphate
Cytidine 3’-monophosphate
Cytidine 5’-monophosphate
Sophorine
C28H33NO7
C4H5N3O
den
g cm –3
239 dec
233 dec
233 dec
153
s H2O
sl H2O; i EtOH,
eth, bz; s acid,
alk
s H2O
vs H2O; sl EtOH
1.67725
s H2O, EtOH
vs H2O, EtOH
vs H2O, EtOH,
MeOH; s bz,
ace
2182
219
270
207
265(1)
280
C15H26O2
C27H29NO10
C5H10N2S2
314.253 cry (DMF
aq)
480-15-9
286.236 pa ye nd (al,
aq HOAc)
887-08-1
238.366 cry
20830-81-3 527.520 red nd
533-74-4
162.276 nd (bz)
C12Br10O
C12Cl10
C10H18
C10H18
C12F10
1163-19-5
2051-24-3
2051-25-4
1647-16-1
434-90-2
959.167 ye pr (tol)
498.658 cry (bz)
138.250
138.250
334.112
305
306(1)
C10H18
493-01-6
138.250 liq
s H2O; sl EtOH,
chl; i eth
sub
s EtOH, eth
277.5
114
208
106
vs ace, eth,
EtOH
1282
reac H2O; s
EtOH
i H2O
i H2O
vs bz
67.3(0.8)
169
164(5)
207(2)
0.75230
0.7525
1.78520
-42.9(0.3)
195.8(0.3)
0.896520 1.481020 i H2O; msc
EtOH; vs eth,
ace, chl
1.432520
4/11/16 11:22 AM
Physical Constants of Organic Compounds
O
2700
3-141
O2N
N
NO2
N
Cl
H
N
N
O2N
N
NO2
O
S
H2N
O
S
Cl
N
N
2702
Cyclotetramethylenetetranitramine
2703
Cyclothiazide
2704
Cycluron
Cl
O
Cyfluthrin
N
H
2705
N
N
2707
Cyhalothrin
2708
Cyhexatin
Cypermethrin
NH2
N
N
N
N
N
H
2709
N
H
2710
Cyprazine
O
N
N
HCl H2N
NH2
2711
Cyproheptadine
S
S
2712
Cyromazine
SH
H2N
NH2 HCl
O
S
HO
O
2713
Cystamine dihydrochloride
OH
NH2
2714
Cysteamine
L-Cysteic acid
NH2
NH2
N
N
O
O
HS
HCl HS
OH
O
2715
2716
L-Cysteine
S
OH
NH2
2717
L-Cysteine, ethyl ester, hydrochloride
S
O
NH2
O
HO
O
HO
OH HCl
HS
NH2
NH2
NH2
O
L-Cystine
HO
O
Cytarabine
Cytidine
O
N
HO
O
O P OH
O
O
O
2721
N
HO
HO P O
O
OH
O
2724
N
O
Cytosine
NH
H 2N
N
N
N
2727
O
O
NH
O
HN
N
N
H
2729
Cytochalasin E
O
N
O
H
2725
N
O
O
O
2726
Cytochalasin B
O
N
O
2728
O
O
H
Cytisine
H
N H
O
OH
2723
N
H
O
NH
5’-Cytidylic acid
N
O
O
O
HN
NH
N
Cytochalasin D
O
N
NH2
O
O
H
O
HO
2731
Daidzein
O
N
2732
O
OH
N
OH
N
Dazomet
OH O
OH
2733
Cl Cl
O
HO
O
O
HO
2734
Dantrolene
Datiscetin
O
2735
Daucol
Cl Cl
2739
Decachlorobiphenyl
2736
2741
1,9-Decadiene
Br
Br
Br
Br
O
Br
F F
F
H
F
F
2740
1,3-Decadiene
Br
Br
Decabromobiphenyl ether
F
Cl
Br
2738
Daunorubicin
F
Cl
Br
Br
HO
NH2
HO
Cl
Cl
Cl
O
S
2737
O
N
O
Cl
O
N
S
NH
OH O
OH
Daminozide
Dactinomycin
O
O
O
H
N
O
2730
Dacarbazine
OH
O
N
O
N
O
HO
N H
N
NH2
O
O
HO
N
O
HO
2722
O
O
OH
3’-Cytidylic acid
O
O
O
N
O
HO
HO P O
O
2’-Cytidylic acid
H
OH
NH2
N
O
HO
OH
2720
NH2
N
HO
N
O
2719
OH
NH2
O
HO
OH
2718
L-Cysteine, hydrochloride
N
O
HO
F F
2742
F
2,2’,3,3’,4,4’,5,5’,6,6’-Decafluoro-1,1’-biphenyl
H
2743
cis-Decahydronaphthalene
Organic
HN
N
Cl
O
O
2706
Cygon
O
Cl
O
O
F
Cl
Sn
O
F
F
O
O
OH
O
S
P
S
O
O
O O
2701
Cyclopropyl methyl ketone
HN
NH
F
Cl
O
Physical Constants of Organic Compounds
3-142
Organic
No.
Name
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
Physical
Form
2744
trans-Decahydronaphthalene
trans-Decalin
C10H18
493-02-7
138.250 liq
2745
2746
Decahydro-2-naphthol
Decamethonium dibromide
Decahydro-β-naphthol
C10H18O
C16H38Br2N2
825-51-4
541-22-0
2747
2748
Decamethylcyclopentasiloxane
Decamethyltetrasiloxane
C10H30O5Si5
C10H30O3Si4
541-02-6
141-62-8
154.249
418.294 cry (MeOH/
ace)
370.770 liq
310.685 liq
2749
Decanal
C10H20O
112-31-2
2750
Decane
C10H22
2751
2752
2753
1,10-Decanediamine
Decanedinitrile
1,10-Decanediol
2754
2755
mp/˚C
bp/˚C
-30.35(0.06) 187.3(0.2)
10914
269 dec
den
g cm –3
-37.0(0.5)
-76
213(3)
194.4(0.1)
156.265 liq
-3.9(0.2)
212(3)
124-18-5
142.282 liq
-29.61(0.02) 174.1(0.1)
646-25-3
1871-96-1
112-47-0
172.311
59.7(0.4)
164.247
8.0(0.5)
174.281 nd (w, dil al) 72.4(0.2)
14012
20416
19220
0.91320
Decamethylene glycol
C10H24N2
C10H16N2
C10H22O2
Decanedioyl dichloride
Decanenitrile
Caprinitrile
C10H16Cl2O2
C10H19N
111-19-3
1975-78-6
239.139
153.265 liq
-1.3
-14.4(0.4)
22075
241(5)
1.121220
0.819920
2756
1-Decanethiol
Decyl mercaptan
C10H22S
143-10-2
174.347 liq
240(11)
0.844320
2757
Decanoic acid
Capric acid
C10H20O2
334-48-5
172.265 nd
-25.290​
(0.001)
31.39(0.02)
270(1)
0.885840
2758
1-Decanol
Capric alcohol
C10H22O
112-30-1
158.281 oily liq
7(1)
229(3)
0.829720
2759
2-Decanol
C10H22O
74742-10-2 158.281 liq
-2(1)
211
0.825020
2760
2761
3-Decanol
4-Decanol
1-Propylheptyl alcohol
C10H22O
C10H22O
1565-81-7
2051-31-2
158.281 liq
158.281 liq
-7.5
-11
217(7)
214(3)
0.82720
0.826120
2762
2763
5-Decanol
2-Decanone
Methyl octyl ketone
C10H22O
C10H20O
5205-34-5
693-54-9
158.281 liq
156.265 nd
8.7
14
216(5)
211(3)
0.82420
0.824820
2764
2765
3-Decanone
4-Decanone
Ethyl heptyl ketone
Hexyl propyl ketone
C10H20O
C10H20O
928-80-3
624-16-8
156.265 liq
156.265 liq
2(4)
-9(4)
212(4)
206.5
0.825120
0.82420
2766
2767
2768
Decanoyl chloride
trans-2-Decenal
1-Decene
Caprinoyl chloride
C10H19ClO
C10H18O
C10H20
112-13-0
3913-81-3
872-05-9
190.710 liq
154.249
140.266 liq
-34.5
2769
2770
2771
cis-2-Decene
trans-2-Decene
cis-5-Decene
C10H20
C10H20
C10H20
20348-51-0 140.266 col liq
20063-97-2 140.266 col liq
7433-78-5 140.266 col liq
-112(2)
174.2(0.7)
173.4(0.5)
170.4(0.8)
2772
trans-5-Decene
C10H20
7433-56-9
140.266 col liq
-73(1)
171.3(0.6)
2773
2774
2775
2776
2777
9-Decenoic acid
9-Decen-1-ol
3-Decen-2-one
Declomycin
Decyl acetate
Caproleic acid
Decylenic alcohol
Heptylidene acetone
Demeclocycline
C10H18O2
C10H20O
C10H18O
C21H21ClN2O8
C12H24O2
14436-32-9
13019-22-2
10519-33-2
127-33-3
112-17-4
170.249
156.265
154.249
464.853 cry
200.318 liq
26.5
15821
236
10215.3
176 dec
-15.0(0.4)
249(1)
2778
Decylamine
1-Decanamine
C10H23N
2016-57-1
157.297
15(1)
217(2)
2779
Decylbenzene
C16H26
104-72-3
218.377 liq
-14.40(0.08) 298(1)
2780
2781
Decylcyclohexane
Decylcyclopentane
C16H32
C15H30
1795-16-0
1795-21-7
224.425 liq
210.399 liq
-1.72(0.05) 298(1)
-22.11(0.05) 279(1)
2782
2783
2784
2785
2786
Decyl decanoate
Decyl formate
11-Decylheneicosane
1-Decylnaphthalene
Decyloxirane
C20H40O2
C11H22O2
C31H64
C20H28
C12H24O
1654-86-0
5451-52-5
55320-06-4
26438-27-7
2855-19-8
312.531
186.292 liq
436.840
268.436
184.318
10(2)
HCP_Section_03.indb 142
Capraldehyde
219(13)
230
-66.21(0.03) 171(1)
9.2(0.4)
15
21915
243
282.010
379
nD
Solubility
0.865925 1.469520 i H2O; vs EtOH,
eth, ace; msc
bz; sl MeOH
0.99625 1.499220
i eth
0.959320 1.398220 i H2O
0.853625 1.389520 i H2O; sl EtOH; s
bz, peth
0.83015 1.428720 i H2O; s EtOH,
eth, ace; sl ctc
0.726625 1.409025 i H2O; msc
EtOH; s eth; sl
ctc
0.91925
1.447420 i H2O; s chl
sl H2O, eth; vs
EtOH; s DMSO;
i lig
1.468418
1.429620 vs ace, eth,
EtOH, chl
1.450920 i H2O; s EtOH,
eth
1.428840 i H2O; vs ace,
bz, eth, EtOH
1.437220 i H2O; msc
EtOH, eth, ace,
bz, chl; s ctc
1.432625 s EtOH, bz; msc
eth, ace; sl ctc
1.43420
1.432020 i H2O; s EtOH,
ctc
1.433320
1.425520 i H2O; s EtOH,
eth; sl ctc
1.425220 s EtOH, eth, ctc
1.424021 i H2O; msc
EtOH, eth
1.441020 s eth, ctc
0.740820 1.421520 i H2O; msc
EtOH, eth
0.744520 1.425820 i H2O; msc
EtOH, eth; sl
ctc
0.740120 1.424320 i H2O; msc
EtOH, eth; sl
ctc
0.923815 1.450715 vs eth, EtOH
0.87625 1.448020
0.847320 1.448020
0.867120 1.427320 i H2O; s EtOH,
eth, bz, ctc,
HOAc
0.793620 1.436920 sl H2O; msc
EtOH, eth, ace,
bz, chl
0.855520 1.483220 vs ace, bz, eth,
EtOH
0.818620 1.453420
0.811020 1.448620 vs ace, bz, eth,
EtOH
0.858620 1.442320 vs eth
0.811620 1.454020
0.932220 1.543520
1.434725 sl ctc
4/11/16 11:22 AM
Physical Constants of Organic Compounds
3-143
Si
O
H
Br
OH
N
Si
O
N
O
Si
2745
2744
Si
2747
2746
Decahydro-2-naphthol
Si
O
Br
H
trans-Decahydronaphthalene
O
Si
O
Si
Si
O
2748
Decamethylcyclopentasiloxane
Decamethonium dibromide
Si
O
Decamethyltetrasiloxane
N
NH2
H2N
O
2749
2750
Decanal
2751
Decane
OH
HO
N
2752
1,10-Decanediamine
2753
Decanedinitrile
1,10-Decanediol
O
N
O
2754
2755
Decanedioyl dichloride
SH
OH
2756
Decanenitrile
2757
1-Decanethiol
Decanoic acid
OH
OH
OH
2758
OH
2760
2759
1-Decanol
2761
3-Decanol
2-Decanol
4-Decanol
O
OH
O
2762
O
2763
5-Decanol
2764
2-Decanone
2765
3-Decanone
4-Decanone
O
Cl
O
2766
2767
Decanoyl chloride
2768
trans-2-Decenal
2769
1-Decene
cis-2-Decene
O
OH
2771
2770
2772
cis-5-Decene
trans-2-Decene
Cl
trans-5-Decene
OH
H
H
OH O HO
N
OH
O
OH
3-Decen-2-one
O
O
NH2
O
2776
2775
9-Decen-1-ol
9-Decenoic acid
NH2
O
OH
2774
2773
2777
Declomycin
2778
Decyl acetate
Decylamine
O
O
2779
2780
Decylbenzene
Decylcyclohexane
2781
2782
Decylcyclopentane
Decyl decanoate
O
O
2783
Decyl formate
O
2784
11-Decylheneicosane
2785
1-Decylnaphthalene
2786
Decyloxirane
Organic
O
Cl
Cl
Physical Constants of Organic Compounds
3-144
No.
Name
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
2787
2788
Decyl vinyl ether
1-Decyne
1-(Ethenyloxy)decane
Octylacetylene
C12H24O
C10H18
765-05-9
764-93-2
2789
5-Decyne
Dibutylacetylene
C10H18
2790
Dehydroabietic acid
8,11,13-Abietatrien-18-oic
acid
2791
Physical
Form
Organic
mp/˚C
bp/˚C
184.318
138.250 liq
-41
-44
10110
174(6)
1942-46-7
138.250 liq
-74(4)
178(3)
C20H28O2
1740-19-8
172
Delphinidin
C15H11ClO7
528-53-0
300.435 cry (EtOH
aq)
338.697
2792
Delphinine
C33H45NO9
561-07-9
599.712 orth (al)
199
2793
2794
Deltamethrin
Demecarium bromide
C22H19Br2NO3
C32H52Br2N4O4
52918-63-5 505.199
56-94-0
716.588 hyg pow
2795
Demeton
C8H19O3PS2
8065-48-3
258.339 oily liq
1342
2796
2797
2798
C6H15O3PS2
C10H13N5O3
C10H16N5O12P3
919-86-8
958-09-8
1927-31-7
C6H8O5
528-81-4
230.285 ye liq
251.242
491.182 cry (EtOH
aq)
160.125 pr (AcOEt)
1181
2799
Demeton-S-methyl
2’-Deoxyadenosine
2’-Deoxyadenosine
5’-triphosphate
6-Deoxy-L-ascorbic acid
168
2800
Deoxycholic acid
C24H40O4
83-44-3
392.573 cry (al)
177
2801
C9H14N3O7P
1032-65-1
307.197 pow
183 dec
50-91-9
154-17-6
902-04-5
246.191 cry
164.156
347.222
150
146.5
2’-Deoxy-5’-guanylic acid
C9H11FN2O5
C6H12O5
C10H14N5O7P
D-Quercitol
N-Methylglucamine
C6H12O5
C7H17NO5
488-73-3
6284-40-8
164.156 pr (w, dil al) 236
195.214 cry (MeOH) 128.5
2807
2808
2809
2’-Deoxycytidine
5’-monophosphate
2’-Deoxy-5-fluorouridine
2-Deoxy-D-glucose
2’-Deoxyguanosine
5’-monophosphate
2-Deoxy-D-chiro-inositol
1-Deoxy-1-(methylamino)-Dglucitol
6-Deoxy-3-O-methylgalactose
D-2-Deoxyribose
Deserpidine
Digitalose
C7H14O5
C5H10O4
C32H38N2O8
4481-08-7
533-67-5
131-01-1
178.183 nd (AcOEt)
134.131
578.652 nd or pr
119
90
230.5
2810
Desethyl atrazine
C6H10ClN5
6190-65-4
187.630 cry
136
2811
Desferrioxamine
C25H48N6O8
70-51-9
2812
2813
2814
2815
2816
2817
Desipramine
Desmedipham
Desmetryne
Desthiobiotin
Dexamethasone
Dexon
2818
2819
2820
2802
2803
2804
2805
2806
Systox
3,12-Dihydroxycholan-24-oic
acid, (3α,5β,12α)
2’-Deoxy-5’-cytidylic acid
Floxuridine
6-Chloro-N-isopropyl-1,3,5triazine-2,4-diamine
Deferoxamine
den
g cm –3
nD
>350
vs H2O, EtOH,
MeOH; s
AcOEt
i H2O; s chl,
ace, eth; vs
EtOH
100.4(0.5)
165 dec
1.2020
1.506320
160 sub
s H2O
1.584513
vs H2O
s H2O
vs H2O
i H2O; s EtOH,
chl
C18H22N2
C16H16N2O4
C8H15N5S
C10H18N2O3
C22H29FO5
C8H10N3NaO3S
Dexpanthenol
C9H19NO4
81-13-0
205.252 hyg oil
C18H28N2O4S
C18H26BrNO
51-63-8
125-69-9
368.491
>300
352.309 wh cry pow 123
2821
Dextroamphetamine sulfate
Dextromethorphan
hydrobromide
Diacetone alcohol
C6H12O2
123-42-2
116.158 liq
-47(2)
167.9
0.938720 1.421320
2822
3,3-Diacetoxy-1-propene
C7H10O4
869-29-4
158.152 liq
-37.6
176(18)
1.076020 1.419320
2823
1,3-Diacetylbenzene
C10H10O2
6781-42-6
162.185
32
15215
2824
2825
1,4-Diacetylbenzene
4-Acetylacetophenone
N,N’-Diacetyl-4,4’-diaminobiphenyl
Diacetylmorphine
Diacetylperoxide
Acetyl peroxide
Dialifor
Diallate
Diallylcyanamide
C10H10O2
C16H16N2O2
1009-61-6
613-35-4
162.185
268.310 nd (HOAc)
113.0
328.3
1283
C21H23NO5
C4H6O4
C14H17ClNO4PS2
C10H17Cl2NOS
C7H10N2
561-27-3
110-22-5
10311-84-9
2303-16-4
538-08-9
369.412 orth
118.089 nd (eth) lf
393.846
270.219
122.167
173
30
68.1(0.5)
27312
6321
2826
2827
2828
2829
2830
HCP_Section_03.indb 144
4-Hydroxy-4-methyl-2-pentanone
vs H2O; sl ace; i
ace, eth
i H2O; s EtOH,
tol
i H2O; s os
sl H2O
vs H2O, ace,
EtOH
560.684 cry (EtOH
aq)
50-47-5
266.381
13684-56-5 300.309
1014-69-3 213.304 cry
533-48-2
214.261 lo nd (H2O)
50-02-2
392.460
140-56-7
251.238 ye-br pow
Sodium dimethylaminobenzenediazosulfonate
Solubility
0.81220 1.434620
0.765520 1.426520 i H2O; s EtOH,
eth
0.769020 1.433120 i H2O; s EtOH,
eth
139
1730.02
121.7(0.5)
85
157
262
s H2O
sl H2O; s DMF
dec
1.2020
1.49720
1.1525
1509
14290
1.5625
vs H2O, EtOH,
MeOH; sl eth
vs H2O
s EtOH, chl; i
eth
msc H2O, EtOH,
eth; s chl
vs ace, bz, eth,
EtOH
sl H2O, peth; s
EtOH, bz, chl,
HOAc
vs EtOH; sl chl
vs bz, chl
vs eth, EtOH
s EtOH; sl eth,
ctc
4/11/16 11:22 AM
Physical Constants of Organic Compounds
3-145
OH
OH
OH
O
HO
OH
OH
O
O
2787
O
N
O
O
O
Br
O
O
O
2793
Delphinine
HO
N
S
2795
Demeton
N
OH
N
O
O
P
O
O
O
P
OH
O
OH
O
O
N
N
P
NH2
N
N
CH2OH
OH
O
H
O
OH
OH
HO
OH
OH
O
HO
O
O
N
O
OH
H
2799
2’-Deoxyadenosine 5’-triphosphate
P
OH
HO
2798
2’-Deoxyadenosine
N
O
OH
2797
Demeton-S-methyl
O
S
O P O
O
Demecarium bromide
S
2796
Br
NH2
NH2
N
N
2794
Deltamethrin
N
Br
O
Br
2792
N
O
N
2801
2800
6-Deoxy-L-ascorbic acid
2’-Deoxycytidine 5’-monophosphate
Deoxycholic acid
O
O
F
HN
O
O
HO
H2N
OH
N
P
O
HO
O
O
OH HO
HO
OH
2802
H
OH
2803
OH
2805
2’-Deoxyguanosine 5’-monophosphate
CH2NHMe
OH
H
OH
OH
CH2OH
O
OH
O
OH
HO
OH
2806
2-Deoxy-D-chiro-inositol
O
HO
OH
2807
1-Deoxy-1-(methylamino)-D-glucitol
2808
6-Deoxy-3-O-methylgalactose
D-2-Deoxyribose
N
H
O
NH2
O
O
O
HO
2804
2-Deoxy-D-glucose
H
O
H
HO
H
H
OH
OH
OH
2’-Deoxy-5-fluorouridine
N
N
OH
O
N
H
N
HN
N
O
O
N
Cl
O
2809
O
N
H2N
N
H
OH
N
H
N
N
OH
Desferrioxamine
O
N
H
N
N
H
N
HO
N
OH
H
NH
O
N
H
N
H
2814
Desmedipham
Desipramine
O
HO
N
S
O
2813
2812
OH
HN
O
N
H
N
OH
2811
Desethyl atrazine
O
O
N
H
O
O
2810
Deserpidine
O
O
2815
Desmetryne
O
N N S O Na
O
N
F
O
2816
Desthiobiotin
2817
Dexamethasone
Dexon
O
O
HBr
OH
HO
O
H
N
OH
O
NH2
2818
2819
Dexpanthenol
0.5 H2SO4
Dextroamphetamine sulfate
H
2820
N
Dextromethorphan hydrobromide
OH O
O
O
O
2821
Diacetone alcohol
O
O
O
2822
2823
3,3-Diacetoxy-1-propene
1,3-Diacetylbenzene
2824
1,4-Diacetylbenzene
O
O
O
O
O
O
HN
NH
2825
N,N’-Diacetyl-4,4’-diaminobiphenyl
O
O
H
N
O
N
O
O
O
2826
Diacetylmorphine
2827
Diacetylperoxide
O
Cl
S
S P O
O
2828
Dialifor
O
Cl
S
N
N
N
Cl
2829
Diallate
2830
Diallylcyanamide
Organic
O
H
O
O P S
O
Delphinidin
O
N
O
2791
Dehydroabietic acid
O
H
H
2790
5-Decyne
1-Decyne
OH
O
2789
2788
Decyl vinyl ether
OH
Physical Constants of Organic Compounds
3-146
Organic
No.
Name
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
2831
Diethylene glycol bis(allyl
carbonate)
C12H18O7
142-22-3
274.267 col liq
2832
2833
2834
Diallyl diethylene glycol
carbonate
Diallyldimethylsilane
Diallyl disulfide
Diallyl ether
C8H16Si
C6H10S2
C6H10O
1113-12-8
2179-57-9
557-40-4
140.299
146.273
98.142 liq
2835
Diallyl fumarate
C10H12O4
2807-54-7
196.200
1403
2836
Diallyl isophthalate
C14H14O4
1087-21-4
246.259
1765
2837
2838
Diallyl maleate
Diallyl oxalate
C10H12O4
C8H10O4
999-21-3
615-99-6
196.200
170.163
12910
217
2839
N,N-Diallyl-2-propen-1-amine Triallylamine
C9H15N
102-70-5
137.222
94
2840
5,5-Diallyl-2,4,6(1H,3H,5H)pyrimidinetrione
Diallyl sulfide
Diallyl trisulfide
Diamantane
1,2-Diamino-9,10-anthracenedione
C10H12N2O3
52-43-7
208.213 lf
172(1)
C6H10S
C6H10S3
C14H20
C14H10N2O2
592-88-1
2050-87-5
2292-79-7
1758-68-5
114.208 liq
178.338
188.309 cry
238.241 viol nd
-85
2841
2842
2843
2844
Allyl ether
Di-2-propenyl 1,3-benzenedicarboxylate
Allobarbital
Congressane
Physical
Form
mp/˚C
bp/˚C
den
g cm –3
-4
1612
1.1420
-6
137.9(0.3)
10048
94(3)
0.767920 1.442020
1.023715
0.826020 1.416320 i H2O; msc
EtOH, eth; vs
ace; s chl
1.076820 1.467025 vs ace, bz, eth,
EtOH
1,4-Diamino-9,10-anthracenedione
C14H10N2O2
128-95-0
238.241 dk viol nd
(py)
268
2846
1,5-Diamino-9,10-anthracenedione
C14H10N2O2
129-44-2
238.241 dk red nd
(al, HOAc)
319
2847
1,8-Diamino-9,10-anthracenedione
C14H10N2O2
129-42-0
238.241 red nd (al,
HOAc)
265
2848
2,6-Diamino-9,10-anthracenedione
C14H10N2O2
131-14-6
238.241 red-br pr
(aq-py)
320 dec
2849
4,4’-Diaminoazobenzene
C12H12N4
538-41-0
2850
3,5-Diaminobenzoic acid
C7H8N2O2
535-87-5
212.250 ye nd (al),
250.5
oran-ye pr
(al)
152.151 nd (+1w)
228
2851
2,4-Diaminobutanoic acid
C4H10N2O2
305-62-4
118.134 hyg cry
118.1
2852
C4H4N4
1187-42-4
108.102
178.5
C14H10N2O4
128-94-9
270.240 bl nd (xyl)
2854
2855
cis-2,3-Diamino-2-butenedinitrile
1,8-Diamino-4,5-dihydroxy9,10-anthracenedione
4,4’-Diaminodiphenyl ether
4,4-Oxydianiline
4,4’-Diaminodiphenylmethane 4,4’-Methylenedianiline
C12H12N2O
C13H14N2
101-80-4
101-77-9
2856
4,4’-Diaminodiphenyl sulfide
C12H12N2S
139-65-1
200.235
192.2(0.2)
198.263 pl or nd (w) 90(1)
pl (bz)
216.301 nd (w)
108.5
2857
2858
3,3’-Diaminodiphenyl sulfone 3,3’-Sulfonyldianiline
meso-2,6-Diaminoheptane2,6-Diaminopimelic acid
dioic acid
1,4-Diamino-2-methoxy-9,10anthracenedione
1,4-Diamino-5-nitro-9,10anthracenedione
2,4-Diaminophenol
C12H12N2O2S
C7H14N2O4
599-61-1
922-54-3
248.300
190.197 nd (w)
168.5
314 dec
C15H12N2O3
2872-48-2
268.267
242(1)
C14H9N3O4
82-33-7
283.239
278
C6H8N2O
95-86-3
124.140 lf
79 dec
C6H10Cl2N2O
137-09-7
197.061 nd
235 dec
Thionine
C12H10ClN3S
581-64-6
263.745
Prontosil
C12H14ClN5O2S
103-12-8
327.790
249.5
Amsonic acid
C3H10N2O
C14H14N2O6S2
616-29-5
81-11-8
90.123 cry
370.400 ye nd
42.8
300
C3H5N5O
645-92-1
127.105 nd (aq
Na2CO3)
dec
2859
2860
2861
2862
2863
2864
2865
2866
2867
2,4-Diaminophenol,
dihydrochloride
3,7-Diaminophenothiazin-5ium chloride
4-[(2,4-Diaminophenyl)­azo]­
benzenesulfonamide
1,3-Diamino-2-propanol
4,4’-Diamino-2,2’-stilbenedisulfonic acid
4,6-Diamino-1,3,5-triazin2(1H)-one
HCP_Section_03.indb 146
4,4’-Thiodianiline
138(5)
11716
Solubility
i H2O; s os
1.07520 1.469920 s chl
1.158220 1.448120 i H2O; s EtOH,
ace, bz; sl chl
0.80920 1.450220 s EtOH, eth,
ace, bz, acid
sl H2O, DMSO; s
EtOH, eth, bz
0.887727 1.487025 vs eth, EtOH
1.084515
vs eth
244.73(0.05)
303.5
2845
2853
150(2)
nD
sl EtOH, eth,
chl, xyl; s py,
con sulf
sl H2O; s EtOH,
bz, PhNO2; vs
py
i H2O; sl EtOH,
eth, ace, bz; s
PhNO2
i H2O; s EtOH,
py; sl eth,
HOAc
sl H2O; s EtOH,
chl, con sulf,
xyl, py
sl H2O, lig; s
EtOH; vs bz,
chl
sl H2O, tfa; s
EtOH; vs eth
s H2O; sl EtOH,
MeOH
sub
1.4120
i H2O; s bz, xyl,
EtOH
>300
379(3)
sl H2O; vs EtOH,
eth, bz
sl H2O; vs EtOH,
eth, bz; s tfa
vs H2O, EtOH
s H2O
vs H2O, ace,
EtOH
vs H2O
sl H2O, EtOH,
eth; s bz, chl,
acid
sl H2O; s EtOH,
ace, oils, fats
i eth, bz
sl H2O
i H2O, EtOH, eth,
bz, HOAc; s
acid, alk
4/11/16 11:22 AM
Physical Constants of Organic Compounds
3-147
O
O
O
O
O
O
O
O
S
Si
O
2831
2832
Diallyl diethylene glycol carbonate
O
S
2833
Diallyldimethylsilane
2834
Diallyl disulfide
O
O
2835
Diallyl ether
Diallyl fumarate
O
O
O
O
O
O
O
2836
2838
Diallyl maleate
O
N
O
O
2837
Diallyl isophthalate
NH
O
O
2839
Diallyl oxalate
N,N-Diallyl-2-propen-1-amine
O
NH2
N
H
O
2840
5,5-Diallyl-2,4,6(1H,3H,5H )-pyrimidinetrione
O
NH2
O
O
NH2
NH2 O
Organic
O
O
NH2
NH2
S
S
2841
S
S
O
2842
Diallyl sulfide
2843
Diallyl trisulfide
NH2 O
NH2
2844
Diamantane
2845
1,2-Diamino-9,10-anthracenedione
O
O
NH2
O
2847
2848
1,8-Diamino-9,10-anthracenedione
NH2
H2N
2849
2,6-Diamino-9,10-anthracenedione
H2N
OH
NH2
NH2
2850
4,4’-Diaminoazobenzene
NH2 O
OH
H2N
N
N
2851
3,5-Diaminobenzoic acid
2,4-Diaminobutanoic acid
NH2
N
N
1,5-Diamino-9,10-anthracenedione
O
H2N
H2N
O
2846
1,4-Diamino-9,10-anthracenedione
O
NH2
OH O
2852
H2N
OH
2853
cis-2,3-Diamino-2-butenedinitrile
NH2
H2N
2854
1,8-Diamino-4,5-dihydroxy-9,10-anthracenedione
NH2
2855
4,4’-Diaminodiphenyl ether
4,4’-Diaminodiphenylmethane
NH2
O
S
H2N
H2N
O
S
O
O
NH2
HO
OH
NH2
NH2
2856
2857
4,4’-Diaminodiphenyl sulfide
O
3,3’-Diaminodiphenyl sulfone
NH2
O
O
NH2
O
2858
NH2
2859
meso-2,6-Diaminoheptanedioic acid
1,4-Diamino-2-methoxy-9,10-anthracenedione
OH
OH
NH2
NH2
N
O
N
O
O
2 HCl
NH2
2861
1,4-Diamino-5-nitro-9,10-anthracenedione
2862
2,4-Diaminophenol
N N
2864
O
S NH2
O
4-[(2,4-Diaminophenyl)azo]benzenesulfonamide
NH2 Cl
S
2863
2,4-Diaminophenol, dihydrochloride
OH
O S O
NH2
H2N
H2N
NH2
NH2
2860
3,7-Diaminophenothiazin-5-ium chloride
NH2
NH2
N
OH
H2N
NH2
2865
1,3-Diamino-2-propanol
O S O
OH
H2N
2866
4,4’-Diamino-2,2’-stilbenedisulfonic acid
O
N
N
H
2867
NH2
4,6-Diamino-1,3,5-triazin-2(1H )-one
Physical Constants of Organic Compounds
3-148
Mol.
Wt.
Physical
Form
Organic
No.
Name
Synonym
Mol. Form.
CAS RN
2868
8,8’-Diapo-ψ,ψ-carotenedioic
acid
Crocetin
C20H24O4
27876-94-4 328.403 brick red
orth
286
2869
Diatrizoic acid
C11H9I3N2O4
117-96-4
300
2870
2871
2872
2873
2874
2875
Diazenedicarboxamide
Diazinon
Diazomethane
Dibenz[a,h]acridine
Dibenz[a,j]acridine
Dibenz[c,h]acridine
N,N’-Diacetyl-3,5-diamino2,4,6-triiodobenzoic acid
Azodicarbonamide
C2H4N4O2
C12H21N2O3PS
CH2N2
C21H13N
C21H13N
C21H13N
123-77-3
333-41-5
334-88-3
226-36-8
224-42-0
224-53-3
2876
Dibenz[a,h]anthracene
C22H14
53-70-3
2877
Dibenz[a,j]anthracene
C22H14
224-41-9
278.346 oran lf or nd 198.2
(bz)
2878
Carbamazepine
C15H12N2O
298-46-4
236.268
190.2
2879
2880
2881
2882
2883
2884
5H-Dibenz[b,f]azepine-5carboxamide
Dibenzepin
7H-Dibenzo[c,g]carbazole
13H-Dibenzo[a,i]carbazole
Dibenzo[b,k]chrysene
Dibenzo[b,e][1,4]dioxin
Dibenzofuran
Diphenylene dioxide
2,2’-Biphenylene oxide
C18H21N3O
C20H13N
C20H13N
C26H16
C12H8O2
C12H8O
4498-32-2
194-59-2
239-64-5
217-54-9
262-12-4
132-64-9
295.379
267.324 cry (EtOH)
267.324
328.405
184.191 nd (MeOH)
168.191 lf or nd (al)
117
157(1)
221.3
400
117.5(0.2)
82.16(0.05)
2885
Dibenzo[a,e]pyrene
Naphtho[1,2,3,4-def]chrysene
C24H14
192-65-4
302.368 pa ye
nd(xyl)
247.0(0.6)
2886
2887
2888
Dibenzo[a,h]pyrene
Dibenzo[a,i]pyrene
Dibenzo[a,l]pyrene
Dibenzo[b,def]chrysene
Benzo[rst]pentaphene
Dibenzo[def,p]chrysene
C24H14
C24H14
C24H14
189-64-0
189-55-9
191-30-0
318(1)
283.6(0.3)
164.5
2750.05
2889
Dibenzothiophene
C12H8S
132-65-0
302.368 oran pl
302.368
302.368 ye pl (bz/
EtOH)
184.257 nd (dil al,
lig)
98.67(0.02)
331.6(0.4)
2890
Dibenz[c,e]oxepin-5,7-dione
C14H8O3
6050-13-1
2891
Dibenzoyl disulfide
Benzoyl disulfide
C14H10O2S2
644-32-6
2892
Dibenzylamine
N-Benzylbenzenemethanamine C14H15N
103-49-1
224.212 nd (HOAc or 217
bz)
274.358 pr(al),
134.5
sc(chlpeth)
197.276
-26(1)
2893
Dibenzyl disulfide
C14H14S2
150-60-7
246.391 lf (al)
68.6(0.2)
2894
N,N’-Dibenzyl-1,2-ethanediamine
Dibenzyl ether
Benzathine
C16H20N2
140-28-3
240.343 oily lig
26
1954
Benzyl ether
C14H14O
103-50-4
198.260 liq
1.8
298
C20H18O
897-78-9
274.356
117.5
19020
C17H16O4
C14H15O3P
C14H14S
-2.5
48.3(0.5)
1872
1620.1
335(6)
152
290 dec
2895
2896
7-Azadibenz[a,j]anthracene
1,2:5,6-Dibenzanthracene
613.913 cry (EtOH
aq)
116.079
304.345
42.040 ye gas
279.335 ye cry
279.335
279.335 ye cry
(EtOH)
278.346 pl (dil ace)
mp/˚C
bp/˚C
Solubility
225(1)
-145
226.6(0.7)
219.6(0.9)
189
870.05
-23
1.108820 1.492220
vs eth, diox
i H2O
269(6)
i H2O; sl EtOH; s
ace, bz, CS2
i H2O, HOAc; sl
EtOH, eth, bz;
s peth
1850.01
i H2O
285.2(0.3)
sub
dec
300 dec
2897
2898
2899
2900
Dibenzyl sulfone
C14H14O2S
15014-25-2 284.307
17176-77-1 262.241
538-74-9
214.326 pl (eth or
chl)
620-32-6
246.325 nd (al-bz)
2901
Dibenzyl sulfoxide
C14H14OS
621-08-9
230.325 lf (al, w)
135(3)
210 dec
2902
2903
N,N’-Dibenzylurea
Dibromoacetic acid
C15H16N2O
C2H2Br2O2
1466-67-7
631-64-1
240.300 nd (al)
217.844 hyg cry
170(1)
49
195250
2904
2905
Dibromoacetonitrile
2,4-Dibromoaniline
C2HBr2N
C6H5Br2N
3252-43-5
615-57-6
2906
2907
3,5-Dibromoaniline
9,10-Dibromoanthracene
C6H5Br2N
C14H8Br2
626-40-4
523-27-3
198.844
250.919 orth bipym 79.5
(chl) nd or
lf (al)
250.919 nd (dil al)
57
336.022 ye nd (to or 226
xyl)
HCP_Section_03.indb 148
nD
sl H2O, EtOH; i
eth, bz; s py;
vs NaOH
2,6-Dibenzylidenecyclohexanone
Dibenzyl malonate
Dibenzyl phosphite
Dibenzyl sulfide
Benzyl sulfide
den
g cm –3
169
15674
sub
1.088699 1.607999 i H2O; s EtOH,
ace, bz; vs
eth, HOAc
sl EtOH, ace, bz,
HOAc; s tol,
con sulf
i H2O; s chl,
MeOH; vs
EtOH, bz
i H2O; sl eth
i H2O; sl EtOH,
eth; s CS2
1.025622 1.578120 i H2O; vs EtOH,
eth; s ctc
sl H2O; s EtOH,
eth, bz, MeOH
1.02420 1.563520 vs bz, eth, EtOH
1.042820 1.561820 i H2O; msc
EtOH, eth; s
ctc
sl EtOH; s bz,
HOAc
1.13725 1.544720
1.552118
1.058350
i H2O; s EtOH,
eth, CS2
i H2O; sl EtOH;
vs ace; s bz,
HOAc
i H2O; vs EtOH,
eth
vs EtOH, HOAc
vs H2O; vs
EtOH, eth
2.36920 1.539320
2.26020
s EtOH, eth, chl,
HOAc
vs EtOH, eth, bz
i H2O; sl EtOH,
eth, bz; s chl
4/11/16 11:22 AM
Physical Constants of Organic Compounds
3-149
O
O
O
HO
OH
O
2868
OH
I
I
N
H
N
H
I
O
O
H2N
S
N
O P O
O
NH2
2870
Diatrizoic acid
N
N
O
2869
8,8’-Diapo-ψ,ψ-carotenedioic acid
N
H
C N
N
2871
Diazenedicarboxamide
2872
Diazinon
Diazomethane
N
N
O
N
2873
2875
Dibenz[a,j]acridine
2876
Dibenz[c,h]acridine
2877
Dibenz[a,h]anthracene
NH2
2878
Dibenz[a,j]anthracene
5H-Dibenz[b,f]azepine-5-carboxamide
Organic
Dibenz[a,h]acridine
2874
N
H
N
O
N
O
N
N
H
N
H
2879
2880
Dibenzepin
2881
7H-Dibenzo[c,g]carbazole
2882
13H-Dibenzo[a,i]carbazole
Dibenzo[b,k]chrysene
O
O
2883
2884
Dibenzo[b,e][1,4]dioxin
Dibenzofuran
O
O
O
S
2885
Dibenzo[a,e]pyrene
2886
2887
Dibenzo[a,h]pyrene
2888
Dibenzo[a,i]pyrene
2889
Dibenzo[a,l]pyrene
O
S
S
S
N
H
O
2891
2892
Dibenzoyl disulfide
S
O
O
O
2896
O
2895
N,N’-Dibenzyl-1,2-ethanediamine
O
P
O
Dibenzyl ether
S
O
O
2897
2,6-Dibenzylidenecyclohexanone
O
2894
Dibenzyl disulfide
O
Dibenz[c,e]oxepin-5,7-dione
H
N
N
H
2893
Dibenzylamine
2890
Dibenzothiophene
2898
Dibenzyl malonate
2899
Dibenzyl phosphite
Dibenzyl sulfone
NH2
S
O
2901
Dibenzyl sulfoxide
N
H
Br
Br
N
H
2902
N,N’-Dibenzylurea
Br
OH
Br
Br
O
Br
O
2900
Dibenzyl sulfide
O
S
NH2
N
2903
Dibromoacetic acid
Br
2904
Dibromoacetonitrile
2905
2,4-Dibromoaniline
Br
Br
2906
3,5-Dibromoaniline
Br
2907
9,10-Dibromoanthracene
Physical Constants of Organic Compounds
3-150
No.
Name
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
2908
o-Dibromobenzene
1,2-Dibromobenzene
C6H4Br2
583-53-9
2909
m-Dibromobenzene
1,3-Dibromobenzene
C6H4Br2
2910
p-Dibromobenzene
1,4-Dibromobenzene
2911
2912
4,4’-Dibromobenzophenone
4,4’-Dibromo-1,1’-biphenyl
Bis(4-bromophenyl) ketone
2913
2915
2916
2917
1,3-Dibromo-2,2Pentaerythritol tetrabromide
bis(bromomethyl)propane
3,5-Dibromo-N-(4Tribromsalan
bromophenyl)-2-hydroxybenzamide
1,1-Dibromobutane
1,2-Dibromobutane
α-Butylene dibromide
1,3-Dibromobutane
2918
Physical
Form
mp/˚C
bp/˚C
235.904
6(2)
220.4(0.3)
108-36-1
235.904 liq
-6.9(0.5)
214(14)
C6H4Br2
106-37-6
235.904 pl
87.3(0.1)
222(3)
C13H8Br2O
C12H8Br2
3988-03-2
92-86-4
177
164
394(24)
357.5
C5H8Br4
3229-00-3
C13H8Br3NO2
87-10-5
340.010 pl (al)
312.000 mcl pr
(MeOH)
387.734 cry (ace), nd
(lig)
449.921
C4H8Br2
C4H8Br2
C4H8Br2
62168-25-6 215.915
533-98-2
215.915 liq
107-80-2
215.915
-65.4(0.4)
158
161(4)
176.4(0.4)
1,4-Dibromobutane
C4H8Br2
110-52-1
215.915 liq
-21.1(0.5)
197(4)
2919
2920
2,3-Dibromobutane
trans-1,4-Dibromo-2-butene
C4H8Br2
C4H6Br2
5408-86-6
821-06-7
215.915 liq
213.899 pl (peth)
-24
53.4
158(5)
203
2921
1,4-Dibromo-2-butyne
C4H4Br2
2219-66-1
211.883
2922
α,α’-Dibromo-d-camphor
C10H14Br2O
514-12-5
310.025
2923
2924
2925
Dibromochlorofluoromethane
1,2-Dibromo-3-chloropropane
1,2-Dibromo-1-chloro-1,2,2trifluoroethane
2,2-Dibromo-2-cyanoacetamide
trans-1,2-Dibromocyclohexane, (±)1,10-Dibromodecane
Decamethylene dibromide
CBr2ClF
C3H5Br2Cl
C2Br2ClF3
353-55-9
96-12-8
354-51-8
226.270
236.333
276.277
C3H2Br2N2O
10222-01-2 241.868 cry (bz)
126
C6H10Br2
5183-77-7
241.951
-2.0
145100
C10H20Br2
4101-68-2
300.074 pl (al)
28
1619
C2H2Br2Cl2
75-81-0
256.751 liq
-26
195
C2H2Br2Cl2
683-68-1
256.751 liq
-26
195
CBr2Cl2
594-18-3
242.725
38
150.2
C2H2Br2F2
75-82-1
223.842 liq
-61.3
92.5
CBr2F2
75-61-6
-110.1
22.79(0.08)
2914
Organic
2926
2927
2928
2929
2930
2931
2932
2933
1,2-Dibromo-1,1-dichloroethane
1,2-Dibromo-1,2-dichloroethane
Dibromodichloromethane
1,2-Dibromo-1,1-difluoroethane
Dibromodifluoromethane
Genetron 132b-B2
160.29(0.05) 305.5
den
g cm –3
nD
226.4(0.5)
9215
61
50
80.3
200(13)
92.8(0.2)
1.78425 1.498825
1.791520 1.402520 i H2O; s eth, chl
1.80020 1.50720 i H2O; s eth, chl;
sl ctc
1.819925 1.516725 i H2O; sl ctc; s
chl
1.789322 1.513322 i H2O; s eth
sl H2O, chl; vs
EtOH, peth; s
ace
2.01418 1.58818 s eth, ace; vs
chl
1.85421
i H2O; vs EtOH,
eth, bz, chl; s
AcOEt
2.317322 1.457020
2.09314 1.55314 i H2O
1.775920 1.544519 vs ace, bz, eth,
EtOH
1.33530 1.492725 i H2O; sl EtOH; s
eth
2.13520 1.566220 vs ace, bz, eth,
EtOH
2.13520 1.566220 i H2O; s EtOH,
eth, ace, bz
2.4225
i H2O; s EtOH,
eth, ace, bz
2.223820 1.445620
C5H6Br2N2O2
77-48-5
C5H10Br2
5434-27-5
229.941
185(11)
2936
1,3-Dibromo-5,5-dimethylDibromantine
2,4-imidazolidinedione
1,3-Dibromo-2,2-dimethylpropane
1,12-Dibromododecane
209.816 vol liq or
gas
285.922
C12H24Br2
3344-70-5
328.127 nd (al,HOAc) 41
21515
2937
1,1-Dibromoethane
Ethylidene dibromide
C2H4Br2
557-91-5
187.861 liq
-63
109(4)
2.055520 1.512820
2938
1,2-Dibromoethane
Ethylene dibromide
C2H4Br2
106-93-4
187.861 liq
9.8(0.1)
131.3(0.3)
2.168325 1.535625
2939
cis-1,2-Dibromoethene
cis-1,2-Dibromoethylene
C2H2Br2
590-11-4
185.845 liq
-53
111(1)
2.246420 1.542820
2940
trans-1,2-Dibromoethene
trans-1,2-Dibromoethylene
C2H2Br2
590-12-5
185.845 liq
-6.5
107(3)
2.230820 1.550518
2941
2942
2943
1,2-Dibromo-1-ethoxyethane
1,2-Dibromoethyl acetate
(1,2-Dibromoethyl)benzene
C4H8Br2O
C4H6Br2O2
C8H8Br2
2983-26-8 231.914
24442-57-7 245.898 liq
93-52-7
263.958
1.732020 1.504420
1.9120
73(1)
8020
89.516
13319
2934
2935
HCP_Section_03.indb 150
Solubility
1.984320 1.615520 i H2O; s EtOH;
msc eth, ace,
bz, ctc
1.952320 1.608317 i H2O; s EtOH;
msc eth
2.26117 1.5742
i H2O; s EtOH,
bz; vs eth,
ace, CS2
vs bz, HOAc, chl
i H2O; sl EtOH; s
bz
2.59615
s EtOH, bz, tol;
sl eth, chl
s H2O, eth, ace,
bz
198 dec
1.677520 1.5090
i H2O; vs EtOH,
chl; s eth,
HOAc
i H2O; s EtOH,
ace, bz; sl chl;
vs eth
vs ace, bz, eth,
EtOH
i H2O; vs EtOH,
eth; s ace, bz,
chl
i H2O; vs EtOH,
eth; s ace, bz,
chl
vs EtOH, chl
s EtOH, eth, bz,
chl, HOAc,
MeOH, lig
4/11/16 11:23 AM
Physical Constants of Organic Compounds
3-151
Br
O
Br
Br
Br
Br
Br
Br
2908
2909
o-Dibromobenzene
2910
m-Dibromobenzene
Br
Br
2912
2911
p-Dibromobenzene
2913
4,4’-Dibromo-1,1’-biphenyl
4,4’-Dibromobenzophenone
1,3-Dibromo-2,2-bis(bromomethyl)propane
Br
Br
Br
Br
2914
2915
3,5-Dibromo-N-(4-bromophenyl)-2-hydroxybenzamide
2916
1,1-Dibromobutane
2921
1,3-Dibromobutane
2922
2919
1,4-Dibromobutane
2,3-Dibromobutane
F F
Br
Br
Cl
Cl
Br
2923
α,α’-Dibromo-d-camphor
1,4-Dibromo-2-butyne
Br
2918
Br
F
Br
O
Br
Br
Br
2917
1,2-Dibromobutane
Br
Br
Br
Br
trans-1,4-Dibromo-2-butene
O
N
Br
Br Br
2925
1,2-Dibromo-3-chloropropane
Br
2920
Cl F
2924
Dibromochlorofluoromethane
Br
1,2-Dibromo-1-chloro-1,2,2-trifluoroethane
Br
2926
2,2-Dibromo-2-cyanoacetamide
Cl
Br
Br
Br
2927
Cl Cl
2928
trans-1,2-Dibromocyclohexane, (±)-
F
F
2932
2931
Dibromodichloromethane
Br
O
N
Br
Br
2933
1,2-Dibromo-1,1-difluoroethane
1,2-Dibromo-1,2-dichloroethane
N
Br
Br
Cl
Br
2930
1,2-Dibromo-1,1-dichloroethane
O
Br
Cl
Br
Cl
2929
1,10-Dibromodecane
F
Br
Br
Br
NH2
Br
2934
Dibromodifluoromethane
Br
Br
Br
2935
1,3-Dibromo-5,5-dimethyl-2,4-imidazolidinedione
2936
1,3-Dibromo-2,2-dimethylpropane
1,12-Dibromododecane
Br
Br
Br
Br
2937
1,1-Dibromoethane
Br
Br
2938
1,2-Dibromoethane
Br
H
H
2939
cis-1,2-Dibromoethene
Br
H
H
2940
Br
trans-1,2-Dibromoethene
O
Br
Br
O
2941
1,2-Dibromo-1-ethoxyethane
Br
Br
O
2942
Br
1,2-Dibromoethyl acetate
2943
(1,2-Dibromoethyl)benzene
Organic
Br
Br
F
Br
Br
N
H
Br
Br
Br
Br
Br
OH O
Br
Br
Physical Constants of Organic Compounds
3-152
No.
Name
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
2944
Dibromofluoromethane
Fluorodibromomethane
CHBr2F
1868-53-7
191.825 liq
2945
2946
1,2-Dibromoheptane
1,7-Dibromoheptane
Heptamethylene dibromide
C7H14Br2
C7H14Br2
42474-21-5 257.994
4549-31-9 257.994
2947
2948
2949
2,3-Dibromoheptane
3,4-Dibromoheptane
1,2-Dibromo-1,1,2,3,3,3hexafluoropropane
1,2-Dibromohexane
1,6-Dibromohexane
C7H14Br2
C7H14Br2
C3Br2F6
21266-88-6 257.994
21266-90-0 257.994
661-95-0
309.830
C6H12Br2
C6H12Br2
624-20-4
629-03-8
3,5-Dibromosalicylaldehyde
C6H12Br2
C7H4Br2O2
3,5-Dibromosalicylic acid
2950
2951
2952
2953
Organic
2954
2955
2956
2957
3,4-Dibromohexane
3,5-Dibromo-2-hydroxybenzaldehyde
3,5-Dibromo-2-hydroxybenzoic acid
3,5-Dibromo-4-hydroxybenzonitrile
Dibromomethane
Physical
Form
mp/˚C
bp/˚C
den
g cm –3
-78
64.9
2.42120
41.7
228
247(12)
1.508620
1.530620
10117
10724
72.8
1.513920
1.518220
2.163020
-1.2
10336
245.5
89583-12-0 243.967
90-59-5
279.914 pa ye pr
86
8013
sub
1.577420 1.502420 vs bz, eth, chl
1.602525 1.505425 i H2O; s eth,
ace, chl; sl ctc
1.602720 1.504320
vs bz, eth, chl
C7H4Br2O3
3147-55-5
295.913 nd
228
Bromoxynil
C7H3Br2NO
1689-84-5
276.913
190.5(0.8)
Methylene bromide
CH2Br2
74-95-3
173.835 liq
-52.1(0.7)
97.0(0.6)
2,5-Dibromotoluene
C7H6Br2
615-59-8
249.931
6(1)
236(11)
2.496920 1.542020 sl H2O; msc
EtOH, eth, ace;
s ctc
1.812717 1.598218 i H2O
C7H6Br2
31543-75-6 249.931
-10(1)
10311
1.817625 1.596425
C7H6Br2
618-31-5
249.931
1.0
15623
6217
265 dec
139(2)
310
1.836528 1.614720 i H2O; msc
EtOH, eth
1.671720 1.572925
s chl
1.782720 1.511920 s EtOH, eth, chl
i H2O; s EtOH,
eth; sl HOAc
sl H2O; s HOAc
243.967
243.967 liq
2959
2960
2961
2962
2963
2,3-Dibromo-2-methylbutane
2,4-Dibromo-6-methylphenol
1,2-Dibromo-2-methylpropane
1,4-Dibromonaphthalene
C5H10Br2
C7H6Br2O
C4H8Br2
C10H6Br2
594-51-4
609-22-3
594-34-3
83-53-4
229.941
265.930 nd (peth)
215.915
285.963
7
58
10.5
83
2964
2,6-Dibromo-4-nitroaniline
C6H4Br2N2O2
827-94-1
207
2965
2,6-Dibromo-4-nitrophenol
C6H3Br2NO3
99-28-5
295.916 ye nd (al,
HOAc)
296.901 pa ye pr or
lf (al)
2966
2967
2968
1,9-Dibromononane
1,4-Dibromooctafluorobutane
1,8-Dibromooctane
C9H18Br2
C4Br2F8
C8H16Br2
4549-33-1
335-48-8
4549-32-0
286.047 liq
359.838
272.021
-22.5
15.5
269(10)
98(25)
271
2969
2970
2971
1,2-Dibromopentane
1,4-Dibromopentane
1,5-Dibromopentane
C5H10Br2
C5H10Br2
C5H10Br2
3234-49-9
626-87-9
111-24-0
229.941
229.941
229.941 liq
-34.4
-40.0(0.4)
179(13)
146150
222.3
2972
2973
2,4-Dibromopentane
2,4-Dibromophenol
C5H10Br2
C6H4Br2O
19398-53-9 229.941
615-58-7
251.903 nd (peth)
40(2)
7521
238.5
2974
2,6-Dibromophenol
C6H4Br2O
608-33-3
251.903 nd (w)
56.5
255
2975
1,2-Dibromopropane
C3H6Br2
78-75-1
201.888 liq
-55.4(0.3)
140(1)
2976
1,3-Dibromopropane
C3H6Br2
109-64-8
201.888 liq
-35(1)
164(1)
2977
2,2-Dibromopropane
C3H6Br2
594-16-1
201.888
2978
2979
2980
2,3-Dibromopropanoic acid
2,3-Dibromo-1-propanol
1,3-Dibromo-2-propanol
C3H4Br2O2
C3H6Br2O
C3H6Br2O
600-05-5
96-13-9
96-21-9
231.871
217.887
217.887 ye liq
2981
C9H15Br6O4P
126-72-7
697.610
2982
2983
2,3-Dibromo-1-propanol,
phosphate (3:1)
1,3-Dibromo-2-propanone
1,1-Dibromo-1-propene
C3H4Br2O
C3H4Br2
816-39-7
215.871 nd
13195-80-7 199.872
2984
2985
1,2-Dibromo-1-propene
2,3-Dibromo-1-propene
C3H4Br2
C3H4Br2
26391-16-2 199.872
513-31-5
199.872
HCP_Section_03.indb 152
Octamethylene dibromide
Propylene dibromide
DBP
Tris(2,3-dibromopropyl)
phosphate
1,3-Dibromoacetone
Solubility
1.468520 i H2O; s EtOH,
eth, ace, bz,
chl
1.498620
1.503420 i H2O; s eth,
ace, bz, ctc,
chl
1.499220
1.501020
i H2O
s ace
1,4-Dibromo-2-methylbenzene
2,4-Dibromo-1-methylbenzene
(Dibromomethyl)benzene
2958
nD
145 dec
i H2O; vs EtOH,
eth; sl ace, bz,
HOAc
113
66.5
16020
219
219 dec
26
9722
125
131.5
142(18)
1.422920
1.459425 1.497125 i H2O; s eth, ctc,
chl
1.66818
1.622220 1.508620
1.692825 1.510225 i H2O; s bz, chl;
sl ctc
1.665920 1.498720
2.070020
sl H2O, ctc; vs
EtOH, eth, bz
s H2O; vs EtOH,
eth
1.932420 1.520120 s EtOH, eth, chl;
sl ctc
1.970125 1.520425 i H2O; s EtOH,
eth, chl; sl ctc
1.88020
vs eth, EtOH,
chl
vs bz, eth, EtOH
2.12020
2.136420 1.549525 vs ace, eth,
EtOH
s chl
2.167018
vs eth, CS2
1.976720 1.526020 sl H2O; s bz,
ctc, chl
2.007620
2.034525 1.541625 i H2O; s eth,
ace, chl
4/11/16 11:23 AM
Physical Constants of Organic Compounds
3-153
Br
Br
F
Br
F Br
F
Br
Br
Br
Br
H
2944
2945
Dibromofluoromethane
Br
2946
1,2-Dibromoheptane
2947
1,7-Dibromoheptane
2948
2,3-Dibromoheptane
Br
Br
Br
F F F F
Br
Br
2949
3,4-Dibromoheptane
1,2-Dibromo-1,1,2,3,3,3-hexafluoropropane
2950
1,2-Dibromohexane
N
HO
O
Br
Br
O
OH
OH
Br
Br
Br
Br
2951
Br
2952
Br
Br
2953
3,4-Dibromohexane
Br
OH
Br
2956
3,5-Dibromo-4-hydroxybenzonitrile
3,5-Dibromo-2-hydroxybenzoic acid
H
H
2955
2954
3,5-Dibromo-2-hydroxybenzaldehyde
Br
2957
Dibromomethane
1,4-Dibromo-2-methylbenzene
Organic
1,6-Dibromohexane
Br
Br
OH
Br
Br
Br
NH2
Br
Br
Br
Br
Br
Br
Br
Br
2958
2,4-Dibromo-1-methylbenzene
2959
2961
2960
(Dibromomethyl)benzene
Br
Br
2,4-Dibromo-6-methylphenol
2,3-Dibromo-2-methylbutane
1,4-Dibromonaphthalene
1,2-Dibromo-2-methylpropane
N
O
Br
2963
2962
O
2964
2,6-Dibromo-4-nitroaniline
OH
Br
Br
F F F F
Br
O
N
Br
O
Br
2965
2966
2,6-Dibromo-4-nitrophenol
Br
2967
1,9-Dibromononane
Br
Br
F F F F
2968
1,4-Dibromooctafluorobutane
Br
Br
Br
2969
1,8-Dibromooctane
1,2-Dibromopentane
Br
2970
1,4-Dibromopentane
OH
Br
Br
Br
Br
2971
1,5-Dibromopentane
OH
Br
Br
O
Br
Br
Br
Br
2972
2973
2,4-Dibromopentane
2,4-Dibromophenol
2974
2,6-Dibromophenol
2975
Br
Br Br
1,2-Dibromopropane
Br
OH
Br
2976
1,3-Dibromopropane
Br
OH
Br
2977
2978
2,2-Dibromopropane
2,3-Dibromopropanoic acid
Br
2979
2,3-Dibromo-1-propanol
Br
Br
Br
Br
Br
OH
2980
1,3-Dibromo-2-propanol
O
O P O
O
Br
2981
Br
Br
2,3-Dibromo-1-propanol, phosphate (3:1)
Br
O
Br
Br
2982
1,3-Dibromo-2-propanone
Br
Br
2983
1,1-Dibromo-1-propene
Br
Br
Br
2984
1,2-Dibromo-1-propene
2985
2,3-Dibromo-1-propene
Physical Constants of Organic Compounds
3-154
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
C5H3Br2N
625-92-3
C9H5Br2NO
521-74-4
Physical
Form
No.
Name
mp/˚C
bp/˚C
2986
3,5-Dibromopyridine
236.893 nd (al)
112
222
2987
5,7-Dibromo-8-quinolinol
Broxyquinoline
302.950 nd (al)
196
sub
2988
2989
2,6-Dibromoquinone-4chlorimide
1,14-Dibromotetradecane
2,6-Dibromo-4-(chloroimino)- C6H2Br2ClNO
2,5-cyclohexadien-1-one
Tetradecamethylene dibromide C14H28Br2
2990
2991
2992
1,2-Dibromotetrafluoroethane Refrigerant 114B2
2,3-Dibromothiophene
2,5-Dibromothiophene
C2Br2F4
C4H2Br2S
C4H2Br2S
299.347 ye pr (al or
HOAc)
37688-96-3 356.180 lf (al-eth)
cry (al)
124-73-2
259.823 liq
3140-93-0 241.932 liq
3141-27-3 241.932 liq
2993
2994
C4H2Br2S
C2HBr2F3
3141-26-2
354-04-1
C7H4Br2O5
602-92-6
2996
3,4-Dibromothiophene
1,2-Dibromo-1,1,2-trifluoro- Halon 2302
ethane
2,6-Dibromo-3,4,5-trihydroxy- Dibromogallic acid
benzoic acid
3,5-Dibromo-L-tyrosine
C9H9Br2NO3
2997
2998
2999
3000
3001
3002
Dibucaine
Dibucaine hydrochloride
1,4-Dibutoxybenzene
1,2-Dibutoxyethane
Dibutoxymethane
Dibutyl adipate
3003
537-45-1
den
g cm –3
83
1908
-110(1)
-17.5
-6
47.1(0.2)
218.5
210.3
2.14223
241.932
241.832
4.5
217(17)
76(4)
2.27427
150
300-38-9
327.912 nd, pr or lf
(w+1)
338.980 nd or pl
Ethylene glycol dibutyl ether
Butylal
Dibutyl hexanedioate
C20H29N3O2
C20H30ClN3O2
C14H22O2
C10H22O2
C9H20O2
C14H26O4
85-79-0
61-12-1
104-36-9
112-48-1
2568-90-3
105-99-7
343.463 hyg cry
379.924
222.324
174.281 liq
160.254 liq
258.354
64
94 dec
45.5
-69.1
-59(1)
-32.4
15815
198(10)
179.7(0.7)
16510
Dibutylamine
N-Butylbutanamine
C8H19N
111-92-2
129.244 liq
-61.8(0.5)
162(2)
3004
3005
3006
Di-sec-butylamine
2-Dibutylaminoethanol
N,N-Dibutylaniline
N-sec-Butyl-2-butanamine
C8H19N
C10H23NO
C14H23N
626-23-3
102-81-8
613-29-6
129.244
173.296
205.340 liq
-32.2(0.2)
135(7)
11418
274.8
3007
1,4-Di-tert-butylbenzene
C14H22
1012-72-2
190.325 nd (MeOH)
77.63(0.04)
237.3(0.5)
3008
2,5-Di-tert-butyl-1,4-benzenediol
Dibutylbis(dodecylthio)­
stannane
Dibutyl carbonate
C14H22O2
88-58-4
213.5
C32H68S2Sn
1185-81-5
222.324 cry (aq
HOAc)
635.722 col liq
C9H18O3
542-52-9
174.237
Organic
3009
3010
Cinchocaine
Dibutyltin bis(dodecyl sulfide)
245
174(14)
3013
C14H20O2
719-22-2
220.308
69
600.01
C17H29NO
88-27-7
263.418 pl (EtOH)
94
17940
C12H20O4Sn
78-04-6
346.995 ye solid
110
3016
2,6-Di-tert-butyl-2,5-cyclohexadiene-1,4-dione
2,6-Di-tert-butyl-4(dimethylaminomethyl)phenol
2,2-Dibutyl-1,3,2-dioxastannepin-4,7-dione
Dibutyl disulfide
C8H18S2
629-45-8
178.359 oil
3017
3018
Di-tert-butyl disulfide
cis-1,2-Di-tert-butylethene
C8H18S2
C10H20
110-06-5
692-47-7
178.359
140.266 liq
3019
Dibutyl ether
C8H18O
142-96-1
130.228 liq
3020
3021
3022
Di-sec-butyl ether
Di-tert-butyl ether
N,N’-Di-tert-butylethylenediamine
2,6-Di-tert-butyl-4-ethylphenol
N,N-Dibutylformamide
Dibutyl fumarate
N,N’-Dibutyl-1,6-hexanediamine
3,5-Di-tert-butyl-2-hydroxybenzoic acid
C8H18O
C8H18O
C10H24N2
6863-58-7
6163-66-2
4062-60-6
C16H26O
3024
3025
3026
3027
HCP_Section_03.indb 154
0.831925 1.411225
0.833920 1.407217
0.961320 1.436920 i H2O; msc
EtOH, eth
0.767020 1.417720 s H2O, ace, bz;
vs EtOH, eth
0.753420 1.416220 vs H2O; s EtOH
0.903720 1.518620 i H2O; msc
EtOH, eth; vs
ace, bz; s ctc
0.985020
i H2O; s EtOH,
eth
0.925120 1.411720 i H2O; s EtOH,
eth
vs EtOH
i H2O; s EtOH,
eth, bz, chl,
HOAc
40
152.5
3023
s chl
s ctc
203(4)
34619-03-9 174.237 cry (al)
2460-77-7 220.308 ye cry (al)
N,N’-Di-tert-butylethanediamine
1.419124
1.0520
C9H18O3
C14H20O2
cis-2,2,5,5-Tetramethyl-3hexene
Butyl ether
1.36125
1.630422
1.628820 i H2O; vs EtOH,
eth; s ctc
1220.3
Di-tert-butyl carbonate
2,5-Di-tert-butyl-2,5-cyclohexadiene-1,4-dione
3015
2.14925
vs eth, EtOH,
chl
i H2O
vs H2O, eth,
EtOH
sl H2O, EtOH; i
eth; s alk, acid
3011
3012
3014
Solubility
sl H2O; s EtOH,
eth
i H2O; s EtOH,
ace, bz, chl,
HOAc; sl eth
vs EtOH
50.4
2995
nD
s tol, hp
236(4)
0.93820
-2.5
8821
144(6)
0.922620
0.74420
-96(3)
141.6(0.3)
130.228 liq
130.228 liq
172.311 cry
53.3
121.9(0.3)
107.1(0.7)
189
0.768420 1.399220 i H2O; msc
EtOH, eth; vs
ace; sl ctc
0.75625
0.765820 1.394920
0.69
4130-42-1
234.376
44
272
C9H19NO
C12H20O4
C14H32N2
761-65-9
105-75-9
4835-11-4
157.253
228.285 liq
228.417
-18.0(0.4)
281(4)
1383.5
C15H22O3
19715-19-6 250.334
163.3
1.492320 i H2O; msc
EtOH, eth
1.489920
1.427020
i alk
s ctc, CS2
0.977520 1.446920 i H2O; s ace, chl
1.447025
s chl
4/11/16 11:23 AM
Physical Constants of Organic Compounds
O
Br
Br
Br
N
Br
N
OH
2986
2987
3,5-Dibromopyridine
N
F
F
Br
Cl
Br
2988
5,7-Dibromo-8-quinolinol
2,6-Dibromoquinone-4-chlorimide
Br
2992
2993
2,5-Dibromothiophene
N
H
N
O
N
OH
OH
NH2
O
OH
2995
1,2-Dibromo-1,1,2-trifluoroethane
2,3-Dibromothiophene
Br
N
2996
2,6-Dibromo-3,4,5-trihydroxybenzoic acid
O
2997
3,5-Dibromo-L-tyrosine
Dibucaine
O
H
N
O
HO
2994
3,4-Dibromothiophene
Br
HO
Br
F
F
S
2991
1,2-Dibromotetrafluoroethane
Br
Br
S
OH
Br
F
Br
S
Br
F
2990
1,14-Dibromotetradecane
Br
Br
Br
F
2989
O
Br
Br
Organic
Br
Br
3-155
N
HCl
O
O
O
2998
Dibucaine hydrochloride
O
O
3000
2999
O
O
3001
1,2-Dibutoxyethane
1,4-Dibutoxybenzene
O
O
O
3002
Dibutoxymethane
Dibutyl adipate
OH
N
N
H
H
N
N
3004
3005
OH
3003
Dibutylamine
Di-sec-butylamine
OH
3006
3007
N,N-Dibutylaniline
2-Dibutylaminoethanol
1,4-Di-tert-butylbenzene
3008
2,5-Di-tert-butyl-1,4-benzenediol
O
O
Sn S
S
O
3009
O
O
O
3010
Dibutylbis(dodecylthio)stannane
O
O
3011
Dibutyl carbonate
3012
Di-tert-butyl carbonate
2,5-Di-tert-butyl-2,5-cyclohexadiene-1,4-dione
OH
O
O
O
Sn
O
N
O
3013
3014
2,6-Di-tert-butyl-2,5-cyclohexadiene-1,4-dione
S
O
2,6-Di-tert-butyl-4-(dimethylaminomethyl)phenol
3015
S
S
3016
2,2-Dibutyl-1,3,2-dioxastannepin-4,7-dione
S
3017
Dibutyl disulfide
Di-tert-butyl disulfide
OH
O
O
3018
cis-1,2-Di-tert-butylethene
3019
3020
Dibutyl ether
Di-sec-butyl ether
H
N
O
3021
N
H
3022
Di-tert-butyl ether
N,N’-Di-tert-butylethylenediamine
3023
2,6-Di-tert-butyl-4-ethylphenol
O
OH
OH
O
O
O
O
N
3024
N,N-Dibutylformamide
H
N
N
H
O
3025
Dibutyl fumarate
3026
N,N’-Dibutyl-1,6-hexanediamine
3027
3,5-Di-tert-butyl-2-hydroxybenzoic acid
Physical Constants of Organic Compounds
3-156
Mol. Form.
CAS RN
Mol.
Wt.
Di-tert-butyl ketone
C9H18O
815-24-7
3029
3030
Dibutyl maleate
Dibutyl malonate
C12H20O4
C11H20O4
3031
3032
3033
Di-tert-butyl malonate
Dibutylmercury
2,4-Di-tert-butyl-5-methylphenol
3034
2,4-Di-tert-butyl-6-methylphenol
2,6-Di-tert-butyl-4-methylphenol
No.
Name
3028
3035
Synonym
DBMC
Physical
Form
Organic
mp/˚C
bp/˚C
142.238 liq
-25.2(0.2)
152(4)
105-76-0
1190-39-2
228.285
216.275 liq
<-80
-95(3)
280
253(11)
C11H20O4
C8H18Hg
C15H24O
541-16-2
629-35-6
497-39-2
216.275
314.82
220.351
-6
62.1
11331
223
282
C15H24O
616-55-7
220.351
51
269
C15H24O
128-37-0
220.351
70.1(0.8)
265
C17H32O4
C10H18O4
2917-73-9
2050-60-4
300.434
202.248 liq
-30.5
1702
244(3)
C8H18O2
110-05-4
146.228 liq
-40
110.0(0.2)
257.5
262(1)
16150
den
g cm –3
nD
0.982420 1.426220 i H2O; s EtOH,
eth, ace, bz,
HOAc, ctc
1.418420 1.418429 s ace, chl
1.777920 1.505720
0.91280
i H2O; s EtOH,
eth, ace, bz,
ctc
0.89180
i alk
0.893775 1.485975 i H2O; s EtOH,
ace, bz, peth; i
alk
sl chl
0.987320 1.423420 i H2O; s EtOH,
eth
0.70420 1.389020 i H2O; msc ace;
s ctc, lig
1.508020
1.508020 sl ctc; i alk
1.500120 sl EtOH; s ctc; i
alk
3036
3037
Dibutyl nonanedioate
Dibutyl oxalate
3038
Di-tert-butyl peroxide
3039
3040
3041
2,6-Di-sec-butylphenol
2,4-Di-tert-butylphenol
2,6-Di-tert-butylphenol
C14H22O
C14H22O
C14H22O
5510-99-6
96-76-4
128-39-2
206.324 liq
206.324
206.324 pr (al)
-42
58(1)
37.5(0.3)
3042
3043
3044
3045
3,5-Di-tert-butylphenol
Dibutyl phosphate
Dibutyl phosphonate
Dibutyl phthalate
C14H22O
C8H19O4P
C8H19O3P
C16H22O4
1138-52-9
107-66-4
1809-19-4
84-74-2
206.324
210.208 oil
194.209 oil
278.344 liq
88
3046
3047
3048
2,6-Di-tert-butylpyridine
Dibutyl sebacate
Dibutyl succinate
C13H21N
C18H34O4
C12H22O4
585-48-8
109-43-3
141-03-7
191.313
314.461 liq
230.301 liq
3049
3050
3051
Di-tert-butyl succinate
Dibutyl sulfate
Dibutyl sulfide
C12H22O4
C8H18O4S
C8H18S
926-26-1
625-22-9
544-40-1
230.301
210.292 liq
146.294 liq
3052
Di-sec-butyl sulfide
C8H18S
626-26-6
146.294
3053
3054
3055
Di-tert-butyl sulfide
Dibutyl sulfite
Dibutyl sulfone
C8H18S
C8H18O3S
C8H18O2S
107-47-1
626-85-7
598-04-9
146.294 liq
194.292
178.293
44(1)
152.3(0.8)
230
291
3056
Dibutyl sulfoxide
C8H18OS
2168-93-6
162.293 nd (dil al)
32(3)
290(13)
3057
Dibutyl tartrate
C12H22O6
87-92-3
262.299 pr
22
320
3058
3059
3060
N,N’-Dibutylthiourea
Dibutyltin dichloride
Dibutyltin dilaurate
C9H20N2S
C8H18Cl2Sn
C32H64O4Sn
109-46-6
683-18-1
77-58-7
188.333 nd (al)
64(1)
303.845 solid
43.0(0.2)
631.558 ye liq or cry 23
3061
Dicapthon
C8H9ClNO5PS
2463-84-5
297.653 cry (MeOH)
50.5(0.9)
3062
3063
3064
Dicentrine
Dichlofenthion
Dichlofluanid
C20H21NO4
C10H13Cl2O3PS
C9H11Cl2FN2O2S2
517-66-8
97-17-6
1085-98-9
339.386
315.153
333.229 wh pow
105.3
3065
3066
Dichloroacetaldehyde
2,2-Dichloroacetamide
C2H2Cl2O
C2H3Cl2NO
79-02-7
683-72-7
112.942
127.957
90.5
234
1.43625
99.4
3067
Dichloroacetic acid
C2H2Cl2O2
79-43-6
128.942 liq
12(3)
193(3)
1.563420 1.465820
3068
3069
Dichloroacetic anhydride
1,1-Dichloroacetone
C4H2Cl4O3
C3H4Cl2O
4124-30-5
513-88-2
239.869
126.969
18.0
215 dec
120
1.57424
1.30418
3070
3071
1,3-Dichloroacetone
Dichloroacetonitrile
C3H4Cl2O
C2HCl2N
534-07-6
3018-12-0
126.969 pr or nd
109.942
45
173.4
112.5
1.382646 1.471640
1.36920 1.439125
HCP_Section_03.indb 156
DTBP
Butyl phthalate
Butyl sebacate
Butyl sulfate
Butyl sulfide
Butyl sulfite
Dibutyldichlorostannane
-35
1360.05
230
338(9)
-9.2(0.5)
-29.2
12020
356(9)
269(3)
1099
1156
-74.97(0.05) 168(4)
Solubility
0.824018 1.419420 i H2O; s EtOH,
eth, ace, chl,
HOAc
1.0620
s ctc, BuOH
0.98525 1.422020
1.046520 1.491120 i H2O; msc
EtOH, eth, bz;
s ctc
0.940515 1.443315 i H2O; s eth, ctc
0.975220 1.429920 i H2O; s EtOH,
eth, bz, ctc
36.5
167(1)
-9.0
0.838620 1.453020 vs eth, EtOH,
chl
0.834820 1.450620 i H2O; vs EtOH,
eth
0.81525 1.450620
0.995720 1.431020 s EtOH, eth
0.988547
i H2O; s EtOH,
eth
0.831723 1.466920 i H2O; s EtOH,
eth
1.090920 1.445120 vs H2O, ace,
EtOH
13510
s hx, eth, thf
i H2O, MeOH; s
eth, bz, ctc
i H2O; s ace, tol,
xyl, AcOEt
s chl
s ctc, CS2
i H2O; s ace,
MeOH, xyl
sl EtOH
s H2O, EtOH,
eth; sl ace
msc H2O, EtOH,
eth; s ace; sl
ctc
sl H2O; s EtOH;
msc eth
s H2O, EtOH, eth
s MeOH
4/11/16 11:23 AM
Physical Constants of Organic Compounds
3-157
O
O
O
O
3028
3029
Di-tert-butyl ketone
O
O
O O
O
3030
Dibutyl maleate
O
O
O
Hg
O
3031
Dibutyl malonate
3032
Di-tert-butyl malonate
Dibutylmercury
OH
OH
OH
O
O
O
3033
3034
2,4-Di-tert-butyl-5-methylphenol
3035
2,4-Di-tert-butyl-6-methylphenol
O
3036
2,6-Di-tert-butyl-4-methylphenol
Dibutyl nonanedioate
OH
OH
OH
O
O
O
O
3037
O
3038
Dibutyl oxalate
OH
Organic
O
3039
Di-tert-butyl peroxide
3040
2,6-Di-sec-butylphenol
3041
2,4-Di-tert-butylphenol
3042
2,6-Di-tert-butylphenol
3,5-Di-tert-butylphenol
O
O
O
O
P
O
O
H
O
P
O
O
OH
3043
3044
Dibutyl phosphate
N
O
3045
Dibutyl phosphonate
O
O
O
O
O
O
O
3049
Dibutyl succinate
S
S
3052
3053
O
Dibutyl sulfide
Di-sec-butyl sulfide
O
OH
O
3055
Dibutyl sulfone
S
O
N
H
3057
Dibutyl sulfoxide
O
S
O
Dibutyl sulfite
OH O
3056
Dibutyl sulfate
3054
Di-tert-butyl sulfide
O
S
O
O
S
Cl
Sn
Cl
N
H
3058
Dibutyl tartrate
O
S
O
O
3050
Di-tert-butyl succinate
S
3051
O
O
O
3048
Dibutyl sebacate
2,6-Di-tert-butylpyridine
O
O
O
3047
3046
Dibutyl phthalate
3059
N,N’-Dibutylthiourea
Dibutyltin dichloride
O
O
O
Sn
O
O
N
3060
O
Dichlofluanid
3065
Dichloroacetaldehyde
Cl
NH2
OH
Cl
Cl
3066
3067
2,2-Dichloroacetamide
Cl
Dichloroacetic acid
Cl
O
O
O
Cl
Dichlofenthion
Cl
Cl
O
3068
P
O
Cl
O
S
3063
Dicentrine
O
Cl
Cl
3062
Dicapthon
O
Cl
3064
O
3061
Dibutyltin dilaurate
Cl
O
O
O
O
N
O S OF
Cl
N
S
Cl
Cl
N
H
O
S
O
P
O
O
Dichloroacetic anhydride
Cl
3069
1,1-Dichloroacetone
Cl
Cl
3070
N
Cl
O
1,3-Dichloroacetone
Cl
3071
Dichloroacetonitrile
Physical Constants of Organic Compounds
3-158
Organic
Mol. Form.
CAS RN
Mol.
Wt.
C2HCl3O
79-36-7
147.387
C2Cl2
C7H5Cl2NO4S
7572-29-4
80-13-7
94.927 liq
270.091 pr (HOAc)
-66
195 dec
33
C6H5Cl2N
608-27-5
162.017 nd (lig)
24
252
2,4-Dichloroaniline
C6H5Cl2N
554-00-7
3077
2,5-Dichloroaniline
C6H5Cl2N
95-82-9
162.017 pr (ace) nd 63(4)
(dil al) (lig)
162.017 nd (lig)
44.9(0.2)
3078
2,6-Dichloroaniline
C6H5Cl2N
608-31-1
162.017
39
3079
3,4-Dichloroaniline
C6H5Cl2N
95-76-1
162.017 nd (lig)
72.0(0.5)
273.0(0.5)
3080
3,5-Dichloroaniline
C6H5Cl2N
626-43-7
52
261
3081
9,10-Dichloroanthracene
C14H8Cl2
605-48-1
3082
1,5-Dichloro-9,10-anthracenedione
C14H6Cl2O2
82-46-2
162.017 nd (lig, dil
al)
247.120 ye nd
(MeCOEt
or CCl4)
277.103 ye nd (to)
3083
C14H6Cl2O2
82-43-9
202.5
C12H8Cl2N2
1602-00-2
277.103 ye nd
(HOAc)
251.111 ye nd (ace)
3085
3086
3087
1,8-Dichloro-9,10-anthracenedione
trans-4,4’-Dichloroazobenzene
4,4’-Dichloroazoxybenzene
2,3-Dichlorobenzaldehyde
2,4-Dichlorobenzaldehyde
C12H8Cl2N2O
C7H4Cl2O
C7H4Cl2O
614-26-6
6334-18-5
874-42-0
267.110 ye nd (EtOH) 158
175.012 cry (dil al)
66
175.012 pr
74.1(0.3)
10515
3088
3089
2,6-Dichlorobenzaldehyde
3,4-Dichlorobenzaldehyde
C7H4Cl2O
C7H4Cl2O
83-38-5
6287-38-3
175.012 nd (lig)
175.012
69(3)
44
247.5
3090
3,5-Dichlorobenzaldehyde
C7H4Cl2O
65
240
3091
3092
2,6-Dichlorobenzamide
o-Dichlorobenzene
1,2-Dichlorobenzene
C7H5Cl2NO
C6H4Cl2
10203-08-4 175.012 nd or lf (dil
HOAc)
2008-58-4 190.027 cry
95-50-1
147.002 liq
198
-17.0(0.1)
180.2(0.3)
3093
m-Dichlorobenzene
1,3-Dichlorobenzene
C6H4Cl2
541-73-1
147.002 liq
-24.8(0.3)
172(2)
3094
p-Dichlorobenzene
1,4-Dichlorobenzene
C6H4Cl2
106-46-7
147.002 mcl pr, lf
(ace)
53.1(0.2)
173.9(0.2)
3095
C6H6Cl2N2
20103-09-7 177.031 pr (w)
170
C6H6Cl2N2
609-20-1
C6H4Cl2O2
177.031 nd, pr (dil
al)
13673-92-2 179.001 pr
125
3097
2,5-Dichloro-1,4-benzenediamine
2,6-Dichloro-1,4-benzenediamine
3,5-Dichloro-1,2-benzenediol
3098
4,5-Dichloro-1,2-benzenediol
C6H4Cl2O2
3428-24-8
116.5(0.2)
3099
4,6-Dichloro-1,3-benzenediol
C6H4Cl2O2
137-19-9
3100
2,5-Dichloro-1,4-benzenediol
C6H4Cl2O2
824-69-1
3101
4,5-Dichloro-1,3-benzenedi- Dichlorphenamide
sulfonamide
2,4-Dichlorobenzenemethanamine
2,4-Dichlorobenzenemethanol 2,4-Dichlorobenzyl alcohol
N,N-Dichlorobenzenesulfonamide
2,5-Dichlorobenzenethiol
2,2’-Dichloro-p-benzidine
[1,1’-Biphenyl]-4,4’-diamine,
2,2’-dichloro3,3’-Dichloro-p-benzidine
[1,1’-Biphenyl]-4,4’-diamine,
3,3’-dichloro-
C6H6Cl2N2O4S2
120-97-8
179.001 nd or pr w,
ace, bz)
305.159
C7H7Cl2N
95-00-1
176.044
12513
C7H6Cl2O
C6H5Cl2NO2S
1777-82-8
473-29-0
177.028
59.5
226.081 ye mcl or pl 76
15025
C6H4Cl2S
C12H10Cl2N2
5858-18-4
84-68-4
11550
C12H10Cl2N2
91-94-1
179.067
253.126 nd (w), pr
(al)
253.126 nd
No.
Name
3072
Dichloroacetyl chloride
3073
3074
3075
Dichloroacetylene
4-[(Dichloroamino)­sulfonyl]­
benzoic acid
2,3-Dichloroaniline
3076
3084
3096
3102
3103
3104
3105
3106
3107
HCP_Section_03.indb 158
Synonym
Halazone
Physical
Form
179.001 pr(chl-CS2)
nd(bzpeth)
179.001
mp/˚C
bp/˚C
108
245
250(21)
213.5
den
g cm –3
nD
Solubility
1.531516 1.459120 dec H2O, EtOH;
msc eth
1.26120 1.4279020 s EtOH, eth, ace
sl H2O, chl; vs
HOAc; i peth
s EtOH, ace; vs
eth; sl bz, ctc,
lig
1.56720
sl H2O, chl; s
EtOH, eth
sl H2O; s EtOH,
eth, bz, chl,
CS2
sl H2O; s EtOH,
eth
s EtOH, eth; sl
bz, chl
i H2O; s EtOH,
eth, ctc, lig
sl EtOH, eth,
chl; s bz
252
i H2O; sl EtOH,
ace; s bz,
HOAc
i H2O; sl EtOH; s
bz, tol, PhNO2
189
vs eth, EtOH
i H2O; s EtOH,
eth, bz, chl,
HOAc
vs eth, EtOH, lig
i H2O; s EtOH,
eth; sl ctc
vs ace, bz, eth,
EtOH
1.305920 1.551520 i H2O; s EtOH,
eth; msc ace,
bz, ctc
1.288420 1.545920 i H2O; s EtOH,
eth, bz; msc
ace
1.247555 1.528520 i H2O; msc
EtOH, ace, bz;
s eth, ctc
s EtOH, eth,
ace, bz
sl H2O; s EtOH;
vs ace
s H2O; vs EtOH,
bz
83.5(0.2)
113
254
172.5
1.815024
vs H2O, EtOH,
eth, ace; sl lig
s H2O; vs EtOH,
eth, ace
228.7
1.576225 s chl
s chl
s EtOH; sl ctc
165
vs eth, EtOH
132.5
i H2O; s EtOH,
bz, HOAc
4/11/16 11:23 AM
Physical Constants of Organic Compounds
3-159
OH
O
NH2
NH2
Cl
Cl
NH2
O
Cl
Cl
3072
Dichloroacetyl chloride
Cl
O S O
N
Cl
Cl
Cl
Cl
3073
3076
2,3-Dichloroaniline
Cl
O
Cl
Cl
Cl
Cl
Cl
Cl
3075
4-[(Dichloroamino)sulfonyl]benzoic acid
NH2
Cl
Cl
3074
Dichloroacetylene
NH2
3077
2,4-Dichloroaniline
Cl
Cl
3078
2,5-Dichloroaniline
O
3079
2,6-Dichloroaniline
3,4-Dichloroaniline
Cl
Cl
NH2
Cl
Cl
Cl
3080
Cl
3081
3,5-Dichloroaniline
O
O
3082
9,10-Dichloroanthracene
Cl
3083
1,5-Dichloro-9,10-anthracenedione
3084
1,8-Dichloro-9,10-anthracenedione
trans-4,4’-Dichloroazobenzene
O
Cl
N
O
Cl
N
O
Cl
O
Cl
Cl
3085
NH2
3087
2,3-Dichlorobenzaldehyde
3088
2,4-Dichlorobenzaldehyde
Cl
Cl
2,6-Dichlorobenzamide
Cl
Cl
OH
OH
Cl
3092
o-Dichlorobenzene
NH2
Cl
3093
3094
m-Dichlorobenzene
p-Dichlorobenzene
NH2
3095
NH2
O S O
Cl
3097
2,6-Dichloro-1,4-benzenediamine
3,5-Dichloro-1,2-benzenediol
NH2
OH
Cl
Cl
Cl
Cl
3096
2,5-Dichloro-1,4-benzenediamine
OH
OH
OH
3,5-Dichlorobenzaldehyde
NH2
NH2
Cl
OH
Cl
3090
3,4-Dichlorobenzaldehyde
Cl
Cl
3091
Cl
3089
2,6-Dichlorobenzaldehyde
Cl
Cl
Cl
Cl
Cl
O
Cl
Cl
3086
4,4’-Dichloroazoxybenzene
O
O
Cl
Cl
O
Cl
3098
4,5-Dichloro-1,2-benzenediol
Cl
Cl
OH
Cl
OH
Cl
3099
3100
4,6-Dichloro-1,3-benzenediol
2,5-Dichloro-1,4-benzenediol
Cl
N
O S O
S
Cl O
NH2
Cl
3101
Cl
3102
4,5-Dichloro-1,3-benzenedisulfonamide
3103
2,4-Dichlorobenzenemethanamine
2,4-Dichlorobenzenemethanol
Cl
SH
H2N
Cl
3104
N,N-Dichlorobenzenesulfonamide
Cl Cl
Cl
3105
2,5-Dichlorobenzenethiol
Cl
NH2
3106
2,2’-Dichloro-p-benzidine
Cl
H2N
NH2
3107
3,3’-Dichloro-p-benzidine
Organic
N N
Physical Constants of Organic Compounds
3-160
Organic
No.
Name
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
3108
3,3’-Dichloro-[1,1’-biphenyl]4,4’-diamine
C12H12Cl4N2
612-83-9
326.048
3109
3,3’-Dichloro-p-benzidine
dihydrochloride
2,4-Dichlorobenzoic acid
C7H4Cl2O2
50-84-0
191.012 nd (w or bz) 164.2
sub
3110
2,5-Dichlorobenzoic acid
C7H4Cl2O2
50-79-3
191.012 nd (w)
154(1)
301
3111
2,6-Dichlorobenzoic acid
C7H4Cl2O2
50-30-6
142(2)
sub
3112
3,4-Dichlorobenzoic acid
C7H4Cl2O2
51-44-5
3113
3,5-Dichlorobenzoic acid
C7H4Cl2O2
51-36-5
191.012 nd (al), pr
(w)
191.012 nd (w, al,
bz)
191.012 nd (al, w)
187.4(0.5)
sub
3114
3115
2,6-Dichlorobenzonitrile
4,4’-Dichlorobenzophenone
Dichlobenil
Bis(4-chlorophenyl) ketone
C7H3Cl2N
C13H8Cl2O
1194-65-6
90-98-2
172.012 cry (peth)
251.108 pl (al)
143.6(0.7)
146.8(0.3)
270
353
1.450020
3116
3,4-Dichlorobenzotrifluoride
1,2-Dichloro-4(trifluoromethyl)benzene
C7H3Cl2F3
328-84-7
215.000 liq
175(3)
1.472925
3117
3118
3119
3120
3121
3122
3123
3124
2,3-Dichlorobenzoyl chloride
2,4-Dichlorobenzoyl chloride
2,5-Dichlorobenzoyl chloride
3,4-Dichlorobenzoyl chloride
2,5-Dichlorobiphenyl
2,6-Dichlorobiphenyl
3,3’-Dichlorobiphenyl
4,4’-Dichlorobiphenyl
C7H3Cl3O
C7H3Cl3O
C7H3Cl3O
C7H3Cl3O
C12H8Cl2
C12H8Cl2
C12H8Cl2
C12H8Cl2
2905-60-4
89-75-8
2905-61-5
3024-72-4
34883-39-1
33146-45-1
2050-67-1
2050-68-2
209.457
209.457
209.457
209.457
223.098
223.098
223.098
223.098
3125
C14H10Cl4
72-54-8
C14H8Cl4
72-55-9
318.026
3127
3128
3129
1,1-Dichloro-2,2-bis(p-chlorophenyl)ethane
2,2-Dichloro-1,1-bis(4-chlorophenyl)ethene
2,3-Dichloro-1,3-butadiene
1,1-Dichlorobutane
Butylidene chloride
1,2-Dichlorobutane
cry
34.7(0.5)
nd (dil al)
29
pr or nd (al, 148(2)
to-peth)
320.041
109(1)
C4H4Cl2
C4H8Cl2
C4H8Cl2
1653-19-6
541-33-3
616-21-7
122.981
127.013
127.013
101(15)
115(6)
123.9(0.8)
3130
1,3-Dichlorobutane
C4H8Cl2
1190-22-3
127.013
133.7(0.7)
3131
3132
3133
3134
3135
1,4-Dichlorobutane
2,2-Dichlorobutane
2,3-Dichlorobutane, (±)1,4-Dichloro-2,3-butanediol
3,4-Dichloro-1-butene
C4H8Cl2
C4H8Cl2
C4H8Cl2
C4H8Cl2O2
C4H6Cl2
110-56-5
4279-22-5
2211-67-8
2419-73-0
760-23-6
127.013
127.013
127.013
159.012
124.997
3136
cis-1,3-Dichloro-2-butene
C4H6Cl2
10075-38-4 124.997
127(16)
3137
trans-1,3-Dichloro-2-butene
C4H6Cl2
7415-31-8
124.997
132
3138
cis-1,4-Dichloro-2-butene
C4H6Cl2
1476-11-5
124.997 liq
-42(2)
149(11)
3139
trans-1,4-Dichloro-2-butene
C4H6Cl2
110-57-6
124.997 col liq
3(2)
155.4
3140
1,4-Dichloro-2-butyne
C4H4Cl2
821-10-3
122.981
3141
2,6-Dichloro-4-(chloroimino)- Gibbs’ reagent
2,5-cyclohexadien-1-one
1,2-Dichloro-4-(chloromethyl)­
benzene
2,4-Dichloro-1-(chloromethyl)­
benzene
Dichloro(chloromethyl)­
methylsilane
Dichloro(2-chlorovinyl)arsine
2,5-Dichloro-2,5-cyclohexadiene-1,4-dione
2,6-Dichloro-2,5-cyclohexadiene-1,4-dione
1,1-Dichlorocyclohexane
cis-1,2-Dichlorocyclohexane
1,10-Dichlorodecane
C6H2Cl3NO
101-38-2
210.445
66
C7H5Cl3
102-47-6
195.474
37.5
C7H5Cl3
94-99-5
195.474
12013
C2H5Cl3Si
1558-33-4
163.506
121.5
1.285820 1.450020
C2H2AsCl3
C6H2Cl2O2
541-25-3
615-93-0
190
1.88820
3126
3142
3143
3144
3145
3146
3147
3148
3149
3150
HCP_Section_03.indb 160
C6H2Cl2O2
C6H10Cl2
C6H10Cl2
C10H20Cl2
Physical
Form
mp/˚C
bp/˚C
den
g cm –3
nD
Solubility
i H2O; vs EtOH
s H2O, EtOH,
eth, bz, chl; sl
ace
sl H2O, DMSO; s
EtOH, eth
s H2O, EtOH,
eth, bz, chl
s H2O, eth; vs
EtOH; sl DMSO
sl H2O, lig,
DMSO; s EtOH,
eth
204.5(0.4)
liq
16.5
liq
25
14014
15034
95.41
242
18230
320
317
i H2O; s EtOH;
vs eth, chl; sl
ace
1.589520 s ctc
1.44200
1931
sl ctc
i H2O
i H2O
vs bz, eth, EtOH
i H2O; sl EtOH,
chl; s bz
sl chl
89.8(0.3)
liq
liq
liq
liq
207.318 liq
176.985 pa ye mcl pr
(al)
697-91-6
176.985 ye orth (lig,
bz)
2108-92-1 153.049 liq
10498-35-8 153.049 liq
2162-98-3 211.172
-38.7(0.4)
-74
-80
126.5
-61(5)
155(3)
102(6)
119
15030
116
164(15)
0.1
162.3
241
i H2O; s EtOH,
ctc
i H2O; sl EtOH; s
eth, chl
sl H2O, EtOH; s
chl
121.8
-36.6(0.1)
-5(3)
15.6(0.5)
1.182920 1.489020 vs chl
1.086320 1.435520 i H2O; s chl
1.111625 1.445020 i H2O; s eth, chl;
sl ctc
1.115820 1.444520 i H2O; s eth, chl;
sl ctc
1.133125 1.452225 i H2O; vs chl
1.104825 1.4295
i H2O; s chl
1.10525 1.440925 i H2O
vs EtOH
1.117020 1.464120 i H2O; s EtOH,
eth, ctc; vs
chl, bz
1.160520 1.473520 vs ace, bz, eth,
EtOH
1.16020 1.471920 vs ace, bz, eth,
EtOH
1.18825 1.488725 vs ace, bz, eth,
EtOH
1.18325 1.487125 vs ace, bz, eth,
EtOH
1.25820 1.505820 s eth, ace; sl
ctc; vs chl
171
191(10)
16728
1.155920 1.480320
1.202120 1.496720 vs bz
0.994525 1.458625
4/11/16 11:23 AM
Physical Constants of Organic Compounds
O
3-161
OH
O
O
Cl
Cl
OH
Cl
HCl H2N
O
Cl
NH2 HCl
3108
3109
3,3’-Dichloro-p-benzidine dihydrochloride
O
Cl
Cl
Cl
3110
2,4-Dichlorobenzoic acid
3111
2,5-Dichlorobenzoic acid
2,6-Dichlorobenzoic acid
O
Cl
Cl
3113
3,4-Dichlorobenzoic acid
O
Cl
O
Cl
3112
Cl
N
OH
Cl
Cl
Cl
OH
OH
3,5-Dichlorobenzoic acid
Cl
Cl
O
Cl
Cl
Cl
Cl
F
Cl
Cl
3114
3115
F
Cl
3116
4,4’-Dichlorobenzophenone
Cl
Cl
3118
3117
3,4-Dichlorobenzotrifluoride
3119
2,4-Dichlorobenzoyl chloride
2,3-Dichlorobenzoyl chloride
2,5-Dichlorobenzoyl chloride
Organic
2,6-Dichlorobenzonitrile
F
Cl
O
Cl
Cl
Cl
Cl
Cl
Cl
Cl
Cl
3120
3,4-Dichlorobenzoyl chloride
Cl
Cl
Cl
3121
3122
2,5-Dichlorobiphenyl
Cl
Cl
3124
3123
2,6-Dichlorobiphenyl
Cl
Cl
4,4’-Dichlorobiphenyl
3,3’-Dichlorobiphenyl
Cl
3125
1,1-Dichloro-2,2-bis(p-chlorophenyl)ethane
Cl
Cl
Cl
Cl
Cl
Cl
3126
3127
2,2-Dichloro-1,1-bis(4-chlorophenyl)ethene
Cl
Cl
Cl
3128
2,3-Dichloro-1,3-butadiene
Cl
1,1-Dichlorobutane
3129
3130
1,2-Dichlorobutane
Cl
Cl
Cl
Cl
1,3-Dichlorobutane
3132
1,4-Dichlorobutane
2,2-Dichlorobutane
OH
Cl
Cl
OH
Cl
Cl
3134
3135
1,4-Dichloro-2,3-butanediol
3136
3,4-Dichloro-1-butene
cis-1,3-Dichloro-2-butene
O
Cl
3137
3139
cis-1,4-Dichloro-2-butene
trans-1,4-Dichloro-2-butene
Cl
3140
1,4-Dichloro-2-butyne
Cl
Cl
Cl
Cl
3141
2,6-Dichloro-4-(chloroimino)-2,5-cyclohexadien-1-one
2,3-Dichlorobutane, (±)-
Cl
Cl
Cl
3138
trans-1,3-Dichloro-2-butene
Cl
Cl
N
Cl
Cl
Cl
Cl
3133
Cl
Cl
Cl
Cl
Cl Cl
3131
3142
1,2-Dichloro-4-(chloromethyl)benzene
Cl
3143
2,4-Dichloro-1-(chloromethyl)benzene
Si Cl
Cl
Cl
Cl
As
Cl
3144
Dichloro(chloromethyl)methylsilane
Cl
3145
Dichloro(2-chlorovinyl)arsine
O
O
Cl
Cl
Cl
Cl Cl
Cl
Cl
Cl
O
O
3146
3147
2,5-Dichloro-2,5-cyclohexadiene-1,4-dione
2,6-Dichloro-2,5-cyclohexadiene-1,4-dione
Cl
Cl
3148
1,1-Dichlorocyclohexane
3149
cis-1,2-Dichlorocyclohexane
3150
1,10-Dichlorodecane
Physical Constants of Organic Compounds
3-162
No.
Name
3151
3152
2,7-Dichlorodibenzo-p-dioxin
C12H6Cl2O2
1,2-Dichloro-4C7H4Cl4
(dichloromethyl)benzene
Dichloro(dichloromethyl)­
C2H4Cl4Si
methylsilane
2,3-Dichloro-5,6-dicyanobenC8Cl2N2O2
zoquinone
Dichlorodiethylsilane
C4H10Cl2Si
1,1-Dichloro-1,2-difluoroethC2H2Cl2F2
ane
1,2-Dichloro-1,1-difluoroethC2H2Cl2F2
ane
1,2-Dichloro-1,2-difluoroethC2H2Cl2F2
ane
1,1-Dichloro-2,2-difluoroeth- 1,1-Dichloro-2,2-difluoroethyl- C2Cl2F2
ene
ene
cis-1,2-Dichloro-1,2-difluoro- Refrigerant 1112
C2Cl2F2
ethene
trans-1,2-Dichloro-1,2C2Cl2F2
difluoroethene
Dichlorodifluoromethane
Refrigerant 12
CCl2F2
3153
3154
3155
3156
3157
3158
3159
3160
Organic
3161
3162
3163
3164
3165
Synonym
2,2-Dichloro-1,1-difluoro-1Methoxyflurane
methoxyethane
2,2’-Dichlorodiisopropyl ether
Mol. Form.
CAS RN
Mol.
Wt.
Physical
Form
33857-26-0 253.081 cry
56961-84-3 229.919
mp/˚C
bp/˚C
den
g cm –3
257
1.51522
149
1.411620 1.470020
nD
1558-31-2
197.951
84-58-2
227.004 ye-oran cry 214.5
vs bz, eth, EtOH
vs bz, HOAc,
diox
1719-53-5 157.114
25915-78-0 134.940 col liq
-96.5
130(2)
48.4
1.050420 1.430920
1649-08-7
134.940 liq
-101.2
47(1)
1.416320 1.3619320 sl H2O
431-06-1
134.940 liq
-101.2
59.6
1.416320 1.361920
79-35-6
-116
19
1.555-20
311-81-9
132.924 vol liq or
gas
132.924 vol liq
-119.6
21.1
1.4950
381-71-5
132.924 vol liq
-93.3
22
1.4940
75-71-8
120.914 col gas
-157.05(0.01) -29.8(0.1)
C3H4Cl2F2O
76-38-0
164.966 col liq
-35
C6H12Cl2O
108-60-1
171.064
C8H8Cl2
1124-05-6
175.056
71
C8H16Cl2
6223-78-5
183.119 lf, nd
63(3)
0.954320
C5H6Cl2N2O2
118-52-5
197.019 pr
132
1.520
C8H8Cl2O
133-53-9
191.055
83
C2H6Cl2Si
C4H6Cl2O2
75-78-5
95-59-0
129.061 liq
156.996
-16
30
C13H10Cl2
C12H10Cl2Si
2051-90-3
80-10-4
237.124
253.199
1.383-20
sl H2O; s EtOH,
eth, HOAc
105
1.4320
1.386120
184(3)
1.10320
1.450520 i H2O; msc
EtOH, eth, ace;
vs bz
s chl
222
3169
3170
1,4-Dichloro-2,5-dimethylbenzene
2,5-Dichloro-2,5-dimethylhexane
1,3-Dichloro-5,5-dimethyl­
hydantoin
2,4-Dichloro-3,5-dimethylphe- Dichloroxylenol
nol
Dichlorodimethylsilane
2,3-Dichloro-1,4-dioxane
3171
3172
Dichlorodiphenylmethane
Dichlorodiphenylsilane
3173
1,1-Dichloroethane
Ethylidene dichloride
C2H4Cl2
75-34-3
98.959
liq
-96.93(0.06) 56.3(0.7)
1.175720
3174
1,2-Dichloroethane
Ethylene dichloride
C2H4Cl2
107-06-2
98.959
liq
-35.6(0.2)
83.4(0.1)
1.245425
3175
2,2-Dichloroethanol
C2H4Cl2O
598-38-9
114.958
147(15)
1.404025
3176
1,1-Dichloroethene
Vinylidene chloride
C2H2Cl2
75-35-4
96.943
liq
-122.5(0.1)
31.6(0.3)
1.21320
3177
cis-1,2-Dichloroethene
cis-1,2-Dichloroethylene
C2H2Cl2
156-59-2
96.943
liq
-80.0(0.2)
60(2)
1.283720
3178
trans-1,2-Dichloroethene
trans-1,2-Dichloroethylene
C2H2Cl2
156-60-5
96.943
liq
-49.8(0.2)
47.64(0.08)
1.256520
3179
3180
3181
1,2-Dichloro-1-ethoxyethane
1,2-Dichloroethyl acetate
Dichloroethylaluminum
32
144(4)
7933
11550
3182
3183
3184
3185
3186
3187
Dichloroethylmethylsilane
2’,7’-Dichlorofluorescein
1,1-Dichloro-1-fluoroethane
1,2-Dichloro-1-fluoroethane
1,1-Dichloro-2-fluoroethene
Dichlorofluoromethane
C3H8Cl2Si
C20H10Cl2O5
C2H3Cl2F
C2H3Cl2F
C2HCl2F
CHCl2F
623-46-1
143.012
10140-87-1 156.996 liq
563-43-9
126.949 hyg solid or
liq
4525-44-4 143.088
76-54-0
401.196
1717-00-6 116.949 liq
430-57-9
116.949 liq
359-02-4
114.933 liq
75-43-4
102.923 col gas
1.137020
Ethylaluminum chloride
C4H8Cl2O
C4H6Cl2O2
C2H5AlCl2
101
1.004720 1.419720
-103.5(0.5)
-60
-108.8
-130.4
32.05(0.09)
74(4)
38(21)
8.9
1.25010
1.381420
1.373216
1.4059
3188
3189
3190
(Dichlorofluoromethyl)benzene
1,1-Dichloro-2-fluoropropene
1,7-Dichloroheptane
C7H5Cl2F
C3H3Cl2F
C7H14Cl2
498-67-9
430-95-5
821-76-1
-26.8
179
78
12435
1.313811
1.302625
1.040825
3166
3167
3168
HCP_Section_03.indb 162
2’,7’-Dichloro-3,6-fluorandiol
HCFC-141b
1,1-Dichloro-2-fluoroethylene
Refrigerant 21
Solubility
210.0(0.5)
179.019 liq
128.960
169.092
70.5(0.5)
8110
1.06425
1.46820
299(17)
304(3)
1.23518
1.20425
vs bz, eth,
EtOH, chl
sl H2O; s chl,
ctc, bz
vs eth
1.403820 dec H2O, EtOH
1.492820 i H2O; vs eth,
ace, bz, ctc,
diox
s eth, bz, ctc
1.580020 s EtOH, eth,
ace, bz, ctc
1.416420 sl H2O; vs EtOH,
eth; s ace, bz
1.442225 sl H2O; vs EtOH;
msc eth; s
ace, bz, chl
1.462625 sl H2O, ctc; s
EtOH, eth
1.424920 i H2O; s EtOH,
ace, bz; vs
eth, chl
1.449020 sl H2O; msc
EtOH, eth, ace;
vs bz, chl
1.445420 sl H2O; msc
EtOH, eth, ace;
vs bz, chl
1.443520 sl chl
1.207
reac H2O
sl DMSO
1.360010 i H2O
1.413220
1.403116
1.37249 i H2O; s EtOH,
eth, ctc, chl,
HOAc
1.518011 vs EtOH
1.419625
1.456525
4/11/16 11:23 AM
Physical Constants of Organic Compounds
3-163
Cl
Cl
Cl
O
Si
Cl
O
Cl
Cl
3151
Cl
Cl
Cl
3153
3152
2,7-Dichlorodibenzo-p-dioxin
Cl
O
N
O
Cl
Cl
F
F
Cl
Cl
F
3156
F
3158
1,2-Dichloro-1,1-difluoroethane
Cl
F
F
Cl
Cl
Cl
3159
1,2-Dichloro-1,2-difluoroethane
3160
1,1-Dichloro-2,2-difluoroethene
cis-1,2-Dichloro-1,2-difluoroethene
Organic
1,1-Dichloro-1,2-difluoroethane
F
Cl
3157
3155
Dichlorodiethylsilane
2,3-Dichloro-5,6-dicyanobenzoquinone
F
F
Si Cl
Cl
Cl
3154
Dichloro(dichloromethyl)methylsilane
1,2-Dichloro-4-(dichloromethyl)benzene
Cl
F
N
Cl
Cl
Cl
F
Cl
Cl
F
F
3161
Cl
3166
3168
1,3-Dichloro-5,5-dimethyl hydantoin
Cl
Cl
3173
3174
1,1-Dichloroethane
1,2-Dichloroethane
Cl
O
Cl
Cl
Cl
3171
2,3-Dichloro-1,4-dioxane
Dichlorodiphenylmethane
Cl
OH
Cl
O
3170
Dichlorodimethylsilane
Cl
Cl
3172
3169
2,4-Dichloro-3,5-dimethylphenol
Cl
Dichlorodiphenylsilane
Cl Si Cl
Cl
3167
2,5-Dichloro-2,5-dimethylhexane
Cl
Si
Cl
O
N
Cl
1,4-Dichloro-2,5-dimethylbenzene
Cl
N
Cl
Cl
3165
2,2’-Dichlorodiisopropyl ether
OH
Cl
O
Cl
3164
2,2-Dichloro-1,1-difluoro-1-methoxyethane
Dichlorodifluoromethane
O
Cl
3163
3162
trans-1,2-Dichloro-1,2-difluoroethene
O
F
Cl
F
Cl
F
Cl
Cl
Cl
3175
3176
2,2-Dichloroethanol
1,1-Dichloroethene
3177
Cl
3178
cis-1,2-Dichloroethene
O
Cl
Cl
Cl
Cl
3179
trans-1,2-Dichloroethene
1,2-Dichloro-1-ethoxyethane
O
O
Cl
Cl
O
3180
1,2-Dichloroethyl acetate
Cl
F
Cl
3186
1,1-Dichloro-2-fluoroethene
Al
Cl
O
Cl
Cl
Si Cl
Cl
3181
3182
Dichloroethylaluminum
O
F
Cl
Cl
F
3187
3185
1,2-Dichloro-1-fluoroethane
Cl
Cl
3188
(Dichlorofluoromethyl)benzene
Cl
3184
F
F
Cl
Cl
Cl
1,1-Dichloro-1-fluoroethane
2’,7’-Dichlorofluorescein
Cl
Dichlorofluoromethane
F
OH
3183
Dichloroethylmethylsilane
H
Cl
HO
Cl
3189
1,1-Dichloro-2-fluoropropene
Cl
Cl
3190
1,7-Dichloroheptane
Physical Constants of Organic Compounds
3-164
No.
Name
3191
1,2-Dichloro-1,2,3,3,4,4hexafluorocyclobutane
1,2-Dichloro-3,3,4,4,5,5hexafluorocyclopentene
1,2-Dichloro-1,1,2,3,3,3hexafluoropropane
1,3-Dichloro-1,1,2,2,3,3hexafluoropropane
1,5-Dichloro-1,1,3,3,5,5hexamethyltrisiloxane
1,2-Dichlorohexane
1,6-Dichlorohexane
3192
3193
3194
3195
3196
3197
3198
3199
Organic
3200
3201
3202
3203
3204
3205
3206
3207
3,5-Dichloro-2-hydroxybenzaldehyde
3,5-Dichloro-2-hydroxybenzoic acid
2,6-Dichloroindophenol,
sodium salt
5,6-Dichloro-1,3-isobenzofurandione
Dichloromethane
1,2-Dichloro-3-methoxybenzene
1,3-Dichloro-2-methoxybenzene
2,4-Dichloro-1-methoxybenzene
3,6-Dichloro-2-methoxybenzoic acid
(Dichloromethyl)benzene
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
C4Cl2F6
356-18-3
C5Cl2F6
Physical
Form
bp/˚C
232.939 liq
-24.2
59.5
706-79-6
244.949 liq
-105.8
90.7
C3Cl2F6
661-97-2
220.928
C3Cl2F6
662-01-1
220.928 liq
-125.4
35.7
1.57320
C6H18Cl2O2Si3
3582-71-6
277.369 liq
-53
184
1.01820
C6H12Cl2
C6H12Cl2
2162-92-7
2163-00-0
155.065
155.065
172.2(0.9)
205(1)
C7H4Cl2O2
90-60-8
C7H4Cl2O3
320-72-9
C12H6Cl2NNaO2
620-45-1
191.012 ye orth
(HOAc)
207.011 nd (dil al)
orth pr
290.078 dk grn cry
1.08515
vs eth, chl
1.067625 1.455525 i H2O; s eth, ctc,
chl
i H2O
942-06-3
217.006 tab or pr (to) 188
313
CH2Cl2
75-09-2
84.933
39.8(0.3)
1.326620 1.424220 sl H2O; msc
EtOH, eth; s
ctc
C7H6Cl2O
1984-59-4
177.028
31.0(0.4)
C7H6Cl2O
1984-65-2
177.028 liq
10
10520
1.291
C7H6Cl2O
553-82-2
177.028 pr
28.5
232
Dicamba
C8H6Cl2O3
1918-00-9
221.038 cry (pent)
114.9(0.8)
Benzal chloride
C7H6Cl2
98-87-3
161.029 liq
-17.0(0.5)
Refrigerant 216
Tillman’s reagent
4,5-Dichlorophthalic anhydride C8H2Cl2O3
Methylene chloride
2,6-Dichloroanisole
liq
95
220.5
-95(2)
205
C7H7Cl2NO2S
473-34-7
240.108 pr(chl-peth) 83
3209
3210
Dichloromethylborane
2,3-Dichloro-2-methylbutane
Methyldichloroborane
Amylene dichloride
CH3BCl2
C5H10Cl2
7318-78-7
507-45-9
96.752 col gas
141.038
11
129
3211
Methoxydichloromethane
C2H4Cl2O
4885-02-3
114.958
86(9)
3212
3213
1,1-Dichloromethyl methyl
ether
2,4-Dichloro-3-methylphenol
2,4-Dichloro-6-methylphenol
C7H6Cl2O
C7H6Cl2O
17788-00-0 177.028 pr (peth)
58
1570-65-6 177.028 nd (w, peth) 55
236
3214
2,6-Dichloro-4-methylphenol
C7H6Cl2O
2432-12-4
177.028 nd (lig)
231
3215
3216
3217
Dichloromethylphenylsilane
C7H8Cl2Si
Dichloromethylphosphine
Methylphosphonous dichloride CH3Cl2P
1,2-Dichloro-2-methylpropane 1,2-Dichloroisobutane
C4H8Cl2
149-74-6
676-83-5
594-37-6
191.131
116.915
127.013
3218
C5H4Cl2N2
1780-31-0
163.004 pl (al)
26
235
C5H4Cl2N2
5424-21-5
163.004 nd (lig)
46.5
219
3220
3221
3222
3223
2,4-Dichloro-5-methylpyrimidine
2,4-Dichloro-6-methylpyrimidine
Dichloromethylsilane
1,2-Dichloronaphthalene
1,3-Dichloronaphthalene
1,4-Dichloronaphthalene
CH4Cl2Si
C10H6Cl2
C10H6Cl2
C10H6Cl2
75-54-7
2050-69-3
2198-75-6
1825-31-6
115.035
197.061
197.061
197.061
liq
pl (al)
nd or pr (al)
nd or pr (al,
ace)
-93
36
62.3
67.5
40.9(0.1)
295(26)
291
288
3224
1,5-Dichloronaphthalene
C10H6Cl2
1825-30-5
107
sub
3225
1,6-Dichloronaphthalene
C10H6Cl2
2050-72-8
49
sub
3226
1,7-Dichloronaphthalene
C10H6Cl2
2050-73-9
63.5
285.5
3227
1,8-Dichloronaphthalene
C10H6Cl2
2050-74-0
89
sub
3228
2,3-Dichloronaphthalene
C10H6Cl2
2050-75-1
197.061 nd or lf (al)
pr (sub)
197.061 nd or pr (al,
peth)
197.061 nd or pr (al,
HOAc)
197.061 orth pl (hx)
nd (al, sub)
197.061 orth lf (al)
206(3)
1250
108(2)
120
i H2O
1.303020
dec H2O
sl H2O; vs EtOH,
eth
s H2O, EtOH,
ace
vs eth, EtOH, tol
1.543020
sl chl
1.5725
Dichloramine-T
39
Solubility
1.654620 1.367620
sub
N,N-Dichloro-4-methylbenzenesulfonamide
HCP_Section_03.indb 164
nD
34(2)
3208
3219
den
g cm –3
mp/˚C
1.2625
1.550220 i H2O; vs eth,
EtOH
i H2O; s EtOH,
eth, bz, ctc,
HOAc
1.069615 1.445018 i H2O; vs eth,
EtOH
1.27125 1.430020
vs eth, chl
sl H2O; vs EtOH,
eth, chl, CS2
i H2O; vs eth,
EtOH, HOAc
1.186620 1.518020
1.30420 1.494020
1.09320 1.437020 i H2O; msc
EtOH, eth, ace,
bz, ctc
sl H2O; vs EtOH,
eth, bz, chl
vs bz, eth,
EtOH, chl
1.10525
1.314749 1.533849 s EtOH, eth
s EtOH
1.299776 1.622876 i H2O; sl EtOH; s
eth, bz, HOAc;
vs ace
1.490020
i H2O; sl EtOH; s
eth
1.2611100 1.6092100 s EtOH, eth, bz,
HOAc
1.2924100 1.6236100 s EtOH, peth
i H2O; sl EtOH;
vs eth
4/11/16 11:23 AM
Physical Constants of Organic Compounds
F
3-165
Cl
F
F
F
F
F
F
F
F
Cl Cl
3191
F
F
F
F
F
3192
1,2-Dichloro-1,2,3,3,4,4-hexafluorocyclobutane
F F
Cl F
Cl
F
F
Cl
F
Cl
F
3193
1,2-Dichloro-3,3,4,4,5,5-hexafluorocyclopentene
3194
1,2-Dichloro-1,1,2,3,3,3-hexafluoropropane
1,3-Dichloro-1,1,2,2,3,3-hexafluoropropane
HO
O
Cl
Si
Cl
F
F
F
O
OH
Si
O
Si
O
Cl
Cl
Cl
Cl
Cl
3195
3196
1,2-Dichlorohexane
Cl
Cl
Cl
3198
1,6-Dichlorohexane
Cl
3199
3,5-Dichloro-2-hydroxybenzaldehyde
3,5-Dichloro-2-hydroxybenzoic acid
Organic
1,5-Dichloro-1,1,3,3,5,5-hexamethyltrisiloxane
3197
OH
Cl
N
O
O Na
2,6-Dichloroindophenol, sodium salt
O
Cl
Cl
H
3202
1,2-Dichloro-3-methoxybenzene
OH
3207
3208
(Dichloromethyl)benzene
Cl
3209
N,N-Dichloro-4-methylbenzenesulfonamide
OH
Dichloromethylborane
3210
2,3-Dichloro-2-methylbutane
Cl
2,4-Dichloro-3-methylphenol
3211
1,1-Dichloromethyl methyl ether
Cl Si Cl
Cl
Cl
Cl
3212
O
Cl
Cl
OH
Cl
Cl
B
Cl
Cl
3205
2,4-Dichloro-1-methoxybenzene
Cl
Cl
3206
1,3-Dichloro-2-methoxybenzene
Cl
Cl
3,6-Dichloro-2-methoxybenzoic acid
Cl
3204
O Cl
O S N
Cl
Cl
O
3203
Dichloromethane
OH
Cl
Cl
O
Cl
5,6-Dichloro-1,3-isobenzofurandione
O
Cl
H
O
3201
Cl
Cl
Cl
O
Cl
3200
O
O
Cl
3213
3214
2,4-Dichloro-6-methylphenol
3215
2,6-Dichloro-4-methylphenol
Dichloromethylphenylsilane
P
Cl
Cl
Cl
3216
Dichloromethylphosphine
3217
1,2-Dichloro-2-methylpropane
Cl
Cl
Cl
N
N
Cl
Si H
Cl
N
N
Cl
3218
2,4-Dichloro-5-methylpyrimidine
Cl
3219
2,4-Dichloro-6-methylpyrimidine
Cl
Cl
Cl
Cl
3220
3221
Dichloromethylsilane
3222
1,2-Dichloronaphthalene
1,3-Dichloronaphthalene
Cl
3223
1,4-Dichloronaphthalene
Cl
Cl
Cl
Cl
Cl
Cl
Cl
Cl
3224
1,5-Dichloronaphthalene
Cl
Cl
3225
1,6-Dichloronaphthalene
3226
1,7-Dichloronaphthalene
3227
1,8-Dichloronaphthalene
3228
2,3-Dichloronaphthalene
Physical Constants of Organic Compounds
3-166
No.
