Chloroethyl chloroformate
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| Names | |||
|---|---|---|---|
| IUPAC names
1-Chloroethyl carbonochloridate 2-Chloroethyl carbonochloridate | |||
| Identifiers | |||
50893-53-3 (1-chloroethyl chloroformate)  627-11-2 (2-chloroethyl chloroformate) | |||
| 3D model (Jmol) | Interactive image Interactive image | ||
| ChemSpider | 454726 (1-chloroethyl chloroformate) 11802 (2-chloroethyl chloroformate) | ||
| ECHA InfoCard | 100.051.650 | ||
| PubChem | 521305 (1-chloroethyl chloroformate) 12305 (2-chloroethyl chloroformate) | ||
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| Properties | |||
| C3H4Cl2O2 | |||
| Molar mass | 142.96 g·mol−1 | ||
| Related compounds | |||
| Related chloroformates |
Chloromethyl chloroformate | ||
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |||
| Infobox references | |||
Chloroethyl chloroformates (chemical formula: C3H4Cl2O2) are a pair of related chemical compounds. They can be used to form protecting groups and as N-dealkylating agents[1].
They are listed as extremely hazardous substances.[2]
References
- ↑ 'A new reagent for the selective, high-yield N-dealkylation of tertiary amines: improved syntheses of naltrexone and nalbuphine' R. A. Olofson, Jonathan T. Martz, Jean Pierre Senet, Marc Piteau, Thierry Malfroot J. Org. Chem., 1984, 49 (11), pp 2081–2082
- ↑ Extremely Hazardous Chemicals
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