Acetyl chloride, dichloro-

• Formula: C₂HCl₃O
• Molecular weight: 147.388
• IUPAC Standard InChI: InChI=1S/C2HCl3O/c3-1(4)2(5)6/h1H Copy

  
• IUPAC Standard InChIKey: FBCCMZVIWNDFMO-UHFFFAOYSA-N Copy
• CAS Registry Number: 79-36-7
• Chemical structure:
  This structure is also available as a 2d Mol file
• Other names: α,α-Dichloroacetyl chloride; Dichloroacetyl chloride; 2,2-Dichloroacetyl chloride; CHCl2COCl; Dichloracetyl chloride; Chlorid kyseliny dichloroctove; Chlorure de dichloracetyle; Dichloroethanoyl chloride; UN 1765; Dichloroacetic acid chloride; Acetyl chloride, 2,2-dichloro-
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• Information on this page:
  • Gas phase thermochemistry data
  • Condensed phase thermochemistry data
  • Phase change data
  • Gas phase ion energetics data
  • References
  • Notes
• Other data available:
  • Reaction thermochemistry data
  • IR Spectrum
  • Mass spectrum (electron ionization)
  • Gas Chromatography
• Data at other public NIST sites:
  • Gas Phase Kinetics Database
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Gas phase thermochemistry data

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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 by: Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein

Condensed phase thermochemistry data

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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 by: Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein

Phase change data

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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

Gas phase ion energetics data

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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 by: Sharon G. Lias, Rhoda D. Levin, and Sherif A. Kafafi

Ionization energy determinations

References

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Pritchard and Skinner, 1950
Pritchard, H.O.; Skinner, H.A., The heats of hydrolysis of the chloro-substituted acetyl chlorides, J. Chem. Soc., 1950, 272-276. [all data]

Cox and Pilcher, 1970
Cox, J.D.; Pilcher, G., Thermochemistry of Organic and Organometallic Compounds, Academic Press, New York, 1970, 1-636. [all data]

Aldrich Chemical Company Inc., 1990
Aldrich Chemical Company Inc., Catalog Handbook of Fine Chemicals, Aldrich Chemical Company, Inc., Milwaukee WI, 1990, 1. [all data]

Weast and Grasselli, 1989
CRC Handbook of Data on Organic Compounds, 2nd Editon, Weast,R.C and Grasselli, J.G., ed(s)., CRC Press, Inc., Boca Raton, FL, 1989, 1. [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]

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]

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]

Katsumata and Kimura, 1975
Katsumata, S.; Kimura, K., Photoelectron spectra and sum rule consideration. Effect of chlorine substitution on ionization energies for chloroethanes, chloroacetaldehydes and chloroacetyl chlorides, J. Electron Spectrosc. Relat. Phenom., 1975, 6, 309. [all data]

Notes

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• Symbols used in this document:
  

  Tboil	Boiling point
  ΔfH°gas	Enthalpy of formation of gas at standard conditions
  ΔfH°liquid	Enthalpy of formation of liquid at standard conditions

• Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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