Name
3229
Synonym
Mol.
Wt.
Physical
Form
Organic
CAS RN
2,6-Dichloronaphthalene
C10H6Cl2
2065-70-5
3230
2,7-Dichloronaphthalene
C10H6Cl2
2198-77-8
197.061 nd or lf (al) 140.5
pl (eth, bz)
197.061 pl or lf (al) 115.0
3231
Dichlone
C10H4Cl2O2
117-80-6
227.044 ye nd (al)
196.4(0.5)
3232
3233
2,3-Dichloro-1,4-naphthalenedione
2,4-Dichloro-1-naphthol
2,6-Dichloro-4-nitroaniline
2,4-Dichloro-α-naphthol
C10H6Cl2O
C6H4Cl2N2O2
2050-76-2
99-30-9
107.5
193.8(0.8)
180
3234
1,2-Dichloro-3-nitrobenzene
C6H3Cl2NO2
3209-22-1
60.7(0.6)
257.5
1.72114
3235
1,2-Dichloro-4-nitrobenzene
C6H3Cl2NO2
99-54-7
213.060 nd (al, bz)
207.014 ye nd (al,
HOAc)
192.000 mcl nd
(peth,
HOAc)
192.000 nd (al)
41.0(0.2)
255.5
1.455875
3236
1,3-Dichloro-5-nitrobenzene
C6H3Cl2NO2
618-62-2
65(2)
3237
1,4-Dichloro-2-nitrobenzene
C6H3Cl2NO2
89-61-2
192.000 mcl pr or lf
(HOAc, al)
192.000 pl or pr (al)
pl (AcOEt)
53.5(0.2)
267(10)
1.43975
3238
2,4-Dichloro-1-nitrobenzene
C6H3Cl2NO2
611-06-3
192.000 nd (al)
33(2)
258.5
1.479080 1.551270
3239
3240
3241
3242
3243
3244
HCFC-225cb
C2H3Cl2NO2
C6H3Cl2NO3
C3H5Cl2NO2
C9H18Cl2
C8H16Cl2
C3HCl2F5
594-72-9
618-80-4
595-44-8
821-99-8
2162-99-4
507-55-1
143.957
207.999 br nd (w)
157.984
197.145
183.119
202.938 liq
Refrigerant 225ca
C3HCl2F5
422-56-0
3246
1,1-Dichloro-1-nitroethane
2,6-Dichloro-4-nitrophenol
1,1-Dichloro-1-nitropropane
1,9-Dichlorononane
1,8-Dichlorooctane
1,3-Dichloro-1,1,2,2,3pentafluoropropane
3,3-Dichloro-1,1,1,2,2pentafluoropropane
1,2-Dichloropentane
C5H10Cl2
3247
1,5-Dichloropentane
3248
3249
Ethide
mp/˚C
bp/˚C
den
g cm –3
Mol. Form.
nD
285
1.4000100
1.439075
123.5
sl EtOH; s eth,
bz, chl, HOAc
vs EtOH; s hx,
HOAc
i H2O; sl EtOH,
eth, bz; s chl
vs bz, eth, EtOH
s EtOH, acid; sl
DMSO
i H2O; s EtOH,
eth, ace, bz,
peth; sl chl
i H2O; s EtOH,
eth; sl ctc
i H2O; s EtOH,
eth
i H2O; s EtOH,
eth, bz, CS2; sl
ctc
i H2O; s EtOH,
eth; sl chl
s ctc
vs eth, chl
s ctc
145
241(12)
246(1)
55(2)
1.82225
1.31220
1.017325 1.458625
1.024825 1.457225
1.5525
202.938 liq
50(2)
1.5425
1674-33-5
141.038
148.2(0.7)
C5H10Cl2
628-76-2
141.038 liq
-72.8
182.9(0.8)
2,3-Dichloropentane
Dichlorophene
C5H10Cl2
C13H10Cl2O2
600-11-3
97-23-4
-77.3
177.5
143(4)
3250
2,3-Dichlorophenol
C6H4Cl2O
576-24-9
141.038 liq
269.123 cry (bz,
peth)
163.001 cry (lig, bz)
3251
2,4-Dichlorophenol
C6H4Cl2O
120-83-2
163.001 hex nd (bz)
43(2)
3252
2,5-Dichlorophenol
C6H4Cl2O
583-78-8
163.001 pr (bz, peth) 57.8(0.3)
222(8)
3253
2,6-Dichlorophenol
C6H4Cl2O
87-65-0
163.001 nd (peth)
226(4)
3254
3,4-Dichlorophenol
C6H4Cl2O
95-77-2
163.001 nd (bz-peth) 67.8(0.3)
253
3255
3,5-Dichlorophenol
C6H4Cl2O
591-35-5
163.001 pr (peth)
67.8(0.3)
233
3256
(2,4-Dichlorophenoxy)acetic
acid
4-(2,4-Dichlorophenoxy)­
butanoic acid
2-(2,4-Dichlorophenoxy)­
propanoic acid
Dichlorophenylarsine
2,4-Dichlorophenyl
benzenesulfonate
2,2-Dichloro-1-phenylethanone
1-(2,4-Dichlorophenyl)­
ethanone
1-(2,5-Dichlorophenyl)­
ethanone
1-(3,4-Dichlorophenyl)­
ethanone
3,4-Dichlorophenyl isocyanate
2,4-D
C8H6Cl2O3
94-75-7
221.038 cry (bz)
140(2)
1600.4
1.087220 1.448520 i H2O; s EtOH;
vs chl
1.095625 1.454525 i H2O; s EtOH,
eth, bz, ctc
1.078920 1.446420 i H2O
i H2O; s EtOH,
ace
s EtOH, eth, bz,
lig
sl H2O; s EtOH,
eth, bz, chl
sl H2O; vs EtOH,
eth; s bz, peth
1.65320
vs EtOH, eth; s
bz, peth
sl H2O; vs EtOH,
eth; s bz, peth
sl H2O; vs EtOH,
eth; s peth
i H2O; s EtOH; sl
bz, DMSO
Butyrac 118
C10H10Cl2O3
94-82-6
249.090
118(2)
Dichlorprop
C9H8Cl2O3
120-36-5
235.064
116.6(0.3)
C6H5AsCl2
C12H8Cl2O3S
696-28-6
97-16-5
222.932 liq
303.161
-19
45.5
256(4)
1.651620 1.638615
Genite
C8H6Cl2O
2648-61-5
189.039 amor
20.5
249
1.34016
C8H6Cl2O
2234-16-4
189.039
33.5
C8H6Cl2O
2476-37-1
189.039
12
11812
C8H6Cl2O
2642-63-9
189.039 nd (peth)
76
13512
102-36-3
188.011 cry
42
11212
3245
3257
3258
3259
3260
3261
3262
3263
3264
3265
3266
3267
1,2-Dichloro-5-isocyanatoben- C7H3Cl2NO
zene
3,5-Dichlorophenyl isocyanate 1,3-Dichloro-5-isocyanatoben- C7H3Cl2NO
zene
N-(3,4-Dichlorophenyl)-2Dicryl
C10H9Cl2NO
methyl-2-propenamide
HCP_Section_03.indb 166
34893-92-0 188.011
2164-09-2
127 exp
Solubility
56.8(0.3)
66.6(0.4)
33
230.090 cry (al-peth) 122.6(0.5)
210
sl H2O, lig; s
EtOH, eth
vs bz, eth, EtOH
s ctc, CS2
1.568620 s EtOH, bz, ctc
1.564020 i H2O
1.32130
1.559530
i H2O; s ctc, lig
1.380
vs ace, EtOH
4/11/16 11:23 AM
Physical Constants of Organic Compounds
3-167
Cl
Cl
3229
3230
Cl
O
N
O
3235
O
N
Cl
O
N
3234
2,6-Dichloro-4-nitroaniline
1,2-Dichloro-3-nitrobenzene
O
O
OH
Cl
NO2
Cl
Cl
Cl
3237
3238
O
3239
2,4-Dichloro-1-nitrobenzene
Cl
N
O
3240
1,1-Dichloro-1-nitroethane
2,6-Dichloro-4-nitrophenol
Organic
1,4-Dichloro-2-nitrobenzene
O
N
O
O
Cl
Cl
1,3-Dichloro-5-nitrobenzene
N
Cl
3233
2,4-Dichloro-1-naphthol
Cl
N
O
3236
1,2-Dichloro-4-nitrobenzene
3232
2,3-Dichloro-1,4-naphthalenedione
Cl
Cl
O
3231
2,7-Dichloronaphthalene
O
Cl
Cl
Cl
Cl
O
Cl
2,6-Dichloronaphthalene
Cl
Cl
Cl
Cl
NH2
OH
O
O
N
F F
Cl
O
Cl Cl
Cl
Cl
3241
Cl
Cl
3242
1,1-Dichloro-1-nitropropane
F
3243
1,3-Dichloro-1,1,2,2,3-pentafluoropropane
HO
Cl
Cl
F
OH
OH
F
F
Cl
OH
Cl
F F
Cl
F
3244
1,8-Dichlorooctane
1,9-Dichlorononane
F
Cl
Cl
Cl
3245
3,3-Dichloro-1,1,1,2,2-pentafluoropropane
Cl
Cl
Cl
3247
3246
1,5-Dichloropentane
1,2-Dichloropentane
Cl
3248
Cl
Cl
3249
2,3-Dichloropentane
Cl
3250
Dichlorophene
3251
2,3-Dichlorophenol
2,4-Dichlorophenol
OH
OH
Cl
Cl
O
Cl
Cl
3252
3253
2,5-Dichlorophenol
Cl
3254
2,6-Dichlorophenol
Cl
Cl
3255
3,4-Dichlorophenol
Cl
Cl
3256
3,5-Dichlorophenol
O
OH
Cl
Cl
O
O
OH
OH
(2,4-Dichlorophenoxy)acetic acid
3257
4-(2,4-Dichlorophenoxy)butanoic acid
O
Cl
Cl
O
O
Cl
As
Cl
O
S O
O
OH
Cl
3258
2-(2,4-Dichlorophenoxy)propanoic acid
3259
Dichlorophenylarsine
O
Cl
Cl
3261
2,4-Dichlorophenyl benzenesulfonate
C
Cl
Cl
Cl
3260
N
O
O
OH
Cl
2,2-Dichloro-1-phenylethanone
3262
1-(2,4-Dichlorophenyl)ethanone
O
O
N
C
O
HN
Cl
Cl
Cl
Cl
3263
1-(2,5-Dichlorophenyl)ethanone
3264
1-(3,4-Dichlorophenyl)ethanone
Cl
Cl
Cl
Cl
Cl
3265
3,4-Dichlorophenyl isocyanate
Cl
3266
3,5-Dichlorophenyl isocyanate
3267
N-(3,4-Dichlorophenyl)-2-methyl-2-propenamide
Physical Constants of Organic Compounds
3-168
Organic
Mol. Form.
CAS RN
Mol.
Wt.
C9H6Cl2O2
1201-99-6
217.049
Phenyldichlorosilane
Propylidene chloride
C6H6Cl2Si
C3H6Cl2
1631-84-1
78-99-9
177.104
112.986
Propylene dichloride
C3H6Cl2
26198-63-0 112.986 liq
-100.53
96.4
1,3-Dichloropropane
C3H6Cl2
142-28-9
112.986 liq
-99.5
120.8(0.3)
3273
2,2-Dichloropropane
C3H6Cl2
594-20-7
112.986 liq
-33.9(0.1)
69.51(0.1)
3274
2,2-Dichloropropanoic acid
C3H4Cl2O2
75-99-0
142.969
187.5
3275
2,3-Dichloro-1-propanol
C3H6Cl2O
616-23-9
128.985 visc
176(5)
3276
1,3-Dichloro-2-propanol
C3H6Cl2O
96-23-1
128.985
171(4)
3277
C9H15Cl6O4P
78-43-3
430.904
1900.1
C3H3Cl3O
7623-13-4
161.414
5317
1.475720 1.476420
3279
2,3-Dichloro-1-propanol,
phosphate (3:1)
2,3-Dichloropropanoyl
chloride
1,1-Dichloropropene
1.22125
dec H2O
1.132120 1.428920 s EtOH, eth, bz,
chl
1.156020 1.439420 sl H2O; s EtOH,
eth, bz, chl
1.178525 1.445525 sl H2O; vs EtOH,
eth; s bz, chl
1.113620 1.414820 i H2O; s EtOH,
bz, chl; msc
eth
1.38912
vs H2O, alk,
EtOH; s eth,
ctc
1.360720 1.481920 sl H2O, lig; msc
EtOH, eth, ace,
bz
1.350617 1.483720 vs H2O, EtOH;
msc eth; s
ace, chl
1.51722
C3H4Cl2
563-58-6
110.970
76(5)
3280
cis-1,2-Dichloropropene
C3H4Cl2
6923-20-2
110.970
105(5)
3281
trans-1,2-Dichloropropene
C3H4Cl2
7069-38-7
110.970
77
3282
cis-1,3-Dichloropropene
cis-1,3-Dichloropropylene
C3H4Cl2
10061-01-5 110.970
104(1)
3283
trans-1,3-Dichloropropene
trans-1,3-Dichloropropylene
C3H4Cl2
10061-02-6 110.970
111(5)
3284
2,3-Dichloropropene
C3H4Cl2
78-88-6
110.970 liq
10
93.0(0.4)
3285
3286
3287
C4H2Cl2N2
C5H3Cl2N
C4H3Cl2N3
141-30-0
2402-78-0
56-05-3
148.978
147.990
163.993
68.8
87
215
890.2
211
3288
3289
3,6-Dichloropyridazine
2,6-Dichloropyridine
4,6-Dichloro-2-pyrimidinamine
2,4-Dichloropyrimidine
4,7-Dichloroquinoline
1.186425 1.443025 i H2O; s eth,
ace, chl
1.454920 i H2O; s ace, bz,
chl
1.181820 1.447120 i H2O; vs EtOH,
ctc, MeOH
1.22420 1.468220 i H2O; s eth, bz,
chl
1.21720 1.473020 i H2O; s eth, bz,
chl
1.21120 1.460320 i H2O; msc
EtOH; s eth,
bz, chl
s chl
C4H2Cl2N2
C9H5Cl2N
3934-20-1
86-98-6
3290
5,7-Dichloro-8-quinolinol
C9H5Cl2NO
773-76-2
148.978
59
198.049 cry (MeOH), 92.4(0.5)
nd (80%
al)
214.048 cry (al)
179.5
3291
2,3-Dichloroquinoxaline
C8H4Cl2N2
2213-63-0
199.037 cry (al, bz)
151.2(0.4)
3292
3293
2,5-Dichlorostyrene
1,2-Dichloro-3,4,5,6-tetrafluorobenzene
1,1-Dichloro-1,2,2,2-tetrafluo- Refrigerant 114a
roethane
C8H6Cl2
C6Cl2F4
1123-84-8
1198-59-0
173.040
218.964
8.0
935
157.7
1.24620
1.579820
C2Cl2F4
374-07-2
170.921 col gas
-56.6
3(1)
1.30920
vs bz, eth, EtOH
3295
1,2-Dichloro-1,1,2,2-tetrafluo- Refrigerant 114
roethane
C2Cl2F4
76-14-2
170.921 col gas
-92.52(0.05) 3.6(0.5)
1.30920
i H2O; vs eth,
EtOH
3296
C4H12Cl2Si2
4342-61-4
187.215
148
C4H12Cl2OSi2
2401-73-2
203.214 liq
-37.5
138
1.03820
3298
1,2-Dichloro-1,1,2,2-tetramethyldisilane
1,3-Dichloro-1,1,3,3-tetramethyldisiloxane
2,5-Dichlorothiophene
1.45525
(p>1
atm)
1.45525
(p>1
atm)
1.01020
C4H2Cl2S
3172-52-9
153.030 liq
-40.5
165(4)
3299
3300
3301
3302
3303
2,3-Dichlorotoluene
2,4-Dichlorotoluene
2,5-Dichlorotoluene
2,6-Dichlorotoluene
3,4-Dichlorotoluene
32768-54-0
95-73-8
19398-61-9
118-69-4
95-75-0
161.029
161.029 liq
161.029
161.029
161.029 liq
6
-13.5
2.5
25.8
-15.2(0.2)
207.5
200(8)
200
194(11)
208(18)
1.442220 1.562620 i H2O; msc
EtOH, eth; s
ctc
1.245820 1.551120 vs bz
1.247620 1.551120 i H2O; s ctc
1.253520 1.544920 i H2O; s bz
1.268620 1.550720 i H2O; s chl
1.256420 1.547120 i H2O; msc
EtOH, eth, ace,
bz, lig, ctc
No.
Name
3268
3269
3270
3-(2,4-Dichlorophenyl)-2propenoic acid
Dichlorophenylsilane
1,1-Dichloropropane
3271
1,2-Dichloropropane, (±)-
3272
3278
3294
3297
HCP_Section_03.indb 168
Synonym
2,2-Dichloropropionic acid
Chloroxine
C7H6Cl2
2,4-Dichloro-1-methylbenzene C7H6Cl2
C7H6Cl2
C7H6Cl2
1,2-Dichloro-4-methylbenzene C7H6Cl2
Physical
Form
mp/˚C
bp/˚C
den
g cm –3
nD
234
Solubility
s DMSO
181
88.4(0.5)
s DMSO
198
14810
sl chl
sl EtOH, ace,
chl, DMSO; s
alk, bz, peth
i H2O; vs EtOH,
bz, chl, HOAc
1.454820
4/11/16 11:23 AM
Physical Constants of Organic Compounds
Cl
HSi
OH
Cl
Cl Cl
Cl
Cl
Cl
Cl
3268
3269
3-(2,4-Dichlorophenyl)-2-propenoic acid
Cl
O
O P O
O
Cl
Cl
3276
1,3-Dichloro-2-propanol
Cl
Cl
3277
3278
2,3-Dichloro-1-propanol, phosphate (3:1)
2,3-Dichloropropanoyl chloride
OH
Cl
Cl
3275
3274
2,2-Dichloropropane
2,3-Dichloro-1-propanol
2,2-Dichloropropanoic acid
Cl
Cl
Cl
Cl
Cl
3273
1,3-Dichloropropane
O
Cl
Cl
O
Cl
3272
1,2-Dichloropropane, (±)-
Cl
Cl
OH
Cl
3271
1,1-Dichloropropane
OH
Cl Cl
Cl
3270
Dichlorophenylsilane
Cl
Cl
Cl
Cl
Cl
Cl
3279
3280
1,1-Dichloropropene
3281
cis-1,2-Dichloropropene
3282
trans-1,2-Dichloropropene
cis-1,3-Dichloropropene
Cl
Cl
Cl
Cl
Cl
Cl
Cl
3283
trans-1,3-Dichloropropene
Cl
3284
N
N
N
Cl
3285
2,3-Dichloropropene
3286
3,6-Dichloropyridazine
Cl
N
2,6-Dichloropyridine
N
Cl
Cl
3291
2,3-Dichloroquinoxaline
N
NH2
Cl
3287
Cl
Cl
N
3288
4,6-Dichloro-2-pyrimidinamine
2,4-Dichloropyrimidine
N
N
OH
3289
3290
4,7-Dichloroquinoline
5,7-Dichloro-8-quinolinol
Cl
F
Cl
F
F
F
F
Cl
N
N
Cl
Cl
Cl
Cl
Cl
F
3292
3293
2,5-Dichlorostyrene
F
F
3294
1,2-Dichloro-3,4,5,6-tetrafluorobenzene
F
Cl
F
Cl
F
Cl
F
Cl
3295
1,1-Dichloro-1,2,2,2-tetrafluoroethane
Si
Si
Cl
3296
1,2-Dichloro-1,1,2,2-tetrafluoroethane
1,2-Dichloro-1,1,2,2-tetramethyldisilane
Cl
Si
Cl
O
Cl
Si
Cl
3297
1,3-Dichloro-1,1,3,3-tetramethyldisiloxane
Cl
S
3298
Cl
2,5-Dichlorothiophene
Cl
3299
2,3-Dichlorotoluene
Cl
Cl
3300
2,4-Dichlorotoluene
Cl
Cl
Cl
Cl
Cl
3301
2,5-Dichlorotoluene
3302
2,6-Dichlorotoluene
3303
3,4-Dichlorotoluene
Organic
O
3-169
Physical Constants of Organic Compounds
3-170
No.
Name
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
3304
Dichlorocyanuric acid
C3HCl2N3O3
2782-57-2
197.964 cry
C7H3Cl5
13014-24-9 264.364
Refrigerant 123a
C2HCl2F3
354-23-4
HCFC-123
C2HCl2F3
306-83-2
Refrigerant 123b
C2HCl2F3
812-04-4
152.930 vol liq or
gas
152.930 vol liq or
gas
152.930
2,4-Dichlorobenzotrifluoride
C7H3Cl2F3
320-60-5
215.000
Chloroflurazole
C8H3Cl2F3N2
3615-21-2
255.024
3311
3312
1,3-Dichloro-1,3,5-triazine2,4,6(1H,3H,5H)-trione
1,2-Dichloro-4(trichloromethyl)benzene
1,2-Dichloro-1,1,2-trifluoroethane
2,2-Dichloro-1,1,1-trifluoroethane
1,1-Dichloro-1,2,2-trifluoroethane
2,4-Dichloro-1(trifluoromethyl)benzene
4,5-Dichloro-2(trifluoromethyl)-1H-benzimidazole
Dichlorovinylmethylsilane
Dichlorvos
124-70-9
62-73-7
141.072
220.976
3313
Diclofop-methyl
3314
3315
3316
3317
Dicrotophos
Dicumarol
Dicyanamide
o-Dicyanobenzene
C3H6Cl2Si
Phosphoric acid, 2,2-dichloro- C4H7Cl2O4P
ethenyl dimethyl ester
Methyl 2-[4-(2,4-dichlorophe- C16H14Cl2O4
noxy)phenoxy]propanoate
C8H16NO5P
C19H12O6
Cyanocyanamide
C2HN3
o-Phthalodinitrile
C8H4N2
3318
m-Dicyanobenzene
m-Phthalodinitrile
3319
p-Dicyanobenzene
p-Phthalodinitrile
3320
3321
Dicyclohexyl adipate
Dicyclohexylamine
3322
Dicyclohexylamine nitrite
3323
3324
3325
3326
3327
3328
Dicyclohexylcarbodiimide
Dicyclohexyl disulfide
Dicyclohexyl ether
Dicyclohexylmethanone
Dicyclohexylphosphine
Dicyclohexyl phthalate
3329
3330
3331
3332
3333
3334
3335
3336
3337
3338
N,N’-Dicyclohexylthiourea
N,N’-Dicyclohexylurea
Dicyclomine hydrochloride
Dicyclopentadiene
Dicyclopentyl ether
Dicyclopropyl ketone
Didecylamine
Didecyl ether
Didecyl phthalate
3’,4’-Didehydro-β,ψ-caroten16’-oic acid
3339
2’,3’-Dideoxyinosine
3340
2,6-Dideoxy-3-O-methyl-ribo- Cymarose
hexose
C7H14O4
3341
3342
Didodecanoyl peroxide
Didodecylamine
C24H46O4
C24H51N
purp nd
(MeOHeth)
69655-05-6 236.227 wh cry
(EtOH aq)
579-04-4
162.184 pr
(eth-peth)
nd (ace)
105-74-8
398.620 wh pl
3007-31-6 353.669
3343
3344
Didodecyl phosphate
Didodecyl phthalate
C24H51O4P
C32H54O4
7057-92-3
2432-90-8
3345
Dieldrin
C12H8Cl6O
3346
Dienestrol
3347
1,2:8,9-Diepoxy-p-menthane
3305
3306
3307
3308
3309
3310
Organic
HCP_Section_03.indb 170
Physical
Form
bp/˚C
den
g cm –3
25.8
283.1
1.591320 1.588620
-78
30.0(0.1)
1.5025
-107
27.8(0.6)
1.463825
mp/˚C
nD
sl H2O
30.2
1.480220
213.5
93.7(0.5)
14020
51338-27-3 341.186
42.1(0.5)
1.086820 1.427020 dec H2O
1.41525
1760.1
141-66-2
66-76-2
504-66-5
91-15-6
237.191
336.294 nd
290
67.049 aq soln only
128.131 nd (w, lig)
140.6(0.9)
400
1.21615
15010
1.125025
C8H4N2
626-17-5
128.131 nd(al)
162
sub
0.99240
C8H4N2
623-26-7
128.131 nd (w,
MeOH)
224
sub
Dicyclohexyl hexanedioate
C18H30O4
N-Cyclohexylcyclohexanamine C12H23N
849-99-0
101-83-7
310.429
181.318 liq
35(1)
-0.1
251(4)
0.912320 1.484220
N-Cyclohexylcyclohexanamine, C12H24N2O2
nitrite
C13H22N2
C12H22S2
C12H22O
C13H22O
C12H23P
C20H26O4
3129-91-7
228.331 cry
179.5(0.6)
538-75-0
2550-40-5
4645-15-2
119-60-8
829-84-5
84-61-7
206.327
230.433 liq
182.302 liq
194.313
198.285
330.418 pr (al)
34.5
1236
19520
242.5
15920
281
2254
0.922720
0.9860
0.90425
1.38320
1212-29-9
2387-23-7
67-92-5
1755-01-7
10137-73-2
1121-37-5
1120-49-6
2456-28-2
84-77-5
514-92-1
240.408
224.342
345.948
132.202
154.249
110.153
297.562
298.546
446.663
564.840
Torularhodin
C13H24N2S
C13H24N2O
C19H36ClNO2
C10H12
C10H18O
C7H10O
C20H43N
C20H42O
C28H46O4
C40H52O2
Didanosine
C10H12N4O3
Dicycloverine hydrochloride
Cyclopentyl ether
N-Decyl-1-decanamine
Lauroyl peroxide
N-Dodecyl-1-dodecanamine
1,2-Benzenedicarboxylic acid,
didodecyl ester
Limonene diepoxide
Solubility
226.6
cry (MeOH)
cry
-36
57
66
180
233.8
165
32
liq
16
2.5
211
170 dec
8013
161
359.0
19615.5
2403
sl H2O, lig; vs
EtOH, bz; s
eth, ace
sl H2O; vs EtOH;
s eth, bz, chl; i
peth
i H2O; sl EtOH,
eth; s bz; vs
HOAc
s chl
sl H2O, ctc; s
EtOH, eth, bz
1.474120
1.486020 s eth, ace, ctc
1.516320
1.43120 i H2O; s EtOH,
eth; sl chl
0.930235 1.505035 vs eth, EtOH
0.97725
1.467020
0.818720
0.963920
vs py, chl, CS2
162
101
vs H2O, ace,
EtOH
49
46.9(0.5)
26327
434.633 cry (MeOH)
502.769
59
22.0
2561
60-57-1
380.909
178.8(0.3)
C18H18O2
84-17-3
266.335 cry (dil al)
227.5
C10H16O2
96-08-2
168.233
242
i H2O; s chl
vs bz, eth,
EtOH, chl
0.938920
1.7525
130 sub
i H2O; sl EtOH; s
ace, bz
vs ace, eth,
EtOH
4/11/16 11:23 AM
Physical Constants of Organic Compounds
3-171
Cl
Cl
O
H
N
N
N
Cl
O
Cl
F
Cl
3304
Cl
Cl
Cl
3306
1,2-Dichloro-4-(trichloromethyl)benzene
F
F
F
F
3307
1,2-Dichloro-1,1,2-trifluoroethane
Cl
Cl
F
Cl
Cl
3305
1,3-Dichloro-1,3,5-triazine-2,4,6(1H,3H,5H )-trione
F
F
Cl
F
O
3308
2,2-Dichloro-1,1,1-trifluoroethane
1,1-Dichloro-1,2,2-trifluoroethane
Cl
Cl
Cl
Cl
Cl
F
F
N
H
F
3309
Si
3310
2,4-Dichloro-1-(trifluoromethyl)benzene
O
Cl
F
F
F
N
O
O
P
O
O
Cl
Cl
3311
4,5-Dichloro-2-(trifluoromethyl)-1H-benzimidazole
O
Cl
O
3312
Dichlorovinylmethylsilane
Cl
O
3313
Dichlorvos
Diclofop-methyl
Organic
N
N
O
O P O
O
OH
N
OH
N
N
N
O
O
OO
3314
N
H
O
3315
Dicrotophos
3316
Dicumarol
O
O
H
N
O
N
N
o-Dicyanobenzene
m-Dicyanobenzene
3317
Dicyanamide
O
3321
Dicyclohexyl adipate
3322
Dicyclohexylamine
3319
p-Dicyanobenzene
N
H
N
HNO2
3320
N
3318
Dicyclohexylamine nitrite
C
N
S S
3323
3324
Dicyclohexylcarbodiimide
Dicyclohexyl disulfide
O
O
O
O
H
P
O
O
3325
3326
Dicyclohexyl ether
3327
Dicyclohexylmethanone
Dicyclohexylphosphine
Dicyclohexyl phthalate
H
N
S
O
3329
3330
N,N’-Dicyclohexylthiourea
N,N’-Dicyclohexylurea
H
HCl
O
3328
H
N
H
N
H
N
N
O
O
H
3331
Dicyclomine hydrochloride
3332
Dicyclopentadiene
HN
O
3333
3334
Dicyclopentyl ether
O
3335
Dicyclopropyl ketone
3336
Didecylamine
Didecyl ether
OH
O
N
O
O
HO
OH
O N
N
N
O
O
3337
3338
Didecyl phthalate
3339
3’,4’-Didehydro-β,ψ-caroten-16’-oic acid
2’,3’-Dideoxyinosine
O
O
HO
OH
O
O
O
O
O
P
HO
O
HN
O
3340
2,6-Dideoxy-3-O-methyl-ribo-hexose
3341
3342
Didodecanoyl peroxide
O
O
O
O
O
Didodecyl phthalate
Didodecyl phosphate
OH
Cl Cl
Cl
H
Cl
H
3344
3343
Didodecylamine
3345
Dieldrin
Cl
Cl
HO
O
O
3346
Dienestrol
3347
1,2:8,9-Diepoxy-p-menthane
Physical Constants of Organic Compounds
3-172
Organic
No.
Name
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
Physical
Form
3348
Diethanolamine
Bis(2-hydroxyethyl)amine
C4H11NO2
111-42-2
105.136
3349
3350
Diethatyl, ethyl ester
4,4’-Diethoxyazobenzene
C16H22ClNO3
C16H18N2O2
38727-55-8 311.804 cry
588-52-3
270.326 ye lf (al)
3351
3352
3,4-Diethoxybenzaldehyde
1,2-Diethoxybenzene
C11H14O3
C10H14O2
2029-94-9
2050-46-6
3353
1,4-Diethoxybenzene
C10H14O2
3354
3355
3356
3357
3358
4,4-Diethoxy-1-butanamine
1,1-Diethoxy-N,N-dimethylmethanamine
Diethoxydimethylsilane
Diethoxydiphenylsilane
2,2-Diethoxyethanamine
3359
1,1-Diethoxyethane
3360
1,2-Diethoxyethane
3361
3362
mp/˚C
bp/˚C
27.9(0.2)
271.2(0.7)
46(1)
162
dec
den
g cm –3
nD
Solubility
1.096620 1.477620 vs H2O, EtOH; sl
eth, bz
279
219
122-95-2
194.227
22
166.217 pr (peth, dil 44
al)
166.217 pl (dil al)
72
C8H19NO2
C7H17NO2
6346-09-4
1188-33-6
161.243
147.216
196
129
0.93325
0.85925
C6H16O2Si
C16H20O2Si
C6H15NO2
78-62-6
2553-19-7
645-36-3
148.276 liq
272.415
133.189 liq
-87
-78
113(3)
296(3)
163
Acetal
C6H14O2
105-57-7
118.174 liq
-106.1(0.6)
102(2)
Ethylene glycol diethyl ether
C6H14O2
629-14-1
118.174 liq
-74.0(0.2)
120.6(0.7)
1,1-Diethoxyethene
Diethoxymethane
C6H12O2
C5H12O2
2678-54-8
462-95-3
116.158
104.148 liq
-66(2)
68100
86(2)
3363
3364
3365
3366
3367
2-(Diethoxymethyl)furan
Diethoxymethylphenylsilane
Diethoxymethylsilane
1,1-Diethoxypentane
1,1-Diethoxypropane
C9H14O3
C11H18O2Si
C5H14O2Si
C9H20O2
C7H16O2
13529-27-6
775-56-4
2031-62-1
3658-79-5
4744-08-5
170.205
210.346
134.250
160.254
132.201
191.5
217(3)
98
5912
121(1)
3368
2,2-Diethoxypropane
C7H16O2
126-84-1
132.201
101(5)
3369
3,3-Diethoxy-1-propene
C7H14O2
3054-95-3
130.185
123.5
3370
3,3-Diethoxy-1-propyne
C7H12O2
10160-87-9 128.169
139
3371
N,N-Diethylacetamide
C6H13NO
685-91-6
115.173
199(10)
3372
Diethyl 2-acetamidomalonate
C9H15NO5
1068-90-2
96.3
3373
3374
3375
N,N-Diethylacetoacetamide
Diethyl acetylphosphonate
Diethyl 2-acetylsuccinate
C8H15NO2
C6H13O4P
C10H16O5
2235-46-3
919-19-7
1115-30-6
217.219 cry
(al,bzpeth)
157.211 liq
180.138
216.231
0.86525 1.381120 s ctc
1.032920 1.526920
0.915925 1.412325 vs H2O, eth,
EtOH, chl
0.825420 1.383420 s H2O, chl; msc
EtOH, eth; vs
ace
0.835125 1.389825 vs ace, bz, eth,
EtOH
0.793220 1.364321
0.831920 1.374818 s H2O; msc
EtOH; vs ace,
bz; sl chl
0.997620 1.445120 vs EtOH
0.962720 1.469020
0.82925
0.82922 1.402922
0.82520 1.392419 s H2O, ace, bz;
vs EtOH, eth
0.820021 1.389120 s EtOH, ace, bz;
vs eth; sl ctc
0.854315 1.400020 sl H2O; msc
EtOH, eth
0.894222 1.414020 vs ace, eth,
EtOH, chl
0.913017 1.437417 s H2O, EtOH;
msc eth, ace,
bz; sl ctc
sl H2O, eth; s
tfa, EtOH
3376
Diethyl adipate
C10H18O4
141-28-6
202.248 liq
-20(2)
3377
Diethyl 2-allylmalonate
C10H16O4
2049-80-1
200.232
3378
Diethylamine
N-Ethylethanamine
C4H11N
109-89-7
73.137
3379
Diethylamine hydrochloride
N-Ethylethanamine
hydrochloride
C4H12ClN
660-68-4
109.598 lf (al-eth)
228.5
3380
3381
(Diethylamino)acetonitrile
4-(Diethylamino)benzaldehyde
C6H12N2
C11H15NO
3010-02-4
120-21-8
112.172
177.243 ye nd (w)
41
169(6)
17210
3382
2-(Diethylamino)-N-(2,6dimethylphenyl)acetamide
2-(Diethylamino)-N-(2,6dimethylphenyl)acetamide,
monohydrochloride
2-Diethylaminoethanol
C14H22N2O
137-58-6
234.337 nd (bz, al)
68(1)
1814
C14H23ClN2O
73-78-9
270.798
128
C6H15NO
100-37-8
117.189 hyg
C8H19NO2
140-82-9
161.243
C9H17NO2
2426-54-2
171.237
3383
3384
3385
3386
2-[2-(Diethylamino)­ethoxy]­
ethanol
2-(Diethylamino)ethyl acrylate
HCP_Section_03.indb 172
Dimethyldiethoxysilane
Acrolein, diethyl acetal
Diethyl hexanedioate
Lidocaine
246
18520
7613
11420
255
250(11)
222.5
liq
-50(2)
1.010022
1.007520 1.508325
i H2O; sl EtOH; s
eth, bz, chl; vs
HOAc
vs EtOH
s EtOH, ctc; vs
eth
vs EtOH; s eth,
bz, ctc, chl
55.4(0.1)
1.427520
1.400720
1.100520 1.420026
1.08120 1.434620 i H2O; s EtOH,
eth, bz; sl chl
1.007620 1.427220 i H2O; s EtOH,
eth
1.009820 1.430520 i H2O; vs EtOH,
eth; s ctc
0.705620 1.386420 vs H2O; msc
EtOH; s eth,
ctc
1.047722
vs H2O, EtOH
0.866020 1.426020 s H2O
vs H2O; s EtOH,
eth, bz, ctc
vs bz, eth,
EtOH, chl
vs H2O
162.13(0.09) 0.892120 1.441220 msc H2O; s
EtOH, eth, ace,
bz, peth; sl ctc
221.5
0.942125 1.448020
<-60
8110
0.93720
1.437625
4/11/16 11:24 AM
Physical Constants of Organic Compounds
3-173
O
O
O
O
N
O
O
O
H
N
HO
OH
3348
3349
Diethanolamine
O
NH2
3355
Diethoxymethane
1,1-Diethoxyethene
3356
3357
O
O
3359
2,2-Diethoxyethanamine
3363
3364
2-(Diethoxymethyl)furan
Diethoxymethylphenylsilane
1,2-Diethoxyethane
O
O
3366
Diethoxymethylsilane
3360
1,1-Diethoxyethane
O
3365
O
O
O
O
O
3367
1,1-Diethoxypentane
O
O
HN
1,1-Diethoxypropane
2,2-Diethoxypropane
O
O P
O
O
N
O
O
O
O
O
O
O
3370
3371
3,3-Diethoxy-1-propyne
3372
N,N-Diethylacetamide
O
3368
O
O
N
3369
O
H Si O
O
O
O
O
1,4-Diethoxybenzene
NH2
3358
Diethoxydiphenylsilane
O
Si
O
3,3-Diethoxy-1-propene
3353
1,2-Diethoxybenzene
O
O
O
3362
3361
O
Diethoxydimethylsilane
O
O
O
3352
3,4-Diethoxybenzaldehyde
Si O
O
1,1-Diethoxy-N,N-dimethylmethanamine
O
3351
O
Si O
N
O
3354
O
O
4,4’-Diethoxyazobenzene
O
4,4-Diethoxy-1-butanamine
O
O
O
3350
Diethatyl, ethyl ester
O
O
N
N
Diethyl 2-acetamidomalonate
O
3373
N,N-Diethylacetoacetamide
3374
Diethyl acetylphosphonate
3375
Diethyl 2-acetylsuccinate
O
O
O
O
O
O
O
O
O
3376
3377
Diethyl adipate
H
N
Diethyl 2-allylmalonate
N
O
3382
2-(Diethylamino)-N-(2,6-dimethylphenyl)acetamide
N
H
N
H
HCl
3378
3379
Diethylamine
H
N
N
O
3383
HCl
2-(Diethylamino)-N-(2,6-dimethylphenyl)acetamide, monohydrochloride
N
Diethylamine hydrochloride
N
N
N
OH
3380
3381
(Diethylamino)acetonitrile
N
O
4-(Diethylamino)benzaldehyde
OH
N
O
O
3384
2-Diethylaminoethanol
3385
2-[2-(Diethylamino)ethoxy]ethanol
3386
2-(Diethylamino)ethyl acrylate
Organic
Cl
Physical Constants of Organic Compounds
3-174
Mol.
Wt.
Physical
Form
No.
Name
Synonym
Mol. Form.
CAS RN
3387
2-Diethylaminoethyl
4-aminobenzoate
2-(N,N-Diethylamino)ethyl
methacrylate
2-(Diethylamino)ethyl
2-phenylbutanoate
4-(Diethylamino)-2-hydroxybenzaldehyde
Diethyl 2-aminomalonate
Procaine
C13H20N2O2
59-46-1
C10H19NO2
105-16-8
C16H25NO2
14007-64-8 263.376
C11H15NO2
17754-90-4 193.243
C7H13NO4
6829-40-9
175.183
C14H17NO2
91-44-1
C10H15NO
91-68-9
C13H19NO
90-84-6
231.291 cry (al,
bz-lig)
165.232 orth bipym
(CS2-lig)
205.296 liq
C7H17NO
622-93-5
131.216
4079-68-9
579-66-8
91-66-7
111.185 liq
149.233
149.233 ye oil
C4H11As
692-42-2
134.052
3388
3389
3390
3391
3392
3393
3394
Butethamate
7-(Diethylamino)-4-methyl2H-1-benzopyran-2-one
3-(Diethylamino)phenol
mp/˚C
236.310 nd (w+2) pl 61
(lig or eth)
185.264
bp/˚C
8010
12216
78
1.10016
276
1.435316 vs H2O, EtOH,
eth; s ace, bz;
i lig
sl H2O; s EtOH,
eth, ace
s H2O, EtOH,
eth, CS2; sl lig
11114
Organic
3396
3397
3398
3-(Diethylamino)-1-propyne
2,6-Diethylaniline
N,N-Diethylaniline
N,N-Diethyl-2-propargylamine C7H13N
C10H15N
C10H15N
3399
Diethylarsine
3400
3401
N,N-Diethylbenzamide
o-Diethylbenzene
1,2-Diethylbenzene
C11H15NO
C10H14
1696-17-9
135-01-3
177.243
134.218 liq
-31.4(0.3)
1325
183.4(0.4)
3402
m-Diethylbenzene
1,3-Diethylbenzene
C10H14
141-93-5
134.218 liq
-83.9(0.2)
181.1(0.5)
3403
p-Diethylbenzene
1,4-Diethylbenzene
C10H14
105-05-5
134.218 liq
-43.3(0.4)
184(1)
3404
C10H16N2
93-05-0
164.247
3405
N,N-Diethyl-1,4-benzenediamine
Diethyl benzylidenemalonate
Diethyl benzalmalonate
C14H16O4
5292-53-5
248.275
3406
3407
3408
Diethyl benzylmalonate
Diethyl benzylphosphonate
Diethylbromoacetamide
2-Bromo-2-ethylbutanamide
C14H18O4
C11H17O3P
C6H12BrNO
607-81-8
1080-32-6
511-70-6
250.291
228.225
194.069
67
3409
Diethyl 2-bromomalonate
Ethyl bromomalonate
C7H11BrO4
685-87-0
239.064
-54
3410
3411
N,N-Diethylbutanamide
Diethyl 2-butylmalonate
1114-76-7
133-08-4
143.227
216.275
3412
3413
3414
3415
Diethyl 2-butynedioate
Diethylcarbamazine citrate
Diethylcarbamic chloride
N,N’-Diethylcarbanilide
C8H17NO
Pentane-1,1-dicarboxylic acid, C11H20O4
diethyl ester
C8H10O4
C16H29N3O8
C5H10ClNO
C17H20N2O
762-21-0
1642-54-2
88-10-8
85-98-3
170.163
391.416 cry
135.592
268.353 cry (al)
0.8
138
3416
Diethyl carbonate
Ethyl carbonate
105-58-8
118.131 liq
-43
3417
Diethyl thiophosphoryl chloride C4H10ClO2PS
2524-04-1
188.613
3418
3419
O,O-Diethyl chloridothionophosphate
Diethylchloroaluminum
Diethyl chloromalonate
3420
3421
Diethyl chlorophosphonate
Diethylcyanamide
3422
Diethyl 1,1-cyclobutanedicarboxylate
1,1-Diethylcyclohexane
Diethyl 1,1-cyclopropanedicarboxylate
Diethyl dibutylmalonate
HCP_Section_03.indb 174
1.490920
65.0
3395
3425
Solubility
0.9230
16811
Diethylpropion
3423
3424
nD
sl H2O; s EtOH,
eth, bz, chl
2-(Diethylamino)-1-phenyl-1propanone
3-(Diethylamino)-1-propanol
C5H10O3
den
g cm –3
189.5
1.5
-21.3(0.2)
120
251(8)
216(1)
105
261
32
21630
0.860020 1.443920 s EtOH; s eth,
ace, bz; sl chl
0.90625 1.545220
0.930720 1.540920 sl H2O; s EtOH,
ace, ctc; vs
eth, chl
1.133824 1.4709
vs ace, bz, eth,
EtOH
0.880020 1.503520 i H2O; msc
EtOH, eth, ace,
bz, lig, ctc
0.860220 1.495520 i H2O; msc
EtOH, eth, ace,
bz, lig, ctc
0.862020 1.496720 i H2O; msc
EtOH, eth, ace,
bz, lig, ctc
vs bz
206
237(8)
1.104520 1.538920 i H2O; s EtOH,
eth, ace, bz
1.07615 1.487220 i H2O; sl chl
1.493020 s ctc
sl H2O, chl; vs
EtOH, eth, bz
1.402225 1.452120 i H2O; msc
EtOH, eth; s
ace, ctc
0.888420 1.440325 vs H2O, EtOH
0.976420 1.425020 vs EtOH, eth
184200
1.007520 1.442520 s EtOH, eth, ctc
300
1102
231(12)
186
71(2)
125.9(0.9)
0.969225 1.384520
453
-74
Diethylaluminum chloride
Ethyl chloromalonate
C4H10AlCl
C7H11ClO4
96-10-6
120.557 col liq
14064-10-9 194.613
Diethoxyphosphoryl chloride
C4H10ClO3P
C5H10N2
814-49-3
617-83-4
172.547
98.146 liq
C10H16O4
3779-29-1
200.232
223(5)
0.96
reac H2O
1.204020 1.432720 i H2O; msc
EtOH, eth, chl;
s CS2
1.20519 1.417020
0.85420 1.412625 i H2O; s EtOH,
eth
1.045620 1.433026 vs EtOH; sl ctc
C10H20
C9H14O4
78-01-3
1559-02-0
140.266
186.205
178(6)
214(7)
1.05525
C15H28O4
596-75-8
272.381
15012
-80.7(0.6)
12750
222
i H2O; vs EtOH;
s chl
i H2O; s EtOH,
eth, chl
s ctc
93.5
187(15)
1.434518 vs EtOH, eth
0.945720 1.434120 i H2O; s EtOH,
eth, ctc
4/11/16 11:24 AM
Physical Constants of Organic Compounds
3-175
O
O
O
O
O
N
OH
N
O
N
H 2N
O
3387
N
3388
2-Diethylaminoethyl 4-aminobenzoate
3389
2-(N,N-Diethylamino)ethyl methacrylate
3390
2-(Diethylamino)ethyl 2-phenylbutanoate
4-(Diethylamino)-2-hydroxybenzaldehyde
OH
O
O
O
O
O
O
N
O
N
N
N
OH
NH2
3391
3393
3392
3394
3-(Diethylamino)phenol
7-(Diethylamino)-4-methyl-2H-1-benzopyran-2-one
3395
2-(Diethylamino)-1-phenyl-1-propanone
3-(Diethylamino)-1-propanol
Organic
Diethyl 2-aminomalonate
NH2
N
O
N
3396
3-(Diethylamino)-1-propyne
N
As
H
N
3398
3397
3400
3399
N,N-Diethylaniline
2,6-Diethylaniline
3401
N,N-Diethylbenzamide
Diethylarsine
3402
o-Diethylbenzene
3403
m-Diethylbenzene
p-Diethylbenzene
NH2
O
O
O
N
O
3404
O
O
3405
N,N-Diethyl-1,4-benzenediamine
O
3406
Diethyl benzylidenemalonate
O
N
O
O
O
N,N-Diethylbutanamide
Diethyl 2-butylmalonate
O,O-Diethyl chloridothionophosphate
Diethyl carbonate
O
O
Diethylchloroaluminum
Diethyl 1,1-cyclobutanedicarboxylate
3414
Cl
O
O P O
Cl
3419
3420
O
Diethyl chloromalonate
O
3423
N
3415
N,N’-Diethylcarbanilide
Diethyl chlorophosphonate
Diethylcyanamide
O
O
3424
Diethyl 1,1-cyclopropanedicarboxylate
N
N
3421
O
O
1,1-Diethylcyclohexane
N
Cl
Diethylcarbamic chloride
O
O
O
O
3422
3413
3418
3409
Diethyl 2-bromomalonate
O
O
3417
N
Diethylcarbamazine citrate
Al
Cl
O
3416
OH
N
Diethyl 2-butynedioate
O
Br
O
OH
O
3412
S
O P Cl
O
O
O
3411
HO
O
O
3410
Diethylbromoacetamide
O
O
OH O
O
N
N
O
3408
Diethyl benzylphosphonate
O
O
O
NH2
Br
3407
Diethyl benzylmalonate
O
O
O
P
O
O
O
O
O
O
3425
Diethyl dibutylmalonate
Physical Constants of Organic Compounds
3-176
CAS RN
Mol.
Wt.
den
g cm –3
1609-47-8
162.140
9318
1.12020
C9H22NO5P
2781-11-5
255.249 liq
1500.01
Diethadione
C8H13NO3
702-54-5
171.194 cry (eth)
97.5
3,5-Diethoxycarbonyl-1,4dihydrocollidine
C14H21NO4
632-93-9
267.322 lt bl flr pl
(al)
131
Diethyldimethylplumbane
C6H16Pb
C13H17NO4
1762-27-2
1149-24-2
295.4
col liq
251.279
71
C12H17NO4
2436-79-5
239.268 nd (dil al)
137.8
C4H10S2
110-81-6
122.252 liq
C16H33NO
C4H10O3
3352-87-2
111-46-6
255.439
106.120 liq
C6H8Cl2O5
106-75-2
231.031 liq
C8H14O5
C18H18O5
C12H26O3
C8H18O3
628-68-2
120-55-8
112-73-2
112-36-7
190.194
314.333
218.332 liq
162.227 liq
Oxydiethylene methacrylate
C12H18O5
2358-84-1
242.268
Diglyme
C6H14O3
111-96-6
134.173 liq
-64.0(0.1)
162(2)
2,2’-Oxybisethanol, dinitrate
C4H8N2O7
C8H18O3
693-21-0
112-34-5
196.116
162.227 liq
-68
440.01
232(4)
C10H20O4
124-17-4
204.264 liq
-32
248(2)
17.5
>270
Name
Synonym
3426
Diethyl dicarbonate
Pyrocarbonic acid diethyl ester C6H10O5
3427
Diethyl [(diethanolamino)­
methyl]phosphonate
5,5-Diethyldihydro-2H-1,3oxazine-2,4(3H)-dione
Diethyl 1,4-dihydro-2,4,6trimethyl-3,5-pyridinedicarboxylate
Diethyldimethyllead
Diethyl 2,6-dimethyl-3,5pyridinedicarboxylate
Diethyl 3,5-dimethylpyrrole2,4-dicarboxylate
3428
3429
3430
3431
3432
Organic
bp/˚C
No.
3433
Diethyl disulfide
3434
3435
N,N-Diethyldodecanamide
Diethylene glycol
3436
Diethylene glycol,
Oxydi-2,1-ethanediyl
bischloroformate
carbonochloridate
Diethylene glycol diacetate
Diethylene glycol dibenzoate
Diethylene glycol dibutyl ether Bis(2-butoxyethyl) ether
Diethylene glycol diethyl ether Bis(2-ethoxyethyl) ether
3437
3438
3439
3440
3441
3442
3443
3444
3445
3446
3447
3448
3449
3450
3451
3452
3453
3454
3455
Diethylene glycol
dimethacrylate
Diethylene glycol dimethyl
ether
Diethylene glycol dinitrate
Diethylene glycol monobutyl
ether
Diethylene glycol monobutyl
ether acetate
Diethylene glycol
monododecanoate
Diethylene glycol monoethyl
ether
Diethylene glycol monoethyl
ether acetate
Diethylene glycol monohexyl
ether
Diethylene glycol monomethyl
ether
Diethylene glycol monopropyl
ether
N,N-Diethyl-1,2-ethanediamine
N,N’-Diethyl-1,2-ethanediamine
Diethyl ether
Diglycol
Mol. Form.
Physical
Form
mp/˚C
5113
301
1.7920
-101.5(0.1)
154.0(0.6)
0.993120 1.507320
-10.3(0.3)
1662
245.5(0.2)
0.84725 1.454520
1.119715 1.447220
1265
1.3920
200
28024
255(4)
185(4)
1.106815 1.434820 vs EtOH
1.169015
vs H2O, EtOH
0.88525 1.423520
0.906320 1.411520 vs H2O, EtOH; s
eth
1.082120 1.457125
18
33.5
-60.2(0.2)
-44.3(0.2)
>200
C16H32O4
141-20-8
288.423 lt ye
C6H14O3
111-90-0
134.173 hyg liq
Carbitol acetate
C8H16O4
112-15-2
176.211 liq
-25
218(1)
2-[2-(Hexyloxy)ethoxy]ethanol
C10H22O3
112-59-4
190.280 col liq
-28
259(2)
2-(2-Methoxyethoxy)ethanol
C5H12O3
111-77-3
120.147
C7H16O3
6881-94-3
148.200 liq
C6H16N2
100-36-7
116.204
144
C6H16N2
111-74-0
116.204
146
Ethyl ether
C4H10O
60-29-7
74.121
2-Ethoxy-1,1bis(ethoxycarbonyl)ethene
C10H16O5
87-13-8
216.231
280 dec
C9H14O4
C9H16O4
1462-12-0
133-13-1
186.205
188.221
11617
208
202(3)
194(2)
liq
-53.3
-116.22(0.04) 34.4(0.5)
3456
3457
3458
Diethyl ethylphenylmalonate
C15H20O4
76-67-5
264.318
17019
3459
Diethyl ethylphosphonate
C6H15O3P
78-38-6
166.155
198
3460
N,N-Diethylformamide
C5H11NO
617-84-5
101.147
175(10)
3461
3462
3463
3464
Diethyl fumarate
Diethyl glutarate
3,4-Diethylhexane
Di-2-ethylhexyl maleate
C8H12O4
C9H16O4
C10H22
C20H36O4
623-91-6
818-38-2
19398-77-7
142-16-5
172.179
188.221 syr liq
142.282
340.498
0.8
-24.1
i H2O; s EtOH,
eth, bz, chl, lig
i H2O; sl EtOH,
eth; s ace, bz,
HOAc
sl H2O; msc
EtOH, eth
s chl
s H2O, EtOH,
eth, chl
1.454220
0.943420 1.409720 msc H2O, EtOH,
eth
0.955320 1.430620 msc H2O; vs
EtOH, eth, ace;
s bz
0.98520 1.426220 vs ace, eth,
EtOH
0.9625
msc EtOH, eth,
ace; s bz, tol
0.988520 1.430020 msc H2O, EtOH,
ace, bz; vs eth
1.009620 1.421320 vs H2O, ace,
eth, EtOH
1.03520
1.426420 msc H2O, ace;
vs EtOH, eth
214.8(0.4)
Diethyl (ethoxymethylene)­
malonate
Diethyl ethylidenemalonate
Diethyl ethylmalonate
HCP_Section_03.indb 176
Solubility
1.396020 vs ace, EtOH,
lig
sl H2O, EtOH,
eth, CS2; vs
chl
2-(2-Butoxyethoxy)ethyl
acetate
2-(2-Hydroxyethoxy)ethyl
laurate
Carbitol
N,N-Diethylethylenediamine
nD
214(5)
237(3)
160(5)
1567
0.828020 1.434020 msc H2O; s
EtOH, eth, ctc,
tol
0.828020 1.434020 vs H2O, eth,
EtOH, tol
0.713820 1.352620 sl H2O; msc
EtOH, bz, eth;
vs ace
1.460020 i H2O; s EtOH,
eth; sl chl
1.040420 1.430817 vs eth, EtOH
1.00620 1.416620 sl H2O; vs EtOH,
eth, ace, chl
1.07120 1.489625 i H2O; s EtOH,
eth; sl chl
1.025920 1.416320 sl H2O; s EtOH,
eth
0.908019 1.432125 msc H2O, ace,
bz; vs EtOH,
eth
1.045220 1.441220 i H2O; s ace, chl
1.022020 1.424120 vs eth
0.747225 1.419020
0.9420
4/11/16 11:24 AM
Physical Constants of Organic Compounds
O
P O
O
OH
O
N
O
O
O
3-177
N
HO
O
3426
O
Pb
N
H
3428
Diethyl [(diethanolamino)methyl]phosphonate
O
O
H
O
O
3427
Diethyl dicarbonate
O
O
3429
5,5-Diethyldihydro-2H-1,3-oxazine-2,4(3H )-dione
3430
Diethyl 1,4-dihydro-2,4,6-trimethyl-3,5-pyridinedicarboxylate
Diethyldimethyllead
O
O
O
O
O
O
O
N
N
H
3431
3432
O
S
3434
Diethyl disulfide
O
Cl
O
O
O
O
O
3440
O
O
Diethylene glycol dimethacrylate
O
N
O
O
O
OH
3444
Diethylene glycol dinitrate
O
Diethylene glycol monobutyl ether
OH
O
3450
O
N
OH
3452
Diethylene glycol monopropyl ether
O
O
O
O
O
O
O
O
O
O
O
O
O
O
3448
Diethylene glycol monoethyl ether acetate
H
N
NH2
N,N-Diethyl-1,2-ethanediamine
O
O
3447
3451
Diethylene glycol monomethyl ether
OH
Diethylene glycol monoethyl ether
O
OH
O
O
OH
3446
Diethylene glycol monohexyl ether
O
O
3443
Diethylene glycol monododecanoate
3449
O
O
O
O
O
O
3445
O
Diethylene glycol dibutyl ether
O
Diethylene glycol monobutyl ether acetate
O
O
N
Diethylene glycol dimethyl ether
O
O
O
3442
O
O
O
O
O
O
3439
Diethylene glycol dibenzoate
3441
Diethylene glycol diethyl ether
O
O
3438
O
O
O
O
O
O
Diethylene glycol diacetate
O
O
Diethylene glycol
O
O
O
3437
Diethylene glycol, bischloroformate
O
O
O
Cl
3436
OH
3435
N,N-Diethyldodecanamide
O
O
O
HO
3433
Diethyl 3,5-dimethylpyrrole-2,4-dicarboxylate
Diethyl 2,6-dimethyl-3,5-pyridinedicarboxylate
N
S
Organic
O
N
H
O
3453
3454
N,N’-Diethyl-1,2-ethanediamine
Diethyl ether
O
P O
O
N
O
O
3455
Diethyl (ethoxymethylene)malonate
3456
3457
Diethyl ethylidenemalonate
Diethyl ethylmalonate
3458
Diethyl ethylphenylmalonate
3459
O
O
O
O
O
3461
Diethyl fumarate
O
O
O
3460
Diethyl ethylphosphonate
N,N-Diethylformamide
O
O
O
O
3462
Diethyl glutarate
3463
3,4-Diethylhexane
3464
Di-2-ethylhexyl maleate
Physical Constants of Organic Compounds
3-178
No.
Name
3465
3466
1,2-Diethylhydrazine
Diethyl 1,2-hydrazinedicarboxylate
Diethyl hydrogen phosphate
N,N-Diethyl-4-hydroxy-3methoxybenzamide
Diethyl iminodiacetate
Diethyl isobutylmalonate
3467
3468
3469
3470
3471
3472
Mol.
Wt.
Physical
Form
mp/˚C
bp/˚C
den
g cm –3
nD
135
85.5
250 dec
0.79726
1.3248
1.420420 vs bz, eth, EtOH
vs eth, EtOH
203 dec
1.180020 1.417020 vs eth
s chl
Synonym
Mol. Form.
CAS RN
Diethyl bicarbamate
C4H12N2
C6H12N2O4
1615-80-1
4114-28-7
Diethyl phosphate
Ethamivan
C4H11O4P
C12H17NO3
598-02-7
304-84-7
C8H15NO4
C11H20O4
6290-05-7 189.210 orth cry
10203-58-4 216.275
247 dec
C12H14O4
C10H16O4
636-53-3
6802-75-1
222.237
200.232
11.5
88.151
176.170 nd (chl), pr
(w)
154.101 syr
223.268
95
298(6)
176.5
Organic
3473
Diethyl isophthalate
Diethyl isopropylidenemalonate
Diethyl isopropylmalonate
Ethyl isopropylmalonate
C10H18O4
759-36-4
202.248
215
3474
Diethyl ketomalonate
Ethyl mesoxalate
C7H10O5
609-09-6
174.151 pa ye grn oil -30
210
3475
3476
Diethyl malate
Diethyl maleate
Diethyl hydroxybutanedioate
C8H14O5
C8H12O4
7554-12-3
141-05-9
190.194
172.179 liq
-8.8
253
222(8)
3477
Diethyl malonate
Ethyl malonate
C7H12O4
105-53-3
160.168 liq
-50(2)
200(3)
3478
3479
Diethyl mercury
Diethylmethylamine
N-Ethyl-N-methylethanamine
C4H10Hg
C5H13N
627-44-1
616-39-7
258.71
87.164
-196
159
65.9(0.3)
3480
N,N-Diethyl-2-methylaniline
C11H17N
606-46-2
163.260 liq
-60
209
3481
N,N-Diethyl-4-methylaniline
C11H17N
613-48-9
163.260
229
3482
N,N-Diethyl-3-methylbenzamide
1,3-Diethyl-5-methylbenzene
DEET
C12H17NO
134-62-3
191.269
16019
C11H16
2050-24-0
148.245 liq
-74.1(0.3)
4-N,N-Diethyl-1,4-diamino-2- C11H19ClN2
methylbenzene, hydrochloride
2051-79-8
214.735 cry
250 dec
Isovaleryl diethylamide
C9H19NO
533-32-4
157.253
3486
N4,N4-Diethyl-2-methyl-1,4benzenediamine,
monohydrochloride
N,N-Diethyl-3-methylbutanamide
Diethyl methylenesuccinate
C9H14O4
2409-52-1
186.205
3487
Diethyl methylmalonate
C8H14O4
609-08-5
174.195
198.1(0.8)
3488
Diethyl methylphosphonate
C5H13O3P
683-08-9
152.129
181(6)
3489
C10H21N3O
90-89-1
199.293
49.5(0.5)
C10H17NO2
125-64-4
183.248
75.5
C14H17N
84-95-7
199.292
3492
N,N-Diethyl-4-methyl-1piperazinecarboxamide
3,3-Diethyl-5-methyl-2,4piperidinedione
N,N-Diethyl-1-naphthalenamine
N,N-Diethyl-4-nitroaniline
C10H14N2O2
2216-15-1
3493
N,N-Diethyl-4-nitrosoaniline
C10H14N2O
120-22-9
3494
Diethyl nonanedioate
Diethyl azelate
C13H24O4
624-17-9
194.230 ye nd (lig) pl 77.5
(al)
178.230 grn mcl pr 87.5
(eth) grn lf
(ace)
244.328 liq
-18.5
289(15)
3495
Diethyl oxalate
Ethyl oxalate
C6H10O4
95-92-1
146.141 liq
186(1)
3496
Diethyl oxobutanedioate
Diethyl oxalacetate
C8H12O5
108-56-5
188.178
13124
3497
Diethyl 3-oxo-1,5-pentanedioate
3,3-Diethylpentane
N’,N’-Diethyl-1,4-pentanediamine
2,2-Diethyl-4-pentenamide
Diethyl 2-pentenedioate
Diethyl 1,3-acetonedicarboxyl- C9H14O5
ate
Tetraethylmethane
C9H20
Novoldiamine
C9H22N2
105-50-0
202.204
250
1067-20-5
140-80-7
128.255 liq
158.284
-33.04(0.06) 146.2(0.3)
201
Novonal
Diethyl glutaconate
512-48-1
2049-67-4
155.237 wh pow
186.205
75.5
3483
3484
3485
3490
3491
3498
3499
3500
3501
HCP_Section_03.indb 178
Diethylcarbamazine
C9H17NO
C9H14O4
liq
58.5
205
0.980420 1.423620 i H2O; vs EtOH,
eth; s chl
1.123917 1.50818 i H2O
1.028218 1.448617 vs ace, EtOH
0.996120 1.418821 sl H2O, ctc; vs
EtOH, eth; s
chl
1.141916 1.431022 vs H2O; s EtOH,
eth, chl; i CS2
1.129020
1.066220 1.441620 i H2O; s EtOH,
eth; sl chl
1.055120 1.413920 sl H2O; msc
EtOH, eth; vs
ace, bz
2.4320
s eth; sl EtOH
0.70325 1.387925 vs H2O, EtOH,
eth
0.928620 1.515320 sl H2O; msc
EtOH, eth; s
ctc
0.924216
sl H2O; msc
EtOH, eth
0.99620 1.521220 vs H2O, bz, eth,
EtOH
0.874820 1.502720 i H2O; msc
EtOH, eth, ace,
bz, lig, ctc
211
0.876420 1.442220 vs eth, EtOH
228
1.046720 1.437720 msc EtOH; s
eth, bz; vs ace
1.022520 1.412620 sl H2O; vs EtOH,
eth, ace, chl
1.040630 1.410130 s H2O, EtOH,
eth; i bz
1103
285
-40.6(0.3)
Solubility
1.01320
1.22525
1.2415
237
1.596120
s H2O, bz, chl,
EtOH
s EtOH, eth, bz;
sl ctc
s EtOH; sl lig
sl H2O; s EtOH,
eth, ace, chl
0.972920 1.435120 i H2O; s EtOH,
eth
1.078520 1.410120 sl H2O; msc
EtOH, eth, ace;
s ctc
1.13120 1.456117 i H2O; msc
EtOH, eth, bz;
vs ace
1.11320
sl H2O; msc
EtOH
0.753620 1.420620 i H2O; s eth, bz
0.81420 1.442920
vs eth, EtOH
1.049620 1.441120 vs eth, EtOH
4/11/16 11:24 AM
Physical Constants of Organic Compounds
3-179
O
O
N
H
H
N
O
3465
H
N
N
H
O
O P O
OH
O
O
3466
1,2-Diethylhydrazine
O
O
OH
3467
Diethyl 1,2-hydrazinedicarboxylate
N
3468
Diethyl hydrogen phosphate
O
H
N
O
O
3469
N,N-Diethyl-4-hydroxy-3-methoxybenzamide
Diethyl iminodiacetate
O
O
O
O
O
O
O
O
O
O
O
O
O
O
O
O
O
O
3471
Diethyl isobutylmalonate
OH
O
O
O
O
3470
O
3472
Diethyl isophthalate
3473
Diethyl isopropylidenemalonate
O
3474
Diethyl isopropylmalonate
3475
Diethyl ketomalonate
Diethyl malate
Organic
O
N
N
O
O
O
O
O
O
O
3476
O
3477
Diethyl maleate
N
Hg
3478
Diethyl malonate
3479
Diethyl mercury
3480
Diethylmethylamine
3481
N,N-Diethyl-2-methylaniline
N,N-Diethyl-4-methylaniline
HCl NH2
O
N
O
O
N
O
O
N
3482
N,N-Diethyl-3-methylbenzamide
3483
1,3-Diethyl-5-methylbenzene
3484
N4,N4-Diethyl-2-methyl-1,4-benzenediamine, monohydrochloride
O
O
3485
N,N-Diethyl-3-methylbutanamide
N
3486
Diethyl methylenesuccinate
O
N
N
O
O
O
O
O P O
O
3487
3488
Diethyl methylmalonate
Diethyl methylphosphonate
N
N
H
N
3489
N,N-Diethyl-4-methyl-1-piperazinecarboxamide
O
3490
3,3-Diethyl-5-methyl-2,4-piperidinedione
3491
N,N-Diethyl-1-naphthalenamine
N
O
O
O
O
N
N
O
3492
O
O
O
O
O
3493
N,N-Diethyl-4-nitroaniline
N,N-Diethyl-4-nitrosoaniline
O
O
Diethyl 3-oxo-1,5-pentanedioate
3498
3499
N1,N1-Diethyl-1,4-pentanediamine
O
3500
2,2-Diethyl-4-pentenamide
O
3496
Diethyl oxobutanedioate
NH2
N
3,3-Diethylpentane
O
3495
Diethyl oxalate
NH2
O
O
O
O
3494
Diethyl nonanedioate
O
3497
O
O
O
O
O
O
3501
Diethyl 2-pentenedioate
Physical Constants of Organic Compounds
3-180
CAS RN
Mol.
Wt.
Physical
Form
mp/˚C
bp/˚C
Diethylperoxide
C4H10O2
628-37-5
90.121
liq
-70
46(9)
N,N-Diethyl-10H-phenothiDiethazine
azine-10-ethanamine
N,N-Diethylbenzhydrylamine
N,N-Diethyl-αphenylbenzenemethanamine
Diethyl phenylmalonate
Diethyl phenylphosphonite
5,5-Diethyl-1-phenylPhenetharbital
2,4,6(1H,3H,5H)-pyrimidinetrione
Diethylphosphine
Diethyl phosphonate
O,O’-Diethyl phosphorodithionate
Diethyl phthalate
C18H22N2S
60-91-3
298.446 oil
C17H21N
519-72-2
239.356
58.5
17017
C13H16O4
C10H15O2P
C14H16N2O3
83-13-6
1638-86-4
357-67-5
236.264
198.199
260.288
16.5
291(17)
235
1.095020 1.497720 vs ace, EtOH
1.03216
vs EtOH
C4H11P
C4H11O3P
C4H11O2PS2
627-49-6
762-04-9
298-06-6
90.104
138.102
186.233
85
546
0.78620
C12H14O4
84-66-2
222.237 liq
-40.5
298(2)
1.23214
C9H15NO2
77-03-2
169.221 nd (w)
104
C7H15NO
C7H18N2
1114-51-8
104-78-9
129.200
130.231
191
165(2)
0.897220
0.82220
C7H12O4
510-20-3
160.168 pr (w,bz)
127 dec
61.3(0.5)
Name
3502
3503
3504
3505
3506
3507
3508
3509
3510
3511
Organic
Mol. Form.
No.
3512
Synonym
178
nD
s ctc
s H2O
1.500021 i H2O; msc
EtOH, eth; s
ace, bz, ctc
vs H2O, EtOH,
chl, MeOH
1.442520 vs EtOH
1.44320
3515
3516
2,2-Diethyl-1,3-propanediol
C7H16O2
115-76-4
132.201
3517
Diethyl 2-propylmalonate
C10H18O4
2163-48-6
202.248
3518
C10H14N2O
59-26-7
25
C10H14N2O
530-40-5
178.230 ye solid or
visc liq
178.230
C9H13NO2
77-04-3
167.205
90.7
3521
N,N-Diethyl-3-pyridinecarbox- Nikethamide
amide
N,N-Diethyl-4-pyridinecarbox- Isonicotinic acid diethylamide
amide
3,3-Diethyl-2,4(1H,3H)Pyrithyldione
pyridinedione
Diethyl sebacate
C14H26O4
110-40-7
258.354
2.5
305
3522
3523
3524
Diethyl selenide
Diethylsilane
trans-Diethylstilbestrol
C4H10Se
C4H12Si
C18H20O2
627-53-2
542-91-6
56-53-1
137.08 pa ye
88.224 liq
268.351 pl (bz)
55
-134.3
172(3)
108
57
3525
Clinestrol
C24H28O4
130-80-3
380.477 pr (MeOH)
104
Mestilbol
C19H22O2
18839-90-2 282.377 nd (bz-peth) 117.5
1900.3
3527
trans-Diethylstilbestrol
dipropanoate
trans-Diethylstilbestrol
monomethyl ether
Diethyl succinate
Ethyl succinate
C8H14O4
123-25-1
174.195 liq
-21.6(0.8)
217(1)
1.040220 1.420120
3528
Diethyl sulfate
C4H10O4S
64-67-5
154.185 oil
-26.0(0.5)
208
1.17225
3529
Diethyl sulfide
Ethyl sulfide
C4H10S
352-93-2
90.187
-103.9(0.1)
92.1(0.2)
0.836220 1.443020
3530
3531
Diethyl sulfite
Diethyl sulfone
Ethyl sulfite
Ethyl sulfone
C4H10O3S
C4H10O2S
623-81-4
597-35-3
138.185
122.186 orth pl
70(4)
158
264(14)
1.120
1.35720
3532
Diethyl sulfoxide
C4H10OS
70-29-1
106.186 syr
14
10425
1.009222
3533
Diethyl DL-tartrate
C8H14O6
57968-71-5 206.193
18.7
281
1.204620 1.443820
3534
3535
Diethyl telluride
Diethyl terephthalate
C4H10Te
C12H14O4
627-54-3
636-09-9
43.2(0.6)
137.5
303(8)
1.59915 1.518215
1.098945
3536
3537
Diethyl thiodipropionate
N,N’-Diethylthiourea
C10H18O4S
C5H12N2S
673-79-0
105-55-5
185.72 red-ye
222.237 mcl pr (al,
peth)
234.313
132.227
17415
287(17)
1.103420 1.465520
76.9(0.4)
3538
C7H19NSi
996-50-9
145.319
126.3
0.762720 1.411220
3539
3540
N,N-Diethyl-1,1,1-trimethylsi- (Diethylamino)trimethylsilane
lanamine
Diethyltrisulfide
N,N-Diethylurea
C4H10S3
C5H12N2O
3600-24-6
634-95-7
154.317
116.161 pl, nd (eth)
8526
950.02
1.108220 1.568913
3541
N,N’-Diethylurea
C5H12N2O
623-76-7
116.161 tab (lig), hyg 110.3(0.4)
nd (al)
263
1.041525 1.461640
3519
3520
3526
HCP_Section_03.indb 180
Diethylmalonic acid
liq
244(12)
1.05020
1.457425
221
0.98920
1.419720
280 dec
1.06025
1.52520
1191
-72.6
75.3(0.2)
Solubility
0.824019 1.371517 sl H2O; msc
EtOH, eth
i H2O; s dil HCl
3,3-Diethyl-2,4-piperidinedione
N,N-Diethylpropanamide
N,N-Diethyl-1,3-propanediamine
Diethylpropanedioic acid
3513
3514
Piperidione
1670.5
den
g cm –3
1.52520
vs H2O, EtOH,
eth; sl bz, chl
vs H2O, EtOH,
eth; s chl
sl H2O; vs EtOH,
eth
sl DMSO
vs H2O, ace,
eth, EtOH
0.964620 1.430620 sl H2O, ctc; s
EtOH, ace; i bz
1.230020 1.476820
0.684320 1.392120 i H2O
vs eth, EtOH,
chl
vs bz, eth, EtOH
1.398920
1.431020
vs ace, eth,
EtOH
i H2O; msc
EtOH, eth; s
ace, chl
i H2O; msc
EtOH, eth
sl H2O, ctc; s
EtOH, eth
s EtOH, eth
s H2O, eth; vs
bz; i peth
vs H2O, eth,
EtOH
sl H2O; msc
EtOH, eth; s
ace, ctc
vs EtOH
i H2O; vs EtOH,
eth
s H2O, EtOH; vs
eth; sl ctc
vs H2O, EtOH,
bz, lig; s eth
vs H2O, EtOH,
eth
4/11/16 11:24 AM
Physical Constants of Organic Compounds
3-181
N
O
N
O
O
O
O
N
O
O
P
O
S
3502
3503
Diethylperoxide
3505
3504
N,N-Diethyl-10H-phenothiazine-10-ethanamine
3506
Diethyl phenylmalonate
N,N-Diethyl-α-phenylbenzenemethanamine
Diethyl phenylphosphonite
O
O
N
H
O
O
O
O P O
H
P
H
3507
3508
5,5-Diethyl-1-phenyl-2,4,6(1H,3H,5H )-pyrimidinetrione
S
O P SH
O
3510
3511
O,O’-Diethyl phosphorodithionate
Diethyl phosphonate
N
H2N
N
HO
O
3513
3514
N,N-Diethylpropanamide
O
OH
O
O
N
OH OH
3515
N,N-Diethyl-1,3-propanediamine
3,3-Diethyl-2,4-piperidinedione
O
O
O
N
3516
Diethylpropanedioic acid
O
3512
Diethyl phthalate
O
O
N
H
O
3509
Diethylphosphine
O
O
O
3517
2,2-Diethyl-1,3-propanediol
3518
Diethyl 2-propylmalonate
N,N-Diethyl-3-pyridinecarboxamide
O
N
O
N
H
N
3519
O
O
O
O
3520
N,N-Diethyl-4-pyridinecarboxamide
3521
3,3-Diethyl-2,4(1H,3H )-pyridinedione
3522
Diethyl sebacate
3523
Diethyl selenide
Diethylsilane
OH
O
OH
Si
H2
Se
O
O
O
O
O
HO
3524
3525
trans-Diethylstilbestrol
O
O
O
3526
trans-Diethylstilbestrol dipropanoate
3527
trans-Diethylstilbestrol monomethyl ether
Diethyl succinate
O
O
O O
S
O
O
S
3528
3529
Diethyl sulfate
O
O
O
S
Diethyl thiodipropionate
O O
S
O
3531
3532
S
O
3530
Diethyl sulfide
Diethyl sulfite
O
N
H
Diethyl sulfone
OH
O
O
OH O
N
H
3537
Diethyl sulfoxide
N,N’-Diethylthiourea
N
N,N-Diethyl-1,1,1-trimethylsilanamine
3534
Diethyl DL-tartrate
Diethyl telluride
N
Si
3538
Te
3533
S
O
3536
O
S
S
S
O
S
3539
Diethyltrisulfide
NH2
O
3540
N,N-Diethylurea
O
O
3535
Diethyl terephthalate
H
N
H
N
O
3541
N,N’-Diethylurea
Organic
N
Physical Constants of Organic Compounds
3-182
Organic
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
Zinc diethyl
C6H13O3P
C4H10Zn
682-30-4
557-20-0
164.139
123.531 col liq
C19H17Cl2N3O3
C18H20N2O4S
119446406.262
68-3
43222-48-6 360.428
158.5(0.5)
C14H9ClF2N2O2
35367-38-5 310.683
228(1)
1,2-Difluorobenzene
C2H2F2O2
C6H5F2N
C6H4F2
381-73-7
367-25-9
367-11-3
96.033 liq
129.108 liq
114.093 liq
-1
-7.5
-47.1(0.1)
m-Difluorobenzene
p-Difluorobenzene
1,3-Difluorobenzene
1,4-Difluorobenzene
C6H4F2
C6H4F2
372-18-9
540-36-3
114.093 liq
114.093 liq
-69.11(0.01) 83.0(0.5)
-23.5(0.2)
88.9(0.3)
3552
4,4’-Difluoro-1,1’-biphenyl
4,4’-Difluorodiphenyl
C12H8F2
398-23-2
190.189 mcl pr (al) lf 90(2)
(w)
254.5
3553
3554
3555
3556
1,1-Difluorocyclohexane
3,3-Difluorocyclopropene
Difluorodimethylsilane
1,5-Difluoro-2,4-dinitrobenzene
Difluorodiphenylsilane
1,1-Difluoroethane
C6H10F2
C3H2F2
C2H6F2Si
C6H2F2N2O4
371-90-4
56830-75-2
353-66-2
327-92-4
120.140 liq
76.045 liq
96.152 col gas
204.088
-87.5
75.5
99.5
34
2.5
1322
C12H10F2Si
C2H4F2
312-40-3
75-37-6
220.290
66.050 col gas
-118.6
246
-24.05
C2H4F2
C2H2F2
C2H2F2
C2H2F2
CH2F2
C3H3F5O
624-72-6
75-38-7
1630-77-9
1630-78-0
75-10-5
1885-48-9
66.050
64.034
64.034
64.034
52.024
150.047
CH3BF2
C6H3F2NO2
C3H6F2
373-64-8
446-35-5
420-45-1
63.843 gas
159.091
80.077 col gas
C3H6F2O
C10H6O4
453-13-4
492-94-4
C10H8N2O4
522-27-0
96.076
190.153 ye nd (al),
cry (bz)
220.182
C13H10O3
886-77-1
No.
Name
3542
3543
Diethyl vinylphosphonate
Diethyl zinc
3544
Difenoconazole
3545
Difenzoquat methyl sulfate
3546
Diflubenzuron
3547
3548
3549
Difluoroacetic acid
2,4-Difluoroaniline
o-Difluorobenzene
3550
3551
3557
3558
3559
3560
3561
3562
3563
3564
1H-Pyrazolium, 1,2-dimethyl3,5-diphenyl-, methyl sulfate
N-[[(4-Chlorophenyl)­amino]­
carbonyl]-2,6difluorobenzamide
Ethylidene difluoride
3565
3566
3567
1,2-Difluoroethane
1,1-Difluoroethene
cis-1,2-Difluoroethene
trans-1,2-Difluoroethene
Difluoromethane
2-(Difluoromethoxy)-1,1,1trifluoroethane
Difluoromethylborane
2,4-Difluoro-1-nitrobenzene
2,2-Difluoropropane
Ethylene difluoride
Vinylidene fluoride
cis-1,2-Difluoroethylene
trans-1,2-Difluoroethylene
Methylene fluoride
Difluoromethyl 2,2,2-trifluoroethyl ether
3568
3569
1,3-Difluoro-2-propanol
Di-2-furanylethanedione
3570
Di-2-furanylethanedione
dioxime
1,5-Di-2-furanyl-1,4-pentadien-3-one
α-Furildioxime
3572
3573
3574
3575
Difurfuryl disulfide
Difurfuryl ether
Digitonin
Digitoxigenin
Furfuryl disulfide
Furfuryl ether
3576
Physical
Form
mp/˚C
1102
-33.34(0.02) 133(6)
76
vol liq
col gas
col gas
col gas
col gas
col liq
bp/˚C
-144
-136.8(0.2)
9.8
-104.8
133
170
93.9(0.5)
-78.5287
207
0(3)
127
166.3
167
1814
C10H10O2S2
C10H10O3
C56H92O29
C23H34O4
10
16713
1012
Digitoxin
C41H64O13
71-63-6
764.939 pr (dil al)
255.5
3577
Digitoxose
C6H12O4
527-52-6
3578
3579
Diglycidyl ether
Diglycolic acid
C6H10O3
C4H6O5
2238-07-5
110-99-6
3580
Digoxigenin
C23H34O5
1672-46-4
148.157 cry (MeOH​ 112
+eth)
130.141
134.088 mcl pr (w + 148
1)
390.513 pr (AcOEt) 222
3581
Digoxin
C41H64O14
3582
Diheptylamine
N-Heptyl-1-heptanamine
3583
3584
3585
3586
Diheptyl ether
Diheptyl phthalate
Diheptyl sulfide
Dihexylamine
Heptyl ether
HCP_Section_03.indb 182
Heptyl sulfide
N-Hexyl-1-hexanamine
sl EtOH
1.14517
0.89625
(p>1
atm)
1.522125
1.3011-72
i H2O; s EtOH
vs EtOH
1.140520 1.508820 i H2O
237.5
253
s EtOH; vs
MeOH
sl H2O; vs EtOH;
s eth, chl,
MeOH, py
vs H2O, ace; s
py, AcOEt
1.119520
C14H31N
20830-75-5 780.939 trc pl (dil al, 249 dec
py)
2470-68-0 213.403 nd
31.5
266(8)
0.795621
C14H30O
C22H34O4
C14H30S
C12H27N
629-64-1
3648-21-3
629-65-2
143-16-8
258(4)
360
295(11)
236
0.800820 1.427520
70
-13.0(0.2)
vs bz, eth, chl
vs eth, EtOH
reac H2O
1.457114 1.514914 sl chl
0.920520 1.290420
(p>1
atm
1.2425
1.372520
sl H2O; s EtOH,
eth, bz, chl
sl EtOH, eth, bz,
lig
vs eth, EtOH,
chl
260
269(18)
214.387
362.503
230.453
185.349 liq
Solubility
1.52625 1.347020
1.26825 1.506320
1.159918 1.445118 i H2O; s ace, bz,
chl
1.157220 1.437420 i H2O; s ace, bz
1.170120 1.442220 i H2O; s ace, bz;
sl ctc
i H2O; vs EtOH,
bz, chl; s eth,
ace
26
-85.5(0.8)
-45(19)
-53.1
-51.65(0.07) 1.2139-52
29.2(0.2)
60.5
Bis(2,3-epoxypropyl) ether
2,2’-Oxydiacetic acid
nD
1.06825 1.429020
1.206520 1.493620 dec H2O; msc
eth, peth, bz
2200.03
214.216 hyg pr
(peth) ye
pr (lig)
4437-20-1 226.315
4437-22-3 178.184
11024-24-1 1229.312
143-62-4
374.514
3571
den
g cm –3
vs H2O, eth,
EtOH
vs EtOH, MeOH;
sl chl
vs EtOH
sl H2O; s EtOH;
vs eth
vs eth, EtOH
0.841620 1.460620 i H2O; s eth
0.788920 1.433920 s EtOH, eth
4/11/16 11:24 AM
Physical Constants of Organic Compounds
3-183
N
N
N
F
O
O
O P O
Cl
O
Cl
Zn
3542
N
SO4 2
O
3543
Diethyl vinylphosphonate
N
H
N
3545
Difenoconazole
O
F
O
3546
Difenzoquat methyl sulfate
OH
F
3547
Diflubenzuron
Difluoroacetic acid
F
NH2
F
F
F F
F F
F
3549
3548
O
N
F
O
F F
Si
3557
F
O
Difluorodimethylsilane
3560
1,2-Difluoroethane
N
F
F
F
3561
1,1-Difluoroethene
F
F
3562
cis-1,2-Difluoroethene
F
3564
B
3563
trans-1,2-Difluoroethene
Difluoromethane
O
F
3565
2-(Difluoromethoxy)-1,1,1-trifluoroethane
O
F
F F
F
F
O
O
O
OH
3567
3566
Difluoromethylborane
H
H
F
F
F
F
N
3555
3,3-Difluorocyclopropene
F
F
3559
1,1-Difluoroethane
O
F
F
F
3558
Difluorodiphenylsilane
3554
1,1-Difluorocyclohexane
F
F
3556
3553
4,4’-Difluoro-1,1’-biphenyl
F
O
1,5-Difluoro-2,4-dinitrobenzene
F
Si F
F
3552
p-Difluorobenzene
m-Difluorobenzene
F
N
3551
3550
o-Difluorobenzene
2,4-Difluoroaniline
F
F
F
F
3568
2,2-Difluoropropane
2,4-Difluoro-1-nitrobenzene
3569
1,3-Difluoro-2-propanol
Di-2-furanylethanedione
OH
O
O
O
N
HO
O
O
3570
3571
Di-2-furanylethanedione dioxime
S S
O
O
O
O
1,5-Di-2-furanyl-1,4-pentadien-3-one
O
3573
3572
Difurfuryl ether
Difurfuryl disulfide
O
O
O
HO
O O
O
O
OH
OH
HO
HO
OH HO
HO
HO
O
O
HO
HO
O
OH
OH
O O
H
O
O
O
O O
OH
O
O
OH
HO
OH
3574
OH
HO
H
OH
3575
Digitonin
3576
Digitoxigenin
Digitoxin
O
O
HO
H
O O OH
OH
OH
HO
O
O
OH
O
O
HO
O
OH
3577
H
N
3582
Diheptylamine
3578
Digitoxose
Diglycidyl ether
O
OH
O
O
O
O O
HO
O
H
OH
3583
Diheptyl ether
O
O O OH
O
HO
O
O
3579
Diglycolic acid
OH
OH
HO
O
O
HO
H
OH
3580
O
3581
Digoxigenin
3584
Digoxin
S
3585
Diheptyl sulfide
Diheptyl phthalate
N
H
3586
Dihexylamine
Organic
F
O
F
O
Cl
3544
Diethyl zinc
H
N
Physical Constants of Organic Compounds
3-184
No.
Name
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
3587
Dihexyl ether
Hexyl ether
C12H26O
112-58-3
186.333
3588
3589
3590
3591
3592
Dihexyl hexanedioate
Dihexyl phthalate
Dihexyl sulfide
15,16-Dihydroaflatoxin G1
9,10-Dihydroanthracene
C18H34O4
C20H30O4
C12H26S
C17H14O7
C14H12
110-33-8
84-75-3
6294-31-1
7241-98-7
613-31-0
314.461 liq
334.450
202.399
330.289
180.245 tab or pr
239.3
109.00(0.01) 305
3593
6,15-Dihydro-5,9,14,18anthrazinetetrone
Indanthrene
C28H14N2O4
81-77-6
442.422 bl nd
485 dec
3594
1,2-Dihydrobenz[j]­
aceanthrylene
Cholanthrene
C20H14
479-23-2
254.325 pa ye lf
(bz-al)
170.4
3595
9,10-Dihydro-9,10[1’,2’]Triptycene
benzenoanthracene
1,3-Dihydro-2H-benzimid2-Benzimidazolethiol
azole-2-thione
1,3-Dihydro-2H-benzimidazol2-one
2,3-Dihydro-1,4-benzodioxin
2,3-Dihydrobenzofuran
Coumaran
C20H14
477-75-8
254.325 cry (cyhex)
253.99(0.01)
C7H6N2S
583-39-1
316.3(0.8)
vs EtOH
C7H6N2O
615-16-7
150.201 pl (dil al or
NH3)
134.135 lf (w or al)
318 dec
sl H2O, eth, bz;
s ace; vs EtOH
C8H8O2
C8H8O
493-09-4
496-16-2
136.149
120.149 liq
-21.5
213(1)
187(19)
1.18020
1.05825
3,4-Dihydro-1H-2-benzopyran Isochroman
3,4-Dihydro-2H-1-benzopyran
3,4-Dihydro-2H-1-benzopyran-2-one
2,3-Dihydro-4H-1-benzopy4-Chromanone
ran-4-one
C9H10O
C9H10O
C9H8O2
493-05-0
493-08-3
119-84-6
134.174
134.174
148.159 lf
4.35(0.02)
-3.31(0.02)
25
11025
215.6(0.8)
272
1.06725
1.07220
1.16918
C9H8O2
491-37-2
148.159
39.1(0.4)
16050
1.1291100
6,7-Dihydrobenzo[b]­thiophen- 4,5,6,7-Tetrahydro-4-benzo4(5H)-one
thiophenone
2,3-Dihydro-4H-1-benzothiopyran-4-one
4,5-Dihydro-2-benzyl-1HTolazoline
imidazole
7,8-Dihydrobiopterin
Dihydrocodeine
C8H8OS
13414-95-4 152.214
C9H8OS
3528-17-4
164.224
29
15412
1.248714 1.639520
C10H12N2
59-98-3
160.215 cry (peth)
67
C9H13N5O3
C18H23NO3
6779-87-9
125-28-0
C17H14
482-66-6
239.231 hyg nd (w)
301.381 cry (aq,
112.5
MeOH)
218.293 nd (al, petr) 135.5
C14H13N
494-19-9
195.260
C15H12O
1210-35-1
208.255
C6H10O3
332-77-4
130.141
C11H13NO3
493-49-2
C11H12N2O
60-80-0
C4H6O2
C15H8O4
543-75-9
117-78-2
C14H8O8S2
117-14-6
9,10-Dihydro-9,10-dioxo-2,6anthracenedisulfonic acid
9,10-Dihydro-9,10-dioxo-1anthracenesulfonic acid
C14H8O8S2
84-50-4
207.226 mcl pr (w,
al)
188.225 lf or sc (eth,
bz)
86.090
252.223 ye nd
(HOAc)
368.339 ye nd (HCl
+4w) pl
(dil HOAc)
368.339
C14H8O5S
82-49-5
9,10-Dihydro-9,10-dioxo-2anthracenesulfonic acid
9,10-Dihydro-9,10-dioxo-1anthracenesulfonic acid,
sodium salt
9,10-Dihydro-9,10-dioxo-2anthracenesulfonic acid,
sodium salt
7,8-Dihydrofolic acid
2,3-Dihydrofuran
C14H8O5S
84-48-0
288.276 lf (HOAc) ye 216.0
lf (conc
HCl, +3w)
288.276 ye lf (+3w)
C14H7NaO5S
128-56-3
310.258 ye lf (w)
vs H2O; s EtOH;
i eth
sl H2O
C14H7NaO5S
131-08-8
310.258
sl DMSO
C19H21N7O6
C4H6O
4033-27-6
1191-99-7
443.413 ye cry
70.090
3596
Organic
3597
3598
3599
3600
3601
3602
3603
3604
3605
3606
3607
3608
3609
3610
3611
3612
3613
3614
3615
3616
3617
3618
3619
3620
3621
3622
3623
3624
Hexyl sulfide
Aflatoxin G2
16,17-Dihydro-15H1,2-Cyclopentenophenancyclopenta[a]phenanthrene
threne
10,11-Dihydro-5H-dibenz[b,f]­
azepine
10,11-Dihydro-5Hdibenzo[a,d]cyclohepten-5one
2,5-Dihydro-2,5-dimethoxyfuran
3,4-Dihydro-6,7-dimethoxyCorydaldine
1(2H)-isoquinolinone
1,2-Dihydro-1,5-dimethyl-2- Antipyrine
phenyl-3H-pyrazol-3-one
2,3-Dihydro-1,4-dioxin
9,10-Dihydro-9,10-dioxo-2anthracenecarboxylic acid
9,10-Dihydro-9,10-dioxo-1,5anthracenedisulfonic acid
HCP_Section_03.indb 184
Sodium anthraquinone-1sulfonate
Physical
Form
mp/˚C
bp/˚C
220(4)
-9
32.4(0.5)
344(16)
2105
230
den
g cm –3
nD
Solubility
0.793620 1.420420 i H2O; s eth; sl
ctc
0.94120
0.841120 1.458620
1.21520
i H2O; s EtOH,
eth, bz, chl
i H2O, EtOH, eth,
ace, bz; s
PhNO2, dil alk
i H2O; s EtOH,
bz, HOAc, lig,
tol
1.548520
1.549720 vs eth, EtOH,
chl
1.544420
1.544420 s H2O; msc os
1.556320 i H2O; sl EtOH,
eth, ctc; s chl
1.5750
s EtOH; vs eth,
ace, bz, chl; sl
ctc
sl chl
s H2O
24815
i H2O; s EtOH,
peth
s chl
2037
1.163520 1.632420
161
1.07325
1.433920
175
108.0(0.2)
319
291
94.1
sub
310 dec
vs H2O, bz, eth,
EtOH
vs H2O, EtOH
1.083620 1.437220 s ctc
sl EtOH, HOAc; i
eth, bz; s ace
vs H2O, EtOH,
HOAc
vs H2O; s EtOH;
i eth, bz
vs H2O, HOAc; s
EtOH
54.5(0.2)
0.92725
1.423920
4/11/16 11:24 AM
Physical Constants of Organic Compounds
3-185
O
O
O
O
O
O
3588
Dihexyl ether
S
O
O
O
3587
3589
Dihexyl hexanedioate
3590
Dihexyl phthalate
Dihexyl sulfide
O
O
H
O
O HN
O
NH O
O
O
O
O
3591
3592
15,16-Dihydroaflatoxin G1
H
N
S
O
3597
1,3-Dihydro-2H-benzimidazole-2-thione
O
O
2,3-Dihydrobenzofuran
3601
3,4-Dihydro-1H-2-benzopyran
3,4-Dihydro-2H-1-benzopyran
O
N
S
O
N
H
S
3604
2,3-Dihydro-4H-1-benzopyran-4-one
O
3600
O
3603
3,4-Dihydro-2H-1-benzopyran-2-one
3599
2,3-Dihydro-1,4-benzodioxin
O
O
O
3598
1,3-Dihydro-2H-benzimidazol-2-one
3602
9,10-Dihydro-9,10[1’,2’]-benzenoanthracene
O
O
N
H
3596
3595
1,2-Dihydrobenz[j]aceanthrylene
6,15-Dihydro-5,9,14,18-anthrazinetetrone
H
N
N
H
3594
3593
9,10-Dihydroanthracene
Organic
H O
3605
6,7-Dihydrobenzo[b]thiophen-4(5H )-one
3606
2,3-Dihydro-4H-1-benzothiopyran-4-one
4,5-Dihydro-2-benzyl-1H-imidazole
O
OH
O
N
OH
N
H
O
NH
N
H
NH2
N
N
H
O
3610
3611
HO
3607
3608
7,8-Dihydrobiopterin
3609
Dihydrocodeine
16,17-Dihydro-15H-cyclopenta[a]phenanthrene
10,11-Dihydro-5H-dibenz[b,f]azepine
10,11-Dihydro-5H-dibenzo[a,d]cyclohepten-5-one
O
O
O
O
O
N
O
O
3612
3614
3,4-Dihydro-6,7-dimethoxy-1(2H )-isoquinolinone
3615
1,2-Dihydro-1,5-dimethyl-2-phenyl-3H-pyrazol-3-one
O
O
S
3617
9,10-Dihydro-9,10-dioxo-1,5-anthracenedisulfonic acid
OH
OO S O
OH
SO3 Na
O
O
O
3618
3619
9,10-Dihydro-9,10-dioxo-2,6-anthracenedisulfonic acid
3621
9,10-Dihydro-9,10-dioxo-1-anthracenesulfonic acid, sodium salt
O
S
OH
O
O
3620
9,10-Dihydro-9,10-dioxo-1-anthracenesulfonic acid
HO
O
SO3 Na
O
O
S
HO
O
9,10-Dihydro-9,10-dioxo-2-anthracenecarboxylic acid
O
O
HO
3616
2,3-Dihydro-1,4-dioxin
OH
OO S O
O S OO
OH
O
O
3613
2,5-Dihydro-2,5-dimethoxyfuran
OH
O
NH
O
O
N
O
O
9,10-Dihydro-9,10-dioxo-2-anthracenesulfonic acid
O
O
N
H
N
H
N
N
H
O
3622
9,10-Dihydro-9,10-dioxo-2-anthracenesulfonic acid, sodium salt
3623
7,8-Dihydrofolic acid
NH
N
NH2
O
3624
2,3-Dihydrofuran
Physical Constants of Organic Compounds
3-186
No.
Name
3625
3626
3628
3629
2,5-Dihydrofuran
2,3-Dihydro-3-hydroxy-1methyl-1H-indole-5,6-dione
2,3-Dihydro-1H-inden-5amine
2,3-Dihydro-1H-inden-1-ol
2,3-Dihydro-1H-inden-5-ol
3630
2,3-Dihydro-1H-inden-1-one
3631
1,3-Dihydro-2H-inden-2-one
3632
1a,6a-Dihydro-6H-indeno[1,2b]oxirene
2,3-Dihydro-1H-indole
3627
3633
Organic
3634
3635
3636
3637
3638
3639
3640
3641
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
Adrenochrome
C4H6O
C9H9NO3
1708-29-8
54-06-8
70.090
179.172
C9H11N
24425-40-9 133.190 nd (peth)
37.5
248
C9H10O
C9H10O
6351-10-6
1470-94-6
134.174 pl (peth)
134.174
55(2)
58
220
253
C9H8O
83-33-0
40(2)
243(8)
1.094340 1.56125
C9H8O
615-13-4
132.159 ta, nd (w +
3)
132.159 nd (al, eth)
58(3)
218 dec
1.071269 1.53867
C9H8O
768-22-9
132.159
24.5
11320
1.125524
C8H9N
496-15-1
119.164
230(13)
1.06920
C8H7NO
C8H7NO
59-48-3
480-91-1
133.148 nd (w)
133.148 nd (w)
1.592320 sl H2O; s eth,
ace, bz
s H2O, EtOH, eth
vs eth, EtOH,
chl
C8H16O2S2
C11H12O2
462-20-4
1078-19-9
C6H10O2
4454-05-1
208.342 ye liq
176.212 cry (MeOH,
lig)
114.142 liq
127(23)
1.006
1.442020
C21H16
56-49-5
268.352 ye nd (bz)
28080
1.2820
C9H10O
1746-11-8
134.174
197.5
1.06125
C5H4O3
2170-03-8
68(1)
C5H6O2
547-65-9
112.084 orth bipym
pr (eth,
chl)
98.101
C5H6O3
4100-80-5
114.100
36.8(0.8)
C5H8O2
1679-47-6
C5H8O2
1679-49-8
C5H8O2
57129-69-8 100.117 liq
Lysidine
C4H8N2
534-26-9
84.120
Methimazole
C4H6N2S
60-56-0
114.169 lf (al)
767-58-8
132.202
1590-08-5
160.212
15
89-36-1
254.262 nd (w+1)
≈300 dec
2-Indanone
1,3-Dihydro-2H-indol-2-one
2,3-Dihydro-1H-isoindol-1one
6,8-Dimercaptooctanoic acid
Dihydro-α-lipoic acid
3,4-Dihydro-6-methoxy-1(2H)- 6-Methoxy-α-tetralone
naphthalenone
3,4-Dihydro-2-methoxy-2Hpyran
1,2-Dihydro-3-methylbenz[j]­ 3-Methylcholanthrene
aceanthrylene
2,3-Dihydro-2-methylbenzofuran
Dihydro-3-methylene-2,5furandione
3642
Dihydro-3-methylene-2(3H)furanone
3643
Dihydro-3-methyl-2,5-furandione
Dihydro-3-methyl-2(3H)2-Methyl-γ-butyrolactone
furanone
Dihydro-4-methyl-2(3H)3-Methyl-γ-butyrolactone
furanone
Dihydro-5-methyl-2(3H)(±)-γ-Valerolactone
furanone, (±)-
3644
3645
3646
3647
3648
3649
3650
3651
3652
3653
3654
3655
3656
3657
3658
3659
3660
3661
4,5-Dihydro-2-methyl-1Himidazole
1,3-Dihydro-1-methyl-2Himidazole-2-thione
α-Methylene butyrolactone
2,3-Dihydro-1-methyl-1HC10H12
indene
3,4-Dihydro-2-methyl-1(2H)C11H12O
naphthalenone
4-(4,5-Dihydro-3-methyl-5C10H10N2O4S
oxo-1H-pyrazol-1-yl)­
benzenesulfonic acid
1,2-Dihydro-5-methyl-25-Hydroxy-3-methyl-1-phenyl- C10H10N2O
phenyl-3H-pyrazol-3-one
pyrazole
2,4-Dihydro-5-methyl-2C10H10N2O
phenyl-3H-pyrazol-3-one
3,6-Dihydro-4-methyl-2HC6H10O
pyran
4,5-Dihydro-2-methylthiazole
C4H7NS
1,2-Dihydronaphthalene
C10H10
1,4-Dihydronaphthalene
C10H10
Δ 2-Dialin
3,4-Dihydro-2(1H)-naphthaleC10H10O
none
1,2-Dihydro-5-nitroacenaphC12H9NO2
thylene
1,6-Dihydro-6-oxo-3-pyridineC6H5NO3
carboxylic acid
Dihydro-5-pentyl-2(3H)furanone
HCP_Section_03.indb 186
4-Hydroxynonanoic acid
lactone
C9H16O2
Physical
Form
mp/˚C
bp/˚C
den
g cm –3
nD
Solubility
1.431120
125 dec
128
151
22723
338
78.1(0.5)
1450.2
17111
178.0(0.2)
i H2O
1.5308
13930
sl eth; vs chl
221(16)
1.120620 1.465020 s H2O, eth, ace,
bz; sl ctc; vs
EtOH
1.2225
100.117 liq
200
1.057020 1.432520
100.117 liq
7611
1.05820
-31
204(4)
107
196.5
146
280 dec
191(7)
1.055120 1.432820 msc H2O; s
EtOH, ace; sl
ctc
vs H2O, EtOH; i
eth; s chl
vs H2O; s EtOH,
chl; sl eth, bz,
lig
0.93825 1.526620 i H2O
13616
1.05725
hyg
8510
vs H2O, EtOH; i
eth, bz
sl H2O, chl; s
eth, ace, bz
vs bz, EtOH, chl
sl H2O, peth; vs
EtOH, eth; s
sulf
sl H2O; vs EtOH,
eth, ace, chl
i H2O; vs EtOH,
eth, ace, chl
s chl
1.433920
1.553520
19735-89-8 174.198
128
287105
1.260020 1.637
89-25-8
127
287105
1.637
174.198 mcl pr (w)
16302-35-5 98.142
2346-00-1
447-53-0
612-17-9
530-93-8
101.171 liq
130.186 liq
130.186 pl
146.185
-101
-8.77(0.05)
24.6(0.9)
18
602-87-9
199.205
103
5006-66-6
139.109 nd(w)
310 dec
104-61-0
156.222 oil
s H2O, EtOH; sl
bz; i peth
118(6)
0.91225
1.449520
145
210.2(0.7)
210(5)
237
1.06725
0.997420
0.992833
1.105527
1.520020
1.581420
1.557720
1.559820 i H2O; s eth, bz
sub
s H2O, EtOH,
eth, lig
sl H2O, tfa; i
EtOH, eth, bz,
chl
13412
4/11/16 11:24 AM
Physical Constants of Organic Compounds
OH
O
3625
H2N
3626
2,5-Dihydrofuran
HO
3627
2,3-Dihydro-3-hydroxy-1-methyl-1H-indole-5,6-dione
3628
2,3-Dihydro-1H-inden-5-amine
3631
3632
O
HS
OH
O
3634
SH
3635
1,3-Dihydro-2H-indol-2-one
3636
2,3-Dihydro-1H-isoindol-1-one
Dihydro-α-lipoic acid
Organic
2,3-Dihydro-1H-indole
2,3-Dihydro-1H-inden-1-one
NH
N
H
3633
1a,6a-Dihydro-6H-indeno[1,2-b]oxirene
3630
2,3-Dihydro-1H-inden-5-ol
O
N
H
1,3-Dihydro-2H-inden-2-one
3629
2,3-Dihydro-1H-inden-1-ol
O
O
O
OH
N
O
O
3-187
O
O
O
3637
3,4-Dihydro-6-methoxy-1(2H )-naphthalenone
O
O
O
3639
3638
3640
1,2-Dihydro-3-methylbenz[j]aceanthrylene
3,4-Dihydro-2-methoxy-2H-pyran
O
O
3641
2,3-Dihydro-2-methylbenzofuran
Dihydro-3-methylene-2,5-furandione
N
O
O
O
3642
Dihydro-3-methylene-2(3H)-furanone
O
O
O
3643
3644
Dihydro-3-methyl-2,5-furandione
O
O
Dihydro-3-methyl-2(3H)-furanone
O
O
3645
O
3646
Dihydro-4-methyl-2(3H )-furanone
3647
Dihydro-5-methyl-2(3H )-furanone, (±)-
4,5-Dihydro-2-methyl-1H-imidazole
H
N
O
NH
N
H
O
S OH
O
N
S
N
O
3648
1,3-Dihydro-1-methyl-2H-imidazole-2-thione
O
N
H
3649
2,3-Dihydro-1-methyl-1H-indene
O
N
3650
3651
3,4-Dihydro-2-methyl-1(2H )-naphthalenone
4-(4,5-Dihydro-3-methyl-5-oxo-1H-pyrazol-1-yl)benzenesulfonic acid
N
N
N
O
3652
1,2-Dihydro-5-methyl-2-phenyl-3H-pyrazol-3-one
3653
2,4-Dihydro-5-methyl-2-phenyl-3H-pyrazol-3-one
S
3654
3655
3,6-Dihydro-4-methyl-2H-pyran
4,5-Dihydro-2-methylthiazole
3656
1,2-Dihydronaphthalene
3657
1,4-Dihydronaphthalene
O
OH
O
O
3658
3,4-Dihydro-2(1H )-naphthalenone
N
3659
O
1,2-Dihydro-5-nitroacenaphthylene
O
N
H
3660
1,6-Dihydro-6-oxo-3-pyridinecarboxylic acid
O
3661
O
Dihydro-5-pentyl-2(3H )-furanone
Physical Constants of Organic Compounds
3-188
No.
Name
3662
3663
9,10-Dihydrophenanthrene
2,3-Dihydro-2-phenyl-4H-1benzopyran-4-one
4,5-Dihydro-2-(phenylmethyl)1H-imidazole, monohydrochloride
4,5-Dihydro-5-phenyl-2oxazolamine
1,4-Dihydro-1-phenyl-5Htetrazole-5-thione
Dihydro-5-propyl-2(3H)furanone
2,3-Dihydro-6-propyl-2thioxo-4(1H)-pyrimidinone
3664
3665
3666
3667
3668
3669
Organic
3670
3671
3672
3673
3674
3675
3676
1,7-Dihydro-6H-purine-6thione
3,4-Dihydro-2H-pyran
3,6-Dihydro-2H-pyran
Dihydro-2H-pyran-2,6(3H)dione
4,5-Dihydro-1H-pyrazole
Mol. Form.
CAS RN
Mol.
Wt.
C14H12
C15H12O2
776-35-2
487-26-3
C10H13ClN2
Aminorex
Synonym
Physical
Form
bp/˚C
180.245 nd (MeOH)
224.255 nd (lig)
33.36(0.05)
76.3(0.5)
16815
59-97-2
196.676
174
C9H10N2O
2207-50-3
162.187 cry (bz)
137
1-Phenyl-5-mercapto-1Htetrazole
γ-Propyl-γ-butyrolactone
C7H6N4S
86-93-1
178.215
145
C7H12O2
105-21-5
128.169
Propylthiouracil
C7H10N2OS
51-52-5
170.231 w pow (w)
6-Mercaptopurine
C5H4N4S
50-44-2
C5H8O
110-87-2
152.178 ye pr (w, + l 313 dec
w)
84.117
85.5(0.2)
0.92119
C5H8O
C5H6O3
3174-74-1
108-55-4
84.117 liq
114.100
95
15815
0.9419
1.411020
C3H6N2
109-98-8
70.093
144
C4H4N2O2
123-33-1
112.087 cry (w)
307
1.020017 1.479617 vs H2O, eth,
EtOH
sl H2O, EtOH, tfa
C4H6N2O2
504-07-4
114.103 nd (w)
275.5
C4H7N
109-96-6
69.106
2-Pyrazoline
1,2-Dihydro-3,6-pyridazinedi- Maleic hydrazide
one
Dihydro-2,4(1H,3H)-pyrimidin- 5,6-Dihydrouracil
edione
2,5-Dihydro-1H-pyrrole
3-Pyrroline
56.3
sl H2O, chl,
DMSO, EtOH; i
eth, bz
i H2O; s alk
90(5)
C9H9NO
C8H6N2O2
553-03-7
147.173 pr (al, eth)
15804-19-0 162.146 nd (w)
163.5
410
3679
3680
Dihydrotachysterol
Dihydrothebaine
C28H46O
C19H23NO3
67-96-9
561-25-1
398.664 cry (MeOH)
313.391
131
162.5
3681
4,5-Dihydro-2-thiazolamine
C3H6N2S
1779-81-3
102.158 nd or lf (bz) 85.3
dec
3682
3683
3684
2,3-Dihydrothiophene
2,5-Dihydrothiophene
2,5-Dihydrothiophene
1,1-dioxide
Dihydro-2(3H)-thiophenone
Dihydro-2-thioxo-4,6(1H,5H)pyrimidinedione
2,3-Dihydro-2-thioxo-4(1H)pyrimidinone
1120-59-8
1708-32-3
77-79-2
86.156
86.156
118.155
112(13)
122.4
3-Sulfolene
C4H6S
C4H6S
C4H6O2S
64.0(0.4)
2-Thiobarbituric acid
C4H6OS
C4H4N2O2S
1003-10-7
504-17-6
102.155
144.152 pl (w)
235 dec
2-Thiouracil
C4H4N2OS
141-90-2
128.152 pr (w, al)
>340 dec
C2H3N3S
3179-31-5
101.130
222.5
C13H15NO
84-83-3
201.264
C18H20
3910-35-8
236.352 tcl pr (al)
52(1)
308.5
C12H15N
147-47-7
173.254
26.5
260
Quinizarin
C14H8O4
81-64-1
240.212 ye red lf
(eth) dk
red nd
240.212 pa ye pl (gl
HOAc)
199.7(0.4)
280
sub
240.212 red or
red-ye nd
or lf (al)
240.212 ye nd (al)
193
sub
3688
3689
3690
3691
3692
1,2-Dihydro-3H-1,2,4triazole-3-thione
(1,3-Dihydro-1,3,3-trimethyl2H-indol-2-ylidene)
acetaldehyde
2,3-Dihydro-1,1,3-trimethyl3-phenyl-1H-indene
1,2-Dihydro-2,2,4-trimethylquinoline
1,4-Dihydroxy-9,10-anthracenedione
3693
1,5-Dihydroxy-9,10-anthracenedione
Anthrarufin
C14H8O4
117-12-4
3694
1,8-Dihydroxy-9,10-anthracenedione
Danthron
C14H8O4
117-10-2
3695
2,6-Dihydroxy-9,10-anthracenedione
C14H8O4
84-60-6
3696
2,7-Dihydroxy-9,10-anthracenedione
C14H8O4
572-93-0
HCP_Section_03.indb 188
Solubility
1.438525
219
3,4-Dihydro-2(1H)-quinolinone Hydrocarbostyril
1,4-Dihydro-2,3-quinoxaline- 2,3-Quinoxalinediol
dione
3687
nD
1.075740 1.641520 s chl
i H2O; s ace, bz;
sl ctc
845
3677
3678
3685
3686
den
g cm –3
mp/˚C
1.440219 s H2O, EtOH; sl
chl
0.909720 1.466420
20145
vs H2O; s EtOH,
chl, MeOH
vs H2O, ace,
eth, EtOH
vs eth, EtOH
vs H2O; sl EtOH,
eth; s bz,
DMSO, HOAc
i H2O; s os
i H2O; s EtOH,
bz, AcOEt
vs H2O, EtOH,
bz, chl
s chl
11152
1.1825
1.523020
sl H2O; s EtOH,
dil alk, dil HCl
sl H2O, EtOH,
DMSO; s anh
HF
s DMSO
s chl
360 dec
240.212 ye nd (+1w, 353.8
dil al) nd
(sub)
sub
1.000920 1.568120 i H2O; s EtOH,
bz, MeOH
s H2O, EtOH,
eth, bz, KOH,
sulf
i H2O; sl EtOH,
eth, ace, CS2;
s bz
i H2O; sl EtOH,
eth; s ace,
HOAc, alk
sl H2O, EtOH; i
eth, bz, chl; s
alk
i H2O; s EtOH; sl
eth, bz, chl
4/11/16 11:24 AM
Physical Constants of Organic Compounds
3-189
O
N
N
O
3663
9,10-Dihydrophenanthrene
3664
2,3-Dihydro-2-phenyl-4H-1-benzopyran-4-one
HN N
N
N
S
3665
4,5-Dihydro-2-(phenylmethyl)-1H-imidazole, monohydrochloride
4,5-Dihydro-5-phenyl-2-oxazolamine
O
S
NH
O
3666
3667
1,4-Dihydro-1-phenyl-5H-tetrazole-5-thione
S
N
H
O
N
N
3668
Dihydro-5-propyl-2(3H)-furanone
H
N
HN
O
3669
2,3-Dihydro-6-propyl-2-thioxo-4(1H )-pyrimidinone
3670
1,7-Dihydro-6H-purine-6-thione
3,4-Dihydro-2H-pyran
Organic
3662
HCl
NH2
O
N
H
O
O
O
O
3671
O
N
H
O
3672
3,6-Dihydro-2H-pyran
N
3673
Dihydro-2H-pyran-2,6(3H )-dione
N
H
O
NH
NH
3674
4,5-Dihydro-1H-pyrazole
O
N
H
N
H
3675
1,2-Dihydro-3,6-pyridazinedione
3676
Dihydro-2,4(1H,3H)-pyrimidinedione
2,5-Dihydro-1H-pyrrole
O
N
H
O
3677
3,4-Dihydro-2(1H)-quinolinone
H
N
O
N
H
O
O
3678
3679
1,4-Dihydro-2,3-quinoxalinedione
N
N
H
O
HO
S
3680
Dihydrotachysterol
NH2
S
3681
Dihydrothebaine
3682
4,5-Dihydro-2-thiazolamine
2,3-Dihydrothiophene
O
O
NH
NH
O
S
3683
S
O
O
S
3684
2,5-Dihydrothiophene
O
3685
2,5-Dihydrothiophene 1,1-dioxide
N
H
3686
Dihydro-2(3H)-thiophenone
S
N
H
S
3687
Dihydro-2-thioxo-4,6(1H,5H )-pyrimidinedione
2,3-Dihydro-2-thioxo-4(1H )-pyrimidinone
S
HN
N
NH
3688
1,2-Dihydro-3H-1,2,4-triazole-3-thione
O
OH
N
O
N
H
3689
3690
(1,3-Dihydro-1,3,3-trimethyl-2H-indol-2-ylidene)acetaldehyde
O
OH
3691
2,3-Dihydro-1,1,3-trimethyl-3-phenyl-1H-indene
OH O
OH
1,2-Dihydro-2,2,4-trimethylquinoline
O
O
OH
HO
OH
HO
O
3692
OH
1,4-Dihydroxy-9,10-anthracenedione
OH O
3693
1,5-Dihydroxy-9,10-anthracenedione
O
3694
1,8-Dihydroxy-9,10-anthracenedione
O
3695
2,6-Dihydroxy-9,10-anthracenedione
O
3696
2,7-Dihydroxy-9,10-anthracenedione
Physical Constants of Organic Compounds
3-190
No.
Name
3697
Mol.
Wt.
Physical
Form
Organic
Mol. Form.
