N -acetylsulfanilyl chloride
Structural formula | ||||||||||||||||||||||
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General | ||||||||||||||||||||||
Surname | N-acetylsulfanilyl chloride | |||||||||||||||||||||
other names |
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Molecular formula | C 8 H 8 ClNO 3 S | |||||||||||||||||||||
Brief description |
white solid with an acetic acid odor |
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properties | ||||||||||||||||||||||
Molar mass | 233.67 g mol −1 | |||||||||||||||||||||
Physical state |
firmly |
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solubility |
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safety instructions | ||||||||||||||||||||||
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Toxicological data | ||||||||||||||||||||||
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . |
N -acetylsulfanilyl chloride is a chemical compound from the group of carboxamides and sulfonyl halides .
Extraction and presentation
N- acetylsulfanilyl chloride can be obtained by reacting acetanilide with chlorosulfonic acid at elevated temperatures.
properties
N -acetylsulfanilyl chloride is a flammable, hardly ignitable, white solid with an acetic acid- like odor that decomposes in water to form hydrochloric and acetic acid. It also decomposes when heated above 146 ° C.
use
N -acetylsulfanilyl chloride is used as an intermediate in the manufacture of other chemical compounds (such as sulfadimidine , dimethylsulfanilamide and sulfanilamide ).
Individual evidence
- ↑ a b c d e f g Entry on N-acetylsulfanilyl chloride in the GESTIS substance database of the IFA , accessed on July 1, 2017(JavaScript required) .
- ↑ Data sheet 4-Acetamidobenzenesulfonyl chloride, 98 +% from AlfaAesar, accessed on July 1, 2017 ( PDF )(JavaScript required) .
- ↑ Entry on 4- (acetylamino) benzenesulfonyl chloride in the Hazardous Substances Data Bank , accessed on July 1, 2017.
- ↑ Data sheet N-Acetylsulfanilyl chloride, 98% from Sigma-Aldrich , accessed on July 1, 2017 ( PDF ).
- ^ Profiles of Drug Substances, Excipients and Related Methodology . Academic Press, 1978, ISBN 978-0-08-086102-9 , pp. 413 ( limited preview in Google Book search).