Acetyl chloride, chloro-
- Formula: C2H2Cl2O
- Molecular weight: 112.943
- IUPAC Standard InChIKey: VGCXGMAHQTYDJK-UHFFFAOYSA-N
- CAS Registry Number: 79-04-9
- Chemical structure:
This structure is also available as a 2d Mol file or as a computed 3d SD file
The 3d structure may be viewed using Java or Javascript. - Other names: α-Chloroacetyl chloride; Chloracetyl chloride; Chloroacetic acid chloride; Chloroacetic chloride; Chloroacetyl chloride; Monochloroacetyl chloride; CH2ClCOCl; Chloroethanoyl chloride; Chlorid kyseliny chloroctove; Chlorure de chloracetyle; UN 1752; Acetyl chloride, 2-chloro-
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Normal boiling point
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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Data compiled as indicated in comments:
BS - Robert L. Brown and Stephen E. Stein
TRC - Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director
Tboil (K) | Reference | Comment |
---|---|---|
378.7 | Aldrich Chemical Company Inc., 1990 | BS |
379. | Landor, Landor, et al., 1977 | Uncertainty assigned by TRC = 3. K; TRC |
378. | Khan and Johnathan, 1969 | Uncertainty assigned by TRC = 2. K; TRC |
378. | Pohloudek-Fabini and Schroepl, 1968 | Uncertainty assigned by TRC = 3. K; TRC |
381. | Lee, 1966 | Uncertainty assigned by TRC = 5. K; TRC |
380. | Aroney, Le Fevre, et al., 1965 | TRC |
381. | Briody and Satchell, 1965 | TRC |
381. | Parrot, Hervien, et al., 1964 | Uncertainty assigned by TRC = 3. K; TRC |
380. | Gross and Gloede, 1963 | Uncertainty assigned by TRC = 5. K; TRC |
378.0 | Euranto and Kujanpaa, 1961 | Uncertainty assigned by TRC = 1. K; TRC |
377. | Ol'dekop and Maier, 1960 | Uncertainty assigned by TRC = 3. K; TRC |
379. | Seryakov, Vaks, et al., 1960 | TRC |
383.15 | Slanina and Hennion, 1937 | Uncertainty assigned by TRC = 3. K; TRC |
379. | Branch and Nixon, 1936 | Uncertainty assigned by TRC = 3. K; TRC |
References
Go To: Top, Normal boiling point, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Aldrich Chemical Company Inc., 1990
Aldrich Chemical Company Inc.,
Catalog Handbook of Fine Chemicals, Aldrich Chemical Company, Inc., Milwaukee WI, 1990, 1. [all data]
Landor, Landor, et al., 1977
Landor, P.D.; Landor, S.R.; Odyek, O.,
Allenes: Synthesis of 1,3,50Trienamides as Potential Insecticides by the Wittig Reaction,
J. Chem. Soc., 1977, 1977, 93-5. [all data]
Khan and Johnathan, 1969
Khan, A.Y.; Johnathan, N.,
Rotational Isomerism in Chloroacetyl Halides,
J. Chem. Phys., 1969, 50, 1801. [all data]
Pohloudek-Fabini and Schroepl, 1968
Pohloudek-Fabini, R.; Schroepl, E.,
Aroyl and Acyl Isothiocyanates I. Synthesis of Acyl and Aroylisothicyanates,
Pharm. Zentralk., 1968, 107, 277-83. [all data]
Lee, 1966
Lee, J.B.,
Preparation of Acyl Halides under Very Mild Conditions,
J. Am. Chem. Soc., 1966, 88, 3440-1. [all data]
Aroney, Le Fevre, et al., 1965
Aroney, M.J.; Le Fevre, R.J.W.; Singh, A.N.,
Molecular polarisability dipole moments, molar kerr constants and apparent conformation of certain alpha-substituted carbonyl compounds,
J. Chem. Soc., 1965, 1965, 564. [all data]
Briody and Satchell, 1965
Briody, J.M.; Satchell, D.P.,
J. Chem. Soc., 1965, 1965, 168-75. [all data]
Parrot, Hervien, et al., 1964
Parrot, J.; Hervien, J.; Ursy, Y.; Paty, M.,
Preparation and Properties of the N-(chloro and bromoacetyl)-piperdines,
Bull. Soc. Chim. Fr., 1964, 1964, 1063-9. [all data]
Gross and Gloede, 1963
Gross, H.; Gloede, J.,
Chem. Ber., 1963, 96, 1387-94. [all data]
Euranto and Kujanpaa, 1961
Euranto, E.; Kujanpaa, T.,
The Preparation of α-Halo-sec-alkyl Esters of Aliphatic Acids,
Acta Chem. Scand., 1961, 15, 1209-14. [all data]
Ol'dekop and Maier, 1960
Ol'dekop, Y.U.; Maier, N.A.,
Reaction of Acetyl Peroxide with Mercuric Acetate and Some Salts of Inorganic Acids,
Zh. Obshch. Khim., 1960, 30, 3472. [all data]
Seryakov, Vaks, et al., 1960
Seryakov, G.V.; Vaks, S.A.; Sidorina, L.S.,
Phase equilibrium of liquid-vapor in systems formed from titanium tetrachloride with chlorides of mono - and tri - chloroacetic acids,
Zh. Obshch. Khim., 1960, 30, 2130-3. [all data]
Slanina and Hennion, 1937
Slanina, S.J.; Hennion, G.F.,
Reactions of Alkenyl Esters Derived from Alkylacetylenes,
J. Am. Chem. Soc., 1937, 59, 855. [all data]
Branch and Nixon, 1936
Branch, G.E.K.; Nixon, A.C.,
The Rate of Alcoholysis of Acyl Chlorides,
J. Am. Chem. Soc., 1936, 58, 2499-2504. [all data]
Notes
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- Symbols used in this document:
Tboil Boiling point - Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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