CAS RN
2,2’-Dihydroxyazobenzene
C12H10N2O2
2050-14-8
3698
2,3-Dihydroxybenzaldehyde
C7H6O3
24677-78-9 138.121 ye nd
108
235
3699
2,4-Dihydroxybenzaldehyde
C7H6O3
95-01-2
138.121 nd (eth-lig)
135
22622
3700
2,5-Dihydroxybenzaldehyde
C7H6O3
1194-98-5
138.121 ye nd (bz)
100.0
3701
3,4-Dihydroxybenzaldehyde
Protocatechualdehyde
C7H6O3
139-85-5
138.121 lf (w, to)
153 dec
3702
N,2-Dihydroxybenzamide
Salicylhydroxamic acid
C7H7NO3
89-73-6
153.136 nd (HOAc)
168
3703
Homogentisic acid
C8H8O4
451-13-8
C7H6O4
303-38-8
3705
2,4-Dihydroxybenzoic acid
β-Resorcylic acid
C7H6O4
89-86-1
168.148 pr (w+1), lf
(al-chl)
154.121 pr or nd
(w+1)
154.121 cry (+w)
153
3704
2,5-Dihydroxybenzeneacetic
acid
2,3-Dihydroxybenzoic acid
3706
2,5-Dihydroxybenzoic acid
Gentisic acid
C7H6O4
490-79-9
154.121 nd or pr (w) 204(3)
3707
2,6-Dihydroxybenzoic acid
C7H6O4
303-07-1
154.121 nd (+w)
171(1)
3708
3,4-Dihydroxybenzoic acid
C7H6O4
99-50-3
202(1)
3709
3,5-Dihydroxybenzoic acid
C7H6O4
99-10-5
154.121 mcl nd
(w+1)
154.121 pr or nd
3710
2,2’-Dihydroxybenzophenone
Bis(2-hydroxyphenyl) ketone
C13H10O3
835-11-0
214.216
59.5
3711
4,4’-Dihydroxybenzophenone
Bis(4-hydroxyphenyl) ketone
C13H10O3
611-99-4
214.216 nd (lig), cry
(w)
210
3712
6,7-Dihydroxy-2H-1-benzopy- Esculetin
ran-2-one
C9H6O4
305-01-1
sub
3713
7,8-Dihydroxy-2H-1-benzopy- Daphnetin
ran-2-one
C9H6O4
486-35-1
178.142 nd (w), pr
276
(HOAc) lf
(sub)
178.142 ye nd (dil al) 262
3714
3715
2,4-Dihydroxybutanoic acid
3,6-Dihydroxycholan-24-oic
acid, (3α,5β,6α)
C4H8O4
C24H40O4
1518-62-3
83-49-8
120.105 liq
392.573 cry (AcOEt)
963
Hyodeoxycholic acid
198.5
3716
3,7-Dihydroxycholan-24-oic
acid, (3α,5β,7β)
3,7-Dihydroxycholan-24-oic
acid, (3α,5β,7α)
Ursodiol
C24H40O4
128-13-2
392.573 pl (al)
203
Chenodiol
C24H40O4
474-25-9
392.573 nd (EtOAc​
+hep)
119
3717
Synonym
β-Resorcylaldehyde
Protocatechuic acid
mp/˚C
214.219 gold-ye lf
173
(bz), nd (al)
bp/˚C
den
g cm –3
1400.001
sub
205(4)
1.54220
229(1)
1.5244
235.3(0.8)
333
1.133131
sub
nD
Solubility
i H2O; sl EtOH,
bz; vs eth; s
con alk
vs ace, EtOH,
HOAc
s H2O, HOAc; vs
EtOH, eth, chl;
sl bz
vs H2O, EtOH,
chl
s H2O; vs EtOH,
eth
sl H2O, DMSO;
vs EtOH, eth; s
HOAc
vs H2O, EtOH,
eth; i bz, chl
s H2O, EtOH,
eth; sl ace
s H2O, EtOH,
eth, bz; i CS2
vs H2O, EtOH,
eth; s ace; i
bz, chl, CS2
s H2O, EtOH,
eth; i chl; sl tfa
sl H2O; vs EtOH;
s eth; i bz
sl H2O, ace; vs
EtOH, eth
i H2O; s EtOH,
eth, chl
sl H2O; s EtOH,
eth, ace; i bz,
CS2
sl H2O, eth; s
EtOH, ace, chl,
AcOEt
s H2O, EtOH; sl
eth, bz, chl,
CS2
sl H2O, eth, ace,
bz; s EtOH,
HOAc
vs EtOH; sl eth
i H2O, bz; vs
EtOH, ace; s
eth, HOAc
sl EtOH, MeOH,
thf, AcOEt
sl H2O, ace,
DMSO; s EtOH,
HOAc; i eth
s H2O, EtOH; sl
eth, ace,
AcOEt; i bz
3718
1,25-Dihydroxycholecalciferol Calcitriol
C27H44O3
32222-06-3 416.636 wh cry pow 115
3719
2,5-Dihydroxy-2,5-cyclohexadiene-1,4-dione
C6H4O4
615-94-1
140.094 dk ye nd
211
3720
2,3-Dihydroxy-2-cyclopenten- Reductic acid
1-one
C5H6O3
80-72-8
114.100
212
3721
2,6-Dihydroxy-2,6-dimethyl- Di(2-hydroxy-2-methylpropyl)
4-heptanone
ketone
2,2’-Dihydroxydiphenylmeth- 2,2’-Methylenebisphenol
ane
4,4’-Dihydroxydiphenyl sulfide 4,4’-Thiobisphenol
C9H18O3
3682-91-5
174.237 pale ye cry
C13H12O2
2467-02-9
200.233
118.3
C12H10O2S
2664-63-3
151
Aloe-emodol
C15H10O5
481-72-1
218.271 mcl pr or lf
(al)
270.237 oran ye nd
(to, al)
Dihydroxymaleic acid
C4H4O6
526-84-1
148.071 pl (w+2)
155 dec
C9H10O5
55-10-7
198.172 sc (bz-eth)
132 dec
sl H2O, eth,
MeOH; s EtOH
vs H2O, ace, eth
C10H8O5
574-84-5
208.168 pl (dil al)
231
vs EtOH
3722
3723
3724
3725
3726
3727
1,8-Dihydroxy-3(hydroxymethyl)-9,10anthracenedione
2,3-Dihydroxymaleic acid
Vanilmandelic acid
α,4-Dihydroxy-3methoxybenzeneacetic acid
7,8-Dihydroxy-6-methoxy-2H- Fraxetin
1-benzopyran-2-one
HCP_Section_03.indb 190
223.5
363
sub
1.28025
sl H2O, EtOH,
eth, CS2
vs bz, eth, EtOH
4/11/16 11:24 AM
Physical Constants of Organic Compounds
3-191
O
O
HO
O
OH
N
N
O
OH
OH
OH
3697
3699
2,3-Dihydroxybenzaldehyde
HO
OH
O
3705
2,3-Dihydroxybenzoic acid
HO
OH
OH
2,4-Dihydroxybenzoic acid
3707
2,5-Dihydroxybenzoic acid
3708
2,6-Dihydroxybenzoic acid
3,4-Dihydroxybenzoic acid
3,5-Dihydroxybenzoic acid
O
HO
3710
HO
OH
3711
2,2’-Dihydroxybenzophenone
O
3713
3715
3,6-Dihydroxycholan-24-oic acid, (3α,5β,6α)
O
HO
3716
3,7-Dihydroxycholan-24-oic acid, (3α,5β,7β)
OH
2,5-Dihydroxy-2,5-cyclohexadiene-1,4-dione
1,25-Dihydroxycholecalciferol
OH
S
O
OH
O
OH
3718
3,7-Dihydroxycholan-24-oic acid, (3α,5β,7α)
OH
HO
3720
OH
HO
3721
2,3-Dihydroxy-2-cyclopenten-1-one
3722
2,6-Dihydroxy-2,6-dimethyl-4-heptanone
OH
3723
2,2’-Dihydroxydiphenylmethane
4,4’-Dihydroxydiphenyl sulfide
OH
OH
HO
OH
1,8-Dihydroxy-3-(hydroxymethyl)-9,10-anthracenedione
OH
OH
HO
OH
O
O
3724
HO
3717
HO
3719
H
OH
H
O
OH
OH
OH
OH
H
3714
2,4-Dihydroxybutanoic acid
O
OH
HO
OH
OH
7,8-Dihydroxy-2H-1-benzopyran-2-one
O
OH
HO
O
OH
6,7-Dihydroxy-2H-1-benzopyran-2-one
OH
O
O
3712
4,4’-Dihydroxybenzophenone
O
O
OH
3709
O
OH
HO
HO
HO
OH
3706
OH
O
HO
H
OH
OH
HO
OH
3704
2,5-Dihydroxybenzeneacetic acid
O
OH
OH
3703
OH O
OH
N,2-Dihydroxybenzamide
3,4-Dihydroxybenzaldehyde
O
O
OH
OH
3702
3701
2,5-Dihydroxybenzaldehyde
O
OH
OH
OH
3700
2,4-Dihydroxybenzaldehyde
HO
O
OH
HO
OH
3698
2,2’-Dihydroxyazobenzene
HO
N
H
OH
OH
O
3725
2,3-Dihydroxymaleic acid
O
HO
O
3726
α,4-Dihydroxy-3-methoxybenzeneacetic acid
O
HO
O
O
OH
3727
7,8-Dihydroxy-6-methoxy-2H-1-benzopyran-2-one
Organic
O
OH
Physical Constants of Organic Compounds
3-192
No.
Name
3728
5,7-Dihydroxy-3-(4methoxyphenyl)-4H-1benzopyran-4-one
(2,6-Dihydroxy-4-methoxyCotoin
phenyl)phenylmethanone
1,7-Dihydroxy-3-methoxy-9H- Gentisin
xanthen-9-one
1,8-Dihydroxy-3-methyl-9,10- Chrysophanic acid
anthracenedione
3729
3730
3731
Synonym
CAS RN
Mol.
Wt.
Physical
Form
C16H12O5
491-80-5
284.263
C14H12O4
479-21-0
C14H10O5
437-50-3
244.243 ye pr (chl) lf 130.5
or nd (w)
258.226 ye orth
266.5
C15H10O4
481-74-3
C8H8O4
480-64-8
254.238 ye hex or
mcl nd
(sub)
168.148 nd (dil
HOAc,
+1w)
192.169 nd (al), lf
(HOAc)
mp/˚C
196
Organic
2107-76-8
3734
6,7-Dihydroxy-4-methyl-2H1-benzopyran-2-one
5,8-Dihydroxy-1,4-naphthalenedione
C10H8O4
529-84-0
192.169 ye nd (dil al) 275
C10H6O4
475-38-7
Chromotropic acid
C10H8O8S2
148-25-4
Alizarin Blue
C17H9NO4
568-02-5
Alizarin Orange
C14H7NO6
568-93-4
190.153 dk red mcl 243(1)
pr (bz) redbr nd (al)
320.296 nd or lf
(w+2)
291.258 br-viol nd
269
(bz)
285.209 oran nd or 244 dec
pl (HOAc)
Phloionic acid
C18H34O6
23843-52-9 346.459 cry (al)
126
9,10-Dihydroxystearic acid
C18H36O4
120-87-6
316.477
90
Chrysin
C15H10O4
480-40-0
254.238 lt ye pr
(MeOH)
285(2)
3739
3740
3741
9,10-Dihydroxyoctadecanedioic acid, (R*,R*)-(±)9,10-Dihydroxyoctadecanoic
acid
5,7-Dihydroxy-2-phenyl-4H1-benzopyran-4-one
3742
1-(2,4-Dihydroxyphenyl)­
ethanone
Resacetophenone
C8H8O3
89-84-9
152.148 nd or lf
146
3743
(2,4-Dihydroxyphenyl)­
phenylmethanone
Benzoresorcinol
C13H10O3
131-56-6
214.216 nd (w)
144
3744
3-(3,4-Dihydroxyphenyl)-2propenoic acid
Dihydroxyphenylstibine oxide
17,21-Dihydroxypregna-1,4diene-3,11,20-trione
17,21-Dihydroxypregn-4-ene3,20-dione
17,21-Dihydroxypregn-4-ene3,11,20-trione
Caffeic acid
C9H8O4
331-39-5
180.158 ye pr, pl (w) 225 dec
Benzenestibonic acid
Prednisone
C6H7O3Sb
C21H26O5
535-46-6
53-03-2
248.878 nd (HOAc)
358.428
139
234 dec
152-58-9
346.461
215
53-06-5
360.444
222
C3H6O3
56-82-6
90.078
145
Glyceric acid
C3H6O4
6000-40-4
nd or pr
(40%
MeOH)
106.078 thick gum
Dihydroxyacetone
C3H6O3
96-26-4
90.078
74(3)
C13H26O4
2277-23-8
246.343 pr (peth)
53
C11H22O4
26402-26-6 218.291 cry (peth)
C10H7NO4
59-00-7
205.168 ye micry cry 289
(w)
C4H6O8
C14H10O9
76-30-2
536-08-3
182.086
322.224 nf (dil al +
1w)
C20H14O5
518-44-5
C2I2
624-74-8
334.322 col or ye nd 126
(eth), pl
(bz)
277.830 orth nd (lig) 81.5
3745
3746
3747
3748
3749
2,3-Dihydroxypropanal, (±)-
3750
2,3-Dihydroxypropanoic acid,
(R)1,3-Dihydroxy-2-propanone
3751
3752
3753
3754
3755
3756
3757
3758
11-Deoxy-17-hydrocorticoste- C21H30O4
rone
Cortisone
C21H28O5
2,3-Dihydroxypropyl
Decanoic acid glycerol
decanoate
monoester
2,3-Dihydroxypropyl octanoate Octanoic acid glycerol
monoester
4,8-Dihydroxy-2-quinolinecar- Xanthurenic acid
boxylic acid
Dihydroxytartaric acid
3,4-Dihydroxy-5-[(3,4,5Digallic acid
trihydroxybenzoyl)oxy]
benzoic acid
2-(3,6-Dihydroxy-9H-xanthen- Fluorescin
9-yl)benzoic acid
Diiodoacetylene
HCP_Section_03.indb 192
sub
0.9225
vs ace, bz, eth,
EtOH
i H2O; vs EtOH; i
ace; s py
vs bz, HOAc
sl H2O, eth, bz,
chl; vs EtOH,
alk
s H2O, EtOH,
HOAc
sl H2O, EtOH,
eth; s HOAc
C10H8O4
3738
Solubility
283
5,7-Dihydroxy-4-methyl-2H1-benzopyran-2-one
3737
nD
s EtOH, eth
3733
4,5-Dihydroxy-2,7-naphthalenedisulfonic acid
5,6-Dihydroxynaphtho[2,3-f]
quinoline-7,12-dione
1,2-Dihydroxy-3-nitro-9,10anthracenedione
den
g cm –3
176 dec
2,4-Dihydroxy-6-methylbenzoic acid
3736
bp/˚C
214.8
3732
3735
o-Orsellinic acid
Mol. Form.
sub
s H2O, alk; i
EtOH, eth
vs bz, gl HOAc
sub
sl H2O; s EtOH,
bz, chl, sulf,
HOAc
1.18141
1450.8
1.45318
i H2O; sl EtOH,
eth
i H2O; s EtOH,
ace; sl eth, bz,
CS2
i H2O, chl; s
EtOH, py; sl
eth, bz
i H2O; s EtOH;
vs eth; sl bz,
chl
vs EtOH
vs ace, EtOH,
chl
sl H2O, eth, bz,
chl; s EtOH,
ace
s H2O; sl EtOH,
eth; i bz, peth,
lig
s H2O, EtOH,
eth, ace; i lig
40
i H2O; s EtOH,
dil HCl; sl eth,
bz
114.5
269 dec
vs ace, EtOH
247(16)
i H2O; s EtOH,
eth, ace, bz,
HOAc
vs ace, bz, eth,
EtOH
4/11/16 11:24 AM
Physical Constants of Organic Compounds
3-193
O
OH O
OH O
O
OH
HO
O
HO
O
3728
5,7-Dihydroxy-3-(4-methoxyphenyl)-4H-1-benzopyran-4-one
OH O
O
OH
3729
(2,6-Dihydroxy-4-methoxyphenyl)phenylmethanone
HO
OH
O
3730
1,7-Dihydroxy-3-methoxy-9H-xanthen-9-one
O
OH
OH
HO
OH
3732
1,8-Dihydroxy-3-methyl-9,10-anthracenedione
2,4-Dihydroxy-6-methylbenzoic acid
OH O
O
HO
O
S
O
HO
O
O
3734
5,7-Dihydroxy-4-methyl-2H-1-benzopyran-2-one
6,7-Dihydroxy-4-methyl-2H-1-benzopyran-2-one
O
OH
S
O
3733
O
OH
OH
N
O
O
OH
OH O
HO
3735
3736
5,8-Dihydroxy-1,4-naphthalenedione
O
O
OH
OH
N
O
O
3737
4,5-Dihydroxy-2,7-naphthalenedisulfonic acid
O
3738
5,6-Dihydroxynaphtho[2,3-f]quinoline-7,12-dione
1,2-Dihydroxy-3-nitro-9,10-anthracenedione
OH
OH
O
OH
HO
OH
OH
O
OH
3739
3740
9,10-Dihydroxyoctadecanedioic acid, (R *,R *)-(±)-
9,10-Dihydroxyoctadecanoic acid
O
OH O
O
OH
O
OH
OH
O
HO
Organic
HO
O
3731
HO
OH
3741
OH
3742
5,7-Dihydroxy-2-phenyl-4H-1-benzopyran-4-one
1-(2,4-Dihydroxyphenyl)ethanone
O
O
HO Sb OH
3744
3-(3,4-Dihydroxyphenyl)-2-propenoic acid
(2,4-Dihydroxyphenyl)phenylmethanone
O
OH
OH
O
OH
3743
O
OH
OH
OH
OH
O
OH
O
3745
3746
Dihydroxyphenylstibine oxide
17,21-Dihydroxypregna-1,4-diene-3,11,20-trione
3747
3749
17,21-Dihydroxypregn-4-ene-3,11,20-trione
2,3-Dihydroxypropanal, (±)-
O
O
HO
3748
17,21-Dihydroxypregn-4-ene-3,20-dione
O
OH
3750
OH
N
OH
O
3754
4,8-Dihydroxy-2-quinolinecarboxylic acid
OH
O HO OH
3755
Dihydroxytartaric acid
2,3-Dihydroxypropyl octanoate
OH
HO
O
HO
HO OH O
3753
2,3-Dihydroxypropyl decanoate
OH
HO
OH
OH
3752
1,3-Dihydroxy-2-propanone
O
OH
O
OH
3751
2,3-Dihydroxypropanoic acid, (R)-
O
OH
O
HO
OH
O
HO
O
O
O
O
OH
O
OH
HO
OH
OH
OH
3756
3,4-Dihydroxy-5-[(3,4,5-trihydroxybenzoyl)oxy]benzoic acid
3757
2-(3,6-Dihydroxy-9H-xanthen-9-yl)benzoic acid
I
I
3758
Diiodoacetylene
Physical Constants of Organic Compounds
3-194
No.
Name
3759
2,4-Diiodoaniline
3760
3761
o-Diiodobenzene
m-Diiodobenzene
3762
p-Diiodobenzene
3763
Synonym
Mol.
Wt.
Physical
Form
Organic
Mol. Form.
CAS RN
C6H5I2N
533-70-0
1,2-Diiodobenzene
1,3-Diiodobenzene
C6H4I2
C6H4I2
615-42-9
626-00-6
1,4-Diiodobenzene
C6H4I2
624-38-4
344.920 br nd or
orth cry
(al)
329.905 pl or pr (lig)
329.905 orth pl or pr
(eth-al)
329.905 orth lf (al)
1,4-Diiodobutane
C4H8I2
628-21-7
309.916
3764
1,2-Diiodoethane
C2H4I2
624-73-7
3765
3766
cis-1,2-Diiodoethene
4,4’-Diiodofluorescein
cis-1,2-Diiodoethylene
C2H2I2
C20H10I2O5
3767
1,6-Diiodohexane
Hexamethylene diiodide
3768
Diiodomethane
3769
mp/˚C
bp/˚C
95.5
23.5(0.7)
34.2(0.6)
den
g cm –3
2.74825
287
285
2.5420
2.4725
129.25(0.05) 285
Solubility
vs ace, bz, eth,
EtOH
1.717920 i H2O; sl EtOH
i H2O; vs eth,
EtOH, chl
i H2O; s EtOH;
vs eth; sl chl
1.618425 i H2O; sl ctc; s
os
1.87120 sl H2O; s EtOH,
eth, ace, chl
i H2O; s eth, chl
sl H2O; s alk,
EtOH
1.583725 i H2O; vs EtOH,
eth
1.741120 sl H2O, ctc; s
EtOH, eth, bz,
chl
vs EtOH
12515 dec
2.349425
200
3.32520
72.516
3.062520
C6H12I2
281.862 ye mcl pr or 83
orth (eth)
590-26-1
279.846
-13(2)
38577-97-8 584.099 oran-red
pow
629-09-4
337.968 nd
9.4(0.5)
16317
2.034225
Methylene iodide
CH2I2
75-11-6
267.836 ye nd or lf
6.0(0.2)
182
3.321120
2,6-Diiodo-4-nitrophenol
Disophenol
C6H3I2NO3
305-85-1
157
3770
3771
3772
1,5-Diiodopentane
1,2-Diiodopropane
1,3-Diiodopropane
Pentamethylene diiodide
628-77-3
598-29-8
627-31-6
9
14920
Trimethylene diiodide
C5H10I2
C3H6I2
C3H6I2
390.902 lt ye cry (gl
HOAc)
323.942
295.889
295.889
-20
222(12)
3773
5,7-Diiodo-8-quinolinol
Iodoquinol
C9H5I2NO
83-73-8
396.951 ye nd
210
(HOAc, xyl)
3774
3,5-Diiodo-L-tyrosine
C9H9I2NO3
300-39-0
213
3775
3776
3777
Diisobutyl adipate
Diisobutylaluminum chloride
Diisobutylaluminum hydride
Diisobutyl hexanedioate
Diisobutyl aluminum chloride
C14H26O4
C8H18AlCl
C8H19Al
141-04-8
1779-25-5
1191-15-7
432.981 ye nd (w,
70% al)
258.354
176.664 hyg col liq
142.219 liq
-40
288(16)
15210
1404
3778
Diisobutylamine
2-Methyl-N-(2-methylpropyl)1-propanamine
C8H19N
110-96-3
129.244 liq
-73.5(0.4)
139.6
3779
Diisobutyl carbonate
C9H18O3
539-92-4
174.237
190(6)
3780
Diisobutyl ether
1,1’-Oxybis[2-methylpropane]
C8H18O
628-55-7
130.228
122.7(0.7)
3781
3782
3783
3784
3785
3786
Diisobutyl phthalate
Diisobutyl sulfide
1,3-Diisocyanatobenzene
1,4-Diisocyanatobenzene
Diisodecyl phthalate
Diisononyl phthalate
Bis(8-methylnonyl)phthalate
Bis(7-methyloctyl)phthalate
C16H22O4
C8H18S
C8H4N2O2
C8H4N2O2
C28H46O4
C26H42O4
84-69-5
592-65-4
123-61-5
104-49-4
26761-40-0
28553-12-0
278.344
146.294
160.130
160.130
446.663
418.609
2.169225 1.598725 i H2O; s eth, chl
2.49018
vs eth, EtOH
2.561225 1.639125 i H2O; s eth, ctc,
chl
sl H2O, bz, chl,
eth; vs EtOH; s
alk
sl H2O; i EtOH,
eth, bz
0.954319 1.430120
0.905
1.450620 s eth, hx
s cyhex, eth, bz,
tol
1.409020 sl H2O, ctc; s
EtOH, eth, ace,
bz
0.913820 1.407220 i H2O; msc
EtOH, eth
0.76115
i H2O; msc
EtOH, eth
1.049015
s ctc
0.836310
3787
3788
3789
Diisooctyl adipate
Diisooctyl phthalate
Diisopentylamine
1330-86-5 370.566
27554-26-3 390.557
544-00-3
157.297 liq
3790
Diisopentyl ether
3-Methyl-N-isopentyl-1butanamine
Diisoamyl ether
C22H42O4
C24H38O4
C10H23N
C10H22O
544-01-4
158.281 col liq
3791
3792
Diisopentyl phthalate
Diisopentyl sulfide
Diisoamyl phthalate
Isopentyl sulfide
C18H26O4
C10H22S
605-50-5
544-02-5
306.397
174.347 liq
-74.6
367(16)
211
3793
Diisopropanolamine
1,1’-Iminobis-2-propanol
C6H15NO2
110-97-4
133.189 cry
44.5
250
3794
Diisopropyl adipate
Diisopropyl hexanedioate
C12H22O4
6938-94-9
230.301
-0.6
1206.5
3795
Diisopropylamine
N-Isopropyl-2-propanamine
C6H15N
108-18-9
101.190 liq
-61
84(3)
3796
3797
2,6-Diisopropylaniline
1,2-Diisopropylbenzene
C12H19N
C12H18
24544-04-5 177.286 liq
577-55-9
162.271 liq
-45
-57(4)
272(9)
204.7(0.6)
3798
1,3-Diisopropylbenzene
C12H18
99-62-7
-63(2)
203(3)
HCP_Section_03.indb 194
Diisooctyl hexanedioate
5.9(0.4)
nD
liq
cry
cry
liq
col liq
162.271 liq
-105.5(0.5)
51
95
-50
296.5
173(4)
1038
11714
2534
-44
2104
370
187(5)
172(2)
0.96620
i H2O; s os
i H2O; s ace,
MeOH; bz, eth
0.767221 1.423520 i H2O; s EtOH;
msc eth
0.777720 1.408520 i H2O; vs ace,
EtOH, chl
1.020916 1.487120 vs EtOH
0.832320 1.452020 i H2O; msc
EtOH; vs eth
0.98920
s H2O, EtOH; sl
eth
0.956920 1.424720 vs ace, eth,
EtOH
0.715320 1.392420 vs ace, bz, eth,
EtOH
0.9425
1.533220
0.870120 1.496020 i H2O; msc
EtOH, eth, ace,
bz, ctc
0.855920 1.488320 i H2O; msc
EtOH, eth, ace,
bz, ctc
4/11/16 11:25 AM
Physical Constants of Organic Compounds
3-195
O
I
I
O
I
I
I
I
I
3759
3760
2,4-Diiodoaniline
3761
o-Diiodobenzene
I
I
3762
m-Diiodobenzene
3763
p-Diiodobenzene
I
I
3764
1,4-Diiodobutane
I
cis-1,2-Diiodoethene
H
O
I
3768
N
3769
Diiodomethane
3770
2,6-Diiodo-4-nitrophenol
I
I
I
I
O
3771
1,5-Diiodopentane
1,2-Diiodopropane
I
N
I
3772
O
OH
NH2
HO
OH
O
O
O
I
3773
1,3-Diiodopropane
1,6-Diiodohexane
O
I
I
I
3767
4,4’-Diiodofluorescein
I
H
I
I
3766
I
I
OH
I
3765
1,2-Diiodoethane
OH
I
O
HO
I
I
5,7-Diiodo-8-quinolinol
3774
3775
3,5-Diiodo-L-tyrosine
Organic
NH2
Diisobutyl adipate
N
C
O
O
O
O
O
Cl
Al
H
Al
H
N
3776
3777
3778
Diisobutylaluminum chloride
N
C
Diisobutylaluminum hydride
Diisobutylamine
O
O
3779
Diisobutyl carbonate
C
O
O
S
3780
3781
3782
Diisobutyl ether
Diisobutyl phthalate
3783
Diisobutyl sulfide
1,3-Diisocyanatobenzene
O
O
O
N
C
O
O
O
O
N
O
O
O
O
O
3785
3784
3786
Diisodecyl phthalate
1,4-Diisocyanatobenzene
O
O
O
3787
Diisononyl phthalate
O
Diisooctyl adipate
O
O
O
O
O
N
H
O
3789
3788
3790
Diisopentylamine
Diisooctyl phthalate
3794
Diisopropyl adipate
3792
Diisopentyl phthalate
Diisopentyl sulfide
H
N
OH
3793
Diisopropanolamine
NH2
O
O
S
3791
Diisopentyl ether
O
O
OH
O
O
N
H
3795
Diisopropylamine
3796
2,6-Diisopropylaniline
3797
1,2-Diisopropylbenzene
3798
1,3-Diisopropylbenzene
Physical Constants of Organic Compounds
3-196
Mol. Form.
CAS RN
Mol.
Wt.
1,4-Diisopropylbenzene
C12H18
100-18-5
C12H18O2
C13H18N2S2
3802
3803
3804
p-Diisopropylbenzene
hydroperoxide
N,N-Diisopropyl-2-benzothiazolesulfenamide
N,N’-Diisopropylcarbodiimide
Diisopropyl disulfide
N,N-Diisopropylethanolamine
3805
Diisopropyl ether
3806
3811
Diisopropyl methylphosphonate
2,6-Diisopropylnaphthalene
Diisopropyl oxalate
Diisopropyl phosphonate
O,O-Diisopropyl phosphorodithioate
Diisopropyl phthalate
3812
No.
Name
3799
3800
Physical
Form
den
g cm –3
mp/˚C
bp/˚C
162.271 liq
-17.0(0.1)
210.3(0.2)
98-49-7
194.270 waxy cry
30.1
1231
0.856820 1.489820 i H2O; msc
EtOH, eth, ace,
bz, ctc
0.993220
i H2O
95-29-4
266.425
59.0
C7H14N2
C6H14S2
N,N-Diisopropyl-2-aminoetha- C8H19NO
nol
Isopropyl ether
C6H14O
693-13-0
4253-89-8
96-80-0
126.199
150.305 liq
145.243
-69.0(0.3)
147
177(1)
195(5)
0.80625 1.432020
0.943520 1.491620
0.82625 1.441720
108-20-3
102.174 liq
-85.37(0.05) 68.4(0.2)
C7H17O3P
1445-75-6
180.182
C16H20
C8H14O4
C6H15O3P
C6H15O2PS2
24157-81-1
615-81-6
1809-20-7
107-56-2
212.330 cry (MeOH)
174.195
166.155
214.286 liq
C14H18O4
605-45-8
250.291
Diisopropyl sulfide
C6H14S
625-80-9
118.240 liq
3813
Diisopropyl tartrate, (±)-
C10H18O6
58167-01-4 234.246
34
3814
Diisopropyl dixanthogen
C8H14O2S4
105-65-7
52
3815
Diisopropyl thioperoxydicarbonate
1,4-Diisothiocyanatobenzene
Bitoscanate
C8H4N2S2
4044-65-9
3816
3817
3818
3819
Diketene
Dilactic acid
Dimefline
Dimefox
3820
Dimemorfan
3821
3823
3824
2,3-Dimercaptobutanedioic
acid, (R*,S*)
1,4-Dimercapto-2,3-butanediol
2,2’-Dimercaptodiethyl ether
2,3-Dimercapto-1-propanol
3825
Dimetan (R)-
3826
Dimethipin
3827
Dimethirimol
3828
2-[(3-Butyl-1-isoquinolinyl)­
C17H24N2O
oxy]-N,N-dimethylethanamine
Dimethoxane
2,6-Dimethyl-1,3-dioxan-4-ol C8H14O4
acetate
2’,5’-Dimethoxyacetophenone
C10H12O3
1,2-Dimethoxy-4-allylbenzene Methyleugenol
C11H14O2
3801
Organic
3807
3808
3809
3810
3822
3829
3830
3831
3832
Synonym
1,2-Benzenedicarboxylic acid,
diisopropyl ester
C4H4O2
C6H10O5
C20H21NO3
Tetramethylphosphorodiamidic C4H12FN2OP
fluoride
3,17-Dimethylmorphinan, (9
C18H25N
α,13 α,14 α)Succimer
C4H6O4S2
2,2’-Oxybispropanoic acid
2-Mercaptoethyl ether
Dimercaprol
189(8)
9740
713
13012
-78.03(0.04) 120.0(0.3)
192.261 nd (ace,
HOAc)
674-82-8
84.074 liq
19201-34-4 162.140 orth
1165-48-6 323.386
115-26-4
154.122 liq
132
36309-01-0 255.399 ye oil
92
304-55-2
193
-6.5
112.5
109.5
127.0(0.6)
1.087720 1.437920
8615
1.115120 1.426720
7634-42-6
C4H10OS2
C3H8OS2
2150-02-9
59-52-9
138.251 liq
124.225
-80
217
830.8
C11H17NO3
122-15-6
211.258 cry
46
17511
42.5
55290-64-7 210.271
165
5221-53-4
209.288 nd
102
86-80-6
272.385
146
828-00-2
174.195 liq
1201-38-3
93-15-2
180.200 cry
178.228 liq
C12H14O4
523-80-8
C8H11NO2
vs H2O, eth
s chl
vs H2O, bz, eth
1330.3
s chl
1563
1.114
1.246320 1.574920 s EtOH, eth,
oils; sl chl
s H2O, cyhex; vs
EtOH, eth, ace
20
1.548620
sl H2O; vs chl,
xyl; s EtOH,
ace
s H2O, EtOH
8610
1.065520 1.431020 msc H2O; s os
21
-2.0
15614
254.7
222.237 nd
29.2(0.2)
294
2735-04-8
153.179 pl (lig)
33.5
262.0
82.5
270(21)
1.139
1.544120
1.039620 1.534020 i H2O; s EtOH,
eth
1.01520 1.536020 vs ace, bz,
EtOH, lig
sl H2O, chl; s
EtOH, eth, bz,
lig
s H2O, EtOH,
chl, lig
s eth, chl
i H2O; s EtOH,
eth, bz; sl chl
sl H2O; s EtOH,
eth
sl H2O, chl; vs
EtOH, eth
3833
3834
2,5-Dimethoxyaniline
C8H11NO2
102-56-7
153.179
3835
3836
3,4-Dimethoxyaniline
2,4-Dimethoxybenzaldehyde
C8H11NO2
C9H10O3
6315-89-5
613-45-6
153.179 lf (eth)
87.5
166.173 nd (al or lig) 72
15914
290
3837
2,5-Dimethoxybenzaldehyde
C9H10O3
93-02-7
166.173
52
270
3838
3,4-Dimethoxybenzaldehyde
C9H10O3
120-14-9
166.173 nd (eth, lig,
to)
43
281
HCP_Section_03.indb 196
1.00220 1.410020 vs eth, EtOH
0.997018
1.0920
s EtOH, bz, ace,
ctc, chl
1.061515 1.490020
275
4,7-Dimethoxy-5-allyl-1,3benzodioxole
2,4-Dimethoxyaniline
Veratraldehyde
0.719225 1.365825 sl H2O; msc
EtOH, eth; s
ace, ctc
16
1.4120
0.814220 1.443820 i H2O; s EtOH,
eth
1.116620
vs ace, eth,
EtOH
s chl
C4H10O2S2
Dimethisoquin
Solubility
70
182.219 wh cry
(MeOH)
154.251
2,3-Dihydro-5,6-dimethyl-1,4- C6H10O4S2
dithiin, 1,1,4,4-tetraoxide
5-Butyl-2-(dimethylamino)-6- C11H19N3O
methylpyrimidin-4(1H)-one
Apiole
270.456
663
nD
4/11/16 11:25 AM
Physical Constants of Organic Compounds
O
3-197
OH
N
S N
S
3799
3800
1,4-Diisopropylbenzene
p-Diisopropylbenzene hydroperoxide
S
N C N
O
3803
3802
3801
3804
Diisopropyl disulfide
N,N’-Diisopropylcarbodiimide
N,N-Diisopropyl-2-benzothiazolesulfenamide
OH
N
S
3805
N,N-Diisopropylethanolamine
Diisopropyl ether
O
O
O P O
O
O
O P O
H
O
O
3806
Diisopropyl methylphosphonate
3807
2,6-Diisopropylnaphthalene
3808
O
3812
Diisopropyl phthalate
O,O-Diisopropyl phosphorodithioate
Diisopropyl phosphonate
S
3811
3810
3809
Diisopropyl oxalate
O
O
S
O P O
SH
Diisopropyl sulfide
O
O
OH
S
O
O
O
S
S
OH O
S
3813
Diisopropyl tartrate, (±)-
N
3814
3820
3815
HO
O
3816
O
O
O
N
N
OH
Dimefox
O O
S
O
HS
SH
O
3821
3822
1,4-Dimercapto-2,3-butanediol
HS
O
HS
OH
2,3-Dimercaptobutanedioic acid, (R *,S*)
N
3819
Dimefline
Dilactic acid
P
F
3818
3817
Diketene
O
O
OH
OH
SH
O
N C S
1,4-Diisothiocyanatobenzene
SH
HO
Dimemorfan
S C N
Diisopropyl thioperoxydicarbonate
O
H
O
O
SH
3823
2,2’-Dimercaptodiethyl ether
OH
O
SH
O
S
O O
N
3825
3824
3826
Dimetan (R)-
2,3-Dimercapto-1-propanol
Dimethipin
O
O
OH
N
N
O
O
N
3827
O
N
3829
Dimethoxane
Dimethisoquin
NH2
O
O
O
O
3830
2’,5’-Dimethoxyacetophenone
3831
1,2-Dimethoxy-4-allylbenzene
3832
4,7-Dimethoxy-5-allyl-1,3-benzodioxole
O
NH2
O
O
O
O
3828
Dimethirimol
O
O
N
O
O
O
NH2
O
O
O
O
3833
2,4-Dimethoxyaniline
O
O
3834
2,5-Dimethoxyaniline
3835
3,4-Dimethoxyaniline
O
O
3836
2,4-Dimethoxybenzaldehyde
O
O
3837
2,5-Dimethoxybenzaldehyde
3838
3,4-Dimethoxybenzaldehyde
Organic
O
Physical Constants of Organic Compounds
3-198
Mol. Form.
CAS RN
Mol.
Wt.
C9H10O3
7311-34-4
C8H10O2
1,3-Dimethoxybenzene
3842
No.
Name
3839
3,5-Dimethoxybenzaldehyde
3840
1,2-Dimethoxybenzene
3841
Physical
Form
den
g cm –3
mp/˚C
bp/˚C
166.173
46.3
15116
91-16-7
138.164 liq
22.5(0.2)
206(1)
1.081025 1.582721
C8H10O2
151-10-0
138.164 liq
-35.3(0.4)
216(5)
1.052125 1.523120
1,4-Dimethoxybenzene
C8H10O2
150-78-7
138.164 lf (w)
56.2(0.7)
213(5)
1.037555
3843
3,4-Dimethoxybenzeneacetic
acid
C10H12O4
93-40-3
98
3844
3,4-Dimethoxybenzeneethanamine
3,4-Dimethoxybenzenemethanamine
3,4-Dimethoxybenzenemethanol
3,3’-Dimethoxybenzidine
Dianisidine
C10H15NO2
120-20-7
196.200 cry
(bz-peth)
nd (w+1)
181.232
C9H13NO2
5763-61-1
167.205
15612
1.14325
C9H12O3
93-03-8
168.189 visc oil
298
1.17817
C14H16N2O2
119-90-4
244.289 lf or nd (w)
137
C16H12N2O4
91-93-0
296.277 cry
112
C9H10O4
91-52-1
182.173
107.2(0.4)
C9H10O4
C9H10O4
1466-76-8
93-07-2
186 dec
181
sub
i H2O; vs EtOH,
eth; sl chl
C9H10O4
1132-21-4
185.5
sub
vs eth, EtOH
3845
3846
Organic
3847
3848
Synonym
Veratrole
16414
nD
s chl
1.55517
3850
3851
2,6-Dimethoxybenzoic acid
3,4-Dimethoxybenzoic acid
3852
3,5-Dimethoxybenzoic acid
3853
4,4’-Dimethoxybenzoin
p-Anisoin
C16H16O4
119-52-8
182.173
182.173 nd (w or
HOAc) orth
(sub)
182.173 nd (w), pr
(al)
272.296 pr (dil al)
3854
5,7-Dimethoxy-2H-1-benzopyran-2-one
Limettin
C11H10O4
487-06-9
206.195 pr or nd (al) 149
200 dec
3855
4,4’-Dimethoxy-1,1’-biphenyl
C14H14O2
2132-80-1
214.260 lf (bz)
175
sub
3856
Dimethoxyborane
C2H7BO2
4542-61-4
73.887
-130.6
25.9
3857
3858
4,4-Dimethoxy-2-butanone
2,6-Dimethoxy-2,5-cyclohexa- 2,6-Dimethoxy-p-quinone
diene-1,4-dione
C6H12O3
C8H8O4
5436-21-5
530-55-2
132.157
168.148 ye mcl pr
(HOAc)
256
505
sub
3859
3860
3861
3862
3863
Dimethoxydimethylsilane
Dimethoxydiphenylsilane
1,1-Dimethoxydodecane
2,2-Dimethoxyethanamine
1,2-Dimethoxyethane
Ethylene glycol dimethyl ether
C4H12O2Si
C14H16O2Si
C14H30O2
C4H11NO2
C4H10O2
1112-39-6
6843-66-9
14620-52-1
22483-09-6
110-71-4
120.223
244.362
230.387
105.136
90.121 liq
-78
-69.0(0.2)
82
286
1335
13795
85.0(0.1)
3864
3865
(2,2-Dimethoxyethyl)benzene
4,8-Dimethoxyfuro[2,3-b]
quinoline
Fagarine
C10H14O2
C13H11NO3
101-48-4
524-15-2
166.217
229.231 pr (al)
142
3866
1,1-Dimethoxyhexadecane
C18H38O2
2791-29-9
286.494
10
1442
C10H12O4
90-24-4
196.200 cry (al)
82
18520
C11H12O3
C10H10O4
2107-69-9
569-31-3
192.211
194.184 wh nd (w)
119.5
102.5
C3H8O2
109-87-5
76.095
-105.11(0.03) 42.3(0.2)
0.859320 1.351320
C9H12O2
494-99-5
152.190 pr (eth)
24
221(4)
1.050925 1.525725
C9H12O2
4179-19-5
152.190
244
1.047815 1.523420
C9H12O2
24599-58-4 152.190
3867
3868
3869
Palmitaldehyde, dimethyl
acetal
2,4-Dimethoxy-6-hydroxyace- Xanthoxylin
tophenone
5,6-Dimethoxy-1-indanone
6,7-Dimethoxy-1(3H)-isoben- Meconin
zofuranone
3870
Dimethoxymethane
3871
1,2-Dimethoxy-4-methylbenzene
1,3-Dimethoxy-5-methylbenzene
1,4-Dimethoxy-2-methylbenzene
3872
3873
Lauraldehyde, dimethyl acetal
HCP_Section_03.indb 198
Methylal
liq
s H2O, EtOH
i H2O; s EtOH,
eth, ace, bz,
chl
3849
vol liq or
gas
sl H2O, peth; s
EtOH, bz
sl H2O; s EtOH,
eth, ctc
sl H2O; s EtOH,
eth, bz, ctc,
sulf
sl H2O; s EtOH,
chl; vs eth, bz
s H2O, chl; vs
EtOH, eth
1.546420 s ctc
3,3’-Dimethoxybenzidine-4,4’diisocyanate
2,4-Dimethoxybenzoic acid
Veratric acid
Solubility
sl H2O; s EtOH,
eth, chl, HOAc
109(3)
sl H2O, chl,
EtOH, eth; s
ace
sl H2O; vs EtOH,
ace, chl; i eth,
lig
i H2O, peth; vs
EtOH, bz, chl;
sl eth
dec H2O
s ctc
sl H2O, EtOH,
eth; s tfa; vs
alk, HOAc
dec H2O
0.864620 1.370820
1.077120 1.544720
1.431025 vs eth, EtOH
0.96625 1.417020
0.863725 1.377025 s H2O, EtOH,
eth, ace, bz,
chl, ctc
193.5
21
0.854220 1.438225
sl H2O, peth; s
EtOH, eth, bz,
chl
vs ace, eth,
EtOH
vs eth, EtOH
sl ctc
sl H2O; s EtOH,
eth, ace, bz,
HOAc, chl
s H2O; vs ace,
bz, eth, EtOH
i H2O; sl ctc; vs
os
vs bz, eth, EtOH
214.0
4/11/16 11:25 AM
Physical Constants of Organic Compounds
3-199
O
O
OH
O
O
O
O
3841
3840
3,5-Dimethoxybenzaldehyde
3842
1,3-Dimethoxybenzene
1,2-Dimethoxybenzene
O
3843
1,4-Dimethoxybenzene
3,4-Dimethoxybenzeneacetic acid
3844
3,4-Dimethoxybenzeneethanamine
OH
O
NH2
O
OH
O
O
O
O
3845
3846
O
3,3’-Dimethoxybenzidine
O
3850
OH
O
3849
3,3’-Dimethoxybenzidine-4,4’-diisocyanate
O
O
3851
OH
O
3852
3,4-Dimethoxybenzoic acid
O
O
O
O
2,6-Dimethoxybenzoic acid
N C O
3848
2,4-Dimethoxybenzoic acid
OH
O
O
O
O C N
NH2
3847
3,4-Dimethoxybenzenemethanol
OH
O
O
H2N
O
3,4-Dimethoxybenzenemethanamine
O
O
3853
3,5-Dimethoxybenzoic acid
O
O
O
3854
4,4’-Dimethoxybenzoin
5,7-Dimethoxy-2H-1-benzopyran-2-one
O
O
3855
4,4’-Dimethoxy-1,1’-biphenyl
O
O
O
H
B
O
O
O
O
3856
3857
Dimethoxyborane
O
O
Si
O
O
Si
O
3858
3859
3860
O
4,4-Dimethoxy-2-butanone
2,6-Dimethoxy-2,5-cyclohexadiene-1,4-dione
Dimethoxydimethylsilane
O
O
3861
Dimethoxydiphenylsilane
1,1-Dimethoxydodecane
O
O
O
O
O
NH2
O
3862
2,2-Dimethoxyethanamine
O
O
3863
3864
1,2-Dimethoxyethane
O
N
O
O
O
O
3865
(2,2-Dimethoxyethyl)benzene
4,8-Dimethoxyfuro[2,3-b]quinoline
O
O
O
O
O
3868
5,6-Dimethoxy-1-indanone
3869
O
O
6,7-Dimethoxy-1(3H )-isobenzofuranone
O
3866
1,1-Dimethoxyhexadecane
O
Dimethoxymethane
3871
2,4-Dimethoxy-6-hydroxyacetophenone
O
O
3870
3867
O
O
O
O
HO
1,2-Dimethoxy-4-methylbenzene
3872
1,3-Dimethoxy-5-methylbenzene
O
3873
1,4-Dimethoxy-2-methylbenzene
Organic
3839
O
O
O
O
O
O
NH2
O
Physical Constants of Organic Compounds
3-200
den
g cm –3
nD
119.163
104
0.89725
1.397220
122-07-6
119.163
140
0.92825
1.411520
C9H14O2Si
C8H9NO4
3027-21-2
709-09-1
182.292
183.162 ye nd (al-w) 98
12979
23015
1.1888133
C8H9NO4
89-39-4
C8H10O3
C8H10O3
C10H12O3
91-10-1
500-99-2
1131-62-0
183.162 gold-ye nd
(dil al)
154.163 mcl pr (w)
154.163
180.200 pr (dil al)
Isoeugenyl methyl ether
C5H12O2
C5H12O2
C5H10O2
C11H14O2
4744-10-9
77-76-9
6044-68-4
6379-72-2
104.148
104.148 liq
102.132
178.228
Apiole (Dill)
C12H14O4
484-31-1
222.237 oil
C10H12O2
6380-23-0
164.201
C4H10O2
534-15-6
90.121
liq
-113.2
63(2)
liq
-19(1)
165.9(0.2)
10.3(0.5)
11513
1.060020 1.428320 i H2O; s EtOH,
eth, ctc, HOAc
7.3(0.4)
0.68040
136(6)
0.864920 1.409520
Name
3874
N-(Dimethoxymethyl)­
Dimethylformamide dimethyl
dimethylamine
acetal
2,2-Dimethoxy-N-methylethanamine
Dimethoxymethylphenylsilane
1,2-Dimethoxy-4-nitrobenzene
3875
3876
3877
3878
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
C5H13NO2
4637-24-5
C5H13NO2
Physical
Form
3888
1,4-Dimethoxy-2-nitrobenzene
2,6-Dimethoxyphenol
3,5-Dimethoxyphenol
1-(3,4-Dimethoxyphenyl)­
ethanone
1,1-Dimethoxypropane
2,2-Dimethoxypropane
3,3-Dimethoxy-1-propene
trans-1,2-Dimethoxy-4-(1propenyl)benzene
4,5-Dimethoxy-6-(2propenyl)-1,3-benzodioxole
1,2-Dimethoxy-4-vinylbenzene
Dimethylacetal
3889
N,N-Dimethylacetamide
N,N-Dimethylethanamide
C4H9NO
127-19-5
87.120
3890
2,7-Dimethyl-3,6-acridinediamine, monohydrochloride
Dimethyl adipate
Acridine Yellow
C15H16ClN3
135-49-9
273.761 red cry pow
Dimethyl 1,6-hexanedioate
C8H14O4
627-93-0
174.195 cry
3879
3880
3881
Organic
bp/˚C
No.
3882
3883
3884
3885
3886
3887
3891
mp/˚C
72.5
56.5
37
51
285
1.159815 1.530517
1.571120 s chl
246.092 cry (MeOH)
3893
C2H7N
124-40-3
45.084
col gas
-93(2)
3894
Dimethylamine hydrochloride
C2H8ClN
506-59-2
81.545
orth nd (al)
171
3895
3896
(Dimethylamino)acetonitrile
4-Acetyl-N,N-dimethylaniline
4’-(Dimethylamino)­
acetophenone
10-[(Dimethylamino)­acetyl]Ahistan
10H-phenothiazine
4-(Dimethylamino)azobenzene
C4H8N2
C10H13NO
926-64-7
2124-31-4
84.120
163.216 nd (w, peth) 105.5
C16H16N2OS
518-61-6
284.375 cry
144.5
C14H15N3
60-11-7
225.289 ye lf (al)
116(1)
4-o-Tolylazo-o-toluidine
C14H15N3
97-56-3
225.289 ye lf (al)
102
Ehrlich’s reagent
C9H11NO
100-10-7
149.189 lf (w)
73.1(0.8)
3898
3899
3900
2’,3-Dimethyl-4-aminoazobenzene
4-(Dimethylamino)­
benzaldehyde
261(22)
19935
287
29.5
358-72-5
3897
1.1666132
18
C5H12O7P2
N-Methylmethanamine
hydrochloride
17617
4-(Dimethylamino)­
benzalrhodanine
C12H12N2OS2
536-17-4
264.365 dp red nd
(xyl)
270 dec
3902
2-(Dimethylamino)benzoic
acid
3-(Dimethylamino)benzoic
acid
4-(Dimethylamino)benzoic
acid
4,4’-Dimethylaminobenzophe- Brilliant Oil Yellow
nonimide
(Dimethylamino)dimethylborane
6-(Dimethylamino)-4,4diphenyl-3-heptanone
6-(Dimethylamino)-4,4Normethadone
diphenyl-3-hexanone
2-(Dimethylamino)ethyl
acrylate
3-[2-(Dimethylamino)­ethyl]Bufotenine
1H-indol-5-ol
C9H11NO2
610-16-2
165.189 pr, nd (eth)
72
C9H11NO2
99-64-9
165.189 nd (w)
152.5
C9H11NO2
619-84-1
165.189 nd (al)
242.5
C17H21N3
492-80-8
136
C4H12BN
1113-30-0
267.369 ye or col pl
(al)
84.956 liq
C21H27NO
76-99-3
309.445
99.5
C20H25NO
467-85-6
295.419 oily liq
C7H13NO2
2439-35-2
143.184
<-60
9550
C12H16N2O
487-93-4
204.267 pr (EtOAc)
146.5
3200.1
3904
3905
3906
3907
3908
3909
3910
HCP_Section_03.indb 200
-92
0.850120 1.366820 s H2O, EtOH,
eth, ctc, chl;
vs ace
0.937225 1.434125 msc H2O, EtOH,
eth, ace, bz,
chl
s hot H2O, EtOH
dec
3901
3903
i H2O; vs EtOH,
eth; s chl; sl
lig
i H2O; s EtOH,
bz, chl, sulf
vs eth, EtOH
s eth, bz; sl lig
vs H2O, bz,
EtOH, chl
0.864820
0.84725 1.378020
0.86225 1.395420
1.052120 1.561620
3,3-Dimethylallyl diphosphate 3-Methyl-2-butenyl
pyrophosphate
Dimethylamine
N-Methylmethanamine
3892
1.479520
88(5)
77.4(0.7)
88
270.5
-47
Solubility
1.35017
vs H2O; s EtOH,
eth
vs H2O, EtOH,
chl
vs H2O, EtOH
vs H2O, eth, lig;
sl chl
i H2O; vs EtOH,
py; s eth; sl
chl, lig
vs eth, EtOH
1.0254100
sub
sl H2O, chl; s
EtOH, eth, ace,
bz
i H2O; sl EtOH,
bz; vs eth, ctc;
s ace
vs H2O, eth,
EtOH
sl H2O, chl; s
EtOH, eth
s EtOH; sl eth
i H2O; s EtOH; sl
eth
vs eth, ace
65
vs EtOH
1653
0.93820
vs eth, EtOH
4/11/16 11:25 AM
Physical Constants of Organic Compounds
3-201
O
N
O
O
O
O
Si
O
H
N
O
O
N
OH
O
O
O
3877
Dimethoxymethylphenylsilane
2,2-Dimethoxy-N-methylethanamine
N-(Dimethoxymethyl)dimethylamine
O
O
3876
3875
3874
O
N
O
O
3879
3878
1,2-Dimethoxy-4-nitrobenzene
2,6-Dimethoxyphenol
1,4-Dimethoxy-2-nitrobenzene
O
OH
O
O
O
O
3880
O
O
3881
3882
1-(3,4-Dimethoxyphenyl)ethanone
O
O
O
3883
1,1-Dimethoxypropane
3884
2,2-Dimethoxypropane
3885
3,3-Dimethoxy-1-propene
trans-1,2-Dimethoxy-4-(1-propenyl)benzene
Organic
3,5-Dimethoxyphenol
O
O O
O
O
O
O
O
O
O
O
3887
3886
3888
1,2-Dimethoxy-4-vinylbenzene
4,5-Dimethoxy-6-(2-propenyl)-1,3-benzodioxole
N
O
3889
Dimethylacetal
HCl
NH2
N
H2N
3890
N,N-Dimethylacetamide
2,7-Dimethyl-3,6-acridinediamine, monohydrochloride
O
O
O
O
O
3891
O
O
O P O P OH
OH OH
H
N
3892
Dimethyl adipate
3893
3,3-Dimethylallyl diphosphate
N
H
N HCl
3894
Dimethylamine
N
N
3895
Dimethylamine hydrochloride
(Dimethylamino)acetonitrile
3896
4’-(Dimethylamino)acetophenone
O
N
O
O
N
N
N
S
3897
N
3898
10-[(Dimethylamino)acetyl]-10H-phenothiazine
NH
N
N
3900
2’,3-Dimethyl-4-aminoazobenzene
4-(Dimethylamino)benzaldehyde
4-(Dimethylamino)benzalrhodanine
NH
OH
N
N
3902
2-(Dimethylamino)benzoic acid
S
3901
OH
O
OH
S
N
N
3899
4-(Dimethylamino)azobenzene
O
O
H2N
N
N
3903
3904
3-(Dimethylamino)benzoic acid
N
N
3905
4-(Dimethylamino)benzoic acid
B
3906
4,4’-Dimethylaminobenzophenonimide
(Dimethylamino)dimethylborane
N
HO
N
O
N
N
O
O
O
3907
6-(Dimethylamino)-4,4-diphenyl-3-heptanone
3908
6-(Dimethylamino)-4,4-diphenyl-3-hexanone
3909
2-(Dimethylamino)ethyl acrylate
N
H
3910
3-[2-(Dimethylamino)ethyl]-1H-indol-5-ol
Physical Constants of Organic Compounds
3-202
No.
Name
3911
3915
2-(Dimethylamino)ethyl
methacrylate
4-[2-(Dimethylamino)­ethyl]­
phenol
N-[2-(Dimethylamino)­ethyl]N,N’,N’-trimethyl-1,2ethanediamine
5-(Dimethylamino)-1-naphthalenesulfonyl chloride
3-(Dimethylamino)phenol
3916
4-(Dimethylamino)phenol
3917
[4-(Dimethylamino)­phenyl]­
phenylmethanone
3918
3927
3-(Dimethylamino)-1-phenyl1-propanone, hydrochloride
3-[4-(Dimethylamino)­phenyl]- 4-(Dimethylamino)­
cinnamaldehyde
2-propenal
3-(Dimethylamino)­
propanenitrile
2-(Dimethylamino)-1-propanol
3-(Dimethylamino)-1-propanol
1-(Dimethylamino)-2-propanol
3-(Dimethylamino)-1-propyne N,N-Dimethyl-2-propargylamine
2-Dimethylaminopurine
N,N-Dimethyl-1H-purin-6amine
2-(p-Dimethylaminostyryl)­
benzothiazole
2,3-Dimethylaniline
2,3-Xylidine
3928
2,4-Dimethylaniline
3929
3912
Synonym
Hordenine
Mol. Form.
CAS RN
Mol.
Wt.
Physical
Form
C8H15NO2
2867-47-2
157.211
C10H15NO
539-15-1
117.5
C9H23N3
3030-47-5
165.232 orth pr (al),
nd (w)
173.299
C12H12ClNO2S
605-65-2
269.747
70
C8H11NO
99-07-0
137.179 nd (lig)
C8H11NO
619-60-3
C15H15NO
mp/˚C
bp/˚C
den
g cm –3
nD
Solubility
636
17311
vs eth, EtOH,
chl
8412
1.441325
86
266.5
137.179
77
16530
530-44-9
225.286 ye lf (al) nd
(peth)
92.5
1.589526 i H2O; s EtOH,
eth, ace, bz,
CS2
sl H2O; s EtOH,
eth
i H2O; sl EtOH;
vs eth; s chl,
peth
C11H16ClNO
879-72-1
213.704
153.5
C11H13NO
6203-18-5
175.227
139.5
C5H10N2
1738-25-6
98.146
177(12)
0.870520
C5H13NO
C5H13NO
C5H13NO
C5H9N
15521-18-3
3179-63-3
108-16-7
7223-38-3
103.163
103.163
103.163
83.132
150.3
163.5
124.5
81(3)
0.882026
s H2O
0.87225 1.436020 s ctc
0.83725 1.419320 s ctc
0.779220 1.419520
C7H9N5
938-55-6
163.180
263
C17H16N2S
1628-58-6
207 dec
C8H11N
87-59-2
280.387 ye nd
(MeOH)
121.180 liq
3(1)
223(17)
2,4-Xylidine
C8H11N
95-68-1
121.180 liq
-13(2)
215(2)
2,5-Dimethylaniline
2,5-Xylidine
C8H11N
95-78-3
121.180 ye lf (lig)
6(1)
214
3930
3931
2,6-Dimethylaniline
3,4-Dimethylaniline
2,6-Xylidine
3,4-Xylidine
C8H11N
C8H11N
87-62-7
95-64-7
121.180 liq
11.0(0.4)
121.180 pl or pr (lig) 49(1)
211(4)
228
3932
3,5-Dimethylaniline
3,5-Xylidine
C8H11N
108-69-0
121.180
217(5)
3933
N,2-Dimethylaniline
C8H11N
611-21-2
121.180
207.5
3934
N,3-Dimethylaniline
C8H11N
696-44-6
121.180
206.5
3935
N,4-Dimethylaniline
C8H11N
623-08-5
121.180
215(20)
3936
N,N-Dimethylaniline
C8H11N
121-69-7
121.180 pa ye
2.1(0.5)
3937
C8H12ClN
5882-44-0
C9H12O
1004-66-6
157.641 hyg pl (w,
bz)
136.190
90
3938
N,N-Dimethylaniline
hydrochloride
2,6-Dimethylanisole
3939
3,5-Dimethylanisole
C9H12O
874-63-5
136.190
194
3940
3941
C16H14
C16H12O2
781-43-1
1519-36-4
C2H7As
593-57-7
206.282
186.4(0.5)
236.265 ye nd (al,
140.5
sub)
105.999 liq, ign in air -136.1
360.0
sub
3942
9,10-Dimethylanthracene
1,4-Dimethyl-9,10-anthracenedione
Dimethylarsine
3943
Dimethylarsinic acid
C2H7AsO2
75-60-5
137.998
199.5(0.6)
>200
3944
2,4-Dimethylbenzaldehyde
C9H10O
15764-16-6 134.174 liq
-9
218
3945
2,5-Dimethylbenzaldehyde
C9H10O
5779-94-2
0.993120 1.568420 sl H2O; vs EtOH,
eth; s ctc
0.972320 1.556920 sl H2O, ctc; s
EtOH, eth, bz
0.979021 1.559121 sl H2O; s eth,
ctc
0.984220 1.561020 vs eth, EtOH
1.07618
sl H2O, chl; s
eth; vs lig
0.970620 1.558120 sl H2O; s eth,
ctc
0.970920 1.564920 i H2O; msc
EtOH, eth; s
ace
0.966020 1.555725 i H2O; msc
EtOH, eth; s
ace
0.934855 1.556820 i H2O; msc
EtOH, eth; s
ace
0.955720 1.558220 sl H2O; s EtOH,
eth, ace, bz;
vs chl
1.115619
vs H2O, EtOH,
chl
0.961914 1.505314 i H2O; s EtOH,
eth, bz, ctc
0.962715 1.511020 i H2O; s EtOH,
eth, bz, CS2; sl
ctc
i H2O
i H2O; sl EtOH; s
bz, xyl, HOAc
1.20829
vs ace, bz, eth,
EtOH
vs H2O; s EtOH;
i eth
s EtOH; s eth,
ace, bz; sl chl
0.950020
vs EtOH; s eth,
ace, bz, ctc
3913
3914
Organic
3919
3920
3921
3922
3923
3924
3925
3926
HCP_Section_03.indb 202
Dansyl chloride
4-(Dimethylamino)­
benzophenone
Cacodylic acid
Isoxylaldehyde
134.174
10(1)
193(1)
183(11)
36
220
4/11/16 11:25 AM
Physical Constants of Organic Compounds
3-203
Cl
O S O
N
O
N
N
3911
3912
2-(Dimethylamino)ethyl methacrylate
N
3913
4-[2-(Dimethylamino)ethyl]phenol
3914
N-[2-(Dimethylamino)ethyl]-N,N’,N’-trimethyl-1,2-ethanediamine
OH
OH
N
N
HO
O
5-(Dimethylamino)-1-naphthalenesulfonyl chloride
O
O
3915
O
N
OH
N
3919
3921
3-(Dimethylamino)propanenitrile
2-(Dimethylamino)-1-propanol
3-(Dimethylamino)-1-phenyl-1-propanone, hydrochloride
N
OH
N
OH
3922
3923
3-(Dimethylamino)-1-propanol
1-(Dimethylamino)-2-propanol
NH2
N
N
N
N
3920
3-[4-(Dimethylamino)phenyl]-2-propenal
3918
[4-(Dimethylamino)phenyl]phenylmethanone
4-(Dimethylamino)phenol
N
N
3917
3916
3-(Dimethylamino)phenol
N
N
N
H
S
3925
2-Dimethylaminopurine
HCl
N
N
N
3924
3-(Dimethylamino)-1-propyne
NH2
NH2
NH2
NH2
NH2
N
3926
3927
2-(p-Dimethylaminostyryl)benzothiazole
3928
2,3-Dimethylaniline
2,4-Dimethylaniline
3929
3930
2,5-Dimethylaniline
3931
2,6-Dimethylaniline
3,4-Dimethylaniline
3932
3,5-Dimethylaniline
NH
NH
N
N
NH
O
O
HCl
3933
N,2-Dimethylaniline
3934
3935
N,3-Dimethylaniline
N,4-Dimethylaniline
3936
N,N-Dimethylaniline
3937
3938
N,N-Dimethylaniline hydrochloride
2,6-Dimethylanisole
3939
3,5-Dimethylanisole
O
O
O
O
3940
9,10-Dimethylanthracene
3941
1,4-Dimethyl-9,10-anthracenedione
H
As
3942
Dimethylarsine
O
As OH
3943
Dimethylarsinic acid
3944
2,4-Dimethylbenzaldehyde
3945
2,5-Dimethylbenzaldehyde
Organic
N
Physical Constants of Organic Compounds
3-204
CAS RN
Mol.
Wt.
3,5-Dimethylbenzaldehyde
C9H10O
5779-95-3
134.174
N,N-Dimethylbenzamide
7,12-Dimethylbenz[a]
9,10-Dimethyl-1,2-benzananthracene
thracene
4,5-Dimethyl-1,2-benzenediamine
N,N-Dimethyl-1,2-benzenediamine
N,N-Dimethyl-1,3-benzenediamine
N,N-Dimethyl-1,4-benzenedi- Dimethyl-p-phenylenediamine
amine
C9H11NO
C20H16
611-74-5
57-97-6
272.0
C8H12N2
3171-45-7
149.189
43.8(0.5)
256.341 pa ye pl (al, 123(1)
HOAc)
136.194
128
C8H12N2
2836-03-5
136.194 oil
218
0.99522
C8H12N2
2836-04-6
136.194
<-20
270
0.99525
C8H12N2
99-98-9
136.194 nd (bz)
53
264(5)
1.03620
207.5
Name
3946
3947
3948
3949
3950
3951
3952
Organic
Mol. Form.
No.
Synonym
Physical
Form
mp/˚C
bp/˚C
9
221(12)
den
g cm –3
nD
Solubility
vs ace, bz, eth,
EtOH
vs ace, bz
sl H2O; vs EtOH,
eth, ace, bz
sl H2O; vs EtOH,
eth
s H2O, chl; vs
EtOH, eth, bz;
sl lig
s H2O, EtOH, eth
3953
2,5-Dimethyl-1,3-benzenediol
C8H10O2
488-87-9
3954
2,6-Dimethyl-1,4-benzenediol
C8H10O2
654-42-2
3955
C10H15N
93-88-9
C10H15N
122-09-8
149.233 oily liq
205
C9H13N
585-32-0
135.206
196.5
0.942320 1.518125
3958
Phenylpropylmethylamine
N,βDimethylbenzeneethanamine
Phentermine
α,αDimethylbenzeneethanamine
α,αDimethylbenzenemethanamine
α,4-Dimethylbenzenemethanol 1-(4-Methylphenyl)ethanol
138.164 nd (bz), pr 163
(w)
138.164 nd (xyl), cry 152.3
(w)
149.233
C9H12O
536-50-5
136.190
215(11)
3959
α,α-Dimethylbenzenemethanol α-Cumyl alcohol
C9H12O
617-94-7
136.190 pr
37(1)
202
3960
α,α-Dimethylbenzenepropanol Benzyl-tert-butanol
C11H16O
103-05-9
164.244 nd
24.5
12113
3961
C8H11NO2S
640-61-9
185.244 pl (dil al)
78.5
C9H10N2
582-60-5
146.188 cry (eth)
205.5
sub
3963
N,4-Dimethylbenzenesulfonamide
5,6-Dimethyl-1H-benzimidazole
2,4-Dimethylbenzoic acid
0.966825 1.524620 i H2O; vs EtOH,
eth
0.973520 1.532520 i H2O; s EtOH,
eth, bz, HOAc
0.962621 1.507721 i H2O; vs EtOH,
eth, ace, bz
1.34025
vs eth, EtOH
C9H10O2
611-01-8
150.174 mcl or tcl
nd (w)
90
268
3964
2,5-Dimethylbenzoic acid
C9H10O2
610-72-0
150.174 nd (al)
132(3)
sub
3965
2,6-Dimethylbenzoic acid
C9H10O2
632-46-2
150.174 nd (lig)
116
277(18)
3966
3,4-Dimethylbenzoic acid
C9H10O2
619-04-5
150.174 pr (al)
163(2)
3967
3,5-Dimethylbenzoic acid
Mesitylenic acid
C9H10O2
499-06-9
150.174 nd (w, al)
171.1
275(19)
3968
4,4’-Dimethylbenzophenone
Bis(4-methylphenyl) ketone
C15H14O
611-97-2
210.271 orth (al)
96.5
339(20)
3969
7,8-Dimethylbenzo[g]­
pteridine-2,4(1H,3H)-dione
2,5-Dimethylbenzoxazole
N,N-Dimethylbenzylamine
Lumichrome
C12H10N4O2
1086-80-2
242.233 ye cry (chl)
300
Dimethylbenzylamine
C9H9NO
C9H13N
5676-58-4
103-83-3
147.173
135.206
218.5
179(15)
1.088018 1.541220
0.9150
1.501120
C11H18N2
103-55-9
178.274
14530
0.934320 1.508920
C16H21N3
91-81-6
255.358 ye oil
1400.1
C9H14O
38651-65-9 138.206 liq
C9H14
529-16-8
C11H18O
3956
3957
3962
3970
3971
3972
Dimedazole
278.5
vs eth, EtOH
3977
N,N-Dimethyl-N’-benzyl-1,2- N-Benzyl-N’,N’-dimethyl-1,2ethanediamine
ethanediamine
N,N-Dimethyl-N’-benzyl-N’-2- Tripelennamine
pyridinyl-1,2-ethanediamine
6,6-Dimethylbicyclo[3.1.1]­
heptan-2-one, (1R)2,3-Dimethylbicyclo[2.2.1]­
2,3-Dimethyl-2-norbornene
hept-2-ene
6,6-Dimethylbicyclo[3.1.1]­
hept-2-ene-2-ethanol
2,2’-Dimethylbiphenyl
3978
3,3’-Dimethylbiphenyl
C14H14
612-75-9
182.261
3979
4,4’-Dimethylbiphenyl
C14H14
613-33-2
182.261 mcl pr (eth) 120.9(0.4)
294(11)
3980
3981
3982
4,4’-Dimethyl-2,2’-bipyridine
2,3-Dimethyl-1,3-butadiene
N,N-Dimethylbutanamide
C12H12N2
C6H10
C6H13NO
1134-35-6
513-81-5
760-79-2
184.236
82.143 liq
115.173 liq
69(1)
186
3973
3974
3975
3976
HCP_Section_03.indb 204
Diisopropenyl
-1
0.91525
vs bz, eth, EtOH
1.06921
1.57625
s H2O, EtOH,
eth, chl, DMSO
sl H2O; s EtOH,
ace, bz, chl,
HOAc, tol
i H2O; s EtOH,
eth, ace, bz
sl H2O, lig; s
EtOH, eth
i H2O; s EtOH,
eth, bz
sl H2O; vs EtOH,
eth
vs ace, bz, eth,
EtOH
sl H2O, EtOH,
chl
s ctc
sl H2O; msc
EtOH, eth
misc H2O
209
0.980720 1.478720 vs eth, EtOH
122.207
140.5
0.869817 1.468817 s eth, ace, bz
128-50-7
166.260
235
0.97325
C14H14
605-39-0
182.261 cry (al)
19.94(0.01)
258(7)
8(4)
289.6(0.2)
0.990620 1.575220 i H2O; vs EtOH,
eth, bz; s ace
0.999520 1.594620 i H2O; vs EtOH,
eth, bz; s ace
0.917121
i H2O; sl EtOH; s
eth, ace, bz,
CS2
s chl
0.722225 1.439420 s ctc
0.906425 1.439125 vs ace, bz, eth,
EtOH
171.5
-76.0(0.1)
-40
1.493020 s chl
4/11/16 11:25 AM
Physical Constants of Organic Compounds
3-205
NH2
O
O
N
N
NH2
NH2
N
NH2
3946
3,5-Dimethylbenzaldehyde
3948
3947
3949
7,12-Dimethylbenz[a]anthracene
N,N-Dimethylbenzamide
N
3951
3950
4,5-Dimethyl-1,2-benzenediamine
N,N-Dimethyl-1,3-benzenediamine
N,N-Dimethyl-1,2-benzenediamine
OH
OH
H
N
NH2
OH
OH
3952
3953
3954
2,5-Dimethyl-1,3-benzenediol
3955
2,6-Dimethyl-1,4-benzenediol
3956
3957
α,α-Dimethylbenzeneethanamine
N,β-Dimethylbenzeneethanamine
α,α-Dimethylbenzenemethanamine
Organic
N,N-Dimethyl-1,4-benzenediamine
NH2
NH2
O
OH
3958
α,4-Dimethylbenzenemethanol
OH
3959
3960
α,α-Dimethylbenzenemethanol
O
OH
S
N
O
N
H
N
H
3961
α,α-Dimethylbenzenepropanol
O
O
O
OH
3962
N,4-Dimethylbenzenesulfonamide
3963
5,6-Dimethyl-1H-benzimidazole
2,4-Dimethylbenzoic acid
OH
OH
O
O
OH
O
N
NH
N
3964
2,5-Dimethylbenzoic acid
3965
3966
2,6-Dimethylbenzoic acid
3,4-Dimethylbenzoic acid
3968
3967
4,4’-Dimethylbenzophenone
3,5-Dimethylbenzoic acid
3970
2,5-Dimethylbenzoxazole
3971
3972
N,N-Dimethylbenzylamine
7,8-Dimethylbenzo[g]pteridine-2,4(1H,3H )-dione
3974
6,6-Dimethylbicyclo[3.1.1]heptan-2-one, (1R)-
N
N
3973
N,N-Dimethyl-N’-benzyl-1,2-ethanediamine
O
O
N
N
H
N
O
N
H
3969
N
N
OH
N,N-Dimethyl-N’-benzyl-N’-2-pyridinyl-1,2-ethanediamine
OH
3975
2,3-Dimethylbicyclo[2.2.1]hept-2-ene
3976
6,6-Dimethylbicyclo[3.1.1]hept-2-ene-2-ethanol
3977
2,2’-Dimethylbiphenyl
3978
3,3’-Dimethylbiphenyl
O
N
3979
4,4’-Dimethylbiphenyl
N
N
3980
4,4’-Dimethyl-2,2’-bipyridine
3981
2,3-Dimethyl-1,3-butadiene
3982
N,N-Dimethylbutanamide
Physical Constants of Organic Compounds
3-206
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
3,3-Dimethyl-2-butanamine
2,2-Dimethylbutane
Neohexane
C6H15N
C6H14
3850-30-4
75-83-2
3985
2,3-Dimethylbutane
Diisopropyl
C6H14
3986
2,3-Dimethyl-2,3-butanediol
Pinacol
3987
3988
No.
Name
3983
3984
Physical
Form
den
g cm –3
Organic
mp/˚C
bp/˚C
101.190 liq
86.175 liq
-20
-99.0(0.4)
101(6)
49.7(0.2)
79-29-8
86.175
-128.1(0.2)
58.0(0.3)
C6H14O2
76-09-5
118.174 nd (al,eth)
43.3(0.2)
174(3)
2,3-Dimethyl-2-butanethiol
2,2-Dimethylbutanoic acid
C6H14S
C6H12O2
1639-01-6
595-37-9
118.240 liq
116.158 liq
3989
2,2-Dimethyl-1-butanol
C6H14O
1185-33-7
102.174
3990
3,3-Dimethyl-1-butanol
Dimbunol
C6H14O
624-95-3
102.174 liq
3991
2,3-Dimethyl-2-butanol
Isopropyldimethylcarbinol
C6H14O
594-60-5
102.174 liq
3992
3,3-Dimethyl-2-butanol, (±)-
C6H14O
20281-91-8 102.174
3993
3,3-Dimethyl-2-butanone
C6H12O
75-97-8
100.158 liq
3994
3995
3,3-Dimethylbutanoyl chloride
2,3-Dimethyl-1-butene
C6H11ClO
C6H12
7065-46-5
563-78-0
134.603
84.159 liq
3996
3,3-Dimethyl-1-butene
C6H12
558-37-2
84.159
liq
3997
2,3-Dimethyl-2-butene
C6H12
563-79-1
84.159
liq
3998
N-(1,3-Dimethylbutyl)-N’phenyl-1,4-benzenediamine
3,3-Dimethyl-1-butyne
Dimethyl 2-butynedioate
Dimethyl cadmium
C18H24N2
793-24-8
268.397
126.1(0.7)
187.87(0.02) 0.927620 1.414520 sl H2O; s EtOH,
eth
<-15
137(1)
0.828320 1.420820 sl H2O; s EtOH,
eth
-60
143(2)
0.84415 1.432315 sl H2O; s EtOH,
eth, ace
-10.5(0.3)
118.7(0.5) 0.823620 1.417620 s H2O; msc
EtOH, eth
5.6
120.4
0.812225 1.414820 sl H2O; vs EtOH,
eth
-51.40(0.05) 106.1(0.2) 0.722925 1.395220 sl H2O; s EtOH,
eth, ace, ctc
129(8)
0.96920 1.421020 vs eth
-157.27(0.09) 55.59(0.04) 0.680320 1.399520 i H2O; s EtOH,
eth, ace, ctc,
CS2
-115.2(0.3) 41.24(0.04) 0.652920 1.376320 i H2O; s EtOH,
eth, ctc, chl
-74.3(0.1)
73.19(0.06) 0.708020 1.412220 i H2O; s EtOH,
eth, ace, chl
46
1641
C6H10
C6H6O4
C2H6Cd
917-92-0
762-42-5
506-82-1
82.143 liq
142.110
142.480
C3H6ClNO
C3H6ClNS
79-44-7
107.539 liq
16420-13-6 123.605 pr
C11H14O4
C3H6O3
39589-98-5 210.227 cry
616-38-6
90.078
3999
4000
4001
4002
4003
Pinacolone
tert-Butylacetylene
Solubility
-15.0(0.5)
-78.2(0.4)
0.662325 1.373620
1.156420 1.443420 s EtOH, eth, ctc
1.984618 1.5488
s peth
-33
42(2)
38(2)
199(9)
105.5 (exp
150)
154(10)
9810
38
-1(10)
13712.5
90.11(0.09)
1.16421 1.485220
1.063625 1.368720
-2.67(0.02)
1.16825
1.454020
4004
4005
Dimethylcarbamic chloride
Dimethylcarbamothioic
chloride
Dimethyl carbate
Dimethyl carbonate
4006
Dimethylcyanamide
C3H6N2
1467-79-4
70.093
4007
C8H8O2
526-86-3
136.149 ye nd
55
C8H8O2
137-18-8
136.149 ye nd (al)
126.0
C8H8O2
527-61-7
136.149 ye nd
72.5
4010
2,3-Dimethyl-2,5-cyclohexadiene-1,4-dione
2,5-Dimethyl-2,5-cyclohexadiene-1,4-dione
2,6-Dimethyl-2,5-cyclohexadiene-1,4-dione
1,1-Dimethylcyclohexane
C8H16
590-66-9
112.213 liq
-33.31(0.04) 119.5(0.3)
4011
cis-1,2-Dimethylcyclohexane
C8H16
2207-01-4
112.213 liq
-49.83(0.04) 129.7(0.6)
4012
trans-1,2-Dimethylcyclohexane
C8H16
6876-23-9
112.213 liq
-88.12(0.02) 123.4(0.3)
4013
cis-1,3-Dimethylcyclohexane
C8H16
638-04-0
112.213 liq
-75.51(0.03) 124.4(0.6)
4014
trans-1,3-Dimethylcyclohexane
cis-1,4-Dimethylcyclohexane
C8H16
2207-03-6
112.213 liq
-90.05(0.03) 120.1(0.7)
C8H16
624-29-3
112.213 liq
-87.4(0.3)
124.3(0.7)
C8H16
2207-04-7
112.213 liq
-36.9(0.2)
119.3(0.5)
C10H16O4
3399-22-2
200.232 ndl (eth)
71
s eth
126-81-8
140.180 nd (w)
52.5(0.5)
sl H2O, eth; s
ace, ctc; vs
chl, HOAc
4008
4009
4015
4016
4017
4018
trans-1,4-Dimethylcyclohexane
Dimethyl trans-1,4-cyclohexanedicarboxylate
5,5-Dimethyl-1,3-cyclohexanedione
HCP_Section_03.indb 206
Dimethylcarbamoyl chloride
liq
nD
0.766820 1.410525 vs H2O
0.644425 1.368820 i H2O; s EtOH,
eth; vs ace,
bz, peth, ctc
0.661620 1.375020 i H2O; s EtOH,
eth; vs ace,
bz, peth, ctc
sl H2O, CS2; vs
EtOH, eth
Methyl carbonate
5,5-Dimethyldihydroresorcinol C8H12O2
162(5)
1.408919
sub
sub
1.047928
vs eth; s chl,
peth
i H2O
i H2O; s EtOH,
eth; sl ctc
vs ace, eth,
EtOH
sl H2O; s EtOH,
eth, chl
sl H2O, EtOH; s
eth, bz, chl
s chl
0.780920 1.429020 i H2O; s EtOH,
eth, ace, bz;
msc ctc
20
20
0.7963
1.4360
i H2O; s EtOH,
bz, ctc; msc
eth, ace
0.776020 1.427020 i H2O; s EtOH,
eth; msc ace,
bz; vs lig
20
20
0.7660
1.4229
i H2O; msc
EtOH, eth, ace,
bz, lig, ctc
0.7915
1.428425
0.782920 1.423020 i H2O; msc
EtOH, eth, ace,
bz, lig, ctc
0.7715
1.418525 i H2O
4/11/16 11:25 AM
Physical Constants of Organic Compounds
3-207
HO
OH
NH2
OH
3983
3,3-Dimethyl-2-butanamine
3985
3984
3986
2,3-Dimethylbutane
2,2-Dimethylbutane
3990
3988
2,3-Dimethyl-2-butanethiol
O
2,2-Dimethylbutanoic acid
3989
2,2-Dimethyl-1-butanol
Cl
O
OH
OH
OH
O
3987
2,3-Dimethyl-2,3-butanediol
OH
3991
3992
2,3-Dimethyl-2-butanol
3993
3,3-Dimethyl-2-butanol, (±)-
3,3-Dimethyl-2-butanone
3994
3995
3,3-Dimethylbutanoyl chloride
2,3-Dimethyl-1-butene
3996
3,3-Dimethyl-1-butene
Organic
3,3-Dimethyl-1-butanol
SH
H
N
O
N
H
3997
2,3-Dimethyl-2-butene
O
3998
O
Dimethyl 2-butynedioate
3,3-Dimethyl-1-butyne
O
S
N
Cl
O
4003
Dimethylcarbamothioic chloride
4001
Dimethyl cadmium
O
O
4004
4002
Dimethylcarbamic chloride
N
O
N
O
4007
Dimethylcyanamide
Dimethyl carbonate
O
O
4006
4005
Dimethyl carbate
Cl
O
O
O
N
Cd
4000
3999
N-(1,3-Dimethylbutyl)-N’-phenyl-1,4-benzenediamine
O
O
2,3-Dimethyl-2,5-cyclohexadiene-1,4-dione
4008
2,5-Dimethyl-2,5-cyclohexadiene-1,4-dione
O
O
4009
2,6-Dimethyl-2,5-cyclohexadiene-1,4-dione
4010
1,1-Dimethylcyclohexane
4011
cis-1,2-Dimethylcyclohexane
4012
trans-1,2-Dimethylcyclohexane
O
4013
cis-1,3-Dimethylcyclohexane
4014
trans-1,3-Dimethylcyclohexane
O
O
O
4015
cis-1,4-Dimethylcyclohexane
4016
trans-1,4-Dimethylcyclohexane
O
O
4017
Dimethyl trans-1,4-cyclohexanedicarboxylate
4018
5,5-Dimethyl-1,3-cyclohexanedione
Physical Constants of Organic Compounds
3-208
CAS RN
Mol.
Wt.
C10H21N
101-40-6
155.281
C8H16O
C8H14O
C8H14O
C8H14O
C8H14O
C8H14
C8H14
C8H12O
767-12-4
1193-47-1
2816-57-1
2979-19-3
4255-62-3
1674-10-8
2808-76-6
1123-09-7
128.212
126.196 liq
126.196
126.196
126.196
110.197 liq
110.197
124.180
C7H14
C7H14
C7H14
1638-26-2
1192-18-3
822-50-4
98.186
98.186
98.186
liq
liq
liq
-69.43(0.01) 87.8(0.3)
-53.67(0.02) 99.5(0.3)
-118(1)
91.9(0.4)
0.749925 1.413620
0.768025 1.422220
0.746825 1.412020
C7H14
C7H14
2532-58-3
1759-58-6
98.186
98.186
liq
liq
-133.67(0.03) 91.7(0.5)
-133.9(0.1) 90.7(0.6)
0.740225 1.408920
0.744325 1.410720
C9H19N
102-45-4
141.254
C7H12
C7H12
C5H10
765-47-9
96.170
16491-15-9 96.170
1630-94-0 70.133
cis-1,2-Dimethylcyclopropane
C5H10
930-18-7
70.133
trans-1,2-Dimethylcyclopropane
Dimethyldecylamine
Dimethyldiacetoxysilane
trans-Dimethyldiazene
C5H10
2402-06-4
70.133
C12H27N
C6H12O4Si
C2H6N2
1120-24-7
2182-66-3
4143-41-3
C6H8O4
Name
4019
4034
4035
4036
Propylhexedrine
N,αDimethylcyclohexaneethanamine
3,3-Dimethylcyclohexanol
2,2-Dimethylcyclohexanone
2,6-Dimethylcyclohexanone
3,3-Dimethylcyclohexanone
4,4-Dimethylcyclohexanone
1,2-Dimethylcyclohexene
1,3-Dimethylcyclohexene
3,5-Dimethyl-2-cyclohexen-1one
1,1-Dimethylcyclopentane
cis-1,2-Dimethylcyclopentane
trans-1,2-Dimethylcyclopentane
cis-1,3-Dimethylcyclopentane
trans-1,3-Dimethylcyclopentane
Cyclopentamine
N,αDimethylcyclopentaneethanamine
1,2-Dimethylcyclopentene
1,5-Dimethylcyclopentene
1,1-Dimethylcyclopropane
4037
4038
4020
4021
4022
4023
4024
4025
4026
4027
4028
4029
4030
Organic
Mol. Form.
No.
4031
4032
4033
4039
4040
4041
4042
4043
4044
4045
4046
4047
4048
4049
4050
Synonym
N,N-Dimethyl-1-decanamine
Bis(acetyloxy)dimethylsilane
Azomethane
2,2-Dimethyl-1,3-dioxaneMeldrum’s acid
4,6-dione
cis-3,6-Dimethyl-1,4-dioxane2,5-dione
2,2-Dimethyl-1,3-dioxolane- Isopropylidene glycerol
4-methanol
Dimethyldiphenoxysilane
2,3-Dimethyl-2,3-diphenylbu- Dicumene
tane
3,3’-Dimethyldiphenylmethane 4,4’-diisocyanate
2,9-Dimethyl-4,7-diphenyl1,10-phenanthroline
Dimethyldiphenylsilane
N,N’-Dimethyl-N,N’-diphenylurea
4051
Dimethyl disulfide
4052
O,O-Dimethyl dithiophosphate O,O-Dimethyl phosphorodithionate
N,N-Dimethyldodecylamine
oxide
1,2-Dimethylenecyclohexane
4053
4054
4055
Methyl disulfide
Physical
Form
mp/˚C
11(2)
-20.5
39
-84.1(0.2)
bp/˚C
den
g cm –3
205
0.850120 1.460020 vs EtOH
186(4)
172
175(15)
180
7314
137(3)
126(4)
208.5
0.912814
0.914520
0.92525
0.90915
0.93220
0.822025
0.79925
0.940020
171
105(3)
99
21(2)
vol liq or
gas
-149.7(0.1)
28(2)
185.349
176.243 liq
58.082 gas
-12.5
-78
234(6)
165
1.5
2033-24-1
144.126
94
C6H8O4
4511-42-6
144.126 orth (eth)
96.8
C6H12O3
100-79-8
132.157
C14H16O2Si
C18H22
3440-02-6
1889-67-4
244.362
238.368 cry (MeOH)
C17H14N2O2
139-25-3
278.305
C26H20N2
4733-39-5
360.450
280 dec
C14H16Si
C15H16N2O
778-24-5
611-92-7
212.363
240.300 pl (al)
121.6(0.7)
277
350
C2H6S2
624-92-0
94.199
-84.67(0.1)
109.72(0.08) 1.062520 1.528920
C2H7O2PS2
756-80-9
158.180 liq
C14H31NO
1643-20-5
229.402 hyg nd (tol)
C8H12
2819-48-9
C4H12N2
-23
119(1)
0.792825 1.444820
0.78020 1.433120
0.660420 1.366820 i H2O; s EtOH;
vs eth, sulf
0.688925 1.382920 i H2O; s EtOH;
vs eth; sl ctc
0.664825 1.371320 vs eth, EtOH
1.054020 1.403020
0.7430
1.419919 vs ace, EtOH,
eth; s ctc, hp
15025
8210
1.06420
1315
1.059925 1.533020
1.438320
s chl
liq
0.986720 1.564420
vs H2O, EtOH,
ace; sl eth, bz,
CS2
i H2O; msc
EtOH, eth
564
1.2920
108.181
125(7)
108-00-9
88.151
104
0.836120 1.471825 i H2O; s EtOH,
eth, bz, chl; vs
ace
0.80325 1.426020
C4H12N2
110-70-3
88.151
120
0.82815
130.7(0.5)
0.886620 1.430020
130.5
4057
Deanol
C4H11NO
108-01-0
89.136
liq
-65(1)
4058
Dimethyl ether
Methyl ether
C2H6O
115-10-6
46.068
col gas
-141.49(0.05) -24.8(0.2)
4059
4060
(1,1-Dimethylethoxy)benzene
[(1,1-Dimethylethoxy)­methyl]­
oxirane
C10H14O
C7H14O2
6669-13-2
7665-72-7
150.217 liq
130.185 liq
HCP_Section_03.indb 208
1.450020
-90.4(0.5)
-118.5(0.5)
-109.0(0.1)
-140.92(0.09) 37(3)
Solubility
1.460615
1.448620
1.446020
1.448217
1.453724
1.462020
1.44920
1.481220 s EtOH, eth
liq
liq
vol liq or
gas
liq
N,N-Dimethyl-1,2-ethanediamine
N,N’-Dimethyl-1,2-ethanediamine
N,N-Dimethylethanolamine
4056
nD
-18.3(0.4)
-70
194(6)
152
s EtOH, eth, dil
HCl
msc H2O, EtOH,
eth; s chl
s H2O, EtOH,
eth, ace, chl;
sl bz
0.921420
0.89820
4/11/16 11:25 AM
Physical Constants of Organic Compounds
3-209
OH
O
O
O
NH
4019
4021
4020
N,α-Dimethylcyclohexaneethanamine
4022
2,2-Dimethylcyclohexanone
3,3-Dimethylcyclohexanol
2,6-Dimethylcyclohexanone
4023
3,3-Dimethylcyclohexanone
O
O
4025
4026
1,2-Dimethylcyclohexene
4027
1,3-Dimethylcyclohexene
4030
4029
1,1-Dimethylcyclopentane
4032
4031
trans-1,2-Dimethylcyclopentane
cis-1,2-Dimethylcyclopentane
4028
3,5-Dimethyl-2-cyclohexen-1-one
trans-1,3-Dimethylcyclopentane
cis-1,3-Dimethylcyclopentane
H
N
4033
4034
N,α-Dimethylcyclopentaneethanamine
4035
1,2-Dimethylcyclopentene
4036
1,5-Dimethylcyclopentene
1,1-Dimethylcyclopropane
4037
cis-1,2-Dimethylcyclopropane
O
O
O
N
4038
4039
trans-1,2-Dimethylcyclopropane
O
O
O
4043
4041
trans-Dimethyldiazene
O
O
O
4042
2,2-Dimethyl-1,3-dioxane-4,6-dione
O
Si
O
4045
4044
cis-3,6-Dimethyl-1,4-dioxane-2,5-dione
O
N N
Dimethyldiacetoxysilane
HO
O
O
4040
Dimethyldecylamine
O
Si
O
Dimethyldiphenoxysilane
2,2-Dimethyl-1,3-dioxolane-4-methanol
4046
2,3-Dimethyl-2,3-diphenylbutane
O
O
C
N
N
C
O
N
4047
N
4048
3,3’-Dimethyldiphenylmethane 4,4’-diisocyanate
S
Si
2,9-Dimethyl-4,7-diphenyl-1,10-phenanthroline
S
O P O
SH
S
4051
Dimethyldiphenylsilane
4053
O,O-Dimethyl dithiophosphate
N,N-Dimethyldodecylamine oxide
N
4050
N,N’-Dimethyl-N,N’-diphenylurea
O
N
4052
Dimethyl disulfide
N
4049
H2N
4054
1,2-Dimethylenecyclohexane
N
4055
N,N-Dimethyl-1,2-ethanediamine
O
H
N
N
H
4056
N,N’-Dimethyl-1,2-ethanediamine
O
N
OH
4057
N,N-Dimethylethanolamine
O
O
4058
Dimethyl ether
4059
(1,1-Dimethylethoxy)benzene
4060
[(1,1-Dimethylethoxy)methyl]oxirane
Organic
4024
4,4-Dimethylcyclohexanone
Physical Constants of Organic Compounds
3-210
Organic
No.
Name
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
Physical
Form
mp/˚C
bp/˚C
4061
N,N-Dimethylformamide
DMF
C3H7NO
68-12-2
73.094
liq
-60.3(0.2)
152.8(0.5)
4062
4063
Dimethyl fumarate
2,5-Dimethylfuran
C6H8O4
C6H8O
624-49-7
625-86-5
144.126
96.127 liq
101.7(0.7)
-62.8
193
96(3)
4064
3,4-Dimethyl-2,5-furandione
C6H6O3
766-39-2
96
223
4065
4066
Dimethyl germanium sulfide
Dimethyl glutarate
C2H6GeS
C7H12O4
126.110 pl or lf (dil
al)
16090-49-6 134.77 col cry
1119-40-0 160.168 liq
54.5
-42.5
302
216(4)
4067
N,N-Dimethylglycine
C4H9NO2
1118-68-9
103.120 hyg nd
(PrOH)
185.5
4068
Dimethylglyoxime
C4H8N2O2
95-45-4
4069
4070
2,6-Dimethyl-1,5-heptadiene
2,2-Dimethylheptane
C9H16
C9H20
6709-39-3
1071-26-7
116.119 nd (to or dil 245.5
234 sub
al)
124.223 liq
-70
143(3)
128.255 liq
-113.05(0.1) 133(1)
4071
2,3-Dimethylheptane
C9H20
3074-71-3
128.255 liq
4072
2,4-Dimethylheptane
C9H20
2213-23-2
128.255
132(2)
4073
2,5-Dimethylheptane
C9H20
2216-30-0
128.255
135(2)
4074
4075
2,6-Dimethylheptane
3,3-Dimethylheptane
C9H20
C9H20
1072-05-5
4032-86-4
128.255 liq
128.255
4076
3,4-Dimethylheptane
C9H20
922-28-1
128.255
140(3)
4077
3,5-Dimethylheptane
C9H20
926-82-9
128.255
135(3)
4078
4,4-Dimethylheptane
C9H20
1068-19-5
128.255
134(3)
4079
Dimethyl heptanedioate
Dimethyl pimelate
C9H16O4
1732-08-7
188.221
4080
4081
2,6-Dimethyl-2-heptanol
2,6-Dimethyl-4-heptanol
Diisobutylcarbinol
C9H20O
C9H20O
13254-34-7 144.254
108-82-7
144.254
4082
4083
3,5-Dimethyl-4-heptanol
2,6-Dimethyl-4-heptanone
Diisobutyl ketone
C9H20O
C9H18O
19549-79-2 144.254
108-83-8
142.238 liq
4084
4085
Isometheptene
C9H16O
C9H19N
106-72-9
503-01-5
140.222 oil
141.254
4086
4087
2,6-Dimethyl-5-heptenal
N,6-Dimethyl-5-hepten-2amine
2,5-Dimethyl-1,5-hexadiene
2,5-Dimethyl-2,4-hexadiene
C8H14
C8H14
627-58-7
764-13-6
110.197 liq
110.197
-75.6(0.2)
13.8(0.3)
4088
2,2-Dimethylhexane
C8H18
590-73-8
114.229 liq
-121.19(0.07) 106.8(0.4)
4089
2,3-Dimethylhexane
C8H18
584-94-1
114.229
4090
4091
2,4-Dimethylhexane
2,5-Dimethylhexane
C8H18
C8H18
589-43-5
592-13-2
114.229
114.229 liq
109.4(0.4)
-91.14(0.02) 109.1(0.7)
4092
3,3-Dimethylhexane
C8H18
563-16-6
114.229 liq
-126.2(0.1)
4093
3,4-Dimethylhexane
C8H18
583-48-2
114.229
4094
2,5-Dimethyl-2,5-hexanediamine
C8H20N2
23578-35-0 144.258
HCP_Section_03.indb 210
Methyl glutarate
Biisobutyl
-116
-103.1(0.5)
-21
140.6(0.9)
135(2)
137(3)
12010
170(11)
193(6)
-46.0(0.2)
179(5)
157(3)
120100
177
114(2)
135.2(0.2)
115.6(0.5)
111.9(0.6)
117.7(0.4)
184
den
g cm –3
nD
Solubility
0.944525 1.430520 msc H2O, EtOH,
eth, ace, bz; sl
lig
1.3720
1.4062111 i H2O; s ace, chl
0.888320 1.436320 i H2O; s EtOH,
eth, ace, bz,
HOAc, chl
1.107100
sl H2O; vs EtOH,
eth, bz, chl
1.087620 1.424220 vs EtOH, eth; s
chl
vs H2O, MeOH;
s EtOH, eth,
ace
i H2O; vs EtOH,
eth; sl bz, tol
0.764825
0.710520 1.401620 i H2O; s eth, ctc;
vs ace, chl;
msc bz
0.726020 1.408820 i H2O; msc
EtOH, eth, ace,
bz, peth, chl
0.711525 1.403420 i H2O; msc
EtOH, eth, ace,
bz, chl, peth
0.719820 1.403320 vs ace, bz, eth,
EtOH
0.708920 1.401120 sl chl
0.725420 1.408720 i H2O; msc
EtOH; s eth; vs
ace, bz
0.731420 1.410820 i H2O; s eth, ctc;
vs ace, chl;
msc bz
0.722520 1.408320 i H2O; s eth, ctc;
vs ace, chl;
msc bz
0.722120 1.407620 i H2O; s eth, ctc;
vs ace, chl;
msc bz
1.062520 1.430920 sl H2O; s EtOH,
eth, bz
0.818620 1.424220
0.811420 1.424220 i H2O; s EtOH,
eth; sl ctc
0.83618 1.428320 sl H2O
0.806220 1.41221 i H2O; msc
EtOH, eth; s
ctc
vs eth, EtOH
0.74320 1.4399521 i H2O; s ace, chl
0.757725 1.478520 i H2O; s EtOH,
eth, bz, chl
0.695320 1.393520 vs ace, bz, eth,
EtOH
0.691225 1.401120 vs ace, bz,
EtOH, lig
0.696225 1.392925
0.690125 1.392520 i H2O; msc
EtOH, ace, bz;
s eth
0.710020 1.400120 i H2O; msc
EtOH; vs eth,
ace, bz
0.715125 1.404120 i H2O; s eth;
msc EtOH,
ace, bz
0.848515 1.445920
4/11/16 11:25 AM
Physical Constants of Organic Compounds
3-211
O
N
O
O
O
O
4061
4062
N,N-Dimethylformamide
O
O
S
Ge
O
O
4064
4063
Dimethyl fumarate
4065
3,4-Dimethyl-2,5-furandione
2,5-Dimethylfuran
HO
O
O
O
Dimethyl germanium sulfide
N
O
O
4066
N
OH
4067
N,N-Dimethylglycine
OH
4068
4069
Dimethylglyoxime
4070
2,6-Dimethyl-1,5-heptadiene
2,2-Dimethylheptane
Organic
Dimethyl glutarate
N
4071
4072
2,3-Dimethylheptane
4073
2,4-Dimethylheptane
4075
4074
2,5-Dimethylheptane
3,3-Dimethylheptane
2,6-Dimethylheptane
O
O
O
O
4076
4077
3,4-Dimethylheptane
4079
4078
3,5-Dimethylheptane
Dimethyl heptanedioate
4,4-Dimethylheptane
OH
OH
OH
O
O
4080
2,6-Dimethyl-2-heptanol
4081
2,6-Dimethyl-4-heptanol
4082
3,5-Dimethyl-4-heptanol
4083
2,6-Dimethyl-4-heptanone
4084
2,6-Dimethyl-5-heptenal
NH
4085
N,6-Dimethyl-5-hepten-2-amine
4086
2,5-Dimethyl-1,5-hexadiene
4087
4088
2,5-Dimethyl-2,4-hexadiene
4089
2,2-Dimethylhexane
2,3-Dimethylhexane
H2N
NH2
4090
2,4-Dimethylhexane
4091
2,5-Dimethylhexane
4092
3,3-Dimethylhexane
4093
3,4-Dimethylhexane
4094
2,5-Dimethyl-2,5-hexanediamine
Physical Constants of Organic Compounds
3-212
bp/˚C
den
g cm –3
233(13)
0.89820
C8H18O
C8H16
C8H16
C8H16
C8H16
C8H16
C8H16
C8H16O
C15H22
146.228 pr (AcOEt) fl 91(2)
(peth)
2370-13-0 130.228
16746-86-4 112.213
7116-86-1 112.213
7145-20-2 112.213 liq
-115.0(0.1)
3404-78-2 112.213
690-92-6
112.213 liq
-137.36(0.09)
690-93-7
112.213
3329-48-4 128.212
644-30-4
202.336
9529
111(2)
102(3)
122(2)
113(2)
105.4(0.8)
100.9(0.2)
146.5
14019
0.717225
0.70525
0.736625
0.718220
0.708625
0.699525
0.838220
0.880520
C8H14O2
142-30-3
142.196
206(9)
0.94720
C2H8N2
57-14-7
60.098
1,2-Dimethylhydrazine
C2H8N2
540-73-8
60.098
C2H10Cl2N2
306-37-6
133.019 pr (w)
4109
1,2-Dimethylhydrazine
dihydrochloride
Dimethyl hydrogen phosphate Dimethyl phosphate
C2H7O4P
813-78-5
126.048
174 dec
1.322520 1.40825
4110
Dimethyl hydrogen phosphite
C2H7O3P
868-85-9
110.049
170.2(0.5)
1.200220 1.403620
4111
1,2-Dimethyl-1H-imidazole
C5H8N2
1739-84-0
96.131
206
1.005111
4112
4113
2,4-Dimethyl-1H-imidazole
5,5-Dimethyl-2,4-imidazolidinedione
C5H8N2
C5H8N2O2
930-62-1
77-71-4
96.131
128.130 pr (dil al)
92
176.1(0.5)
4114
4115
4116
4117
N,N-Dimethyltryptamine
C11H14
C10H11N
C10H11N
C12H16N2
4912-92-9
875-30-9
91-55-4
61-50-7
146.229
145.201 nd
145.201
188.268
142
107.5
46
Gramine
C11H14N2
87-52-5
Guaiazulene
C10H10O4
C15H18
1459-93-4
489-84-9
174.242 nd or pl
138.5
(ace)
194.184 nd(dil al)
68(1)
198.304 bl-viol pl (al) 31.5
285.1(0.4)
16712
1.19420
0.97320
Cadalene
C15H18
483-78-3
198.304
294
0.966725 1.578525
C10H22
13475-79-1 142.282 liq
-81.7(0.2)
157(4)
0.754525 1.424620
4123
4124
4125
1,1-Dimethylindan
1,3-Dimethyl-1H-indole
2,3-Dimethyl-1H-indole
N,N-Dimethyl-1H-indole-3ethanamine
N,N-Dimethyl-1H-indole-3methanamine
Dimethyl isophthalate
1,4-Dimethyl-7-isopropylazulene
1,6-Dimethyl-4-isopropylnaphthalene
2,4-Dimethyl-3-isopropylpentane
3,5-Dimethylisoxazole
Dimethylmagnesium
Dimethyl maleate
C5H7NO
C2H6Mg
C6H8O4
300-87-8
2999-74-8
624-48-6
97.116
54.374 solid
144.126 liq
142(7)
0.9925
Magnesium dimethyl
Methyl cis-butenedioate
220 dec
-19(1)
202(2)
4126
Dimethyl malonate
Methyl malonate
C5H8O4
108-59-8
132.116 liq
-62(1)
181.1(0.6)
4127
4128
Dimethylmalonic acid
Dimethyl mercury
Dimethylpropanedioc acid
Mercury dimethyl
C5H8O4
C2H6Hg
595-46-0
593-74-8
132.116 pr (bz/peth) 191(2)
230.66 liq
93
4129
Dimethyl citraconate
C7H10O4
617-54-9
158.152
210.5
4130
Dimethyl cis-2-methyl-2butenedioate
Dimethyl methylenesuccinate
C7H10O4
617-52-7
4131
Dimethyl methylmalonate
C6H10O4
609-02-9
158.152 hyg mcl
(MeOH)
146.141
4132
4133
Dimethyl methylphosphonate
trans-2,2-Dimethyl-3-(2methyl-1-propenyl)
cyclopropanecarboxylic acid
Dimethyl 2-methylsuccinate
Dimethyl p-(methylthio)phenyl
phosphate
C3H9O3P
C10H16O2
756-79-6
4638-92-0
124.075
168.233 pr
1.160620 1.441620 sl H2O, lig; s
eth, ctc
1.52820 1.413520 sl H2O; msc
EtOH; vs ace,
bz; s chl
s hot H2O
3.1725
1.545220 i H2O; vs EtOH,
eth
1.115320 1.447320 vs ace, eth,
EtOH
1.124118 1.445720 s EtOH, eth,
MeOH; vs ace
1.097720 1.412820 vs ace, eth,
EtOH, chl
1.168420 1.409930 s H2O, EtOH, eth
vs eth, EtOH,
chl
C7H12O4
C9H13O4PS
1604-11-1
3254-63-5
160.168
248.235 liq
C6H13NO
141-91-3
115.173 liq
No.
Name
Synonym
Mol. Form.
CAS RN
4095
2,5-Dimethyl-2,5-hexanediol
1,1,4,4-Tetramethyl-1,4butanediol
C8H18O2
110-03-2
4096
4097
4098
4099
4100
4101
4102
4103
4104
2,2-Dimethyl-1-hexanol
2,3-Dimethyl-1-hexene
5,5-Dimethyl-1-hexene
2,3-Dimethyl-2-hexene
2,5-Dimethyl-2-hexene
cis-2,2-Dimethyl-3-hexene
trans-2,2-Dimethyl-3-hexene
3,5-Dimethyl-1-hexen-3-ol
1-(1,5-Dimethyl-4-hexenyl)-4- α-Curcumene
methylbenzene
2,5-Dimethyl-3-hexyne-2,5diol
4106
1,1-Dimethylhydrazine
4107
4108
4105
Organic
4118
4119
4120
4121
4122
4134
4135
4136
2,6-Dimethylmorpholine
HCP_Section_03.indb 212
UDMH
Mol.
Wt.
Physical
Form
mp/˚C
95(2)
liq, fumes in -57.15(0.08) 62.4(0.8)
air
fumes (air) -8.86(0.09) 82(3)
0.79122
nD
s H2O; vs EtOH,
bz, chl
1.411320
1.404920
1.426820
1.414020
1.409920
1.406320
1.434220
1.498920 i H2O; s bz
1.407522
0.827420 1.420920
170 dec
38
267
sub
194.0(0.8)
258.5
284(20)
208
177(15)
20.0
168.7(0.7)
245
196
-88
147(18)
Solubility
s H2O, chl; vs
EtOH, eth, ace,
bz
vs H2O, EtOH,
eth, MeOH
msc H2O, EtOH,
eth
vs H2O, EtOH
vs H2O, ace,
EtOH
s EtOH, py; sl
ctc
vs H2O, eth,
EtOH
vs H2O, EtOH,
eth, ace, bz,
chl; s DMSO
0.91920
1.513525
s eth
1.07625
1.27321
1.516820
i H2O; s EtOH,
eth, chl; i peth
sl H2O
s EtOH, eth,
AcOEt
vs oils
1.442120
1.420020
0.932920 1.446020
sl H2O; s ace,
EtOH, diox,
ctc, xyl
msc H2O, EtOH,
bz, lig; s ace;
sl chl
4/11/16 11:25 AM
Physical Constants of Organic Compounds
3-213
HO
OH
OH
4095
4096
2,5-Dimethyl-2,5-hexanediol
4097
2,2-Dimethyl-1-hexanol
4098
2,3-Dimethyl-1-hexene
4099
5,5-Dimethyl-1-hexene
4100
2,3-Dimethyl-2-hexene
2,5-Dimethyl-2-hexene
4101
cis-2,2-Dimethyl-3-hexene
HO
NH2
N
OH
N
H
4108
4110
4111
NH
O
N
H
N
H
4112
1,2-Dimethyl-1H-imidazole
4107
1,2-Dimethylhydrazine
O
N
N
Dimethyl hydrogen phosphite
Dimethyl hydrogen phosphate
1,1-Dimethylhydrazine
N
O P O
H
4109
1,2-Dimethylhydrazine dihydrochloride
4106
2,5-Dimethyl-3-hexyne-2,5-diol
O
O
O P O
OH
2 HCl
4105
1-(1,5-Dimethyl-4-hexenyl)-4-methylbenzene
3,5-Dimethyl-1-hexen-3-ol
trans-2,2-Dimethyl-3-hexene
H
N
4104
4103
4102
H
N
N
H
Organic
OH
4113
2,4-Dimethyl-1H-imidazole
5,5-Dimethyl-2,4-imidazolidinedione
O
O
N
N
H
N
4114
1,1-Dimethylindan
4115
4117
2,3-Dimethyl-1H-indole
4120
4121
O
1,6-Dimethyl-4-isopropylnaphthalene
O
O
O
O
4126
Dimethyl malonate
4122
2,4-Dimethyl-3-isopropylpentane
N,N-Dimethyl-1H-indole-3-methanamine
HO
OH
4127
O
4123
Dimethylmalonic acid
O
Hg
4128
Dimethyl mercury
O
O
Dimethylmagnesium
O
O
O
O O
4129
Dimethyl cis-2-methyl-2-butenedioate
4130
Dimethyl methylenesuccinate
O
O
O
4133
trans-2,2-Dimethyl-3-(2-methyl-1-propenyl)cyclopropanecarboxylic acid
O
4134
Dimethyl 2-methylsuccinate
O
4131
Dimethyl methylmalonate
O
O P O
O
O
OH
O
O
S
O
O O
4124
3,5-Dimethylisoxazole
4119
Dimethyl isophthalate
O
Mg
O
O
O
4118
N,N-Dimethyl-1H-indole-3-ethanamine
N
1,4-Dimethyl-7-isopropylazulene
O
N
H
N
H
4116
1,3-Dimethyl-1H-indole
N
4125
Dimethyl maleate
O
O P O
4132
Dimethyl methylphosphonate
H
N
O
4135
Dimethyl p-(methylthio)phenyl phosphate
4136
2,6-Dimethylmorpholine
Physical Constants of Organic Compounds
3-214
No.
Name
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
4137
Dimethyl morpholinophosphoramidate
1,2-Dimethylnaphthalene
1,3-Dimethylnaphthalene
1,4-Dimethylnaphthalene
Dimethyl 4-morpholinylphosphonate
C6H14NO4P
597-25-1
195.153 liq
C12H12
C12H12
C12H12
573-98-8
575-41-7
571-58-4
156.223
156.223 liq
156.223
-3.0(0.7)
-6
7.6(0.4)
267(5)
265(5)
264(5)
C12H12
C12H12
C12H12
C12H12
C12H12
C12H12
C12H12
C12H13N
571-61-9
575-43-9
575-37-1
569-41-5
581-40-8
581-42-0
582-16-1
86-56-6
156.223
156.223
156.223
156.223
156.223
156.223
156.223
171.238
81.5(0.9)
-16.2(0.5)
-13.9
63.16(0.05)
104.3(0.3)
110.1(0.2)
96(1)
267(4)
263(4)
263(6)
276(3)
267(2)
253(3)
262.4(0.3)
250
C12H13N
2436-85-3
171.238 dk red nd
41.5(0.5)
304(15)
C8H10N2O2
610-17-3
166.177 ye-oran
-20
14620
60(2)
282.5
4138
4139
4140
4141
4142
4143
4144
4145
4146
4147
4148
Physical
Form
mp/˚C
bp/˚C
den
g cm –3
nD
Solubility
961
Organic
1.017920 1.616620 i H2O; s eth, bz
1.014420 1.614020 i H2O; s eth, bz
1.016620 1.612720 i H2O; vs EtOH;
msc eth, ace,
bz, ctc
i H2O; vs bz, eth
1.002120 1.616620 i H2O; s eth, bz
1.011520 1.608320 i H2O; s eth, bz
1.00320
i H2O; s eth, bz
1.00320 1.506020 i H2O; vs bz, eth
1.00320
i H2O
1.00320
1.042320 1.62415 i H2O; s EtOH,
eth, ctc
1.027960 1.644353 i H2O; s EtOH,
eth
1.179420 1.610220 s H2O, eth; vs
EtOH, chl
1.31317
i H2O; s EtOH,
eth
i H2O; s EtOH,
eth, HOAc
1.140220 1.544120 i H2O; s EtOH,
ctc
1.11215 1.520220 i H2O; msc EtOH
1.11215 1.520220 i H2O; vs EtOH;
s ctc
i H2O; vs EtOH,
eth
1.13215 1.541320 i H2O; s EtOH
1.13515 1.547325 i H2O; s eth,
ace, bz, chl
vs eth, EtOH
4150
1,5-Dimethylnaphthalene
1,6-Dimethylnaphthalene
1,7-Dimethylnaphthalene
1,8-Dimethylnaphthalene
2,3-Dimethylnaphthalene
2,6-Dimethylnaphthalene
2,7-Dimethylnaphthalene
N,N-Dimethyl-1-naphthylamine
N,N-Dimethyl-2-naphthylamine
N,N-Dimethyl-2-nitroaniline
4151
N,N-Dimethyl-3-nitroaniline
C8H10N2O2
619-31-8
4152
N,N-Dimethyl-4-nitroaniline
C8H10N2O2
100-23-2
166.177 red mcl pr
(eth)
166.177 ye nd (al)
4153
1,2-Dimethyl-3-nitrobenzene
C8H9NO2
83-41-0
151.163 nd (al)
14(1)
240
4154
4155
1,2-Dimethyl-4-nitrobenzene
1,3-Dimethyl-2-nitrobenzene
C8H9NO2
C8H9NO2
99-51-4
81-20-9
151.163 ye pr (al)
151.163
28(1)
15.2(0.7)
251
226
4156
1,3-Dimethyl-5-nitrobenzene
C8H9NO2
99-12-7
151.163 nd (al)
75
274
4157
4158
1,4-Dimethyl-2-nitrobenzene
2,4-Dimethyl-1-nitrobenzene
C8H9NO2
C8H9NO2
89-58-7
89-87-2
151.163 pa ye liq
151.163
-25
9.6(0.2)
240.5
243(2)
4159
1,2-Dimethyl-5-nitro-1Himidazole
N,N-Dimethyl-4-[2-(4-nitrophenyl)ethenyl]aniline
N,4-Dimethyl-N-nitrosobenzenesulfonamide
Dimethyl nonanedioate
C5H7N3O2
551-92-8
141.129 nd (w)
138.5
C16H16N2O2
4584-57-0
268.310
258.3
p-Tolylsulfonylmethylnitrosamide
Methyl azelate
C8H10N2O3S
80-11-5
214.241 cry
60
C11H20O4
1732-10-1
216.275
-0.8
Myrtenal
C10H14O
564-94-3
150.217 unstab oil
9915
C10H16O
106-26-3
152.233
12020
Citral
C10H16O
141-27-5
152.233
229
Citronellene
Geranic acid
C10H18
C10H16O2
2436-90-0
459-80-3
138.250
168.233 oil
0.886920 1.486920 i H2O; msc
EtOH, eth
0.888820 1.489820 i H2O; msc
EtOH, eth
0.760120 1.436220
Nerol
C10H18O
106-25-2
154.249
225
0.875620 1.474620 vs EtOH
C12H20O2
141-12-8
196.286
13425
0.90515
C11H18O2
105-86-2
182.260
229 dec
C10H22
C10H22
C10H22
C10H22
C10H22
C10H22
C10H22
C10H22
C10H18O4
15869-87-1
7146-60-3
4032-94-4
15869-89-3
2051-30-1
1072-16-8
15869-92-8
15869-94-0
1732-09-8
142.282
142.282
142.282
142.282
142.282
142.282 liq
142.282
142.282
202.248 liq
154(5)
164(3)
154(3)
157(4)
158(2)
160(1)
162(7)
160.8
259(8)
C10H22O2
C10H20O2
C10H22O
C10H22O
107-74-4
29662-90-6
2370-14-1
106-21-8
174.281
172.265
158.281 liq
158.281
0.908625 1.465920 i H2O; vs EtOH;
s eth, ace
0.720825 1.408220
0.737720 1.414620
0.722625 1.409120
0.726425 1.411220
0.731320 1.409720
0.720225 1.408620 s eth, HOAc
0.741025 1.418220
0.732425 1.413920
1.021720 1.434120 i H2O; s EtOH,
eth, ace; sl ctc
0.93720 1.459920 sl bz, tol
4149
4160
4161
4162
4163
4171
4172
4173
4174
4175
4176
4177
4178
4179
6,6-Dimethyl-2-norpinene-2carboxaldehyde
cis-3,7-Dimethyl-2,6-octadienal
trans-3,7-Dimethyl-2,6octadienal
3,7-Dimethyl-1,6-octadiene
3,7-Dimethyl-2,6-octadienoic
acid
cis-3,7-Dimethyl-2,6-octadien-1-ol
cis-3,7-Dimethyl-2,6-octadien-1-ol acetate
trans-3,7-Dimethyl-2,6octadien-1-ol formate
2,2-Dimethyloctane
2,3-Dimethyloctane
2,4-Dimethyloctane
2,5-Dimethyloctane
2,6-Dimethyloctane
2,7-Dimethyloctane
3,4-Dimethyloctane
3,6-Dimethyloctane
Dimethyl octanedioate
4180
4181
4182
4183
3,7-Dimethyl-1,7-octanediol
2,2-Dimethyloctanoic acid
2,2-Dimethyl-1-octanol
3,7-Dimethyl-1-octanol
4164
4165
4166
4167
4168
4169
4170
HCP_Section_03.indb 214
Guajen
4-Nitro-o-xylene
Dimetridazole
Dimethyl suberate
liq
liq
lf (al)
viol flr cry
164(1)
<-15
-54(1)
6(1)
15620
265
14013
211(6)
224(11)
1.008220 1.436720
0.8420
0.83225
i H2O; vs EtOH,
eth
i H2O; s EtOH,
ace, bz, ctc
1.45220
1.43825
s eth
4/11/16 11:25 AM
Physical Constants of Organic Compounds
3-215
O
O P O
N
O
4138
Dimethyl morpholinophosphoramidate
4139
1,2-Dimethylnaphthalene
4140
1,3-Dimethylnaphthalene
4141
1,4-Dimethylnaphthalene
4142
1,5-Dimethylnaphthalene
1,6-Dimethylnaphthalene
4143
1,7-Dimethylnaphthalene
N
N
O
N
N
4144
4145
1,8-Dimethylnaphthalene
4146
2,3-Dimethylnaphthalene
4147
2,6-Dimethylnaphthalene
4149
N,N-Dimethyl-1-naphthylamine
N,N-Dimethyl-2-naphthylamine
4150
N,N-Dimethyl-2-nitroaniline
N
N
N
O
O
O
4151
N
N
O
O
4152
N,N-Dimethyl-3-nitroaniline
O
N
O
O
4153
N,N-Dimethyl-4-nitroaniline
1,2-Dimethyl-3-nitrobenzene
N
O
N
O
4158
1,3-Dimethyl-5-nitrobenzene
4157
1,4-Dimethyl-2-nitrobenzene
O
N
N
O
N
O
O
O
O
O
4160
1,2-Dimethyl-5-nitro-1H-imidazole
O
N
O
4156
1,3-Dimethyl-2-nitrobenzene
O O
S
N
4159
2,4-Dimethyl-1-nitrobenzene
O
O
4155
1,2-Dimethyl-4-nitrobenzene
N
N
O
O
N
O
4154
O
N
O
4148
2,7-Dimethylnaphthalene
O
Organic
4137
4161
N,N-Dimethyl-4-[2-(4-nitrophenyl)ethenyl]aniline
4162
N,4-Dimethyl-N-nitrosobenzenesulfonamide
Dimethyl nonanedioate
O
O
O
OH
O
4164
4163
4165
cis-3,7-Dimethyl-2,6-octadienal
6,6-Dimethyl-2-norpinene-2-carboxaldehyde
4166
trans-3,7-Dimethyl-2,6-octadienal
3,7-Dimethyl-1,6-octadiene
4167
3,7-Dimethyl-2,6-octadienoic acid
O
OH
O
O
4168
cis-3,7-Dimethyl-2,6-octadien-1-ol
trans-3,7-Dimethyl-2,6-octadien-1-ol formate
cis-3,7-Dimethyl-2,6-octadien-1-ol acetate
4173
4174
2,4-Dimethyloctane
4175
2,5-Dimethyloctane
4176
2,6-Dimethyloctane
2,7-Dimethyloctane
O
O
O
HO
4179
4180
3,7-Dimethyl-1,7-octanediol
4171
2,2-Dimethyloctane
4177
3,4-Dimethyloctane
4172
2,3-Dimethyloctane
4178
3,6-Dimethyloctane
O
OH
4181
2,2-Dimethyloctanoic acid
OH
OH
OH
O
Dimethyl octanedioate
O
4170
4169
4182
2,2-Dimethyl-1-octanol
4183
3,7-Dimethyl-1-octanol
Physical Constants of Organic Compounds
3-216
No.
