N -chloroaniline
| Structural formula | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|
|
||||||||||
| General | ||||||||||
| Surname | N -chloroaniline | |||||||||
| other names |
|
|||||||||
| Molecular formula | C 6 H 6 ClN | |||||||||
| External identifiers / databases | ||||||||||
|
||||||||||
| properties | ||||||||||
| Molar mass | 127.57 g mol −1 | |||||||||
| solubility |
rapidly decomposes in water |
|||||||||
| safety instructions | ||||||||||
|
||||||||||
| As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . | ||||||||||
N -chloroaniline is a chemical compound from the group of chloramines .
Extraction and presentation
N -chloroaniline can be obtained by reacting aniline with tert-butyl hypochlorite .
use
N -chloroaniline is used for the production of indoles and oxindoles by the Gassman indole synthesis or the Gassman oxindole synthesis .
Individual evidence
- ↑ S. Gangolli, Royal Society of Chemistry (Great Britain): The Dictionary of Substances and Their Effects: C . Royal Society of Chemistry, 1999, ISBN 0-85404-813-8 , pp. 280 ( limited preview in Google Book search).
- ↑ This substance has either not yet been classified with regard to its hazardousness or a reliable and citable source has not yet been found.
- ↑ a b Jie Jack Li: Name Reactions in Heterocyclic Chemistry II . John Wiley & Sons, 2011, ISBN 1-118-09285-6 , pp. 134 ( limited preview in Google Book search).
- ^ William J. Houlihan: The Chemistry of Heterocyclic Compounds, Indoles . John Wiley & Sons, 2009, ISBN 0-470-18842-1 , pp. 216 ( limited preview in Google Book search).