Propanoyl chloride
- Formula: C3H5ClO
- Molecular weight: 92.524
- IUPAC Standard InChIKey: RZWZRACFZGVKFM-UHFFFAOYSA-N
- CAS Registry Number: 79-03-8
- Chemical structure:
This structure is also available as a 2d Mol file - Other names: Propionyl chloride; Propionic chloride; Propionic acid chloride; UN 1815
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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 |
---|---|---|
351.2 | Aldrich Chemical Company Inc., 1990 | BS |
347. | Valitova, Popova, et al., 1990 | Uncertainty assigned by TRC = 4. K; TRC |
353.2 | Weast and Grasselli, 1989 | BS |
351. | Hoffmann and Haase, 1981 | Uncertainty assigned by TRC = 4. K; TRC |
355. | Lee, 1966 | Uncertainty assigned by TRC = 5. K; TRC |
343. | Briody and Satchell, 1965 | Uncertainty assigned by TRC = 4. K; TRC |
353. | Mamedov, 1964 | Uncertainty assigned by TRC = 3. K; TRC |
352. | Rylski, 1962 | Uncertainty assigned by TRC = 5. K; TRC |
351. | Yamase, 1961 | Uncertainty assigned by TRC = 3. K; TRC |
352.5 | Von Reis, 1881 | Uncertainty assigned by TRC = 0.6 K; TRC |
353. | Sestini, 1869 | Uncertainty assigned by TRC = 4. K; TRC |
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.
Aldrich Chemical Company Inc., 1990
Aldrich Chemical Company Inc.,
Catalog Handbook of Fine Chemicals, Aldrich Chemical Company, Inc., Milwaukee WI, 1990, 1. [all data]
Valitova, Popova, et al., 1990
Valitova, L.A.; Popova, E.V.; Ibragimov, Sh.N.; Ivanov, B.E.,
Izv. Akad. Nauk SSSR, Ser. Khim., 1990, 2, 428-32. [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]
Hoffmann and Haase, 1981
Hoffmann, H.M.R.; Haase, K.,
Synthesis, 1981, 9, 715-9. [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]
Briody and Satchell, 1965
Briody, J.M.; Satchell, D.P.,
J. Chem. Soc., 1965, 1965, 168-75. [all data]
Mamedov, 1964
Mamedov, G.Kh.,
Synthesis and Study of Aromatic Ketones,
Azber. Khim. Zh., 1964, 1964, 25-8. [all data]
Rylski, 1962
Rylski, L.,
Synthesis of 4-(9-Fluorenyl), 4-(9-Xanthyl)- and 4-(benzhydryl)- Derivatives of N-Methylpiperidin-4-ol I. The Fluorenyl Derivatives,
Acta Polon. Pharm., 1962, 19, 447-52. [all data]
Yamase, 1961
Yamase, Y.,
Friedel-Crafts Acylation II. Relative Reactivity for Some Acyl Halides,
Bull. Chem. Soc. Jpn., 1961, 34, 480-84. [all data]
Von Reis, 1881
Von Reis, M.A.,
IV. The Specific Heat of Liquid Organic Compounds and its Relation to Molecular Weight.,
Ann. Phys. (Leipzig), 1881, 13, 447. [all data]
Sestini, 1869
Sestini,
Bull. Soc. Chim. Fr., 1869, 11, 470. [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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