Name
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
4184
4185
4186
4187
2,6-Dimethyl-2-octanol
3,6-Dimethyl-3-octanol
3,7-Dimethyl-3-octanol
cis-3,7-Dimethyl-1,3,6octatriene
trans-3,7-Dimethyl-1,3,6octatriene
3,7-Dimethyl-1,3,7-octatriene
Tetrahydromyrcenol
cis-β-Ocimene
C10H22O
C10H22O
C10H22O
C10H16
18479-57-7
151-19-9
78-69-3
3338-55-4
158.281
158.281 liq
158.281
136.234
trans-β-Ocimene
C10H16
3779-61-1
136.234
α-Ocimene
C10H16
502-99-8
136.234
cis, cis-2,6-Dimethyl-2,4,6octatriene
trans,trans-2,6-Dimethyl2,4,6-octatriene
3,7-Dimethyl-6-octenal
cis-allo-Ocimene
C10H16
17202-20-9 136.234 liq
trans-allo-Ocimene
C10H16
3016-19-1
136.234 liq
Citronellal
C10H18O
106-23-0
Citronellic acid
Citronellol, (+)
C10H20
C10H18O2
C10H20O
Citronellol, (-)
4188
4189
4190
4191
4192
Organic
4193
4194
4195
4196
4197
4198
4199
4200
3,7-Dimethyl-1-octene
3,7-Dimethyl-6-octenoic acid
3,7-Dimethyl-6-octen-1-ol,
(R)3,7-Dimethyl-6-octen-1-ol,
(S)3,7-Dimethyl-7-octen-1-ol,
(S)3,7-Dimethyl-6-octen-3-ol
3,7-Dimethyl-6-octen-1-ol,
acetate
Dimethyloldihydroxyethyleneurea
Physical
Form
mp/˚C
bp/˚C
-67.5
80.510
198(13)
205.1
den
g cm –3
177 dec
0.800020 1.486220 i H2O; s EtOH,
eth, chl, HOAc
188
0.811820 1.544620
205(2)
0.85320
4984-01-4
502-47-6
1117-61-9
154.249 nd or orth
cry
140.266 col liq
170.249
156.265 oil
155(7)
257
224
C10H20O
7540-51-4
156.265 oil
224
0.739620 1.421220
0.923421
0.855020 1.456520 sl H2O; msc
EtOH, eth
0.85918 1.457618 vs eth, EtOH
Rhodinol
C10H20O
6812-78-8
156.265
11412
0.854920 1.455620 vs eth, EtOH
C10H20O
C12H22O2
18479-51-1 156.265
150-84-5
198.302
9414
11510
0.869515 1.456915
Citronellol acetate
163.4(0.5)
1.171660 1.37982
78(6)
5815
51(2)
60(4)
56(10)
189
0.83425
15025
1.18525
94(2)
141100
0.734323 1.439023
0.896225 1.441925 vs H2O, eth,
EtOH
0.673920 1.382220 i H2O; s EtOH,
eth; msc ace,
bz, hp, chl
0.690825 1.389425 i H2O; s EtOH,
eth; msc ace,
bz, chl
0.672720 1.381520 i H2O; s EtOH,
eth; msc ace,
bz, chl, hp
0.693620 1.390920 i H2O; s EtOH,
eth; msc ace,
bz, hp, chl
4,5-Dihydroxy-1,3C5H10N2O5
bis(hydroxymethyl)-2-imidazolidinone
C4H6O4
-35.4
1854-26-8
178.143 hyg cry
553-90-2
118.089 mcl tab
51(2)
C5H7NO3
695-53-4
129.115
76.5
C5H10O
C5H8O2
C4H8O
C4H8O
C4H8O
C6H10O3
6921-35-3
1955-45-9
558-30-5
1758-33-4
6189-41-9
815-17-8
86.132
100.117
72.106
72.106 liq
72.106 liq
130.141
C9H15NO2
2873-97-4
169.221
Dimethyl 1,3-acetonedicarbox- C7H10O5
ylate
C7H12
C7H15NO
1830-54-2
174.151
1000-86-8
6225-06-5
96.170 liq
129.200
-116.0(0.3)
-51
-123.71(0.04) 79.2(0.3)
Dimethyl oxalate
4202
4211
4212
5,5-Dimethyl-2,4-oxazolidinedione
3,3-Dimethyloxetane
3,3-Dimethyl-2-oxetanone
2,2-Dimethyloxirane
cis-2,3-Dimethyloxirane
trans-2,3-Dimethyloxirane
3,3-Dimethyl-2-oxobutanoic
acid
N-(1,1-Dimethyl-3-oxobutyl)2-propenamide
Dimethyl 3-oxo-1,5-pentanedioate
2,4-Dimethyl-1,3-pentadiene
N,N-Dimethylpentanamide
4213
2,2-Dimethylpentane
C7H16
590-35-2
100.202 liq
4214
2,3-Dimethylpentane
C7H16
565-59-3
100.202
4215
2,4-Dimethylpentane
C7H16
108-08-7
100.202 liq
-119.16(0.02) 80.4(0.5)
4216
3,3-Dimethylpentane
C7H16
562-49-2
100.202 liq
-134.4(0.4)
86.0(0.6)
4217
C7H10O3
4160-82-1
142.152
125.8
18125
4218
3,3-Dimethylpentanedioic acid Dihydro-4,4-dimethyl-2Hanhydride
pyran-2,6(3H)-dione
3,3-Dimethylpentanedioic acid
C7H12O4
4839-46-7
103.5
126415
1.427820
4219
4220
4221
4222
2,2-Dimethylpentanoic acid
2,2-Dimethyl-1-pentanol
2,3-Dimethyl-2-pentanol
2,4-Dimethyl-2-pentanol
C7H14O2
C7H16O
C7H16O
C7H16O
1185-39-3
2370-12-9
4911-70-0
625-06-9
160.168 mcl pl, nd
(bz)
130.185 liq
116.201
116.201
116.201
989
0.918920
<-20
133(3)
4223
2,2-Dimethyl-3-pentanol
C7H16O
3970-62-5
116.201 liq
9.3(0.5)
136(2)
4224
2,3-Dimethyl-3-pentanol
C7H16O
595-41-5
116.201
<-30
140(4)
4209
4210
HCP_Section_03.indb 216
Solubility
0.79920
4201
4203
4204
4205
4206
4207
4208
nD
0.802325 1.422025
0.834722 1.437020
0.82625 1.43325
0.79920
Dimethadione
2-Methyl-1,2-epoxypropane
Diacetone acrylamide
-83.4(0.5)
-85
90.5
89.8(0.6)
1.447320 sl H2O; s EtOH
sl H2O; s EtOH,
eth, ace, chl
1.396520
0.811220 1.371222 s EtOH, eth
0.822625 1.380220 vs eth, ace, bz
0.801025 1.373620 vs eth, ace, bz
sl H2O; s eth,
bz, chl, CS2
s chl
1.443420
vs H2O, EtOH,
eth; sl bz; i lig
s chl
0.80420
sl H2O
0.810320 1.417220 sl H2O; s EtOH,
eth, ctc
0.825320 1.422320 i H2O; s EtOH,
eth
0.83320 1.428720 sl H2O, bz; s
EtOH, eth
4/11/16 11:25 AM
Physical Constants of Organic Compounds
3-217
HO
HO
OH
4184
4185
2,6-Dimethyl-2-octanol
4186
3,6-Dimethyl-3-octanol
4187
3,7-Dimethyl-3-octanol
4188
cis-3,7-Dimethyl-1,3,6-octatriene
trans-3,7-Dimethyl-1,3,6-octatriene
4189
3,7-Dimethyl-1,3,7-octatriene
OH
O
O
4190
4191
4192
trans,trans-2,6-Dimethyl-2,4,6-octatriene
4193
3,7-Dimethyl-6-octenal
4194
3,7-Dimethyl-1-octene
3,7-Dimethyl-6-octenoic acid
Organic
cis, cis-2,6-Dimethyl-2,4,6-octatriene
OH
OH
O
OH
O
HO
4196
4195
3,7-Dimethyl-6-octen-1-ol, (S)-
3,7-Dimethyl-6-octen-1-ol, (R)-
HO
4198
4197
4199
3,7-Dimethyl-6-octen-3-ol
3,7-Dimethyl-7-octen-1-ol, (S)-
3,7-Dimethyl-6-octen-1-ol, acetate
OH
HO
O
O
N
O
OH
O
O
4200
O
4201
Dimethyloldihydroxyethyleneurea
H
O
N
O
O
4202
Dimethyl oxalate
O
4207
trans-2,3-Dimethyloxirane
4208
4209
2,2-Dimethyloxirane
O
N
O
O
4210
N-(1,1-Dimethyl-3-oxobutyl)-2-propenamide
4211
Dimethyl 3-oxo-1,5-pentanedioate
2,4-Dimethyl-1,3-pentadiene
HO
O
4213
2,2-Dimethylpentane
4214
2,3-Dimethylpentane
4215
2,4-Dimethylpentane
4216
O
4217
3,3-Dimethylpentane
4206
cis-2,3-Dimethyloxirane
O
O
O
4205
3,3-Dimethyl-2-oxetanone
O
O
3,3-Dimethyl-2-oxobutanoic acid
4204
3,3-Dimethyloxetane
H
N
OH
O
O
O
4203
5,5-Dimethyl-2,4-oxazolidinedione
O
O
O
3,3-Dimethylpentanedioic acid anhydride
OH
O
O
4212
N,N-Dimethylpentanamide
O
4218
3,3-Dimethylpentanedioic acid
OH
O
4219
2,2-Dimethylpentanoic acid
HO
HO
OH
4220
2,2-Dimethyl-1-pentanol
OH
4221
2,3-Dimethyl-2-pentanol
4222
2,4-Dimethyl-2-pentanol
4223
2,2-Dimethyl-3-pentanol
OH
4224
2,3-Dimethyl-3-pentanol
Physical Constants of Organic Compounds
3-218
Mol. Form.
CAS RN
Mol.
Wt.
2,4-Dimethyl-3-pentanol
C7H16O
600-36-2
4226
4227
4,4-Dimethyl-2-pentanone
2,2-Dimethyl-3-pentanone
C7H14O
C7H14O
4228
2,4-Dimethyl-3-pentanone
4229
No.
Name
4225
Physical
Form
Organic
mp/˚C
bp/˚C
116.201
<-70
142(2)
590-50-1
564-04-5
114.185 liq
114.185 liq
-64
-45
124(2)
125(3)
C7H14O
565-80-0
114.185 liq
-68.4(0.6)
125.2(0.3)
2,3-Dimethyl-1-pentene
C7H14
3404-72-6
98.186
liq
-137(5)
84(1)
4230
2,4-Dimethyl-1-pentene
C7H14
2213-32-3
98.186
liq
-124.1(0.1)
81.6(0.9)
4231
3,3-Dimethyl-1-pentene
C7H14
3404-73-7
98.186
liq
-134.4(0.1)
77(2)
4232
4233
3,4-Dimethyl-1-pentene
4,4-Dimethyl-1-pentene
C7H14
C7H14
7385-78-6
762-62-9
98.186
98.186
liq
-136.6(0.1)
82(4)
72.5(0.2)
4234
2,3-Dimethyl-2-pentene
C7H14
10574-37-5 98.186
liq
-118.3(0.1)
96(2)
4235
2,4-Dimethyl-2-pentene
C7H14
625-65-0
98.186
liq
-127.6(0.2)
83.3(0.7)
4236
4237
4238
4239
cis-3,4-Dimethyl-2-pentene
trans-3,4-Dimethyl-2-pentene
cis-4,4-Dimethyl-2-pentene
trans-4,4-Dimethyl-2-pentene
C7H14
C7H14
C7H14
C7H14
4914-91-4
4914-92-5
762-63-0
690-08-4
98.186
98.186
98.186
98.186
liq
liq
liq
liq
-124.2(0.1)
-113.4(0.1)
-135.5(0.1)
-115.2(0.1)
92(4)
91(3)
80.4(0.9)
76.7(0.8)
4240
4241
4,4-Dimethyl-1-pentyne
4,4-Dimethyl-2-pentyne
C7H12
C7H12
13361-63-2 96.170
999-78-0
96.170
liq
liq
-75.7
-82(2)
75(3)
83(4)
4242
Dimethylperoxide
C2H6O2
690-02-8
-100
-3(12)
4243
2,9-Dimethyl-1,10-phenanthroline
3,4-Dimethylphenol phosphate
(3:1)
5-(2,5-Dimethylphenoxy)-2,2dimethylpentanoic acid
N-(2,4-Dimethylphenyl)­
acetamide
1-[(2,4-Dimethylphenyl)­azo]2-naphthol
1-[(2,5-Dimethylphenyl)­azo]2-naphthol
1-(2,4-Dimethylphenyl)­
ethanone
1-(2,5-Dimethylphenyl)­
ethanone
1-(3,4-Dimethylphenyl)­
ethanone
C14H12N2
484-11-7
C24H27O4P
3862-11-1
C15H22O3
4244
4245
4246
4247
4248
4249
4250
4251
4252
4258
4259
4260
4,4-Dimethyl-1-phenyl-1penten-3-one
2,2-Dimethyl-1-phenyl-1propanone
3,5-Dimethyl-1-phenyl-1Hpyrazole
4,4-Dimethyl-1-phenyl-3pyrazolidinone
N,N-Dimethyl-γ-phenyl-2pyridinepropanamine
1,3-Dimethyl-3-phenyl-2,5pyrrolidinedione
Dimethylphenylsilane
N,N-Dimethyl-N’-phenylurea
Dimethylphosphine
4261
Dimethylphosphinic acid
4253
4254
4255
4256
4257
HCP_Section_03.indb 218
Synonym
Diisopropyl ketone
Neocuproine
62.068
vol liq or
gas
208.258 cry, 1/2w
(w, lig)
410.442
nD
Solubility
0.828820 1.425020 sl H2O; s EtOH,
eth
0.80925 1.403620
0.812520 1.406520 sl H2O; s EtOH,
eth, ace, chl
0.810820 1.399920 sl H2O; msc
EtOH, eth; s
bz; sl ctc
0.705120 1.403320 i H2O; msc
EtOH, eth; vs
dil sulf
0.694320 1.398620 i H2O; msc
EtOH, eth; s
bz, ctc, chl
0.697420 1.398420 i H2O; msc
EtOH, eth; s
bz, chl
0.693425 1.399220
0.682720 1.381820 i H2O; msc
EtOH, eth; s
bz, ctc, chl
0.727720 1.420820 i H2O; s EtOH,
eth, bz, chl
0.695420 1.404020 i H2O; s EtOH,
eth, bz, ctc
0.709225 1.410420
0.712425 1.412820
0.695125 1.402620
0.688920 1.398220 i H2O; s EtOH,
eth, bz, chl
0.714220 1.398320 vs bz, eth, chl
0.717620 1.407120 i H2O; s eth, bz,
chl; sl ctc
0.86770 1.35030 sl EtOH, eth; s
tol, HOAc
163(1)
72
2617
25812-30-0 250.334 cry
62.0(0.5)
1590.02
C10H13NO
2050-43-3
163.216 nd (al)
129.3
17010
1-(2,4-Xylylazo)-2-naphthol
C18H16N2O
3118-97-6
276.332 red nd (al)
166
1-(2,5-Xylylazo)-2-naphthol
C18H16N2O
85-82-5
276.332 nd (al)
153
2,4-Dimethylacetophenone
C10H12O
89-74-7
148.201
2,5-Dimethylacetophenone
C10H12O
2142-73-6
148.201 liq
3,4-Dimethylacetophenone
C10H12O
3637-01-2
C13H16O
Gemfibrozil
den
g cm –3
i H2O; sl EtOH,
chl, hx; s bz
vs EtOH, chl
vs eth, EtOH
228
1.012115 1.534020 vs eth, EtOH
-18.1(0.7)
232.5
148.201 liq
-5(1)
245(11)
538-44-3
188.265
43
15425
0.996319 1.529120 i H2O; vs EtOH,
eth, bz, CS2
1.009014 1.541315 i H2O; vs EtOH,
eth, bz; s ctc,
HOAc
0.950846 1.552325
C11H14O
938-16-9
162.228
220
0.96326
C11H12N2
1131-16-4
172.226
272
1.056620 1.573819 vs eth, EtOH,
chl
4,4-Dimethylphenidone
C11H14N2O
2654-58-2
190.241
Pheniramine
C16H20N2
86-21-5
240.343
18113
1.008125 1.551925 vs bz, eth,
EtOH, chl
Methsuximide
C12H13NO2
77-41-8
203.237
Fenuron
C8H12Si
C9H12N2O
C2H7P
766-77-8
101-42-8
676-59-5
C2H7O2P
3283-12-3
136.267
164.203 cry (hx)
62.051 vol liq or
gas
94.050 cry (bz)
1.508619 s ace
176
52.5
1210.1
159(3)
0.889120 1.499520 i H2O
132.9(0.5)
25
92
377
i H2O; s EtOH,
eth
vs H2O, EtOH,
eth; s bz
4/11/16 11:26 AM
Physical Constants of Organic Compounds
O
OH
4225
4226
2,4-Dimethyl-3-pentanol
4,4-Dimethyl-2-pentanone
4234
4233
2,3-Dimethyl-2-pentene
O
O
4227
4228
2,2-Dimethyl-3-pentanone
4229
2,4-Dimethyl-3-pentanone
4235
2,4-Dimethyl-2-pentene
2,3-Dimethyl-1-pentene
4236
4230
4237
cis-3,4-Dimethyl-2-pentene
4232
4231
2,4-Dimethyl-1-pentene
3,4-Dimethyl-1-pentene
3,3-Dimethyl-1-pentene
4238
trans-3,4-Dimethyl-2-pentene
4239
cis-4,4-Dimethyl-2-pentene
trans-4,4-Dimethyl-2-pentene
Organic
4,4-Dimethyl-1-pentene
3-219
O
O P O
O
O
4240
4241
4,4-Dimethyl-1-pentyne
N
O
4242
4,4-Dimethyl-2-pentyne
Dimethylperoxide
O
OH
N
O
4243
2,9-Dimethyl-1,10-phenanthroline
4244
4245
3,4-Dimethylphenol phosphate (3:1)
5-(2,5-Dimethylphenoxy)-2,2-dimethylpentanoic acid
O
O
HN
N
N
N
N
4246
N-(2,4-Dimethylphenyl)acetamide
O
OH
OH
4247
1-[(2,4-Dimethylphenyl)azo]-2-naphthol
4248
4249
1-[(2,5-Dimethylphenyl)azo]-2-naphthol
4250
1-(2,4-Dimethylphenyl)ethanone
1-(2,5-Dimethylphenyl)ethanone
O
O
O
4251
1-(3,4-Dimethylphenyl)ethanone
4252
4253
4,4-Dimethyl-1-phenyl-1-penten-3-one
2,2-Dimethyl-1-phenyl-1-propanone
H
Si
N
N
4256
N,N-Dimethyl-γ-phenyl-2-pyridinepropanamine
O
N
O
N
4257
O
1,3-Dimethyl-3-phenyl-2,5-pyrrolidinedione
4258
N
4254
H
N
4,4-Dimethyl-1-phenyl-3-pyrazolidinone
N
4259
N,N-Dimethyl-N’-phenylurea
N H
4255
3,5-Dimethyl-1-phenyl-1H-pyrazole
O
Dimethylphenylsilane
N
H
P
4260
Dimethylphosphine
O
P OH
4261
Dimethylphosphinic acid
Physical Constants of Organic Compounds
3-220
Organic
Mol. Form.
CAS RN
Mol.
Wt.
bp/˚C
den
g cm –3
C2H6ClO2PS
2524-03-0
160.560 hyg liq
nD
6812
1.322
1.482020
C10H10O4
131-11-3
194.184 pa ye
1.03(0.02)
282.7(0.2)
114.188 liq
-1.0(0.3)
129.8(0.8)
114
164(19)
2512-81-4
114.188 orth bipym
nd or pr
(chl)
113.201
1.190520 1.513820 i H2O; msc
EtOH, eth; s
bz; sl ctc
0.860020 1.447420 vs H2O, EtOH,
eth
1.472020 vs H2O, EtOH,
chl; sl eth, bz
1,4-Dimethylpiperazine
C6H14N2
106-58-1
4265
cis-2,5-Dimethylpiperazine
C6H14N2
6284-84-0
4266
1,2-Dimethylpiperidine, (±)-
C7H15N
4267
2,6-Dimethylpiperidine
C7H15N
504-03-0
113.201
4268
4269
4270
4271
4272
4273
3,5-Lupetidine
Pivaldehyde
4274
3,5-Dimethylpiperidine
2,2-Dimethylpropanal
2,2-Dimethylpropanamide
N,N-Dimethylpropanamide
N,N-Dimethyl-1-propanamine
N,N-Dimethyl-1,3-propanediamine
2,2-Dimethyl-1,3-propanediol
C7H15N
C5H10O
C5H11NO
C5H11NO
C5H13N
C5H14N2
35794-11-7
630-19-3
754-10-9
758-96-3
926-63-6
109-55-7
113.201
86.132
101.147
101.147 liq
87.164
102.178
Neopentyl glycol
C5H12O2
126-30-7
4275
4276
4277
2,2-Dimethylpropanenitrile
2,2-Dimethyl-1-propanethiol
2,2-Dimethylpropanoic acid
tert-Butyl cyanide
Neopentyl mercaptan
Trimethylacetic acid
C5H9N
C5H12S
C5H10O2
4278
2,2-Dimethyl-1-propanol
Neopentyl alcohol
4279
4286
4287
4288
2,2-Dimethylpropanoyl
chloride
N,N-Dimethyl-2-propenamide
2,2-Dimethylpropylamine
(1,1-Dimethylpropyl)benzene
(2,2-Dimethylpropyl)benzene
4-(1,1-Dimethylpropyl)­
cyclohexanone
1,1-Dimethylpropyl
3-methylbutanoate
2-(1,1-Dimethylpropyl)phenol
4-(1,1-Dimethylpropyl)phenol
4,6-Dimethyl-2H-pyran-2-one
4289
No.
Name
Synonym
4262
4263
O,O-Dimethyl phosphorochlo- Dimethyl chlorothiophosphate
ridothioate
Dimethyl phthalate
Methyl phthalate
4264
Physical
Form
mp/˚C
Solubility
127.5
0.82415
128(5)
0.815825
144(5)
74(2)
0.85325
0.792317
-45
176(7)
65(3)
129(13)
0.926920
0.715220 1.386020 vs bz, eth, EtOH
0.827220
104.148 nd (bz)
129.3(0.9)
207(14)
630-18-2
1679-08-9
75-98-9
83.132
104.214 liq
102.132 nd
18.97(0.05)
36(1)
C5H12O
75-84-3
88.148
55(3)
Pivalic acid chloride
C5H9ClO
3282-30-2
120.577
105.2(0.2) 0.758625 1.377420
103.6(0.8)
164.20(0.02) 0.90550 1.393130 sl H2O; vs EtOH,
eth
112(1)
0.81220
sl H2O; vs EtOH,
eth; s ctc
104(4)
1.00320 1.413920 vs eth
N,N-Dimethylacrylamide
2,2-Dimethyl-1-propanamine
C5H9NO
C5H13N
C11H16
C11H16
C11H20O
2680-03-7
5813-64-9
2049-95-8
1007-26-7
16587-71-6
99.131 liq
87.164
148.245
148.245
168.276
8120
82(7)
191(3)
186(4)
12516
0.96225
0.745520
0.874820
0.858118
0.92025
tert-Pentyl isopentanoate
C10H20O2
542-37-0
172.265
188(13)
0.87290
p-tert-Pentylphenol
C11H16O
C11H16O
C7H8O2
3279-27-4
80-46-6
675-09-2
164.244
164.244
124.138 lf (eth)
92.7(1)
51.5
262(9)
245
2,6-Dimethyl-4H-pyran-4-one
C7H8O2
1004-36-0
124.138 pl, nd (sub)
132.1(0.2)
251
0.9953137
4290
4291
2,3-Dimethylpyrazine
2,5-Dimethylpyrazine
C6H8N2
C6H8N2
5910-89-4
123-32-0
108.141
108.141
15
161(16)
152(4)
1.02810
0.988720 1.498020
4292
2,6-Dimethylpyrazine
C6H8N2
108-50-9
108.141 pr
47.5
155.6
0.964750
4293
4294
1,3-Dimethyl-1H-pyrazole
3,5-Dimethyl-1H-pyrazole
C5H8N2
C5H8N2
694-48-4
67-51-6
96.131
96.131
107.5
137
218
0.956117 1.473415
0.883916
4295
4296
4297
4298
2,7-Dimethylpyrene
4,6-Dimethyl-2-pyridinamine
N,N-Dimethyl-2-pyridinamine
N,N-Dimethyl-4-pyridinamine
C18H14
C7H10N2
C7H10N2
C7H10N2
15679-24-0
5407-87-4
5683-33-0
1122-58-3
230.304
122.167
122.167
122.167 pl (eth)
4299
4300
2,3-Dimethylpyridine
2,4-Dimethylpyridine
2,3-Lutidine
2,4-Lutidine
C7H9N
C7H9N
583-61-9
108-47-4
107.153
107.153 liq
4301
2,5-Dimethylpyridine
2,5-Lutidine
C7H9N
589-93-5
107.153 liq
4302
2,6-Dimethylpyridine
2,6-Lutidine
C7H9N
108-48-5
107.153 liq
4303
3,4-Dimethylpyridine
3,4-Lutidine
C7H9N
583-58-4
107.153 liq
4280
4281
4282
4283
4284
4285
HCP_Section_03.indb 220
Dimethylpropylamine
cry (peth,
al)
1(2)
96
1.439520 vs H2O, eth,
EtOH
1.437720 msc H2O, EtOH,
eth; sl ctc; s
acid
1.445420
1.379120 s EtOH, eth
s tfa
s H2O, bz, chl;
vs EtOH, eth
1.473020
1.402320 vs eth
1.495820
1.488418
1.467720
vs EtOH
sl ctc
230
61
182
113.9(0.2)
vs H2O, eth,
EtOH
s H2O, EtOH,
eth, ace
s H2O, EtOH, eth
msc H2O, EtOH,
eth; s ace, chl
s H2O, EtOH,
eth; sl ctc
vs H2O
s H2O, ace; vs
EtOH, eth, bz,
MeOH
235
196
1.014914 1.566320 s EtOH, eth, bz
vs H2O, EtOH,
bz, chl; s eth
161.1(0.4) 0.931925 1.505720 s H2O, EtOH, eth
-63.80(0.03) 158.4(0.3) 0.930920 1.501020 vs H2O, EtOH,
eth; s ace
-14.08(0.03) 157.00(0.05) 0.929720 1.500620 sl H2O; vs EtOH;
msc eth; s ace
-6.12(0.03) 144.0(0.1) 0.922620 1.495320 msc H2O; sl
EtOH; s eth,
ace, chl
-10.45(0.03) 179.1(0.3) 0.928120 1.509620 sl H2O, ctc; s
EtOH, eth, ace,
chl
4/11/16 11:26 AM
Physical Constants of Organic Compounds
3-221
O
S
O P O
Cl
4262
4263
4264
Dimethyl phthalate
4269
4267
1,2-Dimethylpiperidine, (±)-
2,6-Dimethylpiperidine
4268
3,5-Dimethylpiperidine
N
N
N
O
O
4270
4271
2,2-Dimethylpropanamide
H2N
N,N-Dimethylpropanamide
4272
N,N-Dimethyl-1-propanamine
N
HO
4273
OH
4274
N,N-Dimethyl-1,3-propanediamine
2,2-Dimethyl-1,3-propanediol
4275
2,2-Dimethylpropanenitrile
Organic
2,2-Dimethylpropanal
4266
cis-2,5-Dimethylpiperazine
N
H
N
H
N
4265
1,4-Dimethylpiperazine
NH2
O
N
H
N
O
O,O-Dimethyl phosphorochloridothioate
H
N
N
O
O
O
O
SH
4276
2,2-Dimethyl-1-propanethiol
OH
4277
2,2-Dimethylpropanoic acid
N
Cl
OH
4278
4279
2,2-Dimethyl-1-propanol
2,2-Dimethylpropanoyl chloride
NH2
O
4280
4281
N,N-Dimethyl-2-propenamide
2,2-Dimethylpropylamine
4282
(1,1-Dimethylpropyl)benzene
OH
O
OH
O
O
O
4283
(2,2-Dimethylpropyl)benzene
4284
4285
4-(1,1-Dimethylpropyl)cyclohexanone
1,1-Dimethylpropyl 3-methylbutanoate
4286
4287
2-(1,1-Dimethylpropyl)phenol
O
4288
4-(1,1-Dimethylpropyl)phenol
4,6-Dimethyl-2H-pyran-2-one
O
O
4289
2,6-Dimethyl-4H-pyran-4-one
N
N
N
N
N
N
4290
2,3-Dimethylpyrazine
4291
2,5-Dimethylpyrazine
4292
2,6-Dimethylpyrazine
N
N
N
H
4293
N
4294
1,3-Dimethyl-1H-pyrazole
3,5-Dimethyl-1H-pyrazole
4295
2,7-Dimethylpyrene
N
N
NH2
4296
4,6-Dimethyl-2-pyridinamine
N
N
4297
N,N-Dimethyl-2-pyridinamine
N
4298
N,N-Dimethyl-4-pyridinamine
N
4299
2,3-Dimethylpyridine
N
4300
2,4-Dimethylpyridine
N
4301
2,5-Dimethylpyridine
N
4302
2,6-Dimethylpyridine
N
4303
3,4-Dimethylpyridine
Physical Constants of Organic Compounds
3-222
No.
Name
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
4304
3,5-Dimethylpyridine
3,5-Lutidine
C7H9N
591-22-0
4305
4306
2,6-Dimethylpyridine-1-oxide
4,6-Dimethyl-2-pyrimidinamine
C7H9NO
C6H9N3
4307
4310
2,6-Dimethyl-4-pyrimidinamine
4,6-Dimethylpyrimidine
1,3-Dimethyl-2,4(1H,3H)pyrimidinedione
2,4-Dimethylpyrrole
4311
2,5-Dimethylpyrrole
4312
4313
1,2-Dimethylpyrrolidine
2,4-Dimethylquinoline
4314
2,6-Dimethylquinoline
4315
2,7-Dimethylquinoline
4316
2,3-Dimethylquinoxaline
4317
Dimethyl sebacate
4318
Physical
Form
den
g cm –3
mp/˚C
bp/˚C
107.153 liq
-6.34(0.03)
171.9(0.1)
1073-23-0
767-15-7
123.152 hyg
123.155
23.3(0.5)
153.5
C6H9N3
461-98-3
183
C6H8N2
C6H8N2O2
1558-17-4
874-14-6
123.155 nd (al), pl
(bz)
108.141
140.140
C6H9N
625-82-1
95.142
C6H9N
625-84-3
95.142
C6H13N
C11H11N
765-48-0
1198-37-4
99.174 oil
157.212 orth pr (eth)
C11H11N
877-43-0
157.212 orth pr (eth) 57.69(0.05)
C11H11N
93-37-8
157.212
61(2)
C10H10N2
2379-55-7
158.199 nd (w+3,
ace)
106.3(0.4)
Dimethyl decanedioate
C12H22O4
106-79-6
230.301 lo pr
26.6(0.5)
Dimethyl selenide
Methyl selenide
C2H6Se
593-79-3
109.03
4319
4320
4321
Dimethylsilane
Dimethylstearylamine
Dimethyl succinate
2-Silapropane
Dymanthine
Methyl succinate
C2H8Si
C20H43N
C6H10O4
1111-74-6
124-28-7
106-65-0
60.171 col gas
297.562
146.141
4322
4323
Dimethylsulfamoyl chloride
Dimethyl sulfate
Dimethylaminosulfonyl chloride C2H6ClNO2S
C2H6O4S
13360-57-1 143.593
77-78-1
126.132 liq
-31.8(0.4)
4324
Dimethyl sulfide
2-Thiapropane
C2H6S
75-18-3
62.134
-98.26(0.04) 37.32(0.05)
4325
4326
4327
4328
Dimethyl sulfite
2,4-Dimethylsulfolane
Dimethyl sulfone
Dimethyl sulfoxide
DMSO
C2H6O3S
C6H12O2S
C2H6O2S
C2H6OS
616-42-2
1003-78-7
67-71-0
67-68-5
110.132
148.223 liq
94.133 pr
78.133
126(2)
-1.5
281
108.83(0.05) 238(5)
18.52(0.05) 191.9(0.9)
4329
Dimethyl L-tartrate
608-68-4
50(form a);
61(form b)
4330
4331
Dimethyl telluride
Dimethyl terephthalate
593-80-6
120-61-6
178.139 (i) cry (bz)
(ii) cry (w)
157.67 pa ye
194.184
4332
Dimethyl tetrachloroterephthalate
2,7-Dimethylthiachromine-8ethanol
C10H6Cl4O4
1861-32-1
331.965
158.2(0.7)
C12H14N4OS
92-35-3
262.330 ye pr (chl)
228.8
sub
C4H6N2S
27464-82-0 114.169
65
202.5
C14H12S2
135-58-0
244.375 nd (HOAc,al) 123
1843
145.60(0.09) 1.056215 1.509120
4308
4309
Organic
4333
Kyanmethin
4-Methylquinaldine
m-Toluquinaldine
Dimethyl 2,3-dihydroxybutane- C6H10O6
dioate, [R-(R*,R*)]C2H6Te
C10H10O4
pa bl flr cry
7.68(0.08)
liq
4334
2,5-Dimethyl-1,3,4-thiadiazole
4335
2,7-Dimethylthianthrene
4336
2,4-Dimethylthiazole
C5H7NS
541-58-2
113.182
4337
4338
4339
4340
4,5-Dimethylthiazole
N,N-Dimethylthioacetamide
Dimethyl thiodipropionate
2,3-Dimethylthiophene
C5H7NS
C4H9NS
C8H14O4S
C6H8S
3581-91-7
631-67-4
4131-74-2
632-16-6
113.182
103.186
206.260
112.193 liq
4341
2,4-Dimethylthiophene
C6H8S
638-00-6
112.193
4342
2,5-Dimethylthiophene
C6H8S
638-02-8
112.193 liq
HCP_Section_03.indb 222
Mesulphen
25
119.3(0.5)
-150
22.9(0.2)
18.6(0.6)
140.602​
(0.004)
83.5
74.5
-49.0(0.6)
nD
Solubility
0.941920 1.506120 s H2O, EtOH,
eth, ace; sl ctc
13322
1.07325 1.570620
s H2O, EtOH,
ace, bz; i eth;
vs chl
sub
sl H2O, EtOH,
bz, chl
159(8)
1.488020 vs H2O
sl EtOH; s eth,
chl
165(7)
0.923620 1.504820 sl H2O; vs EtOH,
eth, bz; s chl
167.43(0.04) 0.935320 1.503620 i H2O; vs EtOH,
eth
104(8)
0.79920
s H2O
267(2)
1.061115 1.607520 sl H2O, chl; vs
EtOH, eth
268.1(0.4)
sl H2O, EtOH,
eth, chl; vs bz
260(19)
sl H2O; s EtOH,
eth, chl
s EtOH, eth,
ace, bz, chl,
acid
17520
0.988228 1.435528 i H2O; s EtOH,
eth, ace, ctc
58(3)
1.407715
vs eth, EtOH,
chl
-20
0.68-80
197(1)
8016
186(3)
280
94
288
1.119820 1.419720 sl H2O, ctc; s
EtOH, ace; vs
eth
1.332220 1.387420 s H2O, eth, bz,
ctc; msc EtOH;
i CS2
0.848320 1.443820 sl H2O; s EtOH,
eth
1.212920 1.408320 s H2O, EtOH, eth
1.136220 1.473220 vs lig
1.1700110 1.4226
s H2O, EtOH, bz
1.101025 1.479320 s H2O, EtOH,
eth, ace, ctc,
AcOEt
1.30645
vs H2O, ace,
eth, EtOH
vs EtOH
1.075141
sl H2O, EtOH,
MeOH; s eth,
chl
s H2O, MeOH; sl
EtOH, eth, ace,
chl
sl H2O, EtOH,
eth
vs ace, eth,
peth, chl
sl H2O; s EtOH,
eth, chl
vs eth, EtOH
158
1.069920
16218
141(7)
1.155920 1.474020
1.002120 1.519220 i H2O; vs EtOH,
eth; s bz
0.993820 1.510420 i H2O; s EtOH,
eth, bz
0.985020 1.512920 i H2O; s EtOH,
eth, bz
137(19)
-62.52(0.05) 139(2)
4/11/16 11:26 AM
Physical Constants of Organic Compounds
3-223
O
NH2
N
N
O
N
4304
N
4305
3,5-Dimethylpyridine
N
NH2
4307
4,6-Dimethyl-2-pyrimidinamine
N
N
N
4306
2,6-Dimethylpyridine-1-oxide
N
N
4308
2,6-Dimethyl-4-pyrimidinamine
O
4309
4,6-Dimethylpyrimidine
1,3-Dimethyl-2,4(1H,3H )-pyrimidinedione
N
N
N
H
4310
2,4-Dimethylpyrrole
4313
1,2-Dimethylpyrrolidine
2,5-Dimethylpyrrole
2,4-Dimethylquinoline
O
O
Se
4317
O
O
4331
Dimethyl terephthalate
N
S
4337
4,5-Dimethylthiazole
4316
2,7-Dimethylquinoline
2,3-Dimethylquinoxaline
O
O
N
4319
Dimethyl selenide
O
O
4320
Dimethylsilane
4321
Dimethylstearylamine
Dimethyl succinate
OH O
O
O O
S
O
O
4323
Dimethyl sulfate
O
O
2,6-Dimethylquinoline
H
4318
Dimethyl sebacate
Dimethylsulfamoyl chloride
N
4315
H
O
4322
N
4314
Si
O
O
Cl
S
N
O
N
N
4312
4311
O
S
4324
4325
Dimethyl sulfide
S
O O
4326
Dimethyl sulfite
2,4-Dimethylsulfolane
O O
S
O
S
4327
4328
Dimethyl sulfone
O
O
O
4329
Dimethyl L-tartrate
Dimethyl sulfoxide
Te
OH
4330
Dimethyl telluride
O
Cl
Cl
Cl
Cl
O
O
S
O
O
4332
Dimethyl tetrachloroterephthalate
S
N
S
HO
4338
N,N-Dimethylthioacetamide
N
S
4333
S
O
4334
2,5-Dimethyl-1,3,4-thiadiazole
S
4335
2,7-Dimethylthianthrene
N
S
4336
2,4-Dimethylthiazole
O
O
4339
S
N N
N
2,7-Dimethylthiachromine-8-ethanol
O
N
N
Dimethyl thiodipropionate
S
4340
2,3-Dimethylthiophene
S
4341
2,4-Dimethylthiophene
S
4342
2,5-Dimethylthiophene
Organic
N
H
Physical Constants of Organic Compounds
3-224
Mol. Form.
CAS RN
Mol.
Wt.
3,4-Dimethylthiophene
C6H8S
632-15-5
112.193
4344
4345
N,N-Dimethylthiourea
N,N’-Dimethylthiourea
C3H8N2S
C3H8N2S
6972-05-0
534-13-4
104.174 cry (w)
104.174 hyg pl
4346
C19H39NO
24602-86-6 297.519
C10H11F3N2O
2164-17-2
232.201
C2H6S3
C13H20O
3658-80-8
141-10-6
126.264
192.297 pa ye oil
4350
2,6-Dimethyl-4-tridecylmorTridemorph
pholine
N,N-Dimethyl-N’-[3Fluometuron
(trifluoromethyl)phenyl]urea
Dimethyl trisulfide
6,10-Dimethyl-3,5,9-undeca- Pseudoionone
trien-2-one
N,N-Dimethylurea
C3H8N2O
598-94-7
88.108
4351
N,N’-Dimethylurea
C3H8N2O
96-31-1
4352
4353
Dimethyl zinc
Dimetilan
C2H6Zn
C10H16N4O3
4354
4355
4356
Dimorpholamine
N,N’-Di-2-naphthyl-1,4benzenediamine
Di-2-naphthyl disulfide
4357
No.
Name
4343
4347
4348
4349
Synonym
Physical
Form
mp/˚C
bp/˚C
den
g cm –3
145
0.99325
vs H2O, EtOH,
ace; sl eth, bz;
i CS2
1411.3
0.86
161(1)
vs ace, EtOH
416
14412
181.2(0.8)
Organic
544-97-8
644-64-4
-43.01(0.02) 43(3)
69
20513
C20H38N4O4
C26H20N2
119-48-2
93-46-9
398.541 cry (peth)
360.450
41.5
235
C20H14S2
5586-15-2
318.455 nd
139.5
N,N’-Di-1-naphthylurea
C21H16N2O
607-56-7
4358
Diniconazole
4359
4360
106(2)
296
269
2290.4
0.898420 1.533520 s EtOH, eth, chl,
MeOH
1.255525
s H2O; sl EtOH,
tfa; i eth
1.14225
vs H2O, EtOH; i
eth; sl chl
1.38610
s eth; msc peth
s H2O, chl,
EtOH, ace, xyl
vs H2O
i EtOH, eth, bz
1.144145
C15H17Cl2N3O
312.364 nd (py,
HOAc)
83657-24-3 326.221 cry
149
Dinitramine
2,3-Dinitroaniline
C11H13F3N4O4
C6H5N3O4
29091-05-2 322.241
602-03-9
183.122
99.3(0.5)
128
1.64650
4361
2,4-Dinitroaniline
C6H5N3O4
97-02-9
180.1(0.5)
1.61514
4362
4363
2,5-Dinitroaniline
2,6-Dinitroaniline
C6H5N3O4
C6H5N3O4
619-18-1
606-22-4
4364
3,5-Dinitroaniline
C6H5N3O4
618-87-1
183.122 ye nd (ace)
grn ye tab
(al)
183.122 oran nd (al)
183.122 gold lf
(HOAc) ye
nd (al)
183.122 ye nd (dil al)
4365
1,5-Dinitro-9,10-anthracenedione
C14H6N2O6
82-35-9
298.207 pa ye nd
(xyl)
385
4366
C14H6N2O6
129-39-5
298.207
312
4367
1,8-Dinitro-9,10-anthracenedione
2,4-Dinitrobenzaldehyde
C7H4N2O5
528-75-6
4368
4369
3,5-Dinitrobenzamide
1,2-Dinitrobenzene
Nitromide
o-Dinitrobenzene
C7H5N3O5
C6H4N2O4
121-81-3
528-29-0
196.117 pa ye pr (al), 71.8(0.7)
pl (bz)
211.132 lf (w)
184
168.107 nd (bz), pl
115.8(0.6)
(al)
sub
4370
1,3-Dinitrobenzene
m-Dinitrobenzene
C6H4N2O4
99-65-0
168.107 orth pl (al)
4371
1,4-Dinitrobenzene
p-Dinitrobenzene
C6H4N2O4
100-25-4
4372
4373
2,4-Dinitroresorcinol
C6H4N2O6
C6H3ClN2O4S
519-44-8
528-76-7
C6H4N2O7S
4375
4376
2,4-Dinitro-1,3-benzenediol
2,4-Dinitrobenzenesulfenyl
chloride
2,4-Dinitrobenzenesulfonic
acid
2,4-Dinitrobenzoic acid
3,4-Dinitrobenzoic acid
4377
4378
4379
1.455520 i H2O; vs EtOH,
eth; i lig
vs py
s H2O, ace,
MeOH, xyl
138.0
138.0(0.5)
i H2O; s EtOH; sl
eth
i H2O; sl EtOH,
ace, HCl
vs EtOH
i H2O, lig; sl
EtOH; s eth, bz
162(1)
1.60150
sub
20015
319(3)
1.3119120 1.56517
89.2(0.5)
296(2)
1.575118
168.107 nd (al)
171.1(0.9)
297
1.62518
147.3(0.4)
99
89-02-1
200.105 ye lf (al)
234.617 ye pr
(bz-peth)
248.170 nd (w+3)
C7H4N2O6
C7H4N2O6
610-30-0
528-45-0
212.116 nd (w)
212.116 cry (dil al)
182.7(0.5)
165.0(0.5)
3,5-Dinitrobenzoic acid
C7H4N2O6
99-34-3
212.116 mcl pr (al)
205
3,5-Dinitrobenzoyl chloride
2,2’-Dinitro-1,1’-biphenyl
C7H3ClN2O5
C12H8N2O4
99-33-2
2436-96-6
230.562 ye nd (bz)
74
244.203 ye mcl pr or 127(1)
nd (al)
HCP_Section_03.indb 224
Solubility
1.520620 i H2O; s EtOH;
vs eth
161.5
63.8(0.6)
mcl pr (al,
chl)
88.108 orth bipym
(chl-eth)
95.478 liq, ign in air
240.259 col solid
4374
nD
108
1.67220
19612
305
1.4525
i H2O; s EtOH,
eth; sl ace, bz
i H2O; sl EtOH,
eth, bz; vs
PhNO2
sl H2O, chl, lig;
s EtOH, eth, bz
vs H2O
i H2O; s EtOH,
bz, chl, AcOEt;
sl DMSO
sl H2O; vs EtOH,
ace, py; s eth,
tol
i H2O; sl EtOH,
chl; s ace, bz,
tol
sl H2O, EtOH
vs bz, chl,
HOAc; sl peth
vs H2O, EtOH; sl
eth; i bz, peth
sl H2O, EtOH, bz
sl H2O; vs EtOH,
eth
sl H2O; vs EtOH,
HOAc
s eth, chl
i H2O; vs EtOH;
s eth, bz; sl
ace, lig
4/11/16 11:26 AM
Physical Constants of Organic Compounds
3-225
H
N
N
O
4343
F
F
4346
N,N’-Dimethylthiourea
N,N-Dimethylthiourea
4347
2,6-Dimethyl-4-tridecylmorpholine
O
N
H
N
NH2
4350
6,10-Dimethyl-3,5,9-undecatrien-2-one
O
Zn
4352
N,N’-Dimethylurea
N,N-Dimethylurea
O
4351
O
O
4349
N
H
N
N
Dimethyl trisulfide
O
O
O
N
O
N
N
O
N
N
4354
4353
Dimethyl zinc
S
4348
N,N-Dimethyl-N’-[3-(trifluoromethyl)phenyl]urea
N
S
S
F
4345
4344
3,4-Dimethylthiophene
N
S
S
S
H
N
H
N
NH2
Dimorpholamine
Dimetilan
Organic
N
O
N
N
N
O
HN
H
N
H
N
OH
Cl
NH
F
S S
4356
N,N’-Di-2-naphthyl-1,4-benzenediamine
N
O
NH2 O
N
O
O
4360
O
N
N
O
4361
2,3-Dinitroaniline
O
O
N
2,4-Dinitrobenzaldehyde
OH
O S OO
N
N
NH2 O
N
N
O
N
O
O
4368
O
O
N
O
N
N
O
N
O
O
N
N
O
N
Dinitramine
O
O
O
1,5-Dinitro-9,10-anthracenedione
O
OH O
N
N
O
O
4371
1,4-Dinitrobenzene
O
2,4-Dinitrobenzoic acid
N
HO
O
4376
3,4-Dinitrobenzoic acid
O
O
N
O
O
4365
4366
1,8-Dinitro-9,10-anthracenedione
Cl
O
N
S
O
N
O
O
4372
O
2,4-Dinitro-1,3-benzenediol
O
O
O
N
O
N
O
4377
O
3,5-Dinitrobenzoic acid
O
N
O
4373
2,4-Dinitrobenzenesulfenyl chloride
Cl
O
O
O
OH
1,3-Dinitrobenzene
O
N
O
O
O
4370
N
O
O
O
3,5-Dinitroaniline
O
O
O
N
4359
Diniconazole
4364
N
O
HO
O
4375
N
O
1,2-Dinitrobenzene
O
N
N
O
4369
3,5-Dinitrobenzamide
O
O
2,6-Dinitroaniline
O
O
2,4-Dinitrobenzenesulfonic acid
O
N
NH2
HO
O
4374
N,N’-Di-1-naphthylurea
4363
2,5-Dinitroaniline
O
4367
O
O
O
O
O
N
O
O
4358
NH2
4362
2,4-Dinitroaniline
O
O
O
O
O
4357
Di-2-naphthyl disulfide
NH2 O
N
O
N
Cl
4355
NH2 O
N
NH2 O
N
F
F
N
O
N
O
4378
O
3,5-Dinitrobenzoyl chloride
O2N NO2
4379
2,2’-Dinitro-1,1’-biphenyl
Physical Constants of Organic Compounds
3-226
Organic
Mol. Form.
CAS RN
Mol.
Wt.
4,4’-Dinitro-1,1’-biphenyl
C12H8N2O4
1528-74-1
244.203 nd (al)
235(6)
4381
1,4-Dinitrobutane
C4H8N2O4
4286-49-1
148.118 pl (al)
33.5(0.5)
4382
4,4’-Dinitrodiphenylamine
4-Nitro-N-(4-nitrophenyl)­
aniline
C12H9N3O4
1821-27-8
259.217 ye nd(al)
210(1)
4383
4,4’-Dinitrodiphenyl ether
Bis(4-nitrophenyl) ether
C12H8N2O5
101-63-3
260.202
143(1)
4384
4,4’-Dinitrodiphenyl sulfide
Bis(4-nitrophenyl) sulfide
C12H8N2O4S
1223-31-0
160.5
4385
1,1-Dinitroethane
C2H4N2O4
600-40-8
4386
4387
1,2-Dinitroethane
Dinitromethane
C2H4N2O4
CH2N2O4
7570-26-5
625-76-3
276.268 oran pl
(HOAc)
120.064 ye mcl (bz,
MeOH)
120.064
106.038 ye nd
4388
1,3-Dinitronaphthalene
C10H6N2O4
606-37-1
4389
1,5-Dinitronaphthalene
C10H6N2O4
605-71-0
4390
1,8-Dinitronaphthalene
C10H6N2O4
4391
2,4-Dinitro-1-naphthol
4392
No.
Name
4380
Synonym
Physical
Form
mp/˚C
38.2(0.4)
<-15
bp/˚C
185.5
1.34924
955
169(11)
1.459720 1.446820
sub
602-38-0
218.166 ye orth pl
(chl)
172(1)
445 dec
C10H6N2O5
605-69-6
138(1)
2,3-Dinitrophenol
C6H4N2O5
66-56-8
234.165 ye nd (al,
chl)
184.106 ye nd (w)
4393
2,4-Dinitrophenol
C6H4N2O5
51-28-5
184.106 pa ye pl or
lf (w)
114(2)
4394
2,5-Dinitrophenol
C6H4N2O5
329-71-5
105.6(0.2)
4395
2,6-Dinitrophenol
C6H4N2O5
573-56-8
4396
4397
4398
3,4-Dinitrophenol
2,4-Dinitrophenol, acetate
4-[(2,4-Dinitrophenyl)­amino]­
phenol
2,4-Dinitro-N-phenylaniline
C6H4N2O5
C8H6N2O6
C12H9N3O5
577-71-9
4232-27-3
119-15-3
184.106 ye mcl pr or
nd (w,lig)
184.106 pa ye orth
nd or lf (dil
al)
184.106 tcl nd (w)
226.143 cry (MeOH)
275.216 red lf
C12H9N3O4
961-68-2
259.217 ye red nd
(al)
159(2)
2,4-Dinitrophenyl
dimethylcarbamodithioate
(2,4-Dinitrophenyl)hydrazine
C9H9N3O4S2
89-37-2
287.315
152.5
C6H6N4O4
119-26-6
198.137 blsh-red (al) 201.6(0.4)
C3H6N2O4
C3H6N2O4
C3H6N2O4
C3H6N2O6
C16H8N2O4
C16H8N2O4
C5H10N6O2
601-76-3
6125-21-9
595-49-3
2736-80-3
42397-64-8
42397-65-9
101-25-7
134.091 liq
134.091
134.091
166.089 wh pl (bz)
292.246
292.246
186.172 cry (MeOH)
C4H8N4O2
C14H10N2O10S2
140-79-4
128-42-7
144.133 pa ye pl (w) 155.9(0.7)
430.366 cry (AcOH) 266
4411
1,1-Dinitropropane
1,3-Dinitropropane
2,2-Dinitropropane
2,2-Dinitro-1,3-propanediol
1,6-Dinitropyrene
1,8-Dinitropyrene
Dinitrosopentamethylenetetramine
1,4-Dinitrosopiperazine
4,4’-Dinitro-2,2’-stilbenedisulfonic acid
Dinobuton
Dessin
C14H18N2O7
973-21-7
60
4412
4413
4414
4415
4416
Dinocap
Dinonyl adipate
Dinonyl ether
Dinonyl phthalate
Dinoseb
C18H24N2O6
C24H46O4
C18H38O
C26H42O4
C10H12N2O5
6119-92-2
151-32-6
2456-27-1
84-76-4
88-85-7
326.302 ye cry
(EtOH)
364.393
398.620
270.494 liq
418.609
240.212
4417
4418
4419
Dioctadecylamine
Dioctylamine
Dioctyl ether
C36H75N
C16H35N
C16H34O
112-99-2
1120-48-5
629-82-3
521.988
241.456 nd
242.440 liq
72.9
20(9)
-7.7(0.4)
4400
4401
4402
4403
4404
4405
4406
4407
4408
4409
4410
HCP_Section_03.indb 226
Dinonyl hexanedioate
Phenol, 2-(1-methylpropyl)4,6-dinitroDistearylamine
N-Octyl-1-octanamine
nD
17613
218.166 ye nd (bz,
148
py-w)
218.166 hex nd (ace, 217(2)
HOAc)
4399
den
g cm –3
371(3)
145.1(0.2)
1.586020
1.68120
sub
-42(1)
-21.4(0.2)
52(2)
142
309(1)
299(1)
207
i H2O; sl EtOH; s
bz, HOAc
i H2O; sl EtOH; s
eth, bz, MeOH
i H2O, tol; sl
EtOH, bz; s
ace, HOAc
i H2O; sl EtOH,
eth; s bz,
HOAc
i H2O; sl EtOH; s
con sulf
sl H2O; s EtOH,
eth
vs eth, EtOH
i H2O; s EtOH,
eth
i H2O; s EtOH,
ace
i H2O; sl EtOH,
ace; s bz, py;
vs eth
i H2O; sl EtOH,
bz; s ace, chl,
py
sl H2O, DMSO;
vs EtOH, eth; s
bz
sl H2O; s EtOH,
eth, ace, bz,
tol, chl, py
vs bz, eth
1.68324
62.4(0.8)
134.4(1)
72.5
195.5
Solubility
i H2O; vs EtOH,
eth; s bz, chl;
sl ctc
vs bz, eth, EtOH
1.67225
s alk
1.5420
194(4)
1031
186.0(0.5)
1.261025 1.433920
1.35326 1.465420
1.3025
i H2O; s EtOH,
ace; sl eth, bz,
DMSO
i H2O; s EtOH,
ace, bz
i H2O; s EtOH; sl
eth, bz, chl,
DMSO
s alk
i H2O; s eth
sl H2O
vs EtOH
1360.01
2051
318
413
43.3(0.5)
0.81
1.435620
1.26545
2682
307.7(0.6)
289(3)
vs chl
0.796326 1.441526 vs eth, EtOH
0.806320 1.432720 sl H2O; s EtOH,
eth, ctc
4/11/16 11:26 AM
Physical Constants of Organic Compounds
O
N
O
O
N
O
4380
H
N
O
O
N
O
O
O
N
O
4385
O
N
N
O
4386
1,1-Dinitroethane
O
O
N
N
O
N
O
O
O
O
4388
N
4389
1,3-Dinitronaphthalene
N
O
4390
1,5-Dinitronaphthalene
OH O
N
O
N
O
O
4391
1,8-Dinitronaphthalene
O
4384
OH O
N
O
N
O
4,4’-Dinitrodiphenyl sulfide
O
N
O
Dinitromethane
N
O
4,4’-Dinitrodiphenyl ether
NO2 NO2
4387
1,2-Dinitroethane
N
S
O
4383
4,4’-Dinitrodiphenylamine
NO2
H
H
NO2
O
O
4382
1,4-Dinitrobutane
O
O
N
O
N
O
4381
4,4’-Dinitro-1,1’-biphenyl
O
O
OH O
N
O
O
2,4-Dinitro-1-naphthol
N
O
4392
O
O
4393
2,3-Dinitrophenol
2,4-Dinitrophenol
Organic
O
N
O
O
N
3-227
O
OH O
N
O
O
O
N
O
O
N
OH O
N
O
O
4394
4395
2,5-Dinitrophenol
N
O
N
O
O
H
N
O
N
O
O
O
N
HO
4397
O
N
O
2,4-Dinitro-N-phenylaniline
4-[(2,4-Dinitrophenyl)amino]phenol
O
N
S
S
N
O
O
N
H2N
O
O
O
4400
NH O
N
N
O
4401
2,4-Dinitrophenyl dimethylcarbamodithioate
O
(2,4-Dinitrophenyl)hydrazine
O
N
O
N
O
O
4402
1,1-Dinitropropane
O
O
N
O
N
O
4403
1,3-Dinitropropane
O2N
HO
O2N
NO2
4404
OH
NO2
N
O
4405
2,2-Dinitropropane
O
4399
4398
2,4-Dinitrophenol, acetate
3,4-Dinitrophenol
N
O
O
O
N
H
N
O
4396
2,6-Dinitrophenol
O
N
O
OH
N
O
O
4406
2,2-Dinitro-1,3-propanediol
1,6-Dinitropyrene
O
O
O
O
N
O
O
N
O
O
N
N
N N
O
4407
N
N N
O
4408
1,8-Dinitropyrene
Dinitrosopentamethylenetetramine
N N
O
S O
O OH O S
HO O
N N
O
4409
1,4-Dinitrosopiperazine
O
N
O
O
O
N
O
O
R = NO2, R' = C8H17
and
R = C8H17, R' = NO2
R
N
4412
Dinobuton
Dinocap
O
O
O
O
O
4413
O
4414
Dinonyl adipate
NH
4417
4418
Dioctylamine
OH
N
O
4416
Dinonyl phthalate
N
H
O
N
O
4415
Dinonyl ether
Dioctadecylamine
O
O
O
O
R'
O
4411
4,4’-Dinitro-2,2’-stilbenedisulfonic acid
O
O
O
4410
O
N
Dinoseb
O
4419
Dioctyl ether
Physical Constants of Organic Compounds
3-228
Organic
No.
Name
Synonym
4420
4421
4422
4423
4424
4425
4426
Dioctyl hexanedioate
Dioctyl maleate
Dioctyl phthalate
Dioctyl sebacate
Dioctyl sulfide
Dioctyl terephthalate
Dioscorine
4427
1,3-Dioxane
4428
1,4-Dioxane
4429
4430
4431
4432
4433
1,4-Dioxane-2,5-dione
1,4-Dioxane-2,6-dione
Dioxathion
1,3-Dioxepane
1,3-Dioxolane
4434
4435
1,3-Dioxol-2-one
Dioxybenzone
4436
4437
4438
4439
Dioxypyramidon
Dipentaerythritol
Dipentene
Dipentylamine
C3H2O3
(2-Hydroxy-4-methoxyphenyl)­ C14H12O4
(2-hydroxyphenyl)methanone
C13H17N3O3
C10H22O7
p-Menthadiene
C10H16
Diamylamine
C10H23N
4440
4441
Dipentyl cis-2-butenedioate
Dipentyl ether
Dipentyl maleate
Amyl ether
4442
4443
4444
4445
4446
4447
2,6-Di-tert-pentyl-4-methylphenol
Di-tert-pentyl peroxide
Dipentyl phthalate
Dipentyl sulfide
Dipentyl sulfoxide
Diphenamid
4448
Diphenidol
4449
Diphenolic acid
2,6-Bis(1,1-dimethylpropyl)-4- C17H28O
methylphenol
C10H22O2
C18H26O4
C10H22S
C10H22OS
Benzeneacetamide,
C16H17NO
N,N-dimethyl-α-phenyl1,1-Diphenyl-4-piperidinyl-1- C21H27NO
butanol
C17H18O4
4450
1,2-Diphenoxyethane
Ethylene glycol diphenyl ether
4451
Mol.
Wt.
Physical
Form
370.566
340.498 liq
390.557
426.673
258.506
390.557 cry
221.296 grn-ye pr
(eth)
1,3-Dioxacyclohexane
C4H8O2
505-22-6
88.106
liq
-45
105(2)
1,4-Dioxacyclohexane
C4H8O2
123-91-1
88.106
col liq
11.75(0.06)
101.2(0.3)
C4H4O4
C4H4O4
C12H26O6P2S4
C5H10O2
C3H6O2
502-97-6
4480-83-5
78-34-2
505-65-7
646-06-0
116.073 lf (al, al-chl)
116.073 cry (bz)
456.538
102.132
74.079 liq
83.0(0.1)
92.5
-20
240.5
-97.21(0.02) 75.3(0.1)
1.06020
872-36-6
131-53-3
86.046 liq
244.243
22
178(6)
1721
1.3525
519-65-3
126-58-9
7705-14-8
2050-92-2
263.292 pr
254.278 cry (w)
136.234 liq
157.297
105.5
221
-95.5
1972
s H2O, EtOH
1.36615
s hot H2O
0.840221 1.472720
0.777120 1.427220 sl H2O; vs EtOH;
msc eth; s ace
0.97420
0.783320 1.411920 i H2O; msc
EtOH, eth; s
chl
0.93125 1.495020
C14H24O4
C10H22O
10099-71-5 256.339 liq
693-65-2
158.281 liq
1912
2420.002
2204
2180.5
20229
425
25
18
34
-69.2(0.5)
56103-67-4 248.403
176(5)
204(4)
16110
187(2)
283
174.281
306.397
174.347
190.346
239.312
-51.3
58
133(2)
972-02-1
309.445 nd (peth)
104.5
126-00-1
286.323 cry (w)
171.5
C14H14O2
104-66-5
214.260 lf (al)
98
N,N-Diphenylacetamide
C14H13NO
519-87-9
211.259 wh cry pow 101.4(0.6)
sub
4452
Diphenylacetylene
C14H10
501-65-5
300
4453
2-(Diphenylacetyl)-1H-indene- Diphenadione
1,3(2H)-dione
Diphenylamine
N-Phenylbenzenamine
C23H16O3
82-66-6
C12H11N
122-39-4
178.229 mcl pr or pl 62(2)
(al)
340.371 pa ye mcl
146.5
(al)
169.222 mcl lf(dil al) 53.2(0.3)
C14H11NO4
579-92-0
257.242 ye cry (al)
C12H10NNaO3S
6152-67-6
271.267 ye cry
C26H18
C12H10AsCl
1499-10-1
712-48-1
C18H16N2
74-31-7
330.421
264.582 orth pl
(peth)
260.333
C20H18O
C19H16S
4455
4456
4457
4458
4459
4460
4461
Diphenylamine-2,2’-dicarboxylic acid
Diphenylamine-4-sulfonic
Sodium diphenylamine-4acid, sodium salt
sulfonate
9,10-Diphenylanthracene
Diphenylarsinous chloride
Chlorodiphenylarsine
N,N’-Diphenyl-1,4-benzenedi- N,N’-Diphenyl-p-phenylenediamine
amine
α,α-Diphenylbenzeneethanol
α,αDiphenylbenzenemethanethiol
HCP_Section_03.indb 228
Triphenylmethyl mercaptan
-55
Solubility
0.907425
s ctc
0.84225 1.461020
1.2162
s H2O, ace, chl,
EtOH; sl eth,
bz
1.028625 1.416520 msc H2O, EtOH,
eth, ace, bz
1.033720 1.422420 msc H2O, EtOH,
eth, ace, bz; s
ctc
vs ace
1.25726
10508-09-5
131-18-0
872-10-6
1986-90-9
957-51-7
4454
1.453920
123-79-5
2915-53-9
117-84-0
2432-87-3
2690-08-6
4654-26-6
3329-91-7
1,3-Dioxacyclopentane
9.6
nD
C22H42O4
C20H36O4
C24H38O4
C26H50O4
C16H34S
C24H38O4
C13H19NO2
Diglycollic anhydride
bp/˚C
0.92225
0.9420
CAS RN
Dioctyl decanedioate
Octyl sulfide
mp/˚C
den
g cm –3
Mol. Form.
5814
20511
863.7
1201
0.80820
s chl
1.397420 msc H2O; s
EtOH, eth, ace
1.409520
s ctc, CS2
0.840720 1.456120 i H2O; s eth
1.1723.3
18212
0.9657100
1.670
vs H2O, ace,
EtOH
i H2O; sl EtOH; s
eth, chl
sl H2O, eth, chl;
s EtOH
i H2O; sl EtOH,
chl; vs eth
vs ace, HOAc
305.1(1)
1.15822
i H2O; vs EtOH,
ace; s eth; sl
chl
237.0(0.2)
44
337
150
2220.5
4428-13-1
274.356 nd(bz-lig) pr 89.5
(peth)
22211
1.482016 1.633256 vs ace, bz, eth,
EtOH
sl EtOH, eth, bz,
chl; i acid
i H2O; vs EtOH;
sl eth, chl,
peth
3695-77-0
276.395
296 dec
105.8
4/11/16 11:26 AM
Physical Constants of Organic Compounds
3-229
O
O
O
O
O
O
O
O
O
O O
4420
O
4421
Dioctyl hexanedioate
4422
Dioctyl maleate
Dioctyl phthalate
O
O
O
O
N
O
O
O
O
S
4423
4424
Dioctyl sebacate
Dioctyl sulfide
O
O
O
O
O
O
4427
4428
4429
1,3-Dioxane
1,4-Dioxane
O
O
O
O
O
O
1,4-Dioxane-2,5-dione
O
P
O
S
OH O
S
O
P
S
O
4431
Dioxathion
1,4-Dioxane-2,6-dione
O
O
O
4430
Dioscorine
Dioctyl terephthalate
S
O
O
4426
4425
Organic
O
O
O
4432
4433
1,3-Dioxepane
OH
O
O
O
O
4435
4434
1,3-Dioxolane
Dioxybenzone
1,3-Dioxol-2-one
O
N
N
N
O
O
HO
OH
HO
O
4436
Dioxypyramidon
O
OH
HO
H
N
OH
4438
4437
4439
Dipentene
Dipentaerythritol
Dipentyl cis-2-butenedioate
O
O
O
Dipentyl ether
O
4440
Dipentylamine
OH
4441
O
O
4442
O
O
O
2,6-Di-tert-pentyl-4-methylphenol
S
O
4443
4444
Di-tert-pentyl peroxide
4445
Dipentyl phthalate
Dipentyl sulfide
O
O
N
4446
O
O
O
S
Dipentyl sulfoxide
OH
N
OH
4447
HO
4448
Diphenamid
4449
Diphenidol
N
O
OH
4450
Diphenolic acid
4451
1,2-Diphenoxyethane
N,N-Diphenylacetamide
O
O
O
H
N
O
OH O
H
N
OH
H
N
SO3 Na
4452
Diphenylacetylene
4453
2-(Diphenylacetyl)-1H-indene-1,3(2H )-dione
Cl
As
4454
Diphenylamine
4457
4458
Diphenylarsinous chloride
Diphenylamine-2,2’-dicarboxylic acid
4456
Diphenylamine-4-sulfonic acid, sodium salt
H
N
SH
N
H
9,10-Diphenylanthracene
4455
4459
N,N’-Diphenyl-1,4-benzenediamine
OH
4460
α,α-Diphenylbenzeneethanol
4461
α,α-Diphenylbenzenemethanethiol
Physical Constants of Organic Compounds
3-230
Organic
Mol. Form.
CAS RN
Mol.
Wt.
N,N’-Diphenyl-[1,1’-biphenyl]- N,N’-Diphenylbenzidine
4,4’-diamine
C24H20N2
531-91-9
336.429 lf or pl
C16H14
538-81-8
206.282 lf (al, HOAc) 149(4)
352
4464
4465
trans,trans-1,4-Diphenyl-1,3butadiene
1,4-Diphenyl-1,3-butadiyne
Diphenyldiacetylene
1,1-Diphenylbutane
C16H10
C16H18
886-66-8
719-79-9
202.250
210.314
287
4466
1,2-Diphenylbutane
C16H18
5223-59-6
210.314
4467
1,4-Diphenylbutane
C16H18
1083-56-3
210.314
52.2(0.1)
316(3)
4468
4469
1,3-Diphenyl-1-butene
trans-1,4-Diphenyl-2-butene1,4-dione
C16H16
C16H12O2
7614-93-9
959-28-4
208.298
236.265 ye nd (al,
bz)
47.5
111
311
4470
4471
4472
1,3-Diphenyl-2-buten-1-one
Diphenylcarbamic chloride
Diphenylcarbazone
C16H14O
C13H10ClNO
C13H12N4O
495-45-4
83-01-2
538-62-5
4473
N,N’-Diphenylcarbodiimide
C13H10N2
622-16-2
222.281
231.677 lf (al)
240.260 oran oran
nd (bz) pr
(al)
194.231
4474
Diphenyl carbonate
Phenyl carbonate
C13H10O3
102-09-0
214.216 nd (al, bz)
4475
sym-Diphenylcarbazide
C13H14N4O
140-22-7
4476
4477
2,2’-Diphenylcarbonic
dihydrazide
Diphenyl chlorophosphonate
Diphenyl diselenide
Phenyl diselenide
C12H10ClO3P
C12H10Se2
2524-64-3
1666-13-3
242.276 cry (al + 1) 170
cry (HOAc)
268.632
312.13 ye nd
63.5
4478
Diphenyl disulfide
Phenyl disulfide
C12H10S2
882-33-7
4479
1,1-Diphenylethane
C14H14
612-00-0
4480
1,2-Diphenylethane
Dibenzyl
C14H14
103-29-7
4481
4482
N,N’-Diphenylethanediamide
N,N’-Diphenyl-1,2-ethanediamine
1,2-Diphenyl-1,2-ethanediol,
(R*,R*)-(±)-
1,2-Dianilinoethane
C14H12N2O2
C14H16N2
620-81-5
150-61-8
C14H14O2
655-48-1
214.260 nd (w,al),tab 122.5
(eth)
>300
C14H12
C12H10O
530-48-3
101-84-8
180.245
170.206
277(17)
258.0(0.1)
1.023220 1.608520
1.066130 1.578725
2325
1.09025
No.
Name
4462
4463
4483
Synonym
Dypnone
Physical
Form
mp/˚C
bp/˚C
den
g cm –3
85.9(0.5)
27
291(9)
342.5
0.992820 1.566420 i H2O; s EtOH,
eth, bz, chl
0.967320 1.555420 i H2O; s EtOH,
eth, bz, chl
0.988020
i H2O; s EtOH,
eth, chl
0.999620 1.59015
sl EtOH; s bz,
HOAc; vs chl; i
lig
1.108015 1.634320 vs eth, EtOH
84.5
157 dec
i H2O; vs EtOH,
bz, chl
169
331
78.9(0.3)
306
1.121587
dec
314272
20211
1.29625
1.55780
60.4(0.5)
310
1.35320
-18.0(0.1)
285.8(0.2)
0.999720 1.575620
182.261 mcl pr
(MeOH)
240.257 lf (bz)
212.290 cry (dil al)
51.18(0.06)
280(3)
0.978025 1.547660
254
74
>360
22912
1,1-Diphenylethene
Diphenyl ether
4486
C20H27O4P
1241-94-7
362.399
4487
Diphenyl 2-ethylhexyl
phosphate
N,N-Diphenylformamide
C13H11NO
607-00-1
197.232 orth (dil al)
73.5
337.5
4488
2,5-Diphenylfuran
C16H12O
955-83-9
91
344
4489
N,N’-Diphenylguanidine
C13H13N3
102-06-7
220.265 nd or lf (dil
al)
211.262 mcl nd (al,
to)
147(1)
170 dec
1.1320
4490
1,6-Diphenyl-1,3,5-hexatriene
C18H16
1720-32-7
232.320 lf (ace)
202(4)
4491
1,1-Diphenylhydrazine
C12H12N2
530-50-7
184.236 tab (lig)
50.5
22040
1.19016
4492
1,2-Diphenylhydrazine
Hydrazobenzene
C12H12N2
122-66-7
184.236 tab (al-eth)
128.7(0.5)
4493
Doxenitoin
C15H14N2O
3254-93-1
238.284 pl (MeOH)
183
4494
4495
4496
5,5-Diphenyl-4-imidazolidinone
Diphenyl isophthalate
Diphenylketene
Diphenyl maleate
C20H14O4
C14H10O
C16H12O4
744-45-6
525-06-4
7242-17-3
318.323
194.228 red-ye liq
268.264 pl (lig)
138
Diphenylethenone
4497
Diphenylmercury
C12H10Hg
587-85-9
354.80
4498
Diphenylmethane
C13H12
101-81-5
168.234 pr nd
HCP_Section_03.indb 230
1,3-Diphenylguanidine
Mercuriodibenzene
1.550020
1.74320
218.337 nd(al) or
orth
182.261 liq
8.2(0.4)
26.865​
(0.003)
73
25.22(0.02)
Solubility
i H2O; sl EtOH,
eth, bz; vs tol,
HOAc
vs bz, eth,
EtOH, peth
4484
4485
Oxybisbenzene
nD
247
sl H2O, EtOH,
eth; s bz
i H2O; s EtOH,
eth, ctc, HOAc
sl H2O, eth; s
EtOH, ace, bz
s tfa
s EtOH, eth, xyl,
MeOH
i H2O; s EtOH,
eth, bz, CS2
i H2O; msc
EtOH, eth; s bz
i H2O; s EtOH,
eth, CS2
vs bz
i H2O; s EtOH,
eth; sl tfa
i H2O, lig; vs
EtOH, eth; s
ace
i H2O; s eth, chl
i H2O; s EtOH,
eth, bz, HOAc;
sl chl
1.51025
i H2O; s EtOH,
eth, bz; sl ctc
i H2O; vs EtOH,
eth; s ace, bz
sl H2O; s EtOH,
ctc chl, tol; vs
eth
i H2O, EtOH, eth,
HOAc; s ace;
sl bz, chl
vs bz, eth,
EtOH, chl
vs EtOH; sl bz,
DMSO; i HOAc
1.15816
s chl
267.5
22615
1.110713 1.61514
20410
2.31825
264.2(0.3)
1.00126
1.575320
vs ace, bz, eth,
EtOH
i H2O; sl EtOH,
eth; s bz, chl
i H2O; s EtOH,
eth, chl
4/11/16 11:26 AM
Physical Constants of Organic Compounds
3-231
H
N
N
H
4462
4463
N,N’-Diphenyl-[1,1’-biphenyl]-4,4’-diamine
4464
trans,trans-1,4-Diphenyl-1,3-butadiene
4465
1,4-Diphenyl-1,3-butadiyne
4466
1,1-Diphenylbutane
O
1,2-Diphenylbutane
O
O
Cl
N
O
4467
4468
1,3-Diphenyl-1-butene
4470
trans-1,4-Diphenyl-2-butene-1,4-dione
1,3-Diphenyl-2-buten-1-one
4471
Diphenylcarbamic chloride
Organic
1,4-Diphenylbutane
4469
O
N
N
N
H
H
N
O
N C
4472
O
N
H
H
N
N
H
4477
4478
4479
4480
1,1-Diphenylethane
Diphenyl chlorophosphonate
O
H
N
S
Diphenyl disulfide
4476
2,2’-Diphenylcarbonic dihydrazide
Diphenyl carbonate
H
N
N
H
O
Diphenyl diselenide
O
O P O
Cl
4475
4474
N,N’-Diphenylcarbodiimide
S
Se
O
4473
Diphenylcarbazone
Se
N
H
N
O
4481
1,2-Diphenylethane
N,N’-Diphenylethanediamide
N
H
4482
N,N’-Diphenyl-1,2-ethanediamine
O
O P O
O
OH
O
O
N
OH
4483
4484
1,2-Diphenyl-1,2-ethanediol, (R *,R *)-(±)-
4485
1,1-Diphenylethene
H
N
O
4486
Diphenyl ether
Diphenyl 2-ethylhexyl phosphate
NH2
N
H
N
H
N
NH
4488
4489
2,5-Diphenylfuran
4490
N,N’-Diphenylguanidine
4491
1,6-Diphenyl-1,3,5-hexatriene
4487
N,N-Diphenylformamide
1,1-Diphenylhydrazine
N
H
4492
1,2-Diphenylhydrazine
O
O
O
H
N
N
H
4493
5,5-Diphenyl-4-imidazolidinone
O
O
C
O
O
O
Hg
O O
4494
Diphenyl isophthalate
4495
Diphenylketene
4496
Diphenyl maleate
4497
Diphenylmercury
4498
Diphenylmethane
Physical Constants of Organic Compounds
3-232
No.
Name
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
4499
4,4’-Diphenylmethane
diisocyanate
Diphenylmethanethione
Methylene diphenyl
diisocyanate
C15H10N2O2
101-68-8
C13H10S
4500
Physical
Form
mp/˚C
bp/˚C
den
g cm –3
250.252
40.41(0.01)
1965
1.19770
1450-31-3
198.283
53.5
17414
C13H12N2
622-15-1
196.247 nd (al)
142
>250
65(1)
302(6)
1.590650 s ace, bz,
PhNO2
sl EtOH, eth,
peth; vs bz,
chl
sl H2O, peth; s
EtOH, ace, bz;
vs eth
sl H2O; vs EtOH,
eth, ctc, chl; s
HOAc
i H2O
nD
Solubility
4501
N,N’-Diphenylmethanimidamide
4502
Diphenylmethanol
Benzohydrol
C13H12O
91-01-0
184.233 nd (lig)
4503
2-(Diphenylmethoxy)-N,Ndimethylethanamine
Diphenyl methylphosphonate
2-(Diphenylmethyl)-1-piperidineethanol
2,5-Diphenyloxazole
Diphenhydramine
C17H21NO
58-73-1
255.355 oil
C13H13O3P
C20H25NO
7526-26-3 248.214
13862-07-2 295.419
35
106.5
20513
1800.1
1.205120
Diphemethoxidine
C15H11NO
92-71-7
221.254 nd (lig)
71(3)
360
C17H14O
538-58-9
dec
C24H16N2
1662-01-7
234.292 pl or lf (ace, 113 dec
AcOEt)
332.397
220 dec
1.0940100 1.6231100 i H2O; vs EtOH,
eth; sl chl
i H2O; sl EtOH,
eth; s ace, chl
C12H10ClP
C12H11O3P
C20H14O4
1079-66-9
4712-55-4
84-62-8
220.634 hyg ye liq
234.187
318.323 pr (al, lig)
12
73
320
21826
25314
1.229
1.22325
Pipradrol
C18H21NO
467-60-7
267.366 cry (hx)
97.5
1081-75-0
778-22-3
120-46-7
196.288 liq
196.288
224.255
6
29.1(0.3)
77(3)
300
281(6)
1.00720 1.576020
0.998020
4504
4505
4506
Organic
4507
4508
4509
4510
4511
4512
1,5-Diphenyl-1,4-pentadien- Dibenzalacetone
3-one
4,7-Diphenyl-1,10-phenanthroline
Diphenylphosphinous chloride Chlorodiphenylphosphine
Diphenyl phosphonate
Diphenyl phthalate
Phenyl phthalate
1653
i H2O; sl EtOH,
eth, ctc
Dibenzoylmethane
C15H16
C15H16
C15H12O2
4516
4517
α,α-Diphenyl-2piperidinemethanol
1,3-Diphenylpropane
2,2-Diphenylpropane
1,3-Diphenyl-1,3-propanedione
1,3-Diphenyl-1-propanone
1,1-Diphenyl-2-propanone
Phenethyl phenyl ketone
1,1-Diphenylacetone
C15H14O
C15H14O
1083-30-3
781-35-1
210.271 lf (EtOH)
210.271
72.5
46
360
307
4518
1,3-Diphenyl-2-propanone
Dibenzyl ketone
C15H14O
102-04-5
34(1)
329(14)
4519
3,3-Diphenyl-2-propenal
β-Phenylcinnamaldehyde
C15H12O
1210-39-5
44.8
20514
4520
1,1-Diphenyl-1-propene
C15H14
778-66-5
210.271 cry (al,
peth)
208.255 pa ye pr
(lig)
194.272
49(5)
289(6)
4521
trans-1,3-Diphenyl-2-propen- Chalcone
1-one
C15H12O
614-47-1
208.255 pa ye lf, pr,
nd (peth)
56(4)
346 dec
4522
C20H25N
3540-95-2
279.420
41.5
2158
C15H12N2
C15H12N2O2
1145-01-3
3426-01-5
C12H10Se
1132-39-4
220.269 cry (al)
252.268 cry (EtOAc,
Diox)
233.17 ye nd (bz)
200
233.5
4525
Fenpiprane
1-(3,3-Diphenylpropyl)­
piperidine
3,5-Diphenyl-1H-pyrazole
1,4-Diphenyl-3,5-pyrazolidin- Phenopyrazone
edione
Diphenyl selenide
4526
4527
4528
Diphenylsilane
Diphenylsilanediol
Diphenyl succinate
C12H12Si
C12H12O2Si
C16H14O4
775-12-2
947-42-2
621-14-7
184.309
216.308
270.280 lf (al)
121
4529
Diphenyl sulfide
C12H10S
139-66-2
186.272 liq
-15.35(0.05) 294.2(0.5)
1.113620
4530
Diphenyl sulfone
C12H10O2S
127-63-9
127(3)
379
1.25220
4531
Diphenyl sulfoxide
C12H10OS
945-51-7
218.271 mcl pr(bz),​
pl(al)
202.271 pr(lig)
70.2(0.2)
34016
4532
N,N’-Diphenylthiourea
sym-Diphenylthiourea
C13H12N2S
102-08-9
228.312
153(1)
4533
1,3-Diphenyl-1-triazene
Diazoaminobenzene
C12H11N3
136-35-6
98
4534
N,N-Diphenylurea
C13H12N2O
603-54-3
197.235 ye lf or pr
(al)
212.246 tab (al)
189
dec
1.27625
4535
N,N’-Diphenylurea
C13H12N2O
102-07-8
212.246 orth pr (al)
236(3)
260 dec
1.23925
4513
4514
4515
4523
4524
HCP_Section_03.indb 232
Phenyl sulfide
Carbanilide
1.3
1.636020
1.557520
s EtOH, eth, chl,
dil NaOH
1.1950
1.536116 s EtOH, eth, bz,
chl, lig
i H2O; s EtOH,
eth, peth
1.025020 1.588020 i H2O; s EtOH,
bz
1.071262
i H2O; sl EtOH; s
eth, bz, chl,
CS2
301.5
1.35120
13416
0.996920
330
1.3225
1.550020 i H2O; msc
EtOH, eth; s
bz, xyl
1.580020 s ctc, CS2
sl DMSO
i H2O; s EtOH,
eth, ace, bz
1.633420 i H2O; s EtOH,
ctc; msc eth,
bz, CS2
i H2O; s EtOH,
eth, bz
vs EtOH, eth,
bz, HOAc; sl
chl; i peth
sl H2O; vs EtOH,
eth, chl, oils
i H2O; vs EtOH,
eth, bz, py
sl H2O; s EtOH,
eth, chl
sl H2O, EtOH; s
eth, py, HOAc;
i bz
4/11/16 11:26 AM
Physical Constants of Organic Compounds
3-233
S
O
C
N
N
C
O
4499
4501
4500
4,4’-Diphenylmethane diisocyanate
N
4502
N,N’-Diphenylmethanimidamide
Diphenylmethanethione
4505
N
4506
4507
2,5-Diphenyloxazole
O
N
4508
1,5-Diphenyl-1,4-pentadien-3-one
4504
Diphenyl methylphosphonate
4509
4,7-Diphenyl-1,10-phenanthroline
Diphenylphosphinous chloride
O
P
OH
4510
Diphenyl phosphonate
Organic
2-(Diphenylmethyl)-1-piperidineethanol
2-(Diphenylmethoxy)-N,N-dimethylethanamine
Cl
P
O
OH
4503
Diphenylmethanol
O
N
O
O P O
N
O
OH
H
N
N
O
N
H
O
O
O
OH
O
O
O
O
4511
4513
4512
α,α-Diphenyl-2-piperidinemethanol
Diphenyl phthalate
1,3-Diphenylpropane
4514
4515
2,2-Diphenylpropane
4516
1,3-Diphenyl-1,3-propanedione
1,3-Diphenyl-1-propanone
O
4517
1,1-Diphenyl-2-propanone
N
O
N
H
O
4518
1,3-Diphenyl-2-propanone
4520
4519
4522
4521
1,1-Diphenyl-1-propene
3,3-Diphenyl-2-propenal
1-(3,3-Diphenylpropyl)piperidine
trans-1,3-Diphenyl-2-propen-1-one
N
4523
3,5-Diphenyl-1H-pyrazole
O
O
N
NH
H
Se
Si
H
O
HO OH
Si
O
O O
S
S
O
O
4524
1,4-Diphenyl-3,5-pyrazolidinedione
4525
4526
Diphenyl selenide
Diphenylsilane
4527
Diphenylsilanediol
4528
4529
Diphenyl succinate
Diphenyl sulfide
4530
Diphenyl sulfone
O
O
S
S
N
H
4531
Diphenyl sulfoxide
N
N
H
4532
N,N’-Diphenylthiourea
N
H
N
4533
1,3-Diphenyl-1-triazene
N
NH2
O
N
H
4534
N,N-Diphenylurea
N
H
4535
N,N’-Diphenylurea
Physical Constants of Organic Compounds
3-234
No.
Name
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
4536
Diphosgene
Carbonochloridic acid,
trichloromethyl ester
C2Cl4O2
503-38-8
4537
4538
4539
4540
4541
C12H24N2
C11H22N2
C13H26N2
C16H10Cl4O5
C10H14O5
4545
4546
1,2-Dipiperidinoethane
1,1’-Dipiperidinomethane
1,1’-Methylenedipiperidine
1,3-Di-4-piperidylpropane
4,4’-Trimethylenedipiperidine
Diploicin
Di-2-propenoyldiethyleneglycol
Di-2-propenoyl-2,2-dimethyl- 2-Propenoic acid,
1,3-propanediol
2,2-dimethyl-1,3-propanediyl
ester
Di-2-propenoyl-1,6-hexane- 2-Propenoic acid,
diol
1,6-hexanediyl ester
Dipropetryn
6-(Ethylthio)-N,N’-diisopropyl1,3,5-triazine-2,4-diamine
1,2-Dipropoxyethane
Dipropoxymethane
Formaldehyde, dipropyl acetal
mp/˚C
bp/˚C
den
g cm –3
197.832 liq
-57
128
1.652514 1.456622 vs eth, EtOH
1932-04-3
880-09-1
16898-52-5
527-93-5
4074-88-8
196.332 liq
182.306
210.358
424.059
214.215
-0.5
265
230
329
0.916025 1.485325
0.926920 1.482020
200
1.111025 1.459525
C11H16O4
2223-82-7
212.243
C12H18O4
13048-33-4 226.269
C11H21N5S
4147-51-7
C8H18O2
C7H16O2
18854-56-3 146.228 liq
505-84-0
132.201 liq
-97.3
161(13)
140.5
4547
4548
N,N-Dipropylacetamide
Dipropyl adipate
Dipropyl hexanedioate
C8H17NO
C12H22O4
1116-24-1
106-19-4
143.227
230.301
-15.7
227(13)
15111
4549
Dipropylamine
N-Propyl-1-propanamine
C6H15N
142-84-7
101.190 liq
-63
107.5(0.9)
4550
4-[(Dipropylamino)­sulfonyl]­
benzoic acid
N,N-Dipropylaniline
Probenecid
C13H19NO4S
57-66-9
285.360
195
C12H19N
2217-07-4
177.286 ye lf
241(4)
EPTC
C9H19NOS
759-94-4
189.318
12720
4553
Dipropylcarbamothioic acid,
S-ethyl ester
Dipropyl carbonate
C7H14O3
623-96-1
146.184
166(4)
4554
4555
Dipropyl disulfide
Dipropylene glycol
C6H14S2
C6H14O3
629-19-6
150.305 liq
25265-71-8 134.173
4556
4557
C20H22O5
C7H16O3
27138-31-4 342.386
34590-94-8 148.200 liq
-80
1971
203(14)
4558
Dipropylene glycol dibenzoate
Dipropylene glycol
1-(2-Methoxyisopropoxy)-2monomethyl ether
propanol
Dipropyl ether
Propyl ether
C6H14O
111-43-3
-114.8(0.4)
90.1(0.3)
4559
4560
Dipropyl fumarate
Dipropyl maleate
C10H16O4
C10H16O4
14595-35-8 200.232
2432-63-5 200.232
4561
Dipropyl oxalate
C8H14O4
615-98-5
174.195 liq
-44.3
212(3)
4562
C9H15NO3
512-12-9
185.220
42.5
1493
4563
4564
4565
5,5-Dipropyl-2,4-oxazolidinedione
Dipropyl succinate
Dipropyl sulfate
Dipropyl sulfide
C10H18O4
C6H14O4S
C6H14S
925-15-5
598-05-0
111-47-7
202.248 liq
182.238
118.240 liq
-5.9
4566
Dipropyl sulfone
C6H14O2S
598-03-8
150.239 cry
28(2)
4567
4568
4569
C6H14OS
C24H40N8O4
C10H8N2O2S2
4253-91-2
58-32-2
3696-28-4
134.239 nd
504.627
252.313 cry (MeOH)
25(1)
163
205
802
4570
4571
4572
4573
4574
4575
Dipropyl sulfoxide
Dipyridamole
Di-2-pyridinyl disulfide,
N,N’-dioxide
2,2’-Dipyrrolylmethane
Diquat
Diquat dibromide
Disodium calcium EDTA
Disodium hydrogen citrate
Disperse Blue No. 1
C9H10N2
C12H12N2
C12H12Br2N2
C10H12CaN2Na2O8
C6H6Na2O7
C14H12N4O2
21211-65-4
2764-72-9
85-00-7
62-33-9
144-33-2
2475-45-8
146.188
184.236
344.044
374.268
236.088
268.271
73
16412
4576
4577
Distearyl thiodipropionate
Disulfiram
C42H82O4S
C10H20N2S4
693-36-7
97-77-8
683.163 cry
296.539
61
71.5
11717
4578
4579
4580
Disulfoton
1,2-Dithiane
1,3-Dithiane
C8H19O2PS3
C4H8S2
C4H8S2
298-04-4
505-20-4
505-23-7
274.405
120.237 nd
120.237
-25
32.5
54.0(0.3)
1080.01
8014
8914
4542
4543
4544
Organic
4551
4552
HCP_Section_03.indb 234
Dipyrithione
Edetate calcium disodium
Sodium acid citrate
1,4,5,8-Tetraamino-9,10anthracenedione
Dioctadecyl thiobispropanoate
Physical
Form
67.1
232
nD
Solubility
vs H2O
1.454225
1.01025
255.384
105.0(0.5)
102.174 liq
-85.4(0.1)
196(1)
231(2)
1105
12612
lf or nd (al)
Cation
248(7)
12020
-102.68(0.04) 142.8(0.8)
337
pow
wh pow (w) 149 dec
red-br nd
331
0.831225 1.401325
0.834520 1.393919 vs ace, bz, eth,
EtOH
0.899217 1.441917 vs EtOH
0.979020 1.431420 vs eth, EtOH,
chl
0.740020 1.405020 s H2O, EtOH;
msc eth; vs
ace, bz
0.910420 1.527120 i H2O; s EtOH,
eth, ace, bz; sl
ctc
0.954630
0.943520 1.400820 sl H2O; msc
EtOH, eth
0.959920 1.498120
1.020620
msc H2O; s
EtOH
0.95
1.419020
0.746620 1.380920 sl H2O; vs eth,
EtOH
1.012920 1.443520 s EtOH, eth
1.024520 1.443420 i H2O; s EtOH,
eth, ace, bz
1.018820 1.415820 sl H2O; msc
EtOH; s eth
1.002020 1.425020 vs ace, bz, eth
1.106420 1.413520 vs peth
0.81417 1.448720 i H2O; s EtOH,
eth
1.027850 1.445630 sl H2O; s EtOH,
eth
0.965420 1.466320 vs eth, EtOH
vs bz, eth, EtOH
1.2420
s H2O
vs H2O
i H2O; s EtOH; sl
eth; vs chl
1.14420
1.598125 s eth, bz, chl
1.598125 vs bz, eth, chl
4/11/16 11:26 AM
Physical Constants of Organic Compounds
3-235
O
O
Cl
Cl
N
Cl
Cl
O
N
N
N
HO
HN
4537
4536
Cl
Cl
4540
1,3-Di-4-piperidylpropane
1,1’-Dipiperidinomethane
O
O
NH
4539
4538
1,2-Dipiperidinoethane
Diphosgene
Cl
O
Cl
Diploicin
HN
O
O
O
O
O
O
O
O
O
O
O
N
H
O
O
4542
4541
N
S
N
4543
Di-2-propenoyl-2,2-dimethyl-1,3-propanediol
Di-2-propenoyldiethyleneglycol
N
4544
Di-2-propenoyl-1,6-hexanediol
Dipropetryn
O
O
O
O
4545
HO
N
O
4546
1,2-Dipropoxyethane
O
O
4547
Dipropoxymethane
H
N
O
4548
N,N-Dipropylacetamide
Organic
O
4549
Dipropyl adipate
Dipropylamine
O
N
O
O S O
N
4550
4551
4-[(Dipropylamino)sulfonyl]benzoic acid
N,N-Dipropylaniline
O
S
O
4553
Dipropylcarbamothioic acid, S-ethyl ester
Dipropyl carbonate
O
O
O
Dipropyl disulfide
O
OH
O
OH
4555
4556
Dipropylene glycol
4557
Dipropylene glycol dibenzoate
O
O
O O
O
4559
O
O
O
4561
Dipropyl maleate
O
NH
O
O
4560
Dipropyl fumarate
Dipropyl ether
O
O
O
4558
Dipropylene glycol monomethyl ether
O
O
S
4554
O
O
O
O
O
4552
O
HO
S
N
4562
Dipropyl oxalate
O
O
4563
5,5-Dipropyl-2,4-oxazolidinedione
Dipropyl succinate
OH
N
N
N
HO
O O
S
O
O
4564
Dipropyl sulfate
4565
4566
Dipropyl sulfide
N
O
OH
4567
Dipropyl sulfone
OH
N
O
S
O O
S
S
N
N
N
N
4568
Dipropyl sulfoxide
S S
N
O
4569
Dipyridamole
Di-2-pyridinyl disulfide, N,N’-dioxide
2
COO
N
H
N
H
4570
2,2’-Dipyrrolylmethane
NH2 O
OOC
2Br
N
N
N
4571
2Na
N
OH
O
OH
2Na
OH
4574
Disodium calcium EDTA
Disodium hydrogen citrate
NH2
S
4575
HO
COO
4573
Diquat dibromide
O
NH2 O
Ca
O
OOC
4572
Diquat
N
N
O
2
NH2
Disperse Blue No. 1
O
N
O
S
4576
Distearyl thiodipropionate
O
S
S
S
4577
Disulfiram
N
S
O P O
S
4578
Disulfoton
S
S
S
S
4579
1,2-Dithiane
S
4580
1,3-Dithiane
Physical Constants of Organic Compounds
3-236
Organic
Mol. Form.
CAS RN
Mol.
Wt.
1,4-Dithiane
C4H8S2
505-29-3
4582
4583
Dithianone
Dithiazanine iodide
C14H4N2O2S2
C23H23IN2S2
3347-22-6
514-73-8
4584
2,2’-Dithiobisbenzoic acid
C14H10O4S2
119-80-2
4585
4586
4587
3,3’-Dithiobispropanoic acid
3,3’-Dithiobis-D-valine
2,5-Dithiobiurea
C6H10O4S2
C10H20N2O4S2
C2H6N4S2
1119-62-6 210.271
20902-45-8 296.407
142-46-1
150.226 nd (w)
156(3)
204.5
214
4588
4589
4590
4591
4592
4593
4,4’-Dithiodimorpholine
1,2-Dithiolane
1,3-Dithiolane
1,3-Dithiolane-2-thione
Dithiopyr
Dithizone
C8H16N2O2S2
C3H6S2
C3H6S2
C3H4S3
C15H16F5NO2S2
C13H12N4S
103-34-4
557-22-2
4829-04-3
822-38-8
97886-45-8
60-10-6
124.5
77
-50
35
65
167 dec
4594
4595
Di(p-tolyl)carbodiimide
1,2-Di(p-tolyl)ethane
C15H14N2
C16H18
726-42-1
538-39-6
236.355
106.210
106.210 liq
136.259
401.416
256.326 bl-blk
(chl-al)
222.285
210.314 lf (al)
4596
N,N’-Di(o-tolyl)guanidine
C15H17N3
97-39-2
239.316 cry (dil al)
179
4597
4598
4599
4600
4601
4602
4603
4604
4605
Ditridecyl phthalate
Diundecyl phthalate
Diuron
o-Divinylbenzene
m-Divinylbenzene
p-Divinylbenzene
cis-1,2-Divinylcyclobutane
trans-1,2-Divinylcyclobutane
Divinyl ether
1,2-Divinylbenzene
1,3-Divinylbenzene
1,4-Divinylbenzene
C34H58O4
C30H50O4
C9H10Cl2N2O
C10H10
C10H10
C10H10
C8H12
C8H12
C4H6O
119-06-2
3648-20-2
330-54-1
91-14-5
108-57-6
105-06-6
16177-46-1
6553-48-6
109-93-3
530.823 liq
474.716 cry (EtOH)
233.093
130.186
130.186
130.186
108.181
108.181
70.090 vol liq or
gas
-52.2(0.2)
30(2)
4606
Divinyl sulfide
Vinyl sulfide
C4H6S
627-51-0
4607
4608
C4H6O2S
C8H18OSi2
4609
4610
Divinyl sulfone
Vinyl sulfone
1,3-Divinyl-1,1,3,3-tetramethyldisiloxane
Djenkolic acid
DMPA
4611
Docosane
4612
Docosanoic acid
4613
1-Docosanol
4614
4615
4616
13-Docosenamide
1-Docosene
cis-13-Docosenoic acid
4617
4618
4619
4620
4621
trans-13-Docosenoic acid
5,7-Dodecadiyne
Dodecamethylcyclohexasiloxane
Dodecamethylpentasiloxane
Dodecanal
4622
No.
Name
4581
Synonym
Diphenyl disulfide-2,2’-dicarboxylic acid
1,2-Hydrazinedicarbothioamide
1,3-Dithiacyclopentane
1,2-Bis(p-tolyl)ethane
Physical
Form
mp/˚C
bp/˚C
120.237 mcl pr
111.4(0.3)
199.5
296.324 nd (ace)
518.476 grn nd
(MeOH)
306.357
220
248 dec
den
g cm –3
nD
sl H2O; s EtOH,
eth, ctc, CS2,
HOAc
i H2O
289.5
58.5
81.8(0.5)
i H2O; s EtOH,
eth
s chl
9027
175
307
1.25917
1.597515 s EtOH, eth, xyl
i H2O; sl EtOH,
eth; s chl, alk
22120
17818
1.150020
i H2O; sl EtOH; s
bz, peth
sl H2O, tfa,
EtOH; vs eth; s
chl
1.1020
2853.5
438(25)
0.95225
-101(1)
8214
12176
9518
3838
112.5
28(3)
0.932522
0.929420
0.91340
0.801020
0.781720
0.77320
86.156
20
84(4)
0.917415
77-77-0
2627-95-4
118.155 liq
186.399 liq
-26
-99.7
234.5
39
1.17725
0.81120
C7H14N2O4S2
C10H14Cl2NO2PS
498-59-9
299-85-4
254.327 nd(w)
314.169 solid
≈325 dec
51.8(0.3)
1502
C22H46
629-97-0
43.8(0.3)
369(5)
0.794420 1.445520
C22H44O2
112-85-6
310.600 pl(to), cry
(eth)
340.583 nd
80.6(0.1)
30660
0.822390 1.4270100
C22H46O
661-19-8
326.599 cry (ace,
chl)
71(1)
1800.22
C22H43NO
C22H44
C22H42O2
112-84-5
1599-67-3
112-86-7
337.582 cry
308.584
338.567 nd (al)
94
38
33.0(0.5)
367
26515
0.79425
0.86055
C22H42O2
C12H18
C12H36O6Si6
506-33-2
1120-29-2
540-97-6
338.567 pl (al)
162.271
444.923 liq
61.9
0.858557
-4.2(0.2)
28230
1038
245.0(0.2)
C12H36O4Si5
C12H24O
141-63-9
112-54-9
384.840 liq
184.318 lf
-80
44(4)
229.9(0.1)
185100
Dodecanamide
C12H25NO
1120-16-7
199.333 nd
101(2)
19912
4623
Dodecane
C12H26
112-40-3
170.334 liq
-9.55(0.02)
216.3(0.2)
4624
4625
1,12-Dodecanediamine
Dodecanedioic acid
C12H28N2
C12H22O4
2783-17-7
693-23-2
200.363
230.301
68(1)
126.6(0.8)
1353
22225
HCP_Section_03.indb 236
Behenic acid
Erucamide
Erucic acid
Brassidic acid
Dibutylbutadiyne
Lauraldehyde
35.5
157(1)
Solubility
1.576720
1.576020
1.583525
1.456320
1.445120
1.398920
s ace, bz
s ace, bz
s ace, bz
i H2O; msc
EtOH, eth, ace,
chl
sl H2O; s ace;
msc EtOH, eth
1.476520
1.412320
sl H2O; vs bz,
ctc, ace
i H2O; s EtOH,
chl; vs eth
sl H2O, EtOH,
eth
sl H2O, eth; vs
EtOH, MeOH; s
chl
1.475820 i H2O; s EtOH,
ctc; vs eth,
MeOH
1.4347100
0.967225 1.401520 i H2O
0.875520 1.392520 s ctc, CS2
0.835215 1.43522 i H2O; sl EtOH; s
eth
1.4287110 i H2O; s EtOH,
ace, ctc; sl
eth, bz
0.749520 1.421020 i H2O; vs EtOH,
eth, ace, ctc,
chl
1.1525
s tfa
4/11/16 11:26 AM
Physical Constants of Organic Compounds
3-237
O
N
S
S
S
N
O
4581
I
N
S
N
4583
Dithianone
OH
S
NH2
O
HO
S
S
4585
2,2’-Dithiobisbenzoic acid
H 2N
N
H
H
N
S
S
NH2
O
S
4587
N S S N
O
S
4588
2,5-Dithiobiurea
S
S
4589
4,4’-Dithiodimorpholine
S
S
4590
1,2-Dithiolane
S
F
F
1,3-Dithiolane
3,3’-Dithiobis-D-valine
S
S
F
F
N
N
F
4592
1,3-Dithiolane-2-thione
OH
NH2
O
N
4591
S
4586
3,3’-Dithiobispropanoic acid
O
S
O
S
O
O
4584
Dithiazanine iodide
HO
OH
O
S
S
4582
1,4-Dithiane
S
HO
N
H
H
N
4593
Dithiopyr
Dithizone
Organic
O
O
H
N
N C N
O
O
H
N
NH
4594
4595
Di(p-tolyl)carbodiimide
1,2-Di(p-tolyl)ethane
O
H
N
Cl
O
O
4598
4600
Diuron
4601
o-Divinylbenzene
O O
4605
4606
4607
Divinyl ether
Divinyl sulfide
Divinyl sulfone
Si
O
4603
p-Divinylbenzene
cis-1,2-Divinylcyclobutane
O
HO
Si
4602
m-Divinylbenzene
O
S
S
Ditridecyl phthalate
N
4599
Diundecyl phthalate
O
4597
N,N’-Di(o-tolyl)guanidine
O
Cl
O
O
4596
S
S
NH2
4608
O
OH
NH2
Cl
Cl
4609
1,3-Divinyl-1,1,3,3-tetramethyldisiloxane
4604
trans-1,2-Divinylcyclobutane
S H
N
P
O
4610
Djenkolic acid
4611
DMPA
Docosane
O
O
O
NH2
OH
OH
OH
4612
4613
Docosanoic acid
4614
1-Docosanol
O
Si
OH
O
4617
4618
trans-13-Docosenoic acid
4615
13-Docosenamide
5,7-Dodecadiyne
Si
O
Si
O
O
Si
O
Si
4616
1-Docosene
cis-13-Docosenoic acid
Si
O
Si
4619
O
Si
O
Si
O
Si
O
Si
O
4620
Dodecamethylcyclohexasiloxane
4621
Dodecamethylpentasiloxane
Dodecanal
O
O
HO
4622
Dodecanamide
NH2
H2N
NH2
4623
Dodecane
4624
1,12-Dodecanediamine
OH
O
4625
Dodecanedioic acid
Physical Constants of Organic Compounds
3-238
No.
Name
4626
1,12-Dodecanediol
4627
Dodecanenitrile
4628
1-Dodecanethiol
4629
Dodecanoic acid
4630
4631
Synonym
Mol. Form.
CAS RN
C12H26O2
5675-51-4
C12H23N
Mol.
Wt.
Physical
Form
mp/˚C
bp/˚C
den
g cm –3
nD
Solubility
Organic
81.3
18912
2437-25-4
202.333 cry (bz, dil
al)
181.318
4.0(0.2)
276.1(0.5)
C12H26S
112-55-0
202.399 liq
-6.7
277(3)
Lauric acid
C12H24O2
143-07-7
200.318 nd (al)
43.82(0.02)
225100
Dodecanoic anhydride
1-Dodecanol
Lauryl alcohol
C24H46O3
C12H26O
645-66-9
112-53-8
382.620 lf (al, eth)
186.333 lf (dil al)
41.8
24.2(0.3)
264.1(0.3)
4632
4633
2-Dodecanol
2-Dodecanone
Decyl methyl ketone
C12H26O
C12H24O
10203-28-8 186.333
6175-49-1 184.318
19
21
249(11)
247(6)
4634
4635
Dodecanoyl chloride
1-Dodecene
C12H23ClO
C12H24
112-16-3
112-41-4
218.763
168.319 liq
-17
14518
-35.19(0.05) 213.4(0.9)
4636
trans-2-Dodecenedioic acid
C12H20O4
6402-36-4
228.285 cry (al,ace)
165.5
4637
2-Dodecenylsuccinic
anhydride
Dodecyl acetate
Dodecyl acrylate
Dodecylamine
C16H26O3
19780-11-1 266.375 hyg cry
42
1815
C14H28O2
C15H28O2
C12H27N
112-66-3
2156-97-0
124-22-1
228.371
240.382
185.349
1.2(0.2)
4
27.8(0.7)
265
1200.8
255(2)
C14H31NO2
C12H28ClN
C18H31N
C18H30
C18H30O3S
2016-56-0
929-73-7
104-42-7
123-01-3
121-65-3
245.402
221.810
261.446
246.431
326.494
69.5
182(2)
41.5
-2(5)
C18H36
C14H28O2S
C16H30O2
C14H28O
C14H30O2
C25H34O3
1795-17-1
3746-39-2
142-90-5
3234-28-4
4536-30-5
2985-59-3
252.479
260.436
254.408
212.371 oil
230.387
382.536
12.6(0.4)
1.5
C18H30O
C17H35N
C12H26O4S
C20H42O5
104-43-8
5917-47-5
151-41-7
5274-68-0
262.430 nd (bz)
253.467 pa ye
266.397 cry
362.544
66
C19H30O5
1166-52-5
338.438
96.5
s ace
C15H34ClN
112-00-5
263.891
246 dec
vs H2O, ace,
EtOH, chl
C12H22
C12H22
765-03-7
6975-99-1
166.303 liq
166.303
-19
2439-10-3
287.442
137.5(0.5)
51-61-6
153.179 pr
113-53-1
544-85-4
295.442
450.866 pl (bz,​chl,​
HOAc,eth)
4638
4639
4640
4641
4642
4643
4644
4645
Lauronitrile
Traumatic acid
Lauryl 2-propenoate
1-Dodecanamine
4658
4659
Dodecylamine, acetate
Dodecylamine hydrochloride
4-Dodecylaniline
Dodecylbenzene
4-Dodecylbenzenesulfonic
acid
Dodecylcyclohexane
Dodecyl mercaptoacetate
Dodecyl methacrylate
Dodecyloxirane
2-(Dodecyloxy)ethanol
4-Dodecyloxy-2-hydroxybenzophenone
4-Dodecylphenol
1-Dodecylpiperidine
Dodecyl sulfate
Dodecyltetraethylene glycol
monoether
Dodecyl 3,4,5-trihydroxybenzoate
Dodecyltrimethylammonium
chloride
1-Dodecyne
6-Dodecyne
4660
Dodine
4661
Dopamine
4662
4663
Dothiepin
Dotriacontane
Dodecylguanidine,
C15H33N3O2
monoacetate
4(2-Aminoethyl)-1,2-benzene- C8H11NO2
diol
C19H21NS
Bicetyl
C32H66
4664
4665
4666
Doxepin
Doxorubicin
Doxorubicin hydrochloride
Adriamycin
Adriamycin hydrochloride
4667
4668
4669
Doxylamine
Drimenin
Dromostanolone propanoate
4646
4647
4648
4649
4650
4651
4652
4653
4654
4655
4656
4657
HCP_Section_03.indb 238
1-Dodecanamine, acetate
Lauryl amine hydrochloride
Laurylbenzene
1,2-Epoxytetradecane
Lauryl sulfate
3,6,9,12-Tetraoxatetracosan1-ol
Decylacetylene
2-Methyl-17-(1-oxopropoxy)­
androstan-3-one, (2α,5α,17β)
21110
329(4)
>205
331
1713
1424
950.4
1430.8
0.824020 1.436120 i H2O; msc
EtOH, eth, ace,
bz, chl
0.84420 1.458920 i H2O; s EtOH,
eth, chl
0.867950 1.418382 i H2O; vs EtOH,
eth; s ace;
msc bz
0.853370 1.429270 vs EtOH
0.830924
i H2O; s EtOH,
eth; sl bz
0.828620 1.440020
0.819820 1.433020 i H2O; s EtOH,
eth, ace; sl ctc
0.916925 1.445820 vs eth
0.758420 1.430020 i H2O; s EtOH,
eth, ace, ctc,
peth
vs eth, EtOH,
chl
0.865222 1.443920
0.872720
0.801520 1.442120 sl H2O; msc
EtOH, eth, bz,
chl
vs H2O, EtOH
vs H2O, EtOH
0.855120 1.482420 i H2O
0.822320 1.455920
0.86620
0.845
1.440820
43.5
1752
1615
0.837820 1.458820
s H2O
24710
56
69.7(0.3)
215
213(9)
1720.05
470(14)
C19H21NO
C27H29NO11
C27H30ClNO11
1668-19-5 279.376 oily liq
23214-92-8 543.519 cry
230
25316-40-9 579.980 oran-red nd 204 dec
1550.03
C17H22N2O
C15H22O2
C23H36O3
469-21-6
2326-89-8
521-12-0
1390.5
1100.1
270.369 liq
234.335 cry
360.530
s tfa
133
130(1)
0.778820 1.434020
0.78520 1.444220 vs ace, eth,
EtOH
0.812420 1.455020 i H2O; sl EtOH,
chl; s eth, ctc;
vs bz
s H2O, MeOH; i
ace, bz, chl,
eth, peth
i H2O
4/11/16 11:27 AM
Physical Constants of Organic Compounds
3-239
O
N
OH
HO
4626
4627
1,12-Dodecanediol
O
OH
SH
4628
Dodecanenitrile
4629
1-Dodecanethiol
Dodecanoic acid
O
O
OH
4630
Dodecanoic anhydride
O
OH
4631
4632
1-Dodecanol
4633
2-Dodecanol
2-Dodecanone
O
O
HO
Cl
OH
O
O
4634
4635
Dodecanoyl chloride
1-Dodecene
4637
trans-2-Dodecenedioic acid
2-Dodecenylsuccinic anhydride
NH2 HO
O
O
NH2
O
4638
4639
Dodecyl acetate
O
4640
Dodecyl acrylate
4641
Dodecylamine
Dodecylamine, acetate
Organic
O
O
O
4636
OH
O S O
NH2
NH2 HCl
4642
4643
Dodecylamine hydrochloride
4644
4-Dodecylaniline
4645
Dodecylbenzene
4-Dodecylbenzenesulfonic acid
O
O
O
4646
4647
Dodecylcyclohexane
O
O
SH
4648
Dodecyl mercaptoacetate
4649
Dodecyl methacrylate
Dodecyloxirane
OH
O HO
N
O
OH
O
4651
4650
4653
4652
4-Dodecyloxy-2-hydroxybenzophenone
2-(Dodecyloxy)ethanol
1-Dodecylpiperidine
4-Dodecylphenol
O
HO
O
O
S
O
O
O
OH
O
O
OH
O
HO
OH
4654
4655
4656
Dodecyltetraethylene glycol monoether
Dodecyl sulfate
Dodecyl 3,4,5-trihydroxybenzoate
H
N
Cl
N
NH2
OH
NH
4657
4658
Dodecyltrimethylammonium chloride
4659
1-Dodecyne
O
4660
6-Dodecyne
Dodine
OH
O
O
OH
N
NH2
N
O
S
OH
4661
4662
Dopamine
O
Dothiepin
OH
O
OH
O
OH
O O
HO
4663
Dotriacontane
OH
O O
O
HO
HO
O
O
OH
NH2
4664
4665
Doxepin
Doxorubicin
OH
O
HCl
N
O
O
O
H
O
NH2
4666
Doxorubicin hydrochloride
N
H
4667
Doxylamine
4668
Drimenin
O
H
4669
Dromostanolone propanoate
Physical Constants of Organic Compounds
3-240
Organic
No.
Name
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
4670
Droperidol
Dehydrobenzperidol
C22H22FN3O2
548-73-2
379.427 cry (w)
146 (hyd)
4671
4672
4673
Dydrogesterone
Dyphylline
Ecgonidine
C21H28O2
C10H14N4O4
C9H13NO2
152-62-5
479-18-5
484-93-5
172(1)
161.5
228 dec
vs H2O
4674
4675
4676
Ecgonine
Echimidine
Echinochrome A
C9H15NO3
C20H31NO7
C12H10O7
481-37-8
520-68-3
517-82-8
205
vs H2O, EtOH
4677
Echitamine
C22H30N2O5
6871-44-9
312.446 cry (ace/hx)
254.243
167.205 cry (MeOH)
(MeOHeth)
185.220 mcl pr
397.463 glass
266.203 red nd
(Diox-w)
402.483
4678
Edrophonium chloride
C10H16ClNO
116-38-1
201.693 cry
162
4679
Efloxate
C19H16O5
119-41-5
324.327
123.7
4680
4681
Eicosamethylnonasiloxane
Eicosane
C20H60O8Si9
C20H42
2652-13-3
112-95-8
681.455
282.547 lf (al)
36.48(0.01)
307.5
344.1(0.9)
4682
Eicosanedioic acid
4683
2-Ethyl-3,5,6,7,8-pentahydroxy-1,4-naphthalenedione
Ethyl [(4-oxo-2-phenyl-4H-1benzopyran-7-yl)oxy]acetate
Physical
Form
mp/˚C
220 dec
bp/˚C
den
g cm –3
nD
Solubility
i H2O; sl EtOH,
eth, bz; s chl,
DMF
120 sub
sl H2O; s EtOH,
ace; vs eth, bz
s H2O, EtOH,
eth, chl, con
sulf; i peth
vs H2O; s EtOH;
i eth, chl
s chl
206
C20H38O4
2424-92-2
342.514 cry (bz,al)
125.5
2332
Eicosanoic acid
1,18-Octadecanedicarboxylic
acid
Arachidic acid
0.917320 1.398020 vs bz
0.788620 1.442520 i H2O; s eth,
peth, bz; sl
chl; vs ace
s eth
C20H40O2
506-30-9
312.531 pl (al)
75.06(0.02)
400(6)
0.8240100 1.425100
4684
1-Eicosanol
Arachic alcohol
C20H42O
629-96-9
298.546 wax (al), cry 63.9(0.9)
(chl)
356
0.840520 1.435020
4685
5,8,11,14-Eicosatetraenoic
acid, (all-cis)
Arachidonic acid
C20H32O2
506-32-1
304.467
-38(2)
1631
0.908220 1.482420
4686
4687
4688
4689
4690
1-Eicosene
cis-9-Eicosenoic acid
trans-9-Eicosenoic acid
cis-11-Eicosenoic acid
Elaidic acid
C20H40
C20H38O2
C20H38O2
C20H38O2
C18H34O2
3452-07-1
29204-02-2
506-31-0
2462-94-4
112-79-8
280.532
310.515
310.515
310.515
282.462 pl (al)
28.5
24.5
54
24
44.0(0.5)
341
2206
0.788230 1.444030
0.888225 1.459725
26715
288100
4691
4692
4693
4694
Elaiomycin
1,3-Elemadien-11-ol
β-Elemene
Embelin
C13H26N2O3
C15H26O
C15H24
C17H26O4
23315-05-1
639-99-6
33880-83-0
550-24-3
258.356 ye oil
222.366 cry (al)
204.352
294.386 oran pl (al)
0.882625
vs EtOH, MeOH
0.873445 1.449945 i H2O; s EtOH,
eth, bz, chl
1.479825 sl H2O; s os
0.934518 1.498018
0.874920 1.493520
vs bz, eth, EtOH
4695
Emetine
C29H40N2O4
483-18-1
480.639 amor pow
74
4696
Emylcamate
C7H15NO2
78-28-4
145.200 nd
57
351
4697
Enallylpropymal
C11H16N2O3
1861-21-8
56.5
17712
4698
4699
4700
4701
Endosulfan
Endosulfan sulfate
Endothall disodium
Endrin
C9H6Cl6O3S
C9H6Cl6O4S
C8H8Na2O5
C12H8Cl6O
115-29-7
1031-07-8
129-67-9
72-20-8
224.256 cry (w, dil
al)
406.925
422.925 cry (cyhex)
230.13
380.909 cry
106
181
144
dec 245
1060.7
4702
4703
Enflurane
Ephedrine, (±)-
C3H2ClF5O
C10H15NO
13838-16-9 184.492 liq
90-81-3
165.232 nd (eth,
peth)
76.5
56.8(0.5)
13512
4704
d-Ephedrine
C10H15NO
321-98-2
165.232 pl (w)
40
225
4705
l-Ephedrine
C10H15NO
299-42-3
165.232 pl (w + 1)
40
225
4706
Ephedrine hydrochloride
C10H16ClNO
50-98-6
201.693 orth nd
219
4707
Epichlorohydrin
C3H5ClO
13403-37-7 92.524
HCP_Section_03.indb 240
Icosane
Gadoleic acid
Gondoic acid
trans-9-Octadecenoic acid
Elemol
2,5-Dihydroxy-3-undecyl-2,5cyclohexadiene-1,4-dione
6’,7’,10,11-Tetramethoxyemetan
3-Methyl-3-pentanol,
carbamate
α-[1-(Methylamino)­ethyl]­
benzenemethanol,
(R*,S*)-(±)α-[1-(Methylamino)­ethyl]­
benzenemethanol,
[S-(R*,S*)]α-[1-(Methylamino)­ethyl]­
benzenemethanol,
[R-(R*,S*)]2-(Methylamino)-1-phenyl-1propanol, hydrochloride
(Chloromethyl)oxirane
liq
52.5
14212
12016
142.5
-26
i H2O; sl EtOH;
vs eth; s bz,
chl
i H2O; sl EtOH,
chl; vs ace; s
bz, peth
i H2O; vs ace,
eth, EtOH,
peth
i H2O; s bz, peth
i H2O; s EtOH,
eth, ace; sl bz,
chl
sl H2O; vs bz,
eth, EtOH
vs bz, eth,
EtOH, chl
1.74520
1.43120
1.512125 1.302520
1.122020
vs ace, bz, xyl;
s ctc, hx
vs os
s H2O, EtOH,
eth, bz, chl
s H2O, EtOH,
eth, bz, chl
1.008522
s H2O, EtOH,
eth, bz, chl
1.020820
111.99(0.05) 1.181220 1.435825 sl H2O; msc
EtOH, eth; s
bz, ctc
4/11/16 11:27 AM
Physical Constants of Organic Compounds
3-241
O
N
F
O
O
N
H
O
N
H
H
4671
Droperidol
N
OH
O
OH
OH
OH
4672
Dydrogesterone
N
O
OH
N
N
O
O
4670
N
N
4673
Dyphylline
4674
Ecgonidine
Ecgonine
O
O
HO
O
O
N
OH
HO
OH
OH
HO
4675
O
Si
O
Si
O
Si
O
N
H
HO
OH
O
4676
4677
Echinochrome A
O
4678
Echitamine
O
O
OH
4679
Edrophonium chloride
Efloxate
O
Si
O
OH
OH
O
Si
Cl
OH O
Echimidine
Si
O
N
N
Organic
O
H
O
OH O
O
Si
O
Si
O
Si
OH
O
4680
4681
Eicosamethylnonasiloxane
4683
4682
Eicosane
Eicosanoic acid
Eicosanedioic acid
OH
O
O
OH
OH
4684
4685
1-Eicosanol
4686
5,8,11,14-Eicosatetraenoic acid, (all-cis)
4687
1-Eicosene
cis-9-Eicosenoic acid
O
O
O
OH
OH
OH
4689
4688
4690
cis-11-Eicosenoic acid
trans-9-Eicosenoic acid
Elaidic acid
O
OH
N
O
OH
N
HO
OH
O
O
4692
4691
4693
4694
β-Elemene
1,3-Elemadien-11-ol
Elaiomycin
Embelin
O
N
O
H
HH
O
HN
NH
NH2
O
O
O
4695
N
O
Cl
Cl
Cl
H
Cl
Cl
Cl
Cl
O
S
O
O
H
O
O
S
O
O
Cl
Cl
4698
Enallylpropymal
Emylcamate
H
Cl
Cl
4697
4696
Emetine
Cl
O
O
H
O
COO Na
COO Na
4699
Endosulfan
4700
Endosulfan sulfate
Endothall disodium
Cl Cl
H Cl
H
O
H
Cl
H Cl
4701
Endrin
OH
F
Cl
Cl
O
F F
4702
Enflurane
F
H
N
OH
H
N
OH
H
N
OH
H
N
O
HCl
F
4703
Ephedrine, (±)-
4704
d-Ephedrine
4705
l-Ephedrine
4706
Ephedrine hydrochloride
Cl
4707
Epichlorohydrin
Physical Constants of Organic Compounds
3-242
Organic
No.
Name
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
4708
Epinephrine
D-Adrenaline
C9H13NO3
51-43-4
183.204 br (in air)
211.5
4709
Epiquinidine
C20H24N2O2
572-59-8
113
4710
1,2-Epoxybutane
Ethyloxirane
C4H8O
106-88-7
324.417 cry (AcOEt)
lf (eth)
72.106 liq
-150
63.4(0.2)
4711
4-Vinyl-1-cyclohexene dioxide C8H12O2
106-87-6
140.180 liq
<-55
227
4712
1,2-Epoxy-4-(epoxyethyl)
cyclohexane
1,2-Epoxyhexadecane
0.829720 1.385120 vs EtOH, ace;
msc eth
1.096620 1.478720 vs H2O
Tetradecyloxirane
C16H32O
7320-37-8
24.1
17812
0.846
4713
4714
4715
4716
4717
4718
1,2-Epoxyoctadecane
2,3-Epoxy-α-pinane
2,3-Epoxypropyl acrylate
2,3-Epoxypropyl methacrylate
Equol
Ergocornine
Hexadecyloxirane
α-Pinene oxide
Glycidyl acrylate
Glycidol methacrylate
C18H36O
C10H16O
C6H8O3
C7H10O3
C14H14O3
C31H39N5O5
7390-81-0
1686-14-2
106-90-1
106-91-2
531-95-3
564-36-3
240.424 hyg cry or
liq
268.478 hyg cry
152.233
128.126
142.152
230.259 cry (aq, al)
561.673 cry (MeOH)
26.1
1370.5
8524
5310
189
1.110920 1.449020 vs bz
1.04220 1.44825 vs bz, eth, EtOH
4719
Ergocorninine
C31H39N5O5
564-37-4
561.673 lo pr (al)
228 dec
4720
Ergocristine
C35H39N5O5
511-08-0
609.716 orth (bz)
175 dec
4721
Ergocristinine
C35H39N5O5
511-07-9
609.716 pr (al)
237 dec
4722
Ergocryptine
C32H41N5O5
511-09-1
575.699 pr (al)
213 dec
4723
4724
4725
Ergocryptinine
Ergometrinine
Ergonovine
C32H41N5O5
C19H23N3O2
C19H23N3O2
511-10-4
479-00-5
60-79-7
575.70 lo pr (al)
325.405 pr (ace)
325.405 pl or nd
245 dec
196 dec
162 dec
4726
Ergosine
C30H37N5O5
561-94-4
228 dec
4727
Ergostane, (5α)
C28H50
511-20-6
4728
4729
Ergostane, (5β)
Ergostan-3-ol, (3β,5α)
C28H50
C28H50O
511-21-7
6538-02-9
4730
Ergosta-5,7,9(11),22-tetraen- Dehydroergosterol
3-ol, (3β,22E)Ergosta-5,7,22-trien-3-ol,
Ergosterol
(3β,22E)-
C28H42O
516-85-8
C28H44O
57-87-4
547.646 pr (MeOH,
AcOEt)
386.697 lf or pl (ace,
ethMeOH)
386.697 nd (ace)
402.696 nd
(MeOHeth)
394.632 lf (al) nd
(eth),pl (al)
396.648 pl (+w, al)
nd (eth)
Pyrocalciferol
C28H44O
128-27-8
396.648 nd (MeOH)
94
Lumisterol
C28H44O
474-69-1
118
Campesterol
396.648 nd
(aceMeOH)
400.680 cry (ace)
400.680 nd (MeOH)
cry (PrOH
400.680 lf or nd
(MeOH)
581.67 nd (al), pr
(bz) pl
(ace)
656.706
581.662 orth pl
(MeOH) pl
(al)
229.299 nd or lf (dil
EtOH)
4731
4732
4733
Ergosta-5,7,22-trien-3-ol,
(3β,10α,22E)Ergosta-5,7,22-trien-3-ol,
(3β,9β,10α,22E)-
Ergometrine
Coproergostane
Ergostanol
Physical
Form
mp/˚C
Solubility
1.2240
85
64
144.5
vs eth, chl
i H2O; s eth, chl
146
2300.5
158(1)
2500.01
γ-Ergostenol
C28H48O
C28H48O
474-62-4
516-78-9
4736
Ergost-8(14)-en-3-ol, (3β,5α)
α-Ergostenol
C28H48O
632-32-6
4737
Ergotamine
C33H35N5O5
113-15-5
4738
4739
Ergotamine tartrate (2:1)
Ergotaminine
C35H38N5O8
C33H35N5O5
379-79-3
639-81-6
4740
Ergothioneine
C9H15N3O2S
497-30-3
4741
Eriochrome Black T
C20H12N3NaO7S
1787-61-7
461.380 br-blk pow
4742
Eriodictyol
C15H12O6
552-58-9
267 dec
4743
Erythorbic acid
C6H8O6
89-65-6
288.252 pl or nd
(EtOH)
176.124 gran cry
4744
β-Erythroidine
C16H19NO3
466-81-9
273.327 cry (al)
99.5
HCP_Section_03.indb 242
nD
i H2O; s EtOH,
ace, bz, chl,
AcOEt
vs ace, bz,
EtOH, chl
i H2O; s EtOH,
ace, chl
i H2O; sl EtOH,
ace, chl
i H2O; s EtOH,
chl
vs ace, chl
vs chl
s H2O, ace; vs
EtOH; sl chl
s ace, chl; sl
MeOH
vs ace, eth, chl
Ergost-5-en-3-ol, (3β,24R)Ergost-7-en-3-ol, (3β,5α)
3’,4’,5,7-Tetrahydroxyflavanone, (S)
Isoascorbic acid
den
g cm –3
sl H2O; i EtOH; s
HOAc, acid
vs EtOH; s eth
189.5
183 dec
4734
4735
Gynergen
bp/˚C
157.5
146
131
213 dec
192 dec
252 dec
290 dec
168
vs ace, bz, eth,
EtOH
i H2O; sl EtOH,
eth, peth; s bz,
chl
i H2O; s EtOH,
chl, MeOH
i H2O; s EtOH,
HOAc; vs eth,
ace, chl
s eth
sl EtOH; s eth,
bz, chl
vs bz, eth, chl
i H2O; sl EtOH,
ace, bz; s chl;
vs py
vs H2O; sl EtOH,
ace; i eth, bz,
chl
s H2O, EtOH,
MeOH
vs EtOH, HOAc
s H2O, py; sl
ace
s H2O, eth, chl;
vs EtOH, bz
4/11/16 11:27 AM
Physical Constants of Organic Compounds
HO
H
N
HO
O
N
H
O
O
O
HO
O
N
4709
4708
4710
Epiquinidine
Epinephrine
4711
1,2-Epoxybutane
4712
1,2-Epoxy-4-(epoxyethyl)cyclohexane
1,2-Epoxyhexadecane
OH
O
O
4713
4714
1,2-Epoxyoctadecane
N
H
2,3-Epoxy-α-pinane
O
O
O
N
HN
N
H
N
O
N
H
HO
N
H
N
H
O
N
H H
H
O
OH
N
N
Ergocryptinine
H
N
H
Ergocryptine
H
O
N
N
H
O
OH
N
H
H
NH
4725
Ergometrinine
H
4727
4726
Ergonovine
Ergostane, (5α)
Ergosine
H
H
HO
H
H
4728
HO
HO
4729
Ergostane, (5β)
4731
4730
Ergostan-3-ol, (3β,5α)
Ergosta-5,7,22-trien-3-ol, (3β,22E )-
Ergosta-5,7,9(11),22-tetraen-3-ol, (3β,22E )-
H
HO
4732
4733
N
H
N
HN
N
H
N
H
N
N
HN
H
1/2
O
HN
N
Ergotamine tartrate (2:1)
N
H
NH
O
OH O
N
HO
OH
N
Ergotaminine
NH
OH
N
O
OH
4739
OH
OH O
O Na
O S O
O
O
OH
HO
4738
Ergotamine
O
N
O
O
OH
4737
Ergost-8(14)-en-3-ol, (3β,5α)
N
O
O
NH
4736
H
Ergost-7-en-3-ol, (3β,5α)
O
O
OH
H
O
4735
Ergost-5-en-3-ol, (3β,24R)-
O
O
H
4734
Ergosta-5,7,22-trien-3-ol, (3β,9β,10α,22E )-
O
HO
HO
HO
HO
Ergosta-5,7,22-trien-3-ol, (3β,10α,22E )-
H
NH
NH
NH
4724
N
O
OH
4722
O
O
N
HH
H
NH
4723
H
N
O
HN
N
Ergocristinine
HO
O
O
O
NH
O
HO
Ergocornine
4721
Ergocristine
NH
N
NH
O
N
NH
O
HN
N
4720
Ergocorninine
O
H
H
4718
HO
NH
4719
O
N
O
OH
N
O
Equol
O
O
N
4717
2,3-Epoxypropyl methacrylate
O
NH
N
H
HO
4716
2,3-Epoxypropyl acrylate
O
O
O
4715
HN
O
OH
O
O
O
H
N
O
O
O
O
O
N
O
N
H
4740
Ergothioneine
HO
HO
SH
O
OH
4741
Eriochrome Black T
4742
Eriodictyol
O
O
O
OH
HO
4743
OH
Erythorbic acid
N
O
O
4744
β-Erythroidine
Organic
OH
3-243
Physical Constants of Organic Compounds
3-244
Organic
No.
Name
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
4745
Erythromycin
Propiocine
C37H67NO13
114-07-8
733.927 cry (w)
4746
4747
Erythromycin ethyl succinate
Erythromycin stearate
C43H75NO16
C55H103NO15
1264-62-6
643-22-1
862.053 cry (ace aq) 222
1018.405 cry
92
4748
4749
4750
4751
Erythrophleine
D-Erythrose
L-Erythrose
D-Erythrose 4-phosphate
C24H39NO5
C4H8O4
C4H8O4
C4H9O7P
36150-73-9
583-50-6
533-49-3
585-18-2
421.571
120.105
120.105
200.084
4752
Erythrosine
4753
4754
L-Erythrulose
Esaprazole
4755
Esculin
4756
Eserine sulfate
4757
4763
Estra-1,3,5(10)-triene-3,17diol, (17α)
Estra-1,3,5(10)-triene-3,17diol (17β)
Estra-1,3,5(10)-triene-3,17diol, (8α,17β)
Estra-1,3,5(10)-triene-3,17diol 3-benzoate, (17β)
Estra-1,3,5(10)-triene3,16,17-triol, (16α,17β)
Estra-1,3,5(10)-triene3,16,17-triol, (16β,17β)
Estrone
4764
4765
4766
4767
Norcassamidine
2,3-Dihydroxy-4(phosphonooxy)butanal
C20H8I4O5
C4H8O4
N-Cyclohexyl-1-piperaC12H23N3O
zineacetamide
6-(β-D-Glucopyranosyloxy)-7- C15H16O9
hydroxy-2H-1-benzopyran-2one
Physostigmine sulfate
C30H44N6O8S
glass
syr
syr
stab in aq
soln only
15905-32-5 835.893 br pow (Na
salt)
533-50-6
120.105 syr
64204-55-3 225.330
C18H24O2
50-28-2
Isoestradiol
C18H24O2
517-04-4
Estradiol benzoate
C25H28O3
50-50-0
Estriol
C18H24O3
50-27-1
16-Epiestriol
C18H24O3
547-81-9
C18H22O2
53-16-7
Ethacrynic acid
Ethalfluralin
Ethambutol
Ethane
C13H12Cl2O4
C13H14F3N3O4
C10H24N2O2
C2H6
58-54-8
55283-68-6
74-55-5
74-84-0
4768
Ethanearsonic acid
C2H7AsO3
507-32-4
4769
Ethanedial dioxime
C2H4N2O2
4770
1,2-Ethanediamine
Ethylenediamine
4771
1,2-Ethanediamine,
dihydrochloride
1,2-Ethanediol
Ethylenediamine dihydrochloride
Ethylene glycol
4760
4761
4762
4772
4773
dec
112
648.770 hyg cry
(ace-eth)
272.383 nd (+1/2 w) 221.5
(80% al)
272.383 pr (80% al), 180(1)
β-Estradiol
dec
1900.5
sl H2O, EtOH,
eth; s chl, py,
HOAc
vs ace, EtOH
i H2O; s EtOH,
ace; sl eth, bz
vs ace, EtOH,
Diox
s EtOH, diox
272.383 cry (dil
181
MeOH-chl)
376.488
198(1)
288.382 lf (al), mcl
288 dec
(dil al)
288.382 cry
290
(MeOH-bz)
270.367 mcl, orth
260.2
(al)
-88.6(0.4)
557-30-2
122.5
57
89
-182.794​
(0.005)
153.997 nd (al), orth 99.5
nd (w)
88.065 orth pl (w) 178 dec
C2H8N2
107-15-3
60.098
116.9(0.5)
C2H10Cl2N2
333-18-6
133.019
C2H6O2
107-21-1
62.068
C16H18O6S2
6315-52-2
370.440 cry (bz)
126.5(0.5)
18.9
-31
liq
11.14(0.05)
1.2725
s EtOH; sl eth,
bz, tfa; vs py
1.23625
i H2O; sl EtOH,
eth, bz; s ace,
diox
256 dec
sl H2O; s bz, chl
i H2O; vs bz
0.5446-89
21012
vs H2O, EtOH
sub
vs H2O, EtOH,
eth
vs H2O; msc
EtOH; i eth, bz;
s ctc
vs H2O
0.897920 1.456520
1.633
liq
-13(1)
197.5(0.1)
1.113520 1.431820 msc H2O, EtOH,
ace; s eth, chl;
sl bz
168(3)
184(4)
1.07025 1.398525 vs eth, EtOH
1.104320 1.415920 vs H2O; msc
EtOH, eth, ace,
bz, CS2
1.093526
i H2O; s eth, chl
vs eth, EtOH
1.1930
1.3580
sl H2O; s EtOH,
eth
0.859478
i H2O, EtOH; s
eth; vs ace
1.05320 1.453225 vs bz, EtOH, lig
1.491820
vs eth, EtOH
0.858178
i H2O, EtOH; vs
eth, ace
0.860080
i H2O, EtOH; s
eth; vs ace,
bz, ctc
Ethylidene diacetate
Ethylene glycol diacetate
C6H10O4
C6H10O4
542-10-9
111-55-7
146.141
146.141 liq
4776
4777
4778
4779
1,2-Ethanediol, diacrylate
1,2-Ethanediol, dibenzoate
1,2-Ethanediol, didodecanoate
1,2-Ethanediol, diformate
Ethylene glycol diacrylate
Ethylene glycol dibenzoate
Ethylene glycol didodecanoate
Ethylene glycol diformate
C8H10O4
C16H14O4
C26H50O4
C4H6O4
2274-11-5
94-49-5
624-04-4
629-15-2
170.163 liq
270.280 orth pr (eth) 73.5
426.673 pl (al)
56.6
118.089
550.6
360 dec
18820
174
4780
1,2-Ethanediol, dihexadecanoate
1,2-Ethanediol, dimethacrylate
1,2-Ethanediol, dinitrate
1,2-Ethanediol, distearate
Ethylene glycol dipalmitate
C34H66O4
624-03-3
69.1(0.5)
Ethylene glycol dimethacrylate C10H14O4
Ethylene glycol dinitrate
C2H4N2O6
Ethylene glycol distearate
C38H74O4
97-90-5
628-96-6
627-83-8
538.886 lf or nd
(al-chl)
198.216 liq
152.062 ye liq
594.993 lf
-40
-22.5(0.6)
75.3(0.5)
260
199(3)
24120
1,2-Ethanediol, ditetradecano- Ethylene glycol ditetradecano- C30H58O4
ate
ate
627-84-9
482.780 cry (eth,
ace)
61.7(0.5)
20820
HCP_Section_03.indb 244
s H2; vs eth,
EtOH
vs H2O, EtOH
205
(pentahydrate)
141
303.138
333.263
204.310 cry
30.069 col gas
Solubility
i H2O; sl EtOH,
eth, chl
s H2O, EtOH
s H2O; vs EtOH
vs H2O, EtOH
s H2O
4774
4775
4784
nD
vs ace, eth,
EtOH, chl
1,2-Ethanediol, bis(4-methylbenzenesulfonate)
1,1-Ethanediol, diacetate
1,2-Ethanediol, diacetate
4781
4782
4783
den
g cm –3
115
64-47-1
57-91-0
bp/˚C
191
340.283 pr (w+2)
C18H24O2
4759
mp/˚C
531-75-9
α-Estradiol
4758
Physical
Form
4/11/16 11:27 AM
Physical Constants of Organic Compounds
O
HO
3-245
O
O
OH
OH
HO
O
O
N
O
HO
O
O
O
OH
O
O
N
O
HO
OH
O
O
O
O
O
O
O
OH
OH
O
O
O
O
HO
OH
OH
O
O
N
O
HO
OH
O
O
O
4745
4746
Erythromycin
O
Erythromycin stearate
O
N
H
CHO
OH
OH
CH2OH
H
H
OH
O
HO
HO
4749
4748
CHO
H
H
CH2OH
4750
D-Erythrose
Erythrophleine
CHO
H
OH
H
OH O
CH2O P OH
OH
OH
HO
OH
4754
I
4752
4753
Erythrosine
L-Erythrulose
.H2SO4
N
O
H
N
HO
2
4755
Esaprazole
COCH2OH
H
CH2OH
HO
O
O
O
I
OH
OH
H
N
OH
N
H
I
O
D-Erythrose 4-phosphate
O O
O
N
HO
4751
L-Erythrose
HO
HN
O
I
4756
Esculin
4757
Eserine sulfate
Estra-1,3,5(10)-triene-3,17-diol, (17α)
OH
OH
OH
OH
O
H
H
OH
O
HO
HO
4758
HO
4759
Estra-1,3,5(10)-triene-3,17-diol (17β)
Estra-1,3,5(10)-triene-3,17-diol, (8α,17β)
OH
H
4760
O
O
O
HO
4762
4763
Estra-1,3,5(10)-triene-3,16,17-triol, (16β,17β)
H
H
H
H
H
4767
F
F
Cl
N
O
F
OH
4765
Ethacrynic acid
HO
N
N
OH
H2N
4769
Ethanearsonic acid
NH2
4766
Ethalfluralin
4770
Ethanedial dioxime
H2N
NH2 2HCl
Ethambutol
O
4771
1,2-Ethanediamine
4772
1,2-Ethanediamine, dihydrochloride
1,2-Ethanediol
O
O
O
OH
HO
H
N
N
H
O
S
4768
Ethane
HO
O
OH
As O
OH
H
O
N
4764
Estrone
N
OH
Cl
HO
Estra-1,3,5(10)-triene-3,16,17-triol, (16α,17β)
O
O
H
OH
4761
Estra-1,3,5(10)-triene-3,17-diol 3-benzoate, (17β)
S
O
4773
1,2-Ethanediol, bis(4-methylbenzenesulfonate)
O
O
O
O
O
O
O
O
O
O
O
O
O
O
4774
4775
1,1-Ethanediol, diacetate
O
O
4776
1,2-Ethanediol, diacetate
1,2-Ethanediol, diacrylate
O
O
O
O
4777
4778
1,2-Ethanediol, dibenzoate
1,2-Ethanediol, didodecanoate
O
O
O
O
O
O
O
O
O
O
O
4779
O
N
O
O
O
4781
4780
1,2-Ethanediol, diformate
O
1,2-Ethanediol, dimethacrylate
1,2-Ethanediol, dihexadecanoate
O
O
O
O
O
O
O
O
4783
1,2-Ethanediol, distearate
4784
1,2-Ethanediol, ditetradecanoate
4782
N
O
1,2-Ethanediol, dinitrate
O
Organic
O
O
4747
Erythromycin ethyl succinate
Physical Constants of Organic Compounds
3-246
Organic
bp/˚C
den
g cm –3
144.218 orth pl or nd 90
(w)
dec
1.42000
542-59-6
104.105
188(2)
1.10815
1,2-Ethanediol, monobenzoate Ethylene glycol monobenzoate C9H10O3
1,2-Ethanediol, monostearate Ethylene glycol monostearate C20H40O3
1,2-Ethanediol, monosulfite
Ethylene glycol monosulfite
C2H4O3S
94-33-7
111-60-4
3741-38-6
166.173
328.530 cry (peth)
108.116 liq
45
60.5
-11
15010
1903
173
1.110130
0.878060 1.431060
1.440220 1.446320
1,2-Diphosphonoethane
C2H8O6P2
6145-31-9
223
1,2-Ethanedisulfonic acid
Ethanedithioamide
Ethylene disulfonic acid
Rubeanic acid
C2H6O6S2
C2H4N2S2
110-04-3
79-40-3
190.029 nd (EtOH/
eth)
190.195
120.196 red cry
4793
1,2-Ethanedithiol
Ethylene dimercaptan
C2H6S2
540-63-6
94.199
-41.2
4794
C6H10O4S2
123-81-9
210.271
4795
4796
4797
1,2-Ethanediyl mercaptoacetate
Ethanesulfonic acid
Ethanesulfonyl chloride
Ethanethiol
C2H6O3S
C2H5ClO2S
C2H6S
594-45-6
594-44-5
75-08-1
110.132 hyg
128.578 pa ye
62.134 liq
-17
4798
Ethanimidamide
C2H6N2
143-37-3
58.082
-35
4799
Ethanimidamide monohydrochloride
Acetamidine hydrochloride
C2H7ClN2
124-42-5
94.543
4800
Ethanol
Ethyl alcohol
C2H6O
64-17-5
46.068
nd or pr (al) 177.5
hyg lo pr
(al)
liq
-114.14(0.03) 78.24(0.09)
4801
Ethanolamine
Glycinol
C2H7NO
141-43-5
61.083
liq
10.4(0.2)
4802
Ethanolamine hydrochloride
2-Aminoethanol hydrochloride
C2H8ClNO
2002-24-6
97.544
hyg cry
(EtOH)
85
4803
4804
Ethanolamine O-sulfate
Ethaverine
C2H7NO4S
C24H29NO4
926-39-6
486-47-5
141.147
395.492
4805
Ethchlorvynol
C7H9ClO
113-18-8
144.598 liq
4806
Ethephon
C2H6ClO3P
16672-87-0 144.494
76.7(0.5)
4807
Ethinylestradiol
2-Aminoethyl sulfate
1-[(3,4-Diethoxyphenyl)­
methyl]-6,7diethoxyisoquinoline
1-Chloro-3-ethyl-1-penten-4yn-ol
Phosphonic acid,
(2-chloroethyl)19-Norpregna-1,3,5(10)-trien20-yne-3,17-diol, (17α)-
C20H24O2
57-63-6
296.404
186(1)
4808
4809
4810
4811
Ethion
D-Ethionine
L-Ethionine
Ethirimol
C9H22O4P2S4
C6H13NO2S
C6H13NO2S
C11H19N3O
563-12-2
535-32-0
13073-35-3
23947-60-6
384.476
163.238 cry (H2O)
163.238 cry (H2O)
209.288
-13
278 dec
273 dec
161.2(0.5)
4812
4813
4814
4815
Ethisterone
Ethoate-methyl
Ethofumesate
Ethoheptazine
434-03-7
116-01-8
26225-79-6
77-15-6
312.446
243.284 cry (tol/hp)
286.344
261.360 liq
272
67
72.5(0.5)
4816
Ethoprop
4817
Ethotoin
C21H28O2
C6H14NO3PS2
C13H18O5S
4-Carbethoxymethyl-4-phenyl- C16H23NO2
azacycloheptane
Phosphorodithioic acid, O-ethyl C8H19O2PS2
S,S-dipropyl ester
C11H12N2O2
4818
Ethoxyacetic acid
4819
4820
4821
4822
4823
4824
No.
Name
Synonym
Mol. Form.
CAS RN
4785
1,2-Ethanediol, dithiocyanate
Ethylene glycol dithiocyanate
C4H4N2S2
629-17-4
4786
1,2-Ethanediol, monoacetate
Ethylene glycol monoacetate
C4H8O3
4787
4788
4789
4790
1,2-Ethanediphosphonic acid
4791
4792
Ethylsulfonic acid
Ethyl mercaptan
3-Ethylhomocysteine, (R)
3-Ethylhomocysteine, (S)
4(1H)-Pyrimidinone,
5-butyl-2-(ethylamino)-6methyl-
Mol.
Wt.
Physical
Form
liq
173
170 dec
144(3)
1231
176.5(1)
-147.89(0.02) 35.0(0.1)
1.23420
1.559020
Solubility
sl H2O, bz; s
EtOH, eth; vs
ace
msc H2O, EtOH,
eth
vs EtOH
sl EtOH; s eth
vs H2O, EtOH,
eth, ace, bz,
AcOEt; sl chl
vs diox
sl H2O, EtOH; s
con sulf
i H2O; s EtOH,
eth, ace, bz;
vs alk
C4H8O3
627-03-2
104.105
4’-Ethoxyacetophenone
Ethoxyacetylene
7-Ethoxy-3,9-acridinediamine Ethacridine
2-Ethoxyaniline
o-Phenetidine
C10H12O2
C4H6O
C15H15N3O
C8H11NO
1676-63-7
927-80-0
442-16-0
94-70-2
164.201 pl (eth)
70.090
253.299 ye nd
137.179
3-Ethoxyaniline
4-Ethoxyaniline
C8H11NO
C8H11NO
621-33-0
156-43-4
137.179
137.179 liq
170.3(0.4)
1.334125 1.433520 vs H2O, EtOH
1.35722 1.453120 vs eth; s CS2
0.831525 1.431020 sl H2O; s EtOH,
eth, ace, dil
alk
sl H2O; s EtOH,
acid
vs H2O, EtOH
0.789320 1.361120 msc H2O, EtOH,
eth, ace, chl; s
bz
1.018020 1.454120 msc H2O, EtOH;
sl eth, lig, bz;
s chl
230 dec
100
s H2O; i EtOH
i H2O; s EtOH; sl
eth, chl
181
13194-48-4 242.340
204.225 pr (w)
HCP_Section_03.indb 246
nD
1381.5
86-35-1
m-Phenetidine
p-Phenetidine
mp/˚C
1.0725
1.47425
1.2
sl chl
1650.3
1.2220
1.2125
1341
1.14
1.03826
880.2
1.09420
1.521026
94
39
i H2O; s os
206.5
1.102120 1.419420
268
50
0.800020 1.379620
226
<-21
233(7)
4.7(0.2)
248
254
1.065216
s hot H2O; vs
EtOH, bz, eth
vs H2O, EtOH,
eth; s chl
vs eth, EtOH
1.556020 sl H2O, ctc; s
EtOH, eth
vs eth, EtOH
1.552820 sl H2O; s EtOH,
eth, chl
4/11/16 11:27 AM
Physical Constants of Organic Compounds
3-247
O
O
N
S
S
N
4785
S
O
4789
O
O
4795
4796
Ethanesulfonic acid
4797
Ethanesulfonyl chloride
O
O
SH
SH
O
4793
4794
1,2-Ethanedithiol
1,2-Ethanediyl mercaptoacetate
NH2
HCl
HN
4798
Ethanethiol
HS
NH2
4792
NH
SH
O
HS
Ethanedithioamide
NH2
Cl
1,2-Ethanediol, monostearate
S
H2N
1,2-Ethanedisulfonic acid
O
S
OH
S
4791
1,2-Ethanediphosphonic acid
O
O
S OH
O
O
HO S
O
4790
1,2-Ethanediol, monosulfite
S
O
P OH
OH
O
HO P
OH
O
4788
1,2-Ethanediol, monobenzoate
1,2-Ethanediol, monoacetate
OH
O
4787
4786
1,2-Ethanediol, dithiocyanate
O
OH
O
OH
O
4800
4799
Ethanimidamide
H2N
OH
4802
4801
Ethanol
Ethanimidamide monohydrochloride
OH HCl
H2N
OH
Ethanolamine hydrochloride
Ethanolamine
O
H2N
OH
N
O
OH
O S O
O
O
Cl
O
4803
4804
Ethanolamine O-sulfate
4805
Ethaverine
H
O
HO P OH
Cl
HO
HO
4806
Ethchlorvynol
4807
Ethephon
Ethinylestradiol
OH
O
S
O P S
O
S
O
S
P O
O
S
O
S
OH
4808
N
H
NH2
4809
Ethion
N
OH
NH2
4810
D-Ethionine
H
H
N
H
4812
4811
L-Ethionine
H
O
Ethisterone
Ethirimol
O
O
O P S
S
O
O
O
N
H
4813
Ethoate-methyl
S
O
O O
N
O
4814
4815
Ethofumesate
N
O
S P S
O
O
4816
Ethoheptazine
O
N
H
4817
Ethoprop
Ethotoin
O
O
OH
4818
Ethoxyacetic acid
NH2
NH2
O
O
O
O
4819
4’-Ethoxyacetophenone
4820
Ethoxyacetylene
NH2
NH2
O
N
4821
7-Ethoxy-3,9-acridinediamine
NH2
O
4822
2-Ethoxyaniline
4823
3-Ethoxyaniline
O
4824
4-Ethoxyaniline
Organic
O
Physical Constants of Organic Compounds
3-248
No.
Name
4825
2-Ethoxybenzaldehyde
4826
4827
4-Ethoxybenzaldehyde
2-Ethoxybenzamide
4828
Ethoxybenzene
4829
Mol. Form.
CAS RN
Mol.
Wt.
C9H10O2
613-69-4
150.174
Ethenzamide
C9H10O2
C9H11NO2
Phenetole
Physical
Form
den
g cm –3
mp/˚C
bp/˚C
21
248
10031-82-0 150.174
938-73-8
165.189 nd (w, al)
13.5
133
249
1.0821
C8H10O
103-73-1
122.164 liq
-29.6(0.4)
169.8(0.2)
0.965120 1.507620
4-Ethoxy-1,2-benzenediamine
C8H12N2O
1197-37-1
152.193
71.5
295
4830
2-Ethoxybenzoic acid
C9H10O3
134-11-2
166.173
20.7
21139
4831
4-Ethoxybenzoic acid
C9H10O3
619-86-3
166.173 nd (w)
199(1)
4832
6-Ethoxy-2-benzothiazolesulfonamide
3-Ethoxy-N,N-diethylaniline
C9H10N2O3S2
452-35-7
258.316
191(1)
C12H19NO
1864-92-2
193.285
286
C7H12O2
103-75-3
128.169
132
0.965825
1.532525 s EtOH, bz,
HOAc
1.439420
Ethoxyquin
C14H19NO
91-53-2
217.307
1242
1.02625
1.56925
Dimethylethoxysilane
C4H12OSi
C16H16O2
14857-34-2 104.223 liq
574-09-4
240.297 nd (lig)
54
19420
C4H11NO
110-76-9
89.136
C4H10O2
110-80-5
90.121
C9H16O4
7328-17-8
188.221
0.7620
1.101617 1.572717 vs bz, eth,
EtOH, lig
0.851220 1.410120 msc H2O, EtOH,
eth; s ace, bz;
sl chl
0.925325 1.405425 vs H2O, ace,
eth, EtOH
1.1325
C6H12O3
111-15-9
C7H12O3
4833
Organic
4834
Synonym
Ethoxzolamide
4838
2-Ethoxy-3,4-dihydro-2Hpyran
6-Ethoxy-1,2-dihydro-2,2,4trimethylquinoline
Ethoxydimethylsilane
2-Ethoxy-1,2-diphenylethanone
2-Ethoxyethanamine
4839
2-Ethoxyethanol
4840
4841
2-(2-Ethoxyethoxy)ethyl
2-propenoate
2-Ethoxyethyl acetate
4842
2-Ethoxyethyl acrylate
4843
3-Ethoxy-2-hydroxybenzaldehyde
3-Ethoxy-4-hydroxybenzalde- Ethyl vanillin
hyde
4-Ethoxy-3-methoxybenzaldehyde
4846
4847
4835
4836
4837
62
108(12)
-70
134.7(0.2)
132.157 liq
-61.7
156.6(0.4)
106-74-1
144.168 liq
-47.3(0.6)
174(2)
C9H10O3
492-88-6
166.173
64.1(0.4)
264
C9H10O3
121-32-4
166.173
76.7(0.4)
285
C10H12O3
120-25-2
180.200 mcl pr
64.5
16813
1-Ethoxy-2-methoxyethane
1-Ethoxy-3-methylbenzene
C5H12O2
C9H12O
5137-45-1
621-32-9
104.148 liq
136.190
88(14)
192
4848
1-Ethoxy-4-methylbenzene
C9H12O
622-60-6
136.190
195(6)
4849
4850
C7H16O
C6H6N2O
919-94-8
123-06-8
116.201
122.124
4851
2-Ethoxy-2-methylbutane
(Ethoxymethylene)­
propanedinitrile
(Ethoxymethyl)oxirane
C5H10O2
4016-11-9
102.132
4852
1-Ethoxynaphthalene
C12H12O
5328-01-8
172.222 nd
5.5
280(8)
4853
2-Ethoxynaphthalene
C12H12O
93-18-5
172.222 pl (al)
37.5
282(8)
4854
4855
4856
2-Ethoxy-5-nitroaniline
1-Ethoxy-2-nitrobenzene
1-Ethoxy-4-nitrobenzene
C8H10N2O3
C8H9NO3
C8H9NO3
136-79-8
610-67-3
100-29-8
182.176 ye nd (dil al) 96.5
167.162 br ye
1.1
167.162 pr (dil al,
60(1)
eth)
20514
267
283(7)
4857
C10H12N2O4
1777-84-0
224.213 nd (dil al)
124.0
4858
N-(4-Ethoxy-3-nitrophenyl)­
acetamide
2-Ethoxyphenol
Catechol monoethyl ether
C8H10O2
94-71-3
138.164
29
4859
3-Ethoxyphenol
Resorcinol monoethyl ether
C8H10O2
621-34-1
138.164
4860
4-Ethoxyphenol
Hydroquinone monoethyl ether C8H10O2
622-62-8
138.164 pr or lf (w)
66.5
248(19)
4861
N-(2-Ethoxyphenyl)acetamide
581-08-8
179.216 lf(dil al)
79
299(13)
4844
4845
HCP_Section_03.indb 248
Ethylene glycol monoethyl
ether
Diethylene glycol ethyl ether
acrylate
Ethylene glycol monoethyl
ether acetate
Ethylene glycol monoethyl
ether acrylate
Ethyl tert-pentyl ether
2,3-Epoxypropyl ethyl ether
5-Nitro-o-phenetidine
C10H13NO2
liq
66
101.5(0.4)
16012
126(18)
nD
Solubility
msc EtOH, eth;
sl chl
vs EtOH, eth, bz
sl H2O, chl; vs
EtOH, eth
i H2O; s EtOH,
eth, ctc
vs H2O; s EtOH,
eth, chl
sl H2O, EtOH,
ctc
sl H2O, tfa; s
EtOH, eth, bz
0.974020 1.405420 vs H2O, ace,
eth, EtOH
0.98320 1.427420
sl H2O; s EtOH,
eth, bz, chl
sl H2O; s EtOH,
eth, bz, chl,
HOAc
0.846025 1.384325
0.94920 1.51320 i H2O; s EtOH,
eth
0.950918 1.505818 i H2O; s EtOH,
eth; sl ctc
0.760625 1.388625 vs eth, EtOH
s EtOH, eth; sl
chl
0.970020 1.432020 s H2O, EtOH,
eth; sl ctc
1.06020 1.595325 i H2O; vs EtOH,
eth
1.064020 1.597536 i H2O; s EtOH,
eth, tol, lig,
CS2
vs eth, EtOH
1.190315 1.542520 vs eth, EtOH
1.1176100
sl H2O, EtOH; vs
eth; msc ace,
bz; s peth
vs ace, bz, EtOH
217(6)
1.090325
251(19)
1.10515
sl H2O, ctc; msc
EtOH, eth
i H2O; s EtOH,
eth, bz; sl chl
sl H2O; vs EtOH,
eth; s chl
i H2O; s EtOH,
eth, chl
4/11/16 11:27 AM
Physical Constants of Organic Compounds
3-249
O
NH2
NH2
O
O
4827
4-Ethoxybenzaldehyde
O
4828
2-Ethoxybenzamide
O
4829
Ethoxybenzene
O
O
4833
6-Ethoxy-2-benzothiazolesulfonamide
2-Ethoxybenzoic acid
4-Ethoxybenzoic acid
O
O
S NH2
O
4832
4831
N
H
O
4834
3-Ethoxy-N,N-diethylaniline
O Si H
4835
2-Ethoxy-3,4-dihydro-2H-pyran
4836
6-Ethoxy-1,2-dihydro-2,2,4-trimethylquinoline
Ethoxydimethylsilane
O
O
O
NH2
O
4837
4838
2-Ethoxy-1,2-diphenylethanone
OH
O
4839
2-Ethoxyethanamine
O
O
O
O
4840
2-Ethoxyethanol
O
O
O
2-(2-Ethoxyethoxy)ethyl 2-propenoate
O
O
4841
4842
2-Ethoxyethyl acetate
2-Ethoxyethyl acrylate
O
O
O
O
OH
O
O
OH
4843
4844
3-Ethoxy-2-hydroxybenzaldehyde
O
O
O
4845
3-Ethoxy-4-hydroxybenzaldehyde
O
O
4846
4-Ethoxy-3-methoxybenzaldehyde
1-Ethoxy-2-methoxyethane
4847
1-Ethoxy-3-methylbenzene
4848
1-Ethoxy-4-methylbenzene
NH2
O
O
O
O
O
N
O
4849
2-Ethoxy-2-methylbutane
O
N
4850
O
4856
1-Ethoxy-4-nitrobenzene
N
2-Ethoxynaphthalene
4854
2-Ethoxy-5-nitroaniline
OH
OH
N-(4-Ethoxy-3-nitrophenyl)acetamide
4855
1-Ethoxy-2-nitrobenzene
O
O
O
4858
2-Ethoxyphenol
O
HN
O
O
4857
4853
1-Ethoxynaphthalene
N
O
N
O
OH
O
O
N
O
4852
(Ethoxymethyl)oxirane
H
N
O
O
4851
(Ethoxymethylene)propanedinitrile
O
O
4859
3-Ethoxyphenol
O
4860
4-Ethoxyphenol
4861
N-(2-Ethoxyphenyl)acetamide
Organic
S
O
4830
4-Ethoxy-1,2-benzenediamine
N
N
OH
OH
O
4826
2-Ethoxybenzaldehyde
O
O
O
4825
O
NH2
O
O
Physical Constants of Organic Compounds
3-250
Organic
Mol. Form.
CAS RN
Mol.
Wt.
N-(4-Ethoxyphenyl)acetamide Phenacetin
C10H13NO2
62-44-2
179.216 mcl pr
135(3)
4863
N-(4-Ethoxyphenyl)-2hydroxypropanamide
p-Lactophenetide
C11H15NO3
539-08-2
209.242
118
4864
(4-Ethoxyphenyl)urea
Dulcin
C9H12N2O2
150-69-6
4865
4866
4867
Actinoquinol
C5H10O2
C5H9NO
C11H11NO4S
4868
3-Ethoxypropanal
3-Ethoxypropanenitrile
8-Ethoxy-5-quinolinesulfonic
acid
Ethoxytrimethylsilane
180.203 lf (dil al), pl
(w)
2806-85-1 102.132
2141-62-0 99.131
15301-40-3 253.275 br nd (w)
C5H14OSi
1825-62-3
118.250
4869
4870
Ethoxytriphenylsilane
N-Ethylacetamide
C20H20OSi
C4H9NO
1516-80-9
625-50-3
304.458
87.120
4871
Ethyl acetate
C4H8O2
141-78-6
88.106
4872
Ethyl acetoacetate
Ethyl 3-oxobutanoate
C6H10O3
141-97-9
130.141 liq
4873
4874
4875
1-(4-Ethylphenyl)ethanone
C10H12O
C10H18O3
C9H16O3
937-30-4
1540-29-0
1522-46-9
148.201
186.248
172.221
11411
221.5
220(14)
4876
4877
4’-Ethylacetophenone
Ethyl 2-acetylhexanoate
Ethyl 2-acetyl-3-methylbutanoate
Ethyl 2-acetylpentanoate
Ethyl 2-acetyl-4-pentenoate
Ethyl 2-allylacetoacetate
C9H16O3
C9H14O3
1540-28-9
610-89-9
172.221
170.205
224
208
4878
Ethyl acrylate
Ethyl propenoate
C5H8O2
140-88-5
100.117 liq
-71(2)
98.9(0.6)
4879
Ethylamine
Ethanamine
C2H7N
75-04-7
45.084
-81(2)
16.6(0.2)
4880
4881
Ethylamine hydrochloride
Ethyl 2-aminoacetate
Ethanamine hydrochloride
Glycine, ethyl ester
C2H8ClN
C4H9NO2
557-66-4
459-73-4
81.545
103.120
4882
4883
Ethyl 2-aminobenzoate
Ethyl 3-aminobenzoate
C9H11NO2
C9H11NO2
87-25-2
582-33-2
165.189
165.189
4884
Ethyl 4-aminobenzoate
C9H11NO2
94-09-7
310
4885
C4H8N2O3
626-36-8
4886
Ethyl (aminocarbonyl)
carbamate
2-(Ethylamino)ethanol
165.189 nd (w), orth 89.6(0.3)
(eth)
132.118 nd (w, bz)
196.5
C4H11NO
110-73-6
89.136
178(8)
4887
2-Ethylaniline
C8H11N
578-54-1
121.180 liq
-47(1)
213(4)
4888
4889
3-Ethylaniline
4-Ethylaniline
C8H11N
C8H11N
587-02-0
589-16-2
121.180 liq
121.180 liq
-64
-5.1(0.3)
214(7)
217.2(0.2)
4890
N-Ethylaniline
C8H11N
103-69-5
121.180 liq
-63.4(0.4)
204(1)
4891
4892
4893
4894
2-Ethyl-9,10-anthracenedione
4-Ethylbenzaldehyde
N-Ethylbenzamide
Ethylbenzene
Phenylethane
C16H12O2
C9H10O
C9H11NO
C8H10
84-51-5
4748-78-1
614-17-5
100-41-4
236.265
134.174
149.189 nd (w)
106.165 liq
108.8
4895
α-Ethylbenzeneacetamide
C10H13NO
90-26-6
163.216 cry
86
18516
4896
4897
α-Ethylbenzeneacetic acid
α-Ethylbenzeneacetonitrile
C10H12O2
C10H11N
90-27-7
769-68-6
164.201 pl (eth)
145.201
47.5
271
241(8)
4898
4-Ethyl-1,3-benzenediol
C8H10O2
2896-60-8
138.164 pr (chl, bz)
98.5
16024
4899
α-Ethylbenzenemethanol
C9H12O
93-54-9
136.190
219
4900
Ethyl benzenesulfonate
C8H10O3S
515-46-8
186.228
15615
No.
Name
4862
HCP_Section_03.indb 250
Synonym
Ethyl aminobenzoate
α-Phenylbutyramide
α-Ethylbenzyl alcohol
Physical
Form
liq
vol liq or
gas
mcl pl (al)
mp/˚C
173.5
bp/˚C
dec
nD
Solubility
1.571
sl H2O, eth, bz;
s EtOH, ace;
vs py
s H2O; vs EtOH;
sl eth, bz, chl,
peth
sl H2O; s EtOH;
vs AcOEt
135.2
171(3)
0.916520
0.928515 1.406820 vs eth, EtOH
s alk
76(3)
0.757320 1.374120 i H2O; s EtOH,
eth, ace
s chl
0.9424
1.433820 msc H2O, EtOH;
s chl, HOAc
0.900320 1.372320 s H2O; msc
EtOH, eth; vs
ace, bz
1.036810 1.417120 s H2O; msc
EtOH, eth; s
bz, chl
286 dec
65
344(3)
205(1)
-83.8(0.3)
77.1(0.2)
-45
180(2)
109.5
149
14.3(0.2)
den
g cm –3
271(20)
294
dec
221
70.5
-94.95(0.02) 136.2(0.4)
0.952320 1.430120 vs ace, eth
0.964818 1.425618 i H2O; msc
EtOH, eth
0.966120 1.425520 vs eth, EtOH
0.989820 1.438818 msc EtOH, eth,
bz
0.923420 1.406820 sl H2O, DMSO;
msc EtOH, eth;
s chl
0.68915 1.366320 msc H2O, EtOH,
eth
1.216020
vs H2O, EtOH
1.027510 1.424210 msc H2O, EtOH,
eth, ace, bz;
vs lig
1.117420 1.564620 vs eth, EtOH
1.17120 1.560022 sl H2O; vs EtOH,
eth; s ctc
i H2O; vs EtOH,
eth; s chl, acid
i H2O, eth; sl
EtOH, bz, tfa
0.91420 1.44420 vs H2O, EtOH,
eth; s chl
0.98322 1.558422 sl H2O, chl; vs
EtOH, eth
0.989625
vs eth, EtOH
0.967920 1.555420 sl H2O, ctc; vs
EtOH, eth
0.962520 1.555920 i H2O; msc
EtOH, eth; vs
ace, bz; s ctc
0.979020
0.862625 1.493025 i H2O; msc
EtOH, eth; sl
chl
s H2O, ctc; sl
ace
s eth, bz, ctc
0.97714
i H2O; s EtOH,
eth, bz
sl H2O, EtOH,
eth
0.991525 1.516923 vs bz, eth,
EtOH, MeOH
1.216720 1.508120 sl H2O; s EtOH;
vs eth, chl
4/11/16 11:27 AM
Physical Constants of Organic Compounds
3-251
O
O
HN
HN
O
O
O
OH
NH2
HN
O
4863
N-(4-Ethoxyphenyl)acetamide
OH
O S O
O
4867
8-Ethoxy-5-quinolinesulfonic acid
Ethoxytrimethylsilane
O
4869
O
O
O
O
O
O
4871
N-Ethylacetamide
O
O
O
O
4870
Ethoxytriphenylsilane
3-Ethoxypropanenitrile
O
O
N
H
4868
4866
3-Ethoxypropanal
O
O
Si
N
4865
(4-Ethoxyphenyl)urea
O
Si
N
O
4864
N-(4-Ethoxyphenyl)-2-hydroxypropanamide
O
O
Ethyl acetate
O
O
Ethyl 2-acetylhexanoate
Ethyl 2-acetyl-3-methylbutanoate
4876
4877
Ethyl 2-acetylpentanoate
4878
Ethyl 2-acetyl-4-pentenoate
NH2 HCl
NH2
O
4875
4’-Ethylacetophenone
Ethyl acetoacetate
O
O
O
4874
4873
4872
4879
Ethyl acrylate
4880
Ethylamine
Ethylamine hydrochloride
O
O
H2N
O
O
O
O
NH2
O
4881
NH2
4882
Ethyl 2-aminoacetate
4883
Ethyl 2-aminobenzoate
H2N
H2N
4884
Ethyl 3-aminobenzoate
O
N
H
H
N
O
4885
Ethyl 4-aminobenzoate
NH2
4887
4888
3-Ethylaniline
4889
4-Ethylaniline
O
N
H
4890
4891
N-Ethylaniline
4892
2-Ethyl-9,10-anthracenedione
4893
4-Ethylbenzaldehyde
N-Ethylbenzamide
OH
NH2
O
4895
α-Ethylbenzeneacetamide
OH
N
O
4896
α-Ethylbenzeneacetic acid
2-(Ethylamino)ethanol
O
O
O
2-Ethylaniline
OH
4886
Ethyl (aminocarbonyl)carbamate
HN
NH2
NH2
O
O
4897
α-Ethylbenzeneacetonitrile
4894
Ethylbenzene
O
O S O
OH
OH
4898
4-Ethyl-1,3-benzenediol
4899
α-Ethylbenzenemethanol
4900
Ethyl benzenesulfonate
Organic
4862
O
Physical Constants of Organic Compounds
3-252
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
Ethyl benzenecarboxylate
C8H10O3S
C9H10N2
C9H10O2
98-69-1
1848-84-6
93-89-0
186.228
146.188
150.174 liq
176.5
-34.5(0.3)
212.5(0.2)
C10H10O4
6951-08-2
194.184 pr
18.5
285.5
C11H12O3
94-02-0
192.211
<0
267 dec
C11H15NO2
C13H14O3
6436-90-4
620-80-4
17750
296
C4H7BrO2
105-36-2
193.243
218.248 orth pl (dil
al)
167.002
60.5
4908
Ethyl N-benzylglycinate
Ethyl 2-benzylideneacetoacetate
Ethyl bromoacetate
4909
4910
Ethyl 4-bromoacetoacetate
Ethyl 4-bromobenzoate
C6H9BrO3
C9H9BrO2
13176-46-0 209.037
5798-75-4 229.070 liq
4911
Ethyl 2-bromobutanoate
C6H11BrO2
533-68-6
4912
4913
C6H11BrO2
C6H9BrO2
2969-81-5 195.054
37746-78-4 193.038
C8H15BrO2
C7H13BrO2
25542-62-5 223.108 cry (peth)
609-12-1
209.081
C6H11BrO2
600-00-0
C5H7BrO3
4918
Ethyl 4-bromobutanoate
Ethyl trans-4-bromo-2butenoate
Ethyl 6-bromohexanoate
Ethyl 6-bromocaproate
Ethyl 2-bromo-3-methylbutanoate
Ethyl 2-bromo-2-methylpropanoate
Ethyl 3-bromo-2-oxopropano- Ethyl 3-bromopyruvate
ate
Ethyl 2-bromopentanoate
4919
4920
Ethyl 5-bromopentanoate
Ethyl 2-bromopropanoate
4921
Ethyl 3-bromopropanoate
4922
2-Ethylbutanal
4923
No.
Name
4901
4902
4903
4-Ethylbenzenesulfonic acid
2-Ethyl-1H-benzimidazole
Ethyl benzoate
4904
Ethyl 1,3-benzodioxole-5carboxylate
Ethyl benzoylacetate
Physical
Form
mp/˚C
bp/˚C
den
g cm –3
nD
Solubility
1.23
192
10014
sl chl
1.041525 1.500720 i H2O; s EtOH,
ace, bz; msc
eth; sl ctc
vs eth, EtOH,
peth
1.120215 1.531715 sl H2O; s EtOH,
eth
1.504120 vs EtOH, eth, bz
i H2O; sl EtOH,
eth, bz; vs chl
1.503220 1.448920 i H2O; msc
EtOH, eth; s
ace; sl ctc
1.527818 1.528120 vs eth, EtOH
1.433217 1.543817 sl H2O; s EtOH,
eth, ace, bz
1.327320 1.447520 i H2O; msc
EtOH, eth; s
chl
1.354020 1.455920
1.40216 1.492520 vs EtOH
12621
186
1.23823 1.456621
1.276020 1.449620 vs eth, EtOH
195.054
178(5)
1.326320 1.444620 i H2O; s EtOH;
msc eth
70-23-5
195.012
879
C7H13BrO2
615-83-8
209.081
191
1.22618
C7H13BrO2
C5H9BrO2
14660-52-7 209.081
535-11-5
181.028
12935
152(13)
1.308520
1.413520
C5H9BrO2
539-74-2
181.028
163(13)
1.412318
Diethylacetaldehyde
C6H12O
97-96-1
100.158
118160
0.811020
Ethyl butanoate
Ethyl butyrate
C6H12O2
105-54-4
116.158 liq
-97(6)
121.1(0.4)
0.873525
4924
2-Ethylbutanoic acid
Diethylacetic acid
C6H12O2
88-09-5
116.158 liq
-31.8(0.5)
193(3)
0.923920
4925
C18H34O6
95-08-9
346.459
4926
2-Ethylbutanoic acid,
triethyleneglycol diester
2-Ethyl-1-butanol
C6H14O
97-95-0
102.174 liq
<-15
155(2)
4927
4928
2-Ethylbutanoyl chloride
2-Ethyl-1-butene
C6H11ClO
C6H12
2736-40-5
760-21-4
134.603
84.159 liq
-132.0(0.2)
140(8)
64.7(0.1)
4929
Ethyl cis-2-butenoate
Ethyl isocrotonate
C6H10O2
6776-19-8
114.142
136
4930
Ethyl trans-2-butenoate
Ethyl crotonate
C6H10O2
623-70-1
114.142
140(5)
4931
4932
Ethyl 3-butenoate
2-Ethylbutyl acetate
C6H10O2
C8H16O2
1617-18-1 114.142
10031-87-5 144.212
4933
4934
4935
4936
4937
2-Ethylbutyl acrylate
2-Ethylbutylamine
Ethyl N-butylcarbamate
Ethyl 2-butynoate
Ethyl carbamate
C9H16O2
C6H15N
C7H15NO2
C6H8O2
C3H7NO2
3953-10-4
617-79-8
591-62-8
4341-76-8
51-79-6
156.222
101.190
145.200
112.127
89.094
4938
4939
9-Ethyl-9H-carbazol-3-amine
9-Ethyl-9H-carbazole
C14H14N2
C14H13N
132-32-1
86-28-2
4940
Ethyl chloroacetate
C4H7ClO2
4941
Ethyl 4-chloroacetoacetate
C6H9ClO3
4905
4906
4907
Organic
4914
4915
4916
4917
HCP_Section_03.indb 252
Ethyl α-bromopropionate
2-Ethylbutyl alcohol
2-Ethyl-1-butanamine
Urethane
159(4)
-18
195.054
11514
263
177
33
1.449620 i H2O; s EtOH,
eth
1.454320 sl ctc
1.449020 i H2O; msc
EtOH, eth; s
chl
1.451620 s EtOH, eth,
ace; sl ctc
1.402520 sl H2O, ctc; msc
EtOH, eth
1.389825 sl H2O, ctc; s
EtOH, eth
1.413220 sl H2O, ctc; msc
EtOH, eth
1813.5
<-100
liq
liq
liq
125
-22
pr (bz, to)
119
161(9)
0.832620 1.422020 sl H2O; s EtOH,
eth, chl
0.982520 1.423420 vs eth
0.689420 1.396920 i H2O; s eth,
ace, bz, chl
0.918220 1.424220 vs ace, eth,
EtOH
0.917520 1.424320 i H2O; s EtOH,
eth
0.912220 1.410520 s EtOH
0.879020 1.410920 i H2O; s EtOH,
eth, ctc
8020
48.25(0.04)
221(12)
163
185
0.943426 1.427826
0.964120 1.437220
0.986221 1.414451 vs H2O, EtOH,
eth, bz, chl,
py; sl lig
210.274
195.260 nd (al)
99
67(1)
19010
1.05980
105-39-5
122.551 liq
-21
144(3)
1.158520
638-07-3
164.586
-8
220 dec
1.21825
1.639480 i H2O; vs EtOH,
eth
1.421520 i H2O; msc
EtOH, eth, ace;
s bz
1.452020
4/11/16 11:27 AM
Physical Constants of Organic Compounds
3-253
OH
O S O
4901
O
O
O
4902
4903
2-Ethyl-1H-benzimidazole
4904
Ethyl benzoate
4905
Ethyl 1,3-benzodioxole-5-carboxylate
Ethyl benzoylacetate
O
O
N
H
O
O
O
4906
O
O
Br
O
4907
Ethyl N-benzylglycinate
O
O
O
O
N
H
4-Ethylbenzenesulfonic acid
O
O
N
O
O
Br
Br
4909
4911
4910
Ethyl 4-bromoacetoacetate
Ethyl 2-bromobutanoate
Ethyl 4-bromobenzoate
Organic
Ethyl bromoacetate
O
O
Br
O
4908
Ethyl 2-benzylideneacetoacetate
O
O
O
Br
O
Br
O
4912
Br
O
4913
Ethyl 4-bromobutanoate
4915
Ethyl 6-bromohexanoate
4917
Br
4918
4920
4924
O
O
OH
4925
2-Ethylbutanoic acid
Cl
4926
2-Ethylbutanoic acid, triethyleneglycol diester
O
O
Ethyl cis-2-butenoate
2-Ethylbutanal
O
O
O
4927
2-Ethyl-1-butanol
O
O
4922
Ethyl 3-bromopropanoate
O
O
4929
4921
Ethyl 2-bromopropanoate
O
O
O
O
O
OH
4923
Br
Br
Ethyl 5-bromopentanoate
O
Ethyl butanoate
O
O
O
4919
Ethyl 2-bromopentanoate
O
Ethyl 2-bromo-2-methylpropanoate
O
Br
Ethyl 3-bromo-2-oxopropanoate
O
4916
Ethyl 2-bromo-3-methylbutanoate
O
O
O
Br
Br
O
O
O
O
O
4914
Ethyl trans-4-bromo-2-butenoate
O
Br
O
4928
2-Ethylbutanoyl chloride
2-Ethyl-1-butene
O
O
O
O
NH2
N
H
O
4930
Ethyl trans-2-butenoate
4931
4932
Ethyl 3-butenoate
4934
4933
2-Ethylbutyl acetate
2-Ethylbutylamine
2-Ethylbutyl acrylate
O
4935
Ethyl N-butylcarbamate
NH2
O
O
O
4936
Ethyl 2-butynoate
H2N
N
N
O
4937
Ethyl carbamate
4938
9-Ethyl-9H-carbazol-3-amine
4939
9-Ethyl-9H-carbazole
O
Cl
O
O
4940
Ethyl chloroacetate
O
Cl
O
4941
Ethyl 4-chloroacetoacetate
Physical Constants of Organic Compounds
3-254
Organic
Mol. Form.
CAS RN
Mol.
Wt.
Ethyl 4-chlorobenzoate
Ethyl 4-chlorobutanoate
C9H9ClO2
C6H11ClO2
7335-27-5
3153-36-4
184.619
150.603
4944
4945
4946
4947
Ethyl chlorofluoroacetate
Ethyl chloroformate
Ethyl 2-chloro-2-oxoacetate
Ethyl 2-chloropropanoate
C4H6ClFO2
C3H5ClO2
C4H5ClO3
C5H9ClO2
401-56-9
541-41-3
4755-77-5
535-13-7
140.541
108.524 liq
136.534 hyg
136.577
4948
Ethyl 3-chloropropanoate
C5H9ClO2
623-71-2
136.577
162
4949
4950
4951
4952
Ethyl chlorosulfinate
Ethyl chlorosulfonate
S-Ethyl chlorothioformate
Ethyl trans-cinnamate
6378-11-6
625-01-4
2941-64-2
4192-77-2
128.578
144.577
124.589 liq
176.212
6.5(0.5)
52.544
152.5
136
270(3)
4953
4954
Ethyl cyanate
Ethyl cyanoacetate
C3H5NO
C5H7NO2
627-48-5
105-56-6
71.078
113.116 liq
-26.1(0.1)
162 dec
216(4)
4955
4956
Ethyl 2-cyanoacrylate
Ethyl 2-cyano-2-propenoate
Ethyl 2-cyano-3,3-diphenyl-2- Etocrilene
propenoate
Ethyl 2-cyano-3-ethoxyacrylate
Ethyl cyanoformate
C6H7NO2
C18H15NO2
7085-85-0
5232-99-5
125.126 liq
277.318
110.5
553
1953
C8H11NO3
94-05-3
169.178
52
190.5
C4H5NO2
623-49-4
99.089
115.5
1.00325
C11H11NO2
4553-07-5
189.211 oil
275 dec
1.09120
C12H11NO2
2025-40-3
1.107625
C6H12
4806-61-5
201.221 (i) nd (al) (ii) 51
oil
84.159 liq
-142.9(0.2)
18815
4961
Ethyl 2-cyano-2-phenylacetate
Ethyl 2-cyano-3-phenyl-2propenoate
Ethylcyclobutane
70(1)
4962
Ethylcyclohexane
C8H16
1678-91-7
112.213 liq
4963
Ethyl cyclohexanecarboxylate
C9H16O2
3289-28-9
156.222
4964
4965
1-Ethylcyclohexene
Ethyl 3-cyclohexene-1carboxylate
Ethyl cyclohexylacetate
Ethylcyclopentane
C8H14
C9H14O2
1453-24-3 110.197 liq
15111-56-5 154.206
-109.9(0.1)
0.728420 1.402020 i H2O; msc
EtOH, eth; s
ace, bz, peth
0.788020 1.433020 i H2O; s EtOH,
ace, bz; vs lig;
msc ctc
0.936220 1.450115 vs ace, eth,
EtOH, chl
0.817625 1.456720
0.968820 1.457820
C10H18O2
C7H14
5452-75-5
1640-89-7
170.249
98.186 liq
211
-138.42(0.02) 103.5(0.6)
C8H12O3
611-10-9
156.179
4969
4970
4971
4972
Ethyl 2-cyclopentanone-1carboxylate
1-Ethylcyclopentene
Ethylcyclopropane
Ethyl cyclopropanecarboxylate
Ethyl decanoate
Ethyl caprate
C7H12
C5H10
C6H10O2
C12H24O2
2146-38-5
1191-96-4
4606-07-9
110-38-3
96.170 liq
70.133 liq
114.142
200.318 liq
-118.8(0.4)
-149.4(0.2)
4973
Ethyl diazoacetate
C4H6N2O2
623-73-4
114.103 ye orth cry
4974
Ethyl dibromoacetate
C4H6Br2O2
617-33-4
245.898
4975
Ethyl 2,3-dibromobutanoate
C6H10Br2O2
609-11-0
273.950 nd
4976
Ethyl 2,4-dibromobutanoate
C6H10Br2O2
4977
4978
4979
Ethyl 2,3-dibromopropanoate
Ethyl 3,6-di(tert-butyl)-1naphthalenesulfonate
Ethyl dichloroacetate
4980
Ethyldichloroarsine
4981
4982
4983
Ethyl dichlorocarbamate
Ethyl 2,3-dichloropropanoate
Ethyl diethoxyacetate
No.
Name
4942
4943
4957
4958
4959
4960
4966
4967
4968
HCP_Section_03.indb 254
Synonym
Ethyl oxalyl chloride
Ethyl α-chloropropionate
C2H5ClO2S
C2H5ClO3S
C3H5ClOS
Ethyl trans-3-phenyl-2-prope- C11H12O2
noate
Ethyl 2-benzylidene-2-cyanoacetate
Diazoacetic ester
Ethyl dibunate
Dichloroethylarsine
Physical
Form
mp/˚C
bp/˚C
237.5
184
-80.6
129
91(2)
137
147(4)
-111.28(0.1) 131.8(0.4)
196(4)
136(3)
194.5
den
g cm –3
nD
Solubility
1.187314
vs EtOH
1.075620 1.431120 vs ace, eth,
EtOH
1.22520 1.392720
1.135220 1.397420 vs bz, eth, chl
1.222620
vs bz, eth
1.079320 1.417820 i H2O; msc
EtOH, eth; sl
ctc
1.108620 1.425420 sl H2O; msc
EtOH, eth
1.283720 1.455025 vs eth
1.350225 1.41620 vs eth, chl, lig
1.19520 1.482020
1.049120 1.559820 i H2O; vs EtOH,
eth, ace; s bz,
ctc
0.8920
1.378825 vs eth, EtOH
1.065420 1.417520 s H2O; vs eth,
EtOH
1.382020 i H2O; s EtOH,
eth, ctc
1.501225 vs ace, bz, eth,
EtOH
1.5033
vs ace, chl
221
0.953714 1.45114
0.766520 1.419820 i H2O; msc
EtOH, eth, ace;
s bz, tol
1.078121 1.451920 s eth, bz
-20(2)
106.2(0.2)
36(2)
128(5)
242(1)
0.793625
0.679025
0.960815
0.865020
-22
140 dec
1.085218
194
1.899120
11330
1.680020
36847-51-5 273.950
14952
1.698720
C5H8Br2O2
C20H28O3S
3674-13-3
5560-69-0
259.925
348.499
214.5
1.796620
C4H6Cl2O2
535-15-9
156.996
155
C2H5AsCl2
598-14-1
174.889
155.3
C3H5Cl2NO2
C5H8Cl2O2
C8H16O4
13698-16-3 157.984
6628-21-3 171.022
6065-82-3 176.211
6618
183(7)
199
1.282720 1.438620 sl H2O; msc
EtOH, eth; s
ace, chl
1.6620
s H2O; misc
EtOH, bz
1.30430 1.459520
1.240120 1.448220 vs eth, EtOH
0.98525 1.410020
58.5
1.441220
1.378620
1.419020
1.425620 i H2O; vs eth,
EtOH, chl
1.460520 sl H2O; msc
EtOH, eth, bz,
lig
1.501713 i H2O; msc
EtOH, eth
sl H2O, ctc; s
EtOH, eth
1.496020 i H2O; s EtOH,
eth
1.500720 s EtOH, eth
s chl
4/11/16 11:27 AM
Physical Constants of Organic Compounds
O
3-255
O
O
O
Cl
O
Cl
Cl
4942
F
O
4943
Ethyl 4-chlorobenzoate
O S
Cl
4949
Cl
Cl
4946
Ethyl chloroformate
O
O
O
4947
Ethyl 2-chloro-2-oxoacetate
O
4948
Ethyl 2-chloropropanoate
Ethyl 3-chloropropanoate
O
O
Cl
4950
O
S
4952
S-Ethyl chlorothioformate
4953
Ethyl trans-cinnamate
O
O
O
4951
Ethyl chlorosulfonate
O
N
O
N
N
4954
Ethyl cyanate
4955
Ethyl cyanoacetate
Ethyl 2-cyanoacrylate
Organic
Ethyl chlorosulfinate
O
O
O
4945
Ethyl chlorofluoroacetate
Cl
O S O
O
O
Cl
4944
Ethyl 4-chlorobutanoate
Cl
O
O
O
N
O
N
O
O
Ethyl 2-cyano-3,3-diphenyl-2-propenoate
4958
Ethyl 2-cyano-3-ethoxyacrylate
O
O
N
4957
O
N
O
O
O
4956
O
N
Ethyl cyanoformate
4959
4960
Ethyl 2-cyano-2-phenylacetate
O
O
4963
4965
4964
Ethyl cyclohexanecarboxylate
O
4966
Ethyl 3-cyclohexene-1-carboxylate
1-Ethylcyclohexene
Ethyl cyclohexylacetate
O
N
O
4970
4971
Ethylcyclopropane
4967
Ethylcyclopentane
O
O
4972
Ethyl cyclopropanecarboxylate
Br
O
N
Ethyl diazoacetate
4968
4969
Ethyl 2-cyclopentanone-1-carboxylate
Br
1-Ethylcyclopentene
O
O
O
Br
O
Br
O
4973
Ethyl decanoate
Ethylcyclohexane
O
O
O
O
4962
Ethylcyclobutane
HO
O
O
4961
Ethyl 2-cyano-3-phenyl-2-propenoate
O
Br
Br
4974
Ethyl dibromoacetate
4975
Ethyl 2,3-dibromobutanoate
4976
Ethyl 2,4-dibromobutanoate
O
O S O
O
O
Br
O
Cl
O
Cl
Br
4977
Ethyl 2,3-dibromopropanoate
O
4978
Ethyl 3,6-di(tert-butyl)-1-naphthalenesulfonate
4979
Ethyl dichloroacetate
Cl
As
4980
Cl
Cl
Ethyldichloroarsine
N
Cl
O
O
O
O
4981
Ethyl dichlorocarbamate
Cl
O
O
O
Cl
4982
Ethyl 2,3-dichloropropanoate
4983
Ethyl diethoxyacetate
Physical Constants of Organic Compounds
3-256
Mol. Form.
CAS RN
Mol.
Wt.
Ethyl diethylmalonate
C11H20O4
77-25-8
216.275
230
4985
4986
Ethyl difluoroacetate
Ethyldifluoroarsine
C4H6F2O2
C2H5AsF2
454-31-9
430-40-0
100
94.3
4987
5-Ethyldihydro-5-sec-butyl-2- Thiobutabarbital
thioxo-4,6(1H,5H)-pyrimidinedione
5-Ethyldihydro-2(3H)-furanone
Ethyl dihydrogen phosphate
C10H16N2O2S
2095-57-0
124.087
141.980 liq, fumes in -38.7
air
228.311
169
C6H10O2
C2H7O4P
695-06-7
1623-14-9
114.142 liq
126.048 hyg cry
-18
218(4)
dec
C12H14N2O2
125-33-7
218.251
281.5
C10H12O4
2524-37-0
No.
Name
4984
4988
4989
4990
Synonym
Physical
Form
mp/˚C
bp/˚C
den
g cm –3
4995
4996
1-Ethyl-3,5-dimethylbenzene
C10H14
934-74-7
134.218 liq
-84.3(0.1)
184(2)
4997
4998
2-Ethyl-1,3-dimethylbenzene
2-Ethyl-1,4-dimethylbenzene
C10H14
C10H14
2870-04-4
1758-88-9
134.218 liq
134.218 liq
-16.3(0.3)
-53.7(0.3)
190(2)
186(2)
4999
5000
3-Ethyl-1,2-dimethylbenzene
4-Ethyl-1,2-dimethylbenzene
C10H14
C10H14
933-98-2
934-80-5
134.218 liq
134.218 liq
-49.5(0.3)
-66.9(0.2)
194(2)
189(2)
5001
N’-Ethyl-N,N-dimethyl-1,2ethanediamine
Ethyl 4,4-dimethyl-3-oxopentanoate
3-Ethyl-2,2-dimethylpentane
3-Ethyl-2,3-dimethylpentane
3-Ethyl-2,4-dimethylpentane
Ethyl 2,2-dimethylpropanoate
3-Ethyl-2,5-dimethylpyrazine
C6H16N2
123-83-1
116.204
C9H16O3
17094-34-7 172.221 liq
C9H20
C9H20
C9H20
C7H14O2
C8H12N2
16747-32-3
16747-33-4
1068-87-7
3938-95-2
13360-65-1
128.255 liq
128.255
128.255 liq
130.185 liq
136.194
134(4)
142(5)
-122.38(0.09) 123(6)
-89.5(0.2)
118.3(0.4)
180.5
0.743820
0.750825
0.736520
0.85620
0.965724
C8H13N
517-22-6
123.196 pr
0
197(6)
0.91320
C9H13NO2
2199-44-2
167.205 cry (al)
125
13510.5
C9H13NO2
2199-51-1
C9H13NO2
2199-52-2
167.205 cry (eth-lig, 78.5
peth)
167.205 orth (al)
117.5
C9H13NO2
2199-53-3
167.205 cry (dil al)
111.3
C7H10O4
C3H6OS2
C2H4
615-79-2
151-01-9
74-85-1
158.152
122.209 unstab liq
28.053 col gas
18
214
-53
25
-169.18(0.02) -103.8(0.3)
C4H8N2S4
111-54-6
212.380 unstab liq
C3H4O3
96-49-1
88.062
C10H16N2O8
60-00-4
292.242 cry (w)
245 dec
C10H18N2Na2O10
6381-92-6
372.237
242 dec
C38H76N2O2
110-30-5
593.022 cry (EtOH)
149
C2H5N
151-56-4
43.068
-78.0(0.5)
4992
Organic
4993
4994
5002
5003
5004
5005
5006
5007
5008
5009
5010
5011
5012
5013
5014
5015
5016
5017
5018
5019
5020
5021
3-Ethyl-2,4-dimethyl-1Hpyrrole
Ethyl 3,5-dimethylpyrrole-2carboxylate
Ethyl 2,4-dimethylpyrrole-3carboxylate
Ethyl 2,5-dimethylpyrrole-3carboxylate
Ethyl 4,5-dimethylpyrrole-3carboxylate
Ethyl 2,4-dioxopentanoate
O-Ethyl dithiocarbonate
Ethylene
Ethylenebisdithiocarbamic
acid
Ethylene carbonate
3-Ethyl-oxylene
Ethyl pivaloylacetate
Ethyl 2,2-dimethylpropionate
Xanthogenic acid
Ethene
Vinylene carbonate
Ethylenediaminetetraacetic
EDTA
acid
Ethylenediaminetetraacetic
EDTA disodium
acid, disodium salt, dihydrate
N,N’-Ethylene distearylamide N,N’-Dioctadecanoylethanediamine
Ethyleneimine
Aziridine
HCP_Section_03.indb 256
Solubility
1.026120 1.449520 vs H2O, EtOH
1.43025 1.427
vs H2O, ace,
eth, EtOH
5-Ethyldihydro-5-phenylPrimidone
4,6(1H,5H)-pyrimidinedione
Ethyl 2,4-dihydroxy-6-methylbenzoate
O-Ethyl S-[2VX Nerve agent
(diisopropylamino)ethyl]
methylphosphonothioate
Ethyldimethylamine
N,N-Dimethylethanamine
Ethyl 4-(dimethylamino)
benzoate
1-Ethyl-2,4-dimethylbenzene
4991
nD
0.964330 1.424020 i H2O; msc
EtOH, eth; s
ctc
1.176520
i H2O
1.70817
196.200 lf (HOAc), pr 132
(al)
50782-69-9 267.369 very toxic
liq
sub
C4H11N
C11H15NO2
598-56-1
73.137 liq
10287-53-3 193.243
-140(4)
66.5
36.5(0.6)
19014
0.67520 1.370525
1.0099100
C10H14
874-41-9
134.218 liq
-62.9(0.2)
188(2)
134.5
0.876320 1.503820 vs ace, bz, eth,
EtOH
0.860825 1.498120 i H2O; msc
EtOH, eth, ace,
bz; s peth, ctc
0.886425 1.510720
0.873225 1.504320 i H2O; msc
EtOH, eth, ace,
bz; s peth, ctc
0.888125 1.511720
0.870625 1.503120 i H2O; msc
EtOH, eth, ace,
bz; s peth, ctc
0.73825 1.422220
8317
0.9718
C11H26NO2PS
-99.4(0.1)
vs eth, EtOH
291
vs eth, EtOH
291
vs EtOH
1.125120 1.475717
0.5678104
mcl pl (al)
liq
36.331​
(0.004)
1.412320
1.422120
1.413120
1.390620 s EtOH, eth
1.501424 sl H2O, EtOH,
eth
1.496120 sl H2O; s EtOH,
eth, bz, chl
s EtOH, ace
vs eth, EtOH,
chl
vs eth, EtOH
1.363-100 i H2O; sl EtOH,
bz, ace; s eth
246(1)
1.321439 1.414850 msc H2O, EtOH,
eth, bz, chl,
AcOEt
54(1)
0.83225
msc H2O; s
EtOH; vs eth;
sl chl
4/11/16 11:28 AM
Physical Constants of Organic Compounds
3-257
O
O
O
O
F
O
O
O
F
As
4985
4986
F
4984
Ethyl diethylmalonate
Ethyl difluoroacetate
F
S
N
H
O
O
4987
Ethyldifluoroarsine
O
4988
5-Ethyldihydro-5-sec-butyl-2-thioxo-4,6(1H,5H )-pyrimidinedione
4989
5-Ethyldihydro-2(3H)-furanone
Ethyl dihydrogen phosphate
O
NH
O
N
H
O
O
HO P OH
O
NH
O
HO
4990
O
OH
4991
N
S
N
4992
Ethyl 2,4-dihydroxy-6-methylbenzoate
4993
O-Ethyl S-[2-(diisopropylamino)ethyl] methylphosphonothioate
Ethyldimethylamine
Organic
5-Ethyldihydro-5-phenyl-4,6(1H,5H )-pyrimidinedione
O
P
O
O
N
4994
Ethyl 4-(dimethylamino)benzoate
4995
N
5000
4996
1-Ethyl-2,4-dimethylbenzene
1-Ethyl-3,5-dimethylbenzene
O
H
N
4998
4999
2-Ethyl-1,4-dimethylbenzene
3-Ethyl-1,2-dimethylbenzene
O
O
5001
4-Ethyl-1,2-dimethylbenzene
4997
2-Ethyl-1,3-dimethylbenzene
5002
N’-Ethyl-N,N-dimethyl-1,2-ethanediamine
Ethyl 4,4-dimethyl-3-oxopentanoate
5003
5004
3-Ethyl-2,2-dimethylpentane
5005
3-Ethyl-2,3-dimethylpentane
3-Ethyl-2,4-dimethylpentane
O
N
O
O
N
5006
5007
Ethyl 2,2-dimethylpropanoate
5008
3-Ethyl-2,5-dimethylpyrazine
O
O
N
H
N
H
N
H
O
5009
3-Ethyl-2,4-dimethyl-1H-pyrrole
5010
Ethyl 3,5-dimethylpyrrole-2-carboxylate
Ethyl 2,4-dimethylpyrrole-3-carboxylate
O
O
O
O
O
N
H
N
H
5011
Ethyl 2,5-dimethylpyrrole-3-carboxylate
S
O
O
5012
O
O
5013
Ethyl 4,5-dimethylpyrrole-3-carboxylate
Ethyl 2,4-dioxopentanoate
SH
5014
O-Ethyl dithiocarbonate
H
H
H
H
5015
Ethylene
S
H
N
HS
N
H
S
5016
SH
Ethylenebisdithiocarbamic acid
O
O
O
5017
Ethylene carbonate
O
HOOC
HOOC
N
N
5018
COO Na
COOH
COOH
Ethylenediaminetetraacetic acid
NH
N
HOOC
N
Na
COOH
2H2O
OOC
NH
N
H
O
5019
Ethylenediaminetetraacetic acid, disodium salt, dihydrate
5020
N,N’-Ethylene distearylamide
5021
Ethyleneimine
Physical Constants of Organic Compounds
3-258
No.
Name
5022
5023
5024
5025
5026
Ethylestrenol
N-Ethyl-1,2-ethanediamine
Ethyl ethoxyacetate
Ethyl 3-ethoxypropanoate
Ethyl 2-ethoxy-1(2H)quinoline­carboxylate
Ethyl 2-ethylacetoacetate
Ethyl ethylcarbamate
5027
5028
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
EEDQ
C20H32O
C4H12N2
C6H12O3
C7H14O3
C14H17NO3
965-90-2
110-72-5
817-95-8
763-69-9
16357-59-8
288.467 cry
88.151
132.157
146.184
247.290
C8H14O3
C5H11NO2
607-97-6
623-78-9
158.195
117.147
C10H20O2
C16H19N
2983-37-1 172.265
64653-59-4 225.329
mp/˚C
bp/˚C
den
g cm –3
129
158
168(2)
1260.1
0.83725 1.438520
0.970220 1.403920 s EtOH, eth, ace
0.949020 1.406520
s chl
197(4)
176
0.984716 1.421425 msc EtOH, eth
0.981320 1.421520 vs H2O, eth,
EtOH
0.858625 1.412325
1.555025 i H2O; vs EtOH,
eth; sl chl; s
acid
1.1520
56.5
9028
336603
Organic
Ethyl 2-ethylhexanoate
2-Ethyl-N-(2-ethylphenyl)­
aniline
5031
C4H10ClOPS
1497-68-3
172.613 liq
5032
5033
5034
O-Ethyl ethylthiophosphonyl
chloride
Ethyl fluoroacetate
Ethyl 4-fluorobenzoate
N-Ethylformamide
C4H7FO2
C9H9FO2
C3H7NO
459-72-3
451-46-7
627-45-2
106.096
168.164 mcl pr (w)
73.094
26
120
210
198
5035
Ethyl formate
C3H6O2
109-94-4
74.079
-79.6(0.5)
54.09(0.1)
5036
2-Ethylfuran
C6H8O
3208-16-0
96.127
5037
Ethyl 2-furancarboxylate
C7H8O3
614-99-3
140.137 lf or pr
34.5
5038
5039
γ-Ethyl L-glutamate
Ethyl heptafluorobutanoate
C7H13NO4
C6H5F7O2
1119-33-1
356-27-4
175.183
242.092
191
5040
5041
3-Ethylheptane
4-Ethylheptane
C9H20
C9H20
15869-80-4 128.255 liq
2216-32-2 128.255
-114.9
143.1(0.7)
141(4)
5042
Ethyl heptanoate
C9H18O2
106-30-9
158.238 liq
-66.2(0.5)
188(2)
5043
5044
5045
C9H18O2
C9H20O
C8H12O2
3274-29-1
597-90-0
2396-84-1
158.238 liq
144.254
140.180
5046
2-Ethylheptanoic acid
4-Ethyl-4-heptanol
Ethyl trans,trans-2,4-hexadie- Ethyl sorbate
noate
2-Ethylhexanal
C8H16O
123-05-7
128.212 liq
5047
3-Ethylhexane
C8H18
619-99-8
114.229
5048
2-Ethyl-1,3-hexanediol
C8H18O2
94-96-2
146.228 liq
-40
243(8)
5049
Ethyl hexanoate
C8H16O2
123-66-0
144.212 liq
-67.6(0.4)
165(1)
5050
2-Ethylhexanoic acid
C8H16O2
149-57-5
144.212
5051
2-Ethyl-1-hexanol
C8H18O
104-76-7
130.228 liq
5052
5053
5054
5055
2-Ethylhexanoyl chloride
2-Ethyl-2-hexenal
Ethyl 3-hexenoate
2-Ethylhexyl acetate
C8H15ClO
C8H14O
C8H14O2
C10H20O2
760-67-8
645-62-5
2396-83-0
103-09-3
162.657
126.196
142.196
172.265 liq
5056
5057
5058
5059
2-Ethylhexyl acrylate
2-Ethylhexylamine
2-Ethylhexyl butyl phthalate
2-Ethylhexyl dihydrogen
phosphate
2-Ethylhexyl diphenyl
phosphite
Ethyl hexyl ether
2-Ethylhexyl 2-hydroxybenzoate
2-Ethylhexyl methacrylate
2-[(2-Ethylhexyl)oxy]ethanol
C11H20O2
2-Ethyl-1-hexanamine
C8H19N
Butyl 2-ethylhexyl phthalate
C20H30O4
Mono(2-ethylhexyl) phosphate C8H19O4P
103-11-7
104-75-6
85-69-8
1070-03-7
184.276
129.244
334.450 col liq
210.208 liq
5061
5062
5063
5064
HCP_Section_03.indb 258
Ethyl 2-furanoate
Ethyl oenanthate
Ethohexadiol
Ethyl hydrosorbate
29
liq
nD
Solubility
77
5029
5030
5060
Ethyl 2-ethylcaproate
Physical
Form
350.7
92(3)
196.8
95
15331
179(7)
195.5
<-100
161(7)
118.5(0.5)
227.5(0.1)
-70
186.2(0.2)
-80
10140
175(1)
166.5
200(1)
-90
12560
172(12)
1.091220 1.375520 vs H2O
1.14625 1.486420 vs eth, EtOH
0.955220 1.432020 msc H2O, EtOH,
eth
0.920820 1.360920 s H2O; msc
EtOH, eth; vs
ace; sl ctc
0.901820 1.440320 s EtOH, eth,
ace, bz
1.117421 1.479721 i H2O; msc
EtOH, eth, ace;
s bz
sl H2O
1.39420 1.301120 sl H2O; s eth,
ace
0.722525 1.409320
0.724125 1.409620 i H2O; s eth;
msc EtOH,
ace, bz
0.881720 1.410020 sl H2O, ctc; s
EtOH, eth
1.425527
0.835020 1.433220 vs eth, EtOH
0.950620 1.495120 vs eth, EtOH,
chl
0.854020 1.414220 i H2O; s EtOH,
eth; sl ctc
0.713620 1.401820 i H2O; msc
EtOH, eth, ace,
bz, chl; s ctc
22
20
0.9325
1.4497
sl H2O; s EtOH,
eth
0.87320 1.407320 sl H2O; vs eth,
EtOH
0.903125 1.424120 s H2O, eth, ctc;
sl EtOH
0.831925 1.430020 i H2O; s EtOH,
eth, ace, bz,
chl
0.93925 1.433520
0.855420
0.895720 1.425520
0.871820 1.420420 i H2O; s EtOH,
eth
0.88025 1.433225
sl H2O
sl H2O
s H2O, bz
Forstab
C20H27O3P
15647-08-2 346.400
1520.15
1.05420
1-Ethoxyhexane
Octisalate
C8H18O
C15H22O3
5756-43-4
118-60-5
130.228
250.334 liq
142(4)
19021
0.772220 1.400820 vs eth, EtOH
1.01
C12H22O2
C10H22O2
688-84-6
1559-35-9
198.302
174.281
12018
231(4)
0.88025
Ethylene glycol mono(2ethylhexyl) ether
1.520727
1.43625
4/11/16 11:28 AM
Physical Constants of Organic Compounds
3-259
OH
H
O
H
N
5022
O
NH2
5023
Ethylestrenol
O
O
O
5024
N-Ethyl-1,2-ethanediamine
5028
O
O
O
5026
Ethyl 3-ethoxypropanoate
5027
Ethyl 2-ethoxy-1(2H )-quinolinecarboxylate
S
O P
Cl
N
H
5029
Ethyl 2-ethylacetoacetate
5030
Ethyl 2-ethylhexanoate
O
F
5031
2-Ethyl-N-(2-ethylphenyl)aniline
O
O
5032
O-Ethyl ethylthiophosphonyl chloride
Ethyl fluoroacetate
N
H
F
5033
Ethyl 4-fluorobenzoate
O
5034
N-Ethylformamide
Organic
Ethyl ethylcarbamate
O
O
O
O
O
N
5025
Ethyl ethoxyacetate
O
O
N
H
O
O
H
O
O
O
O
O
O
O
5035
NH2
5037
2-Ethylfuran
F
F
O
O
5036
Ethyl formate
F F
HO
O
F
F F
5039
5038
γ-Ethyl L-glutamate
Ethyl 2-furancarboxylate
O
Ethyl heptafluorobutanoate
5040
5041
3-Ethylheptane
4-Ethylheptane
O
O
OH
O
OH
O
O
O
5043
5042
Ethyl heptanoate
5044
2-Ethylheptanoic acid
5045
4-Ethyl-4-heptanol
O
OH
OH
O
5046
Ethyl trans,trans-2,4-hexadienoate
2-Ethylhexanal
O
O
Cl
OH
OH
O
O
5048
2-Ethyl-1,3-hexanediol
5047
3-Ethylhexane
5049
5050
Ethyl hexanoate
5051
2-Ethylhexanoic acid
2-Ethyl-1-hexanol
5052
2-Ethylhexanoyl chloride
5053
2-Ethyl-2-hexenal
O
5054
Ethyl 3-hexenoate
O
O
O
O
O
O
O
NH2
O
O P OH
OH
O
5055
2-Ethylhexyl acetate
5057
5056
2-Ethylhexylamine
2-Ethylhexyl acrylate
O
P O
O
O
O
5058
2-Ethylhexyl butyl phthalate
5059
2-Ethylhexyl dihydrogen phosphate
O
OH
O
O
OH
O
5060
2-Ethylhexyl diphenyl phosphite
5061
Ethyl hexyl ether
5062
2-Ethylhexyl 2-hydroxybenzoate
5063
2-Ethylhexyl methacrylate
5064
2-[(2-Ethylhexyl)oxy]ethanol
Physical Constants of Organic Compounds
3-260
Organic
Mol. Form.
CAS RN
Mol.
Wt.
C2H8N2
624-80-6
60.098
Ethyl carbazate
C3H8N2O2
4114-31-2
104.108 cry
Ethyl hydrogen hexanedioate
C8H14O4
626-86-8
285
0.979620 1.431120
C6H8O4
2459-05-4
174.195 hyg cry (eth, 29
peth)
144.126
70
14716
1.110987
C6H10O4
1070-34-4
146.141 pr or nd
8
17242
1.146620 1.432720
C2H6O2
3031-74-1
62.068
-100
95(8)
0.933220 1.380020
C4H8O3
C9H10O3
623-50-7
7781-98-8
104.105
166.173 pl (bz)
156(3)
74
1.082623 1.418020
1.0680131
C9H10O3
120-47-8
166.173 cry (dil al)
117
Ethyl 3-hydroxybutanoate, (±)-
C6H12O3
35608-64-1 132.157
185
1.01720
5075
Ethyl 2-hydroxy-3-butenoate
C6H10O3
91890-87-8 130.141
173 dec
1.047015 1.43613
5076
Cyclobutyrol
C10H18O3
512-16-3
186.248 cry
(eth-peth)
81.5
16424
1.001018 1.468018
N,N-Diethylhydroxylamine
C4H11NO
C8H16O2
C10H12O4
3710-84-7
496-03-7
617-05-0
89.136
144.212
196.200 nd (dil al)
10
131.0(0.3)
13850
292
0.866920 1.419520
C20H38O3
55066-53-0 326.514
25813
0.918020 1.461822
5081
5082
α-Ethyl-1hydroxycyclohexaneacetic
acid
N-Ethyl-N-hydroxyethanamine
2-Ethyl-3-hydroxyhexanal
Ethyl 4-hydroxy-3-methoxybenzoate
Ethyl cis-12-hydroxy-9octadecenoate, (R)Ethylidenecyclohexane
5-Ethylidene-2-norbornene
C8H14
C9H12
1003-64-1 110.197
16219-75-3 120.191 liq
137(3)
146
0.82225
0.893
5083
5084
5085
5086
1-Ethyl-1H-imidazole
Ethyl iodoacetate
Ethyl isobutylcarbamate
Ethyl isocyanate
C5H8N2
C4H7IO2
C7H15NO2
C3H5NO
7098-07-9
623-48-3
539-89-9
109-90-0
96.131
214.002 oil
145.200
71.078
208
179(7)
11030
56(1)
0.99925
1.817313 1.507913
0.943220 1.428820
0.903120 1.380820
5087
Ethyl isocyanide
C3H5N
624-79-3
55.079
<-66
79
0.740220 1.362220
5088
C10H9NO2
5022-29-7
175.184 nd (al)
79
285.5
5089
5090
5091
N-Ethyl-1H-isoindole-1,3(2H)dione
Ethyl isopentyl ether
Ethylisopropylamine
N-Ethyl-2-propanamine
1-Ethyl-2-isopropylbenzene
C7H16O
C5H13N
C11H16
628-04-6
116.201
19961-27-4 87.164
18970-44-0 148.245
112(5)
68(7)
193(7)
0.88820
5092
Ethyl isopropyl ether
C5H12O
625-54-7
88.148
54(3)
0.72025
5093
Ethyldiisopropylamine
C8H19N
7087-68-5
129.244
114(10)
0.74225
5094
5095
N-Ethyl-N-isopropyl-2propanamine
Ethyl isopropyl sulfide
Ethyl isothiocyanate
C5H12S
C3H5NS
5145-99-3
542-85-8
104.214 liq
87.144 liq
-122.2(0.2)
-5.9
107.3(0.6)
140(9)
5096
Ethyl lactate
Ethyl 2-hydroxypropionate
C5H10O3
2676-33-7
118.131 liq
-26
151(7)
5097
Ethyl laurate
C14H28O2
106-33-2
228.371 liq
-1.8(0.4)
276(3)
5098
5099
Ethyl levulinate
Ethyl mercaptoacetate
C7H12O3
C4H8O2S
539-88-8
623-51-8
144.168
120.171
205.8
157
5100
Ethyl methacrylate
C6H10O2
97-63-2
114.142
116(19)
0.824620
0.999020 1.513020 i H2O; msc
EtOH, eth
1.032820 1.412420 vs H2O, eth,
EtOH
0.861820 1.431120 i H2O; vs EtOH;
msc eth; sl ctc
1.011120 1.422920 vs H2O, EtOH
1.096415 1.458220 s EtOH, eth; sl
ctc
0.913520 1.414720 sl H2O, chl; msc
EtOH, eth
5101
5102
5103
C3H8O3S
C9H12O
C10H14O2
62-50-0
1515-95-3
5349-60-0
124.159
136.190
166.217
8610
196(8)
14320
5104
5105
Ethyl methanesulfonate
1-Ethyl-4-methoxybenzene
α-Ethyl-4methoxybenzenemethanol
Ethyl 2-methoxybenzoate
Ethyl 4-methoxybenzoate
C10H12O3
C10H12O3
7335-26-4
94-30-4
180.200
180.200
7.5
262(7)
266(19)
5106
4-Ethyl-2-methoxyphenol
C9H12O2
2785-89-9
152.190 liq
-7
236.5
No.
Name
5065
Ethylhydrazine
5066
Ethyl hydrazinecarboxylate
5067
Ethyl hydrogen adipate
5068
Ethyl hydrogen fumarate
5069
Ethyl hydrogen succinate
5070
Ethyl hydroperoxide
5071
5072
Ethyl hydroxyacetate
Ethyl 3-hydroxybenzoate
5073
Ethyl 4-hydroxybenzoate
5074
5077
5078
5079
5080
HCP_Section_03.indb 260
Synonym
Butanedioic acid, monoethyl
ester
Ethyl hydrogen peroxide
Ethylparaben
Ethyl ricinoleate
5-Ethylidenebicyclo[2.2.1]­
hept-2-ene
Isobutyl urethane
Ethyl 2-methyl-2-propenoate
Physical
Form
mp/˚C
bp/˚C
den
g cm –3
nD
101
liq
45.8(0.4)
44
<-65
198 dec
297.5
1.418220
Solubility
vs H2O, ace,
eth, EtOH
s EtOH, eth; sl
chl
s EtOH, eth,
peth
s EtOH, ace; sl
chl
vs H2O, eth,
EtOH
vs H2O, bz, eth,
EtOH
vs eth, EtOH
sl H2O, chl; s
EtOH, eth
sl H2O, chl, tfa;
vs EtOH, eth; i
CS2
s H2O, EtOH; sl
ctc
vs H2O, eth,
EtOH
vs ace, eth,
EtOH, chl
i H2O; vs EtOH,
eth; s chl
0.768821
1.461820
1.490020
msc H2O
s EtOH, eth
vs eth, EtOH
i H2O; msc
EtOH, eth
vs H2O; msc
EtOH, eth; s
ace
s EtOH, eth
vs eth, EtOH
1.387225
1.50820 vs ace, bz, eth,
EtOH
1.369825 s H2O, ace, chl;
msc EtOH, eth
1.413820 s ctc
0.962415 1.512020 vs bz, eth
1.527720 s ctc
1.112420 1.522420 vs eth, EtOH
1.103820 1.525420 i H2O; s EtOH,
eth
1.093118
4/11/16 11:28 AM
Physical Constants of Organic Compounds
O
O
H2N
H2N
N
H
5065
HO
N
H
O
O
O
HO
O
O
5067
Ethyl hydrazinecarboxylate
O
O
O
HO
O
5066
Ethylhydrazine
3-261
5068
Ethyl hydrogen adipate
O
O
O
O
5069
Ethyl hydrogen fumarate
OH
5070
Ethyl hydrogen succinate
Ethyl hydroperoxide
HO
O
5071
Ethyl hydroxyacetate
O
O
O
HO
OH O
O
OH
OH
5073
5072
5075
5076
5077
α-Ethyl-1-hydroxycyclohexaneacetic acid
Ethyl 2-hydroxy-3-butenoate
N-Ethyl-N-hydroxyethanamine
Organic
Ethyl 3-hydroxybutanoate, (±)-
N
OH
O
OH
5074
Ethyl 4-hydroxybenzoate
Ethyl 3-hydroxybenzoate
OH
O
O
O
O
OH
O
O
OH
OH
5078
O
5079
2-Ethyl-3-hydroxyhexanal
5080
Ethyl 4-hydroxy-3-methoxybenzoate
5081
Ethyl cis-12-hydroxy-9-octadecenoate, (R)-
5082
Ethylidenecyclohexane
5-Ethylidene-2-norbornene
O
N
O
O
N
I
5083
N
H
O
5084
1-Ethyl-1H-imidazole
N
O
N C O
5085
Ethyl iodoacetate
N
5086
Ethyl isobutylcarbamate
O
C
5087
Ethyl isocyanate
Ethyl isocyanide
N
H
O
5088
5089
N-Ethyl-1H-isoindole-1,3(2H )-dione
Ethyl isopentyl ether
5090
Ethylisopropylamine
O
N
O
O
5091
5092
1-Ethyl-2-isopropylbenzene
N C S
S
5093
Ethyl isopropyl ether
5094
N-Ethyl-N-isopropyl-2-propanamine
5095
Ethyl isopropyl sulfide
Ethyl isothiocyanate
O
O
HS
O
O
5097
5098
Ethyl laurate
O
O
O
O
O
5099
Ethyl levulinate
5100
Ethyl mercaptoacetate
Ethyl methacrylate
OH
5096
Ethyl lactate
O
O S O
5101
Ethyl methanesulfonate
OH
OH
O
O
O
O
5102
1-Ethyl-4-methoxybenzene
O
5103
α-Ethyl-4-methoxybenzenemethanol
O
O
5104
Ethyl 2-methoxybenzoate
O
O
5105
Ethyl 4-methoxybenzoate
5106
4-Ethyl-2-methoxyphenol
Physical Constants of Organic Compounds
3-262
No.
Name
5107
5108
Ethyl (4-methoxyphenyl)­
acetate
Ethyl 2-methylacetoacetate
5109
N-Ethyl-2-methylallylamine
5110
5-Ethyl-5-(2-methylallyl)-2thiobarbituric acid
Ethylmethylamine
5111
5112
5113
5114
5115
5116
5117
Organic
5118
Ethylmethylamine
hydrochloride
2-Ethyl-6-methylaniline
N-Ethyl-2-methylaniline
N-Ethyl-3-methylaniline
N-Ethyl-4-methylaniline
N-Ethyl-N-methylaniline
Synonym
bp/˚C
den
g cm –3
nD
14062-18-1 194.227
13970
1.09725
1.507520
609-14-3
187
0.994120 1.418520 sl H2O; s EtOH,
eth; vs ace
0.753
1.422120 msc H2O
Mol. Form.
CAS RN
C11H14O3
C7H12O3
N-Ethyl-2-methyl-2-propen-1- C6H13N
amine
Methallatal
C10H14N2O2S
Mol.
Wt.
Physical
Form
mp/˚C
144.168
18328-90-0 99.174
115-56-0
226.295
liq
104.7
160.5
N-Methylethanamine
C3H9N
624-78-2
59.110
N-Methylethanamine
hydrochloride
C3H10ClN
624-60-2
95.571
C9H13N
C9H13N
C9H13N
C9H13N
C9H13N
24549-06-2
94-68-8
102-27-2
622-57-1
613-97-8
135.206 liq
135.206
135.206
135.206
135.206
C11H17N
457-87-4
163.260
C9H13NO2S
80-39-7
199.270
64
C10H12N2
5805-76-5
160.215
51
296
1.07325
C10H12O2
87-24-1
164.201
<-10
227(8)
1.032521 1.50722
C10H12O2
94-08-6
164.201
236(7)
1.026918 1.508918
C7H14O2
108-64-5
130.185 liq
-99.3
135(3)
0.865620 1.396220
<-20
207
86.3(0.5)
1.425020
0.715020 1.41020
156
0.920020 1.434020
153.5
0.919921 1.434520
N-Ethyl-4-toluidine
N-Ethylamphetamine
Solubility
34.2(0.2)
pl (al-eth)
128
-33
<-15
vs H2O, ace,
eth, EtOH
vs H2O, EtOH; i
eth; s chl
1.087420
231
216
221
217
204(5)
0.96825 1.552520
0.94825 1.545620
0.926315 1.545120
0.939116
0.9255
10514
s EtOH, eth
s EtOH, eth
s EtOH, eth
i H2O; msc
EtOH, eth; s
ctc
1.498625
5121
N-Ethyl-αmethylbenzeneethanamine
N-Ethyl-4-methylbenzenesulfonamide
1-Ethyl-2-methyl-1H-benzimidazole
Ethyl 2-methylbenzoate
5122
Ethyl 4-methylbenzoate
5123
Ethyl 3-methylbutanoate
5124
5125
2-Ethyl-2-methylbutanoic acid
2-Ethyl-3-methyl-1-butene
C7H14O2
C7H14
19889-37-3 130.185
7357-93-9 98.186
5126
Ethyl trans-2-methyl-2butenoate
Ethyl 3-methyl-2-butenoate
5-Ethyl-5-(1-methylbutyl)2,4,6(1H,3H,5H)-pyrimidinetrione
Ethyl N-methylcarbamate
Ethyl methyl carbonate
trans-1-Ethyl-4-methylcyclohexane
1-Ethyl-1-methylcyclopentane
C7H12O2
5837-78-5
128.169
C7H12O2
C11H18N2O3
638-10-8
76-74-4
128.169
226.272
130(1)
C4H9NO2
C4H8O3
C9H18
105-40-8
623-53-0
6236-88-0
103.120
104.105 liq
126.239 liq
-14
-80.8
169(5)
107.5
147(6)
1.011520 1.418320 vs H2O, EtOH
1.01220 1.377820 vs eth, EtOH
0.779820 1.430420
C8H16
16747-50-5 112.213 liq
-143.8(0.2)
121.5(0.6)
cis-1-Ethyl-2-methylcyclopentane
trans-1-Ethyl-2-methylcyclopentane
cis-1-Ethyl-3-methylcyclopentane
trans-1-Ethyl-3-methylcyclopentane
1-Ethyl-1-methylcyclopropane
2-Ethyl-2-methyl-1,3-dioxolane
Ethyl methyl ether
C8H16
930-89-2
112.213 liq
-105.9(0.1)
128(1)
0.776725 1.427220 vs ace, bz, eth,
EtOH
0.785220 1.429320
C8H16
930-90-5
112.213 liq
-109(5)
121(4)
0.764925 1.421920
C8H16
2613-66-3
112.213
121(4)
C8H16
2613-65-2
112.213 liq
C6H12
C6H12O2
5119
5120
5127
5128
5129
5130
5131
5132
5133
5134
5135
Ethyl isovalerate
s EtOH
i H2O; msc
EtOH, eth
i H2O; msc
EtOH, eth
sl H2O; vs EtOH,
eth
vs EtOH
i H2O; s eth,
ace, bz, chl
sl H2O; s EtOH,
eth
-108
121(4)
0.772420 1.420320 vs ace, bz, eth,
EtOH
0.761920 1.418620
53778-43-1 84.159 liq
126-39-6
116.158
-130.2(0.2)
57(4)
119(3)
0.696825 1.388720
0.936020
C3H8O
540-67-0
60.095
-113
6(2)
0.72510
1.34204
C9H20
C9H20
C9H20
C9H20
C9H18O2
C8H14O3
16789-46-1
3074-76-8
3074-77-9
3074-75-7
1561-10-0
7152-15-0
128.255
128.255
128.255
128.255
158.238
158.195 liq
-9
138(4)
140(3)
140(4)
134(3)
180
173
0.731020
0.737125
0.742020
0.719525
0.870820
0.9825
1.410620
1.414020
1.413420
1.406320
1.405120
1.25020
5146
3-Ethyl-2-methylhexane
3-Ethyl-3-methylhexane
3-Ethyl-4-methylhexane
2,3-Diethylpentane
4-Ethyl-2-methylhexane
Ethyl 4-methylhexanoate
Ethyl 4-methylcaproate
Ethyl 4-methyl-3-oxopentanoate
3-Ethyl-2-methylpentane
2-Methyl-3-ethylpentane
C8H18
609-26-7
114.229 liq
-115.0(0.1)
115.6(0.6)
5147
3-Ethyl-3-methylpentane
C8H18
1067-08-9
114.229 liq
-90.8(0.1)
118.2(0.9)
5148
Ethyl 4-methylpentanoate
C8H16O2
25415-67-2 144.212
0.719320 1.404020 i H2O; s eth;
msc EtOH,
ace, bz
0.727420 1.407820 i H2O; s eth;
msc EtOH,
ace, bz
0.870520 1.405020
5136
5137
5138
5139
5140
5141
5142
5143
5144
5145
HCP_Section_03.indb 262
3-Methyl-3-ethylpentane
col gas
163
s H2O, ace, chl;
msc EtOH, eth
4/11/16 11:28 AM
Physical Constants of Organic Compounds
3-263
O
NH
O
O
O
O
5107
5108
Ethyl (4-methoxyphenyl)acetate
NH2
H
N
5113
5114
5120
1-Ethyl-2-methyl-1H-benzimidazole
Ethylmethylamine
5112
Ethylmethylamine hydrochloride
H
N
N
5116
5118
5117
N-Ethyl-4-methylaniline
N-Ethyl-α-methylbenzeneethanamine
N-Ethyl-N-methylaniline
O
O
O
5119
N-Ethyl-4-methylbenzenesulfonamide
O
O
O
N
5111
5-Ethyl-5-(2-methylallyl)-2-thiobarbituric acid
H
N
N-Ethyl-3-methylaniline
N
N HCl
H
N
H
NH
O S O
5115
N-Ethyl-2-methylaniline
S
5110
N-Ethyl-2-methylallylamine
H
N
H
N
2-Ethyl-6-methylaniline
5109
Ethyl 2-methylacetoacetate
N
H
O
OH
O
5121
Ethyl 2-methylbenzoate
5122
5123
Ethyl 4-methylbenzoate
5124
Ethyl 3-methylbutanoate
2-Ethyl-2-methylbutanoic acid
5125
2-Ethyl-3-methyl-1-butene
O
O
NH
O
O
5126
Ethyl trans-2-methyl-2-butenoate
5131
trans-1-Ethyl-4-methylcyclohexane
O
O
5127
N
H
O
N
H
O
5128
Ethyl 3-methyl-2-butenoate
5132
5133
O
5129
5-Ethyl-5-(1-methylbutyl)-2,4,6(1H,3H,5H )-pyrimidinetrione
1-Ethyl-1-methylcyclopentane
O
O
Ethyl N-methylcarbamate
5134
cis-1-Ethyl-2-methylcyclopentane
O
5130
Ethyl methyl carbonate
5135
trans-1-Ethyl-2-methylcyclopentane
cis-1-Ethyl-3-methylcyclopentane
O
O
O
5136
trans-1-Ethyl-3-methylcyclopentane
5137
1-Ethyl-1-methylcyclopropane
5138
2-Ethyl-2-methyl-1,3-dioxolane
O
O
5143
5144
Ethyl 4-methylhexanoate
5140
Ethyl methyl ether
3-Ethyl-2-methylhexane
5141
3-Ethyl-3-methylhexane
5142
3-Ethyl-4-methylhexane
O
O
O
O
O
4-Ethyl-2-methylhexane
5139
5145
Ethyl 4-methyl-3-oxopentanoate
5146
3-Ethyl-2-methylpentane
5147
3-Ethyl-3-methylpentane
5148
Ethyl 4-methylpentanoate
Organic
O
O
Physical Constants of Organic Compounds
3-264
No.
Name
5149
5150
5153
3-Ethyl-2-methyl-1-pentene
2-[Ethyl(3-methylphenyl)­
amino]ethanol
Ethyl 3-methyl-3-phenyloxiranecarboxylate
4-Ethyl-4-methyl-2,6-piperidinedione
Ethyl 2-methylpropanoate
5154
5155
Mol.
Wt.
Physical
Form
Mol. Form.
CAS RN
C8H16
C11H17NO
19780-66-6 112.213 liq
91-88-3
179.259
Ethyl 3-methyl-3-phenylglycidate
Bemegride
C12H14O3
77-83-8
206.237
C8H13NO2
64-65-3
Ethyl isobutanoate
C6H12O2
97-62-1
155.195 pl (w,
ace-eth)
116.158 liq
2-Ethyl-5-methylpyrazine
3-Ethyl-4-methylpyridine
3-Ethyl-4-picoline
C7H10N2
C8H11N
5156
4-Ethyl-2-methylpyridine
4-Ethyl-2-picoline
5157
Ethosuximide
5158
3-Ethyl-3-methyl-2,5-pyrrolidinedione
Ethyl methyl sulfide
5159
5151
5152
Synonym
mp/˚C
bp/˚C
den
g cm –3
-112.9(0.1)
109.2(0.9)
1181.5
0.726220 1.414020
1.554020 s ctc
273.5
1.04420
nD
Solubility
1.518220
Organic
126.5
100 sub
-97.8(0.4)
111(2)
0.86820
13360-64-0 122.167 liq
529-21-5
121.180
7956
198
0.928617
C8H11N
536-88-9
121.180
180(6)
0.913025
C7H11NO2
77-67-8
C3H8S
624-89-5
141.168 cry
(ace-eth)
76.161 liq
N-Ethylmorpholine
C6H13NO
100-74-3
115.173
5160
Ethyl myristate
C16H32O2
124-06-1
256.424
12.3(0.8)
308(3)
5161
5162
N-Ethyl-1-naphthalenamine
1-Ethylnaphthalene
C12H13N
C12H12
118-44-5
1127-76-0
171.238
156.223 liq
-13.9(0.2)
305
258(3)
5163
2-Ethylnaphthalene
C12H12
939-27-5
156.223 liq
-7.4(0.9)
259(2)
5164
5165
Ethyl 1-naphthylacetate
Ethyl nitrate
C14H14O2
C2H5NO3
2122-70-5
625-58-1
214.260 oil
91.066 liq
88.5
-94.51(0.1)
22220
89(2)
5166
Ethyl nitrite
C2H5NO2
109-95-5
75.067
5167
Ethyl nitroacetate
C4H7NO4
626-35-7
133.104
5168
1-Ethyl-2-nitrobenzene
C8H9NO2
612-22-6
151.163 liq
-12.2(0.2)
232.5
5169
1-Ethyl-4-nitrobenzene
C8H9NO2
100-12-9
151.163 liq
-12.3
245.5
5170
Ethyl 3-nitrobenzoate
C9H9NO4
618-98-4
195.172
47
297
5171
Ethyl 4-nitrobenzoate
C9H9NO4
99-77-4
195.172
57
186.3
5172
O-Ethyl O-p-nitrophenyl
benzenethiophosphonate
2-Ethyl-2-nitro-1,3-propanediol
Ethyl 2-nitropropanoate
N-Ethyl-N-nitrosourea
Ethyl nonanoate
C14H14NO4PS
2104-64-5
323.304
39.2(0.3)
C5H11NO4
597-09-1
149.146 nd (w)
57.5
C5H9NO4
C3H7N3O2
C11H22O2
2531-80-8
759-73-9
123-29-5
147.130
117.107
186.292 liq
190.5
1.421020
100 dec
-44.4(0.3)
224(5)
0.865720 1.422020
C9H14
C20H36O2
15403-89-1 122.207 liq
544-35-4
308.499 ye or col
-55(5)
143.6
351(10)
0.86
1.463020
0.886520
vs eth, EtOH
C20H34O2
1191-41-9
306.483
357(10)
0.891920 1.469420 vs eth, EtOH
C20H38O2
C10H22
C10H22
C10H20O2
6114-18-7
5881-17-4
15869-86-0
106-32-1
310.515
142.282
142.282
172.265 liq
21815
165(6)
163(6)
206(1)
0.866425
0.735925
0.734325
0.86618
1.448025 vs eth, EtOH
1.415620
1.415120
1.417820 i H2O; vs EtOH,
eth; sl ctc
C10H22S
C20H38O2
C8H14O3
C7H12O3
C10H10O3
3698-94-0
111-62-6
13984-57-1
4949-44-4
1603-79-8
174.347 liq
310.515
158.195
144.168
178.184
10914
357(9)
221.5
191
256.5
0.872020
0.98925
1.012020
1.122225
1.451520 vs eth, EtOH
1.427720
1.423020 vs bz, eth, EtOH
1.519025
5173
5174
5175
5176
5177
5178
N-Nitroso-N-ethylurea
5180
5181
5182
5183
5-Ethyl-2-norbornene
Ethyl cis,cis-9,12-octadecadi- Ethyl linoleate
enoate
Ethyl cis,cis,cis-9,12,15Ethyl linolenate
octadecatrienoate
Ethyl trans-9-octadecenoate
3-Ethyloctane
4-Ethyloctane
Ethyl octanoate
5184
5185
5186
5187
5188
Ethyl 1-octyl sulfide
Ethyl oleate
Ethyl 5-oxohexanoate
Ethyl 3-oxopentanoate
Ethyl 2-oxo-2-phenylacetate
5179
HCP_Section_03.indb 264
1-(Ethylthio)octane
Ethyl cis-9-octadecenoate
Ethyl phenylglyoxylate
s chl
1.386918 sl H2O, ctc; msc
EtOH, eth; s
ace
sl H2O; s EtOH,
eth, chl; vs
ace
vs ace, bz, eth,
EtOH
vs H2O
64.5
-105.89(0.1) 66.6(0.3)
145(5)
ye vol liq or
gas
17.5(0.4)
10625
5.1(0.3)
-44.7(0.3)
-21(2)
0.842220 1.440420 i H2O; msc
EtOH; s eth,
chl
0.899620 1.440020 msc H2O, EtOH,
eth; s ace, bz
0.857325 1.436220 i H2O; s EtOH,
ctc, lig; sl eth
1.065215 1.647715 vs eth, EtOH
1.008220 1.606220 i H2O; msc
EtOH, eth
0.992220 1.599920 i H2O; msc
EtOH, eth; sl
chl
s EtOH, eth
1.108420 1.385220 s H2O; msc
EtOH, eth
0.89915 1.341810 msc EtOH, eth
1.195320 1.425020 sl H2O; msc
EtOH; vs eth; s
dil alk
1.120720 1.535620 i H2O; vs EtOH,
eth; s ace; sl
ctc
1.119220 1.545520 i H2O; vs EtOH,
eth; s ace; sl
ctc
i H2O; vs EtOH,
eth
i H2O; s EtOH,
eth
1.2725
1.597830 vs bz, eth, EtOH
dec
vs H2O, eth,
EtOH
vs bz, eth, EtOH
s chl
i H2O; s EtOH,
eth, ace, ctc
4/11/16 11:28 AM
Physical Constants of Organic Compounds
N
3-265
O
OH
O
O
O
5149
5151
5150
3-Ethyl-2-methyl-1-pentene
O
N
O
5152
Ethyl 3-methyl-3-phenyloxiranecarboxylate
2-[Ethyl(3-methylphenyl)amino]ethanol
O
N
H
N
5154
5153
4-Ethyl-4-methyl-2,6-piperidinedione
2-Ethyl-5-methylpyrazine
Ethyl 2-methylpropanoate
N
O
N
N
5155
5156
3-Ethyl-4-methylpyridine
S
5159
Ethyl methyl sulfide
5160
N-Ethylmorpholine
Ethyl myristate
Organic
3-Ethyl-3-methyl-2,5-pyrrolidinedione
O
O
5158
5157
4-Ethyl-2-methylpyridine
O
O
N
H
O
NH
O
O
5161
5162
N-Ethyl-1-naphthalenamine
O
5164
5163
1-Ethylnaphthalene
O
O
N
O
N
O
5169
O
O
O
5170
1-Ethyl-4-nitrobenzene
N
O
5171
Ethyl 3-nitrobenzoate
N
O
O
5166
Ethyl nitrate
O
O
N
5167
Ethyl nitrite
N
O
O
Ethyl nitroacetate
O
5168
1-Ethyl-2-nitrobenzene
O
O
O
O
O
5165
Ethyl 1-naphthylacetate
2-Ethylnaphthalene
O
N
S
N
O
O
P
HO
O
O
N
O
O
5172
Ethyl 4-nitrobenzoate
OH
O
5173
O-Ethyl O-p-nitrophenyl benzenethiophosphonate
N
O
N
Ethyl 2-nitropropanoate
5175
N-Ethyl-N-nitrosourea
O
O
NH2
O
5174
2-Ethyl-2-nitro-1,3-propanediol
O
N
O
O
O
O
5176
5177
Ethyl nonanoate
5178
5-Ethyl-2-norbornene
5179
Ethyl cis,cis-9,12-octadecadienoate
Ethyl cis,cis,cis-9,12,15-octadecatrienoate
O
O
O
O
5180
5181
Ethyl trans-9-octadecenoate
5182
3-Ethyloctane
5183
4-Ethyloctane
Ethyl octanoate
O
O
O
O
O
S
5184
Ethyl 1-octyl sulfide
O
O
5185
Ethyl oleate
5186
Ethyl 5-oxohexanoate
O
O
O
5187
Ethyl 3-oxopentanoate
O
5188
Ethyl 2-oxo-2-phenylacetate
Physical Constants of Organic Compounds
3-266
Organic
No.
Name
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
5189
Ethyl 2-oxopropanoate
Ethyl pyruvate
C5H8O3
617-35-6
116.116 liq
5190
Ethyl palmitate
C18H36O2
628-97-7
284.478
5191
3-Ethylpentane
C7H16
617-78-7
100.202
5192
3-Ethyl-2,4-pentanedione
C7H12O2
1540-34-7
128.169
5193
Ethyl pentanoate
C7H14O2
539-82-2
130.185
5194
3-Ethyl-3-pentanol
C7H16O
597-49-9
116.201
5195
5196
5197
2-Ethyl-1-pentene
3-Ethyl-1-pentene
3-Ethyl-2-pentene
C7H14
C7H14
C7H14
3404-71-5
4038-04-4
816-79-5
98.186
98.186
98.186
5198
5199
5200
Ethyl pentyl ether
Ethyl 2-pentynoate
2-Ethylphenol
C7H16O
C7H10O2
C8H10O
17952-11-3 116.201
55314-57-3 126.153
90-00-6
122.164
5201
3-Ethylphenol
C8H10O
620-17-7
122.164
5202
4-Ethylphenol
C8H10O
123-07-9
122.164
5203
5204
5205
5206
5207
Ethyl phenoxyacetate
N-Ethyl-N-phenylacetamide
Ethyl phenylacetate
2-(Ethylphenylamino)ethanol
Ethyl phenylcarbamate
C10H12O3
C10H13NO
Benzeneacetic acid, ethyl ester C10H12O2
C10H15NO
Phenylurethane
C9H11NO2
2555-49-9
529-65-7
101-97-3
92-50-2
101-99-5
180.200
163.216
164.201
165.232
165.189
5208
5209
5210
C9H11NO
C10H13NO2
C16H18
6780-49-0
2216-92-4
7439-15-8
149.189
179.216
210.314
5211
5212
Ethyl N-phenylformimidate
Ethyl N-phenylglycinate
1-(4-Ethylphenyl)-2-phenylethane
Ethyl 3-phenylpropanoate
Ethyl 3-phenylpropynoate
2021-28-5
2216-94-6
178.228
174.196
5213
Ethyl phenyl sulfone
599-70-2
170.229 lf (dil al)
5214
Ethylphosphonic acid
6779-09-5
110.049 hyg pl or nd 61.5
3358
5215
5216
Ethyl phosphorodichloridate
5-Ethyl-2-picoline
Ethylphosphoric acid dichloride C2H5Cl2O2P
C8H11N
1498-51-7
104-90-5
162.940
121.180
6210
178(3)
5217
Ethyl 1-piperazinecarboxylate
1-Carbethoxypiperazine
C7H14N2O2
120-43-4
158.198
237
5218
5219
1-Ethylpiperidine
Ethyl 4-piperidinecarboxylate
C7H15N
C8H15NO2
766-09-6
1126-09-6
113.201
157.211 col oil
133(3)
10010
5220
5221
5222
Ethyl 1-piperidinepropanoate
1-Ethyl-3-piperidinol
N-Ethyl-1-propanamine
C10H19NO2
C7H15NO
C5H13N
19653-33-9 185.264
13444-24-1 129.200
20193-20-8 87.164
5223
Ethylpropanedioic acid
C5H8O4
601-75-2
132.116 pr (w+1)
112(2)
1800.05
5224
Ethyl propanoate
C5H10O2
105-37-3
102.132 liq
-73.6(0.5)
98.9(0.2)
5225
Ethyl propyl ether
C5H12O
628-32-0
88.148
-127.5(0.1)
63(3)
5226
5227
5228
5229
2-(1-Ethylpropyl)pyridine
4-(1-Ethylpropyl)pyridine
Ethyl propyl sulfide
Ethyl 2-propynoate
C10H15N
C10H15N
C5H12S
C5H6O2
7399-50-0
35182-51-5
4110-50-3
623-47-2
149.233
149.233
104.214 liq
98.101
5230
2-Ethylpyrazine
C6H8N2
13925-00-3 108.141
HCP_Section_03.indb 266
Ethyl valerate
C11H14O2
Ethyl phenylacetylenecarboxyl- C11H10O2
ate
C8H10O2S
C2H7O3P
Ethyl propionate
(Ethoxycarbonyl)acetylene
Physical
Form
mp/˚C
bp/˚C
-50
155(4)
den
g cm –3
nD
Solubility
1.059615 1.405220 sl H2O; s ace;
msc EtOH, eth
nd
24.2(0.4)
334(7)
0.857725 1.434734 i H2O; s EtOH,
eth, ace, bz,
chl
liq
-118.55(0.01) 93.4(0.4)
0.698220 1.393420 i H2O; s EtOH,
eth; msc ace,
bz, hp, chl
179(11)
0.953119 1.440819 vs eth, EtOH,
chl
liq
-91.2
142(3)
0.877020 1.412020 i H2O; msc
EtOH, eth; sl
ctc
liq
-13(2)
142(3)
0.840722 1.429420 sl H2O; s EtOH,
eth
94(2)
0.707920 1.40520 vs bz, eth, EtOH
liq
-127.51(0.09) 84(2)
0.691725 1.398220
95(1)
0.720420 1.414820 i H2O; s EtOH,
eth, bz, chl
118(4)
0.762220 1.392720 vs eth, EtOH
6718
0.96225
18
204.5(0.1) 1.014625 1.536720 vs ace, bz, eth,
EtOH
liq
0(8)
218.4(0.1) 1.028320
sl H2O, chl; vs
EtOH, eth
nd
45.0(0.3)
217.97(0.06)
1.523925 sl H2O, chl; vs
EtOH, eth, bz;
s ace
247
1.095830 1.508020
55
260
0.993860
s H2O, eth, ctc
liq
-29.4
228(2)
1.033320 1.498020 vs eth, EtOH
s chl
wh nd (w) pl 53(1)
237 dec
1.106430 1.537630 i H2O; vs EtOH,
(dil al)
eth; s bz; sl
ctc
214
1.005120 1.527920 s eth, bz
lf (dil al)
58
273.5
vs eth, EtOH
cry
294
1.02850
42
247(3)
265
1.014720 1.495420 vs eth, EtOH
1.05525 1.552020 s eth
16012
1.141020
217
9415
85(8)
liq
195.4
125.5
217
-117.03(0.05) 118.5(0.8)
119(5)
vs bz, eth,
EtOH, chl
vs H2O, eth,
EtOH
1.433820
0.920220 1.497120 sl H2O; s EtOH,
eth, bz; vs ace
1.476025 vs H2O, eth,
EtOH
0.823720 1.448020
1.459120 vs H2O, bz, eth,
EtOH
0.962725 1.452525 vs H2O
1.477714
0.720417 1.385825 sl H2O; vs ace,
EtOH
vs H2O; s EtOH,
eth, bz; i ace;
sl tfa
0.884325 1.383920 sl H2O, ctc; msc
EtOH, eth; s
ace
0.738620 1.369520 vs eth, EtOH,
HOAc
0.898120 1.485025
0.908525 1.4090525
0.837020 1.446220 s EtOH
0.964516 1.410520 i H2O; vs EtOH,
eth, chl
112200
4/11/16 11:28 AM
Physical Constants of Organic Compounds
3-267
O
O
O
O
O
O
O
O
O
5189
5190
Ethyl 2-oxopropanoate
5191
Ethyl palmitate
5192
3-Ethylpentane
5193
3-Ethyl-2,4-pentanedione
Ethyl pentanoate
OH
5194
3-Ethyl-3-pentanol
OH
O
O
5195
5196
5197
3-Ethyl-1-pentene
5198
3-Ethyl-2-pentene
5199
Ethyl pentyl ether
O
N
5200
Ethyl 2-pentynoate
N
5204
N-Ethyl-N-phenylacetamide
5201
2-Ethylphenol
H
N
OH
5202
3-Ethylphenol
O
4-Ethylphenol
N
5203
Ethyl phenoxyacetate
O
H
N
O
O
O
O
O
O
O
O
2-Ethyl-1-pentene
O
OH
5205
5206
Ethyl phenylacetate
5207
2-(Ethylphenylamino)ethanol
5208
Ethyl phenylcarbamate
O
O
O O
S
O
O
5209
Ethyl N-phenylformimidate
Ethyl N-phenylglycinate
O
HO P OH
O
Cl P Cl
O
5214
5215
N
5210
1-(4-Ethylphenyl)-2-phenylethane
5211
Ethyl 3-phenylpropanoate
Ethyl phenyl sulfone
Ethylphosphonic acid
5-Ethyl-2-picoline
O
N
N
5218
1-Ethylpiperidine
O
O
N
H
O
Ethyl 1-piperazinecarboxylate
5219
Ethyl 4-piperidinecarboxylate
N
5220
Ethyl 1-piperidinepropanoate
O
O
5224
5225
Ethyl propyl ether
O
5221
1-Ethyl-3-piperidinol
5222
N-Ethyl-1-propanamine
N
2-(1-Ethylpropyl)pyridine
5227
4-(1-Ethylpropyl)pyridine
S
O
5228
5229
Ethyl propyl sulfide
OH
5223
Ethylpropanedioic acid
N
O
5226
O
HO
H
N
O
N
Ethyl propanoate
Ethyl phosphorodichloridate
5216
OH
N
5217
5213
Ethyl 3-phenylpropynoate
O
H
N
O
5212
Ethyl 2-propynoate
N
5230
2-Ethylpyrazine
Organic
OH
Physical Constants of Organic Compounds
3-268
Mol. Form.
CAS RN
Mol.
Wt.
2-Ethylpyridine
C7H9N
100-71-0
5232
3-Ethylpyridine
C7H9N
5233
4-Ethylpyridine
5234
5235
2-Ethyl-4-pyridinecarbothioamide
Ethyl 2-pyridinecarboxylate
5236
Ethyl 3-pyridinecarboxylate
5237
No.
Name
5231
Physical
Form
Organic
mp/˚C
bp/˚C
107.153 liq
-63.0(0.5)
149(1)
536-78-7
107.153 liq
-76.9(0.5)
166(2)
C7H9N
536-75-4
107.153 liq
-90.5(0.5)
168(2)
Ethionamide
C8H10N2S
536-33-4
166.243
163
Ethyl 2-picolinate
C8H9NO2
2524-52-9
151.163 ye cry in air 1
243
Ethyl nicotinate
C8H9NO2
614-18-6
151.163
8.5
221(20)
Ethyl 4-pyridinecarboxylate
C8H9NO2
1570-45-2
151.163
23
221(11)
5238
N-Ethylpyridinium bromide
C7H10BrN
1906-79-2
188.065 cry (al)
111.5
5239
5240
1-Ethyl-1H-pyrrole
1-Ethyl-1H-pyrrole-2,5-dione
C6H9N
C6H7NO2
617-92-5
128-53-0
95.142
125.126 cry (bz)
45.5
5241
C7H16N2
26116-12-1 128.215
C17H19N3O2
76058-33-8 297.352
135
5243
1-Ethyl-2-pyrrolidinemethanamine
Ethyl Red
2-(4-Diethylaminophenylazo)­
benzoic acid
Ethyl salicylate
C9H10O3
118-61-6
166.173
45
15010
5244
5245
Ethyl silicate
Ethyl stearate
Tetraethoxysilane
Ethyl octadecanoate
C8H20O4Si
C20H40O2
78-10-4
111-61-5
208.329 liq
312.531
-82.2(0.1)
33.1(0.7)
168(1)
356(6)
5246
5247
5248
5249
5250
5251
2-Ethylstyrene
3-Ethylstyrene
4-Ethylstyrene
Ethyl sulfate
2-(Ethylsulfonyl)ethanol
2-Ethyl-5-(3-sulfophenyl)­
isoxazolium hydroxide, inner
salt
Ethyl tartrate
2-Ethyltetrahydrofuran
7564-63-8
7525-62-4
3454-07-7
540-82-9
513-12-2
4156-16-5
132.202 liq
132.202 liq
132.202 liq
126.132
138.185
253.275
-75.6(0.5)
-101.3(0.6)
-49.7(0.5)
189(1)
190(2)
192(9)
280 dec
Ethylsulfonylethyl alcohol
Woodward’s Reagent K
C10H12
C10H12
C10H12
C2H6O4S
C4H10O3S
C11H11NO4S
C6H10O6
C6H12O
608-89-9
1003-30-1
178.139
100.158
90
5242
5252
5253
Synonym
N-Ethylmaleimide
Ethyl tartrate, acid
130(5)
5916
107(7)
C4H7N3S
14068-53-2 129.184
5255
C4H8OS
625-60-5
104.171
5256
(Ethylthio)acetic acid
C4H8O2S
627-04-3
120.171
-8.5
16483
5257
5258
(Ethylthio)benzene
Ethyl thiocyanate
C8H10S
C3H5NS
622-38-8
542-90-5
138.230
87.144 liq
-85.5(0.5)
207(1)
144(7)
5259
2-(Ethylthio)ethanol
C4H10OS
110-77-0
106.186 liq
-100
175(3)
5260
5261
1-(Ethylthio)-4-methylbenzene
2-Ethylthiophene
C9H12S
C6H8S
622-63-9
872-55-9
152.256
112.193
220
136(1)
5262
Ethyl thiophene-2-carboxylate
C7H8O2S
2810-04-0
156.203
218
5263
C5H7NOS2
7648-01-3
161.246
35.5
5264
3-Ethyl-2-thioxo-4-thiazolidinone
2-Ethyltoluene
C9H12
611-14-3
120.191 liq
-80.7(0.4)
165.1(0.4)
5265
3-Ethyltoluene
C9H12
620-14-4
120.191 liq
-95.7(0.2)
161.3(0.5)
5266
4-Ethyltoluene
C9H12
622-96-8
120.191 liq
-62.7(0.5)
162.0(0.6)
HCP_Section_03.indb 268
Thiophenetole
3-Ethylrhodanine
nD
Solubility
0.950225 1.496420 s H2O; msc
EtOH; vs eth,
ace; sl ctc
0.953925 1.502120 s H2O, EtOH,
eth; vs ace; sl
ctc
0.941720 1.500920 s H2O, EtOH,
eth; vs ace; sl
ctc
1.119420 1.510420 vs H2O, eth,
EtOH
1.107020 1.502420 vs H2O, EtOH,
eth, bz; sl ctc
1.009115 1.501720 sl H2O; s EtOH,
bz; vs eth, chl
s H2O, EtOH; i
eth
0.900920 1.484120 vs EtOH
sl H2O; vs EtOH,
eth; s chl
0.88725 1.466520
1.132620 1.529620 i H2O; msc
EtOH; vs eth; s
ctc
0.932020 1.392820 dec H2O
1.05720 1.434940 i H2O; s EtOH,
eth, chl; vs
ace
0.901725 1.538020
0.894520 1.535120
0.888425 1.537620
1.365720 1.410520 vs H2O
sl chl
dec 207
5-Ethyl-1,3,4-thiadiazol-2amine
S-Ethyl thioacetate
5254
den
g cm –3
vs H2O, EtOH
0.857019 1.414719 vs ace, bz, eth,
EtOH
200.8
114(3)
0.979220 1.458321 i H2O; vs EtOH,
eth
1.149720
vs H2O, EtOH,
eth
1.021120 1.567020 s EtOH
1.00723 1.468415 i H2O; msc
EtOH, eth; s
chl
1.016620 1.486720 sl H2O; s EtOH;
vs ace
0.999620 1.55520
0.993020 1.512220 i H2O; vs EtOH,
eth
1.162316 1.524820 s EtOH, ace; sl
ctc
0.880720 1.504620 i H2O; msc
EtOH, eth, ace,
bz, peth, ctc
0.864520 1.496620 i H2O; vs EtOH,
eth; msc ace,
bz
0.861420 1.495920 i H2O; vs EtOH,
eth; msc ace,
bz
4/11/16 11:28 AM
Physical Constants of Organic Compounds
3-269
S
NH2
5231
5232
2-Ethylpyridine
N
N
N
5233
3-Ethylpyridine
O
5234
4-Ethylpyridine
N
N
5235
2-Ethyl-4-pyridinecarbothioamide
O
O
O
N
N
O
O
5236
Ethyl 2-pyridinecarboxylate
Ethyl 3-pyridinecarboxylate
5237
Ethyl 4-pyridinecarboxylate
HO
O
N
Br
5238
N-Ethylpyridinium bromide
5239
N
O
N
5240
1-Ethyl-1H-pyrrole
5241
1-Ethyl-1H-pyrrole-2,5-dione
O
O Si O
O
OH O
N
N
NH2
N
5242
1-Ethyl-2-pyrrolidinemethanamine
O
5243
Ethyl Red
Ethyl salicylate
O
O
5244
5245
Ethyl silicate
5246
Ethyl stearate
5247
2-Ethylstyrene
3-Ethylstyrene
O
O O
S
O
OH
5250
Ethyl sulfate
5254
5-Ethyl-1,3,4-thiadiazol-2-amine
5255
S-Ethyl thioacetate
OH
5256
5257
(Ethylthio)benzene
O
5252
5253
Ethyl tartrate
N
S
(Ethylthio)acetic acid
OH
OH O
S
O
S
S
N
2-Ethyl-5-(3-sulfophenyl)isoxazolium hydroxide, inner salt
O
NH2
OH
O
5251
2-(Ethylsulfonyl)ethanol
N N
O
O
S
O
O
O O
5249
S
OH
S
5258
Ethyl thiocyanate
5248
4-Ethylstyrene
2-Ethyltetrahydrofuran
S
S
OH
5259
2-(Ethylthio)ethanol
5260
1-(Ethylthio)-4-methylbenzene
O
S
5261
2-Ethylthiophene
N
O
S
O
5262
Ethyl thiophene-2-carboxylate
S
5263
S
3-Ethyl-2-thioxo-4-thiazolidinone
5264
2-Ethyltoluene
5265
3-Ethyltoluene
5266
4-Ethyltoluene
Organic
N
O
Physical Constants of Organic Compounds
3-270
Mol. Form.
CAS RN
Mol.
Wt.
Ethyl p-toluenesulfonate
C9H12O3S
80-40-0
200.254
5268
Ethyl trichloroacetate
C4H5Cl3O2
515-84-4
191.441
5269
5270
Ethyl trifluoroacetate
Ethyl 4,4,4-trifluoroacetoacetate
Ethyl trifluoromethanesulfonate
Ethyl 3,4,5-trihydroxybenzoate
C4H5F3O2
C6H7F3O3
383-63-1
372-31-6
142.077
184.113 liq
C3H5F3O3S
425-75-2
178.130
C9H10O5
831-61-8
No.
Name
5267
5271
5272
5273
5274
Synonym
Physical
Form
bp/˚C
den
g cm –3
33(4)
17315
1.16648
167(3)
1.383620 1.450520
61
132
1.19420 1.30820
1.258615 1.378315 s EtOH, eth
115
1.37400
s eth
sl H2O, chl; s
EtOH, eth,
AcOEt
vs EtOH
vs ace, bz, eth,
EtOH
vs ace, bz, eth,
EtOH
-39.1
nD
C5H14O3Si
C11H16
198.172 mcl pr (w+2 163.0
1/2) nd
(chl)
5314-55-6 150.249
17851-27-3 148.245 liq
-13.4(0.7)
122.9(0.8)
212(1)
0.948820 1.383820
0.88320 1.507520
C11H16
3982-67-0
148.245 liq
-15.5(0.3)
211(1)
0.88320
2710.5
214
1.8820
Solubility
i H2O; s EtOH,
eth, AcOEt; sl
ctc
i H2O; s EtOH,
eth, bz; sl chl
C5H14Pb
C9H15N
C6H11O3P
1762-26-1
520-69-4
824-11-3
281.4
col liq
137.222 lf (eth)
162.123
66.5
53.7
5279
Ethyltrimethoxysilane
1-Ethyl-2,4,5-trimethylbenzene
2-Ethyl-1,3,5-trimethylbenzene
Ethyltrimethyllead
Ethyltrimethylplumbane
3-Ethyl-2,4,5-trimethylpyrrole
4-Ethyl-2,6,7-trioxa-1-phos- Trimethylolpropane phosphite
phabicyclo[2.2.2]octane
Ethyl undecanoate
Ethyl undecylate
C13H26O2
627-90-7
214.344
-16(6)
13114
5280
Ethyl 10-undecenoate
C13H24O2
692-86-4
212.329 liq
-38
264.5
5281
N-Ethylurea
C3H8N2O
625-52-5
88.108
94(2)
dec
5282
Ethyl vinyl ether
C4H8O
109-92-2
72.106
-115.8(0.4)
36(2)
5283
Ethyl Violet
C31H42ClN3
2390-59-2
5284
5285
α-Ethynylbenzenemethanol
α-Ethynylbenzenemethanol
carbamate
1-Ethynylcyclohexanamine
1-Ethynylcyclohexanol
1-Phenylpropargyl alcohol
Carfimate
C9H8O
C10H9NO2
4187-87-5
3567-38-2
492.138 gray-viol
cry
132.159 pr
175.184 cry (al)
22
86.5
11412
1.065520 1.550820
C8H13N
C8H12O
30389-18-5 123.196
78-27-3
124.180 cry (peth)
31(3)
6520
174
Ethinamate
C9H13NO2
126-52-3
97
1203
C7H10O
C10H10O
17356-19-3 110.153
127-66-2
146.185
27
52(3)
157.5
217.5
5291
5292
5293
1-Ethynylcyclohexanol,
carbamate
1-Ethynylcyclopentanol
α-Ethynyl-αmethylbenzenemethanol
Ethynylsilane
Etioporphyrin
Etofylline
0.91325 1.481720
0.987320 1.482220 i H2O; s EtOH,
bz, peth; sl chl
1.444121 sl H2O; vs EtOH;
s hx
0.96225 1.475120
1.031420
C2H4Si
C32H38N4
C9H12N4O3
1066-27-9
448-71-5
519-37-9
56.139 col gas
478.671
224.216
362
158
5294
Etoglucid
C12H22O6
1954-28-5
262.299 col liq
-13
5295
5296
5297
Etoposide
Etrimfos
Eucalyptol
C29H32O13
C10H17N2O4PS
C10H18O
33419-42-0 588.556 cry (MeOH)
38260-54-7 292.291
470-82-6
154.249 oil
≈243
-1.7
1.4(0.3)
5298
Euparin
C13H12O3
532-48-9
216.232
121.5
5299
Evan’s Blue
C34H24N6Na4O14S4
314-13-6
960.806
5300
5301
Evodiamine
Famotidine
C19H17N3O
C8H15N7O2S3
518-17-2
303.357 ye lf (al)
76824-35-6 337.446 cry
28
170.6(0.6)
5302
5303
Famphur
α-Farnesene
C10H16NO5PS2
C15H24
52-85-7
502-61-4
57(2)
5304
5305
5306
β-Farnesene
Farnesic acid
2-cis,6-trans-Farnesol
C15H24
C15H24O2
C15H26O
18794-84-8 204.352
7548-13-2 236.351 oil
3790-71-4 222.366 oil
1219
20416
15612
5307
2-trans,6-trans-Farnesol
C15H26O
106-28-5
16010
5275
Organic
mp/˚C
5276
5277
5278
5286
5287
5288
5289
5290
HCP_Section_03.indb 270
Ethoxyethylene
Silylacetylene
Oxirane, 2,2’-(2,5,8,11-tetraoxadodecane-1,12-diyl)bis-
Cineole
1-[6-Hydroxy-2-(1methylvinyl)-5-benzofuranyl]
ethanone
nd (bz,
al-eth)
liq
167.205 nd
325.342
204.352
222.366 oil
1.507420
s chl
0.863320 1.428520 i H2O; s EtOH,
eth, ace, bz
0.882715 1.444925 i H2O; s EtOH,
eth, HOAc; sl
ctc
1.213018
vs H2O, EtOH,
bz; s eth; i CS2
0.758920 1.376720 sl H2O, ctc; s
EtOH; msc eth
s H2O, EtOH
-22.5
vs H2O; s EtOH;
sl eth, bz
1962
1.131220 1.462220
176(4)
s MeOH
1.19520
0.926720 1.458620 i H2O; s EtOH,
eth, chl; sl ctc
s eth, bz, chl; sl
NaOH
s H2O, EtOH,
acid
i EtOH, chl; vs
DMF; s HOAc;
sl MeOH
13012
0.841020 1.483620 i H2O; s eth,
ace; msc peth,
lig
0.836320 1.489920 vs ace, eth, chl
0.890820 1.487720 vs ace, eth,
EtOH
0.88820 1.487720 i H2O; vs EtOH;
s eth, ace
4/11/16 11:28 AM
Physical Constants of Organic Compounds
3-271
O
O S O
O
Cl
5267
F
O
Cl
F
5268
Ethyl p-toluenesulfonate
O
O
O
Cl
F
F
O
F
5269
Ethyl trichloroacetate
O
F
F
O
F
5270
Ethyl trifluoroacetate
O
S
O
O
O
Si O
O
OH
HO
F
OH
5271
Ethyl 4,4,4-trifluoroacetoacetate
O
5272
Ethyl trifluoromethanesulfonate
5273
Ethyl 3,4,5-trihydroxybenzoate
Ethyltrimethoxysilane
O
N
H
Pb
5274
5275
1-Ethyl-2,4,5-trimethylbenzene
5276
2-Ethyl-1,3,5-trimethylbenzene
Ethyltrimethyllead
P
O
5277
O
5278
3-Ethyl-2,4,5-trimethylpyrrole
4-Ethyl-2,6,7-trioxa-1-phosphabicyclo[2.2.2]octane
O
O
O
N
H
O
O
5279
5280
Ethyl undecanoate
Cl
N
Organic
N
NH2
O
5281
Ethyl 10-undecenoate
N
5282
N-Ethylurea
5283
Ethyl vinyl ether
Ethyl Violet
O
OH
O
NH2
O
HO
H2N
O
HO
H 2N
5284
5285
α-Ethynylbenzenemethanol
5286
α-Ethynylbenzenemethanol carbamate
5287
1-Ethynylcyclohexanamine
5288
1-Ethynylcyclohexanol
5289
1-Ethynylcyclohexanol, carbamate
1-Ethynylcyclopentanol
O
O
H
OH
O
HO
O
O
O
OH
NH N
O
O
N HN
OH
5290
S
O
5293
Etioporphyrin
O
HO
S
O
5296
5297
Etrimfos
N
N
OH NH2 O
OH
S
O
O
S
O
OH
5299
Evan’s Blue
S
N
N
S
O
OH
Euparin
O
N
H
H
N
5295
Etoposide
N
5298
Eucalyptol
O
OH
O
NH2 OH
O
O
HO
O
Etoglucid
O
N
O
5294
Etofylline
O
O
O
O
O
O
P
N
O
5292
Ethynylsilane
O
N
N
O
5291
α-Ethynyl-α-methylbenzenemethanol
O
N
N
SiH3
H
O
P
O
NH2
O
N
O S O
NH2
5300
S
5301
Evodiamine
NH2
N
S
Famotidine
N
NH2
O S O
N
5302
5303
α-Farnesene
Famphur
5304
β-Farnesene
O
OH
5305
Farnesic acid
OH
5306
2-cis,6-trans-Farnesol
OH
5307
2-trans,6-trans-Farnesol
Physical Constants of Organic Compounds
3-272
No.
Name
Synonym
Mol. Form.
5308
5309
5310
5311
5312
Farnesol acetate
Fenadiazole
Fenamiphos
Fenarimol
Fenbuconazole
C17H28O2
2-(1,2,4-Oxadiazol-2-yl)phenol C8H6N2O2
C13H22NO3PS
C17H12Cl2N2O
C20H19ClN4
5313
Fenbutatin oxide
5314
α-Fenchol, (±)-
Distannoxane, hexakis(2methyl-2-phenylpropyl)1,3,3-Trimethylbicyclo[2.2.1]­
heptan-2-ol, endo-(±)
5315
CAS RN
Mol.
Wt.
Physical
Form
mp/˚C
Organic
36386-49-9 154.249
41.5(0.2)
199.5
0.942040
(±)-Fenchone
C10H16O
18492-37-0 152.233 oily liq
6.1
193.5
0.949215 1.470220 i H2O; vs EtOH;
s eth, ace
5316
5317
5318
Fenfluramine
Fenitrothion
Fenoxaprop-ethyl
C12H16F3N
C9H12NO5PS
C18H16ClNO5
458-24-2
231.257 cry (AcOEt)
122-14-5
277.234
82110-72-3 361.777
85
11012
1180.05
2000.001
5319
Fenoxycarb
C17H19NO4
79127-80-3 301.338
53
5320
5321
5322
5323
5324
5325
Fenpropathrin
Fensulfothion
Fentanyl
Fenthion
Fenvalerate
Ferbam
C22H23NO3
C11H17O4PS2
C22H28N2O
C10H15O3PS2
C25H22ClNO3
C9H18FeN3S6
64257-84-7
115-90-2
437-38-7
55-38-9
51630-58-1
14484-64-1
349.423
308.354
336.469
278.328
419.901
416.494
49.3(0.4)
5326
Ferrocene
102-54-5
186.031 oran
needles
175(1)
5327
Ferrous gluconate
C12H22FeO14
5328
Ferrous lactate
C6H10FeO6
5329
5330
Fichtelite
Finasteride
5331
Fisetin
5332
5333
Flavine adenine dinucleotide
Florantyrone
5334
5335
5336
5337
5338
5339
Fluazipop-butyl
Flubenzimine
Fluchloralin
Flucythrinate
Fludrocortisone
Flumethiazide
5340
5341
Fluocinolone acetonide
Fluoranthene
5342
9H-Fluoren-2-amine
5343
9H-Fluorene
5344
5345
FAD
Cythrin
Trifluoromethylthiazide
1.1520
C15H10O6
528-48-3
286.236 lt ye nd (dil
al, + 1 w)
C27H33N9O15P2
C20H14O3
146-14-5
519-95-9
C19H20F3NO4
C17H10F6N4S
C12H13ClF3N3O4
C26H23F2NO4
C21H29FO5
C8H6F3N3O4S2
79241-46-6
37893-02-0
33245-39-5
70124-77-5
127-31-1
148-56-1
785.550 ye cry (w)
302.323 ye cry
(HOAc)
383.362 pale ye liq
416.343 ye cry
355.697
451.463
380.450 cry (EtOH)
329.277 cry
67-73-2
206-44-0
C13H10
86-73-7
9H-Fluorene-9-carboxylic acid
9H-Fluorene-2,7-diamine
2,7-Diaminofluorene
C14H10O2
C13H12N2
1989-33-9
525-64-4
5346
5347
9H-Fluorene-9-methanol
9H-Fluoren-9-ol
C14H12O
C13H10O
5348
9H-Fluoren-9-one
5349
Fluorescein
452.488 cry (ace/hx)
202.250 pa ye nd or
pl (al)
181.233 pl or nd (dil
al)
166.218 lf (al)
210.228
196.247 nd (w), pr
(bz), pl
(eth)
24324-17-2 196.244
1689-64-1 182.217 hex nd (w,
peth)
C13H8O
486-25-9
C20H12O5
2321-07-5
180.202 ye orth
bipym (al,
bz-peth)
332.306 red orth pr
vs eth, EtOH
1.322725
sl H2O, hx; s
eth; vs ace, tol
1400.01
1.1525
1.20220
870.01
dec
1.24620
1.1525
180 dec
C19H34
C23H36N2O2
153-78-6
HCP_Section_03.indb 272
16810
1800.1
249
i H2O; s EtOH,
eth, bz, dil
HNO3
s H2O; i EtOH
299-29-6
C13H11N
Fluorenone
85.2(0.5)
7.5
446.140 ye-gray
pow (w)
5905-52-2 233.984 grn-wh pow
(hyd)
2221-95-6 262.473 cry
46
98319-26-7 372.544 wh cry
252(1)
C24H30F2O6
1,2-(1,8-Naphthylene)benzene C16H10
2,2’-Methylenebiphenyl
145.8(0.5)
Solubility
C10H18O
18-Norabietane
Proscar
1052.68
nD
C60H78OSn2
Iron, tris(dimethyl­carba­
modithioato-S,S’)-, (OC-6-11)Dicyclopentadienyl iron
C10H10Fe
112
49
118
125
den
g cm –3
29548-30-9
1008-65-7
22224-92-6
60168-88-9
11436943-6
13356-08-6
Ethyl 2-(4-phenoxyphenoxy)
ethylcarbamate
264.403
162.146 cry
303.358
331.195
350.845
bp/˚C
s H2O; i EtOH
23643
0.938022 1.505220
sl H2O; s chl,
EtOH, MeOH,
DMSO
i H2O; s EtOH,
ace; sl eth, bz,
peth
330
208
s EtOH, MeOH
5
119
47.7(0.5)
sl H2O
1080.35
1.18922
261 dec
306
266 dec
110.2(0.2)
sl H2O; i bz, tol;
s MeOH, EtOH,
DMF
380(5)
1.2520
114.76(0.03) 294(2)
1.2030
130.3
230(1)
166
i H2O; s EtOH,
chl
103.42(0.08)
154(2)
84(1)
315 dec
i H2O; s EtOH,
eth, bz, chl, CS2
i H2O; s EtOH,
eth, ctc, CS2
i H2O; sl EtOH; s
eth, ace, bz,
CS2
343.1(0.6)
1.130099 1.630999
sl H2O, peth,
EtOH; s eth,
ace; vs bz
i H2O; s EtOH,
ace, bz; vs tol;
sl ctc
sl H2O, EtOH,
eth; vs ace; s
py, MeOH
4/11/16 11:28 AM
Physical Constants of Organic Compounds
3-273
N
Cl
O
5308
O
S
O
O
N
5310
Fenadiazole
O
5313
5314
F
5315
α-Fenchol, (±)-
Fenbutatin oxide
F
N
O
O
O
O
5317
Fenfluramine
O
O
Cl
5316
(±)-Fenchone
P
O
N
O
Fenbuconazole
S
O
O
F
5312
Fenarimol
H
N
OH
N
5311
Fenamiphos
Sn O Sn
Cl
Cl
N
5309
Farnesol acetate
H
N
P
N N
5318
Fenitrothion
Fenoxaprop-ethyl
O
O
O
H
N
O
O
O
O
O
N
N
O
5323
Fentanyl
Fensulfothion
P
O
5322
5321
Fenpropathrin
S
O
O
S
5320
Fenoxycarb
P
O
S
O
N
5319
S
O
Fenthion
N
S
S
N
O
O
Cl
S
O
H
HO
H
H
S
Fe
S
S
N
N
Fe
5325
5324
5326
Ferbam
Fenvalerate
COO
OH
H
OH
OH
CH2OH
Fe2
Fe 2
O
OH
5327
Ferrocene
H
O
2
5328
Ferrous gluconate
5329
Ferrous lactate
Fichtelite
O
N
N
N
CH2
OH
OH
OH O
H
N
O
O
HO
N
H
H
OH
O
O
NH2
5330
N
N
O
OH
O
HO
OH
5331
Finasteride
N
N
O
O P O P O
OH OH
OH
O
H
N
OH
O
5332
Fisetin
5333
Flavine adenine dinucleotide
Florantyrone
Cl
F
N
F
O
O
N
O
O
F
N
F
F
F
5334
O
N
F
F
S
F
F
HO
F
O
S
H2N
H
F
O
5338
NH
S
O O
5339
Fludrocortisone
H
N
O
F
F
F
O
O
N
5337
Flucythrinate
OH
O
O
F
NH2
O
F
5340
Flumethiazide
O
O
Fluchloralin
HO
F F
OH
O
5336
Flubenzimine
O
O
N
F
O
HO
N
N
5335
Fluazipop-butyl
O
N
5341
Fluocinolone acetonide
5342
Fluoranthene
5343
9H-Fluoren-2-amine
9H-Fluorene
O
O
OH
OH
H2N
OH
O
O
NH2
HO
5344
9H-Fluorene-9-carboxylic acid
5345
9H-Fluorene-2,7-diamine
5346
9H-Fluorene-9-methanol
5347
9H-Fluoren-9-ol
5348
9H-Fluoren-9-one
O
5349
Fluorescein
OH
Organic
O
O
OH
N N
OH
Physical Constants of Organic Compounds
3-274
Organic
No.
Name
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
5350
Fluorescein sodium
C.I. Acid Yellow 73
C20H10Na2O5
518-47-8
376.270 ye pow
5351
2-Fluoroacetamide
Fluoroacetic acid amide
C2H4FNO
640-19-7
77.057
5352
5353
5354
5355
Fluoroacetic acid
Fluoroacetyl chloride
Fluoroacetylene
2-Fluoroaniline
Fluoroethanoic acid
C2H3FO2
C2H2ClFO
C2HF
C6H6FN
144-49-0
359-06-8
2713-09-9
348-54-9
78.042
96.487
44.027
111.117
5356
3-Fluoroaniline
C6H6FN
372-19-0
111.117
5357
4-Fluoroaniline
C6H6FN
371-40-4
111.117 pa ye liq
-1.9(0.5)
5358
5359
5360
5361
2-Fluorobenzaldehyde
3-Fluorobenzaldehyde
4-Fluorobenzaldehyde
Fluorobenzene
C7H5FO
C7H5FO
C7H5FO
C6H5F
446-52-6
456-48-4
459-57-4
462-06-6
124.112 liq
124.112
124.112 liq
96.102 liq
-44.5
5362
5363
5364
5365
5366
5367
C8H7FO2
C8H6FN
C8H6FN
C7H8FN
C7H7FO
C6H4ClFO2S
405-50-5
326-62-5
459-22-3
140-75-0
459-56-3
349-88-2
154.139 cry (chl)
135.139
135.139
125.144
126.128
194.611 pl or nd
94(3)
23
30
5368
4-Fluorobenzeneacetic acid
2-Fluorobenzeneacetonitrile
4-Fluorobenzeneacetonitrile
4-Fluorobenzenemethanamine
4-Fluorobenzenemethanol
4-Fluorobenzenesulfonyl
chloride
2-Fluorobenzoic acid
C7H5FO2
445-29-4
140.112 nd (a)
124.2(0.8)
1.46025
5369
5370
3-Fluorobenzoic acid
4-Fluorobenzoic acid
C7H5FO2
C7H5FO2
455-38-9
456-22-4
123.6(0.4)
183.9(0.6)
1.47425
1.47925
5371
5372
5373
5374
5375
5376
2-Fluorobenzonitrile
4-Fluorobenzonitrile
2-Fluorobenzoyl chloride
3-Fluorobenzoyl chloride
4-Fluorobenzoyl chloride
2-Fluoro-1,1’-biphenyl
C7H4FN
C7H4FN
C7H4ClFO
C7H4ClFO
C7H4ClFO
C12H9F
394-47-8
1194-02-1
393-52-2
1711-07-5
403-43-0
321-60-8
140.112 lf (w)
140.112 pr (w), mcl
pr (w)
121.112
121.112 nd (peth)
158.557
158.557 liq
158.557
172.197
34.8
2.0
-30
9
73.5
9322
188.8
9115
189
8220
248
1.107055
1.32825
1.30425
1.34225
1.245225
5377
4-Fluoro-1,1’-biphenyl
C12H9F
324-74-3
172.197 pr
74.2
253
1.24725
5378
5379
1-Fluorobutane
2-Fluorobutane
Butyl fluoride
sec-Butyl fluoride
C4H9F
C4H9F
2366-52-1
359-01-3
76.112
76.112
-134
-121.4
31(8)
23(9)
0.778920
0.755925
5380
5381
5382
Fluorocyclohexane
1-Fluorocyclohexene
5-Fluorocytosine
Cyclohexyl fluoride
372-46-3
694-51-9
2022-85-7
102.149
100.133
129.092 wh cry
13
103(5)
96.5
0.927920 1.414620 i H2O; s py
1.444125
5383
5384
1-Fluorodecane
Fluorodifen
C10H21F
C13H7F3N2O5
334-56-5
160.272 liq
15457-05-3 328.200
-35
91.7(0.5)
189(8)
0.819420 1.4085
5385
5386
1-Fluoro-2,4-dinitrobenzene
Fluoroethane
4-Amino-5-fluoro-2-hydroxypyrimidine
Decyl fluoride
2-Nitro-1-(4-nitrophenoxy)-4(trifluoromethyl)benzene
2,4-Dinitrophenyl fluoride
Ethyl fluoride
C6H11F
C6H9F
C4H4FN3O
C6H3FN2O4
C2H5F
70-34-8
353-36-6
186.097
48.059 col gas
25.8
-143.2
296
-37.7(0.3)
5387
2-Fluoroethanol
Ethylene fluorohydrin
C2H5FO
371-62-0
64.058
liq
-26.4
85(14)
5388
Fluoroethene
Vinyl fluoride
C2H3F
75-02-5
46.043
col gas
-160.5
-72
5389
1-Fluoroheptane
C7H15F
661-11-0
118.192 liq
-73
122(9)
5390
5391
5392
1-Fluorohexane
1-Fluoro-2-iodobenzene
1-Fluoro-4-iodobenzene
C6H13F
C6H4FI
C6H4FI
373-14-8
348-52-7
352-34-1
104.165 liq
221.998 liq
221.998 liq
-103
-41.5
-27
88(8)
188.6
183
5393
1-Fluoro-3-isothiocyanatobenzene
1-Fluoro-4-isothiocyanatobenzene
C7H4FNS
404-72-8
153.177
1.471854 1.569020 s EtOH; sl chl
0.718220 1.265620 sl H2O; vs EtOH,
(p>1
eth
atm
1.104020 1.364718 msc H2O, EtOH,
eth; vs ace; sl
chl
i H2O; s EtOH,
ace
0.806220 1.385420 i H2O; s eth,
ace, bz; vs
peth
0.799520 1.373820 s eth, bz
1.591020 s ace, bz, chl
1.952315 1.527022 i H2O; s EtOH,
eth, ace
1.2725
1.618620
C7H4FNS
1544-68-9
153.177
5394
HCP_Section_03.indb 274
Fluoroethyne
Phenyl fluoride
Hexyl fluoride
Physical
Form
nd
liq
gas
pa ye liq
mp/˚C
bp/˚C
108
sub
35.2
168
72
-74(15)
175
-196
-29(1)
188
liq
vol liq or
gas
182
175
173
-10
181.5
-42.18(0.05) 84.7(0.3)
86.0
1642
232
228
183
210
1069
den
g cm –3
nD
Solubility
s H2O, EtOH,
glycerol, dil
acid
s H2O, ace; sl
chl
s H2O, EtOH
1.369336
1.151321 1.542120 i H2O; s EtOH,
eth; sl ctc
1.156119 1.543620 sl H2O, chl; s
EtOH, eth
1.172520 1.519520 sl H2O, ctc; s
EtOH, eth
1.17825 1.523420
1.1725
1.520620
1.181019
1.022520 1.468430 sl H2O; vs bz,
eth, EtOH, lig
1.05925 1.500920
1.139020 1.500220
1.513920
1.508020
vs bz, eth, chl
sl H2O; vs EtOH,
eth; i bz; s chl
sl H2O; s eth
sl H2O, ace; s
EtOH, eth
1.492555 sl chl; s peth
1.536520
1.528520
1.529620
s EtOH, eth, chl,
peth; sl lig
sl EtOH; s eth,
gl HOAc
1.339620 vs EtOH
296 dec
227
27
vs eth
228
4/11/16 11:28 AM
Physical Constants of Organic Compounds
3-275
O
NH2
O
O
Na O
F
O Na
O
O
5350
F
NH2
5351
Fluorescein sodium
F
5352
2-Fluoroacetamide
F
O
OH
Cl
5353
Fluoroacetic acid
O
NH2
NH2
Fluoroacetyl chloride
F
F
5354
5355
Fluoroacetylene
5356
2-Fluoroaniline
5357
3-Fluoroaniline
5358
4-Fluoroaniline
2-Fluorobenzaldehyde
N
O
NH2
N
O
F
OH
F
F
5359
3-Fluorobenzaldehyde
5360
5361
4-Fluorobenzaldehyde
5362
Fluorobenzene
4-Fluorobenzeneacetic acid
Cl
O S O
OH
F
O
5363
O
OH
F
N
O
4-Fluorobenzenemethanol
O
F
F
F
5368
4-Fluorobenzenesulfonyl chloride
Cl
F
F
5367
4-Fluorobenzenemethanamine
N
OH
OH
F
5366
F
5365
4-Fluorobenzeneacetonitrile
2-Fluorobenzeneacetonitrile
O
O
F
5364
2-Fluorobenzoic acid
5369
3-Fluorobenzoic acid
F
5370
5371
4-Fluorobenzoic acid
2-Fluorobenzonitrile
5372
5373
4-Fluorobenzonitrile
2-Fluorobenzoyl chloride
Cl
NH2
Cl
F
F
F
5374
3-Fluorobenzoyl chloride
5375
5376
4-Fluorobenzoyl chloride
N
O
N
F
O
O
O
F
N
O
F
5383
5384
1-Fluorodecane
Fluorodifen
5378
4-Fluoro-1,1’-biphenyl
F
F
O
N
F
N
N
H
F
F
5377
2-Fluoro-1,1’-biphenyl
O
F
F
F
5379
1-Fluorobutane
5380
2-Fluorobutane
Fluorocyclohexane
5381
1-Fluorocyclohexene
O
5382
5-Fluorocytosine
O
O
5385
1-Fluoro-2,4-dinitrobenzene
F
F
5386
OH
5387
Fluoroethane
2-Fluoroethanol
F
F
5388
Fluoroethene
5389
1-Fluoroheptane
F
F
F
F
I
F
5390
1-Fluorohexane
N
I
5391
1-Fluoro-2-iodobenzene
5392
1-Fluoro-4-iodobenzene
5393
C
S
1-Fluoro-3-isothiocyanatobenzene
N
C
S
5394
1-Fluoro-4-isothiocyanatobenzene
Organic
F
O
F
F
Physical Constants of Organic Compounds
3-276
Organic
No.
Name
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
Physical
Form
mp/˚C
bp/˚C
5395
Fluoromethane
Methyl fluoride
CH3F
593-53-3
34.033
col gas
-143.3
-78.4
5396
5397
5398
5399
1-Fluoro-2-methoxybenzene
1-Fluoro-3-methoxybenzene
1-Fluoro-4-methoxybenzene
4-Fluoro-2-methylaniline
C7H7FO
C7H7FO
C7H7FO
C7H8FN
321-28-8
456-49-5
459-60-9
452-71-1
126.128 liq
126.128 liq
126.128 liq
125.144
-39
-35
-45
14.2
154.5
159
157
9416
0.55725
(p>1
atm)
1.548917
1.10425
1.178118
1.126318
5400
5401
C7H7F
C7H6FNO2
350-50-5
446-34-4
110.129 liq
155.127 nd (al)
-35
53.2
142(2)
973
1.022825
1.438025
5402
5403
(Fluoromethyl)benzene
2-Fluoro-4-methyl-1-nitroben- 3-Fluoro-4-nitrotoluene
zene
2-Fluoro-2-methylpropane
tert-Butyl fluoride
1-Fluoronaphthalene
C4H9F
C10H7F
353-61-7
321-38-0
76.112 col gas
146.161 liq
-14.0(0.2)
12.1
213(14)
5404
2-Fluoronaphthalene
C10H7F
323-09-1
146.161 nd (al)
58(1)
212
5405
5406
1-Fluoro-2-nitrobenzene
1-Fluoro-3-nitrobenzene
o-Fluoronitrobenzene
m-Fluoronitrobenzene
C6H4FNO2
C6H4FNO2
1493-27-2
402-67-5
141.100 ye liq
141.100 ye cry
-6
41
215 dec
197(9)
5407
1-Fluoro-4-nitrobenzene
p-Fluoronitrobenzene
C6H4FNO2
350-46-9
141.100 ye nd
26.5(0.5)
205
5408
5409
5410
5411
5412
1-Fluorooctane
1-Fluoropentane
2-Fluorophenol
3-Fluorophenol
4-Fluorophenol
Octyl fluoride
Pentyl fluoride
C8H17F
C5H11F
C6H5FO
C6H5FO
C6H5FO
463-11-6
592-50-7
367-12-4
372-20-3
371-41-5
132.219 liq
90.139 liq
112.101
112.101
112.101
-64
-120
16.1(0.5)
14(1)
48(1)
146(9)
63(3)
151(4)
178
185.5
5413
5414
5415
2-Fluoro-1-phenylethanone
1-(4-Fluorophenyl)ethanone
1-Fluoropropane
C8H7FO
C8H7FO
C3H7F
450-95-3
403-42-9
460-13-9
138.139 pl
138.139 liq
62.086 col gas
29
-45
-159
9012
196
-3(2)
5416
5417
5418
5419
5420
5421
2-Fluoropropane
1-Fluoro-2-propanone
cis-1-Fluoropropene
trans-1-Fluoropropene
2-Fluoropropene
3-Fluoropropene
C3H7F
C3H5FO
C3H5F
C3H5F
C3H5F
C3H5F
420-26-8
430-51-3
19184-10-2
20327-65-5
1184-60-7
818-92-8
62.086
76.069
60.070
60.070
60.070
60.070
5422
5423
5424
2-Fluoropyridine
3-Fluoropyridine
2-Fluorotoluene
o-Tolyl fluoride
C5H4FN
C5H4FN
C7H7F
372-48-5
372-47-4
95-52-3
97.091
97.091 liq
110.129 liq
-62.5(0.5)
125
107
114(2)
5425
3-Fluorotoluene
m-Tolyl fluoride
C7H7F
352-70-5
110.129 liq
-89.2(0.4)
116(2)
5426
4-Fluorotoluene
p-Tolyl fluoride
C7H7F
352-32-9
110.129 liq
-56.6(0.1)
116.6(0.4)
5427
C7H4Cl3F
488-98-2
213.464
9512
C7H4F4
392-85-8
164.101
114.5
1.29325
C7H4F4
401-80-9
164.101 liq
-81.5
100.6(1)
1.302117
C7H4F4
402-44-8
164.101 liq
-41.7
103.5
1.29325
5431
1-Fluoro-2-(trichloromethyl)­
benzene
1-Fluoro-2-(trifluoromethyl)­
benzene
1-Fluoro-3-(trifluoromethyl)­
benzene
1-Fluoro-4-(trifluoromethyl)­
benzene
Fluorotrimethylsilane
1.128020 1.457420
1.130
1.472020
1.004113 1.470420 i H2O; vs EtOH,
eth
0.997420 1.469120 i H2O; vs EtOH,
eth
0.997520 1.469920 i H2O; vs EtOH,
eth
1.45325 1.543220
Trimethylsilyl fluoride
C3H9FSi
420-56-4
92.187
5432
5-Fluorouracil
5-Fluoro-2,4(1H,3H)-Pyrimidinedione
C4H3FN2O2
5433
5434
5435
5436
5437
5438
Fluoxetine
Fluoxymesterone
Fluphenazine
Fluprednisolone
Flurandrenolide
Flurazepam
5439
5440
Fluridone
Fluroxypyr
5428
5429
5430
HCP_Section_03.indb 276
Propyl fluoride
Isopropyl fluoride
Fluoroacetone
Fludroxycortide
[(4-Amino-3,5-dichloro-6fluoro-2-pyridyl)oxy]acetic
acid
C17H18F3NO
C20H29FO3
C22H26F3N3OS
C21H27FO5
C24H33FO6
C21H23ClFN3O
C19H14F3NO
C7H5Cl2FN2O3
gas
col gas
col gas
col gas
col gas
-10(3)
77
-15(16)
den
g cm –3
nD
Solubility
1.167425 sl H2O, bz, chl;
vs EtOH, eth
1.496917 i H2O; s eth, ctc
1.487620
1.488618 s eth
1.536318 s eth, ace, bz,
ctc
1.489225 s ctc
1.132220 1.593920 i H2O; s EtOH,
eth, bz, chl,
HOAc
i H2O; s EtOH,
eth, bz, chl,
HOAc
1.328518 1.548917 vs eth, EtOH
1.325419 1.526215 i H2O; s EtOH,
eth; sl bz
1.330020 1.531620 i H2O; s EtOH,
eth; sl ctc
0.811620 1.394620
0.790720 1.35912- vs eth, EtOH
1.12025 1.514420 s H2O
1.23825 1.514020
1.188956
sl H2O; s ace,
peth
1.15220 1.520020
1.138225 1.508125 i H2O; s bz, chl
0.759620 1.311520 sl H2O; vs EtOH,
(p>1
eth
atm
sl H2O
1.028820 1.370020
≈-20
-24
-7(15)
vol liq or
gas
51-21-8
130.077 cry (w,
284(4)
MeOH-eth)
54910-89-3 309.326 oil
76-43-7
336.440
270
69-23-8
437.520
53-34-9
378.434
210
1524-88-5 436.513 cry (ace/hx) 251
17617-23-1 387.878 wh rods
80
(eth/peth)
59756-60-4 329.315
155
69377-81-7 255.030
232
sl H2O; vs EtOH,
eth; s chl
1.404025
1.402520
16.4
369(11)
2510.3
4/11/16 11:29 AM
Physical Constants of Organic Compounds
3-277
F
H
H
O
NH2
F
O
O
H
5395
5396
1-Fluoro-2-methoxybenzene
5397
5398
1-Fluoro-3-methoxybenzene
F
O
N
F
F
5404
5399
1-Fluoro-4-methoxybenzene
2-Fluoronaphthalene
5400
4-Fluoro-2-methylaniline
5401
(Fluoromethyl)benzene
5402
2-Fluoro-4-methyl-1-nitrobenzene
2-Fluoro-2-methylpropane
F
OH
OH
O
N
O
5405
F
O
O
5406
1-Fluoro-2-nitrobenzene
N
O
1-Fluoro-3-nitrobenzene
F
F
5407
5408
1-Fluoro-4-nitrobenzene
5409
1-Fluorooctane
1-Fluoropentane
F
5410
5411
2-Fluorophenol
3-Fluorophenol
Organic
1-Fluoronaphthalene
F
F
F
5403
O
F
O
F
Fluoromethane
N
F
F
OH
O
O
F
F
F
5412
5413
4-Fluorophenol
2-Fluoro-1-phenylethanone
5414
5415
1-(4-Fluorophenyl)ethanone
F
O
F
F
F
F
1-Fluoropropane
5416
5417
2-Fluoropropane
1-Fluoro-2-propanone
F
F
5418
5419
cis-1-Fluoropropene
trans-1-Fluoropropene
5420
5421
2-Fluoropropene
3-Fluoropropene
F
F
F
N
F
F
N
5422
5423
2-Fluoropyridine
3-Fluoropyridine
Cl
F
5424
Cl
Cl
F
F
F
5425
2-Fluorotoluene
F
F
F
5426
3-Fluorotoluene
5427
4-Fluorotoluene
5428
1-Fluoro-2-(trichloromethyl)benzene
1-Fluoro-2-(trifluoromethyl)benzene
F
F
5429
1-Fluoro-3-(trifluoromethyl)benzene
OH
N
F
HO
O
F
F
F
N
F
Si
F
5430
1-Fluoro-4-(trifluoromethyl)benzene
N
H
5431
O
F
F
HO
OH
OH
HO
H
H
F
O
5433
F
5436
Fluprednisolone
O
S
5434
5435
Fluoxymesterone
O
O
N
Cl
F
5437
F
F
Fluphenazine
O
N
F
Flurandrenolide
F
N
N
O
O
H
Fluoxetine
5-Fluorouracil
O
HO
F
OH
O
H
N
O
H
5432
Fluorotrimethylsilane
N
5438
Flurazepam
F
F
F
N
5439
Fluridone
NH2
Cl
F
Cl
N
OH
O
O
5440
Fluroxypyr
Physical Constants of Organic Compounds
3-278
Organic
No.
Name
Synonym
Mol. Form.
CAS RN
5441
Fluvalinate
C26H22ClF3N2O3
10285106-9
59-30-3
5442
Folic acid
Vitamin Bc
5443
Folinic acid
5444
Folpet
5445
5446
Fomesafen
Fomocaine
5447
Fonofos
5448
Formaldehyde
5-Formyl-5,6,7,8-tetrahydrofo- C20H23N7O7
lic acid
1H-Isoindole-1,3(2H)-dione,
C9H4Cl3NO2S
2-[(trichloromethyl)thio]C15H10ClF3N2O6S
4-[3-[4-(Phenoxymethyl)­
C20H25NO2
phenyl]propyl]morpholine
Phosphonodithioic acid, ethyl-, C10H15OPS2
O-ethyl S-phenyl ester
Methanal
CH2O
5449
Formaldehyde oxime
Formaldoxime
5450
Formamide
5451
Formamidinesulfinic acid
5452
Formetanate hydrochloride
5453
Formic acid
5454
5455
N-Formimidoyl-L-glutamic
acid
Formononetin
5456
5457
C19H19N7O6
Mol.
Wt.
Physical
Form
mp/˚C
502.912
250 dec
58-05-9
441.397 ye-oran nd
(w)
473.440 cry (w + 3)
133-07-3
296.558
181.0(0.6)
72178-02-0 438.762
17692-39-6 311.419 col cry
bp/˚C
den
g cm –3
>450
1.2925
245 dec
220
53
1.2820
2391.1
246.329
50-00-0
30.026
CH3NO
75-17-2
45.041
Methanamide
CH3NO
75-12-7
45.041
Aminoiminomethanesulfinic
acid
CH4N2O2S
1758-73-2
108.120 nd (al)
C11H16ClN3O2
23422-53-9 257.717 pow
201 dec
Methanoic acid
CH2O2
64-18-6
46.026
8.3(0.2)
N-(Iminomethyl)-L-glutamic
acid
7-Hydroxy-3-(4methoxyphenyl)-4H-1benzopyran-4-one
C6H10N2O4
816-90-0
174.154
90
C16H12O4
485-72-3
268.264
256.5
Formothion
2-Formylbenzoic acid
C6H12NO4PS2
C8H6O3
2540-82-1
119-67-5
257.267 visc ye oil
150.132
25.5
100.5(0.2)
5458
3-Formylbenzoic acid
C8H6O3
619-21-6
150.132 nd (w)
175.0(0.2)
5459
4-Formylbenzoic acid
C8H6O3
619-66-9
150.132
249.8(0.5)
5460
3-Formylbenzonitrile
C8H5NO
24964-64-5 131.132
76.5
210
5461
4-Formylbenzonitrile
C8H5NO
105-07-7
131.132
100.5
13312
5462
C10H10O5
519-05-1
210.183 nd (w)
150
C11H10FeO
CHFO
C9H9NO2
C6H18AlO9P3
12093-10-6
1493-02-3
122-85-0
39148-24-8
214.041
48.016 col gas
163.173 pr (w)
354.105
118.5
-142.2
158.0
>300
5467
6-Formyl-2,3-dimethoxyben- Opianic acid
zoic acid
Formylferrocene
Formyl fluoride
Fluoroformaldehyde
N-(4-Formylphenyl)acetamide
Fosetyl-Al
Aluminum tris(O-ethylphosphonate)
Fosthietan
C6H12NO3PS2
21548-32-3 241.268 ye oil
5468
5469
5470
5471
Fraxin
DL-Fructose
L-Fructose
β-D-Fructose
C16H18O10
C6H12O6
C6H12O6
C6H12O6
524-30-1
6035-50-3
7776-48-9
53188-23-1
370.308
180.155
180.155
180.155
5472
5473
D-Fructose 6-phosphate
Fucoxanthin
Hexose monophosphate
C6H13O9P
C42H58O6
643-13-0
3351-86-8
5474
Fulminic acid
Carbyloxime
CHNO
506-85-4
260.135
658.906 red pl (eth)
hex pl (dil
al)
43.025
5475
5476
Fulvene
Fumaric acid
trans-2-Butenedioic acid
C6H6
C4H4O4
497-20-1
110-17-8
78.112
116.073 nd, mcl pr
or lf (w)
5477
Fumigatin
C8H8O4
484-89-9
168.148 br nd or pl
(peth)
5463
5464
5465
5466
HCP_Section_03.indb 278
α-Acrose
β-Levulose
3-Hydroxy-2-methoxy-5methyl-2,5-cyclohexadiene1,4-dione
col liq
col liq
ye nd (al)
nd
wh cry
pr or nd (w)
orth pr (al)
1300.1
1.1625
-92
-19.1(0.5)
0.815-20
1.3
10915
1.13325
2.57(0.02)
217(3)
1.133420 1.447220
144 dec
101
700.1
-26.5
vs H2O; s
MeOH; sl ace,
hx, chl
msc H2O, EtOH,
eth; vs ace; s
bz, tol
1.371420
1.36120
1.40425
1.554120 sl H2O; misc os
s H2O; vs EtOH,
eth
vs H2O, eth,
EtOH
sl H2O; vs EtOH;
s eth, chl
vs H2O, EtOH,
eth, chl
s H2O; vs EtOH,
eth, chl
s EtOH, eth
1.1950-30
vs H2O, bz
205
130
102
103 dec
1.534825 s ace, chl,
MeOH, tol
1.66516
1.6020
168
unstable in
pure form
116
s H2O, EtOH,
chl; msc eth,
ace, bz
s H2O; vs EtOH,
eth
msc H2O, EtOH;
sl eth; s ace; i
bz, chl
vs H2O; i eth, bz
1.22020
1.325
122(103)
Solubility
vs py, EtOH,
HOAc
sl H2O
944-22-9
col gas
nD
s H2O
vs H2O, ace; s
EtOH, MeOH,
py
vs H2O
vs eth, EtOH
s eth
756
165 sub
0.824120 1.492020 i H2O; s bz, chl
1.63520
sl H2O, eth, ace;
s EtOH, con
sulf
vs ace, bz, eth,
EtOH
4/11/16 11:29 AM
Physical Constants of Organic Compounds
3-279
N
O
H2N
O
O
N
N
N
HN
F
H
N
N
O
F
5441
N
H
N
N
O
OH
O
H
N
N
H
O
H
N
OH
F
Cl
H2N
O
OH
5442
Fluvalinate
Cl
O
O
N S
F
F
Cl
O Cl Cl
F
5444
P
S
N
5446
Fomesafen
H
5447
Fomocaine
HO
O
O
H
5448
Fonofos
N
H
H
5449
Formaldehyde
Formaldehyde oxime
Organic
Folpet
S
O
O
5445
OH
Folinic acid
O
O
S
N
H
NO2
OH
O
5443
Folic acid
O
O
H
N
O
O
O
N
H
NH
O
H
HO
NH2
5450
S
O
N
O
OH
H
5452
Formamidinesulfinic acid
HN
OH
5453
Formetanate hydrochloride
O
O
N
O
NH
O
HO
2-Formylbenzoic acid
O
O
O
5459
5460
4-Formylbenzoic acid
5461
3-Formylbenzonitrile
4-Formylbenzonitrile
OH
OH
O
PH
5470
L-Fructose
Al
O
O
OH
O
OH
OH
5463
6-Formyl-2,3-dimethoxybenzoic acid
HO
HO
Formyl fluoride
O
5462
Formylferrocene
O
O
F
Fe
O
HN
5464
O
O
O
H
Formothion
OH
O
3-Formylbenzoic acid
O
5456
Formononetin
N
5458
N
O
N
OH
OH
O
S
O P S
O
5455
N-Formimidoyl-L-glutamic acid
O
5457
O
5454
Formic acid
O
O
OH
OH
O
NH2
5451
Formamide
HCl
3
S
5466
N-(4-Formylphenyl)acetamide
HO
OH
OH
OH
OH
HO
OH
5468
5469
Fraxin
DL-Fructose
H
O
OH
O
O
OH
O
OH
5472
β-D-Fructose
O
HO
OH
O OH
HO
OH
5471
O
O
HO
Fosthietan
O
HO P O
OH
O OH
HO
O
5467
Fosetyl-Al
O
HO
OH
S
3
5465
O
N P O
O
5473
D-Fructose 6-phosphate
Fucoxanthin
O
O
O
HO
5474
Fulminic acid
OH
O
N O
5475
Fulvene
OH
O
5476
Fumaric acid
5477
Fumigatin
Physical Constants of Organic Compounds
3-280
Organic
No.
Name
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
Physical
Form
mp/˚C
5478
Furan
Oxacyclopentadiene
C4H4O
110-00-9
68.074
liq
-85.58(0.05) 31.3(0.2)
5479
2-Furanacetic acid
C6H6O3
2745-26-8
126.110 lf(peth)
68.5
1020.4
5480
5481
2-Furancarbonitrile
2-Furancarbonyl chloride
2-Furoyl chloride
C5H3NO
C5H3ClO2
617-90-3
527-69-5
93.084
130.530 liq
-1.0
147
173
5482
5483
3-Furancarboxaldehyde
2-Furancarboxylic acid
2-Furoic acid
C5H4O2
C5H4O3
498-60-2
88-14-2
145
231
5484
3-Furancarboxylic acid
C5H4O3
488-93-7
96.085
112.084 mcl nd or lf 130(3)
(w)
112.084 nd (w)
121.7(0.6)
5485
5486
2,5-Furandicarboxylic acid
2-Furanmethanamine
C6H4O5
C5H7NO
3238-40-2
617-89-0
156.093 nd (w), lf (al) 342
97.116
sub
145.5
5487
2-Furanmethanediol diacetate
C9H10O5
613-75-2
220
5488
5489
2-Furanmethanethiol
2-Furanmethanol acetate
C5H6OS
C7H8O3
98-02-2
623-17-6
198.172 nd or pl
(eth-peth)
114.166
140.137
5490
5491
4-(2-Furanyl)-2-butanone
4-(2-Furanyl)-3-buten-2-one
C8H10O2
C8H8O2
699-17-2
623-15-4
138.164 oil
136.149
39.5
203
229 dec
5492
1-(2-Furanyl)ethanone
C6H6O2
1192-62-7
110.111 cry (lig)
28.5(0.4)
175
5493
5494
2-Furanylmethyl pentanoate
3-(2-Furanyl)-1-phenyl-2propen-1-one
1-(2-Furanyl)-1-propanone
1-(2-Furanyl)-2-propanone
3-(2-Furanyl)-2-propenal
C10H14O3
C13H10O2
36701-01-6 182.216
717-21-5
198.217
47
228
317
C7H8O2
C7H8O2
C7H6O2
3194-15-8
6975-60-6
623-30-3
124.138 cry
124.138
122.122
28
29
52(1)
8814
179.5
13514
C7H5NO
C7H6O3
7187-01-1
539-47-9
119.121
138.121 nd (w)
38
141(3)
96
286
C8H7N3O5
67-45-8
225.159
255
C21H31NO4
C5H4O2
2385-81-1
98-01-1
361.476
96.085 liq
28
-38.3(0.8)
2100.5
161.5(0.3)
-14.5(0.2)
168(2)
5495
5496
5497
5498
5499
Dehydromucic acid
Furfurylamine
Furfuryl valerate
2-Furfuryl methyl ketone
52(1)
5501
5502
5503
Furfuryl alcohol
2-Furanmethanol
C5H6O2
98-00-0
98.101
5504
Furfuryl propanoate
2-Furanmethanol, propanoate
C8H10O3
623-19-8
154.163
5505
Furoin
1,2-Di-2-furanyl-2-hydroxyethanone
C10H8O4
552-86-3
192.169 nd (al)
135(3)
5506
5507
5508
5509
Furonazide
Furosemide
Fursultiamine
Furylfuramide, (E)-
C12H11N3O2
C12H11ClN2O5S
C17H26N4O3S2
C11H8N2O5
3460-67-1
54-31-9
804-30-8
18819-45-9
229.234
330.743
398.543 col pr
248.192 cry
202.3
204 dec
132 dec
154
5510
5511
5512
Fusarenon X
Galactaric acid
Galactitol
C17H22O8
C6H10O8
C6H14O6
182
255 dec
187.2(0.4)
5513
D-Galactonic acid, γ-lactone
5514
5515
α-D-Galactopyranose
4-O-β-D-Galactopyranosyl-Dgluconic acid
C6H12O6
C12H22O12
23255-69-8 354.352 cry
526-99-8
210.138 pr (w)
608-66-2
182.171 cry (dil
MeOH)
2782-07-2 178.139 nd (w+1),
nd (al)
3646-73-9 180.155
96-82-2
358.296 syr
5516
D-Galactose
C6H12O6
59-23-4
170
5517
D-Galacturonic acid
C6H10O7
685-73-4
HCP_Section_03.indb 280
2-(2-Furanyl)-3-(5-nitro-2furanyl)-2-propenamide
Mucic acid
Dulcose
C6H10O6
Lactobionic acid
col-ye liq
180.155 pl or pr (al)
pr or nd
(w+1)
194.139 nd (w)
105 sub
157
182(6)
3-(2-Furanyl)-2-propenenitrile 2-Furanacrylonitrile
3-(2-Furanyl)-2-propenoic
2-Furanacrylic acid
acid
Furazolidone
3-[[(5-Nitro-2-furanyl)­
methylene]amino]-2-oxazolidinone
Furethidine
Furfural
2-Furaldehyde
5500
bp/˚C
195
112
2771
den
g cm –3
nD
Solubility
0.951420 1.421420 sl H2O, chl; vs
EtOH, eth; s
ace, bz
s H2O, bz,
MeOH, peth
1.082220 1.479820 s EtOH, eth
1.32425 1.531020 i H2O; s eth, chl;
sl ctc
1.11020 1.494520
s H2O, EtOH; vs
eth; sl ace
sl H2O; s EtOH,
AcOEt; vs eth
1.740020
sl H2O, EtOH
1.099520 1.490820 msc H2O, EtOH;
s eth, chl
vs bz, eth, EtOH
1.131920 1.532920 i H2O; sl chl
1.117520 1.432720 i H2O; s EtOH,
eth
1.036119 1.469617
1.049657 1.578845 i H2O; vs EtOH,
eth, chl; s peth
1.09820 1.501720 i H2O; s EtOH,
eth
1.028420
vs eth, EtOH
1.114020
s EtOH, eth
1.062628 1.492225 s eth; sl ctc
1.10420 1.503520
i H2O; msc
EtOH; s eth; sl
chl
1.582425 vs tol
vs eth, EtOH
1.521920
1.159420 1.526120 s H2O, bz, chl;
vs EtOH, ace;
msc eth
1.129620 1.486920 msc H2O; vs
EtOH, eth; s
chl
20
1.1085
sl H2O; s EtOH,
ace; msc eth
sl H2O, EtOH,
chl; s eth,
MeOH
1.29
sl H2O
1.4720
s H2O; sl EtOH,
py; i eth, bz
vs H2O
167
166 (β)
vs H2O; sl EtOH,
MeOH, HOAc; i
eth
vs H2O; sl EtOH;
i eth, bz; s py
s H2O, EtOH; i
eth
4/11/16 11:29 AM
Physical Constants of Organic Compounds
3-281
O
O
5478
O
OH
O
O
O
5479
Furan
O
5483
3-Furancarboxaldehyde
HO
5484
2-Furancarboxylic acid
OH
O
O
O
O
5485
3-Furancarboxylic acid
2,5-Furandicarboxylic acid
O
O
NH2
O
O
O
5489
2-Furanmethanethiol
O
O
O
O
5488
O
5490
2-Furanmethanol acetate
O
5491
4-(2-Furanyl)-2-butanone
5492
4-(2-Furanyl)-3-buten-2-one
1-(2-Furanyl)ethanone
Organic
2-Furanmethanediol diacetate
O
O
SH
O
5487
2-Furanmethanamine
O
5482
2-Furancarbonyl chloride
OH
OH
O
5481
2-Furancarbonitrile
O
5486
O
O
N
5480
2-Furanacetic acid
O
Cl
O
O
O
O
O
5493
O
O
5494
2-Furanylmethyl pentanoate
O
O
3-(2-Furanyl)-1-phenyl-2-propen-1-one
5495
5496
1-(2-Furanyl)-1-propanone
O
O
O
5497
1-(2-Furanyl)-2-propanone
N
5498
3-(2-Furanyl)-2-propenal
3-(2-Furanyl)-2-propenenitrile
O
O
O
OH
O
O
N
O
O
H2N
N
5506
H
HO
HO
H
5511
Galactaric acid
S
H
HO
HO
H
5512
Galactitol
H
O
O
OH
O
OH
H
OH
CH2OH
5513
D-Galactonic acid, γ-lactone
HO
HO
O
OH
OH
OH
5514
α-D-Galactopyranose
O
OH
O
OH
CH2OH
OH
5515
4-O-β-D-Galactopyranosyl-D-gluconic acid
O
O
Fusarenon X
COOH
OH
HO
H
OH
5510
Furylfuramide, (E )-
HO
H
O
HO
HO
NH2
5509
HO
O
O
O
N
Fursultiamine
Furoin
O
N
O
5508
5505
Furfuryl propanoate
NH2
Cl
Furosemide
CH2OH
OH
H
H
OH
CH2OH
N
S
5507
Furonazide
COOH
OH
H
H
OH
COOH
O
S
O
N
O
O
O
OH
5504
Furfuryl alcohol
O
O
O
5503
OH
O
O
OH
O
Furfural
Furethidine
OH
H
N
O
O
5502
5501
Furazolidone
O
N
O
O
5500
3-(2-Furanyl)-2-propenoic acid
H
N
O
O
5499
O
O
N
O
N N
O
H
HO
HO
H
CHO
OH
H
H
OH
CH2OH
5516
D-Galactose
H
HO
HO
H
CHO
OH
H
H
OH
COOH
5517
D-Galacturonic acid
Physical Constants of Organic Compounds
3-282
Organic
No.
Name
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
5518
Galanthamine
Lycoremine
C17H21NO3
357-70-0
287.354 cry (bz)
126.5
5519
Galipine
2-[2-(3,4-Dimethoxyphenyl)­
ethyl]-4-methoxyquinoline
C20H21NO3
525-68-8
115.5
5520
Gallamine triethiodide
C30H60I3N3O3
65-29-2
323.386 pr (al, eth)
nd (peth)
891.528
5521
Gallein
C20H12O7
2103-64-2
364.31
>300
5522
5523
5524
Ganciclovir
Gardol
Gelsemine
C9H13N5O4
C15H28NNaO3
C20H22N2O2
br-red pow
(+1.5w)
red (anh)
82410-32-0 255.231 cry (MeOH)
137-16-6
293.378
509-15-9
322.401 cry (ace)
5525
C20H23ClN2O2
35306-33-3 358.862
326
5526
Gelsemine, monohydrochloride
Genistein
C15H10O5
446-72-0
270.237 nd(eth),
pr(dil al)
301 dec
5527
β-Gentiobiose
C12H22O11
554-91-6
342.296 cry (EtOH)
192
5528
Geraniol
C10H18O
106-24-1
154.249 oil
<-15
5529
5530
5531
Geranyl 2-methylpropanoate
Geranyl acetate
Germine
C14H24O2
C12H20O2
C27H43NO8
220
5532
Gibberellic acid
C19H22O6
2345-26-8 224.340
16409-44-2 196.286
508-65-6
509.632 pr or cry
(MeOH)
77-06-5
346.374 cry (EtOAc)
5533
Gitoxigenin
C23H34O5
545-26-6
234
5534
Gitoxin
C41H64O14
4562-36-1
5535
d-Glaucine
C21H25NO4
475-81-0
5536
D-Glucaric acid
D-Tetrahydroxyadipic acid
C6H10O8
87-73-0
390.513 pr (AcOEt)
pr (+w, dil
al)
780.939 pr
(chlMeOH)
355.429 pl, pr (eth,
AcOEt)
210.138 nd (45% al)
5537
5538
D-Glucitol
D-Glucitol, hexaacetate
Sorbitol
Sorbitol hexaacetate
C6H14O6
C18H26O12
50-70-4
7208-47-1
182.171 nd (w)
434.392 pr (w)
97(3)
98(3)
5539
D-Gluconic acid
C6H12O7
526-95-4
196.155 nd (al-eth)
131(2)
5540
β-D-Glucopyranose
C6H12O6
492-61-5
5541
6-O-α-D-Glucopyranosyl-Dfructose
2-(β-D-Glucopyranosyloxy)­
benzaldehyde
7-(β-D-Glucopyranosyloxy)2H-1-benzopyran-2-one
2-(β-D-Glucopyranosyloxy)-2methylpropanenitrile
1-[4-(β-D-Glucopyranosyloxy)­
phenyl]ethanone
5542
5543
5544
5545
5,7-Dihydroxy-3-(4hydroxyphenyl)-4H-1-benzopyran-4-one
6-O-β-D-Glucopyranosyl-Dglucose
Physical
Form
mp/˚C
bp/˚C
den
g cm –3
Solubility
vs ace, EtOH,
chl
vs ace, bz, eth,
EtOH
vs H2O, EtOH; sl
eth, ace, bz,
chl
vs ace, EtOH
147.5
250 dec
sl H2O
vs ace, bz, eth,
EtOH
s H2O; sl EtOH
178
229(2)
0.889420 1.476620
13613
11512
0.899715 1.457620
0.916315 1.462420
s hot H2O, hot
MeOH
i H2O; s EtOH,
eth, ace, chl
s bz, MeOH, alk,
acid
vs ace, EtOH,
MeOH
i H2O; sl eth; s
chl
234
285 dec
120
125.5
149
2953.5
1.48920
1.3020
1.333020
vs ace, EtOH,
chl
vs H2O, EtOH; sl
eth, chl
vs H2O, ace
sl H2O, eth; vs
EtOH; s chl,
AcOEt
s H2O; sl EtOH; i
eth, bz
Palatinose
C12H22O11
180.155 cry (hot
EtOH)
13718-94-0 342.296
Helicin
C13H16O7
618-65-5
284.262 nd (w)
175
vs H2O, EtOH
Skimmin
C15H16O8
93-39-0
324.283 cry (w + 1)
220
Linamarin
C10H17NO6
554-35-8
247.245 nd (w, al)
145
s H2O, EtOH; i
eth, chl
vs ace
Picein
C14H18O7
530-14-3
298.289 nd (w+1),
195.5
nd (MeOH)
s H2O
5546
α-D-Glucose
C6H12O6
26655-34-5 180.155
5547
α-D-Glucose pentaacetate
C16H22O11
604-68-2
390.339 pl or nd (al) 132.0(0.5)
sub
5548
β-D-Glucose pentaacetate
C16H22O11
604-69-3
390.339 nd (al)
sub
5549
5550
5551
α-D-Glucose 1-phosphate
D-Glucuronic acid
D-Glucuronic acid γ-lactone
C6H13O9P
C6H10O7
C6H8O6
59-56-3
260.135
6556-12-3 194.139 nd (al)
32449-92-6 176.124 mcl pl (w)
cry (al)
165
177.5
1.7620
5552
DL-Glutamic acid
C5H9NO4
617-65-2
199 dec
1.460120
HCP_Section_03.indb 282
nD
Cori ester
D-Glucuronolactone
147.130 orth (al,w)
146 dec
134
1.562018
1.274020
sl H2O; s EtOH,
eth, HOAc; i
chl
vs H2O; sl EtOH;
i ace, AcOEt; s
py
sl H2O, EtOH,
CS2; s eth, chl,
HOAc
i H2O; sl EtOH,
peth, eth; s bz;
msc chl
vs H2O
vs H2O, EtOH
s H2O; sl EtOH,
DMSO, MeOH;
i bz
sl H2O, eth; i
EtOH, CS2, lig
4/11/16 11:29 AM
Physical Constants of Organic Compounds
3-283
I
N
O
O
N
O
OH
O
N
O
5519
Galanthamine
5520
Galipine
H
N
H
O
N
Na
N
H
O
5523
H
H
O
Gallein
OH HO
OH
5526
N
H
OH
HO
O
5529
Geraniol
O
HO
O
H
OH
H
OH
H
HO
OH
OH
H
HO
OH
H
O
OH
5532
Germine
Geranyl acetate
H
O
O
5531
5530
Geranyl 2-methylpropanoate
5527
β-Gentiobiose
Genistein
H
5528
OH
O
HO
5525
O
O OH
OH
HO
Gelsemine, monohydrochloride
O
O O
OH
OH O
N
HCl
H
Gelsemine
Ganciclovir
HO
H
O
5524
Gardol
5522
H
N
O
OH
OH
5521
Gallamine triethiodide
O
O
O
O
I
O
5518
N
N
H2N
N
N
N
OH
O
N
H
Organic
O
OH
HO
O
OH
O
O
I
Gibberellic acid
O
O
OH
H
OH
O
O O
O
O O
H
OH
O
N
H
O
OH
O O
O
HO
H
COOH
OH
H
OH
OH
COOH
H
HO
H
H
OH
OH
HO
H
O
OH
5533
5534
Gitoxigenin
5535
Gitoxin
5536
d-Glaucine
D-Glucaric acid
H
HO
H
H
CH2OH
OH
H
OH
OH
CH2OH
CH2OAc
OAc
H
OAc
OAc
CH2OAc
H
AcO
H
H
5537
5538
D-Glucitol
D-Glucitol, hexaacetate
HO
H
HO
H
H
COOH
OH
H
OH
OH
CH2OH
O
HO
OH
HO
O OH
OH
O
OH
O
HO
5539
5540
O
O
HO
OH
OH
5542
6-O-α-D-Glucopyranosyl-D-fructose
O
OH
HO
5541
β-D-Glucopyranose
D-Gluconic acid
O
OH
HO
OH
HO
O O
OH
HO
O
HO
OH
5543
2-(β-D-Glucopyranosyloxy)benzaldehyde
7-(β-D-Glucopyranosyloxy)-2H-1-benzopyran-2-one
O
HO
OH
O O
N
5544
5545
1-[4-(β-D-Glucopyranosyloxy)phenyl]ethanone
HO
O OAc
OAc
AcO
OAc
5548
β-D-Glucose pentaacetate
HO
O
O
OH
HO
O P OH
OH OH
5549
α-D-Glucose 1-phosphate
H
HO
H
H
CHO
OH
H
OH
OH
COOH
5550
D-Glucuronic acid
AcO
OH
OH
OH
2-(β-D-Glucopyranosyloxy)-2-methylpropanenitrile
OAc
OH
HO
OH
O
O
OH
HO
AcO
AcO
HO
HO
O O
5546
OAc
OAc
5547
α-D-Glucose
α-D-Glucose pentaacetate
O
C
O
HO
O
OH
OH
OH
5551
D-Glucuronic acid γ-lactone
OH
O
O
NH2
5552
DL-Glutamic acid
Physical Constants of Organic Compounds
3-284
Organic
Mol. Form.
CAS RN
Mol.
Wt.
D-Glutamic acid
C5H9NO4
6893-26-1
147.130 lf (w)
5554
5555
5556
L-Glutamic acid
(S)-2-Aminopentanedioic acid
L-Glutamic acid, hydrochloride
L-Glutamine
2-Aminoglutaramic acid
C5H9NO4
C5H10ClNO4
C5H10N2O3
56-86-0
138-15-8
56-85-9
147.130 orth (dil al) 160 dec
183.591 orth pl (w) 214 dec
146.144 nd (w, dil al) 182(3)
175 sub
1.53820
5557
Glutaric acid
Pentanedioic acid
C5H8O4
110-94-1
132.116 nd (bz)
273(10)
1.42915
5558
Glutathione
C10H17N3O6S
70-18-8
307.323 cry (50% al) 195
5559
Glutathione disulfide
L-γ-Glutamyl-Lcysteinylglycine
L-γ-Glutamyl-Lcysteinylglycine disulfide
C20H32N6O12S2
179
5560
Glutethimide
C13H15NO2
27025-41-8 612.631 cry (EtOH
aq)
77-21-4
217.264 cry (eth)
5561
Glycerol
1,2,3-Propanetriol
C3H8O3
56-81-5
92.094
18.2(0.4)
5562
Glycerol 1-acetate
1,2,3-Propanetriol 1-acetate,
(±)
C5H10O4
106-61-6
134.131
5563
5564
Glycerol 1-butanoate
Glycerol 1,3-dinitrate
C7H14O4
C3H6N2O7
557-25-5
623-87-0
5565
C39H72O5
2465-32-9
5566
Glycerol 1,3-di-9-octadecenoate, cis,cis
Glycerol 1-oleate
1-Monoolein
C21H40O4
111-03-5
162.184
182.089 pr (w), cry
(eth)
620.986 cry (eth/
EtOH)
356.541 pl (al)
5567
5568
5569
5570
L-Glycerol 1-phosphate
Glycerol tridecanoate
Glycerol trielaidate
Glycerol trilaurate
C3H9O6P
C33H62O6
C57H104O6
C39H74O6
5746-57-6
621-71-6
537-39-3
538-24-9
172.073 syr
554.841 cry (peth)
885.432
639.001 nd (al)
5571
5572
Glycerol tri-3-methylbutanoate Triisovalerin
Glycerol trioleate
Triolein
C18H32O6
C57H104O6
620-63-3
122-32-7
344.443
885.432 col-ye oil
5.3(0.6)
332.5
23718
5573
Glycerol tripalmitate
Tripalmitin
C51H98O6
555-44-2
807.320 nd (eth)
66(2)
624(28)
5574
Glycerol tristearate
Tristearin
C57H110O6
555-43-1
891.479
5575
Glycerol tritetradecanoate
Trimyristin
C45H86O6
555-45-3
723.161 wh-ye solid 57.0(0.2)
5576
Glycerone phosphate
C3H7O6P
57-04-5
170.058
5577
Glycine
1-Hydroxy-3-(phosphonooxy)2-propanone
Aminoacetic acid
vs bz, eth, chl
0.898655 1.440460 i H2O; s EtOH,
eth, peth; vs
ace, bz
0.998420 1.435420 vs eth, EtOH
0.91515 1.467615 i H2O; sl EtOH;
vs eth; s chl,
peth
0.875270 1.438180 i H2O; sl EtOH;
vs eth; s bz,
chl
0.855990 1.439580 i H2O, EtOH; sl
bz, ctc; s ace,
chl
0.884860 1.442860 i H2O; sl EtOH,
lig; s eth, ace,
bz
dec H2O
C2H5NO2
56-40-6
75.067
1.16120
5578
C4H10ClNO2
623-33-6
5579
Glycine, ethyl ester,
hydrochloride
Glycine, hydrochloride
C2H6ClNO2
6000-43-7
5580
Glycocholic acid
C26H43NO6
475-31-0
111.528 hyg orth nd 200.5
(w)
465.622 nd (w)
166.5
5581
Glycocyamine
C3H7N3O2
352-97-6
117.107 pl or nd (w) 282
5582
Glycogen
(C6H10O5)x
9005-79-2
162.140 wh pow
5583
5584
Glycolaldehyde
Glycolic acid
C2H4O2
C2H4O3
141-46-8
79-14-1
60.052
76.051
5585
N-Glycolylneuraminic acid
C11H19NO10
1113-83-3
325.270
186
5586
5587
Glycopyrrolate
Glycylalanine
C19H28BrNO3
C5H10N2O3
596-51-0
1188-01-8
398.334
146.144
192.5
237 dec
5588
L-Glycylasparagine
C6H11N3O4
1999-33-3
216
5589
N-Glycylglycine
189.169 nd (EtOH
aq)
132.118
s H2O; i EtOH,
eth
s H2O; sl EtOH
220(1)
s H2O
No.
Name
5553
HCP_Section_03.indb 284
Synonym
1,2,3-Propanetriol,
1,3-dinitrate
α-Glycerophosphoric acid
Decanoic acid glycerol triester
Trielaidin
Trilaurin
Ethyl aminoacetate
hydrochloride
Guanidinoacetic acid
N-(Hydroxyacetyl)neuraminic
acid
N-Alanylglycine
2-(Aminoacetamido)acetic acid C4H8N2O3
556-50-3
Physical
Form
syr, orth pl
mp/˚C
bp/˚C
213 dec
97.9(0.3)
nD
1.53820
1.4188106
85(1)
26
Solubility
sl H2O; i EtOH,
eth, ace, bz,
HOAc, MeOH
sl H2O
vs H2O, EtOH
s H2O; i EtOH,
eth, bz, MeOH
vs H2O, EtOH,
eth; i bz; s chl,
lig
vs H2O; i EtOH,
eth; s DMF
i H2O; s EtOH;
vs eth, ace
msc H2O, EtOH;
sl eth; i bz,
ctc, chl
vs H2O, EtOH
289(3)
1.261320 1.474620
158165
1.206020 1.415720
280
14815
1.12918
1.52320
2393
0.942020 1.462620 i H2O; s EtOH,
eth, chl
dec H2O
1.453120 vs H2O, EtOH
1.471520 vs H2O, eth,
EtOH
50.1
35
31(1)
585(27)
mcl or trg pr 290 dec
(dil al)
139.581
144
pl
orth nd (w)
lf (eth)
den
g cm –3
97
79.5
vs H2O; i EtOH,
eth; sl ace, py
vs H2O, EtOH
vs H2O
1.366100
100
1.477219
sl H2O, eth; vs
EtOH
sl H2O, EtOH,
eth
vs H2O; i EtOH,
eth
s chl
s H2O, EtOH, eth
4/11/16 11:29 AM
Physical Constants of Organic Compounds
3-285
O
OH
OH
O
OH
O
OH
O
O
NH2
O
HCl
O
OH
O
O
NH2
O
5556
L-Glutamic acid, hydrochloride
OH
HO
H
N
O
SH
NH2
O
O
5557
L-Glutamine
OH
HN
5558
Glutaric acid
Glutathione
OH
HN
H
N
O
5555
L-Glutamic acid
OH
NH2
NH2
5554
D-Glutamic acid
HO
O
NH2
5553
O
OH
OH
O
NH2
O
S
S
O
H2N
O
NH
OH
OH
N
H
O
O
O
O
N
H
O
5559
HO
O
5561
O
O
O
N
O
O
5563
Glycerol 1-acetate
O
N
O
OH
OH
5562
Glycerol
Glutethimide
HO
OH
OH
5560
Glutathione disulfide
HO
OH
O
5564
Glycerol 1-butanoate
Glycerol 1,3-dinitrate
Organic
O
O
OH
O
O
HO
O
O
O P OH
OH
OH
HO
OH
O
5565
5566
Glycerol 1,3-di-9-octadecenoate, cis,cis
5567
Glycerol 1-oleate
O
L-Glycerol 1-phosphate
O
O
O
O
O
O
O
O
O
O
O
O
O
O
O
O
O
5568
O
5569
Glycerol tridecanoate
5570
Glycerol trielaidate
O
O
O
O
O
O
O
O
O
O
Glycerol tri-3-methylbutanoate
O
O
O
5571
Glycerol trilaurate
O
O
O
O
O
O
O
O
O
O
5572
5573
Glycerol trioleate
5574
Glycerol tripalmitate
Glycerol tristearate
O
O
O
O
O
O
O P OH
OH
HO
O
O
5575
O
H2N
5576
Glycerol tritetradecanoate
O
HCl H2N
OH
5577
Glycerone phosphate
O
HCl H2N
O
5578
Glycine
OH
5579
Glycine, ethyl ester, hydrochloride
Glycine, hydrochloride
O
HO
N
H
H
HO
OH
O
O
NH2
HN
OH
H
5580
OH
OH
OH
O
O
N-Glycolylneuraminic acid
OH
HO
x
5582
H
N
O
N
Br
5586
Glycopyrrolate
H2N
OH
H
N
5587
OH
NH2
O
5588
Glycolic acid
O
O
O
Glycylalanine
O
5584
Glycolaldehyde
H2N
O
OH
HO
O
5583
Glycogen
O
OH
O O
OH
OH
HO
5585
O
Glycocyamine
O
NH
HO
5581
Glycocholic acid
HO
N
H
OH
OH
L-Glycylasparagine
H
N
H2N
O
5589
N-Glycylglycine
OH
O
Physical Constants of Organic Compounds
3-286
Organic
Mol. Form.
CAS RN
Mol.
Wt.
N-(N-Glycylglycyl)glycine
C6H11N3O4
556-33-2
189.169 nd (dil al)
246 dec
5591
N-Glycyl-L-leucine
C8H16N2O3
869-19-2
256 dec
5592
5593
5594
N-Glycyl-L-phenylalanine
N-Glycylserine, (DL)Glycyrrhizic acid
C11H14N2O3
C5H10N2O4
C42H62O16
3321-03-7
687-38-7
1405-86-3
5595
Glyodin
C22H44N2O2
556-22-9
188.224 pl (dil al) pl
(dil al)
222.240
162.144
822.931 pl or pr
(HOAc)
368.596
5596
Glyoxal
C2H2O2
107-22-2
58.036
15
5597
5598
Glyoxal bis(2-hydroxyanil)
Glyoxylic acid
2,2’-Benzoxazoline
C14H12N2O2
C2H2O3
1149-16-2
298-12-4
5599
5600
Glycine, N-(phosphonomethyl)- C3H8NO5P
C6H17N2O5P
5601
Glyphosate
Glyphosate isopropylamine
salt
Glyphosine
5602
No.
Name
5590
Synonym
1H-Imidazole, 2-heptadecyl4,5-dihydro-, monoacetate
Physical
Form
ye pr
240.257
74.035 orth pr
(w+1/2)
1071-83-6 169.074
38641-94-0 228.183 cry
C4H11NO8P2
2439-99-8
263.080 wh cry
Grayanotoxin I
C22H36O7
4720-09-6
5603
Griseofulvin, (+)
C17H17ClO6
126-07-8
412.517 cry (AcOEt/
C5H12)
352.766 oct or orth
cry (bz)
5604
Guaiol
C15H26O
489-86-1
5605
5606
Guanabenz
Guanadrel sulfate (2:1)
C8H8Cl2N4
C20H40N6O8S
5607
Guanethidine
C10H22N4
5608
5609
Guanidine
Aminomethanamidine
Guanidine monohydrochloride
CH5N3
CH6ClN3
5610
5611
5612
CH6N4O3
C2H12N6O4S
C3H9N3O3S
5613
5614
Guanidine mononitrate
Guanidine sulfate (2:1)
2-Guanidinoethanesulfonic
acid
3-Guanidinopropanoic acid
Guanine
5051-62-7 231.083 wh solid
22195-34-2 524.632 cry (MeOH/
EtOH)
55-65-2
198.309 wh cry
(MeOH)
113-00-8
59.071 cry
50-01-1
95.532 orth bipym
(al)
506-93-4
122.084 lf (w)
594-14-9
216.219
543-18-0
167.186 cry (EtOH,
ace)
353-09-3
131.133 cry (EtOH)
73-40-5
151.127 nd or pl (aq
NH3)
5615
Guanosine
Glycine, N,Nbis(phosphonomethyl)-
Taurocyamine
N-Amidino-β-alanine
C4H9N3O2
C5H5N5O
C10H13N5O5
118-00-3
283.241 nd (w)
C10H15N5O11P2
146-91-8
443.201 amorp solid
C10H14N5O8P
C10H12N5Na2O8P
85-32-5
5550-12-9
363.221 hyg cry
407.185
C37H35N2NaO6S2
C6H12O6
C6H12O6
C21H23ClFNO2
C13H14N2O
4680-78-8
4205-23-6
6027-89-0
52-86-8
304-21-2
690.803
180.155
180.155
375.865
214.262
C12H10N2
486-84-0
5626
5627
2-Amino-1,9-dihydro-9-β-Dribofuranosyl-6H-purin-6-one
Guanosine 5’-diphosphate
Guanosine 5’-(trihydrogen
diphosphate)
Guanosine 5’-monophosphate 5’-Guanylic acid
Guanosine 5’-monophosphate, 5’-Guanylic acid, disodium salt
disodium salt
Guinea Green B
C.I. Acid Green 3
D-Gulose
L-Gulose
Haloperidol
Harmaline
4,9-Dihydro-7-methoxy-1methyl-3H-pyrido[3,4-b]­
indole
Harman
1-Methyl-9H-pyrido[3,4-b]­
indole
Harmine
7-Methoxy-1-methyl-9Hpyrido[3,4-b]indole
HC Blue No. 1
HC Blue No. 2
5628
5629
5630
Hectane
Hederagenin
Helenalin
C100H202
C30H48O4
C15H18O4
5631
5632
Helminthosporal
Helvolic acid
C15H22O2
C33H44O8
5616
5617
5618
5619
5620
5621
5622
5623
5624
5625
HCP_Section_03.indb 286
222.366 trg pr (al)
C13H12N2O
C11H17N3O4
C12H19N3O5
mp/˚C
bp/˚C
den
g cm –3
nD
Solubility
s H2O; i EtOH,
eth
vs H2O; i EtOH
267.0(0.5)
198 dec
220 dec
s H2O
vs H2O, EtOH; i
eth
1.035
50.4
20
1.1420
202
98
1.382620 vs H2O; s EtOH,
eth
s DMSO
vs H2O; sl EtOH,
eth, bz
230 dec
vs H2O
s H2O
268
220
91
288 dec
0.9074100 1.4716100
i H2O; sl EtOH,
eth, ace, bz,
AcOEt, chl
i H2O; s EtOH,
eth
228 dec
214
226
50
184(1)
214.5(0.6)
292 dec
227
210
360 dec
1.35420
dec
vs H2O, EtOH
sub
i H2O, HOAc; sl
EtOH, eth; s
alk, acid
sl H2O; i EtOH,
eth; vs HOAc
239 dec
190 dec
195 dec
dk grn pow
syr
syr
sl H2O
sl H2O
dec
dec
151.5
tab (MeOH) 230
orth pr (al)
182.220 bl flr orth
cry (hp)
442-51-3
212.246 orth (al), pr
(MeOH)
2784-94-3 255.271 blk cry
33229-34-4 285.296 dk bl-blk
cry
6703-98-6 1404.67
465-99-6
472.700 pr (al)
6754-13-8 262.302 cry (EtOH)
236.5
723-61-5
234.335
29400-42-8 568.697 nd (dil
HOAc)
58
212 dec
273
vs H2O, EtOH
vs H2O, EtOH
s H2O; sl EtOH
vs H2O
vs H2O
sl H2O, EtOH,
eth; s chl, py
sub
sl H2O, chl,
EtOH, eth; s py
100
110
115.2(0.4)
333
226
sl H2O; s EtOH,
chl
1170.015
sl H2O, EtOH; s
eth, ace, bz,
diox
4/11/16 11:29 AM
Physical Constants of Organic Compounds
O
H
N
H2N
OH
N
H
O
O
OH
OH
O
5591
HO
OH
O
O
H
N
H2N
OH
OH
O
5592
O O
O O
O
HO
OH
OH
5593
N-Glycyl-L-phenylalanine
5595
Glyodin
O
OH
HO
HO
O
O
H
N
H3CCOOH
H
N-Glycyl-L-leucine
H2N
N
H
O
5590
N-(N-Glycylglycyl)glycine
N
O
O
H
N
H2N
3-287
O
5594
N-Glycylserine, (DL)-
5596
Glycyrrhizic acid
Glyoxal
OH
OH
N
O
O
O
5597
OH
5598
Glyoxal bis(2-hydroxyanil)
O
HO
P
N
OH H
HO
O
5599
Glyoxylic acid
O
O
N
Cl
OH
5603
H2N
5609
NH2
HNO3
H2N
5602
H
N
H2N
O
O
HO P O P O
OH OH
N
O
OH
N
N
H2N
O
HO P O
OH
O
HO
5615
H
OH
H2SO4
N
H
HN
2
2-Guanidinoethanesulfonic acid
N
N
N
N
2Na
O
H2N
O
O P O
O
NH2
HN
N
H
Guanidine
H
O
O
H
N
N
N
N
H 2N
5613
5614
3-Guanidinopropanoic acid
Guanine
O
O S O
O Na
O S O
N
N
O
HO
OH
5618
Guanosine 5’-monophosphate
NH2
5608
OH
N
N
OH
5617
Guanosine 5’-diphosphate
N
N
H2N
Guanethidine
5612
H
NH
NH2
NH
O
HO
5616
Guanosine
H
N
5607
O
OH
S
O
NH2
Guanidine sulfate (2:1)
N
N
H2SO4
2
O
N
NH2
Guanadrel sulfate (2:1)
NH2
O
O
HO
OH
Grayanotoxin I
5606
5611
Guanidine mononitrate
N
H
O
Guanabenz
5610
Guanidine monohydrochloride
N
O
O
5601
NH
NH
NH
HCl
NH2
5605
Guaiol
NH
N
HO
HO
Glyphosine
O
H
N
Cl
5604
Griseofulvin, (+)
NH2
OH
O
P OH
OH
N
NH
O O
O
H2N
HO
P
N
OH H
O
HO P
OH
NH3
Glyphosate isopropylamine salt
O
H
O
5600
Glyphosate
Cl
H2N
O
OH
OH
H
HO
5619
Guanosine 5’-monophosphate, disodium salt
Guinea Green B
Cl
H
H
HO
H
CHO
OH
OH
H
OH
CH2OH
CHO
H
H
OH
H
CH2OH
HO
HO
H
HO
5620
HO
O
O
5621
D-Gulose
F
N
5622
L-Gulose
HO
N
N
O
HO
HO
N
O
N
HO
5626
N
H
O
5625
Harmine
OH
O
H3C(CH2)98CH3
5628
HC Blue No. 2
O
Hectane
H
H
COOH
O
O
CH2OH
5629
Hederagenin
OH
O
H
HO
N
N
H
Harman
5627
HC Blue No. 1
N
5624
Harmaline
H
N
O
N
5623
Haloperidol
H
N
N
H
O
OH
5630
Helenalin
O
O
O
H
O
O
O
5631
Helminthosporal
5632
Helvolic acid
O
Organic
O
N
Physical Constants of Organic Compounds
3-288
Organic
Mol. Form.
CAS RN
Mol.
Wt.
Hematein
C16H12O6
475-25-2
300.262 red-br cry
5634
Hematin
C34H33FeN4O5
15489-90-4 633.495 br pow (py)
>200
5635
Hematoporphyrin
C34H38N4O6
172.5
5636
Hematoxylin
C16H14O6
14459-29-1 598.689 deep red
cry
517-28-2
302.278 ye cry
5637
Hemin
C34H32ClFeN4O4
5638
Heneicosane
5639
Hentriacontane
5640
5641
5642
No.
Name
5633
Synonym
Physical
Form
mp/˚C
bp/˚C
den
g cm –3
nD
250 dec
i H2O, eth, bz,
chl; sl EtOH,
HOAc
i H2O, eth; s
EtOH, alk; sl
py, HOAc
i H2O; s EtOH; sl
eth, chl
sl H2O, eth; s
alk, EtOH
140
C21H44
16009-13-5 651.941 long blades >300
(gl HOAc)
629-94-7
296.574 cry (w)
40.4(0.3)
359(6)
C31H64
630-04-6
436.840 lf (AcOEt)
68(1)
458
Heptachlor
C10H5Cl7
76-44-8
373.318 wh cry
95.8(0.3)
C10H5Cl7O
C12H3Cl7
1024-57-3 389.317
52663-71-5 395.323 cry
162.8(0.3)
122.2(0.5)
C3HCl7
3849-33-0
285.211
11
249
5644
5645
Heptachlor epoxide
2,2’,3,3’,4,4’,6-Heptachlorobiphenyl
1,1,1,2,3,3,3-Heptachloropropane
Heptacontane
Heptacosane
C70H142
C27H56
7719-93-9
593-49-7
106(4)
58.8(0.1)
647
442
5646
Heptadecanal
C17H34O
629-90-3
36(3)
20426
5647
1-Heptadecanamine
C17H37N
4200-95-7
983.876
380.734 cry (al, bz) lf
(AcOEt)
254.451 nd (peth),
cry (al)
255.483
49(1)
336(2)
5648
Heptadecane
C17H36
629-78-7
240.468 hex lf
21.97(0.05)
303(2)
5649
Heptadecanenitrile
C17H33N
5399-02-0
251.451 cry (al)
34.0(0.7)
349
5650
Heptadecanoic acid
Margaric acid
C17H34O2
506-12-7
270.451 pl (peth)
61.08(0.04)
227100
5651
1-Heptadecanol
Margaryl alcohol
C17H36O
1454-85-9
53(1)
324
5652
2-Heptadecanone
Pentadecyl methyl ketone
C17H34O
2922-51-2
256.467 lf (al), cry
(ace)
254.451 pl (dil al)
48.2(0.3)
320(13)
5653
9-Heptadecanone
C17H34O
540-08-9
254.451 pl (MeOH)
50.7(0.2)
251.5
5654
1-Heptadecene
Hexahydroaplotaxene
C17H34
6765-39-5
238.452
10.7(0.6)
301(3)
5655
5656
5657
5658
Heptadecylbenzene
trans,trans-2,4-Heptadienal
1,6-Heptadiene
1,6-Heptadiyne
1-Phenylheptadecane
C23H40
C7H10O
C7H12
C7H8
14752-75-1
4313-03-5
3070-53-9
2396-63-6
316.564
110.153
96.170 liq
92.139 liq
19.7(0.4)
-84.8(0.6)
402(13)
84.5
89(3)
111(1)
5659
Heptafluorobutanoic acid
C4HF7O2
375-22-4
214.039 liq
-17.5
121.5(0.2)
1.65120
1.29525
5660
5661
C8F14O3
C4H3F7O
336-59-4
375-01-9
410.062 liq
200.055
-43
106.5
95(4)
1.66520
1.60020
1.28520
1.29420
C4ClF7O
C10H11F7O2
375-16-6
232.484
17587-22-3 296.182
38
39(10)
465
1.5520
1.27325
1.28820
1.376620
C3F7I
C3HF7
677-69-0
431-89-0
295.925
170.029 col gas
38
-16.34
1.329820
-126.8
C16H34
4390-04-9
226.441
246(1)
C7H22O2Si3
1873-88-7
222.506
143(1)
5668
Heptafluorobutanoic anhydride
2,2,3,3,4,4,4-Heptafluoro-1butanol
Heptafluorobutanoyl chloride
6,6,7,7,8,8,8-Heptafluoro-2,2dimethyl-3,5-octanedione
Heptafluoro-2-iodopropane
Perfluoroisopropyl iodide
1,1,1,2,3,3,3-Heptafluoropro- Refrigerant 227ea
pane
2,2,4,4,6,8,8-Heptamethylnonane
1,1,1,3,5,5,5-Heptamethyltrisiloxane
Heptanal
Heptaldehyde
C7H14O
111-71-7
114.185 liq
-43.94(0.02) 153(3)
5669
Heptanal oxime
Enanthaldoxime
C7H15NO
629-31-2
129.200 pl (al)
57.5
5670
2-Heptanamine
Tuaminoheptane
C7H17N
123-82-0
115.217
5643
5662
5663
5664
5665
5666
5667
HCP_Section_03.indb 288
Untriacontane
Margaric aldehyde
Solubility
0.791920 1.444120 i H2O; sl EtOH; s
peth
0.78168 1.427890 sl EtOH, eth, bz,
chl; s peth
1.579
vs bz, eth,
EtOH, lig
i H2O
195
141(4)
1.792134 1.542721 vs chl
0.779660 1.434565 i H2O, EtOH; sl
eth
vs bz, eth
0.851020 1.451020 i H2O; s EtOH,
eth
0.778020 1.436920 i H2O; sl EtOH,
ctc; s eth
0.831520 1.446720 i H2O; sl EtOH,
chl; vs eth
0.853260 1.434260 i H2O; sl EtOH; s
eth, ace, bz,
chl
0.847520
i H2O; s EtOH,
eth
0.804948
i H2O; sl EtOH; s
ace, peth; vs
bz, eth
0.814048
sl EtOH; s
MeOH
0.785220 1.443220 i H2O; vs eth; s
bz; msc lig
0.854620 1.481020
0.88125 1.531520
0.816417 1.45117
i H2O; s bz,
HOAc
s H2O, eth, tol; i
peth
s EtOH, ace
0.819420 1.381820
0.813225 1.411320 sl H2O, ctc; msc
EtOH, eth
0.858355 1.421020 sl H2O; s EtOH,
eth
0.766519 1.419919 sl H2O, chl; s
EtOH, eth,
peth
4/11/16 11:29 AM
Physical Constants of Organic Compounds
3-289
OH
O
HO
N
OH
N
NH N
N
N HN
Fe
N
OH
HO
OH
Cl
N
Fe
N
N
N
H
OH
OH
HO
O
OH
HO
O
HO
5633
O
HO
O
5634
Hematein
HO
O
Hematin
Cl
H
Cl H
Cl
Heneicosane
Cl
Cl
Cl
Cl
Cl
O
Hemin
Cl
H
Cl
O
Cl Cl
Cl
Cl
Cl
Cl
5641
Heptachlor
Cl
Cl
Cl H
Cl
5640
Hentriacontane
HO
5637
Hematoxylin
Cl
Cl
5639
O
5636
Hematoporphyrin
5638
HO
OH
5635
Cl
Cl
Cl
O
5642
Heptachlor epoxide
2,2’,3,3’,4,4’,6-Heptachlorobiphenyl
Cl
Cl
Cl
H3C(CH2)68CH3
5643
5644
1,1,1,2,3,3,3-Heptachloropropane
O
5645
5646
Heptacosane
Heptacontane
Heptadecanal
NH2
N
5647
5648
1-Heptadecanamine
5649
Heptadecane
Heptadecanenitrile
OH
O
OH
O
5650
5651
Heptadecanoic acid
5652
1-Heptadecanol
2-Heptadecanone
O
5653
5654
9-Heptadecanone
5655
1-Heptadecene
Heptadecylbenzene
F
F
O
5657
trans,trans-2,4-Heptadienal
F
F F
OH
F F
5661
2,2,3,3,4,4,4-Heptafluoro-1-butanol
5658
1,6-Heptadiene
F
F
F
1,6-Heptadiyne
F F
Cl
F F
O
5662
Heptafluorobutanoyl chloride
F
F
F
F
F
O
O
5663
6,6,7,7,8,8,8-Heptafluoro-2,2-dimethyl-3,5-octanedione
5666
5667
1,1,1,3,5,5,5-Heptamethyltrisiloxane
5668
F F
F F
F
O
O
F
F
F F
O
5660
Heptafluorobutanoic anhydride
F
F
F
F
F
F
F
F
F I
F
5664
5665
Heptafluoro-2-iodopropane
N
O
Heptanal
F
F F
O
Heptafluorobutanoic acid
F F
F F
F
F
OH
5659
O Si H
Si O
Si
2,2,4,4,6,8,8-Heptamethylnonane
F F
F F
5656
F
F
F
5669
Heptanal oxime
F
F
1,1,1,2,3,3,3-Heptafluoropropane
NH2
OH
5670
2-Heptanamine
Organic
HO
Physical Constants of Organic Compounds
3-290
No.
Name
5671
5672
Mol.
Wt.
Physical
Form
Organic
Mol. Form.
CAS RN
4-Heptanamine
Heptane
C7H17N
C7H16
16751-59-0 115.217
142-82-5
100.202 liq
5673
5674
1,7-Heptanediamine
Heptanedinitrile
C7H18N2
C7H10N2
646-19-5
646-20-8
130.231
122.167
25.3(0.4)
-31.4(0.4)
224
15514
5675
Heptanedioic acid
C7H12O4
111-16-0
160.168 pr (w)
104.4(0.3)
342.0
5676
5677
5678
5679
5680
1,7-Heptanediol
2,3-Heptanedione
3,5-Heptanedione
Heptanedioyl dichloride
Heptanenitrile
C7H16O2
C7H12O2
C7H12O2
C7H10Cl2O2
C7H13N
629-30-1
96-04-8
7424-54-6
142-79-0
629-08-3
132.201
128.169
128.169
197.059
111.185 liq
21.9(0.2)
262
144
170(8)
13715
183(2)
5681
1-Heptanethiol
C7H16S
1639-09-4
132.267 liq
-43.22(0.02) 176.9(0.7)
5682
2,4,6-Heptanetrione
C7H10O3
626-53-9
142.152 lf
49
12110
5683
Heptanoic acid
C7H14O2
111-14-8
130.185 liq
-7.17(0.05)
222(2)
5684
Heptanoic anhydride
C14H26O3
626-27-7
242.354 liq
-12.4(0.5)
269.5
5685
1-Heptanol
C7H16O
111-70-6
116.201 liq
-33.2(0.1)
178(1)
5686
2-Heptanol, (±)-
C7H16O
52390-72-4 116.201
5687
3-Heptanol, (S)-
Ethylbutylcarbinol
C7H16O
26549-25-7 116.201 liq
-70
163(2)
5688
4-Heptanol
Dipropylcarbinol
C7H16O
589-55-9
116.201 liq
-41.2
161(2)
5689
2-Heptanone
Methyl pentyl ketone
C7H14O
110-43-0
114.185 liq
-34.7(0.4)
151.0(0.3)
5690
3-Heptanone
Ethyl butyl ketone
C7H14O
106-35-4
114.185 liq
-37.2(0.4)
146(2)
5691
4-Heptanone
Dipropyl ketone
C7H14O
123-19-3
114.185 liq
-32.1(0.8)
144(1)
5692
Heptanoyl chloride
C7H13ClO
2528-61-2
148.630 liq
-83.8
125.2
5693
5694
2-Heptenal
1-Heptene
C7H12O
C7H14
2463-63-0
592-76-7
112.169
98.186 liq
166
-118.83(0.06) 94(1)
5695
cis-2-Heptene
C7H14
6443-92-1
98.186
5696
trans-2-Heptene
C7H14
14686-13-6 98.186
liq
-109.47(0.09) 98(2)
5697
cis-3-Heptene
C7H14
7642-10-6
98.186
liq
-136.6
5698
trans-3-Heptene
C7H14
14686-14-7 98.186
liq
-136.64(0.09) 96(2)
5699
5700
5701
5702
6-Heptenoic acid
1-Hepten-4-ol
trans-2-Hepten-1-ol
Heptyl acetate
C7H12O2
C7H14O
C7H14O
C9H18O2
1119-60-4
3521-91-3
33467-76-4
112-06-1
128.169 liq
114.185
114.185
158.238 liq
-6.5
-50.3(0.6)
226
152.1
178
192.2(0.8)
5703
Heptylamine
C7H17N
111-68-2
115.217 liq
-23.0(0.6)
153(2)
5704
5705
5706
5707
Heptylbenzene
Heptyl butanoate
Heptylcyclohexane
Heptylcyclopentane
C13H20
C11H22O2
C13H26
C12H24
1078-71-3
5870-93-9
5617-41-4
5617-42-5
176.298
186.292
182.345
168.319
-48
-57.5(0.5)
-40.3(1)
-61.0(0.2)
242(4)
225.2(0.4)
244(2)
224(6)
5708
5-Heptyldihydro-2(3H)furanone
Heptyl formate
C11H20O2
104-67-6
184.276
286
C8H16O2
112-23-2
144.212
184(6)
5709
HCP_Section_03.indb 290
Synonym
Pimelic acid
Acetyl valeryl
Dipropionylmethane
Heptyl mercaptan
Enanthic acid
Heptyl alcohol
Butylacrolein
1-Heptanamine
4-Hydroxyundecanoic acid
lactone
mp/˚C
-90.549​
(0.002)
-63.8(0.4)
bp/˚C
140(6)
98.38(0.07)
159
97(2)
liq
liq
liq
liq
96(2)
den
g cm –3
nD
Solubility
0.76720 1.417220
0.679525 1.385525 i H2O; vs EtOH;
msc eth, bz,
chl; s ctc
s EtOH, eth, ace
0.94918 1.447220 i H2O; msc
EtOH, eth, chl
1.32915
s H2O, EtOH,
eth; i bz
0.956925 1.452025 vs eth, EtOH
0.91918 1.415018
0.94520
0.810620 1.410430 i H2O; s eth,
ace, bz, HOAc
0.842720 1.452120 i H2O; msc
EtOH, eth; s
chl
1.059940 1.493020 vs H2O, eth,
EtOH
0.912425 1.417020 sl H2O, ctc; s
EtOH, eth, ace
0.932120 1.433515 i H2O; s EtOH,
eth
0.821920 1.424920 sl H2O, ctc; msc
EtOH, eth
0.816720 1.421020 sl H2O, ctc; s
EtOH, eth
0.822720 1.420120 sl H2O, ctc; s
EtOH, eth
0.818320 1.420520 sl H2O; s EtOH,
eth
0.811120 1.408820 vs H2O; s EtOH,
eth
0.818320 1.405720 sl H2O, ctc; msc
EtOH, eth
0.817420 1.406920 i H2O; msc
EtOH, eth; s
ctc
0.959020 1.434518 s eth; sl ctc; vs
lig
0.86417 1.446817
0.697020 1.399820 i H2O; s EtOH,
eth; sl ctc
0.70820 1.40620 i H2O; s EtOH,
eth, ace, bz,
chl; sl ctc
0.701220 1.404520 i H2O; s EtOH,
eth, ace, bz,
peth, chl
0.703020 1.405920 i H2O; s EtOH,
eth, ace, bz,
peth, chl
0.698120 1.404320 i H2O; s EtOH,
eth, ace, bz,
chl; sl ctc
0.951514 1.440414
0.838422 1.434720
0.851620 1.446020 s EtOH, ace
0.875015 1.415020 i H2O; s EtOH,
eth, ctc
0.775420 1.425120 sl H2O, chl; msc
EtOH, eth
0.856720 1.486520 i H2O; s bz, chl
0.863720 1.423120 vs EtOH
0.810920 1.448420
0.801020 1.442120 vs ace, bz, eth,
EtOH
0.949420 1.451220 vs EtOH
0.878420 1.414020 i H2O; msc
EtOH, eth
4/11/16 11:29 AM
Physical Constants of Organic Compounds
3-291
HO
NH2
H2N
5672
5671
5673
Heptane
4-Heptanamine
N
N
NH2
OH
O
5674
1,7-Heptanediamine
O
5675
Heptanedinitrile
Heptanedioic acid
O
Cl
HO
O
OH
5676
O
5677
5678
2,3-Heptanedione
O
3,5-Heptanedione
SH
N
5679
5680
Heptanedioyl dichloride
5681
Heptanenitrile
1-Heptanethiol
Organic
1,7-Heptanediol
Cl
O
O
O
O
O
O
O
O
OH
5682
5683
2,4,6-Heptanetrione
OH
O
OH
5684
Heptanoic acid
5685
Heptanoic anhydride
OH
O
OH
5688
3-Heptanol, (S)-
5689
4-Heptanol
2-Heptanone
2-Heptanol, (±)-
Cl
O
O
O
5687
5686
1-Heptanol
5690
5691
3-Heptanone
O
5692
4-Heptanone
5693
Heptanoyl chloride
2-Heptenal
OH
OH
O
5694
5695
1-Heptene
5696
cis-2-Heptene
trans-2-Heptene
5697
5698
cis-3-Heptene
5699
trans-3-Heptene
O
OH
5701
trans-2-Hepten-1-ol
Heptylcyclohexane
1-Hepten-4-ol
O
NH2
O
5702
O
5703
Heptyl acetate
5704
Heptylamine
Heptylbenzene
O
5706
5700
6-Heptenoic acid
5707
Heptylcyclopentane
5708
5-Heptyldihydro-2(3H )-furanone
5705
Heptyl butanoate
O
O
5709
Heptyl formate
O
Physical Constants of Organic Compounds
3-292
Mol. Form.
CAS RN
Mol.
Wt.
Heptyl pentanoate
C12H24O2
5451-80-9
C12H22O2
5712
6-Heptyltetrahydro-2H-pyran- 5-Dodecanolide
2-one
1-Heptyne
5713
2-Heptyne
5714
3-Heptyne
5715
No.
Name
5710
5711
Physical
Form
den
g cm –3
Organic
mp/˚C
bp/˚C
200.318 liq
-46.4(0.5)
241(4)
713-95-1
198.302 liq
-12
1010.03
C7H12
628-71-7
96.170
-80.9(0.2)
99.8(0.3)
1-Methyl-2-butylacetylene
C7H12
1119-65-9
96.170
1-Ethyl-2-propylacetylene
C7H12
2586-89-2
96.170
Hesperetin
C16H14O6
520-33-2
5716
Hesperidin
C28H34O15
520-26-3
5717
Hexabromobenzene
C6Br6
87-82-1
302.278 pl (dil al +
1/2 w)
610.561 wh nd (dil
MeOH,
HOAc)
551.488 mcl nd (bz)
5718
C12H4Br6
59080-40-9 627.584 cry (ctc)
160
C12H18Br6
3194-55-6
641.695 cry
167
5720
2,2’,4,4’,5,5’-Hexabromobiphenyl
1,2,5,6,9,10-Hexabromocyclododecane
Hexabromoethane
C2Br6
594-73-0
503.445 orth pr (bz)
5721
5722
Hexabutyldistannoxane
Hexacene
C24H54OSn2
C26H16
56-35-9
258-31-1
5723
5724
Hexachloroacetone
Hexachlorobenzene
C3Cl6O
C6Cl6
116-16-5
118-74-1
596.105 liq
328.405 dk bl-grn
cry (sub)
264.749 liq
284.782 nd (sub)
5725
2,2’,3,3’,4,4’-Hexachlorobiphenyl
2,2’,4,4’,6,6’-Hexachlorobiphenyl
2,2’,3,3’,6,6’-Hexachlorobiphenyl
2,2’,4,4’,5,5’-Hexachlorobiphenyl
Hexachloro-1,3-butadiene
C12H4Cl6
38380-07-3 360.878 cry
151.7(0.5)
C12H4Cl6
33979-03-2 360.878 cry
113.7(0.5)
i H2O
C12H4Cl6
38411-22-2 360.878 cry (hx)
112.0(0.5)
i H2O
C12H4Cl6
35065-27-1 360.878 cry
103.5
C4Cl6
87-68-3
260.761 liq
-21
216(2)
Lindane
C6H6Cl6
58-89-9
290.830 nd (al)
115(2)
311(12)
α-Hexachlorocyclohexane
C6H6Cl6
319-84-6
290.830 cry
157.4(0.7)
β-Hexachlorocyclohexane
C6H6Cl6
319-85-7
δ-Lindane
C6H6Cl6
319-86-8
290.830 cry (bz, al,
xyl)
290.830 pl
137.0(0.2)
600.36
Perchlorocyclopentadiene
C5Cl6
77-47-4
272.772 ye grn liq
-9
239
1.701925 1.565820
C12H2Cl6O2
57653-85-7 390.861 cry
285
C12H2Cl6O2
19408-74-3 390.861 cry
243
C2Cl6
67-72-1
236.739 orth (al-eth) 186.8(0.2)
184.7 sp
2.09120
214.2(0.8)
1.763220 1.509120
415(11)
0.778360 1.435760 vs bz, lig, chl
5719
5726
5727
5728
5729
5730
Synonym
Bis(tributyltin) oxide
Perchlorobenzene
liq
113.6(0.3)
liq
-130.5
109.2(0.4)
226(2)
205 sub
327
i H2O; sl EtOH,
eth; s bz, chl
200 dec
3.82320
1.863
-45
380
22510
sub
1.1720
1.4870
-1.0
230(3)
203
325
1.743412 1.511220 sl H2O; s ace
2.04423 1.569123 i H2O; sl EtOH; s
eth, chl; vs bz
i H2O
5738
Hexachlorophene
C13H6Cl6O2
70-30-4
406.904 nd (bz)
165.0(0.3)
5739
5740
5741
Hexachloropropene
Hexacontane
Hexacosane
C3Cl6
C60H122
C26H54
1888-71-7
7667-80-3
630-01-3
-72.9
100(2)
56.09(0.04)
5742
Hexacosanoic acid
C26H52O2
506-46-7
248.750 liq
843.611
366.707 mcl, tcl or
orth (bz)
cry (eth)
396.690
5743
1-Hexacosanol
C26H54O
506-52-5
80(1)
30520 dec
5744
5745
Hexadecamethylheptasiloxane
Hexadecanal
C16H48O6Si7
C16H32O
541-01-5
629-80-1
382.706 orth pl (dil
al)
533.147 liq
240.424 pl (eth), nd
(peth)
-78
36(5)
286.8(0.2)
20029
5733
5734
5735
5736
HCP_Section_03.indb 292
Perchloroethane
Cerotic acid
0.732820 1.408720 sl H2O; msc
EtOH, eth; s
bz, chl, peth
0.74425 1.423020 i H2O; msc
EtOH, eth; s
bz, chl, peth
0.733625 1.418920 i H2O; msc
EtOH, eth; s
bz, chl, peth
vs eth, EtOH
vs py, EtOH,
HOAc
5737
5732
Solubility
262
1,2,3,4,5,6-Hexachlorocyclohexane, (1α,2α,3β,4α,5α,6β)
1,2,3,4,5,6-Hexachlorocyclohexane, (1α,2α,3β,4α,5β,6β)
1,2,3,4,5,6-Hexachlorocyclohexane, (1α,2β,3α,4β,5α,6β)
1,2,3,4,5,6-Hexachlorocyclohexane, (1α,2α,3α,4β,5α,6β)
Hexachloro-1,3-cyclopentadiene
1,2,3,6,7,8-Hexachloro­
dibenzo-p-dioxin
1,2,3,7,8,9-Hexachloro­
dibenzo-p-dioxin
Hexachloroethane
5731
nD
0.862320 1.425415 vs ace, eth,
EtOH
600.50
87.7(0.5)
sl EtOH, eth,
CS2
i H2O, EtOH
1.55625
1.554220 i H2O; s EtOH,
eth
vs ace, bz
1.8919
i H2O; sl EtOH,
bz, chl, HOAc
i H2O; vs EtOH,
eth; s bz; sl liq
HF
i H2O; s EtOH,
eth, ace, chl,
dil alk
i H2O; s ctc, chl
0.8198100 1.4301100 i H2O; vs EtOH,
eth
i H2O; s EtOH,
eth
0.901220 1.396520 vs bz, lig
i H2O; s EtOH,
eth, ace, bz
4/11/16 11:29 AM
Physical Constants of Organic Compounds
3-293
O
O
O
O
5712
5711
5710
5714
5713
1-Heptyne
6-Heptyltetrahydro-2H-pyran-2-one
Heptyl pentanoate
3-Heptyne
2-Heptyne
CH3
O
OH O
OH HO
OH O
HO
O
O O
HO
O
Br
OH
Br Br
Br
O
HO
O
Br
OH
O
Br
OH
5715
5717
Br
5718
Hexabromobenzene
2,2’,4,4’,5,5’-Hexabromobiphenyl
Organic
Hesperidin
Br
Br
Br
5716
Hesperetin
Br
Br
OH
Br
Br
Cl
Br
Sn
Br Br
Br
Br
O
Sn
Cl
Cl
Br
Br
Br Br
Br
5719
1,2,5,6,9,10-Hexabromocyclododecane
5720
5721
Hexabromoethane
Cl Cl
Cl
Cl
2,2’,3,3’,4,4’-Hexachlorobiphenyl
Cl Cl
Cl Cl
5726
5727
2,2’,4,4’,6,6’-Hexachlorobiphenyl
Cl
Cl
Cl
Cl
Cl
Cl
Cl
5729
Cl
Cl
Cl
Cl
Cl
Cl
OH
Cl
Cl
Cl
Cl
5732
1,2,3,4,5,6-Hexachlorocyclohexane, (1α,2β,3α,4β,5α,6β)
Cl
Cl
Cl
Cl
Cl
Cl
O
Cl
Cl
5735
Hexachloro-1,3-cyclopentadiene
Cl
O
Cl
O
Cl
Cl
Cl
Cl
Cl
Cl
5734
1,2,3,4,5,6-Hexachlorocyclohexane, (1α,2α,3α,4β,5α,6β)
Cl
Cl
O
Cl
Cl
Cl
Cl
Cl
5731
Cl
5733
2,2’,4,4’,5,5’-Hexachlorobiphenyl
1,2,3,4,5,6-Hexachlorocyclohexane, (1α,2α,3β,4α,5β,6β)
Cl Cl
Cl
Cl
5728
Cl
5730
Cl
Cl
Cl
Cl
1,2,3,4,5,6-Hexachlorocyclohexane, (1α,2α,3β,4α,5α,6β)
Cl
5724
Hexachlorobenzene
Cl Cl
2,2’,3,3’,6,6’-Hexachlorobiphenyl
Cl
Hexachloro-1,3-butadiene
Cl
Cl
Cl
Cl
Cl
Cl
Cl
Cl
Cl
Cl
5725
Cl Cl
Cl
Hexachloroacetone
Hexacene
Cl
Cl
Cl
Cl
Cl
5723
5722
Hexabutyldistannoxane
Cl Cl
Cl
Cl
O
5736
1,2,3,6,7,8-Hexachlorodibenzo-p-dioxin
Cl
Cl
Cl
5737
1,2,3,7,8,9-Hexachlorodibenzo-p-dioxin
Hexachloroethane
OH
Cl
Cl
Cl
Cl
Cl
5738
5739
Hexachloropropene
OH
5743
1-Hexacosanol
Cl
Cl Cl Cl
Cl
Hexachlorophene
O
Cl
Cl
OH
H3C(CH2)58CH3
5740
5741
Hexacontane
Hexacosane
Si
O
Si
O
Si
O
Si
O
5744
Si
O
Si
Hexadecamethylheptasiloxane
O
5742
Hexacosanoic acid
O
Si
5745
Hexadecanal
Physical Constants of Organic Compounds
3-294
Organic
mp/˚C
bp/˚C
den
g cm –3
255.439 lf
105(3)
23612
1.000020
544-76-3
226.441 lf (HOAc)
18.18(0.02)
286.9(0.7)
0.770125 1.432925
C16H30O4
C16H31N
505-54-4
629-79-8
286.407 pl (al)
237.424 hex
122(1)
31.4(0.4)
333
0.830320 1.445020
Cetyl mercaptan
C16H34S
2917-26-2
258.506 cry (lig)
19
1250.5
Hexadecanoic acid
Palmitic acid
C16H32O2
57-10-3
256.424 nd (al)
62.49(0.02)
351(6)
0.852762 1.4334560
5752
5753
Hexadecanoic anhydride
1-Hexadecanol
Cetyl alcohol
C32H62O3
C16H34O
623-65-4
494.832 lf (peth)
36653-82-4 242.440 fl (AcOEt)
64
49.30(0.01)
325(2)
0.838883 1.436468
0.818750 1.428379
5754
5755
5756
3-Hexadecanone
Hexadecanoyl chloride
1-Hexadecene
1-Cetene
C16H32O
C16H31ClO
C16H32
18787-64-9 240.424 lf (peth)
112-67-4
274.869
629-73-2
224.425 lf
43
12
4.2(0.1)
18417
19920
285(1)
0.901625 1.451420
0.781120 1.441220
5757
5758
cis-9-Hexadecenoic acid
Hexadecyl acetate
Palmitoleic acid
C16H30O2
C18H36O2
373-49-9
629-70-9
254.408
284.478
2(2)
-18.5
1821
222205
5759
Hexadecylamine
1-Hexadecanamine
C16H35N
143-27-1
241.456 lf
46(2)
321(3)
5760
Hexadecylbenzene
C22H38
1459-09-2
302.537
26.4(0.4)
385
5761
Hexadecyldimethylamine
C18H39N
112-69-6
269.510
C32H64O2
C27H40O3
540-10-3
531-84-0
480.849 mcl lf
412.605 grn-wh fl
C19H38O3
35274-05-6 314.503 wax
41(1)
21910
C20H38O2
2495-27-4
310.515
24
1832
C19H40O3
506-03-6
316.519 lf (hx)
64
1200.005
C21H38BrN
140-72-7
384.438
61
C21H38ClN
123-03-5
339.987 wh pow
81(3)
C34H68O2
1190-63-2
No.
Name
5746
Hexadecanamide
5747
Hexadecane
5748
5749
Hexadecanedioic acid
Hexadecanenitrile
5750
1-Hexadecanethiol
5751
Synonym
Cetane
5769
N,N-Dimethyl-1-hexadecanamine
Hexadecyl hexadecanoate
Cetyl palmitate
Hexadecyl 3-hydroxy-2Hexadecyl 3-hydroxy-2naphthalenecarboxylate
naphthoate
Hexadecyl 2-hydroxypropano- Cetyl lactate
ate
Hexadecyl 2-methyl-2-propenoate
3-(Hexadecyloxy)-1,2Chimyl alcohol
propanediol, (S)1-Hexadecylpyridinium
bromide
1-Hexadecylpyridinium
Cetylpyridinium chloride
chloride
Hexadecyl stearate
Cetyl stearate
5770
5771
5772
5773
5774
5775
5776
5777
5778
5779
Hexadecyltrichlorosilane
Hexadecyl vinyl ether
1-Hexadecyne
trans,trans-2,4-Hexadienal
1,2-Hexadiene
cis-1,3-Hexadiene
trans-1,3-Hexadiene
cis-1,4-Hexadiene
trans-1,4-Hexadiene
1,5-Hexadiene
5780
5762
5763
5764
5765
5766
5767
5768
Mol. Form.
CAS RN
Mol.
Wt.
C16H33NO
629-54-9
C16H34
Physical
Form
C16H33Cl3Si
C18H36O
C16H30
C6H8O
C6H10
C6H10
C6H10
C6H10
C6H10
C6H10
cis,cis-2,4-Hexadiene
C6H10
6108-61-8
82.143
liq
5781
trans,cis-2,4-Hexadiene
C6H10
5194-50-3
82.143
liq
5782
trans,trans-2,4-Hexadiene
C6H10
5194-51-4
82.143
liq
5783
2,4-Hexadienoic acid
Sorbic acid
C6H8O2
110-44-1
5784
2,4-Hexadien-1-ol
Sorbic alcohol
C6H10O
5785
trans,trans-2,4-Hexadienoyl
chloride
1,5-Hexadien-3-yne
1,5-Hexadiyne
5786
5787
HCP_Section_03.indb 294
Sorbinaldehyde
Propylallene
Biallyl
Divinylacetylene
Bipropargyl
Solubility
i H2O; sl EtOH,
bz, ace, eth
i H2O; sl EtOH;
msc eth; s ctc
vs ace, EtOH
i H2O; vs EtOH,
eth, ace, bz,
chl
i H2O; sl EtOH,
ctc; s eth
i H2O; s EtOH,
ace, bz; msc
eth; vs chl
vs eth
i H2O; sl EtOH;
vs eth, bz, chl;
s ace
s chl
vs eth
i H2O; s EtOH,
eth, ctc, peth
0.857425 1.443820 i H2O; sl EtOH; s
ctc
0.812920 1.449620 i H2O; vs EtOH,
eth, bz; s ace
0.854720 1.481320 i H2O; sl EtOH;
vs eth, bz, CS2
330.0
508.903 lf or pl (eth,
HOAc)
5894-60-0 359.878
822-28-6
268.478
629-74-3
222.409
142-83-6
96.127 liq
592-44-9
82.143
14596-92-0 82.143
20237-34-7 82.143 liq
7318-67-4 82.143
7319-00-8 82.143 liq
592-42-7
82.143 liq
1-(Ethenyloxy)hexadecane
nD
43.9(0.2)
72.5
0.98920
1.439870 vs eth, EtOH
vs bz, HOAc
1.441040
0.8720
vs ace, peth,
chl
vs H2O, chl
56.8(0.5)
1.441070 vs ace, eth, chl
269
1602
284
174
76(3)
73(3)
71.5(0.8)
70(13)
65.0(0.5)
59.2(0.4)
0.82127
0.796520
0.89820
0.714920
0.703325
0.699525
0.69525
0.69525
0.687825
85(3)
0.729825 1.460620
-96.1(0.4)
83(3)
0.718525 1.456020
-44.9(0.4)
82.4(0.7)
0.710125 1.451020
228 dec
1.20419
111-28-4
112.127 nd (dil al) nd 134.5
(w)
98.142 nd
29(2)
7612
0.896723 1.498120
C6H7ClO
2614-88-2
130.572
8222
1.066619 1.554520
C6H6
C6H6
821-08-9
628-16-0
78.112
78.112
85(3)
88(3)
0.785120 1.503520 i H2O; s bz
0.804920 1.438023 i H2O; s EtOH,
eth, ace, bz
liq
liq
16
15(2)
-16.5
-102.4(0.6)
-138.7
-140.7(0.1)
-88
-5.5(0.2)
1.444425
1.444020
1.538420
1.428220
1.437920
1.440620
1.404920
1.410420
1.404220
vs bz
vs eth, chl
vs eth
i H2O; s EtOH,
eth, bz, chl; sl
ctc
i H2O; s EtOH,
eth, chl
i H2O; s EtOH,
eth, chl
i H2O; s EtOH,
eth, chl
s H2O, EtOH,
chl; vs eth
i H2O; s EtOH,
eth
vs ace
4/11/16 11:30 AM
Physical Constants of Organic Compounds
3-295
O
O
O
OH
OH
NH2
N
O
5746
5748
5747
Hexadecanamide
5749
Hexadecanedioic acid
Hexadecane
OH
SH
5750
Hexadecanenitrile
5751
1-Hexadecanethiol
Hexadecanoic acid
O
O
O
O
O
Cl
OH
O
OH
5752
5753
1-Hexadecanol
5756
5755
3-Hexadecanone
5757
1-Hexadecene
Hexadecanoyl chloride
cis-9-Hexadecenoic acid
Organic
Hexadecanoic anhydride
5754
O
O
NH2
N
5758
5759
Hexadecyl acetate
5760
Hexadecylamine
5761
Hexadecylbenzene
Hexadecyldimethylamine
O
O
O
O
O
O
OH
OH
5762
5763
Hexadecyl hexadecanoate
5764
Hexadecyl 3-hydroxy-2-naphthalenecarboxylate
Hexadecyl 2-hydroxypropanoate
O
OH
O
O
5765
N
Br
OH
5766
Hexadecyl 2-methyl-2-propenoate
5767
3-(Hexadecyloxy)-1,2-propanediol, (S)-
1-Hexadecylpyridinium bromide
O
Cl
N
Cl
Si Cl
Cl
O
5769
5768
5770
Hexadecyl stearate
1-Hexadecylpyridinium chloride
Hexadecyltrichlorosilane
5772
Hexadecyl vinyl ether
5776
trans-1,3-Hexadiene
5773
1-Hexadecyne
5777
5778
cis-1,4-Hexadiene
5779
trans-1,4-Hexadiene
5783
1,2-Hexadiene
5780
1,5-Hexadiene
cis,cis-2,4-Hexadiene
5775
cis-1,3-Hexadiene
5781
trans,cis-2,4-Hexadiene
O
OH
5782
5774
trans,trans-2,4-Hexadienal
O
trans,trans-2,4-Hexadiene
C
O
O
5771
2,4-Hexadienoic acid
Cl
OH
5784
2,4-Hexadien-1-ol
5785
trans,trans-2,4-Hexadienoyl chloride
5786
1,5-Hexadien-3-yne
5787
1,5-Hexadiyne
Physical Constants of Organic Compounds
3-296
No.
Name
Synonym
Mol. Form.
CAS RN
5788
5789
2,4-Hexadiyne
Hexaethylbenzene
Dimethyldiacetylene
C6H6
C18H30
2809-69-0
604-88-6
5790
5791
5792
5793
5794
5795
Hexaethyldisiloxane
Hexaethyl tetraphosphate
Hexafluorenium bromide
Hexafluoroacetylacetone
Hexafluorobenzene
1,1,2,3,4,4-Hexafluoro-1,3butadiene
1,1,1,4,4,4-Hexafluoro-2butyne
Hexafluorocyclobutene
Hexafluoroethane
C12H30OSi2
C12H30O13P4
C36H42Br2N2
C5H2F6O2
C6F6
C4F6
5796
5797
5798
Organic
5799
5800
5801
5802
5803
5804
5805
5806
5807
5808
5809
5810
5811
5812
bp/˚C
64.67(0.01)
129(1)
129.5(0.2)
298(3)
994-49-0
757-58-4
317-52-2
1522-22-1
392-56-3
685-63-2
78.112 pr (sub)
246.431 mcl pr (al or
bz)
246.536
506.253 hyg
662.539 cry (PrOH)
208.059
186.054 liq
162.033 col gas
C4F6
692-50-2
C4F6
C2F6
1,1,1,2,3,3-Hexafluoropropane Refrigerant 236ea
1,1,1,3,3,3-Hexafluoropropane Refrigerant 236fa
1,1,1,3,3,3-Hexafluoro-2propanol
Hexahydro-1H-azepine
Hexamethylenimine
Hexahydro-1H-1,4-diazepine
1,5a,6,9,9a,9b-Hexahydro4a(4H)-dibenzofurancarboxaldehyde
cis-1,2,3,5,6,8a-Hexahydro4,7-dimethyl-1-isopropylnaphthalene, (1S)1,2,4a,5,8,8a-Hexahydro-4,7dimethyl-1-isopropylnaphthalene, [1S-(1α,4aβ,8aα)]
Hexahydro-1,3-isobenzofuran- Hexahydrophthalic anhydride
dione
Hexahydro-1-methyl-1H-1,4diazepine
2,3,4,6,7,8-Hexa­hydro­
pyrrolo[1,2-a]pyrimidine
Hexahydro-1,3,5-trinitroCyclonite
1,3,5-triazine
Hexahydro-1,3,5-triphenyl1,3,5-triazine
1,2,3,5,6,7-Hexahydroxy9,10-anthracenedione
Ethyl tetraphosphate
Perfluorobenzene
Perfluoroethane
5823
5824
5825
5826
5827
HCP_Section_03.indb 296
252(7)
150 dec
vs EtOH, eth
0.8305130 1.4736130 i H2O; s EtOH,
sulf; vs eth, bz
0.845720 1.434020
1.291727 1.427327 vs ace, bz, EtOH
5.10(0.01)
-132
69(2)
80.2(0.2)
5.4(0.2)
1.48520 1.333320
1.617520 1.377720
1.4735
1.378-20
162.033 col gas
-117.4
-24.6
697-11-0
76-16-4
162.033 col gas
138.011 col gas
-60
-100.015​
(0.005)
2(5)
-78.1(0.1)
1.602-20
1.590-78
C3H2F6
C3H2F6
C3H2F6O
431-63-0
690-39-1
920-66-1
152.038 col gas
152.038 col gas
168.037 liq
6.2
-1.4(0.2)
59(3)
1.50260
1.43430
1.460021
C6H13N
111-49-9
99.174
136(2)
0.864322 1.463120 s H2O; vs EtOH,
eth
C5H12N2
C13H16O2
505-66-8
126-15-8
100.162 hyg
204.265 liq
C15H24
483-76-1
C15H24
-40
188
-93.6
-2.0
40.5
-80
s EtOH, eth,
ace, ctc, HOAc
1.298-20
i H2O; sl EtOH,
eth
12512
0.916015 1.508915
523-47-7
204.352
274
0.923020 1.505920 vs eth, lig
C8H10O3
85-42-7
154.163
C6H14N2
4318-37-0
114.188
154
0.911120 1.476920
C7H12N2
3001-72-7
124.183
967
1.00525
C3H6N6O6
121-82-4
222.116 orth cry
(ace)
203.4(0.9)
C21H21N3
91-78-1
315.412
144
Rufigallol
C14H8O8
82-12-2
Mellitene
C12H18
87-85-4
304.209 red rhom,
red-ye nd
(sub)
162.271 orth pr or
nd (al)
C6H21N3Si3
1009-93-4
C6H18O3Si3
C6H18Si2
32
1.525420 i H2O
14518
1.519020
1.8220
i H2O, EtOH, bz;
sl eth, MeOH;
s ace, HOAc
i H2O; sl EtOH; s
eth, ace, bz, tol
i H2O; sl EtOH,
eth; s ace, alk
i H2O; s EtOH,
eth, ace, bz,
HOAc, chl
185
sub
165.6(0.7)
268(3)
1.063025
219.508 liq
-18.7(0.2)
187(1)
0.919620 1.44820
541-05-9
1450-14-2
222.462
146.378
63.7(0.4)
14.4(0.6)
(6-Aminohexyl)carbamic acid
C6H18SSi2
C6H19NSi2
C6H18OSi2
C7H16N2O2
3385-94-2
999-97-3
107-46-0
143-06-6
178.443
161.393
162.377 liq
160.214 cry
-68.2(0.1)
150
135.1(0.4) 1.120020
i H2O
112.65(0.07) 0.724722 1.422920 i H2O; s eth,
ace, bz; dec
alk
162.5
0.85120
125(1)
0.774125 1.409020
100.5(0.3) 0.763820 1.377420 i H2O
Methenamine
C8H12N2O2
C6H12N4
822-06-0
100-97-0
168.193
140.186 orth (al)
>250
12210
sub
C9H18N6O6
C6H18N3OP
531-18-0
680-31-9
306.275
179.200 col liq
137
7.2
235(13)
C6H18N3P
1608-26-0
163.201
C30H62
111-01-3
422.813 liq
-38
420(6)
C6H12O
66-25-1
100.158 liq
-58.2(0.2)
129.6(0.4)
Hexamethylolmelamine
Hexamethylphosphoric
Tris(dimethylamino)phosphine
triamide
oxide
Hexamethylphosphorous
Tris(dimethylamino)phosphine
triamide
2,6,10,15,19,23-Hexamethyl- Squalane
tetracosane
Hexanal
Solubility
204.352
2,2,4,4,6,6-Hexamethylcyclotrisilazane
Hexamethylcyclotrisiloxane
Dimethylsiloxane cyclic trimer
Hexamethyldisilane
5821
5822
nD
1.1020
5814
Hexamethyldisilathiane
Hexamethyldisilazane
Hexamethyldisiloxane
Hexamethylenediamine
carbamate
Hexamethylene diisocyanate
Hexamethylenetetramine
den
g cm –3
169
307
Hexamethylbenzene
5817
5818
5819
5820
Physical
Form
mp/˚C
5813
5815
5816
Mol.
Wt.
Caproaldehyde
1.052820 1.458520
1.331-5
vs H2O; s EtOH,
ace, chl; sl
eth, bz
vs H2O
1.0320
1.457920 s EtOH, eth
s chl
0.811515 1.453015 i H2O; sl EtOH,
ace; s eth, chl;
msc bz
0.833520 1.403920 sl H2O; vs EtOH,
eth; s ace, bz
4/11/16 11:30 AM
Physical Constants of Organic Compounds
Si
5789
5788
F
F
F
F
5795
F
F
F
F
F
F
F
F
5796
5792
F
F
O
F
F
F
F
F
F
5798
5793
5794
Hexafluoroacetylacetone
F
F
F
F
F
5799
Hexafluoroethane
F
F
Hexafluorobenzene
OH
F
F
F
F
F
F
F
Hexafluorocyclobutene
F
F
Hexafluorenium bromide
F
5797
1,1,1,4,4,4-Hexafluoro-2-butyne
O
F
F
F
F
F
F
5800
1,1,1,2,3,3-Hexafluoropropane
F
F
F
F
5801
1,1,1,3,3,3-Hexafluoropropane
1,1,1,3,3,3-Hexafluoro-2-propanol
Organic
1,1,2,3,4,4-Hexafluoro-1,3-butadiene
F
N
Br
5791
F
Br
N
Hexaethyl tetraphosphate
F
F
F
Si
Hexaethyldisiloxane
F
F
O
O
O
O
P
P
P
P
O
O
O
O
O
O
O
O
O
5790
Hexaethylbenzene
2,4-Hexadiyne
O
3-297
NH
N
H
O
N
H
5802
5803
Hexahydro-1H-azepine
H
O
5804
Hexahydro-1H-1,4-diazepine
5805
1,5a,6,9,9a,9b-Hexahydro-4a(4H )-dibenzofurancarboxaldehyde
H
cis-1,2,3,5,6,8a-Hexahydro-4,7-dimethyl-1-isopropylnaphthalene, (1S)-
O
NH
O
H
O
5806
1,2,4a,5,8,8a-Hexahydro-4,7-dimethyl-1-isopropylnaphthalene, [1S-(1α,4aβ,8aα)]
O
O
N
O
N
N
N
N
O
N
O
5816
N
Hexahydro-1,3,5-triphenyl-1,3,5-triazine
Si
S
Si
Si
5817
Hexamethyldisilane
HO
2,3,4,6,7,8-Hexahydropyrrolo[1,2-a]pyrimidine
Si
HN
OH
OH O
Si Si
Hexamethyldisilathiane
N
Hexahydro-1-methyl-1H-1,4-diazepine
OH
HO
5811
Hexahydro-1,3,5-trinitro-1,3,5-triazine
N
5809
OH
HO
N
N
5808
Hexahydro-1,3-isobenzofurandione
O
N
5810
HO
5807
O
N
N
N
H
N
5812
5813
1,2,3,5,6,7-Hexahydroxy-9,10-anthracenedione
H
N
Si
Si
5814
Hexamethylbenzene
2,2,4,4,6,6-Hexamethylcyclotrisilazane
O
Si
5818
Hexamethyldisilazane
Si
O
Si
5819
Hexamethyldisiloxane
H2N
N
H
OH
O
C
5820
N
N
C
O
Si
Hexamethylene diisocyanate
Si
O
5815
Hexamethylcyclotrisiloxane
N
N
N
5821
Hexamethylenediamine carbamate
O
Si
O
NH
N
5822
Hexamethylenetetramine
OH
N
N
HO
N
OH
OH
5823
Hexamethylolmelamine
O
N P N
N
5824
Hexamethylphosphoric triamide
N
N
P
N
5825
Hexamethylphosphorous triamide
O
5826
2,6,10,15,19,23-Hexamethyltetracosane
5827
Hexanal
Physical Constants of Organic Compounds
3-298
Mol. Form.
CAS RN
Mol.
Wt.
Organic
mp/˚C
bp/˚C
den
g cm –3
Hexanamide
C6H13NO
628-02-4
115.173 cry (ace)
101(1)
258(6)
0.99920
5829
Hexane
C6H14
110-54-3
86.175
-95.27(0.02) 68.72(0.06)
0.660625
5830
5831
5832
Hexanedial
Hexanediamide
1,6-Hexanediamine
1072-21-5
628-94-4
124-09-4
-8
225.9(0.4)
38.8(0.6)
Hexanedioic acid, dihydrazide
1,2-Hexanediol
1,6-Hexanediol
Hexamethylene glycol
C6H14N4O2
C6H14O2
C6H14O2
1071-93-8
6920-22-5
629-11-8
114.142
144.171 pl
116.204 orth bipym
pl
174.201
118.174
118.174
1.00319
Hexamethylenediamine
C6H10O2
C6H12N2O2
C6H16N2
5833
5834
5835
181.8
45
41.5(0.5)
234(8)
208
1.07925
5836
2,5-Hexanediol
Diisopropanol
C6H14O2
2935-44-6
118.174 cry (eth)
43
229(7)
0.961020
5837
5838
5839
5840
1,6-Hexanediol dimethacrylate
2,3-Hexanedione
2,4-Hexanedione
2,5-Hexanedione
Hexamethylene methacrylate
Acetylbutyryl
Propionylacetone
Acetonylacetone
C14H22O4
C6H10O2
C6H10O2
C6H10O2
6606-59-3
3848-24-6
3002-24-2
110-13-4
254.323
114.142
114.142 oil
114.142 liq
-5.5
128
160
194
5841
5842
5843
5844
3,4-Hexanedione
Hexanedioyl dichloride
1,6-Hexanedithiol
Hexanenitrile
Bipropionyl
4437-51-8
111-50-2
1191-43-1
628-73-9
114.142 liq
183.033
150.305 liq
97.158 liq
-10
Capronitrile
C6H10O2
C6H8Cl2O2
C6H14S2
C6H11N
5845
1-Hexanethiol
Hexyl mercaptan
C6H14S
111-31-9
118.240 liq
-80.52(0.02) 152.7(0.6)
5846
2-Hexanethiol
C6H14S
1679-06-7
118.240 liq
-147.0(0.4)
139(1)
5847
5848
1,2,6-Hexanetriol
Hexanoic acid
1,2,6-Trihydroxyhexane
Caproic acid
C6H14O3
C6H12O2
106-69-4
142-62-1
134.173
116.158 liq
-4.1(0.7)
1703
204.9(0.6)
5849
5850
Hexanoic anhydride
1-Hexanol
Caproyl alcohol
C12H22O3
C6H14O
2051-49-2
111-27-3
214.301
102.174 liq
-41
-46.4(0.9)
267(9)
156.9(0.7)
5851
2-Hexanol
C6H14O
20281-86-1 102.174
138(6)
5852
3-Hexanol
C6H14O
17015-11-1 102.174
143(2)
5853
2-Hexanone
Butyl methyl ketone
C6H12O
591-78-6
100.158 liq
-55.45(0.05) 127.6(0.1)
5854
3-Hexanone
Ethyl propyl ketone
C6H12O
589-38-8
100.158 liq
-55.4(0.2)
123.5(0.3)
5855
5856
5857
Hexanoyl chloride
Hexatriacontane
cis-1,3,5-Hexatriene
Caproyl chloride
C6H11ClO
C36H74
C6H8
142-61-0
630-06-8
2612-46-6
134.603 liq
506.973
80.128 liq
-87
75.81(0.04)
-12
153
298.43
82.2(0.9)
5858
trans-1,3,5-Hexatriene
C6H8
821-07-8
80.128
-12
79(4)
5859
5860
5861
5862
Hexazinone
trans-2-Hexenal
cis-3-Hexenal
1-Hexene
C12H20N4O2
C6H10O
C6H10O
C6H12
51235-04-2
6728-26-3
6789-80-6
592-41-6
252.313
98.142
98.142
84.159 liq
117.2(0.5)
5863
cis-2-Hexene
C6H12
7688-21-3
84.159
liq
-141.12(0.04) 68.9(0.5)
5864
trans-2-Hexene
C6H12
4050-45-7
84.159
liq
-133.1(0.3)
67.85(0.09)
5865
cis-3-Hexene
C6H12
7642-09-3
84.159
liq
-138.7(0.7)
66.4(0.5)
5866
trans-3-Hexene
C6H12
13269-52-8 84.159
liq
-113.7(0.5)
67.06(0.09)
5867
5868
5869
5870
5871
trans-3-Hexenedinitrile
2-Hexenoic acid
3-Hexenoic acid
5-Hexenoic acid
1-Hexen-3-ol
C6H6N2
C6H10O2
C6H10O2
C6H10O2
C6H12O
1119-85-3
1191-04-4
4219-24-3
1577-22-6
4798-44-1
No.
Name
5828
HCP_Section_03.indb 298
Synonym
trans-1,4-Dicyano-2-butene
Hydrosorbic acid
5-Hexanoic acid
Physical
Form
liq
liq
106.125 cry
114.142 nd (w, al)
114.142
114.142 liq
100.158
-21
-80.3
939
197(2)
130
12612
237
163.5(0.3)
dec
146.5
121
-139.76(0.05) 63.4(0.1)
76
36.5
12
-37
216.5
208
203
134(7)
nD
Solubility
1.4200110 vs bz, eth,
EtOH, chl
1.372725 i H2O; vs EtOH;
s eth, chl
1.435020 vs bz, eth, EtOH
vs EtOH
vs H2O; s EtOH,
bz
1.443120
1.457925 s H2O, EtOH,
ace; sl eth; i
bz
1.447520 s H2O, EtOH,
eth; sl ctc
0.99825
0.93419
0.95920 1.451620
0.737020 1.423220 vs H2O, bz, eth,
EtOH
0.94121 1.413021
sl chl
0.988625 1.511020
0.805120 1.406820 i H2O; s EtOH,
eth; sl chl
0.842420 1.449620 i H2O; vs EtOH,
eth
0.834520 1.445120 i H2O; s EtOH,
eth, bz
1.104920 1.5820
0.921225 1.416320 sl H2O; s EtOH,
eth, chl
0.924015 1.429720 vs eth, EtOH
0.813620 1.417820 sl H2O; s EtOH,
ace, chl; msc
eth, bz
0.815920 1.414420 sl H2O, ctc; s
EtOH, eth
0.818220 1.416720 sl H2O; s EtOH,
ace; msc eth
0.811320 1.400720 sl H2O; s ace;
msc EtOH, eth
0.811820 1.400420 sl H2O; s ace;
msc EtOH, eth
0.978420 1.426420 s eth, ace
0.780380 1.439780
0.717520 1.457720 i H2O; s EtOH,
ace, chl, peth
0.736915 1.513520 i H2O; s EtOH,
ace, chl, peth
1.25
0.849120 1.448020
0.853322 1.430021
0.668525 1.385225 i H2O; vs bz,
eth, EtOH,
peth
0.682425 1.397920 i H2O; s EtOH,
eth, bz, chl, lig
0.673325 1.393620 i H2O; s EtOH,
eth, bz, chl, lig
0.677820 1.394720 i H2O; s EtOH,
eth, bz, chl, lig
0.677220 1.394320 i H2O; s EtOH,
eth, bz, chl, lig
0.96520
0.964023
0.961020
0.83422
1.446040 vs eth
1.493520
1.434320 vs eth, EtOH
1.429718 sl H2O; vs ace,
eth, EtOH
4/11/16 11:30 AM
Physical Constants of Organic Compounds
3-299
O
O
O
NH2
5828
5829
Hexanamide
O
H2N
H
N
N
H
O
5831
Hexanedial
5832
Hexanediamide
1,6-Hexanediamine
O
OH
OH
NH2
O
OH
O
OH
5835
5834
5837
5836
1,6-Hexanediol
1,6-Hexanediol dimethacrylate
2,5-Hexanediol
Organic
1,2-Hexanediol
O
O
HO
OH
5833
Hexanedioic acid, dihydrazide
NH2
H2N
O
5830
Hexane
NH2
H2N
O
O
O
O
O
O
O
5838
5839
2,3-Hexanedione
5840
2,4-Hexanedione
2,5-Hexanedione
1-Hexanethiol
2-Hexanethiol
2-Hexanol
Hexanoic acid
1-Hexanol
O
Cl
5853
3-Hexanol
OH
5850
Hexanoic anhydride
O
5852
O
5849
O
OH
Hexanenitrile
O
5848
1,2,6-Hexanetriol
OH
5851
O
O
5847
5844
1,6-Hexanedithiol
OH
OH
N
SH
5843
Hexanedioyl dichloride
OH
5846
HS
5842
3,4-Hexanedione
HO
SH
Cl
O
5841
SH
5845
O
Cl
O
5854
2-Hexanone
5855
3-Hexanone
5856
Hexanoyl chloride
Hexatriacontane
O
N
O
5857
cis-1,3,5-Hexatriene
N
N
O
N
O
5859
5858
5860
Hexazinone
trans-1,3,5-Hexatriene
5861
trans-2-Hexenal
N
5866
trans-3-Hexene
1-Hexene
O
N
5865
cis-3-Hexene
5862
cis-3-Hexenal
5868
2-Hexenoic acid
OH
OH
5869
3-Hexenoic acid
5864
trans-2-Hexene
O
O
OH
5867
trans-3-Hexenedinitrile
5863
cis-2-Hexene
5870
5-Hexenoic acid
OH
5871
1-Hexen-3-ol
Physical Constants of Organic Compounds
3-300
Organic
Mol. Form.
CAS RN
Mol.
Wt.
cis-2-Hexen-1-ol
C6H12O
928-94-9
100.158
157
5873
5874
trans-2-Hexen-1-ol
cis-3-Hexen-1-ol
C6H12O
C6H12O
928-95-0
928-96-1
100.158
100.158
172(8)
157(9)
5875
5876
5877
5878
5879
5880
5881
5882
trans-3-Hexen-1-ol
trans-4-Hexen-1-ol
4-Hexen-2-ol
5-Hexen-2-ol
cis-3-Hexen-1-ol, acetate
trans-2-Hexen-1-ol, acetate
5-Hexen-2-one
4-Hexen-3-one
C6H12O
C6H12O
C6H12O
C6H12O
C8H14O2
C8H14O2
C6H10O
C6H10O
928-97-2
928-92-7
52387-50-5
626-94-8
3681-71-8
2497-18-9
109-49-9
2497-21-4
100.158
100.158
100.158
100.158
142.196 liq
142.196 liq
98.142
98.142
153(7)
159
137.5
139(6)
6612
165(11)
129.1(0.5)
138(7)
5883
Hexestrol
C18H22O2
84-16-2
270.367 nd (bz)
186.5
5884
5885
5886
Hexobarbital
Hexocyclium methyl sulfate
Hexyl acetate
C12H16N2O3
C21H36N2O5S
C8H16O2
56-29-1
115-63-9
142-92-7
236.266
428.586 cry
144.212 liq
145(1)
205
-61.0(0.2)
5887
sec-Hexyl acetate
4-Methyl-2-pentyl acetate
C8H16O2
108-84-9
144.212
5888
5889
Hexyl acrylate
Hexylamine
1-Hexanamine
C9H16O2
C6H15N
2499-95-8
111-26-2
156.222
101.190 liq
-45
-21(1)
401
132(1)
5890
Hexylbenzene
C12H18
1077-16-3
162.271 liq
-63.4(0.2)
226(2)
5891
4-Hexyl-1,3-benzenediol
C12H18O2
136-77-6
194.270 nd (bz)
68.3(0.2)
334
5892
Hexyl benzoate
C13H18O2
6789-88-4
206.281
5893
Hexyl butanoate
C10H20O2
2639-63-6
172.265 liq
-78.0(0.5)
207(3)
5894
5895
Hexylcyclohexane
Hexylcyclopentane
C12H24
C11H22
4292-75-5
4457-00-5
168.319 liq
154.293 liq
-47.5(0.2)
-73
225(1)
206(10)
5896
5897
2-Hexyldecanoic acid
Hexyl formate
C16H32O2
C7H14O2
25354-97-6 256.424 visc oil
629-33-4
130.185 liq
-62.6(0.4)
1450.02
154(5)
5898
Hexyl hexanoate
C12H24O2
6378-65-0
200.318 liq
-55.2(0.4)
241(4)
5899
5900
Hexyl isocyanate
Hexyl methacrylate
C7H13NO
C10H18O2
2525-62-4
142-09-6
127.184
170.249
5901
5902
5903
Hexyl methyl ether
1-Hexylnaphthalene
Hexyl octanoate
C7H16O
C16H20
C14H28O2
4747-07-3
2876-53-1
1117-55-1
116.201
212.330 liq
228.371 liq
-18
-31(1)
125(4)
322(9)
277(5)
5904
5905
4-(Hexyloxy)benzoic acid
2-(Hexyloxy)ethanol
C13H18O3
C8H18O2
1142-39-8
112-25-4
222.280 cry
146.228 liq
106
-45.1
208(2)
5906
Hexyl pentanoate
C11H22O2
1117-59-5
186.292 liq
-63.0(0.5)
225(4)
5907
5908
4-Hexylphenol
Hexyl propanoate
C12H18O
C9H18O2
2446-69-7
2445-76-3
178.270
158.238 liq
-57.5(0.5)
1489
188(3)
5909
C16H24
66325-11-9 216.362 liq
5910
1-Hexyl-1,2,3,4-tetrahydronaphthalene
1-Hexyne
Butylacetylene
C6H10
693-02-7
82.143
liq
-132.1(0.4)
71.2(0.3)
5911
2-Hexyne
1-Methyl-2-propylacetylene
C6H10
764-35-2
82.143
liq
-89.5(0.4)
84.3(0.5)
5912
3-Hexyne
Diethylacetylene
C6H10
928-49-4
82.143
liq
-104(3)
81.5(0.6)
5913
5914
3-Hexyne-2,5-diol
3-Hexyn-1-ol
3-Hexynol
C6H10O2
C6H10O
3031-66-1
1002-28-4
114.142
98.142
No.
Name
5872
HCP_Section_03.indb 300
Synonym
4-Hexylresorcinol
Hexyl caproate
Ethylene glycol monohexyl
ether
Physical
Form
mp/˚C
bp/˚C
171.1(0.7)
147.5
272
447
162
305
12115
162
den
g cm –3
nD
Solubility
0.847220 1.439720 s H2O; vs EtOH;
s eth, ace; sl
ctc
0.849016 1.434020
0.847822 1.438020 s H2O; vs EtOH,
eth
1.437420
0.851320 1.440220
0.840518 1.439220 sl H2O
0.84216
sl H2O
0.898
1.427020
0.83327 1.417827
0.855920 1.438820 s EtOH, eth; vs
ace
vs ace, eth,
EtOH
sl chl; i eth
0.877915 1.409220 i H2O; vs eth,
EtOH
0.880525 1.398020 sl H2O; vs eth,
EtOH
0.87820
0.766020 1.418020 sl H2O; msc
EtOH, eth; s
chl
0.857520 1.486420 i H2O; msc eth;
s bz, peth
vs ace, eth,
EtOH, chl
0.979320
i H2O; s EtOH,
ace
0.865220 1.416015 i H2O; s EtOH; sl
chl
0.807620 1.446220
0.796520 1.439220 vs ace, bz, eth,
EtOH
1.443224
0.881320 1.407120 i H2O; msc
EtOH, eth
0.86518 1.426415 vs ace, bz, eth,
EtOH
0.88025
1.42925
vs ace, bz, eth,
EtOH
0.956620 1.564720
0.860320 1.432325 i H2O; s EtOH,
eth, ace
0.887820 1.429120 sl H2O; vs EtOH,
eth
0.863520 1.422815 vs ace, eth,
EtOH
0.869820 1.416215 i H2O; s EtOH,
eth, ace,
AcOEt
0.917625 1.512725
0.715525 1.398920 i H2O; s EtOH,
eth, bz, chl; sl
ctc
20
20
0.7315
1.4138
i H2O; msc
EtOH, eth; s
bz, chl, peth
0.723120 1.411520 i H2O; s EtOH,
eth, bz, chl,
peth
1.018020 1.469120
0.898220 1.453020
4/11/16 11:30 AM
Physical Constants of Organic Compounds
OH
3-301
OH
OH
OH
5872
5873
cis-2-Hexen-1-ol
5874
trans-2-Hexen-1-ol
5875
cis-3-Hexen-1-ol
OH
OH
OH
5876
trans-3-Hexen-1-ol
5877
trans-4-Hexen-1-ol
5878
4-Hexen-2-ol
5-Hexen-2-ol
O
OH
O
NH
O
O
O
O
HO
O
5880
cis-3-Hexen-1-ol, acetate
O
O S O
O
5881
trans-2-Hexen-1-ol, acetate
5882
5-Hexen-2-one
5883
4-Hexen-3-one
N
O
5884
Hexestrol
Hexobarbital
Organic
5879
O
N
N
HO
O
O
O
5885
5886
Hexocyclium methyl sulfate
O
O
Hexyl acetate
NH2
O
5887
5889
5888
sec-Hexyl acetate
5890
Hexylamine
Hexyl acrylate
Hexylbenzene
OH
O
OH
O
O
O
5891
5892
4-Hexyl-1,3-benzenediol
5893
Hexyl benzoate
O
5894
Hexyl butanoate
OH
5895
Hexylcyclohexane
Hexylcyclopentane
O
O
5896
5897
2-Hexyldecanoic acid
N
O
O
5898
Hexyl formate
O
5899
Hexyl hexanoate
Hexyl isocyanate
O
O
C
OH
O
O
5900
5901
Hexyl methacrylate
O
O
O
5903
5902
Hexyl methyl ether
Hexyl octanoate
1-Hexylnaphthalene
5904
4-(Hexyloxy)benzoic acid
OH
O
O
OH
O
O
5905
5906
2-(Hexyloxy)ethanol
Hexyl pentanoate
O
5907
5908
4-Hexylphenol
Hexyl propanoate
HO
5909
1-Hexyl-1,2,3,4-tetrahydronaphthalene
OH
OH
5910
1-Hexyne
5911
2-Hexyne
5912
3-Hexyne
5913
3-Hexyne-2,5-diol
5914
3-Hexyn-1-ol
Physical Constants of Organic Compounds
3-302
Synonym
Organic
Mol. Form.
CAS RN
Mol.
Wt.
C6H10O
C6H8O
C5H9N3
105-31-7
2550-28-9
51-45-6
98.142 liq
96.127
111.145 wh nd (chl)
C6H9N3O2
71-00-1
155.154 nd or pl (dil 287 dec
al)
C6H10ClN3O2
645-35-2
191.615
245 dec
C16H21NO3
87-00-3
275.343 pr (al, eth)
99.5
C16H22BrNO3
51-56-9
848-53-3
454-29-5
356.255 orth pym or 217 dec
pl (w)
314.852 oil
135.185
272 dec
6027-13-0
135.185 platelets
232
870-93-9
672-15-1
268.354
119.119 pr (90% al)
264
203 dec
No.
Name
5915
5916
5917
1-Hexyn-3-ol
5-Hexyn-2-one
Histamine
5918
L-Histidine
5919
5920
L-Histidine, monohydrochloride
Homatropine
5921
Homatropine hydrobromide
Tropanol mandelate
5922
5923
Homochlorocyclizine
DL-Homocysteine
5924
L-Homocysteine
5925
5926
Homocystine
L-Homoserine
5927
5928
Humulene
Humulon
C19H23ClN2
DL-2-Amino-4-mercaptobuta- C4H9NO2S
noic acid
L-2-Amino-4-mercaptobutaC4H9NO2S
noic acid
C8H16N2O4S2
2-Amino-4-hydroxybutanoic
C4H9NO3
acid, (S)
C15H24
C21H30O5
5929
Hydralazine
1-Hydrazinophthalazine
5930
5931
5932
Hydramethylnon
Hydrastine
Hydrastinine
5933
5934
Hydrazinecarbothioamide
Hydrazinecarboxaldehyde
5935
Hydrazinecarboxamide
5936
5937
5940
Hydrazinecarboximidamide
1,2-Hydrazinedicarboxaldehyde
1,2-Hydrazinedicarboxamide
4-Hydrazinobenzenesulfonic
acid
4-Hydrazinobenzoic acid
5941
Glyoxaline-5-alanine
Physical
Form
mp/˚C
bp/˚C
-80
142
149
20918
83
s H2O; i eth, bz
sl H2O; i eth, bz
vs H2O; sl EtOH;
i eth, bz
86-54-4
172
CH5N3O
160.177 ye cry
(MeOH)
67485-29-4 494.476
118-08-1
383.395 ye pr (al)
6592-85-4 207.226 nd (lig), cry
(eth)
79-19-6
91.136 lo nd (w)
624-84-0
60.055 ye lf or nd
(al)
57-56-7
75.070 pr (al)
CH6N4
C2H4N2O2
79-17-4
628-36-4
74.086
88.065
dec
161.0
C2H6N4O2
C6H8N2O3S
110-21-4
98-71-5
118.095 pl (w)
188.204 nd, lf (w)
248(1)
286
C7H8N2O2
619-67-0
221 dec
2-Hydrazinoethanol
C2H8N2O
109-84-2
152.151 ye nd or pl
(w)
76.097 liq
5942
5943
5944
5945
Hydrindantin
Hydrochlorothiazide
Hydrocinchonidine
Hydrocinchonine
C18H10O6
C7H8ClN3O4S2
C19H24N2O
C19H24N2O
5103-42-4
58-93-5
485-64-3
485-65-4
322.268 pr (ace)
297.740
296.406 lf (al)
296.406 pr
250 dec
274
229
268.5
5946
5947
Hydrocodone
Hydrocortisone
C18H21NO3
C21H30O5
125-29-1
50-23-7
198
220
5948
5949
Hydrocortisone 21-acetate
Hydrocotarnine
C23H32O6
C12H15NO3
50-03-3
550-10-7
299.365
362.460 pl (al or
i-PrOH)
404.496
221.252
5950
5951
Hydroflumethiazide
Hydrofuramide
C8H8F3N3O4S2
C15H12N2O3
135-09-1
494-47-3
331.293
268.267 nd (al)
270.5
117
5952
Hydrogen cyanide
CHN
74-90-8
27.026
-13.28(0.09) 25.63(0.04)
5953
Hydrohydrastinine
5954
5955
5956
Hydromorphone
Hydroprene
Hydroquinidine
5957
Hydroquinine
5938
5939
HCP_Section_03.indb 302
Thiosemicarbazide
Aminoguanidine
Phenylhydrazine-4-sulfonic
acid
Cortisol acetate
Hydrocyanic acid
CH5N3S
CH4N2O
C17H19NO3
C17H30O2
C20H26N2O2
vol liq or
gas
494-55-3
191.227 nd (lig), cry
(peth)
466-99-9
285.338 cry (EtOH)
41096-46-2 266.419
1435-55-8 326.432 nd (al)
C20H26N2O2
522-66-7
C11H13NO2
7,8-Dihydromorphin-6-one
cry
pr (al)
12310
0.890520 1.503820
sl H2O; s EtOH,
eth, ace, bz,
alk
s acid
193.3(0.5)
132
116.5
183
54
96
-70
1.4848
i H2O; s ace, bz
s H2O; vs EtOH,
eth, chl
vs H2O, EtOH
vs bz, eth,
EtOH, chl
vs H2O; s EtOH;
i eth, bz, chl
vs H2O, EtOH
vs H2O; sl EtOH,
DMSO; i eth
1.60417
sl H2O, EtOH
sl H2O; i eth
219
1.11925
vs H2O, EtOH,
MeOH
vs EtOH
s H2O; sl EtOH; i
eth
i H2O; s EtOH
sl H2O; s EtOH,
diox, HOAc
223 dec
56
66
Solubility
1770.8
66.5
C25H24F6N4
C21H21NO6
C11H13NO3
nD
0.870420 1.434025 s ctc
0.906520 1.436620
s H2O, EtOH,
chl; sl eth
s H2O; sl EtOH; i
eth, ace, bz,
chl
s H2O
sl H2O, bz; s
EtOH, eth, ace,
chl
vs H2O, EtOH
6753-98-6 204.352
26472-41-3 362.460 ye cry (eth)
C8H8N4
den
g cm –3
1.28920
i H2O; s EtOH,
eth, ace, bz,
chl
0.687620 1.261420
303
i H2O; vs EtOH,
eth
msc H2O, EtOH,
eth
vs ace, bz, eth,
EtOH
266.5
17419
168.5
326.432 nd (eth, chl) 172.5
0.895520
s EtOH, eth,
ace, chl
vs ace, eth,
EtOH, chl
4/11/16 11:30 AM
Physical Constants of Organic Compounds
3-303
N
N
O
H2N
HO
N
O
OH
N
NH2
N
H
5915
5916
1-Hexyn-3-ol
5-Hexyn-2-one
O
O
N
H
5919
L-Histidine
Histamine
NH2
OH
OH
N
HO
HCl
N
H
5918
5917
HBr
O
L-Histidine, monohydrochloride
O
O
5920
5921
Homatropine
Homatropine hydrobromide
Cl
N
HS
OH
N
OH
NH2
5922
OH
S
NH2
HO
OH
O
5924
NH2
5925
L-Homocysteine
5926
Homocystine
5927
L-Homoserine
Humulene
Organic
DL-Homocysteine
O
NH2
S
HO
NH2
5923
Homochlorocyclizine
O
O
O
HS
HN
OH O
HO
O
N
N
N
N
O
HO
NH
F
HN
F
NH2
F
O
O
F
O
H2N
OH
5932
5931
Hydramethylnon
S
N
O
O
O
5930
Hydralazine
N
H
H
F
F
5929
5928
Humulon
O
Hydrazinecarbothioamide
OH
O S O
O
H
O
N
H
NH2
H2N
5934
Hydrazinecarboxaldehyde
NH
NH2
N
H
H2N
5935
N
H
5936
Hydrazinecarboxamide
H
N
O
NH2
O
N
H
H2N
O
5937
Hydrazinecarboximidamide
N
H
H
N
O
OH
NH2
HN
O
5938
1,2-Hydrazinedicarboxaldehyde
NH2
5933
Hydrastinine
Hydrastine
N
H
HN
NH2
5939
1,2-Hydrazinedicarboxamide
NH2
5940
4-Hydrazinobenzenesulfonic acid
4-Hydrazinobenzoic acid
O
O
O
Cl
OH
H2N
H
N
H2N
HO
OH
O
5941
S
S
O O
O
5942
2-Hydrazinoethanol
H
N
HO
H
N
H
N
O
NH
H
O O
N
5943
Hydrindantin
HO
Hydrochlorothiazide
O
N
5944
5945
Hydrocinchonidine
N
5946
Hydrocinchonine
Hydrocodone
O
O
HO
O
OH
OH
HO
H
O
OH
H
F
O
O
O
5947
5948
Hydrocortisone
F
H2N
N
O
O
Hydrocortisone 21-acetate
H
N
F
S
S
O O
5949
O
NH
N
O
O
O O
5950
Hydrocotarnine
N
HC N
5951
Hydroflumethiazide
5952
Hydrofuramide
Hydrogen cyanide
HO
HO
O
O
N
O
5953
Hydrohydrastinine
H
O
N
O
O
5954
Hydromorphone
5955
Hydroprene
H
O
N
5956
HO
N
Hydroquinidine
H
O
N
N
5957
Hydroquinine
Physical Constants of Organic Compounds
3-304
bp/˚C
den
g cm –3
nD
Solubility
288(5)
1.33020
1.63225
s H2O, eth; vs
EtOH, ace; i bz
C2H3NO
110.111 mcl pr (sub) 173(2)
nd(w) pr
(MeOH)
13422-51-0 1346.355 red cry (ace 200 dec
aq)
107-16-4
57.051
<-72
C8H8O2
582-24-1
12512
Stanolone
C19H30O2
521-18-6
Androsterone
C19H30O2
53-41-8
290.440 lf or nd (al,
ace)
185
Epiandrosterone
C19H30O2
481-29-8
290.440 cry
(bz-peth,
ace)
288.424 nd (dil ace)
178
Name
Synonym
Mol. Form.
CAS RN
5958
p-Hydroquinone
1,4-Benzenediol
C6H6O2
123-31-9
5959
Hydroxocobalamin
Vitamin B-12a
C62H89CoN13O15P
5960
Hydroxyacetonitrile
Glyconitrile
5961
(Hydroxyacetyl)benzene
5962
17-Hydroxyandrostan-3-one,
(5α,17β)
3-Hydroxyandrostan-17-one,
(3α,5α)
5963
Organic
mp/˚C
No.
Mol.
Wt.
Physical
Form
136.149 hex pl (al), 90
pl (w or dil
al)
290.440
181
183 dec
sl H2O, chl; s
EtOH, eth, ace,
bz
3-Hydroxyandrostan-17-one,
(3β,5α)
5965
17-Hydroxyandrost-4-en-3Testosterone
one, (17β)
1-Hydroxy-9,10-anthracenedione
C19H28O2
58-22-0
C14H8O3
129-43-1
224.212 red-oran nd 193.8
(al)
sub
5967
2-Hydroxy-9,10-anthracenedione
C14H8O3
605-32-3
306
sub
5968
3-Hydroxybenzaldehyde
3-Formylphenol
C7H6O2
100-83-4
224.212 ye pl or nd
(al or
HOAc)
122.122 nd (w)
106.0(0.2)
240
5969
4-Hydroxybenzaldehyde
4-Formylphenol
C7H6O2
123-08-0
122.122 nd (w)
116.0(0.2)
5970
C14H12N2O2
959-36-4
240.257
214
5971
2-Hydroxybenzaldehyde,
[(2-hydroxyphenyl)­
methylene]hydrazone
2-Hydroxybenzamide
C7H7NO2
65-45-2
137.137
140(2)
5972
N-Hydroxybenzamide
C7H7NO2
495-18-1
131 exp
5973
C8H8O3
611-72-3
5974
α-Hydroxybenzeneacetic acid, DL-Mandelic acid
(±)2-Hydroxybenzeneacetic acid
137.137 orth ta, lf
(eth)
152.148 orth pl
C8H8O3
614-75-5
152.148
147(3)
240
5975
3-Hydroxybenzeneacetic acid
C8H8O3
621-37-4
152.148 nd (bz-lig)
132
19011
5976
4-Hydroxybenzeneacetic acid
C8H8O3
156-38-7
152.148 nd (w)
150.2(0.8)
sub
5977
α-Hydroxybenzeneacetonitrile
Mandelonitrile
C8H7NO
532-28-5
133.148 ye oily liq
-10
5978
2-Hydroxybenzenecarbodithioic acid
4-Hydroxy-1,3-benzenedicarboxylic acid
Dithiosalicylic acid
C7H6OS2
527-89-9
170.252 oran-ye nd
49
4-Hydroxyisophthalic acid
C8H6O5
636-46-4
182.131 nd(w), lf (dil 310
al)
C8H6O5
618-83-7
Phenoldisulfonic acid
C6H6O7S2
96-77-5
182.131 nd(w+2)
cr(aq-al)
254.238 nd (w)
Salicyl alcohol
C8H10O2
C7H8O2
501-94-0
90-01-7
5979
5980
Salicylamide
5982
5983
5-Hydroxy-1,3-benzenedicarboxylic acid
4-Hydroxy-1,3-benzenedisulfonic acid
4-Hydroxybenzeneethanol
2-Hydroxybenzenemethanol
5984
3-Hydroxybenzenemethanol
3-Hydroxybenzyl alcohol
C7H8O2
620-24-6
5985
4-Hydroxybenzenemethanol
4-Hydroxybenzyl alcohol
C7H8O2
5986
4-Hydroxybenzenepropanoic
acid
α-Hydroxybenzenepropanoic
acid, (±)3-Hydroxybenzenesulfonic
acid
4-Hydroxybenzenesulfonic
acid
p-Hydroxyhydrocinnamic acid
5981
5987
5988
5989
HCP_Section_03.indb 304
1.096399
135 sub
5964
5966
1.411719
s H2O, EtOH; i
ace, eth, bz
vs H2O, EtOH,
eth; i bz, chl
s H2O, EtOH,
eth, chl; sl lig
151.0(0.3)
1.1179130
1.129130
181.514
118.6(1)
1.175140
1.289020
1.12
1.5705130
i H2O; s EtOH,
eth, ace
i H2O; s EtOH,
eth, bz; sl liq
NH3
i H2O; s EtOH,
eth, aq NH3,
KOH
sl H2O; s EtOH,
eth, ace, bz; i
lig
sl H2O, ace; vs
EtOH, eth; s bz
i H2O; s EtOH,
chl; vs bz, alk
sl H2O, eth,
DMSO; s EtOH
s H2O, EtOH; sl
eth, bz
s H2O, eth,
EtOH, i-PrOH
sl H2O, chl; s
eth
vs H2O, EtOH,
eth; s bz; sl lig
sl H2O; vs EtOH,
eth
i H2O; vs chl,
eth, EtOH
vs bz, eth, EtOH
i H2O, chl; vs
EtOH, eth; s
HOAc
vs bz, eth, EtOH
sub
>100 dec
vs H2O, EtOH
90(3)
87
310.0
sub
1.161325
73
300 dec
1.16125
623-05-2
138.164
124.138 lf (bz), nd or
pl (w, eth)
124.138 nd (bz), cry
(CCl4)
124.138 pr or nd (w)
124.5
252
C9H10O3
501-97-3
166.173
129.3(0.5)
20914
(±)-3-Phenyllactic acid
C9H10O3
828-01-3
m-Phenolsulfonic acid
C6H6O4S
585-38-6
166.173 cry (chl, bz), 98
pr (w)
174.175 nd (w+2)
p-Phenolsulfonic acid
C6H6O4S
98-67-9
174.175 nd
14915
s H2O, EtOH,
eth, bz; vs chl
vs H2O, EtOH,
eth; sl chl
vs H2O, EtOH,
bz, chl; s eth;
sl DMSO
s H2O, EtOH,
eth, bz; i CS2
vs H2O, ace,
eth, EtOH
vs H2O, EtOH
4/11/16 11:30 AM
Physical Constants of Organic Compounds
O
NH2
3-305
NH2
O
O
H 2N
H
H2N
OH
N
O
Co
NH2
N
N
N
O
O
NH2
O
N
NH
O
OH
H
5958
OH
OH
O
N
5959
5960
Hydroxocobalamin
5961
Hydroxyacetonitrile
HO
H
5962
(Hydroxyacetyl)benzene
H
5963
17-Hydroxyandrostan-3-one, (5α,17β)
3-Hydroxyandrostan-17-one, (3α,5α)
Organic
p-Hydroquinone
O
O
HO
O
HO
OH
N
O
P O HO
O
O
OH
O
O
O
OH
H
HO
H
O
5964
5966
17-Hydroxyandrost-4-en-3-one, (17β)
N
5967
1-Hydroxy-9,10-anthracenedione
O
OH
N
OH
2-Hydroxybenzaldehyde, [(2-hydroxyphenyl)methylene]hydrazone
OH
OH
OH
O
OH
O
5972
2-Hydroxybenzamide
4-Hydroxybenzaldehyde
OH
N
H
OH
5969
3-Hydroxybenzaldehyde
O
5971
OH
5968
2-Hydroxy-9,10-anthracenedione
NH2
5970
OH
O
O
5965
3-Hydroxyandrostan-17-one, (3β,5α)
O
OH
5973
α-Hydroxybenzeneacetic acid, (±)-
N-Hydroxybenzamide
5974
2-Hydroxybenzeneacetic acid
O
OH
OH
OH
SH
OH
O
HO
5975
3-Hydroxybenzeneacetic acid
O
OH
OH
O
S
OH
N
5976
OH O
5977
5978
α-Hydroxybenzeneacetonitrile
4-Hydroxybenzeneacetic acid
5979
2-Hydroxybenzenecarbodithioic acid
4-Hydroxy-1,3-benzenedicarboxylic acid
OH
O S O
OH
OH
OH
O
OH
HO
O
OH
5980
S
O OH
5981
5-Hydroxy-1,3-benzenedicarboxylic acid
4-Hydroxy-1,3-benzenedisulfonic acid
OH
OH
5982
4-Hydroxybenzeneethanol
OH
O
5985
4-Hydroxybenzenemethanol
5983
2-Hydroxybenzenemethanol
5986
4-Hydroxybenzenepropanoic acid
3-Hydroxybenzenemethanol
OH
OH
HO
5984
OH
O S O
OH
O S O
O
OH
OH
OH
HO
5987
α-Hydroxybenzenepropanoic acid, (±)-
OH
5988
3-Hydroxybenzenesulfonic acid
OH
5989
4-Hydroxybenzenesulfonic acid
Physical Constants of Organic Compounds
3-306
Mol.
Wt.
Physical
Form
mp/˚C
bp/˚C
den
g cm –3
nD
Solubility
158.6(0.5)
21120
1.44320
1.565
sl H2O, bz, chl,
ctc; vs EtOH,
eth, ace
sl H2O; s EtOH,
eth, ace; i bz
sl H2O, bz; vs
EtOH; s eth,
ace
vs bz, EtOH
Organic
No.
Name
Synonym
Mol. Form.
CAS RN
5990
2-Hydroxybenzoic acid
Salicylic acid
C7H6O3
69-72-7
138.121 nd (w), mcl
pr (al)
5991
3-Hydroxybenzoic acid
C7H6O3
99-06-9
5992
4-Hydroxybenzoic acid
C7H6O3
99-96-7
5993
C7H8N2O2
936-02-7
5994
2-Hydroxybenzoic acid,
hydrazide
2-Hydroxybenzonitrile
138.121 nd (w) pl, pr 201.3(0.2)
(al)
138.121 pr or pl (w, 213(2)
al) cry
(ace)
152.151
148
C7H5NO
611-20-1
119.121
5995
3-Hydroxybenzonitrile
C7H5NO
873-62-1
5996
4-Hydroxybenzonitrile
C7H5NO
767-00-0
119.121 pr (al, eth) lf 82.8
(w)
119.121 lf (w)
113
5997
4-Hydroxybenzophenone
C13H10O2
1137-42-4
5998
C9H6O3
6003
4-Hydroxy-2H-1-benzopyran2-one
7-Hydroxy-2H-1-benzopyran- Umbelliferone
2-one
1-Hydroxy-1H-benzotriazole
2-Hydroxybenzoyl chloride
4-Salicyloylmorpholine
4-(2-Hydroxybenzoyl)­
morpholine
2-Hydroxybiphenyl
[1,1’-Biphenyl]-2-ol
6004
3-Hydroxybiphenyl
6005
98
1.48525
1.4625
14914
1481
1.1052100 1.5372100 sl H2O; vs EtOH,
eth, bz, chl
vs H2O, EtOH,
eth, bz, chl
sl H2O, DMSO;
vs EtOH, eth,
chl
1.133172
sl H2O; vs EtOH,
eth, HOAc
s H2O, EtOH,
eth; sl DMSO
vs EtOH, HOAc,
chl
135
1076-38-6
198.217 nd (al), pr
(dil al)
162.142 nd (w)
C9H6O3
93-35-6
162.142 nd (w)
230.5
sub
C6H5N3O
C7H5ClO2
C11H10NO3
2592-95-2
1441-87-8
3202-84-4
135.123
156.567
204.202
157.8
19
9215
1.311220 1.581220 vs eth
s DMSO
C12H10O
90-43-7
170.206
57.6(0.7)
281(3)
1.21325
[1,1’-Biphenyl]-3-ol
C12H10O
580-51-8
170.206
78
>300
4-Hydroxybiphenyl
[1,1’-Biphenyl]-4-ol
C12H10O
92-69-3
170.206
170.0(0.5)
305
6006
3-Hydroxybutanal
Aldol
C4H8O2
107-89-1
88.106
6007
6008
2-Hydroxybutanoic acid, (±)3-Hydroxybutanoic acid, (±)-
C4H8O3
C4H8O3
600-15-7
625-71-8
104.105
104.105
6009
6010
4-Hydroxybutanoic acid
1-Hydroxy-2-butanone
C4H8O3
C4H8O2
591-81-1
5077-67-8
104.105
88.106
6011
3-Hydroxy-2-butanone, (±)-
C4H8O2
52217-02-4 88.106
6012
4-Hydroxy-2-butanone
C4H8O2
590-90-9
6013
6014
6015
2-Hydroxy-3-butenenitrile
4-Hydroxybutyramide
3-Hydroxycamphor
5999
6000
6001
6002
6016
6017
6018
6019
6020
6021
6022
6023
6024
6025
4-Hydroxyphenyl phenyl
ketone
Acetoin
C4H5NO
C4H9NO2
3-Hydroxy-1,7,7-trimethylbicy- C10H16O2
clo[2.2.1]heptan-2-one
3-Hydroxycholan-24-oic acid, Lithocholic acid
C24H40O3
(3α,5β)
Hydroxycodeinone
2-Hydroxycyclodecanone
2-Hydroxy-2,4,6-cycloheptatrien-1-one
1-Hydroxycyclohexanecarbonitrile
2-Hydroxycyclohexanone
1-(1-Hydroxycyclohexyl)­
ethanone
4-Hydroxydecanoic acid
γ-lactone
2-Hydroxy-3,5-diiodobenzoic
acid
4-Hydroxy-3,5-diiodobenzoic
acid
HCP_Section_03.indb 306
213.5
8320
1.10320
44.2
49
260 dec
13012
1.12520
<-17
180 dec
160
15
88.106
148
182
5809-59-6 83.089 liq
927-60-6
103.120
52
10373-81-6 168.233 nd (bz-peth) 205.5
1.027220 1.418920 vs H2O, EtOH,
eth
1.004420 1.417120 msc H2O; sl
EtOH, eth; s
ace, chl; i lig
1.023320 1.458514 msc H2O, EtOH,
eth; vs ace
vs eth, EtOH,
chl
i H2O, lig; s
EtOH, chl,
HOAc; sl eth
376.573 hex lf (al) pr 188(4)
(dil al)
C18H19NO4
C10H18O2
C7H6O2
508-54-3
96-00-4
533-75-5
313.349
170.249 cry (peth)
122.122 nd
275 dec
38.5
50(1)
13614
40 sub
C7H11NO
931-97-5
125.168
35
13220
C6H10O2
533-60-8
114.142 nd (al)
C8H14O2
1123-27-9
142.196
125.5
5-Hexyldihydro-2(3H)-furanone C10H18O2
706-14-9
170.249 liq
301(8)
C7H4I2O3
133-91-5
389.914 nd (al)
235.5
C7H4I2O3
618-76-8
389.914
237
3,5-Diiodosalicylic acid
1.442420
9417
434-13-9
Sebacoin
1.423820
i H2O; s EtOH,
ace, bz; vs
eth, py
sl H2O; vs EtOH,
eth, bz, py; s
chl
sl H2O, DMSO;
vs EtOH, eth,
chl, py
msc H2O, EtOH;
s eth; vs ace
s H2O, EtOH, eth
vs H2O, EtOH,
eth; i bz
260 dec
s H2O, eth, ace
1.017220 1.469320 vs H2O, eth
1.024825
1.478521 vs H2O, EtOH; i
eth, bz, peth
1.467025 vs eth, EtOH
sl H2O; vs EtOH,
eth; i bz, chl
i H2O; vs EtOH,
eth; sl bz, chl,
lig
4/11/16 11:30 AM
Physical Constants of Organic Compounds
O
OH
N
O
OH
NH2
NH
O
OH
N
N
OH
OH
OH
5990
2-Hydroxybenzoic acid
OH
5991
3-Hydroxybenzoic acid
O
5993
4-Hydroxybenzoic acid
5994
2-Hydroxybenzoic acid, hydrazide
5995
2-Hydroxybenzonitrile
OH
O
O
N
5997
O
HO
5998
4-Hydroxybenzophenone
O
Cl
5999
4-Hydroxy-2H-1-benzopyran-2-one
6004
2-Hydroxybiphenyl
4-(2-Hydroxybenzoyl)morpholine
3-Hydroxybutanal
4-Hydroxybiphenyl
O
6013
4-Hydroxy-2-butanone
HO
OH
6009
4-Hydroxybutanoic acid
OH
O
HO
N
6012
3-Hydroxy-2-butanone, (±)-
3-Hydroxybutanoic acid, (±)-
OH
HO
6011
6008
2-Hydroxybutanoic acid, (±)-
O
O
OH
6007
OH
1-Hydroxy-2-butanone
OH
6002
OH O
OH
6006
OH
O
2-Hydroxybenzoyl chloride
OH
O
6005
3-Hydroxybiphenyl
6010
6001
1-Hydroxy-1H-benzotriazole
OH
OH
6003
N
O
OH
HO
O
O
6000
7-Hydroxy-2H-1-benzopyran-2-one
4-Hydroxybenzonitrile
OH
N
OH
O
5996
3-Hydroxybenzonitrile
N
HO
OH
OH
5992
NH2
O
6014
2-Hydroxy-3-butenenitrile
6015
4-Hydroxybutyramide
3-Hydroxycamphor
O
O
OH
H
O
OH
HO
O
H
6016
Hydroxycodeinone
6018
2-Hydroxycyclodecanone
6019
2-Hydroxy-2,4,6-cycloheptatrien-1-one
6020
1-Hydroxycyclohexanecarbonitrile
O
O
O
OH
O
6021
6022
1-(1-Hydroxycyclohexyl)ethanone
OH
OH
OH
OH
O
2-Hydroxycyclohexanone
N
HO
OH
OH
6017
3-Hydroxycholan-24-oic acid, (3α,5β)
O
O
N
6023
O
4-Hydroxydecanoic acid γ-lactone
I
I
I
6024
2-Hydroxy-3,5-diiodobenzoic acid
I
OH
6025
4-Hydroxy-3,5-diiodobenzoic acid
Organic
HO
O
3-307
Physical Constants of Organic Compounds
3-308
No.
Name
6026
4-Hydroxy-3,5-diiodobenzonitrile
Iodoalphionic acid
4-Hydroxy-3,5-diiodo-αphenylbenzenepropanoic
acid
2-Hydroxy-4,6-dimethoxybenzaldehyde
6027
6028
6029
4-Hydroxy-3,5-dimethoxybenzaldehyde
6030
4-Hydroxy-3,5-dimethoxybenzoic acid
7-Hydroxy-3,7-dimethyloctanal
3-Hydroxy-2,2-dimethylpropanal
2-Hydroxy-3,5-dinitrobenzoic
acid
11-Hydroxy-9,15-dioxoprosta5,13-dien-1-oic acid,
(5Z,11α,13E)1-Hydroxy-1,1-diphosphonoethane
3-Hydroxyestra-1,3,5,7,9pentaen-17-one
3-Hydroxyestra-1,3,5(10),7tetraen-17-one
6031
6032
Organic
6033
6034
6035
6036
6037
6038
6039
6040
6041
6042
6043
6044
6045
Synonym
Syringaldehyde
Hydroxypivaldehyde
Mol. Form.
CAS RN
Mol.
Wt.
Physical
Form
C7H3I2NO
1689-83-4
370.914
215.8(0.5)
C15H12I2O3
577-91-3
494.063
164
C9H10O4
708-76-9
182.173
70
19325
C9H10O4
134-96-3
182.173 br nd (lig)
113
19214
C9H10O5
530-57-4
198.172 nd (w)
204.5
C10H20O2
107-75-5
172.265
C5H10O2
597-31-9
102.132 nd (w)
C7H4N2O7
609-99-4
mp/˚C
bp/˚C
15-Oxo-prostaglandin E2
C20H30O5
Etidronic acid
C2H8O7P2
2809-21-4
206.028 cry (w)
105
s H2O, EtOH,
MeOH
sl EtOH, ace,
chl
sl H2O; s EtOH,
ace, diox,
AcOEt
Equilenin
C18H18O2
517-09-9
266.335
258.5
170 sub
Equilin
C18H20O2
474-86-2
268.351 pl (AcOEt)
239
170 sub
C5H8O3
C14H29NO2
818-61-1
142-78-9
116.116 liq
243.386
88.5
C10H18N2O7
150-39-0
278.259 cry
165 dec
C9H10O4
87-28-5
182.173
37
C6H10O3
868-77-9
C10H9NO3
C6H11NO2
191
1.01123
17315
1.252615
130.141
10313
1.07920
3891-07-4
3445-11-2
191.183 nd (al), lf (w) 130.3
129.157
20
295
1.143520
C7H6O4
149-29-1
154.121 pl or pr (eth, 111
chl)
272.423
96.5
6047
6048
6049
2-Hydroxyhexanoic acid
6-Hydroxyhexanoic acid
3-Hydroxy-2-(hydroxymethyl)- Dimethylolpropionic acid
2-methylpropanoic acid
5-Hydroxy-2-(hydroxymethyl)- Kojic acid
4H-pyran-4-one
C6H12O3
C6H12O3
C5H10O4
6064-63-7
1191-25-9
4767-03-7
132.157 pr (eth)
132.157 liq
134.131
60
195.5(0.5)
C6H6O4
501-30-4
142.110 pr nd (ace)
153.5
C9H6INO4S
547-91-1
351.118 ye pr, lf (al)
260 dec
C8H5NO3
524-38-9
163.131
232
C10H12O2
499-44-5
164.201 pa ye (peth) 51(2)
C15H24N2O2
15358-48-2 264.364 cry (ace)
169.5
CH5NO
C8H8O3
593-77-1
148-53-8
87.5
40.5(0.4)
C8H8O3
673-22-3
C8H8O3
672-13-9
47.057 hyg nd
152.148 lt ye lf, grn
nd (w, lig)
152.148 nd (w), cry
(al)
152.148 ye liq (w)
4
247.5
C8H8O3
621-59-0
152.148
117(3)
17915
6052
2-Hydroxy-1H-isoindole1,3(2H)-dione
2-Hydroxy-4-isopropyl-2,4,6cycloheptatrien-1-one
Hydroxylupanine
6053
6054
6055
6056
6057
6058
6059
N-Hydroxymethanamine
2-Hydroxy-3-methoxybenzaldehyde
2-Hydroxy-4-methoxybenzaldehyde
2-Hydroxy-5-methoxybenzaldehyde
3-Hydroxy-4-methoxybenzaldehyde
HCP_Section_03.indb 308
N-Methylhydroxylamine
1.451520
s H2O, EtOH,
eth, ace, bz; i
peth
i H2O; s EtOH,
ace; sl eth, bz
vs H2O
506-13-8
Ferron
sl H2O; vs EtOH,
eth, bz, chl
sl H2O
C16H32O3
8-Hydroxy-7-iodo-5-quinolinesulfonic acid
0.922020 1.449420 sl H2O; s EtOH,
ace
s H2O, EtOH,
eth, bz
16-Hydroxyhexadecanoic acid 16-Hydroxypalmitic acid
6051
i H2O; vs EtOH,
eth, bz, chl,
HOAc
sl H2O, lig; vs
EtOH, eth, bz,
chl
sl H2O; vs EtOH
182
6046
6050
Solubility
173
228.116 ye nd or pl
(+1w)
26441-05-4 350.449 cry
2-Hydroxyethyl acrylate
2-Hydroxyethyl 2-propenoate
N-(2-Hydroxyethyl)­
dodecanamide
N-(2-Hydroxyethyl)­
ethylenediaminetriacetic acid
2-Hydroxyethyl 2-hydroxyben- Glycol salicylate
zoate
2-Hydroxyethyl methacrylate Ethylene glycol monomethacrylate
N-(2-Hydroxyethyl)phthalimide
1-(2-Hydroxyethyl)-2-pyrrolidinone
4-Hydroxy-4H-furo[3,2-c]­
Patulin
pyran-2(6H)-one
nD
i H2O; s EtOH,
eth; sl bz, chl
1033
89.5
den
g cm –3
sl H2O, bz; s
EtOH, eth, ace,
DMSO
sl H2O, EtOH; i
eth, bz, chl; s
con sulf
s DMSO
13710
1.060665
62.515
265.5
1.000320 1.416420
42.0
1.19625
sl H2O, bz, lig; s
ctc
vs H2O, EtOH,
chl
vs H2O, EtOH
sl H2O, lig; vs
EtOH, eth, ctc
s EtOH, eth, bz,
lig
vs eth, EtOH
sl H2O; s EtOH,
eth, bz, HOAc;
vs chl
4/11/16 11:30 AM
Physical Constants of Organic Compounds
3-309
N
O
O
I
OH
OH
HO
I
I
6026
O
OH
6028
6027
4-Hydroxy-3,5-diiodobenzonitrile
O
O
I
OH
HO
O
O
6029
2-Hydroxy-4,6-dimethoxybenzaldehyde
4-Hydroxy-3,5-diiodo-α-phenylbenzenepropanoic acid
4-Hydroxy-3,5-dimethoxybenzaldehyde
HO
O
O
OH
O
OH
OH
6030
6031
4-Hydroxy-3,5-dimethoxybenzoic acid
6032
7-Hydroxy-3,7-dimethyloctanal
O
O
HO
N
O
O
6033
3-Hydroxy-2,2-dimethylpropanal
2-Hydroxy-3,5-dinitrobenzoic acid
O
O
O
OH
HO
HO
N
O
HO
P
HO
O
O
6034
OH
P
OH
O
HO
11-Hydroxy-9,15-dioxoprosta-5,13-dien-1-oic acid, (5Z,11α,13E )-
HO
6036
6035
6037
3-Hydroxyestra-1,3,5,7,9-pentaen-17-one
1-Hydroxy-1,1-diphosphonoethane
3-Hydroxyestra-1,3,5(10),7-tetraen-17-one
COOH
H
N
O
HO
O
OH
OH
O
6042
2-Hydroxyethyl 2-hydroxybenzoate
OH
O
N
OH
O
O
6044
N-(2-Hydroxyethyl)phthalimide
6045
1-(2-Hydroxyethyl)-2-pyrrolidinone
4-Hydroxy-4H-furo[3,2-c]pyran-2(6H )-one
HO
O
O
HO
HO
OH
6046
6047
O
HO
O
6050
5-Hydroxy-2-(hydroxymethyl)-4H-pyran-4-one
6052
2-Hydroxy-1H-isoindole-1,3(2H )-dione
OH
6055
N-Hydroxymethanamine
O
6056
2-Hydroxy-3-methoxybenzaldehyde
H
O
6057
2-Hydroxy-4-methoxybenzaldehyde
OH
6054
Hydroxylupanine
O
O
OH
OH
N
O
6053
2-Hydroxy-4-isopropyl-2,4,6-cycloheptatrien-1-one
O
O
H
N
H
N
O
OH
8-Hydroxy-7-iodo-5-quinolinesulfonic acid
OH
N OH
N
6051
3-Hydroxy-2-(hydroxymethyl)-2-methylpropanoic acid
O
O
I
6049
6-Hydroxyhexanoic acid
OH
O S O
OH
O
OH
6048
2-Hydroxyhexanoic acid
OH
HO
O
OH
OH
16-Hydroxyhexadecanoic acid
O
O
OH
6043
2-Hydroxyethyl methacrylate
6041
N-(2-Hydroxyethyl)ethylenediaminetriacetic acid
O
N
OH
O
6040
N-(2-Hydroxyethyl)dodecanamide
O
COOH
HO
6039
2-Hydroxyethyl acrylate
OH O
N
O
6038
N
HOOC
OH
OH
O
O
6058
2-Hydroxy-5-methoxybenzaldehyde
6059
3-Hydroxy-4-methoxybenzaldehyde
Organic
O
O
O
Physical Constants of Organic Compounds
3-310
No.
Name
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
6060
4-Hydroxy-3-methoxybenzaldehyde
Vanillin
C8H8O3
121-33-5
6061
4-Hydroxy-3-methoxybenzeneacetic acid
4-Hydroxy-3-methoxybenzenemethanol
4-Hydroxy-3-methoxybenzenepropanol
2-Hydroxy-5-methoxybenzoic
acid
4-Hydroxy-3-methoxybenzoic
acid
7-Hydroxy-6-methoxy-2H-1benzopyran-2-one
4-(4-Hydroxy-3methoxyphenyl)-2-butanone
1-(2-Hydroxy-4-methoxyphenyl)ethanone
1-(4-Hydroxy-3-methoxyphenyl)ethanone
Homovanillic acid
C9H10O4
6062
6063
6064
6065
6066
6067
Organic
6068
6069
6070
6071
6072
6073
6074
6075
6076
6077
6078
6079
6080
6081
6082
6083
6084
6085
6086
6087
6088
6089
6090
6091
6092
(2-Hydroxy-4-methoxyphenyl)­
phenylmethanone
3-(4-Hydroxy-3methoxyphenyl)-2-propenal
N-Hydroxymethylamine
hydrochloride
4-Hydroxy-α-[(methylamino)­
methyl]benzenemethanol
17-Hydroxy-17-methylandrostan-3-one, (5α,17β)
N-Hydroxy-4-methylaniline
2-Hydroxy-5-methylbenzaldehyde
α-(Hydroxymethyl)­
benzeneacetic acid, (±)α-Hydroxy-αmethylbenzeneacetic acid,
(±)2-Hydroxy-5-methyl-1,3benzenedimethanol
2-(Hydroxymethyl)-1,4benzenediol
2-Hydroxy-5-methylbenzoic
acid
2-Hydroxy-3-methylbenzoic
acid
2-Hydroxy-4-methylbenzoic
acid
7-Hydroxy-4-methyl-2H-1benzopyran-2-one
3-Hydroxy-3-methylbutanoic
acid
3-Hydroxy-3-methyl-2butanone
2-Hydroxy-3-methyl-2cyclopenten-1-one
5-(Hydroxymethyl)-2-furancarboxaldehyde
2-Hydroxy-6-methyl-3isopropylbenzoic acid
2-Hydroxy-3-methyl-6isopropyl-2-cyclohexen-1one
2-(Hydroxymethyl)-2-methyl1,3-propanediol
2-Hydroxy-3-methyl-1,4naphthalenedione
HCP_Section_03.indb 310
Physical
Form
mp/˚C
bp/˚C
den
g cm –3
152.148 tetr (w, lig)
81(1)
285
1.05625
306-08-1
182.173
143.5
C8H10O3
498-00-0
115
dec
C10H14O3
2305-13-7
154.163 pr (w), nd
(bz)
182.216
65
19715
C8H8O4
2612-02-4
168.148
142
Vanillic acid
C8H8O4
121-34-6
168.148 wh nd
212(1)
Scopoletin
C10H8O4
92-61-5
192.169 nd or pr (al) 204
Zingerone
C11H14O3
122-48-5
40.5
18714
C9H10O3
552-41-0
194.227 cry (ace,
eth)
166.173 nd (al)
52.5
15820
Apocynin
C9H10O3
498-02-2
166.173 pr (w)
115
297
Oxybenzone
C14H12O3
131-57-7
228.243
65.5
1.310281 1.545281 vs bz, eth,
EtOH, chl
sl H2O; s EtOH,
ace, bz; vs
eth, chl
s ctc
C10H10O3
458-36-6
178.184 cry (bz)
84
1.1562102
CH6ClNO
4229-44-1
83.518
83.5
C9H13NO2
94-07-5
167.205
184.5
Mestanolone
C20H32O2
521-11-9
304.467
192.5
C7H9NO
623-10-9
123.152 lf (bz)
96
117 dec
C8H8O2
613-84-3
136.149 pl (aq, al)
55.1(0.2)
217.5
Tropic acid
C9H10O3
552-63-6
118
dec
Atrolactic acid
C9H10O3
4607-38-9
166.173 nd, pl (al,
bz, w)
166.173 nd, pl (lig)
C9H12O3
91-04-3
168.189
130.5
Gentisyl alcohol
C7H8O3
495-08-9
140.137 nd (chl)
100
p-Cresotic acid
C8H8O3
89-56-5
152.148
152.5(0.2)
o-Cresotic acid
C8H8O3
83-40-9
152.148
167.0(0.2)
m-Cresotic acid
C8H8O3
50-85-1
152.148 cry, lf
177.8(0.2)
Hymecromone
C10H8O3
90-33-5
176.169 nd (al)
194.5
C5H10O3
625-08-1
118.131
<-32
C5H10O2
115-22-0
102.132
C6H8O2
80-71-7
112.127
104.8
5-(Hydroxymethyl)-2-furaldehyde
o-Thymotic acid
C6H6O3
67-47-0
C11H14O3
548-51-6
Diosphenol
C10H16O2
490-03-9
126.110 nd
(eth-peth)
194.227 nd (w, bz,
lig)
168.233
C5H12O3
77-85-0
C11H8O3
483-55-6
Solubility
sl H2O; vs EtOH,
eth, ace; s bz,
lig
1.554525
sub
N-Methylhydroxylamine
hydrochloride
Synephrine
Phthiocol
nD
s H2O, EtOH,
eth, bz
vs eth, EtOH
sl H2O; vs EtOH;
s eth, DMSO
sl H2O, EtOH; s
chl; i bz, CS2
vs eth
vs bz, eth, EtOH
sl AcOEt
1.091359 1.54759
94
75 sub
vs eth, EtOH,
chl
vs eth, EtOH,
chl
vs H2O, eth,
EtOH
vs ace, bz
vs H2O, EtOH,
chl
sl H2O; s EtOH,
eth, bz, chl; i
CS2
sl H2O; s EtOH,
eth, bz, chl
sl H2O; s EtOH,
bz, chl; vs eth
sl H2O, eth, chl;
s EtOH, alk,
HOAc
vs H2O, eth,
EtOH
s chl
16212
0.938420 1.508120
148.4(0.5)
0.952620
31.5
1151
127
sub
1.206225 1.562718 s H2O, EtOH, bz,
chl; sl eth, ctc
vs bz, eth, EtOH
83
10910
120.147 wh pow or
nd (al)
199(2)
13615
188.180 ye pr
(eth-peth)
173.5
sub
msc H2O, EtOH;
i eth, bz; vs
HOAc
vs ace, eth
4/11/16 11:30 AM
Physical Constants of Organic Compounds
3-311
HO
O
OH
O
HO
O
6060
4-Hydroxy-3-methoxybenzaldehyde
6062
4-Hydroxy-3-methoxybenzeneacetic acid
O
6063
4-Hydroxy-3-methoxybenzenemethanol
OH
O
O
OH
6061
OH
HO
O
O
OH
OH
O
OH
6064
4-Hydroxy-3-methoxybenzenepropanol
2-Hydroxy-5-methoxybenzoic acid
O
O
O
O
HO
O
HO
OH
6065
O
O
6067
6066
6068
4-(4-Hydroxy-3-methoxyphenyl)-2-butanone
7-Hydroxy-6-methoxy-2H-1-benzopyran-2-one
O
OH
1-(2-Hydroxy-4-methoxyphenyl)ethanone
6069
1-(4-Hydroxy-3-methoxyphenyl)ethanone
Organic
4-Hydroxy-3-methoxybenzoic acid
HO
O
O
O
OH
O
HO
O
O
OH
6070
HO
6071
(2-Hydroxy-4-methoxyphenyl)phenylmethanone
HN
HO
HCl
6072
3-(4-Hydroxy-3-methoxyphenyl)-2-propenal
OH
H
N
6073
N-Hydroxymethylamine hydrochloride
4-Hydroxy-α-[(methylamino)methyl]benzenemethanol
OH
OH
O
OH
O
H
17-Hydroxy-17-methylandrostan-3-one, (5α,17β)
6075
6076
N-Hydroxy-4-methylaniline
OH
OH
α-(Hydroxymethyl)benzeneacetic acid, (±)-
2-Hydroxy-5-methyl-1,3-benzenedimethanol
O
OH
OH
OH
6080
6081
6082
2-Hydroxy-5-methylbenzoic acid
2-Hydroxy-3-methylbenzoic acid
6084
7-Hydroxy-4-methyl-2H-1-benzopyran-2-one
OH
O
O
HO
HO
OH
6085
6086
3-Hydroxy-3-methylbutanoic acid
3-Hydroxy-3-methyl-2-butanone
6083
2-Hydroxy-4-methylbenzoic acid
O
O
6087
2-Hydroxy-3-methyl-2-cyclopenten-1-one
O
O
O
6088
5-(Hydroxymethyl)-2-furancarboxaldehyde
O
OH
OH
O
OH
HO
OH
OH
6089
OH
OH
OH
2-(Hydroxymethyl)-1,4-benzenediol
HO
O
α-Hydroxy-α-methylbenzeneacetic acid, (±)-
HO
6079
HO
6078
O
O
OH
OH
O
6077
2-Hydroxy-5-methylbenzaldehyde
OH
OH
HO
OH
OH
O
6074
H
N
2-Hydroxy-6-methyl-3-isopropylbenzoic acid
6090
2-Hydroxy-3-methyl-6-isopropyl-2-cyclohexen-1-one
6091
2-(Hydroxymethyl)-2-methyl-1,3-propanediol
O
6092
2-Hydroxy-3-methyl-1,4-naphthalenedione
Physical Constants of Organic Compounds
3-312
Mol.
Wt.
Physical
Form
Name
Synonym
Mol. Form.
CAS RN
6093
5-Hydroxy-2-methyl-1,4naphthalenedione
Plumbagin
C11H8O3
481-42-5
6094
2-(Hydroxymethyl)-2-nitroTris(hydroxymethyl)­
1,3-propanediol
nitromethane
2-Hydroxy-4-methylpentanoic L-Leucic acid
acid, (S)1-(2-Hydroxy-4methylphenyl)­ethanone
1-(2-Hydroxy-5methylphenyl)­ethanone
2-(Hydroxymethyl)­phenyl-β-D- Salicin
glucopyranoside
1-(2-Hydroxy-5methylphenyl)-1-propanone
N-(Hydroxymethyl)phthalimide
C4H9NO5
126-11-4
C6H12O3
13748-90-8 132.157 orth (eth)
81.5
C9H10O2
6921-64-8
150.174
21
245
1.101210 1.552713
C9H10O2
1450-72-2
150.174 pr (lig)
50
210
1.079753
C13H18O7
138-52-3
240 dec
1.43420
C10H12O2
938-45-4
286.278 orth nd or lf 207
(w)
164.201
1.0
12916.5
1.084114 1.54913
C9H7NO3
118-29-6
177.157 lf, pr (to)
3-Hydroxy-2-methylpropanal
2-Hydroxy-2-methylpropanoic
acid
3-Hydroxy-2-methylpropanoic
acid
N-(Hydroxymethyl)-2-propen- N-(Hydroxymethyl)acrylamide
amide
4-Hydroxy-6-methyl-2HTriacetic acid lactone
pyran-2-one
3-Hydroxy-2-methyl-4HMaltol
pyran-4-one
C4H8O2
C4H8O3
C4H8O3
38433-80-6 88.106 oil
594-61-6
104.105 hyg pr (eth) 80(3)
nd (bz)
2068-83-9 104.105 oil
C4H7NO2
924-42-5
101.105 cry
76
C6H6O3
675-10-5
126.110
189 dec
C6H6O3
118-71-8
126.110 mcl pr (chl)
5-Hydroxy-6-methyl-3,4pyridinedimethanol
4-Hydroxy-1-methyl-2quinolinone
2-Hydroxy-4-(methylthio)­
butanoic acid
3-Hydroxy-α-methyl-Ltyrosine
(Hydroxymethyl)urea
C8H11NO3
65-23-6
6095
6096
6097
6098
6099
6100
Organic
6101
6102
6103
6104
6105
6106
6107
6108
6109
6110
6111
Pyridoxin
4-Hydroxy-N-methylcarbostyril C10H9NO2
mp/˚C
188.180 gold pr or
78.5
oran-ye nd
(dil al)
151.118 nd or pr
165
bp/˚C
den
g cm –3
No.
nD
Solubility
sub
vs ace, bz, eth,
EtOH
dec
vs H2O, eth,
EtOH
vs H2O, eth,
EtOH
141.5
vs bz, eth,
EtOH, chl
vs H2O, EtOH,
HOAc
s chl
i H2O, eth, ctc;
sl EtOH, bz; s
tol
212
vs H2O, EtOH,
eth; sl bz
161.5
93 sub
sl H2O, eth, bz;
vs chl; s alk;
peth
169.178 nd (HOAc)
160
1400.0001
1677-46-9
175.184
265
Methionine hydroxy analog
C5H10O3S
583-91-5
150.196 oil
Methyldopa
C10H13NO4
555-30-6
211.215 cry (MeOH)
300 dec
C2H6N2O2
1000-82-4
90.081
111
pr (al)
sl DMSO
6112
2-Hydroxy-1-naphthalenecarboxaldehyde
C11H8O2
708-06-5
172.181 pr (al), nd
(AcOEt)
83
6113
2-Hydroxy-1-naphthalenecar- 2-Hydroxy-1-naphthoic acid
boxylic acid
C11H8O3
2283-08-1
188.180
157.3
6114
1-Hydroxy-2-naphthalenecar- 1-Hydroxy-2-naphthoic acid
boxylic acid
3-Hydroxy-2-naphthalenecar- 3-Hydroxy-2-naphthoic acid
boxylic acid
C11H8O3
86-48-6
C11H8O3
92-70-6
188.180 cry (al) nd 195
(al, eth, bz)
188.180 nd (dil al) ye 222.5
lf (dil al)
6116
2-Hydroxy-1,4-naphthalenedi- Lawsone
one
C10H6O3
83-72-7
174.153 ye pr (HOAc) 195 dec
6117
5-Hydroxy-1,4-naphthalenedi- Juglone
one
C10H6O3
481-39-0
174.153 ye nd (bz)
peth)
6118
7-Hydroxy-1,3-naphthalenedisulfonic acid
3-Hydroxy-2,7-naphthalenedisulfonic acid
6-Hydroxy-2-naphthalenepropanoic acid
4-Hydroxy-1-naphthalenesulfonic acid
7-Hydroxy-1-naphthalenesulfonic acid
1-Hydroxy-2-naphthalenesulfonic acid
6-Hydroxy-2-naphthalenesulfonic acid
Hydroxynaphthol blue,
trisodium salt
2-Naphthol-6,8-disulfonic acid C10H8O7S2
118-32-1
304.297
2-Naphthol-3,6-disulfonic acid C10H8O7S2
148-75-4
304.297 hyg nd
vs py, EtOH,
MeOH
vs H2O; i eth
s H2O
6115
6119
6120
6121
6122
6123
6124
6125
HCP_Section_03.indb 312
155
dec
Allenolic acid
C13H12O3
553-39-9
1-Naphthol-4-sulfonic acid
C10H8O4S
84-87-7
216.232 cry (dil
180.5
MeOH)
224.234 tab or pl (w) 170 dec
Croceic acid
C10H8O4S
132-57-0
224.234
1-Naphthol-2-sulfonic acid
C10H8O4S
567-18-0
224.234 pl (w)
2-Naphthol-6-sulfonic acid
C10H8O4S
93-01-6
224.234 lf, cry (w+1) 125
C20H14N2Na3O11S3
63451-35-4 620.471 dk red cry
>250
19227
vs H2O; s EtOH,
MeOH, HOAc; i
eth
i H2O; s EtOH,
eth, aq alk,
sulf, peth
sl H2O; vs EtOH;
s eth, ace, bz,
lig, chl
sl H2O; vs EtOH,
eth; s bz
sl H2O; vs EtOH,
eth; s bz, chl,
tol
vs EtOH; i eth,
bz, chl; s
HOAc
i H2O; s EtOH,
eth, bz; vs chl;
sl lig
s H2O
sub
vs H2O, EtOH
sl H2O, dil HCl;
s EtOH; i eth
vs H2O, EtOH; i
eth; s HOAc
4/11/16 11:31 AM
Physical Constants of Organic Compounds
3-313
O
HO
O2N
OH O
6093
5-Hydroxy-2-methyl-1,4-naphthalenedione
O
O
O
OH
OH
OH
OH
OH
6094
6095
2-(Hydroxymethyl)-2-nitro-1,3-propanediol
OH
6096
2-Hydroxy-4-methylpentanoic acid, (S)-
6097
1-(2-Hydroxy-4-methylphenyl)ethanone
1-(2-Hydroxy-5-methylphenyl)ethanone
OH
O
O
O
O OH
OH
O
OH
N
HO
6098
6099
6100
1-(2-Hydroxy-5-methylphenyl)-1-propanone
OH
O
HO
6101
N-(Hydroxymethyl)phthalimide
6102
3-Hydroxy-2-methylpropanal
2-Hydroxy-2-methylpropanoic acid
Organic
2-(Hydroxymethyl)phenyl-β-D-glucopyranoside
HO
O
OH
OH
HO
O
HO
O
O
HO
OH
OH
OH
N
H
6103
3-Hydroxy-2-methylpropanoic acid
O
6104
O
O
6107
3-Hydroxy-2-methyl-4H-pyran-4-one
4-Hydroxy-6-methyl-2H-pyran-2-one
OH
N
6106
6105
N-(Hydroxymethyl)-2-propenamide
HO
5-Hydroxy-6-methyl-3,4-pyridinedimethanol
O
OH
S
H2N
OH
OH
6108
4-Hydroxy-1-methyl-2-quinolinone
O
H 2N
HO
OH
O
N
O
OH
O
6109
6110
2-Hydroxy-4-(methylthio)butanoic acid
OH
N
H
OH
6111
3-Hydroxy-α-methyl-L-tyrosine
6112
(Hydroxymethyl)urea
2-Hydroxy-1-naphthalenecarboxaldehyde
O
O
HO
O
OH
OH
O
OH O
OH
OH
OH
6113
2-Hydroxy-1-naphthalenecarboxylic acid
6114
1-Hydroxy-2-naphthalenecarboxylic acid
OH O
O
6115
6116
3-Hydroxy-2-naphthalenecarboxylic acid
6117
2-Hydroxy-1,4-naphthalenedione
5-Hydroxy-1,4-naphthalenedione
OH
O S O
OH
O S O
HO
O
S
O
OH
6118
7-Hydroxy-1,3-naphthalenedisulfonic acid
O
HO
O
S
S
O
O
OH
OH
O
OH
OH
HO
6119
6120
3-Hydroxy-2,7-naphthalenedisulfonic acid
6121
6-Hydroxy-2-naphthalenepropanoic acid
4-Hydroxy-1-naphthalenesulfonic acid
NaO3S
SO3Na
OH
N
OH
O S O
HO
HO O
S
O
OH
O
S
OH
O
7-Hydroxy-1-naphthalenesulfonic acid
6123
1-Hydroxy-2-naphthalenesulfonic acid
HO
SO3Na
HO
6122
N
6124
6-Hydroxy-2-naphthalenesulfonic acid
6125
Hydroxynaphthol blue, trisodium salt
Physical Constants of Organic Compounds
3-314
Mol. Form.
CAS RN
Mol.
Wt.
Physical
Form
mp/˚C
bp/˚C
C12H11NO2
117-93-1
201.221 lf (w, dil al)
235 dec
sub
C12H10O2
711-79-5
98.6(0.2)
325 dec
C7H5NO4
5274-70-4
109.5
vs bz, EtOH
C7H5NO4
97-51-8
s ace
C7H5NO5
85-38-1
148
6131
2-Hydroxy-5-nitrobenzoic acid 5-Nitrosalicylic acid
C7H5NO5
96-97-9
167.120 cry (dil
HOAc)
183.119 ye nd
(HOAc,
w+1)
183.119 nd (w)
127.0
6130
2-Hydroxy-3-nitrobenzaldehyde
2-Hydroxy-5-nitrobenzaldehyde
2-Hydroxy-3-nitrobenzoic acid 3-Nitrosalicylic acid
186.206 pr (bz, lig)
grn-ye nd
(al)
167.120 nd (HOAc)
6132
2-Hydroxy-1,2,3-nonadecane- Agaricic acid
tricarboxylic acid
12-Hydroxyoctadecanoic acid 12-Hydroxysteric acid
C22H40O7
666-99-9
416.549 cry pow
142 dec
C18H36O3
106-14-9
300.477 cry (al)
82
cis-12-Hydroxy-9-octadecenoic acid, (R)2-Hydroxyoctanoic acid
Ricinoleic acid
C18H34O3
141-22-0
298.461 visc liq
-8.28(0.02)
22710
C8H16O3
617-73-2
160.211 pl
70
16210
sl H2O; vs EtOH,
eth; s ace, bz,
chl
sl H2O; vs EtOH,
eth, ace, bz; s
chl
s H2O; sl EtOH,
eth; i bz, chl
i H2O; s EtOH,
eth, chl
i H2O; vs eth,
EtOH
sl H2O, chl; vs
EtOH, eth
5-Hydroxy-4-octanone
[2-Hydroxy-4-(octyloxy)­
phenyl]phenylmethanone
3-Hydroxy-2-oxopropanoic
acid
3-Hydroxy-4-oxo-4H-pyran2,6-dicarboxylic acid
Butyroin
Octabenzone
C8H16O2
C21H26O3
496-77-5
1843-05-6
144.212 liq
326.429
-10
48.5
185
Hydroxypyruvic acid
C3H4O4
1113-60-6
104.062
81 dec
Meconic acid
C7H4O7
497-59-6
120 dec
C5H10O3
C5H10O2
617-31-2
1071-73-4
200.103 orth pl (w,
dil HCl)
(+3w)
118.131 hyg pl
102.132
C12H7NO3
635-78-9
No.
Name
6126
N-(2-Hydroxy-1-naphthyl)­
acetamide
1-(1-Hydroxy-2-naphthyl)­
ethanone
6127
6128
6129
Organic
6133
6134
6135
6136
6137
6138
6139
Synonym
229.5
34
den
g cm –3
nD
vs ace, bz, eth,
EtOH
vs bz, HOAc
1.65020
sub
209
Solubility
0.945021 1.471621
0.910716 1.434516
sl H2O, MeOH,
ace, eth; s
EtOH, bz
s H2O, EtOH, eth
msc H2O; s
EtOH, eth
i H2O; sl EtOH; i
eth; vs alk
6140
6141
2-Hydroxypentanoic acid
5-Hydroxy-2-pentanone
6142
7-Hydroxy-3H-phenoxazin-3one
6143
N-(2-Hydroxyphenyl)­
acetamide
C8H9NO2
614-80-2
213.189 br nd
(PhNO2) pr
(HCl)
151.163 pl (dil al)
209
6144
N-(3-Hydroxyphenyl)­
acetamide
C8H9NO2
621-42-1
151.163 nd (w)
148.5
6145
N-(4-Hydroxyphenyl)­
acetamide
2-[(4-Hydroxyphenyl)­azo]­
benzoic acid
2-Hydroxy-N-phenylbenzamide
N-Hydroxy-N-phenylbenzamide
α-Hydroxy-αphenylbenzeneacetic acid
C8H9NO2
103-90-2
151.163 mcl pr (w)
168.0(0.5)
C13H10N2O3
1634-82-8
242.229
206
sl DMSO
C13H11NO2
87-17-2
213.232 pr (w, al)
136.5
s H2O; sl EtOH,
eth, bz, chl
C13H11NO2
304-88-1
213.232
121(1)
C14H12O3
76-93-7
228.243 mcl nd (w)
149(2)
C15H10O3
577-85-5
238.238 pa ye nd (al) 169.5
sl H2O, ace; vs
EtOH, eth; s
con sulf
s EtOH
C10H13NO2
101-91-7
179.216 nd (w)
139.5
vs H2O, EtOH
6146
6147
6148
6149
6150
Resorufine
Acetaminophen
Salicylanilide
Benzilic acid
1.29321
180 dec
C10H12O2
5471-51-2
164.201
82.5
6153
3-Hydroxy-2-phenyl-4H-1benzopyran-4-one
N-(4-Hydroxyphenyl)­
4’-Hydroxybutyranilide
butanamide
4-(4-Hydroxyphenyl)-2butanone
1-(2-Hydroxyphenyl)ethanone 2-Hydroxyacetophenone
C8H8O2
118-93-4
136.149
2.5
218
6154
1-(3-Hydroxyphenyl)ethanone 3-Hydroxyacetophenone
C8H8O2
121-71-1
136.149 nd or lf
94(3)
296
6155
1-(4-Hydroxyphenyl)ethanone 4-Hydroxyacetophenone
C8H8O2
99-93-4
108.2(0.5)
1473
6156
4-Hydroxyphenyl-β-Dglucopyranoside
Arbutin
C12H16O7
497-76-7
136.149 nd (eth, dil
al)
272.251 nd (w+1)
6157
2-(4-Hydroxyphenyl)-Dglycine
Oxfenicine
C8H9NO3
22818-40-2 167.162 cry
6151
6152
HCP_Section_03.indb 314
199.5
1.007120 1.439020
sl H2O; vs EtOH,
eth, bz; s
DMSO
vs H2O, EtOH; sl
eth, bz, chl,
DMSO
i H2O; vs EtOH
1.130720 1.558420 vs eth, EtOH,
HOAc
1.0992109 1.5348109 sl H2O; vs EtOH,
eth, bz, chl; i
lig
1.1090109 1.5577109 sl H2O, DMSO;
vs EtOH, eth
vs H2O; s EtOH;
sl eth; i bz,
chl, CS2
240 dec
4/11/16 11:31 AM
Physical Constants of Organic Compounds
3-315
OH
N
O
6126
6127
N-(2-Hydroxy-1-naphthyl)acetamide
O
O
6128
1-(1-Hydroxy-2-naphthyl)ethanone
OH
OH
OH
OH O
NH
O
O
O
O
OH
6129
2-Hydroxy-3-nitrobenzaldehyde
O
N
O
N
O
6130
2-Hydroxy-5-nitrobenzaldehyde
2-Hydroxy-3-nitrobenzoic acid
OH
O
OH
O
O
COOH
N
O
6131
OH
COOH
COOH
HO
OH
6132
2-Hydroxy-5-nitrobenzoic acid
6133
12-Hydroxyoctadecanoic acid
Organic
2-Hydroxy-1,2,3-nonadecanetricarboxylic acid
O
O
OH
OH O
O
O
OH
OH
HO
OH
6134
6135
cis-12-Hydroxy-9-octadecenoic acid, (R)-
6136
2-Hydroxyoctanoic acid
6137
5-Hydroxy-4-octanone
OH
O
O
OH
[2-Hydroxy-4-(octyloxy)phenyl]phenylmethanone
6138
3-Hydroxy-2-oxopropanoic acid
O
OH
HO
O
O
O
OH
O
OH
O
HO
OH
6139
6140
3-Hydroxy-4-oxo-4H-pyran-2,6-dicarboxylic acid
HO
6141
2-Hydroxypentanoic acid
H
N
HO
OH
6144
N-(3-Hydroxyphenyl)acetamide
O
N
H
OH
OH
6145
6143
N-(2-Hydroxyphenyl)acetamide
O
O
6146
N-(4-Hydroxyphenyl)acetamide
O
OH
O
7-Hydroxy-3H-phenoxazin-3-one
N
N
O
HO
O
6142
5-Hydroxy-2-pentanone
H
N
O
H
N
N
N
OH
6147
2-[(4-Hydroxyphenyl)azo]benzoic acid
2-Hydroxy-N-phenylbenzamide
6148
N-Hydroxy-N-phenylbenzamide
O
O
HO
OH
O
O
HO
6149
α-Hydroxy-α-phenylbenzeneacetic acid
6150
3-Hydroxy-2-phenyl-4H-1-benzopyran-4-one
HO
6151
N-(4-Hydroxyphenyl)butanamide
O
4-(4-Hydroxyphenyl)-2-butanone
O
HO
1-(3-Hydroxyphenyl)ethanone
6153
1-(2-Hydroxyphenyl)ethanone
OH
HO
6155
1-(4-Hydroxyphenyl)ethanone
NH2
O
OH
6154
OH
6152
HO
O
OH
O
O
H
N
OH
6156
OH
OH
4-Hydroxyphenyl-β-D-glucopyranoside
O
HO
6157
2-(4-Hydroxyphenyl)-D-glycine
Physical Constants of Organic Compounds
3-316
No.
Name
6158
N-(4-Hydroxyphenyl)glycine
6159
2-(2-Hydroxyphenyl)-2-(4hydroxyphenyl)propane
2-[[(2-Hydroxyphenyl)­imino]­
methyl]phenol
N-Hydroxy-N-(phenylmethyl)­
benzenemethanamine
N-(4-Hydroxyphenyl)­
octadecanamide
3-(4-Hydroxyphenyl)-2oxopropanoic acid
(2-Hydroxyphenyl)­
phenylmethanone
6160
6161
6162
6163
6164
6165
Organic
6166
6167
6168
6169
6170
6171
6172
6173
6174
6175
1-(2-Hydroxyphenyl)-3phenyl-2-propen-1-one
2-Hydroxy-1-phenyl-1-propanone
1-(2-Hydroxyphenyl)-1propanone
1-(4-Hydroxyphenyl)-1propanone
3-(4-Hydroxyphenyl)-2propenoic acid
3-Hydroxy-2-phenyl-4-quinolinecarboxylic acid
N-Hydroxypiperidine
3-Hydroxypregnan-20-one,
(3α,5α)
3-Hydroxypregnan-20-one,
(3β,5α)
17-Hydroxypregn-4-ene-3,20dione
21-Hydroxypregn-4-ene-3,20dione
Mol. Form.
CAS RN
Mol.
Wt.
Physical
Form
mp/˚C
C8H9NO3
122-87-2
167.162 lf (w) pl (w)
246 dec
C15H16O2
837-08-1
228.287 cry (bz)
111
1761-56-4
213.232
185
C14H15NO
621-07-8
213.275
122.5
C24H41NO2
103-99-1
375.589
133.8
4-Hydroxy-αoxobenzenepropanoic acid
2-Hydroxybenzophenone
C9H8O4
156-39-8
180.158 cry (w)
220 dec
C13H10O2
117-99-7
198.217 pl (dil al)
35(3)
2’-Hydroxychalcone
C15H12O2
1214-47-7
224.255
90
C9H10O2
5650-40-8
150.174 ye oil
251
C9H10O2
610-99-1
150.174
15080
Paroxypropione
C9H10O2
70-70-2
p-Coumaric acid
C9H8O3
7400-08-0
150.174 wh nd or pl 149
(w)
164.158 nd
212(11)
Oxycinchophen
C16H11NO3
485-89-2
265.263 ye pr (al)
206 dec
1-Piperidinol
Allopregnan-3α-ol-20-one
C5H11NO
C21H34O2
4801-58-5
516-54-1
101.147 hyg
318.494 cry (al)
39.3
177
Allopregnan-3β-ol-20-one
C21H34O2
516-55-2
318.494
170(15)
17α-Hydroxyprogesterone
C21H30O3
68-96-2
330.461
Deoxycorticosterone
C21H30O3
64-85-7
330.461 pl (eth)
141.5
11-Dehydrocorticosterone
C21H28O4
72-23-1
183.5
C5H9NO3
C5H9NO3
618-27-9
51-35-4
Synonym
2,4’-Isopropylidenediphenol
N-Salicylidene-o-aminophenol C13H11NO2
bp/˚C
den
g cm –3
nD
sl H2O, EtOH; i
eth; s AcOEt,
chl
s chl
239.510
i H2O; sl eth, bz,
chl; s ace
s H2O; dec alk
250560
i H2O; vs EtOH,
eth, bz; sl chl,
peth
1.108518 1.53623
1.550120 sl H2O; s EtOH,
eth, ctc, alk
sl H2O, ace; s
EtOH, eth, alk
vs eth, EtOH
vs bz, EtOH,
HOAc
110
55
sl chl
sl H2O, eth; vs
EtOH, ace; s
chl
i H2O; s EtOH,
ace, bz
6176
21-Hydroxypregn-4-ene3,11,20-trione
6177
6178
cis-4-Hydroxy-L-proline
trans-4-Hydroxy-L-proline
6179
3-Hydroxypropanal
Hydracrolein
C3H6O2
2134-29-4
344.445 pr (ace-w,
al,
ace-eth)
131.130 nd (w+1)
131.130 lf (dil al) pr
(w)
74.079
6180
Hydroxypropanedioic acid
Tartronic acid
C3H4O5
80-69-3
120.061 pr (w+1)
157
sub
6181
2-Hydroxypropanenitrile
Acetaldehyde cyanohydrin
C3H5NO
78-97-7
71.078
liq
-40.0(0.5)
184(3)
0.987720 1.405818
6182
3-Hydroxypropanenitrile
Hydracrylonitrile
C3H5NO
109-78-4
71.078
liq
-46
218(5)
1.040425 1.424820
6183
3-Hydroxypropanoic acid
Hydracrylic acid
C3H6O3
503-66-2
90.078
syr
6184
1-Hydroxy-2-propanone
Acetone alcohol
C3H6O2
116-09-6
74.079
hyg liq
6185
4-(3-Hydroxy-1-propenyl)-2- Coniferyl alcohol
methoxyphenol
2-Hydroxypropyl acrylate
(2-Hydroxypropyl)­
trimethylammonium chloride
3-Hydroxy-1H-pyridin-2-one
1-Hydroxy-2,5-pyrrolidinedi- N-Hydroxysuccinimide
one
4-Hydroxy-2-quinolinecarbox- Kynurenic acid
ylic acid
8-Hydroxy-5-quinolinesulfonic
acid
C10H12O3
458-35-5
C6H10O3
C6H16ClNO
999-61-1
2382-43-6
C5H5NO2
C4H5NO3
16867-04-2 111.100
6066-82-6 115.088 hyg
245 dec
96.3
C10H7NO3
492-27-3
282.5
C9H7NO4S
84-88-8
C9H7NO2
86-95-3
6186
6187
6188
6189
6190
6191
6192
4-Hydroxy-2-quinolinone
HCP_Section_03.indb 316
2,4-Quinolinediol
Solubility
239.5
274
vs H2O
vs H2O; sl EtOH
9018
dec
-17
145.5
180.200 pr (eth-lig)
74
1643
130.141 liq
153.650 pr (Bu OH)
165
702
dec
189.168 ye nd (+w,
dil al)
225.222 ye lf, nd (+
1w) (dil
HCl)
161.158
322.5
353(4)
1.448920
1.080520 1.429520
vs ace, eth,
EtOH
s H2O, EtOH; sl
eth
msc H2O, EtOH;
s eth, chl; i
CS2, peth
msc H2O, EtOH;
sl eth; s chl; i
CS2
vs H2O; s EtOH;
msc eth
vs H2O, EtOH,
eth
i H2O; s EtOH,
alk; vs eth
vs H2O, EtOH
sl DMSO
sl H2O; s EtOH; i
eth; vs alk
sl H2O
sl EtOH, PhNO2,
gl HOAc
4/11/16 11:31 AM
Physical Constants of Organic Compounds
OH
O
H
N
3-317
N
OH
OH
HO
6158
OH
6159
N-(4-Hydroxyphenyl)glycine
N
OH
HO
6160
2(2-Hydroxyphenyl)-2(4-hydroxyphenyl)propane
6161
2-[[(2-Hydroxyphenyl)imino]methyl]phenol
N-Hydroxy-N-(phenylmethyl)benzenemethanamine
O
H
N
OH O
OH
O
HO
6162
6163
N-(4-Hydroxyphenyl)octadecanamide
6164
3-(4-Hydroxyphenyl)-2-oxopropanoic acid
O
(2-Hydroxyphenyl)phenylmethanone
O
O
O
Organic
O
HO
O
OH
OH
OH
6165
6166
1-(2-Hydroxyphenyl)-3-phenyl-2-propen-1-one
O
OH
6167
2-Hydroxy-1-phenyl-1-propanone
HO
HO
6168
1-(2-Hydroxyphenyl)-1-propanone
3-(4-Hydroxyphenyl)-2-propenoic acid
O
O
OH
6169
1-(4-Hydroxyphenyl)-1-propanone
O
OH
OH
N
N
OH
6170
6171
3-Hydroxy-2-phenyl-4-quinolinecarboxylic acid
O
HO
6172
N-Hydroxypiperidine
O
OH
HO
H
H
O
6175
6176
21-Hydroxypregn-4-ene-3,20-dione
O
H
O
6178
cis-4-Hydroxy-L-proline
trans-4-Hydroxy-L-proline
OH
O
N
6182
3-Hydroxypropanenitrile
HO
6174
17-Hydroxypregn-4-ene-3,20-dione
OH
OH
N
6177
21-Hydroxypregn-4-ene-3,11,20-trione
HO
O
3-Hydroxypregnan-20-one, (3β,5α)
HO
OH
N
O
H
6173
3-Hydroxypregnan-20-one, (3α,5α)
OH
O
H
HO
H
O
HO
6183
6184
3-Hydroxypropanoic acid
1-Hydroxy-2-propanone
HO
O
O
6179
OH
OH
N
O
6180
3-Hydroxypropanal
6181
Hydroxypropanedioic acid
2-Hydroxypropanenitrile
O
O
OH
OH
HO
Cl
O
N
OH
6185
4-(3-Hydroxy-1-propenyl)-2-methoxyphenol
6186
2-Hydroxypropyl acrylate
OH
O S O
OH
OH
6187
(2-Hydroxypropyl)trimethylammonium chloride
OH
OH
N
H
O
6188
3-Hydroxy-1H-pyridin-2-one
O
N
OH
6189
O
1-Hydroxy-2,5-pyrrolidinedione
OH
N
O
6190
4-Hydroxy-2-quinolinecarboxylic acid
N
OH
6191
8-Hydroxy-5-quinolinesulfonic acid
N
H
6192
O
4-Hydroxy-2-quinolinone
Physical Constants of Organic Compounds
3-318
No.
Name
6193
3-Hydroxyspirostan-12-one,
Hecogenin
(3β,5α,25R)4-Hydroxystyrene
4-Vinylphenol
2-Hydroxy-5-sulfobenzoic acid 5-Sulfosalicylic acid
6194
6195
6196
6197
6198
6199
6200
6201
6202
Synonym
2-Hydroxy-5-sulfobenzoic acid 5-Sulfosalicylic acid dihydrate
dihydrate
4-Hydroxy-2,2,6,6-tetrameth- 2,2,6,6-Tetramethyl-4-piperidylpiperidine
inol
5-Hydroxytryptamine
3-(2-Aminoethyl)indol-5-ol
5-Hydroxy-DL-tryptophan
Organic
Mol. Form.
CAS RN
Mol.
Wt.
Physical
Form
C27H42O4
467-55-0
430.620 pl (eth)
266.5
C8H8O
C7H6O6S
2628-17-3
97-05-2
120.149
218.184 hyg nd
72(2)
120
C7H10O8S
5965-83-3
254.214 wh cry (w)
C9H19NO
2403-88-5
157.253
C10H12N2O
C11H12N2O3
50-67-9
114-03-4
CH4N2O2
C21H27ClN2O2
C14H17O5PS
127-07-1
68-88-2
299-45-6
176.214
220.224 rod or nd
(al)
76.055 nd (al)
374.904 oil
328.321 nd
C15H22O5
C17H23NO3
mp/˚C
130
141
6205
Hypoglycin A
C7H11NO2
6206
Hypoxanthine
C5H4N4O
57377-32-9 282.333 cry
101-31-5
289.370 tetr nd (dil
al)
156-56-9
141.168 ye pl (Me
aq)
68-94-0
136.112 oct nd (w)
6207
Ibuprofen
C13H18O2
15687-27-1 206.281 col cry
6208
6209
6210
6211
6212
6213
6214
6215
Icosylamine
D-Idose
L-Idose
Imazalil
Imazapyr
Imazaquin
Imazethapyr
Imidazole
C20H43N
C6H12O6
C6H12O6
C14H14Cl2N2O
C13H15N3O3
C17H17N3O3
C15H19N3O3
C3H4N2
10525-37-8
5978-95-0
5934-56-5
35554-44-0
81334-34-1
81335-37-7
81335-77-5
288-32-4
297.562
180.155 syr
180.155 syr
297.179
261.276
311.335
289.330
68.077 mcl pr (bz)
50.2(0.5)
171
221
173
89.52(0.04)
6216
1H-Imidazole-4,5-dicarboxylic
acid
1H-Imidazole-4-ethanamine,
dihydrochloride
C5H4N2O4
570-22-9
156.097 pr
290 dec
C5H11Cl2N3
56-92-8
184.066 pl
(ethHOAc), pr
(w)
100.076 nd (MeOH),
lf (w)
251.3
6217
1,3-Diazole
38
213.5
dec
2200.5
2101.0 dec
vs H2O
1.26038
1.568537 vs H2O; sl peth
sl H2O, eth, bz;
vs EtOH, chl
150 dec
sl H2O; s alk, dil
acid
sl H2O; s os
75(1)
389(15)
vs H2O
vs H2O
Hydantoin
C3H4N2O2
461-72-3
6219
2-Imidazolidinethione
Ethylene thiourea
C3H6N2S
96-45-7
102.158 nd (al), pr
(al)
203
6220
6221
Imidazolidinetrione
2-Imidazolidinone
Parabanic acid
Ethylene urea
C3H2N2O3
C3H6N2O
120-89-8
120-93-4
114.059 mcl nd (w)
86.092
247(3)
131.7(0.5)
6222
Imidodicarbonic diamide
Biuret
C2H5N3O2
108-19-0
190 dec
6223
6224
3,3’-Iminobispropanenitrile
Iminodiacetic acid
Bis(2-cyanoethyl)amine
Diglycine
C6H9N3
C4H7NO4
111-94-4
142-73-4
103.080 pl (al), nd
(w+1)
123.155
133.104 orth pr
6225
Iminodiacetic acid, dinitrile
2,2’-Iminobisacetonitrile
C4H5N3
628-87-5
95.103
78
6226
6227
Imipramine
Imipramine hydrochloride
Tofranil
C19H24N2
C19H25ClN2
50-49-7
113-52-0
280.407
316.868
174.5
6228
Imperatorin
C16H14O4
482-44-0
270.280 cry (al)
102
6229
Indaconitine
C34H47NO10
4491-19-4
629.738 cry
202 dec
6230
Indalone
C12H18O4
532-34-3
226.269 ye-red liq
6231
Indan
C9H10
496-11-7
118.175 liq
6232
1-Indanamine
1-Aminoindane
C9H11N
34698-41-4 133.190
6233
1H-Indazole
1H-Benzopyrazole
C7H6N2
271-44-3
HCP_Section_03.indb 318
vs H2O; vs
EtOH, eth
vs H2O; vs
EtOH, eth
282
2,4-Imidazolidinedione
118.136 nd (al, w)
Solubility
vs ace, eth,
EtOH
108.5
6218
Butopyronoxyl
nD
s H2O
6203
6204
2-(4-Isobutylphenyl)propanoic
acid
1-Eicosanamine
den
g cm –3
300 dec
Hydroxyurea
Hydroxyzine
Hymecromone O,O-diethyl
phosphorothioate
Hymenoxone
Hyoscyamine
Tropine tropate
bp/˚C
dec
1.24323
257
1.0303101 1.4801101 vs H2O, EtOH; s
eth, ace, py; sl
bz
1.74925
sl H2O, py; i
EtOH, eth, bz
1.4320
vs H2O, MeOH
220
-6(1)
247.5
s H2O, EtOH,
alk; sl eth; i
peth
vs H2O; s EtOH;
i eth, bz, chl;
sl DMSO
s H2O; vs EtOH
vs H2O, EtOH; sl
eth, chl
sl H2O; vs EtOH;
i eth
100 sub
1625
1.016520
sl H2O; i EtOH,
eth
s H2O, EtOH; sl
eth, bz, chl
1600.1
263
-51.34(0.02) 177.8(0.4)
221
146.1(0.6)
269
1.05720
1.47525
0.963920 1.537820
1.03815
1.561320
vs H2O; s EtOH;
sl ace
sl H2O; s EtOH,
eth, bz, peth;
vs chl
vs eth, EtOH,
chl
i H2O; vs EtOH,
eth, chl
i H2O; msc
EtOH, eth; sl
chl
sl H2O; s eth,
ace, bz
s H2O, EtOH, eth
4/11/16 11:31 AM
Physical Constants of Organic Compounds
O
O
O
OH
O
H
HO
3-319
O
6193
6194
3-Hydroxyspirostan-12-one, (3β,5α,25R)-
O
S
HO
O
6195
4-Hydroxystyrene
2H2O
OH
O
S
HO
O
OH
H
OH
OH
OH
N
H
6197
6196
2-Hydroxy-5-sulfobenzoic acid
4-Hydroxy-2,2,6,6-tetramethylpiperidine
2-Hydroxy-5-sulfobenzoic acid dihydrate
Cl
NH2
O
HO
N
HO
OH
NH2
N
H
N
H
6198
O
HO
6199
N
NH2
O
6200
5-Hydroxy-DL-tryptophan
OH
6201
Hydroxyurea
O
O
O
O
6202
Hydroxyzine
O
OH
6203
Hymecromone O,O-diethyl phosphorothioate
Hymenoxone
Organic
5-Hydroxytryptamine
N
H
H
HO
O
O P O
S
N
OH
NH2
O
H
OH
O
6205
Hyoscyamine
H
N
N
N
N
O
6204
O
OH
Hypoglycin A
NH2
O
6206
6207
Hypoxanthine
6208
Ibuprofen
Icosylamine
N
HO
H
HO
H
CHO
H
OH
H
OH
CH2OH
H
HO
H
HO
6209
N
CHO
OH
H
OH
H
CH2OH
D-Idose
N
H
Cl
6211
L-Idose
Imazalil
6216
O
O
N
H
N
N
O
N
H
6222
HO
6223
Imidodicarbonic diamide
O
O
O
O
6228
O
6220
HCl
N
6227
Imipramine
Imipramine hydrochloride
O
O
NH2
O
O
O
6229
Indaconitine
6221
N
6226
Iminodiacetic acid, dinitrile
O
2-Imidazolidinone
N
O
HO
N
H
O
O
H
N
O
Imperatorin
H
NH
O
N
H
Imidazolidinetrione
N
6225
Iminodiacetic acid
O
OH
O
OH
H
N
6215
Imidazole
H
N
6224
3,3’-Iminobispropanenitrile
O
2-Imidazolidinethione
O
N
O
N
6219
2,4-Imidazolidinedione
H
N
O
S
N
H
N
H
Imazethapyr
H
O
N
N
6214
N
6218
1H-Imidazole-4-ethanamine, dihydrochloride
NH2
H
N
H
6217
1H-Imidazole-4,5-dicarboxylic acid
H
O
Imazaquin
N
2HCl
N
H
N
H
O
H2N
N
N
6213
Imazapyr
OH
N
N
H
O
O
H 2N
N
O
OH
N
N
N
6212
OH
O
HO
OH
N
Cl
6210
O
O
O
6230
Indalone
6231
Indan
6232
1-Indanamine
N
N
H
6233
1H-Indazole
Physical Constants of Organic Compounds
3-320
No.
Name
Synonym
Mol. Form.
6234
1H-Indazol-3-ol
1,2-Dihydro-3H-indazol-3-one C7H6N2O
6235
Indene
Indonaphthene
6236
1H-Indene-1,3(2H)-dione
6237
6241
6242
6243
1H-Indene-1,2,3-trione
monohydrate
Indeno[1,2,3-cd]pyrene
Indigo
5,5’-Indigodisulfonic acid,
disodium salt
Indocyanine green
1H-Indol-5-amine
1H-Indole
6244
CAS RN
Physical
Form
mp/˚C
bp/˚C
den
g cm –3
nD
C9H8
95-13-6
C9H6O2
606-23-5
146.143 nd (eth, lig)
Ninhydrin
C9H6O4
485-47-2
1,10-(1,2-Phenylene)pyrene
Indigo Carmine
C22H12
C16H10N2O2
C16H8N2Na2O8S2
193-39-5
482-89-3
860-22-0
178.142 pa ye pr (w, 242 dec
al)
276.330 ye cry (cy) 164(2)
262.262 dk bl pow
390 dec
466.353 dk-bl pow
2,3-Benzopyrrole
C43H47N2NaO6S2
C8H8N2
C8H7N
3599-32-4
5192-03-0
120-72-9
774.962 grn pow
132.163
117.149 lf (w, peth)
cry (eth)
244 dec
132
52.3(0.6)
1H-Indole-3-acetic acid
Indoleacetic acid
C10H9NO2
87-51-4
175.184 lf (bz), pl
(chl)
168.5
6245
6246
1H-Indole-3-acetonitrile
1H-Indole-3-butanoic acid
Indolebutyric acid
C10H8N2
C12H13NO2
771-51-7
133-32-4
156.184
203.237
36
124.5
6247
6248
1H-Indole-3-carboxaldehyde
1H-Indole-2,3-dione
Isatin
C9H7NO
C8H5NO2
487-89-8
91-56-5
145.158
197.8
147.132 oran mcl pr 201(1)
6249
Isatin, 3-thiosemicarbazone
C9H8N4OS
487-16-1
220.251
Tryptamine hydrochloride
C10H13ClN2
343-94-2
6251
1H-Indole-2,3-dione,
3-thiosemicarbazone
1H-Indole-3-ethanamine,
monohydrochloride
1H-Indole-3-ethanol
Tryptophol
C10H11NO
526-55-6
196.676 nd (al-bz or 255
lig)
161.200 pr (bz-peth) 59
6252
1H-Indole-3-lactic acid, (S)-
α-Hydroxy-1H-indole-3propanoic acid
C11H11NO3
7417-65-4
205.210 cry (peth)
100
6253
1H-Indole-3-propanoic acid
C11H11NO2
830-96-6
189.211
134.5
6254
6255
6256
6257
Indolizine
1H-Indol-3-ol, acetate
1-(1H-Indol-3-yl)ethanone
1-(1H-Indol-3-yl)-2-propanone 3-Indolylacetone
C8H7N
C10H9NO2
C10H9NO
C11H11NO
274-40-8
608-08-2
703-80-0
1201-26-9
75
129
192.3
116
6258
C11H9NO2
1204-06-4
6259
6260
3-(1H-Indol-3-yl)-2-propenoic 3-Indolylacrylic acid
acid
Indomethacin
Inosine
Hypoxanthine riboside
117.149 pl
175.184
159.184 nd (bz)
173.211 br orth (bz),
nd (aq
MeOH)
187.195
C19H16ClNO4
C10H12N4O5
53-86-1
58-63-9
160(1)
218 dec
sl H2O; vs EtOH
6261
Inosine 5’-monophosphate
5’-Inosinic acid
C10H13N4O8P
131-99-7
6262
myo-Inositol
(1α,2α,3α,4β,5α,6β)Cyclohexanehexol
C6H12O6
87-89-8
357.788
268.226 pl (w + 2),
nd (80%
al)
348.206 visc liq or
glass
180.155 cry (w)
223.8(0.4)
vs H2O; sl EtOH,
eth
s H2O
6263
Iocetamic acid
C12H13I3N2O3
16034-77-8 613.955 wh-ye pow
225
6264
Iodipamide
C20H14I6N2O6
606-17-7
1139.761
307 dec
6265
6266
2-Iodoacetamide
Iodoacetic acid
C2H4INO
C2H3IO2
144-48-9
64-69-7
184.963
185.948
93.0
82.5
6267
6268
6269
6270
Iodoacetone
Iodoacetonitrile
Iodoacetylene
2-Iodoaniline
C3H5IO
C2H2IN
C2HI
C6H6IN
3019-04-3
624-75-9
14545-08-5
615-43-0
183.975
166.948
151.933
219.023 nd (dil al)
56.5(0.4)
6271
3-Iodoaniline
C6H6IN
626-01-7
219.023 lf
33
Organic
6250
HCP_Section_03.indb 320
252.5
Solubility
134.135 nd or lf
(MeOH) pl
or nd (al)
116.160 liq
6238
6239
6240
7364-25-2
Mol.
Wt.
-1.45(0.02)
129(3)
sl H2O, eth; s
MeOH, EtOH
182.5(0.4)
0.996025 1.576820 i H2O; msc
EtOH, eth; s
ace, bz, py; sl
chl
1.3721
sl H2O, ctc; vs
EtOH; s eth,
bz, alk
vs H2O; s EtOH,
alk; sl eth
300 sub
sl H2O, EtOH; i
os
254(3)
1.2225
s H2O, bz; vs
EtOH, eth, tol;
sl ctc
i H2O; vs EtOH;
s eth, ace, bz;
sl chl
1600.2
vs bz; s DMSO;
i peth
s H2O, ace, bz;
vs EtOH; sl eth
283
vs ace, EtOH
1742
vs ace, eth,
EtOH, chl
205
sl H2O, DMSO;
vs EtOH, eth,
ace, bz
i H2O; s EtOH
14410
vs EtOH
185 dec
1.752
i H2O; sl EtOH,
bz, eth, ace
i H2O, bz; sl
EtOH, eth, ace
s H2O; sl tfa
s H2O, EtOH,
peth; sl eth,
chl
s EtOH
dec
6212
185
32
14515
2.1715
2.30725
1.574420
1.681120
sl H2O; vs EtOH,
eth, ace
i H2O; s EtOH,
chl
4/11/16 11:31 AM
Physical Constants of Organic Compounds
O
O
O
OH
OH
N
N
H
6234
6235
1H-Indazol-3-ol
6236
Indene
6237
1H-Indene-1,3(2H )-dione
Na O3S
O
Indeno[1,2,3-cd]pyrene
H2N
S
O3Na
6240
O
S
O
O
O
N
H
Na
6241
O
O
6244
1H-Indole
N NH
O
N
6243
1H-Indol-5-amine
1H-Indole-3-acetic acid
S
O
N
H
N
H
N
H
N
H
6242
Indocyanine green
OH
6245
Indigo
OH
O
S
O
O
5,5’-Indigodisulfonic acid, disodium salt
6247
1H-Indole-3-butanoic acid
N
H
N
H
6248
1H-Indole-3-carboxaldehyde
NH2 HCl
NH2
O
N
H
N
H
6246
1H-Indole-3-acetonitrile
O
6239
N
H
N
N
H
6238
1H-Indene-1,2,3-trione monohydrate
N
O
N
H
O
O
H
N
6249
1H-Indole-2,3-dione
6250
1H-Indole-2,3-dione, 3-thiosemicarbazone
1H-Indole-3-ethanamine, monohydrochloride
HO
OH
O
O
O
O
OH
N
H
N
H
6251
N
H
6252
1H-Indole-3-ethanol
N
H
N
6253
1H-Indole-3-lactic acid, (S)-
6254
1H-Indole-3-propanoic acid
H
OH
O
O
H
6258
O
I
N
N
O
O
OH
HO
O
I
OH
OH
N
I
HO
NH2
6259
O
H
N
I
6264
Iodipamide
OH
HO
6260
OH
6261
Inosine
Inosine 5’-monophosphate
I
OH
6262
6263
myo-Inositol
Iocetamic acid
OH
I
I
NH2
NH2
N
H
O
HO
Indomethacin
O
O
OH
Cl
O
3-(1H-Indol-3-yl)-2-propenoic acid
I
1-(1H-Indol-3-yl)-2-propanone
N
N
O
HO P O
OH
N
N
OH
6257
1-(1H-Indol-3-yl)ethanone
O
N
HO
6256
1H-Indol-3-ol, acetate
N
N
O
N
H
N
H
6255
Indolizine
O
HO
N
H
O
O
OH
O
I
I
O
NH2
6265
2-Iodoacetamide
I
I
O
I
OH
6266
Iodoacetic acid
6267
Iodoacetone
I
N
6268
Iodoacetonitrile
I
6269
Iodoacetylene
I
6270
2-Iodoaniline
6271
3-Iodoaniline
Organic
OH
3-321
Physical Constants of Organic Compounds
3-322
Organic
Mol. Form.
CAS RN
Mol.
Wt.
4-Iodoaniline
C6H6IN
540-37-4
219.023 nd (w)
6273
6274
2-Iodobenzaldehyde
4-Iodobenzaldehyde
C7H5IO
C7H5IO
26260-02-6 232.018
15164-44-0 232.018
37
77.5
12914
265
6275
Iodobenzene
Phenyl iodide
C6H5I
591-50-4
204.008 liq
-30.7(0.5)
188.5(0.6)
6276
6277
C7H7IO
C6H4ClIO2S
5159-41-1
98-61-3
234.034
302.517
92
85
14832
Pipsyl chloride
6278
2-Iodobenzenemethanol
4-Iodobenzenesulfonyl
chloride
2-Iodobenzoic acid
C7H5IO2
88-67-5
248.018 nd (w)
161.6(0.5)
exp
6279
3-Iodobenzoic acid
C7H5IO2
618-51-9
248.018 mcl pr (ace) 186.7(0.8)
329(19)
6280
4-Iodobenzoic acid
C7H5IO2
619-58-9
316(17)
6281
6282
6283
6284
4-Iodobenzonitrile
2-Iodobenzoyl chloride
4-Iodobenzoyl chloride
2-Iodo-1,1’-biphenyl
C7H4IN
C7H4ClIO
C7H4ClIO
C12H9I
3058-39-7
609-67-6
1711-02-0
2113-51-1
248.018 mcl pr (dil
al) lf (sub)
229.018
266.463
266.463
280.103
6285
6286
3-Iodo-1,1’-biphenyl
4-Iodo-1,1’-biphenyl
C12H9I
C12H9I
26.5
113.5
18816
320
6287
1-Iodobutane
Butyl iodide
C4H9I
20442-79-9 280.103
1591-31-7 280.103 nd (al,
HOAc)
542-69-8
184.018 liq
-103.5(0.4)
130(2)
6288
2-Iodobutane, (±)-
(±)-sec-Butyl iodide
C4H9I
52152-71-3 184.018 liq
-104.2(0.4)
118(3)
6289
Iodocyclohexane
Cyclohexyl iodide
C6H11I
626-62-0
210.055
178(5)
6290
Iodocyclopentane
Cyclopentyl iodide
C5H9I
1556-18-9
196.029
166.5
6291
1-Iododecane
C10H21I
2050-77-3
268.178 liq
6292
6293
6294
6295
1-Iodo-2,4-dimethylbenzene
2-Iodo-1,3-dimethylbenzene
2-Iodo-1,4-dimethylbenzene
1-Iodo-2,2-dimethylpropane
C8H9I
C8H9I
C8H9I
C5H11I
4214-28-2
608-28-6
1122-42-5
15501-33-4
232.061
232.061 oil
232.061
198.045
6296
1-Iodododecane
Lauryl iodide
C12H25I
4292-19-7
296.231
0.3
285(12)
6297
Iodoethane
Ethyl iodide
C2H5I
75-03-6
155.965 liq
-111.0(0.4)
72(1)
6298
2-Iodoethanol
C2H5IO
624-76-0
171.964
6299
6300
6301
C2H3I
C8H9I
C6H11IO3
593-66-8
153.949
17376-04-4 232.061 liq
5634-39-9 258.053 pale ye liq
6302
Iodoethene
Vinyl iodide
(2-Iodoethyl)benzene
2-(1-Iodoethyl)-1,3-dioxolane- Iodinated glycerol
4-methanol
Iodofenphos
C8H8Cl2IO3PS
18181-70-9 412.997 wh cry
76
6303
1-Iodoheptane
C7H15I
4282-40-0
-48.2
201(6)
6304
6305
3-Iodoheptane
1-Iodohexadecane
C7H15I
C16H33I
31294-92-5 226.098
544-77-4
352.337 pa ye liq
20(3)
8930
357
6306
6307
1-Iodohexane
Iodomethane
Hexyl iodide
Methyl iodide
C6H13I
CH3I
638-45-9
74-88-4
212.071 liq
141.939 liq
-74.1(0.6)
-66(2)
182(3)
42.4(0.2)
6308
1-Iodo-2-methoxybenzene
o-Iodoanisole
C7H7IO
529-28-2
234.034
6309
6310
1-Iodo-3-methoxybenzene
1-Iodo-4-methoxybenzene
m-Iodoanisole
p-Iodoanisole
C7H7IO
C7H7IO
766-85-8
696-62-8
234.034
234.034 lf (al), nd
(MeOH)
No.
Name
6272
HCP_Section_03.indb 322
Synonym
Physical
Form
226.098 liq
mp/˚C
bp/˚C
den
g cm –3
nD
62.9(0.4)
270.6(0.3)
127.5
38.3
64.5(0.8)
-16.3
11.2(0.4)
15927
16432
19036
263.7
231(7)
228(3)
232(11)
130(13)
155(15)
57(4)
12213
241
53
244.5
247(4)
1.830820 1.620020
Solubility
sl H2O, peth; s
EtOH, eth
sl H2O; s ace
sl H2O; s EtOH,
bz
i H2O; s EtOH;
msc eth, ace,
bz, ctc
1.634920
2.2525
2.18420
sl H2O, ace; vs
EtOH, eth
sl H2O, eth; vs
EtOH
i H2O; sl EtOH; s
eth, DMSO
1.551125 1.662020 i H2O; s EtOH,
eth, bz, HOAc
1.596725
i H2O; s EtOH,
eth, bz, HOAc
1.615420 1.500120 i H2O; msc
EtOH, eth; vs
chl
1.592020 1.499120 i H2O; msc
EtOH, eth; vs
chl
1.624420 1.547720 i H2O; s EtOH,
eth, ace, bz
1.709620 1.544720 i H2O; s eth, bz;
sl ctc
1.254620 1.485820 i H2O; s EtOH,
eth, ctc
1.628216 1.600816 i H2O; s ace, bz
1.615820 1.603520 i H2O; s ace, bz
1.616817 1.599217 i H2O; s ace, bz
1.494020 1.489020 i H2O; s EtOH,
eth
1.199920 1.484020 i H2O; s EtOH,
MeOH; msc
eth, ace, ctc
1.935720 1.513320 sl H2O; msc
EtOH; s eth,
chl
2.196720 1.571320 vs H2O, eth,
EtOH
2.03720 1.538520 vs eth, EtOH
1.603
1.601020
1.797
1.547
s eth, chl, thf,
AcOEt
i H2O; s ace,
xyl; sl EtOH
1.371925 1.490420 i H2O; s EtOH,
eth, ace, chl;
sl ctc
1.367620
1.121325 1.479720 i H2O; sl EtOH; s
eth, ace; msc
bz; vs chl
1.430525 1.492820 i H2O
2.278920 1.530820 sl H2O; s ace,
bz, chl; msc
EtOH, eth
1.820
vs EtOH, eth,
ace, bz, chl, lig
1.965020
vs EtOH, eth
s EtOH, eth, chl
4/11/16 11:31 AM
Physical Constants of Organic Compounds
3-323
Cl
O S O
O
NH2
O
OH
I
O
I
I
I
I
I
6272
4-Iodoaniline
O
6274
6273
6275
4-Iodobenzaldehyde
2-Iodobenzaldehyde
O
O
6276
Iodobenzene
N
OH
I
2-Iodobenzoic acid
4-Iodobenzenesulfonyl chloride
3-Iodobenzoic acid
Cl
I
I
I
I
6282
6283
2-Iodobenzoyl chloride
4-Iodobenzonitrile
6279
Cl
I
6281
4-Iodobenzoic acid
I
6278
6277
2-Iodobenzenemethanol
I
6280
OH
6285
6284
4-Iodobenzoyl chloride
6286
3-Iodo-1,1’-biphenyl
2-Iodo-1,1’-biphenyl
4-Iodo-1,1’-biphenyl
I
6287
1-Iodobutane
I
I
I
I
I
I
6288
6290
6289
2-Iodobutane, (±)-
6291
Iodocyclopentane
Iodocyclohexane
6292
1-Iododecane
6293
1-Iodo-2,4-dimethylbenzene
2-Iodo-1,3-dimethylbenzene
I
I
I
O
O
6296
1-Iodo-2,2-dimethylpropane
2-Iodo-1,4-dimethylbenzene
HO
I
6295
6294
Cl
O
I
I
6301
Cl
I
I
6297
1-Iodododecane
I
6299
6298
Iodoethane
Iodoethene
2-Iodoethanol
O
P
O
S
6300
(2-Iodoethyl)benzene
I
6302
2-(1-Iodoethyl)-1,3-dioxolane-4-methanol
OH
I
6303
Iodofenphos
6304
1-Iodoheptane
3-Iodoheptane
I
H
H
I
I
6305
1-Iodohexadecane
6306
1-Iodohexane
I
I
I
O
O
H
6307
Iodomethane
6308
1-Iodo-2-methoxybenzene
6309
1-Iodo-3-methoxybenzene
O
6310
1-Iodo-4-methoxybenzene
Organic
I
O
OH
Physical Constants of Organic Compounds
3-324
Organic
Mol. Form.
CAS RN
Mol.
Wt.
1-Iodo-2-methylbenzene
C7H7I
615-37-2
218.035
6312
1-Iodo-3-methylbenzene
C7H7I
625-95-6
218.035 liq
6313
(Iodomethyl)benzene
C7H7I
620-05-3
6314
1-Iodo-3-methylbutane
Isopentyl iodide
C5H11I
541-28-6
218.035 col or ye nd 26.3(0.2)
(MeOH)
198.045
6315
2-Iodo-2-methylbutane
tert-Pentyl iodide
C5H11I
594-38-7
198.045
124.5
6316
6317
6318
6319
1-Iodo-2-methylpropane
2-Iodo-2-methylpropane
Iodomethylsilane
1-Iodonaphthalene
Isobutyl iodide
tert-Butyl iodide
C4H9I
C4H9I
CH5ISi
C10H7I
513-38-2
558-17-8
18089-64-0
90-14-2
184.018
184.018 liq
172.041 col liq
254.067
-33.6(0.4)
-109.5
7(1)
121(1)
98(6)
71.8
303(77)
6320
2-Iodonaphthalene
C10H7I
612-55-5
254.067 lf (dil al)
54.3(0.5)
308
6321
1-Iodo-2-nitrobenzene
C6H4INO2
609-73-4
50(1)
290
6322
1-Iodo-3-nitrobenzene
C6H4INO2
645-00-1
249.006 ye orth nd
(al)
249.006 mcl pr
36(1)
280
6323
1-Iodo-4-nitrobenzene
C6H4INO2
636-98-6
249.006 ye nd (al)
173(2)
288
6324
6325
1-Iodononane
1-Iodooctadecane
C9H19I
C18H37I
4282-42-2
629-93-6
-20
34(2)
245.0
379(20)
6326
6327
1-Iodooctane
2-Iodooctane, (±)-
C8H17I
C8H17I
254.151 col liq
380.391 lf (lig), nd
(ace,
al-ace)
629-27-6
240.125 liq
36049-78-2 240.125
-45.7(0.5)
226(4)
212(12)
6328
6329
6330
1-Iodopentane
3-Iodopentane
2-Iodophenol
C5H11I
C5H11I
C6H5IO
628-17-1
1809-05-8
533-58-4
198.045 liq
198.045
220.007 nd
-85.6
43
156(8)
141(11)
186160
6331
3-Iodophenol
C6H5IO
626-02-8
220.007 nd (lig)
118
186100
6332
4-Iodophenol
C6H5IO
540-38-5
93.5
1395 dec
6333
6334
1-(3-Iodophenyl)ethanone
1-(4-Iodophenyl)ethanone
3-Iodoacetophenone
4-Iodoacetophenone
C8H7IO
C8H7IO
220.007 nd (w or
sub)
14452-30-3 246.045
13329-40-3 246.045
86
1298
15318
6335
1-Iodopropane
Propyl iodide
C3H7I
107-08-4
169.992 liq
-101.4(0.4)
102(2)
6336
2-Iodopropane
Isopropyl iodide
C3H7I
75-30-9
169.992 liq
-90.4(0.9)
89(3)
6337
3-Iodopropanoic acid
C3H5IO2
141-76-4
199.975 lf (w)
85
6338
6339
3-Iodo-1-propanol
3-Iodopropene
C3H7IO
C3H5I
627-32-7
556-56-9
185.991 visc oil
167.976 ye liq
-98(2)
6340
2-Iodopyridine
C5H4IN
5029-67-4
204.997
6341
C4H3IN2O2
696-07-1
237.983
275 dec
6342
5-Iodo-2,4(1H,3H)-pyrimidine- 5-Iodouracil
dione
1-Iodo-2,5-pyrrolidinedione
N-Iodosuccinimide
C4H4INO2
516-12-1
224.985 cry (ace)
200.5
6343
Iodosylbenzene
C6H5IO
536-80-1
220.007 ye pow
210 exp
6344
2-Iodothiophene
C4H3IS
3437-95-4
210.036 liq
-40
167(8)
2.059525 1.646525
6345
4-Iodotoluene
C7H7I
624-31-7
218.035 lf (al)
33.6(0.2)
214(4)
1.67820
6346
6347
L-3-Iodotyrosine
trans-α-Ionone, (±)-
C9H10INO3
C13H20O
70-78-0
307.084 cry (w)
30685-95-1 192.297
14628
0.929821 1.504120 vs ace, eth,
EtOH
No.
Name
6311
HCP_Section_03.indb 324
Synonym
2-Octyl iodide, (±)
Amyl iodide
Allyl iodide
Physical
Form
mp/˚C
-27.2
bp/˚C
den
g cm –3
211.5
1.71320
218(19)
1.70520
9310
1.733525
145(2)
1.511820 1.493920 sl H2O, ctc; msc
EtOH, eth
1.493720 1.498120 i H2O; msc
EtOH, eth
1.603520 1.495920
1.57125 1.491820 msc EtOH, eth
226
102(9)
10015
nD
Solubility
1.607920 i H2O; msc
EtOH, eth
1.605320 i H2O; msc
EtOH, eth
1.633425 vs bz, eth, EtOH
1.739920 1.702620 i H2O; msc
EtOH, eth, bz,
CS2
1.631999 1.666299 i H2O; vs EtOH,
eth, HOAc
1.918675
i H2O; s EtOH,
eth
1.947750
i H2O; s EtOH,
eth
1.8090155
i H2O; s EtOH,
HOAc; sl
DMSO
1.283625 1.484825
1.099420 1.481020 i H2O; sl EtOH,
eth
1.329820 1.488520 s EtOH, eth
1.325120 1.489620 i H2O; s EtOH,
eth, lig
1.516120 1.495920 s chl
1.517620 1.497420 vs ace, bz, eth
1.875780
s H2O; vs EtOH,
eth, CS2
sl H2O; s EtOH,
eth
1.8573112
sl H2O; vs EtOH,
eth
1.62220 s bz
s EtOH, bz, CS2,
HOAc; sl lig,
eth
1.748920 1.505820 sl H2O, ctc; msc
EtOH, eth
1.704220 1.502820 sl H2O; msc
EtOH, eth, bz,
chl
sl H2O, chl; vs
EtOH; s eth,
ace
1.997620 1.558520
1.84812 1.554021 i H2O; s EtOH,
eth, chl
1.92825 1.636620 s EtOH, eth,
ace, bz
2.24525
vs H2O; s EtOH,
ace; sl eth,
DMSO
s H2O, EtOH; i
eth, ace, bz,
peth
vs EtOH, eth; sl
chl
i H2O; s EtOH,
eth, CS2; sl chl
205 dec
4/11/16 11:31 AM
Physical Constants of Organic Compounds
I
I
6312
1-Iodo-2-methylbenzene
6313
1-Iodo-3-methylbenzene
6314
(Iodomethyl)benzene
I
I
I
6311
6316
6315
1-Iodo-3-methylbutane
1-Iodo-2-methylpropane
2-Iodo-2-methylbutane
I
I
I
H
Si I
H
I
6317
6318
2-Iodo-2-methylpropane
I
I
6319
Iodomethylsilane
6320
1-Iodonaphthalene
O
N
O
6321
2-Iodonaphthalene
I
O
N
1-Iodo-2-nitrobenzene
O
6323
1-Iodo-3-nitrobenzene
1-Iodo-4-nitrobenzene
I
6326
1-Iodooctadecane
6327
1-Iodooctane
2-Iodooctane, (±)-
O
OH
OH
OH
N
I
6325
1-Iodononane
O
6322
I
6324
O
O
I
I
I
6328
I
6329
1-Iodopentane
6330
3-Iodopentane
6331
2-Iodophenol
3-Iodophenol
I
6333
4-Iodophenol
I
I
I
6332
6334
1-(3-Iodophenyl)ethanone
6335
1-(4-Iodophenyl)ethanone
1-Iodopropane
O
I
O
I
I
6336
OH
6337
2-Iodopropane
3-Iodopropanoic acid
I
N
I
OH
6338
3-Iodo-1-propanol
6339
6341
2-Iodopyridine
5-Iodo-2,4(1H,3H )-pyrimidinedione
O
O
I
O
N
I
6342
S
6343
Iodosylbenzene
O
OH
O
1-Iodo-2,5-pyrrolidinedione
H
O
N
H
I
6340
3-Iodopropene
N
6344
I
2-Iodothiophene
NH2
HO
I
6345
4-Iodotoluene
I
6346
L-3-Iodotyrosine
6347
trans-α-Ionone, (±)-
Organic
I
3-325
Physical Constants of Organic Compounds
3-326
Organic
Mol. Form.
CAS RN
Mol.
Wt.
trans-β-Ionone
C13H20O
79-77-6
192.297
6349
Iopanoic acid
C11H12I3NO2
96-83-3
570.932 wh solid
6350
Iophendylate
C19H29IO2
99-79-6
416.336 visc liq
6351
Iopodic acid
C12H13I3N2O2
5587-89-3
597.956 cry
6352
6353
Iprodione
Iridomyrmecin
C13H13Cl2N3O3
C10H16O2
36734-19-7 330.166
485-43-8
168.233 pr
6354
α-Irone
C14H22O
79-69-6
206.324
900.4
0.936220 1.500220
6355
β-Irone
C14H22O
79-70-9
206.324
12511
0.943421 1.516225 sl H2O; vs EtOH,
eth, bz, chl
6356
Iron hydrocarbonyl
C4H2FeO4
-70
6357
6358
6359
Iron nonacarbonyl
Iron(III) NTA
Iron pentacarbonyl
6360
Iron(III) 2,4-pentanedioate
Ferric acetylacetonate
C15H21FeO6
6361
Isanic acid
C18H26O2
6362
6363
6364
6365
6366
Isatidine
Isaxonine
Isazophos
Isobenzan
1(3H)-Isobenzofuranone
17-Octadecene-9,11-diynoic
acid
Retrorsine N-oxide
N-Isopropyl-2-pyrimidinamine
12002-28-7 169.902 col liq;
unstab
15321-51-4 363.781 oran-ye cry
16448-54-7 243.960 solid
13463-40-6 195.896 col to ye
oily liq
14024-18-1 353.169 red-oran
cry
506-25-2
274.398 cry
C18H25NO7
C7H11N3
C9H17ClN3O3PS
C9H4Cl8O
C8H6O2
15503-86-3
4214-72-6
67329-04-8
297-78-9
87-41-2
145
28
6367
Isoborneol
C10H18O
24393-70-2 154.249 tab (peth)
6368
Isobornyl thiocyanoacetate
C13H19NO2S
115-31-1
6369
6370
6-Isobornyl-3,4-xylenol
Isobutanal
Xibornol
2-Methyl-1-propanal
C18H26O
C4H8O
13741-18-9 258.398 cry
78-84-2
72.106 liq
95
-72.1(0.2)
6371
Isobutane
2-Methylpropane
C4H10
75-28-5
58.122
col gas
-159.59(0.02) -11.7(0.5)
6372
Isobutene
2-Methyl-1-propene
C4H8
115-11-7
56.107
col gas
-140.7(0.2)
-7.0(0.2)
6373
Isobutyl acetate
2-Methylpropyl acetate
C6H12O2
110-19-0
116.158 liq
-97.1(0.5)
116.9(0.6)
6374
Isobutyl acrylate
C7H12O2
106-63-8
128.169 liq
-61
137.0(0.8)
6375
Albutoin
C10H16N2OS
830-89-7
212.311
210.5
6376
6377
6378
5-Isobutyl-3-allyl-2-thioxo-4imidazolidinone
Isobutylamine
Isobutyl 4-aminobenzoate
Isobutylbenzene
2-Methyl-1-propanamine
Isobutyl p-aminobenzoate
(2-Methylpropyl)benzene
C4H11N
C11H15NO2
C10H14
78-81-9
94-14-4
538-93-2
73.137 liq
193.243
134.218 liq
-86(1)
64.5
-51.6(0.2)
6379
Isobutyl benzoate
C11H14O2
120-50-3
178.228
240(2)
6380
Isobutyl butanoate
C8H16O2
539-90-2
144.212
157(1)
6381
6382
Isobutyl carbamate
Isobutyl chlorocarbonate
C5H11NO2
C5H9ClO2
543-28-2
543-27-1
117.147 lf
136.577
6383
Isobutyl 2-chloropropanoate
C7H13ClO2
6384
Isobutyl 3-chloropropanoate
C7H13ClO2
114489164.630
96-2
62108-68-3 164.630
No.
Name
6348
HCP_Section_03.indb 326
Synonym
Ethyl 10-(4-iodophenyl)­
undecanoate
Ipodate
Hexahydro-4,7dimethylcyclopenta[c]­pyran3(1H)-one
4-(2,5,6,6-Tetramethyl-2cyclohexen-1-yl)-3-buten-2one
4-(2,5,6,6-Tetramethyl-1cyclohexen-1-yl)-3-buten-2one
Hydrogen
tetracarbonylferrate(II)
Diiron nonacarbonyl
Nitrilotriacetatoiron(III)
1,7,7-Trimethylbicyclo[2.2.1]­
heptan-2-ol, exo-(±)
C9Fe2O9
C6H6FeNO6
C5FeO5
Physical
Form
367.395 cry
137.182
313.741
411.751 cry (hp)
134.133 nd or pl (w)
mp/˚C
bp/˚C
den
g cm –3
12410
0.94520
1971
1.2520
156
168
136
61
1061.5
Solubility
1.519820 sl H2O; msc
EtOH, eth; s
chl
i H2O; s dil alk,
EtOH
1.52525 sl H2O; s EtOH,
bz, chl
i H2O; vs EtOH,
MeOH, chl,
ace
1.460765 sl H2O; s eth
dec
100 dec
-20
nD
s alk
2.85
103
1.520
1.45322
s H2O
i H2O; sl EtOH; s
bz, ace, ctc
188(1)
5.24
39.5
0.930945 1.4914850 s ace, EtOH,
i-PrOH; sl peth
9312
170
1.2220
122.2(0.3)
75
292(2)
1.163699 1.53699
212
sub
1.1020
950.06
1.146525 1.51225
1673
64.1(0.2)
1.024020 1.538220
0.789120 1.373020 s H2O, eth, ace,
chl; sl ctc
0.551025 1.3518-25 sl H2O; s EtOH,
(p>1
eth, chl
atm
0.58925 1.3926-25 i H2O; vs EtOH,
(p>1
eth; s bz, sulf
atm)
0.871220 1.390220 sl H2O, ctc; msc
EtOH, eth; s
ace
0.889620 1.415020 sl H2O; s EtOH,
eth, MeOH
253.361 ye oily liq
67
s eth, bz, xyl, tol
s H2O; vs EtOH,
eth; sl chl
i H2O; vs EtOH,
eth, chl; sl bz
i H2O; vs EtOH,
bz, chl, peth
68.8(0.1)
0.72425
172.7(0.4)
176
0.853220 1.486620 i H2O; msc
EtOH, eth, ace,
bz, peth, ctc
0.999020
i H2O; msc
EtOH, eth; s
ace, chl
18
20
0.8364
1.4032
sl H2O; msc
EtOH, eth
1.409876 vs eth, EtOH
1.042618 1.407118 s EtOH, bz, chl;
msc eth
1.031220 1.424720
191.3
1.032320 1.429520 vs eth, EtOH
207
128.8
1.398819
4/11/16 11:31 AM
Physical Constants of Organic Compounds
3-327
Cl
O
O
I
NH2
6348
H
I
Iopanoic acid
O
O
OC
OC Fe
OC
H2Fe(CO)4
6354
6355
α-Irone
Iridomyrmecin
Iron hydrocarbonyl
O
O
O
O
O H
6360
Cl
6361
6358
6359
Iron(III) NTA
Iron pentacarbonyl
OH
O
O
N
6362
Isanic acid
CO
OC
Fe CO
OC
CO
N
O
Fe
O
O
O
N
Cl
N
H
6363
Isatidine
N
S
O P O
O
N
6364
Isaxonine
Isazophos
Cl
Cl
Cl
O
N
O
O
Iron(III) 2,4-pentanedioate
O
N
OH
O
O
Iron nonacarbonyl
HO
Fe
CO
Fe CO
CO
Iprodione
6357
O
O
O
O
6356
β-Irone
6352
Iopodic acid
O
6353
O
6351
O
H
N
H
N
Iophendylate
O
N
N
6350
Cl
N
I
O
6349
trans-β-Ionone
I
O
I
I
O
OH
OH
O
O
Cl
Cl
O
Cl
Cl
6365
Isobenzan
OH
O
6366
6367
1(3H )-Isobenzofuranone
Isoborneol
O
N
O
S
Isobornyl thiocyanoacetate
6369
O
6374
Isobutyl acrylate
6375
6380
Isobutyl butanoate
H2N
Isobutane
6373
Isobutene
Isobutyl acetate
O
O
H2N
NH2
6376
6377
Isobutylamine
O
O
Isobutanal
6372
O
S
5-Isobutyl-3-allyl-2-thioxo-4-imidazolidinone
O
6371
O
N
N
H
6370
6-Isobornyl-3,4-xylenol
O
O
O
O
OH
O
6368
6378
Isobutyl 4-aminobenzoate
6381
Isobutyl carbamate
Cl
Isobutyl benzoate
O
O
O
6379
Isobutylbenzene
O
6382
Isobutyl chlorocarbonate
O
O
Cl
6383
Isobutyl 2-chloropropanoate
Cl
O
6384
Isobutyl 3-chloropropanoate
Organic
I
Physical Constants of Organic Compounds
3-328
CAS RN
Mol.
Wt.
C10H20
1678-98-4
C9H18
C6H15N
Organic
Name
6385
Isobutylcyclohexane
6386
6387
Isobutylcyclopentane
Isobutyldimethylamine
6388
Isobutyl formate
N,N,2-Trimethyl-1-propanamine
2-Methylpropyl formate
6389
Isobutyl heptanoate
6390
Isobutyl 2-hydroxybenzoate
6391
Isobutyl isobutanoate
6392
6393
Isobutyl isocyanate
Isobutyl isothiocyanate
6394
Isobutyl methacrylate
C5H9NO
1-Isothiocyanato-2-methylpro- C5H9NS
pane
C8H14O2
6395
Isobutyl 3-methylbutanoate
Isobutyl isovalerate
6396
6397
6398
Physical
Form
mp/˚C
bp/˚C
140.266 liq
-95
171.3
3788-32-7
7239-24-9
126.239 liq
101.190
-115.2(0.1)
148(5)
80(4)
C5H10O2
542-55-2
102.132 liq
-95.5(0.7)
98.4(0.3)
Isobutyl enanthate
C11H22O2
7779-80-8
186.292
Isobutyl salicylate
C11H14O3
87-19-4
194.227
5.9
261
C8H16O2
97-85-8
144.212 liq
-80.6(0.2)
148(3)
1873-29-6
591-82-2
99.131
115.197
106
160
97-86-9
142.196
153(17)
C9H18O2
589-59-3
158.238
169(3)
Isobutyl methyl ether
Isobutyl nitrate
Isobutyl nitrite
C5H12O
C4H9NO3
C4H9NO2
625-44-5
543-29-3
542-56-3
88.148
119.119
103.120 col liq
58.6
123.4
68(3)
6399
Isobutyl pentanoate
C9H18O2
10588-10-0 158.238
183(9)
6400
Isobutyl phenylacetate
C12H16O2
102-13-6
192.254
247
6401
Isobutyl propanoate
C7H14O2
540-42-1
130.185 liq
-71.4(0.4)
136(2)
6402
6403
6404
6405
Isobutyl stearate
Isobutyl thiocyanate
Isobutyl trichloroacetate
Isobutyl vinyl ether
C22H44O2
C5H9NS
C6H9Cl3O2
C6H12O
646-13-9
591-84-4
33560-15-5
109-53-5
340.583 wax
115.197 liq
219.493
100.158 liq
28.9
-58.9(0.5)
22315
175(7)
188
83(3)
6406
6407
Isocitric acid
Isocorybulbine
C6H8O7
C21H25NO4
320-77-4
192.124 ye syr
22672-74-8 355.429 lf (al)
105
187.5
6408
6409
Isocorydine
2-Isocyanato-1,3-dimethylbenzene
1-Isocyanato-2-methoxybenzene
1-Isocyanato-3-methoxybenzene
1-Isocyanato-2-methylbenzene
1-Isocyanato-3-methylbenzene
1-Isocyanato-4-methylbenzene
2-Isocyanato-2-methylpropane
1-Isocyanatonaphthalene
1-Isocyanato-2-nitrobenzene
C20H23NO4
2,6-Dimethylphenyl isocyanate C9H9NO
475-67-2
341.402 pl
28556-81-2 147.173 liq
185
1-Isocyanato-3-nitrobenzene
1-Isocyanato-4-nitrobenzene
2-Isocyanatopropane
1-Isocyanato-3(trifluoromethyl)benzene
Isocyanobenzene
Isocyanomethane
(Isocyanomethyl)benzene
2-Isocyanopropane
6410
6411
6412
6413
6414
6415
6416
6417
6418
6419
6420
6421
6422
6423
6424
6425
HCP_Section_03.indb 328
Synonym
Mol. Form.
No.
Isobutyl propionate
208
-112
nD
Solubility
0.795220 1.438620 i H2O; s EtOH,
ace, chl; vs
eth, bz
0.776925 1.429820
0.709720 1.390720 vs H2O
0.877620 1.385720 sl H2O, chl; msc
EtOH, eth; vs
ace
0.859320
vs ace, bz, eth,
EtOH
1.063920 1.508720 i H2O; s EtOH,
eth, ctc
0.854220 1.399920 sl H2O, ctc; s
EtOH, ace;
msc eth
0.963114 1.500514
0.885820 1.419920 i H2O; msc
EtOH, eth
0.85320 1.405720 i H2O; msc
EtOH, eth; vs
ace; s chl
0.731120
vs eth, EtOH
1.015220 1.402820
0.869922 1.371522 sl H2O; s EtOH,
eth
0.862525 1.404620 i H2O; msc
EtOH; s eth,
ace
0.99918
i H2O; s EtOH,
eth
0.8880
1.397320 sl H2O; vs EtOH,
eth; s ace, bz,
chl, ctc
0.849820
vs eth
vs eth, EtOH
1.263620 1.448320 vs bz, eth, EtOH
0.764520 1.396620 sl H2O; vs EtOH,
ace, bz; msc
eth
1.04520
i H2O; s EtOH,
chl, acid
vs chl
10013
C8H7NO2
700-87-8
C8H7NO2
18908-07-1 149.148
10215
C8H7NO
614-68-6
133.148
185
C8H7NO
621-29-4
133.148
196.5
C8H7NO
622-58-2
133.148
187
tert-Butyl isocyanate
C5H9NO
1609-86-5
99.131
1-Naphthyl isocyanate
2-Nitrophenyl isocyanate
C11H7NO
C7H4N2O3
86-84-0
3320-86-3
3-Nitrophenyl isocyanate
4-Nitrophenyl isocyanate
Isopropyl isocyanate
3-(Trifluoromethyl)phenyl
isocyanate
Phenyl isocyanide
Methyl isocyanide
Benzyl isocyanide
Isopropyl isocyanide
C7H4N2O3
C7H4N2O3
C4H7NO
C8H4F3NO
3320-87-4
100-28-7
1795-48-8
329-01-1
169.180
164.118 wh nd
(peth)
164.118 wh lf (lig)
164.118 pa ye nd
85.105
187.119
C7H5N
C2H3N
C8H7N
C4H7N
931-54-4
593-75-9
10340-91-7
598-45-8
103.122 unstab liq
41.052
117.149
69.106
2-Tolyl isocyanate
den
g cm –3
149.148
9417
85.5
41
51
57
-45(3)
1.528220 i H2O; s eth
1.033020
vs bz, eth
0.86707
269
13718
13011
16220
74.5
5411
8040
exp
199 dec
87
vs bz, eth
1.406120
1.177420
s eth, bz
vs bz, eth, chl
vs bz, eth, chl
vs bz, eth, chl
0.86625 1.382520
1.345520 1.469020
0.9815
0.7564
0.97215 1.519320
0.759625
i H2O; msc
EtOH, eth
4/11/16 11:31 AM
Physical Constants of Organic Compounds
3-329
O
O
H
N
6385
6386
Isobutylcyclohexane
6387
Isobutylcyclopentane
Isobutyldimethylamine
O
N
C
6393
6389
Isobutyl formate
O
O
O
6395
6394
6396
Isobutyl 3-methylbutanoate
Isobutyl methacrylate
6390
Isobutyl heptanoate
Isobutyl methyl ether
N
O
N
O
OH
6391
Isobutyl 2-hydroxybenzoate
Isobutyl isobutanoate
O
N
6398
6397
O
6399
Isobutyl nitrite
Isobutyl nitrate
O
O
O
O
Isobutyl isocyanate
O
O
C
6392
6400
Isobutyl pentanoate
Isobutyl phenylacetate
Organic
Isobutyl isothiocyanate
O
6388
O
O
O
O
O
S
O
O
O
O
O
Cl
Cl
S
N
O
6401
6403
6402
Isobutyl propanoate
O
N
HO
H
O
O
HO
O
O
6407
C
Isocorydine
O
N
C
6413
O
N
6414
6415
1-Isocyanato-4-nitrobenzene
C
2-Isocyanatopropane
6411
1-Isocyanato-2-methoxybenzene
6412
1-Isocyanato-3-methoxybenzene
1-Isocyanato-2-methylbenzene
C
O
O
C
O
N
N
6416
N
O
6417
1-Isocyanatonaphthalene
C
O
N
O
O
6418
1-Isocyanato-2-nitrobenzene
1-Isocyanato-3-nitrobenzene
C
N
F
F
6420
O
O
O
O
C
C
O
6410
O
2-Isocyanato-2-methylpropane
N
6419
O
O
2-Isocyanato-1,3-dimethylbenzene
O
C
C
O
1-Isocyanato-4-methylbenzene
N
N
Isocitric acid
N
N
1-Isocyanato-3-methylbenzene
C
O
6406
Isobutyl vinyl ether
O
6409
N
N
C
C
OH
OH
6405
Isobutyl trichloroacetate
N
N
6408
Isocorybulbine
N
N
H
OH
O
O
O
O
O
O
Cl
6404
Isobutyl thiocyanate
Isobutyl stearate
HO
6421
N
F
1-Isocyanato-3-(trifluoromethyl)benzene
N C
6422
Isocyanobenzene
6423
Isocyanomethane
6424
C
(Isocyanomethyl)benzene
C
N
6425
2-Isocyanopropane
Physical Constants of Organic Compounds
3-330
Organic
No.
Name
6426
6427
6428
6429
6430
6431
6432
Isodecyl acrylate
Isodecyl diphenyl phosphate
Isodecyl methacrylate
8-Isoestrone
Isoeugenol
Isofenphos
Isoflurophate
6433
1H-Isoindole-1,3(2H)-dione
6434
Isolan
6435
6436
DL-Isoleucine
L-Isoleucine
6437
6438
Isolongifolene
Isolysergic acid
6439
α-Isomaltose
6440
Isoniazid
6441
Synonym
Phthalimide
2-Amino-3-methylpentanoic
acid
Mol. Form.
CAS RN
Mol.
Wt.
C13H24O2
C22H31O4P
C14H26O2
C18H22O2
C10H12O2
C15H24NO4PS
C6H14FO3P
1330-61-6
29761-21-5
29964-84-9
517-06-6
97-54-1
25311-71-1
55-91-4
C8H5NO2
85-41-6
C10H17N3O2
Physical
Form
den
g cm –3
nD
15850
24910 dec
12610
0.88520
1.441620
264(6)
1200.01
629
1.08025
1.13420
1.05525
1182.5
1.0720
mp/˚C
bp/˚C
212.329
390.452
226.355
270.367 pr (MeOH)
164.201
345.395
184.145
-100
238(1)
119-38-0
147.132 nd (w), pr
(HOAc) lf
(sub)
211.261 col liq
C6H13NO2
C6H13NO2
443-79-8
73-32-5
131.173
131.173
292 dec
284 dec
C15H24
C16H16N2O2
1135-66-6
478-95-5
204.352 liq
268.310 cry (w+2)
218 dec
342.296
120
C6H7N3O
54-85-3
137.139 cry (al)
171.4
Isopentane
C5H12
78-78-4
72.149
-159.8(0.2)
27.83(0.06)
6442
Isopentyl acetate
Isoamyl acetate
C7H14O2
123-92-2
vol liq or
gas
130.185 liq
-78.5
141.6(0.7)
6443
Isopentylbenzene
C11H16
2049-94-7
148.245
196(7)
6444
Isopentyl butanoate
C9H18O2
106-27-4
158.238
184.8(0.3)
6445
Isopentyl formate
C6H12O2
110-45-2
116.158 liq
6446
Isopentyl hexanoate
C11H22O2
2198-61-0
186.292
225.5
6447
C13H18O3
5421-04-5
222.280 oily liq
17211
6448
6449
6450
Isopentyl
Isopentyl mandelate
α-hydroxybenzeneacetate
Isopentyl isopentanoate
Isopentyl isovalerate
Isopentyl lactate
Isopentyl 2-methylpropanoate Isopentyl isobutyrate
C10H20O2
C8H16O3
C9H18O2
659-70-1
172.265
19329-89-6 160.211
2050-01-3 158.238
190(3)
202.4
169(4)
6451
Isopentyl nitrite
C5H11NO2
110-46-3
117.147
99(3)
6452
6453
6454
Isopentyl pentanoate
Isopentyl propanoate
Isopentyl salicylate
C10H20O2
C8H16O2
C12H16O3
2050-09-1
105-68-0
87-20-7
172.265
144.212
208.253
193(6)
173(4)
278
6455
6456
Isopentyl trichloroacetate
Isophorone
6457
6458
Isophorone diisocyanate
Isophthalic acid
6459
Isopilosine
C16H18N2O3
6460
Isopropalin
6461
Isopropamide iodide
Benzenamine,
C15H23N3O4
4-(1-methylethyl)-2,6-dinitroN,N-dipropylC23H33IN2O
6462
Isopropenyl acetate
6463
Isopropenylbenzene
6464
p-Isopropenylisopropylbenzene
p-Isopropenylstyrene
4-Isopropoxydiphenylamine
6465
6466
HCP_Section_03.indb 330
α-Methyl styrene
4-Isopropoxy-N-phenylaniline
msc H2O; s
EtOH, xyl
sl H2O, EtOH; s
py
499-40-1
C7H11Cl3O2
3,5,5-Trimethyl-2-cyclohexen- C9H14O
1-one
C12H18N2O2
1,3-Benzenedicarboxylic acid C8H6O4
1.383025 sl H2O, lig; s
eth; vs oils
vs bz
820.4
C12H22O11
Isoamyl nitrite
vs eth, Diox
1.573919 vs eth, EtOH
s H2O; i EtOH
6-O-α-D-Glucopyranosyl-Dglucose
4-Pyridinecarboxylic acid
hydrazide
2-Methylbutane
Isopentyl caproate
0.87620
254
<-12
Solubility
-93.5
vs H2O, EtOH
124.0(0.8)
0.620120 1.353720 i H2O; msc
EtOH, eth
0.87615 1.400020 sl H2O; msc
EtOH, eth; s
ace, chl
0.85620 1.486710 i H2O; s EtOH,
eth; vs bz
0.86519 1.411020 i H2O; vs EtOH,
eth
0.87720 1.396720 sl H2O, ctc; s
EtOH; msc eth
0.86120
i H2O; s EtOH,
eth
0.858319 1.413019
0.958925 1.424025 vs eth, EtOH
0.862720
sl H2O; s EtOH,
eth, ace
0.882820 1.391820 sl H2O; msc
EtOH, eth
57392-55-9 233.520
78-59-1
138.206 liq
-8.1
217
214.8(0.7)
0.869720 1.406920 vs eth, EtOH
1.053520 1.508020 i H2O; vs EtOH;
s eth, chl; sl
ctc
1.231420 1.452120 vs eth, EtOH
0.925520 1.476618
4098-71-9
121-91-5
60
348.0(0.2)
217100
sub
1.06220
1.53825
222.283 liq
166.132 nd (w, al)
sl H2O; s EtOH,
HOAc; i eth,
bz, lig
vs EtOH
491-88-3
286.325 pl (al), pr (w, 187
dil al)
33820-53-0 309.362 red-oran liq
i H2O; s os
71-81-8
480.424 cry or pow
190
C5H8O2
108-22-5
100.117 liq
-92.9
C9H10
98-83-9
118.175 liq
-22.36(0.05) 165.4(0.3)
0.910620 1.538620
C12H16
2388-14-9
160.255 liq
-30.6
222(1)
0.893620 1.523820
C11H12
C15H17NO
16262-48-9 144.213 liq
101-73-5
227.302
242
0.93
97.4(0.9)
0.909020 1.403320
s H2O, EtOH,
MeOH; i chl
sl H2O; s EtOH,
chl, ace; vs
eth
i H2O; s EtOH,
eth; msc ace,
bz, ctc
vs ace, bz, eth,
EtOH
1.568420
83
4/11/16 11:32 AM
Physical Constants of Organic Compounds
3-331
OH
O
O
O P O
O
O
O
O
HO
O
6426
6427
Isodecyl acrylate
O
H
6428
Isodecyl diphenyl phosphate
6429
Isodecyl methacrylate
6430
8-Isoestrone
Isoeugenol
O
H
S
N
P
O
O
HO
O
O
NH
N
6431
6432
N
N
OH
OH
NH2
6433
Isoflurophate
O
O
O
O
Isofenphos
H
6434
1H-Isoindole-1,3(2H)-dione
6435
Isolan
N
H
NH2
6436
DL-Isoleucine
6437
L-Isoleucine
6438
Isolongifolene
Isolysergic acid
HO
O
OH
HO
HO
O
H
N
O
O
NH2
OH
N
HO
6439
6441
Isoniazid
Isopentane
OH
6442
Isopentyl acetate
O
O
O
O
6447
6448
Isopentyl α-hydroxybenzeneacetate
6443
Isopentyl isopentanoate
6444
Isopentylbenzene
N
O
O
OH
6449
Isopentyl lactate
6450
6451
Isopentyl 2-methylpropanoate
N
C
Isopentyl nitrite
O
6454
N
C
O
O
6455
Isopentyl salicylate
O
NH2 N
Isopentyl trichloroacetate
O
6456
Isophorone
O
O
O
O
6452
6453
Isopentyl pentanoate
HO
Cl Cl
O
6446
Isopentyl hexanoate
Isopentyl propanoate
OH
O
O
Cl
O
Isopentyl formate
O
O
OH O
O
6445
Isopentyl butanoate
O
O
O
H
O
O
6440
α-Isomaltose
O
O
O
OH
HO
O
O
6458
Isophorone diisocyanate
O
N
N
O
N
6459
Isophthalic acid
6460
Isopilosine
I
Isopropalin
H
N
O
O
6461
Isopropamide iodide
O
N
N
OH
6457
O
H
6462
Isopropenyl acetate
O
6463
Isopropenylbenzene
6464
p-Isopropenylisopropylbenzene
6465
p-Isopropenylstyrene
6466
4-Isopropoxydiphenylamine
O
Organic
O
O P F
O
O
N
O
Physical Constants of Organic Compounds
3-332
Organic
Mol. Form.
CAS RN
Mol.
Wt.
C5H12O2
109-59-1
104.148
1-Cyano-2-isopropoxyethane
1-Methylethyl acetate
C6H11NO
C5H10O2
110-47-4
108-21-4
113.157
102.132 liq
Isopropyl acrylate
Isopropylamine
Isopropyl 2-propenoate
2-Propanamine
C6H10O2
C3H9N
689-12-3
75-31-0
114.142 liq
59.110 liq
6472
6473
Isopropylamine hydrochloride
2-(Isopropylamino)ethanol
2-Propanamine hydrochloride
C3H10ClN
C5H13NO
15572-56-2 95.571
109-56-8
103.163
6474
2-Isopropylaniline
C9H13N
643-28-7
135.206
221
6475
6476
4-Isopropylaniline
N-Isopropylaniline
Cumidine
C9H13N
C9H13N
99-88-7
768-52-5
135.206
135.206
228(3)
203
6477
4-Isopropylbenzaldehyde
Cuminaldehyde
C10H12O
122-03-2
148.201
226(5)
6478
Isopropylbenzene
Cumene
C9H12
98-82-8
120.191 liq
6479
Cumene hydroperoxide
C9H12O2
80-15-9
152.190 liq
6480
Isopropylbenzene
hydroperoxide
4-Isopropylbenzenemethanol
Cumic alcohol
C10H14O
536-60-7
150.217
6481
α-Isopropylbenzenemethanol
1-Phenyl-2-methylpropyl
alcohol
C10H14O
611-69-8
150.217
223
6482
Isopropyl benzoate
C10H12O2
939-48-0
164.201
218(1)
6483
4-Isopropylbenzoic acid
C10H12O2
536-66-3
164.201 tcl pl (al)
6484
6485
6486
6487
6488
Isopropyl butanoate
Isopropyl carbamate
Isopropyl chloroacetate
Isopropyl chloroformate
Isopropyl 2-chloropropanoate
C7H14O2
C4H9NO2
C5H9ClO2
C4H7ClO2
C6H11ClO2
638-11-9
1746-77-6
105-48-6
108-23-6
40058-87-5
130.185
103.120 nd
136.577
122.551
150.603
6489
Isopropylcyclohexane
C9H18
696-29-7
126.239 liq
-89.9(0.5)
154.4(0.4)
6490
6491
4-Isopropylcyclohexanone
Isopropylcyclopentane
C9H16O
C8H16
5432-85-9
3875-51-2
140.222
112.213 liq
-111.5(0.1)
214
126.4(0.8)
6492
6493
C6H12
C11H12Cl2O3
3638-35-5
94-11-1
84.159 liq
263.117
-113.00(0.09) 58(2)
5
1401
Pramiverin
C21H27N
14334-40-8 293.446
6495
6496
Isopropylcyclopropane
Isopropyl (2,4-dichlorophenoxy)acetate
N-Isopropyl-4,4-diphenylcyclohexanamine
Isopropyl dodecanoate
Isopropyl formate
Isopropyl laurate
C15H30O2
C4H8O2
10233-13-3 242.398
625-55-8
88.106
19660
68(2)
6497
Isopropyl 2-furancarboxylate
Isopropyl 2-furanoate
C8H10O3
6270-34-4
154.163
198.5
6498
Isopropyl glycidyl ether
(1-Methylethoxy)methyloxirane C6H12O2
4016-14-2
116.158
138(18)
6499
6500
4-Isopropylheptane
Isopropylhydrazine
6501
Isopropyl 2-hydroxybenzoate
6502
Isopropyl isobutanoate
6503
Isopropyl lactate
6504
Isopropyl methacrylate
6505
6506
Isopropyl methanesulfonate
Isopropylmethylamine
No.
Name
6467
2-Isopropoxyethanol
6468
6469
3-Isopropoxypropanenitrile
Isopropyl acetate
6470
6471
6494
HCP_Section_03.indb 332
Synonym
Cumic acid
Physical
Form
mp/˚C
bp/˚C
141.6(0.4)
-73.4
-95.119​
(0.001)
164
128.5
6510
88.6(0.2)
51103
31.8(0.2)
169(4)
-96.01(0.05) 152.4(0.2)
153
28
117(2)
93
70
249
301(20)
129(3)
183
150(5)
105
151.5
nD
Solubility
0.903020 1.409520 msc H2O, EtOH,
eth; s ace
s chl
0.866225 1.374625 s H2O, EtOH,
ace, chl; msc
eth
0.689120 1.374220 msc H2O, EtOH,
eth; vs ace; s
bz, chl
s DMSO
0.897020 1.439520 msc H2O, EtOH,
eth
0.976012
i H2O; s eth, bz,
ctc
0.95320
0.952625 1.538020 s EtOH, eth,
ace, bz
0.975520 1.530120 i H2O; s EtOH,
eth; sl ctc
0.864025 1.491520 i H2O; msc
EtOH, eth, ace,
bz, peth, ctc
1.0320
0.981820 1.521020 i H2O; msc
EtOH, eth; vs
bz
0.986914 1.519314 i H2O; s EtOH,
ace
1.016315 1.489020 i H2O; s EtOH,
eth, ace
1.1624
sl H2O; vs EtOH,
eth; s peth
0.858820 1.393620 i H2O; s EtOH
0.995166
1.088820 1.438220 vs eth
1.401320 vs eth
1.031520 1.414920 i H2O; s EtOH,
eth
0.802320 1.441020 i H2O; vs EtOH,
eth; msc ace,
bz
0.909930 1.455225
0.776520 1.425820 i H2O; msc
EtOH, ace, ctc;
s eth, bz
0.693625 1.386520
1.2625
1.520925
1650.05
C10H22
C3H10N2
52896-87-4 142.282
2257-52-5 74.124 liq
161(6)
107
Isopropyl salicylate
C10H12O3
607-85-2
180.200
238
Isopropyl isobutyrate
C7H14O2
617-50-5
130.185
123(9)
C6H12O3
617-51-6
132.157
167
4655-34-9
128.169
130(17)
926-06-7
4747-21-1
138.185
73.137
826
53.3(0.3)
Isopropyl 2-methyl-2-propeno- C7H12O2
ate
C4H10O3S
Methylisopropylamine
C4H11N
den
g cm –3
0.853620 1.428025 vs eth, EtOH
0.872820 1.367820 sl H2O; msc
EtOH, eth; vs
ace; s chl
1.065524 1.468224 i H2O; s EtOH,
eth, ace, bz
0.918620
s H2O, ace,
EtOH
0.735425 1.415320
s H2O, bz, EtOH;
sl eth
1.072920 1.506520 i H2O; msc
EtOH, eth
0.847121
i H2O; s EtOH,
eth, ace
0.998020 1.408225 vs H2O, bz, eth,
EtOH
0.884720 1.412220 vs ace, bz, eth,
EtOH
4/11/16 11:32 AM
Physical Constants of Organic Compounds
3-333
NH2
OH
O
O
N
O
O
6467
6468
2-Isopropoxyethanol
O
6470
Isopropyl acetate
6471
Isopropyl acrylate
6472
Isopropylamine
6476
6475
6477
N-Isopropylaniline
6478
OH
OH
6479
Isopropylbenzene
2-Isopropylaniline
6480
Isopropylbenzene hydroperoxide
6481
α-Isopropylbenzenemethanol
4-Isopropylbenzenemethanol
Organic
4-Isopropylbenzaldehyde
6474
2-(Isopropylamino)ethanol
OH
O
HN
4-Isopropylaniline
6473
Isopropylamine hydrochloride
O
NH2
OH
N
H
O
6469
3-Isopropoxypropanenitrile
NH2 HCl
NH2
O
OH
O
O
O
O
O
H2N
O
6482
6483
Isopropyl benzoate
Cl
O
6485
6484
4-Isopropylbenzoic acid
O
O
Cl
6486
Isopropyl carbamate
Isopropyl butanoate
O
O
Cl
O
6488
6487
Isopropyl chloroacetate
Isopropyl 2-chloropropanoate
Isopropyl chloroformate
HN
O
O
O
Cl
6490
6489
O
H
O
6495
6501
Isopropyl 2-hydroxybenzoate
O
6502
Isopropyl isobutanoate
6498
Isopropyl 2-furancarboxylate
O
O
HN
O
6497
Isopropyl formate
O
O
NH2
O
6496
Isopropyl dodecanoate
OH
O
N-Isopropyl-4,4-diphenylcyclohexanamine
Isopropyl (2,4-dichlorophenoxy)acetate
O
O
6494
6493
Isopropylcyclopropane
Isopropylcyclopentane
O
O
6492
6491
4-Isopropylcyclohexanone
Isopropylcyclohexane
O
Cl
Isopropyl glycidyl ether
O
O
OH
6503
Isopropyl lactate
O
6504
Isopropyl methacrylate
6499
4-Isopropylheptane
O
O S O
6505
Isopropyl methanesulfonate
6500
Isopropylhydrazine
N
H
6506
Isopropylmethylamine
Physical Constants of Organic Compounds
3-334
No.
Name
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
6507
1-Isopropyl-2-methylbenzene
o-Cymene
C10H14
527-84-4
6508
1-Isopropyl-3-methylbenzene
m-Cymene
C10H14
6509
1-Isopropyl-4-methylbenzene
p-Cymene
6510
6511
Physical
Form
den
g cm –3
mp/˚C
bp/˚C
134.218 liq
-71.5(0.1)
178(2)
535-77-3
134.218 liq
-63.8(0.1)
175(4)
C10H14
99-87-6
134.218 liq
-68.1(0.3)
177(2)
Isopropyl 3-methylbutanoate
C8H16O2
32665-23-9 144.212
147(9)
C10H16
4221-98-1
136.234
173
Homocamfin
C10H16O
535-86-4
152.233 pa ye
244
0.934021 1.486521 vs ace, EtOH
(±)-Piperitone
C10H16O
6091-52-7
152.233 liq
232.5
0.933120 1.484520 vs ace, EtOH
6514
5-Isopropyl-2-methyl-1,3cyclohexadiene, (R)5-Isopropyl-3-methyl-2cyclohexen-1-one, (±)6-Isopropyl-3-methyl-2cyclohexen-1-one, (±)Isopropyl methyl ether
0.876620 1.500620 i H2O; msc
EtOH, eth, ace,
bz, peth, ctc
0.861020 1.493020 i H2O; msc
EtOH, eth, ace,
bz, peth, ctc
0.857320 1.490920 i H2O; msc
EtOH, eth, ace,
bz, peth, ctc
0.853817 1.396020 vs ace, eth,
EtOH
0.842120 1.477219
2-Methoxypropane
C4H10O
598-53-8
74.121
30.8(0.5)
6515
5-Isopropyl-2-methylphenol
Carvacrol
C10H14O
499-75-2
150.217 nd
2.5(0.2)
0.723715 1.357620 sl H2O; msc
EtOH, eth
0.977220 1.523020 sl H2O; s EtOH,
eth, ctc; vs
ace
6516
C8H12N2O
2814-20-2
152.193 cry
173
6517
6518
6519
2-Isopropyl-6-methyl-4pyrimidinol
Isopropyl methyl sulfide
1-Isopropylnaphthalene
2-Isopropylnaphthalene
C4H10S
C13H14
C13H14
1551-21-9
6158-45-8
2027-17-0
90.187 liq
170.250 liq
170.250
-101.47(0.06) 84.7(0.5)
-15.6(0.2)
271(2)
15.0(0.4)
268(2)
6520
6521
Isopropyl nitrate
Isopropyl nitrite
C3H7NO3
C3H7NO2
1712-64-7
541-42-4
105.093
89.094 pa ye oil
6522
1-Isopropyl-4-nitrobenzene
C9H11NO2
1817-47-6
165.189 pa ye oil
6523
C6H14N2O
601-77-4
130.187 cry (eth,w)
48
6524
6525
N-Isopropyl-N-nitroso-2propanamine
Isopropyl 3-oxobutanoate
Isopropyl palmitate
C7H12O3
C19H38O2
542-08-5
142-91-6
144.168 liq
298.504
-27.3
12.8(0.5)
6526
Isopropyl pentanoate
C8H16O2
18362-97-5 144.212
6527
2-Isopropylphenol
C9H12O
88-69-7
136.190
17(1)
6528
6529
3-Isopropylphenol
4-Isopropylphenol
C9H12O
C9H12O
618-45-1
99-89-8
136.190
136.190 nd (peth)
25.7(0.5)
62(2)
6530
C15H18N2
101-72-4
226.317
72.5
6531
6532
6533
N-Isopropyl-N’-phenyl-1,4benzenediamine
Isopropyl phenylcarbamate
Propham
1-(4-Isopropylphenyl)ethanone
Isopropyl propanoate
C10H13NO2
C11H14O
C6H12O2
122-42-9
645-13-6
637-78-5
179.216 wh nd (al)
162.228
116.158
85(2)
6534
6535
6536
6537
N-Isopropyl-2-propenamide
Isopropylpropylamine
Isopropyl propyl sulfide
4-Isopropylpyridine
C6H11NO
C6H15N
C6H14S
C8H11N
2210-25-5
21968-17-2
5008-73-1
696-30-0
113.157
101.190
118.240
121.180 liq
64.5
6538
Isopropyl nicotinate
C9H11NO2
553-60-6
165.189
6539
6540
Isopropyl 3-pyridinecarboxylate
Isopropyl silicate
Isopropyl stearate
Tetra(isopropoxy)silane
C12H28O4Si
C21H42O2
1992-48-9
112-10-7
264.434
326.557
6541
4-Isopropylstyrene
C11H14
2055-40-5
146.229 liq
6542
Isopropyl tetradecanoate
C17H34O2
110-27-0
6543
6544
6545
(Isopropylthio)benzene
Isopropyl trichloroacetate
Isopropylurea
C9H12S
C5H7Cl3O2
C4H10N2O
6546
Isopropyl vinyl ether
C5H10O
6512
6513
Organic
HCP_Section_03.indb 334
Isopropyl acetoacetate
Isopropyl hexadecanoate
N-Propyl-2-propanamine
Isopropyl myristate
2-(Ethenyloxy)propane
-19
241.5(0.5)
nD
Solubility
0.829120 1.493220 s EtOH, eth, ace
0.995620 1.595220
0.975320 1.584820 i H2O; vs EtOH,
eth; s bz
101(2)
1.03419 1.391216 s EtOH, eth
34(2)
0.868415
i H2O; s EtOH,
eth
1229
1.08420 1.536720 i H2O; s ace, bz,
lig
194.5
0.942220
sl H2O; s EtOH,
eth, bz
186
0.983520 1.417320 vs eth, EtOH, lig
1602
0.840438 1.436425 vs ace, bz, eth,
EtOH
0.857920 1.406120 i H2O; s EtOH,
eth, ace
213.84(0.08) 1.01220 1.531520 sl H2O; s EtOH,
eth, bz, ctc
230(3)
1.526120 vs eth
228.0(0.1) 0.99020 1.522820 sl H2O; s EtOH,
chl
1482
250(13)
110(4)
11015
96.2(0.3)
132.0(0.8)
182(4)
1.0920
1.498991 vs bz, EtOH
0.975315 1.523520
0.866020 1.387220 sl H2O; msc
EtOH, eth
12630
0.826920
0.938225 1.496220 sl H2O; msc
EtOH, eth; vs
ace
1.062420 1.492620
24.1(0.5)
184
2076
0.877020
0.840338
-44.7
207(1)
0.885020 1.528920
270.451
19320
0.853220 1.432525
3019-20-3
3974-99-0
691-60-1
152.256
205.468
102.134 nd
208
174(7)
1030.1
926-65-8
86.132
0.985220 1.546420
1.291125 1.442820 vs bz, eth, EtOH
s H2O, EtOH,
chl, ace; sl eth
0.753420 1.384020 vs ace, bz, eth,
EtOH
liq
-54.9(0.5)
-140
56(4)
s ctc, CS2
vs ace, eth,
EtOH, chl
vs ace, bz, eth,
EtOH
i H2O; s EtOH,
eth, chl; vs
ace, bz
4/11/16 11:32 AM
Physical Constants of Organic Compounds
3-335
O
O
6508
6507
6509
1-Isopropyl-3-methylbenzene
1-Isopropyl-2-methylbenzene
6510
1-Isopropyl-4-methylbenzene
6511
Isopropyl 3-methylbutanoate
5-Isopropyl-2-methyl-1,3-cyclohexadiene, (R)-
OH
O
OH
O
N
N
O
6512
6513
6-Isopropyl-3-methyl-2-cyclohexen-1-one, (±)-
6515
Isopropyl methyl ether
6516
5-Isopropyl-2-methylphenol
2-Isopropyl-6-methyl-4-pyrimidinol
Organic
5-Isopropyl-3-methyl-2-cyclohexen-1-one, (±)-
6514
O
S
6517
6518
Isopropyl methyl sulfide
O
O
6520
6519
1-Isopropylnaphthalene
O
N
O
O
6521
Isopropyl nitrate
2-Isopropylnaphthalene
N
N
N
N
O
6522
Isopropyl nitrite
1-Isopropyl-4-nitrobenzene
N-Isopropyl-N-nitroso-2-propanamine
OH
OH
H
N
N
H
O
6525
6526
Isopropyl palmitate
6527
Isopropyl pentanoate
6528
2-Isopropylphenol
3-Isopropylphenol
6529
4-Isopropylphenol
O
6530
6532
6533
1-(4-Isopropylphenyl)ethanone
Isopropyl propanoate
6534
N-Isopropyl-2-propenamide
6535
O
6540
6536
Isopropyl propyl sulfide
S
O
O
O
Isopropyl stearate
O
Isopropylpropylamine
6541
4-Isopropylstyrene
6542
Isopropyl tetradecanoate
6537
6538
4-Isopropylpyridine
Isopropyl 3-pyridinecarboxylate
O
Cl
6543
6539
Isopropyl silicate
O
O
Cl Cl
(Isopropylthio)benzene
6531
Isopropyl phenylcarbamate
N
N
S
O
O
O Si O
O
O
H
N
N
H
O
Isopropyl 3-oxobutanoate
O
N-Isopropyl-N’-phenyl-1,4-benzenediamine
O
O
6524
H
N
O
O
O
O
6523
OH
O
O
O
6544
Isopropyl trichloroacetate
H2N
N
H
6545
Isopropylurea
O
6546
Isopropyl vinyl ether
Physical Constants of Organic Compounds
3-336
Organic
No.
Name
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
6547
Isoproterenol
4-[1-Hydroxy-2[isopropylamino]­ethyl]-1,2benzenediol
C11H17NO3
7683-59-2
211.258
170.5
6548
6549
Isopsoralen
1-Isoquinolinamine
C11H6O3
C9H8N2
523-50-2
1532-84-9
186.164
144.173 pl(w)
139
123
1648
6550
6551
3-Isoquinolinamine
Isoquinoline
C9H8N2
C9H7N
25475-67-6 144.173
119-65-3
129.159 hyg pl
178.5
26.46(0.01)
243.2(0.6)
6552
7-Isoquinolinol
C9H7NO
7651-83-4
145.158
230
6553
6554
Isosorbide
Isosorbide dinitrate
C6H10O4
C6H8N2O8
652-67-5
87-33-2
146.141
236.136 col cry
63
52
6555
6556
Isosystox
Isothebaine
C8H19O3PS2
C19H21NO3
126-75-0
568-21-8
258.339 liq
311.375 orth cry (al) 203.5
6557
6558
6559
Isothiocyanic acid
L-Isovaline
Isoxaben
CHNS
C5H11NO2
C18H24N2O4
3129-90-6 59.091 unstab gas
595-40-4
117.147 nd (w)
82558-50-7 332.395 wh cry
≈300
173
6560
6561
6562
6563
6564
Isoxazole
Isoxsuprine
Jacobine
Javanicin
Jervine
C3H3NO
C18H23NO3
C18H25NO6
C15H14O6
C27H39NO3
288-14-2
395-28-8
6870-67-3
476-45-9
469-59-0
69.062
301.381 cry
351.395 pl (EtOH)
290.268 red cry (al)
425.604
103.0
228
208 dec
243 dec
6565
Kaempferol
C15H10O6
520-18-3
286.236 ye nd (al, + 277
1 w)
6566
Kainic acid
C10H15NO4
487-79-6
6567
6568
6569
Kanamycin A
Kepone
Ketamine
6570
6571
Ketene
Khellin
463-51-4
82-02-0
213.231 cry (EtOH
aq)
484.499 cry (EtOH)
490.636
237.725 cry
(ethpentane)
42.036 col gas
260.242 eth, al
6572
L-Kynurenine
343-65-7
208.213 lf (+l/2w)
6573
6574
Labetalol
DL-Lactic acid
6575
6576
6577
6578
6579
D-Lactic acid
L-Lactic acid
Lactofen
δ-Lactone-D-gluconic acid
α-Lactose
6580
Benzo[c]pyridine
1,4:3,6-Dianhydroglucitol
Demeton-S
2-Amino-2-methylbutyric acid
1-Oxa-2-azacyclopentadiene
C18H36N4O11
Chlordecone
C10Cl10O
2-(2-Chlorophenyl)-2C13H16ClNO
(methylamino)cyclohexanone,
(±)
C2H2O
4,9-Dimethoxy-7-methyl-5H- C14H12O5
furo[3,2-g][1]benzopyran-5one
Benzenebutanoic acid,
C10H12N2O3
α,2-diamino-γ-oxoC19H24N2O3
2-Hydroxypropanoic acid, (±) C3H6O3
59-01-8
143-50-0
6740-88-1
Physical
Form
mp/˚C
bp/˚C
den
g cm –3
sl H2O, eth; vs
EtOH
1.091030 1.614820 i H2O; vs EtOH,
chl; msc eth,
bz
sl H2O, eth; s
EtOH
1332
1.07820
253 dec
350 dec
92.5
1.6125
-49.7(0.4)
1900.05
sl eth, ace
i H2O; s EtOH,
ace; sl eth, chl
194 dec
sl H2O
C3H6O3
C3H6O3
C19H15ClF3NO7
C6H10O6
C12H22O11
10326-41-7
79-33-4
77501-63-4
90-80-2
14641-93-1
90.078
90.078
461.773
178.139
342.296
53
53
93
β-D-Lactose
C12H22O11
5965-66-2
342.296
254
1.5920
6581
α-Lactose monohydrate
C12H24O12
5989-81-1
360.312 mcl (w)
201 dec
1.54720
6582
Lactulose
C12H22O11
4618-18-2
6583
Laminaribiose
6584
Lanosta-8,24-dien-3-ol, (3β)
6585
6586
6587
Lantadene A
Lantadene B
L-Lanthionine
6588
Lapachol
HCP_Section_03.indb 336
δ-D-Gluconolactone
4-O-β-D-Galactopyranosyl-Dfructose
3-O-β-D-Glucopyranosyl-Dglucose
Lanosterol
Rehmannic acid
L-Cysteine, S-(2-amino-2carboxyethyl)-, (R)2-Hydroxy-3-(3-methyl-2butenyl)-1,4-naphthalenedione
12215
1032
1.206021 1.439220 vs H2O, EtOH; sl
eth
vs H2O, EtOH
vs H2O, EtOH
222.8
169
C12H22O11
342.296 hx pl
(MeOH)
34980-39-7 342.296
C30H50O
79-63-0
140.5
C35H52O5
C35H52O5
C6H12N2O4S
467-81-2
467-82-3
922-55-4
426.717 nd (eth), cry
(MeOHace)
552.785 cry (MeOH)
552.785 cry (EtOH)
208.235 hex pl
C15H14O3
84-79-7
242.270 ye pr (eth,
bz) pl (al)
139.5
1.429817
s EtOH; sl eth
s EtOAc, MeCN,
MeOH
s H2O
s alk
i H2O; s EtOH,
ace, chl; sl eth
sl H2O, chl; vs
EtOH, eth, ace;
i bz
s H2O; i EtOH
164
16.9(0.2)
pl (chl)
hyg pr (eth)
ye pow (bz)
nd (al)
wh pow
vs EtOH, eth,
ace
s H2O
i H2O; msc
EtOH, chl; sl
eth; s MeOH
1.13221
36894-69-6 328.405 cry (MeOH)
598-82-3
90.078 ye cry
D-Hydroxypropanoic acid
L-2-Hydroxypropanoic acid
Solubility
1702
95.4(0.7)
-151
154 dec
nD
vs H2O; sl EtOH;
i eth, chl
vs H2O; sl EtOH;
i eth, chl
vs H2O; i EtOH,
eth, chl, MeOH
vs H2O
205
297
302
294 dec
vs eth, EtOH,
chl
sl H2O
i H2O; s EtOH,
eth, bz, chl; vs
HOAc
4/11/16 11:32 AM
Physical Constants of Organic Compounds
HO
OH H
N
HO
3-337
N
O
O
HO
O
NH2
6548
6547
N
6549
Isopsoralen
Isoproterenol
NH2
N
1-Isoquinolinamine
6552
Isoquinoline
3-Isoquinolinamine
O
N
HO
6551
6550
H
O
N O
O
O
H
O
O
O
H
O N
OH
O
6554
6553
7-Isoquinolinol
H
Isosorbide dinitrate
Isosorbide
O
6556
6557
Isothebaine
O
O
OH H
N
N
O
6559
6558
Isothiocyanic acid
N
H
O
O
O H
O
HO
H
N
O
HO
OH O
6562
6564
Javanicin
OH
O
6566
6565
Jervine
OH
N
H
OH
6563
Jacobine
O
OH
O
O
Isoxsuprine
OH O
H H
N
O
OH O
6561
Isoxazole
OH
O
O
HO
6560
Isoxaben
L-Isovaline
N
Kainic acid
Kaempferol
HO
O
NH2
HO
H2N
OH
O
O
OH
HO
OH
O
Cl
Cl
Cl
Cl
HO
H2N
O
Cl
Cl
Cl
O
OH
Labetalol
6575
DL-Lactic acid
HO
OH
OH
6574
OH
D-Lactic acid
OH
OH
O O
OH
HO
O O
OH
HO
OH
OH
6579
OH
OH
6580
α-Lactose
6584
Lanosta-8,24-dien-3-ol, (3β)
6585
Lantadene A
OH
OH
HO
HO
O O
O
O
O
OH
O
O
O
OH
H
O
6583
Laminaribiose
O
6586
OH
O
O
HO
S
NH2
Lantadene B
OH
OH
OH
OH
6582
Lactulose
O
O
H
δ-Lactone-D-gluconic acid
OH
O
HO
OH
6578
HO
O
OH
O
HO
OH
H2O
α-Lactose monohydrate
H
HO
HO
OH
OH
6581
β-D-Lactose
O
HO
O
OH
O
OH
O
Lactofen
HO
O O
HO
O
O
O
6577
L-Lactic acid
HO
OH
OH
F
HO
O OH
HO
N
O
6576
HO
O
F
F
L-Kynurenine
O
O
OH
6572
Khellin
O
OH
OH
6573
HO
6571
Ketene
O
NH2
O
6570
Cl
NH2
HO
O
H2C C O
H
N
HO
NH2
OH
O
Ketamine
O
O
O
6569
Kepone
Kanamycin A
O
Cl
NH
6568
6567
OH
O
Cl
Cl
NH2
O
Cl
6587
OH
NH2
L-Lanthionine
O
6588
Lapachol
Organic
OH
NH2
HN C S
6555
O
O
S
Isosystox
O
O
N
H
HO
O
O
O P O
S
Physical Constants of Organic Compounds
3-338
No.
Name
6589
Synonym
Mol.
Wt.
Physical
Form
Organic
Mol. Form.
CAS RN
Lappaconitine
C32H44N2O8
32854-75-4 584.699 hex pl (al)
6590
Lasiocarpine
C21H33NO7
303-34-4
6591
6592
Laudanidine
Laudanine
C20H25NO4
C20H25NO4
301-21-3
85-64-3
6593
Laudanosine
C21H27NO4
6594
Laureline
C19H19NO3
6595
Laurocapram
6596
6597
Lead
bis(dimethyldithiocarbamate)
Ledol
6598
6599
mp/˚C
bp/˚C
den
g cm –3
nD
Solubility
1.4701
i H2O; sl EtOH,
eth; s bz, chl
sl H2O; s EtOH,
bz, eth
vs H2O, bz
sl H2O, EtOH,
eth; s bz, chl
vs ace, eth,
EtOH, chl
i H2O; s EtOH,
eth, dil acid,
con sulf
i H2O
217.5
411.490 col pl (peth) 95.5
C18H35NO
343.418 hex pr (al)
343.418 ye wh pr (dil
al, al-chl)
2688-77-9 357.444 nd (peth), pr
(al)
81-38-9
309.359 tab (al)
cubes
(peth)
59227-89-3 281.477 col liq
-7
C6H12N2PbS4
19010-66-3 447.6
258
C15H26O
577-27-5
Lenacil
Leptophos
C13H18N2O2
C13H10BrCl2O2PS
2164-08-1 234.294
21609-90-5 412.066 tan waxy
solid
290
74.0(0.5)
6600
DL-Leucine
C6H13NO2
328-39-2
131.173 lf (w)
293
sub
6601
6602
D-Leucine
L-Leucine
C6H13NO2
C6H13NO2
328-38-1
61-90-5
293
293
sub
sub
6603
N-Leucylglycine
C8H16N2O3
686-50-0
131.173 pl (al)
131.173 hex pl (dil
al)
188.224
6604
6605
6606
Leuprolide
Leurosine
Levallorphan
17-Allylmorphinan-3-ol
C59H84N16O12
C46H56N4O9
C19H25NO
6607
Levodopa
L-3,4-Dihydroxyphenylalanine
C9H11NO4
6608
6609
6610
Levopimaric acid
Levorphanol
d-Limonene
17-Methylmorphinan-3-ol
p-Mentha-1,8-diene, (R)
C20H30O2
C17H23NO
C10H16
53714-56-0 1209.398 fluffy solid
23360-92-1 808.959 cry
152-02-3
283.408 cry (EtOH
aq)
59-92-7
197.188 pl (dil al) pr
or nd
(w+SO2)
79-54-9
302.451 orth cry
77-07-6
257.371 cry
5989-27-5 136.234 oil
6611
l-Limonene
p-Mentha-1,8-diene, (S)
C10H16
5989-54-8
6612
Linalol
C10H18O
22564-99-4 154.249
198
6613
Linalyl acetate
3,7-Dimethyl-1,6-octadien3-ol, (±)3,7-Dimethyl-1,6-octadien3-yl acetate
0.841120 1.473020 i H2O; msc
EtOH, eth; s
ctc
0.84320 1.474620 i H2O; vs eth,
EtOH
0.87015 1.4627
C12H20O2
115-95-7
196.286 liq
221(6)
0.89520
6614
Lincomycin
C18H34N2O6S
154-21-2
406.537 amor solid
6615
Linoleic acid
C18H32O2
60-33-3
280.446 col liq
-6.9(0.7)
22916
0.902220
6616
Linolenic acid
C18H30O2
463-40-1
278.430
-10(2)
23117
0.916420
6617
6618
Linuron
Liothyronine
C9H10Cl2N2O2
C15H12I3NO4
330-55-2
6893-02-3
249.093
650.974 cry
92.9(1)
236 dec
6619
6620
Lipoamide
α-Lipoic acid
940-69-2
62-46-4
205.341 cry
206.326 ye nd
128
61
6621
Lisinopril
6622
Lithium oxalate
C2Li2O4
30903-87-8 101.901 col cry
dec
6623
Lobelanidine
C22H29NO2
552-72-7
339.471 sc (al, eth)
150
6624
Lobelanine
C22H25NO2
579-21-5
99
6625
Lobeline
C22H27NO2
90-69-7
335.440 nd (eth,
peth)
337.455 nd (al, bz)
6626
Loflucarban
C13H9Cl2FN2S
790-69-2
315.192
163.5
HCP_Section_03.indb 338
1-Dodecylhexahydro-2Hazepin-2-one
2-Amino-4-methylpentanoic
acid
cis,cis-9,12-Octadecadienoic
acid
cis,cis,cis-9,12,15-Octadecatrienoic acid
1,2-Dithiolane-3-pentanamide C8H15NOS2
1,2-Dithiolane-3-pentanoic
C8H14O2S2
acid
C21H35N3O7
pale ye nd
222.366 nd (al)
184.5
167
1.2620
89
114
105
16050
0.91
292
0.9078100 1.4667110 vs ace, eth,
EtOH
1.3225
vs py
1.5325
i H2O; vs bz; s
ace, 2-PrOH,
xyl
1.29318
s H2O; sl EtOH; i
eth
sl H2O
1.29318
sl H2O; i EtOH,
eth
s H2O; sl EtOH,
eth; i ace, bz,
chl
248 dec
203
181
s H2O; i EtOH,
eth, ace, bz; s
alk, MeOH
277(2)
150
198
-74.0(0.6)
136.234 oil
177.6(0.5)
178(1)
i H2O, EtOH; s
dil alk
162
i H2O
83915-83-7 441.519 wh cry pow 159
130.5
1.446020 i H2O; misc
EtOH, eth
sl H2O; s EtOH,
ace, chl
1.469920 vs ace, bz, eth,
EtOH
1.480020 i H2O; s EtOH,
eth; sl bz
2.12117
i EtOH, chl, ace;
sl MeOH
s H2O; i EtOH,
eth
i H2O; s EtOH; sl
eth; vs ace,
bz, py
vs ace, bz,
EtOH, chl
sl H2O; s EtOH,
eth, bz, chl; vs
ace
4/11/16 11:32 AM
Physical Constants of Organic Compounds
O
HO
3-339
O
O
N
O
O
OH
H
O
O
H
O
NH
O
O
N
H
O
O
OH
O
6591
Lasiocarpine
O
OH
O
6590
Lappaconitine
6592
Laudanidine
Laudanine
O
N
H
O
H
O
N
O
Br
Cl
O
N
Pb
S
6595
6594
Laudanosine
Cl
S
O
6593
NH2
6599
6597
6600
Lenacil
O
NH2
NH2
6601
OH
O
6602
D-Leucine
O
H
N
OH
NH2
DL-Leucine
6598
Ledol
OH
O
N
H
S
O
OH
Leptophos
H
N
Lead bis(dimethyldithiocarbamate)
O
O
N
S
6596
Laurocapram
Laureline
S
O P
O
OH
H
N
O
N
O
OH
HO
N
6589
O
Organic
O
6603
L-Leucine
N-Leucylglycine
N
O
O
N
H
H
N
HO
O
O
O
O
N
H
HO
O
H-5-oxoPro-His-Trp-Ser-Tyr-D-Leu-Leu-Arg-Pro-NHEt
6604
OH
O
N
O
H
6605
Leuprolide
NH2
HO
OH
6607
6606
Leurosine
Levodopa
Levallorphan
HO
O
H
HO
6608
O
N
6609
Levopimaric acid
O
HO
6610
Levorphanol
6612
6611
d-Limonene
6613
Linalol
l-Limonene
Linalyl acetate
CH3
HO C H
N
NH C H
O HO
O
O
OH
OH
S
OH
H
N
O
OH
N
O
O
Cl
Cl
6614
6615
Lincomycin
6617
6616
Linoleic acid
Linuron
Linolenic acid
NH2
I
O
NH2
HO
I
O
OH
I
6618
HS
S
SH
S
6620
N
O
HO
O
O
O
O
2Li
O
6621
α-Lipoic acid
Lipoamide
OH
N
H
OH
NH2
6619
Liothyronine
O
O
O
6622
Lisinopril
Lithium oxalate
Cl
OH
OH
H N H
6623
Lobelanidine
O
O
H
N
H
6624
Lobelanine
OH
H
H
N
6625
Lobeline
O
F
S
N
H
N
H
6626
Loflucarban
Cl
Physical Constants of Organic Compounds
3-340
Mol.
Wt.
Physical
Form
den
g cm –3
258
0.931918 1.504020 i H2O; s bz
Organic
Name
Synonym
Mol. Form.
CAS RN
6627
6628
6629
Longifolene
Loratadine
Lovastatin
Kuromatsuene
Claritin
Mevacor
C15H24
C22H23ClN2O2
C24H36O5
475-20-7
204.352
79794-75-5 382.883 cry (MeCN) 132
75330-75-5 404.540 wh cry (ace 179(1)
aq)
6630
6631
6632
Lovozal
Loxapine
Loxoprofen
C15H7Cl2F3N2O2
C18H18ClN3O
C15H18O3
14255-88-0 375.130 ye cry
103
1977-10-2 327.808 ye cry (peth) 109.5
68767-14-6 246.302 col oil
110
1920.3
6633
Luciculine
C22H35NO3
5008-52-6
6634
6635
Lunacrine
Lup-20(29)-ene-3,28-diol, (3β) Betulin
C16H19NO3
C30H50O2
6636
Lup-20(29)-en-3-ol, (3β)
6637
α-Methyl-4-[(2oxocyclopentyl)­methyl]
benzeneacetic acid
Napelline
mp/˚C
bp/˚C
No.
nD
Solubility
i H2O; vs chl; s
DMF; sl ace,
EtOH
s ace, diox
149
1650.02
82-40-6
473-98-3
361.518 cry (+1w,
ace)
273.327
442.717 nd (al +1)
256(2)
240 sub
C30H50O
545-47-1
426.717 nd (al, ace)
216
Lupulon
C26H38O4
468-28-0
414.578 pr (MeOH)
93
6638
Luteolin
C15H10O6
491-70-3
286.236 ye nd (dil al, 328(1)
+ 1 w)
6639
6640
Luteoskyrin
Lycodine
C30H22O12
C16H22N2
21884-44-6 574.489 ye nd (EtOH) 278 dec
20316-18-1 242.359 orth pr
99
1901.0
s H2O, chl, eth,
EtOH; i peth
6641
6642
Lycomarasmine
Lycorine
C9H15N3O7
C16H17NO4
7611-43-0
476-28-8
277.231
287.311 pr (al, py)
228 dec
280
sub
6643
Lysergamide
C16H17N3O
478-94-4
137.5
6644
Lysergic acid
C16H16N2O2
82-58-6
6645
6646
6647
6648
Lysergide
DL-Lysine
D-Lysine
L-Lysine
50-37-3
70-54-2
923-27-3
56-87-1
267.325 cry (MeOH),
pr (aq,
ace)
268.310 lf or hex sc
(w)
323.432
146.187
146.187
146.187 nd (w, dil al)
i H2O; sl EtOH,
eth, chl
sl EtOH, ace, os
6649
6650
6651
6652
L-Lysine, hydrochloride
D-Lyxose
L-Lyxose
Maclurin
C6H15ClN2O2
C5H10O5
C5H10O5
C13H10O6
10098-89-2
1114-34-7
1949-78-6
519-34-6
182.648
150.130
150.130
262.214 ye nd (al)
263 dec
108
110
222.5
6653
6654
Magenta base
Magenta I
C20H19N3
C20H20ClN3
3248-93-9
632-99-5
301.385 br-red cry
337.846 grn cry
186 dec
200 dec
6655
6656
Magnesium stearate
Malachite Green
Magnesium octadecanoate
C36H70MgO4
C23H25ClN2
557-04-0
569-64-2
591.244 wh pow
364.911 grn cry
132
6657
Malaoxon
(Dimethoxyphosphinylthio)­
butanedioic acid
C10H19O7PS
1634-78-2
314.293 liq
6658
Malathion
C10H19O6PS2
121-75-5
330.358 ye-br liq
3.0(0.4)
6659
Maleic acid
C4H4O4
110-16-7
116.073 mcl pr (w)
143.5(0.5)
6660
Maleic anhydride
C4H2O3
108-31-6
98.057
6661
6662
Maleonitrile
Malic acid
cis-Butenedinitrile
Hydroxybutanedioic acid
C4H2N2
C4H6O5
928-53-0
617-48-1
78.072 pr (EtOH)
134.088
31.5
132
6663
6664
Malonaldehyde
Malonic acid
1,3-Propanedial
C3H4O2
C3H4O4
542-78-9
141-82-2
72.063 hyg nd
104.062 tcl (al)
73
135(1)
6665
Malononitrile
C3H2N2
109-77-3
66.061
31.83(0.02)
6666
6667
6668
Maltopentaose
α-Maltose
6-O-α-Maltosyl-β-cyclodextrin
C30H52O26
C12H22O11
C54H90O45
34620-76-3 828.718 cry (w)
4482-75-1 342.296 nd (al)
1047231459.266 cry (MeOH)
60-6
HCP_Section_03.indb 340
Lupeol
8,8’-Dihydroxyrugulosin
C20H25N3O
2,6-Diaminohexanoic acid, (±) C6H14N2O2
2,6-Diaminohexanoic acid, (D) C6H14N2O2
2,6-Diaminohexanoic acid, (L) C6H14N2O2
(3,4-Dihydroxyphenyl)­(2,4,6trihydroxyphenyl)methanone
Rosaniline
Rosaniline hydrochloride
cis-2-Butenedioic acid
vs EtOH
0.9457218 1.4910218
240 dec
s chl
i H2O; sl EtOH,
bz; s eth,
AcOEt, lig
i H2O; vs EtOH,
eth, ace, bz,
chl
i H2O; s EtOH,
peth, hx
sl H2O; s EtOH,
eth, alk, con
sulf
sl H2O, eth, bz;
s EtOH, py
82
224
218 dec
224 dec
sl H2O
s H2O
s H2O; i EtOH,
eth, ace, bz
1.54520
vs eth, EtOH
sl H2O, EtOH; i
eth
i H2O; reac acid
vs H2O, EtOH,
MeOH
1320.1
nd (chl, eth) 52.56(0.04)
78 (hyd)
162.5
1560.7 dec
202
1.207620 1.496020 sl H2O; s EtOH,
eth, bz
1.59020
vs H2O, EtOH,
ace; s eth; i
bz, chl
1.31460
s H2O; s eth,
ace, chl; sl lig
11120
1.60120
s H2O; vs eth,
EtOH, MeOH
sub
1.61910
219(3)
1.191020 1.414634
vs H2O, py; s
EtOH, eth; i bz
s H2O, ace, bz,
chl; vs EtOH,
eth
1.54620
vs H2O
4/11/16 11:32 AM
Physical Constants of Organic Compounds
3-341
HO
Cl
N
O
N
F
Cl
N
F
F
O
O
Cl
N
O
O
O
N
N
6627
6628
6629
6630
Lovastatin
6633
O
O
H
O
O
N
HO
O
OH
HO
6634
6635
Lunacrine
6636
Lup-20(29)-ene-3,28-diol, (3β)
6637
Lup-20(29)-en-3-ol, (3β)
Lupulon
Organic
Luciculine
Loxoprofen
OH
N
OH
6632
Loxapine
H
O
H
6631
Lovozal
OH
H
OH
O
O
Loratadine
OH
O
Cl
O
Longifolene
O
N
OH O
OH
OH O
HO
OH
O
O
OH O HO
HO
OH O
OH
6638
HO
H
O
HO
N
OH
OH
H
N
N
H
HO
6640
O
N
NH
Lycodine
N
N
H
Lycomarasmine
Lycorine
O
OH
NH2
HCl
6649
CHO
H
H
OH
CH2OH
H
H
HO
6650
L-Lysine, hydrochloride
CHO
OH
OH
H
CH2OH
O
6648
D-Lysine
L-Lysine
HO
HO
NH2
OH
6654
Magenta base
N
Cl
Magenta I
O
O
O
O
P
S
O
6656
Magnesium stearate
Malachite Green
O
O
O
S
P
O
S
O
O
6657
6658
2
6655
O
O
Mg 2
HCl
NH2
6653
Maclurin
N
O
NH
OH
6652
L-Lyxose
O
H2N
NH
HO
6651
D-Lyxose
NH2
6647
DL-Lysine
H2N
HO
HO
H
OH
NH2
6646
Lysergide
O
H2N
OH
NH2
6645
6644
H2N
OH
NH
Lysergic acid
H2N
N
6642
H
NH
O
H
O
O
6643
H
O
NH2
6641
H2N
Lysergamide
HO
O
O
O
N
OH
Luteoskyrin
O
O
N
H
6639
Luteolin
H2N
H
Malaoxon
Malathion
OH O
O
HO
O
O
OH HO
6659
HO
OH
HO
OH
OH
O
OH
6666
Maltopentaose
3
OH
OH
O
OH
O
HO
OH
6667
α-Maltose
OH
OH
OH
OH
OH
Malononitrile
HO
OH
HO
O
O
O
OH
O
OH
OH
O
OH
N
6665
Malonic acid
O
O
HO
N
OH
6664
HO
O
O
O
HO
Malonaldehyde
HO
O
O
6663
Malic acid
HO
O
O
O
6662
Maleonitrile
HO
O
O
OH
O
N
6661
Maleic anhydride
HO
OH
N
6660
Maleic acid
HO
O
O
OH
O
OH
5
OH
O
6668
6-O-α-Maltosyl-β-cyclodextrin
Physical Constants of Organic Compounds
3-342
No.
Name
6669
6670
Maltotetraose
Malvidin chloride
6671
Mandelic acid
6672
Mandelonitrile glucoside
6673
Maneb
6674
Manganese(II) acetate
6675
6676
6678
Manganese carbonyl
Manganese cyclopentadienyl
tricarbonyl
Manganese 2-methylcyclopentadienyl tricarbonyl
D-Mannitol
6679
6680
Synonym
α-Hydroxybenzeneacetic acid
Mol.
Wt.
Physical
Form
Mol. Form.
CAS RN
C24H42O21
C17H15ClO7
34612-38-9 666.577 amorp solid 170 dec
643-84-5
366.750
>300
C8H8O3
611-72-3
C14H17NO6
138-53-4
152.148 orth pl
mp/˚C
bp/˚C
118.6(1)
den
g cm –3
C4H6MnN2S4
C4H6O4Mn
638-38-0
C10Mn2O10
C8H5MnO3
10170-69-1 389.977 ye mcl cry
12079-65-1 204.062 pale ye cry
154
77(2)
C9H7MnO3
12108-13-3 218.088 ye liq
1.5
233
1.38820
Cordycepic acid
C6H14O6
69-65-8
164.1(0.1)
2953.5
1.48920
D-Mannitol hexanitrate
D-Mannose
C6H8N6O18
C6H12O6
111(1)
118(2)
exp
Seminose
182.171 orth nd or
pr (w)
15825-70-4 452.157 nd (al)
3458-28-4 180.155 nd or orth
pr (al)
1.820
1.53920
6681
6682
L-Mannose
Matridin-15-one
C6H12O6
C15H24N2O
10030-80-5 180.155 cry (al)
519-02-8
248.364 α-nd or pl;
β-orth pr
132
Matrine
6683
6684
Mazindol
Mebendazole
C16H13ClN2O
C16H13N3O3
6685
Mebhydroline
C19H20N2
22232-71-9 284.739 cry (ace/hx) 198
31431-39-7 295.292 cry (HOAc/ 288.5
MeOH)
524-81-2
276.375 cry
95
6686
6687
6688
6689
Mecarbam
Meclizine
Medroxyprogesterone
Mefenamic acid
C10H20NO5PS2
C25H27ClN2
C22H32O3
C15H15NO2
2595-54-2
569-65-3
520-85-4
61-68-7
6690
Mefloquine
C17H16F6N2O
178.2
6691
6692
6693
Mefluidide
Melezitose
α-D-Melibiose
C11H13F3N2O3S
C18H32O16
C12H22O11
53230-10-7 378.311 cry (MeOH
aq)
53780-34-0 310.292
597-12-6
504.437 cry (w+2)
585-99-9
342.296
6694
Melinamide
C26H41NO
14417-88-0 383.610 oil
<4
6695
Melphalan
C13H18Cl2N2O2
148-82-3
305.200 nd
183 dec
6696
6697
6698
Menaquinone 7
Menazon
p-Menthane hydroperoxide
C46H64O2
C6H12N5O2PS2
C10H20O2
2124-57-4
78-57-9
80-47-7
648.999 cry
281.296 cry (MeOH)
172.265
54
160
6699
p-Menth-8-en-2-one
7764-50-3
152.233
6700
Menthol 3-methylbutanoate
6701
6702
6703
Meperidine
Mephenytoin
Mephobarbital
6704
6705
Mephosfolan
Mepiquat chloride
6706
Mepivacaine
6707
Mepivacaine monohydrochloride
Mercaptoacetic acid,
2-ethylhexyl ester
2-Mercaptobenzoic acid
6677
Organic
6708
6709
HCP_Section_03.indb 342
Dimanganese decacarbonyl
2-[(2,3-Dimethylphenyl)­
amino]­benzoic acid
6-O-α-D-Galactopyranosyl-Dglucose
N-(1-Phenylethyl)-9,12octadecadieneamide, (Z,Z)L-Phenylalanine, 4-[bis(2chloroethyl)amino]Vitamin K2(35)
1-Methyl-1-(4-methylcyclohexyl)ethyl hydroperoxide
2-Methyl-5-(1-methylethenyl)­ C10H16O
cyclohexanone
Menthol, isovalerate
C15H28O2
Pethidine
Piperidinium, 1,1-dimethyl-,
chloride
N-(2,6-Dimethylphenyl)-1methyl-2-piperidinecarboxamide
Carbocaine hydrochloride
o-Thiosalicylic acid
173.027 red cry (w)
329.374 ye oil
390.948
344.487
241.286 hyg cry
210
i H2O; misc bz
1.3330
1.528625
2111
1440.02
230
1.22320
214.5
230 dec
184.3(0.5)
153
1.556525
2020.07
vs H2O; sl EtOH,
py; i eth
vs bz, eth, EtOH
vs H2O; sl EtOH,
MeOH; i eth,
bz
vs H2O
s H2O, eth, ace;
vs EtOH, bz; sl
peth
i H2O; s EtOH
i H2O, EtOH, eth,
chl
i H2O; sl eth; vs
EtOH, ace,
MeOH
sl H2O
s CS2
vs chl
s alk; sl eth, chl
vs H2O
vs H2O; sl EtOH;
dec acid
1.505023
i H2O; s EtOH
sl H2O; s thf
259
0.92
223.0
16409-46-4 240.382
247.334
218.251
246.261 wh cry (w)
s H2O, MeOH,
HOAc; i ace
i H2O; s os
s os
1.75
2236
Solubility
sl H2O; s EtOH,
MeOH
s H2O, eth,
EtOH, i-PrOH
vs H2O, EtOH
1.289020
295.288 wh nd or pl 122
(al)
12427-38-2 265.302
dec 200
Manganese,
[[1,2-ethanediylbis­
[carbamodithioato]](2-)]-
nD
1299
30
136
176
0.90815
1.448620 i H2O; s EtOH,
ace
C15H21NO2
C12H14N2O2
C13H14N2O3
57-42-1
50-12-4
115-38-8
1555
C8H16NO3PS2
C7H16ClN
950-10-7
269.322 ye liq
24307-26-4 149.662
223
C15H22N2O
96-88-8
246.348 cry (eth)
150.5
s CS2
C15H23ClN2O
1722-62-9
282.809 cry
263
s H2O
C10H20O2S
7659-86-1
204.330
C7H6O2S
147-93-3
154.187 lf or nd (al,
w, HOAc)
1200.001
133.5
168.5
sub
1.535426
sl H2O, eth, chl;
vs EtOH
s ace, EtOH, bz
0.9720
s H2O, EtOH,
eth; sl DMSO,
lig
4/11/16 11:32 AM
Physical Constants of Organic Compounds
3-343
N
OH
HO
HO
OH
HO
O
O
O
OH
OH
O
HO
OH
OH
O
OH
OH
HN
S
S
O
S
S
Mn2
O
6673
2
6674
Maneb
Mandelonitrile glucoside
CO
Mn CO
CO
6675
Manganese(II) acetate
6672
Mandelic acid
CO CO
OC
CO
OC Mn Mn CO
OC
CO
CO CO
NH
OH
6671
Malvidin chloride
Mn
HO
O
6670
Maltotetraose
OH
OH
O
6669
O
O
OH
OH
OH
2
HO
O
O
Cl
HO
CO
Mn CO
CO
6676
Manganese carbonyl
6677
Manganese cyclopentadienyl tricarbonyl
Manganese 2-methylcyclopentadienyl tricarbonyl
N
HO
HO
H
H
O2NO
O2NO
H
H
6678
CH2ONO2
H
H
ONO2
ONO2
CH2ONO2
HO
HO
H
H
6679
D-Mannitol
CHO
H
H
OH
OH
CH2OH
H
H
HO
HO
6680
D-Mannitol hexanitrate
CHO
OH
OH
H
H
CH2OH
O
H
6681
D-Mannose
N
H
O
HO
H
Cl
O
S P S
O
6685
O
Mazindol
Mebendazole
O
OH
Cl
O
H
N
O
O
6686
Mebhydroline
HO
O
N
O
6684
N
N
O
N
H
6683
Matridin-15-one
N
H
N
N
6682
L-Mannose
N
N
N
H
Organic
CH2OH
H
H
OH
OH
CH2OH
6688
6687
Mecarbam
6689
Medroxyprogesterone
Meclizine
Mefenamic acid
HO
HO
HO
N
F
F
F
F
O
O
N
H H
F
H
N
S
O O
O
F
F
HN
6690
F
F
HO
HO
HO
OH
O
O
O
OH
HO
O
O
OH
OH
OH
OH
OH
OH
6692
Mefluidide
6693
α-D-Melibiose
Melezitose
O
O
O
H
OH
Cl
N
H
O
OH
HO
O
6691
Mefloquine
HO
OH
OH
NH2
N
N
O
Cl
6694
H2N
6696
6695
Melinamide
O
P
O
S
S
7
NH2
6697
Menaquinone 7
Melphalan
N
N
Menazon
O
O
O
p-Menthane hydroperoxide
S
O
N P O
O
6704
Mephosfolan
6700
p-Menth-8-en-2-one
N
Cl
6705
Mepiquat chloride
6706
Mepivacaine
HCl
H
N
N
N
NH
O
6702
Meperidine
H
N
O
O
6701
Menthol 3-methylbutanoate
N
NH
N
OH
6699
O
O
O
6698
S
O
Mephenytoin
N
O
6703
Mephobarbital
O
O
HS
O
OH
SH
O
O
6707
Mepivacaine monohydrochloride
6708
Mercaptoacetic acid, 2-ethylhexyl ester
6709
2-Mercaptobenzoic acid
Physical Constants of Organic Compounds
3-344
No.
Name
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
6710
Mercaptobenzthiazyl ether
2,2’-Dithiobis[benzothiazole]
C14H8N2S4
120-78-5
332.487 ye nd
6711
2-Mercaptoethanol
C2H6OS
60-24-2
78.133
6712
C4H8O2S
4695-31-2
120.171
47
C12H11NOS
93-42-5
217.286
111.5
6714
6715
2-Mercapto-2-methylpropanoic acid
2-Mercapto-N-2-naphthylacetamide
2-Mercaptophenol
4-Mercaptophenol
C6H6OS
C6H6OS
1121-24-0
637-89-8
126.176 oil
126.176 cry
5.5
29.5
6716
3-Mercapto-1,2-propanediol
C3H8O2S
96-27-5
108.160 visc
6717
3-Mercaptopropanoic acid
C3H6O2S
107-96-0
106.144 amor
6718
6719
6720
3-Mercapto-D-valine
Mercury(II) benzoate
Mercury(II) oleate
Penicillamine
Mercuric benzoate
Mercuric oleate
C5H11NO2S
C14H10HgO4
C36H66HgO4
52-67-5
583-15-3
1191-80-6
149.212
198.5
442.82 cry pow (w) ≈125
763.50 ye-br solid
6721
6722
Mercury(II) phenyl acetate
Merphos
C8H8HgO2
C12H27PS3
62-38-4
150-50-5
336.74
298.511
6723
Mesityl oxide
Phenylmercuric acetate
Phosphorotrithious acid,
S,S,S-tributyl ester
Isobutenyl methyl ketone
C6H10O
141-79-7
98.142
6724
6725
Mesoridazine
Mestranol
C21H26N2OS2
C21H26O2
5588-33-0
72-33-3
386.573 oil
310.430 cry
154(1)
6726
[2.2]Metacyclophane
C16H16
2319-97-3
208.298 orth pr
131(1)
6727
6728
Metalaxyl
Metaldehyde
C15H21NO4
(C2H4O)x
57837-19-1 279.333
73.0(0.5)
37273-91-9 44.052 tetr nd or pr 246
(al)
6729
Metanil Yellow
C18H14N3NaO3S
587-98-4
375.377 br-ye pow
6730
Metaraminol
54-49-9
6731
6732
Metaxalone
Methacholine chloride
2-Amino-1-(3-hydroxyphenyl)- C9H13NO2
1-propanol, (1R,2S)
C12H15NO3
C8H18ClNO2
1665-48-1
62-51-1
167.205 hyg cry
(HCl)
221.252 cry (AcOEt)
195.688 hyg cry
122
172
2231.5
6733
Methacrylic acid
2-Methylpropenoic acid
C4H6O2
79-41-4
86.090
14.6(0.8)
160(1)
6734
6735
Methacycline
Methadone hydrochloride
C22H22N2O8
C21H28ClNO
914-00-1
1095-90-5
442.418 cry
345.906 pl (al-eth)
6736
Methallenestril
C18H22O3
517-18-0
6737
Methamidophos
Phosphoramidothioic acid,
O,S-dimethyl ester
6738
6739
Methamphetamine
Methamphetamine
hydrochloride
537-46-2
51-57-0
149.233
185.694
6740
6741
Methandrostenolone
Methane
C10H15N
C10H16ClN
N,αDimethylbenzeneethanamine,
hydrochloride, (S)C20H28O2
CH4
72-63-9
74-82-8
300.435
16.043 col gas
CH5AsO3
CH4O6S2
CH4O3S
CH3ClO2S
124-58-3
503-40-2
75-75-2
124-63-0
139.971
176.169
96.106
114.552
Methyl mercaptan
CH3FO2S
CH4S
558-25-8
74-93-1
98.097
48.108
Formamidine
Formamidine acetate
CH4N2
C3H8N2O2
463-52-5
3473-63-0
44.056 pr
104.108
6713
Organic
6742
6743
6744
6745
Methanearsonic acid
Methanedisulfonic acid
Methanesulfonic acid
Methanesulfonyl chloride
6746
6747
Methanesulfonyl fluoride
Methanethiol
6748
6749
Methanimidamide
Methanimidamide,
monoacetate
HCP_Section_03.indb 344
Thionalide
Thioglycerol
Tricyclo[9.3.1.1]hexadeca1(15),4,6,8(16),11,13hexaene
Metacetaldehyde (polymer)
6-(Dimethylamino)-4,4-diphenyl-3-heptanone
hydrochloride
Methionic acid
Methylsulfonic acid
C2H8NO2PS
Physical
Form
mp/˚C
bp/˚C
180
liq
pr
286.366 cry (MeOH
aq)
10265-92-6 141.130
nD
1.50
150.0(0.9)
16.5(0.5)
den
g cm –3
1.114320 1.499620
10115
217
16745
1.23710
1.128525 1.510125
1001
1.245520 1.526820
11115
1.21821
1.49420
Solubility
i H2O; sl EtOH,
bz, ctc, ace
s H2O, EtOH,
eth, bz
vs H2O
i H2O; vs EtOH,
os
vs bz, eth, EtOH
s H2O, EtOH,
alk, con sulf
sl H2O, eth, bz,
chl; msc EtOH;
vs ace
s H2O, EtOH,
eth, ctc
i EtOH
i H2O; sl EtOH,
eth
i H2O; s chl
153
100
1370.7
1.0220
-52.8(0.4)
129.7(0.4)
0.865320 1.444020 s H2O, ace; msc
EtOH, eth
i H2O; s diox,
eth, EtOH, chl
sl EtOH; s bz,
eth
290
115 sub
i H2O, ace; sl
EtOH, eth, bz,
chl
vs H2O, EtOH; s
bz, eth; sl ace
s H2O
1.015320 1.431420
vs H2O, EtOH,
chl
s H2O, chl; msc
EtOH, eth
205 dec
235
vs H2O, EtOH
139
s eth
46.7(0.5)
1.3120
212
174(1)
166
-182.4566​
(0.0003)
160.5
98
20
col gas
vs H2O, EtOH,
chl
-161.5(0.2)
162
16710
159(3)
123.5
-122.98(0.09) 6.0(0.1)
81
161.5
0.4228-
dec
1.481218 1.431718
1.480518 1.457320
0.866520
sl H2O, ace; s
EtOH, eth, bz,
tol, MeOH
s H2O, EtOH
i H2O; s HNO3
s H2O
i H2O; s EtOH,
eth
sl H2O, chl; vs
EtOH, eth
vs H2O, EtOH
vs H2O
4/11/16 11:32 AM
Physical Constants of Organic Compounds
3-345
OH
N
N
S S
SH
S
OH
HS
S
6710
HS
H
N
OH
HS
OH
2-Mercaptophenol
4-Mercaptophenol
O
O
Hg2
OH
NH2
OH
6717
3-Mercapto-1,2-propanediol
6715
O
HS
O
6716
6714
2-Mercapto-N-2-naphthylacetamide
2-Mercapto-2-methylpropanoic acid
OH
SH
6713
6712
2-Mercaptoethanol
SH
SH
O
O
6711
Mercaptobenzthiazyl ether
HO
2
6718
3-Mercaptopropanoic acid
6719
3-Mercapto-D-valine
Mercury(II) benzoate
Organic
O
O
Hg
O
Hg
O
O
S
6720
6721
Mercury(II) oleate
O
S
6722
Mercury(II) phenyl acetate
N
6723
Merphos
Mesityl oxide
HO
O
S
N
S
P
O
O
O
H
N
O
S
6724
6726
6725
Mesoridazine
H
N
OH
O
H
OH N
H
O
6731
Metaraminol
O
N
Metaxalone
HO
OH O
6733
Methacrylic acid
O
HCl
O
O
O P S
NH2
O
6735
Methacycline
OH
Cl
Methacholine chloride
OH
6734
N
6732
NH2
OH O
O
O
6730
OH
Metaldehyde
O
OH
Metanil Yellow
6728
Metalaxyl
O
NH2
6729
O
NH
N
SO3Na
6727
[2.2]Metacyclophane
Mestranol
N
O
O
O
O
O
6736
Methadone hydrochloride
HN
6737
Methallenestril
6738
Methamidophos
Methamphetamine
SO3H
SO3H
H
O
S OH
O
OH
H
HN
6739
HCl
Methamphetamine hydrochloride
O
S Cl
O
6745
Methanesulfonyl chloride
O
6740
Methandrostenolone
O
S F
O
6746
Methanesulfonyl fluoride
O
H
H
As OH
H
H
OH
6741
6742
Methane
H
6743
Methanearsonic acid
6744
Methanedisulfonic acid
Methanesulfonic acid
H
H
O
SH
H
6747
Methanethiol
H2N
NH
6748
Methanimidamide
H2N
NH
6749
OH
Methanimidamide, monoacetate
Physical Constants of Organic Compounds
3-346
Organic
No.
Name
Synonym
Mol. Form.
CAS RN
Mol.
Wt.
Physical
Form
mp/˚C
bp/˚C
6750
Methanol
Methyl alcohol
CH4O
67-56-1
32.042
liq
-97.5(0.1)
64.5(0.7)
6751
Methantheline bromide
C21H26BrNO3
53-46-3
420.340 cry (i-PrOH) 174.5
6752
6753
Methapyrilene
Metharbital
C14H19N3S
C9H14N2O3
91-80-5
50-11-3
261.386
198.218 nd
6754
6755
6756
Methazolamide
Methazole
Methenamine allyl iodide
C5H8N4O3S2
C9H6Cl2N2O3
C9H17IN4
554-57-4
236.273 cry (w)
20354-26-1 261.061
36895-62-2 308.162 cry
213 dec
123.9(0.5)
148 dec
6757
Methestrol
C20H26O2
130-73-4
145
6758
6759
Methidathion
Methiocarb
C6H11N2O4PS3
C11H15NO2S
950-37-8
2032-65-7
298.419 cry (dil
HOAc)
302.330
225.308
6760
L-Methionine
C5H11NO2S
63-68-3
149.212 hex pl (dil
al)
281 dec
6761
6762
6763
6764
6765
6766
Methocarbamol
Methomyl
Methoprene
Methoprotryne
Methotrexate
Methoxamine hydrochloride
Guaifenesin-1-carbamate
C11H15NO5
C5H10N2O2S
C19H34O3
C11H21N5OS
C20H22N8O5
C11H18ClNO3
532-03-6
16752-77-5
40596-69-8
841-06-5
59-05-2
61-16-5
241.241
162.210
310.471
271.383
454.440
247.719
93
79(2)
6767
Methoxsalen
9-Methoxy-7H-furo[3,2-g]­[1]­
benzopyran-7-one
C12H8O4
298-81-7
6768
Methoxyacetaldehyde
6769
6770
5,5-Diethyl-1-methyl2,4,6(1H,3H,5H)-pyrimidinetrione
Allylhexamethylenetetramine
iodide
Phenol, 3,5-dimethyl-4(methylthio)-, methylcarbamate
cry (bz)
1743
150.5
nD
vs H2O; i chl,
eth
42.5(0.5)
121.5(0.4)
s H2O; i EtOH,
eth, ace, bz,
peth; sl HOAc
s EtOH
1.294624
0.92620
69
190 dec
214
sl H2O; s os
C3H6O2
216.190 pr (dil al) nd 148
(peth)
10312-83-1 74.079
92(4)
1.00525
Methoxyacetic acid
Methoxyacetonitrile
C3H6O3
C3H5NO
625-45-6
1738-36-9
204(3)
121(4)
1.176820 1.416820
0.949220 1.383120
6771
Methoxyacetyl chloride
C3H5ClO2
38870-89-2 108.524
112(7)
1.187120 1.419920
6772
2-Methoxyaniline
o-Anisidine
C7H9NO
90-04-0
123.152 ye liq
6.2
221(7)
1.092320 1.571510
6773
3-Methoxyaniline
m-Anisidine
C7H9NO
536-90-3
123.152 liq
-1
251
1.09620
1.579420
6774
4-Methoxyaniline
p-Anisidine
C7H9NO
104-94-9
123.152 orth pl
57.8(0.9)
243(6)
1.07157
1.555960
6775
o-Anisidine hydrochloride
C7H10ClNO
134-29-2
159.613 nd
225
C15H10O3
82-39-3
238.238
170.3
6777
2-Methoxyaniline
hydrochloride
1-Methoxy-9,10-anthracenedione
2-Methoxybenzaldehyde
C8H8O2
135-02-4
136.149 pr
37.5(0.5)
6778
3-Methoxybenzaldehyde
C8H8O2
591-31-1
136.149
6779
4-Methoxybenzaldehyde
C8H8O2
123-11-5
136.149 liq
6780
4-Methoxybenzamide
C8H9NO2
3424-93-9
6781
C9H10O2
6782
4-Methoxybenzeneacetaldehyde
2-Methoxybenzeneacetic acid
6783
6784
6785
6776
6786
90.078
71.078
hyg
1.395020
243(4)
1.132620 1.560020
220(5)
1.118720 1.553020
0
255(5)
1.11915
1.573020
166.5
295
5703-26-4
151.163 nd or tab
(w)
150.174
1.09620
1.535920
C9H10O3
93-25-4
166.173 nd (w)
124
1002
4-Methoxybenzeneacetic acid
C9H10O3
104-01-8
166.173 pl (w)
84.9(0.5)
1382
4-Methoxybenzeneacetonitrile
4-Methoxy-1,2-benzenedi4-Methoxy-o-phenylenediamine
amine
4-Methoxy-1,3-benzenedi4-Methoxy-m-phenylenediamine
amine
C9H9NO
C7H10N2O
104-47-2
102-51-2
147.173
138.166 grn pl
51
286.5
20021
C7H10N2O
615-05-4
138.166 nd (eth)
67.5
HCP_Section_03.indb 346
p-Anisaldehyde
Solubility
0.791420 1.328820 msc H2O, EtOH,
eth, ace; vs
bz; s chl
s H2O, EtOH,
chl; i eth
1.591520
s H2O; sl chl
1.2425
1000.05
cry
ye cry (w)
cry
den
g cm –3
255.5
1.084520 1.530920
vs H2O; i