Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C8H8ClNO3S |
| Molecular Weight | 233.672 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(=O)NC1=CC=C(C=C1)S(Cl)(=O)=O
InChI
InChIKey=GRDXCFKBQWDAJH-UHFFFAOYSA-N
InChI=1S/C8H8ClNO3S/c1-6(11)10-7-2-4-8(5-3-7)14(9,12)13/h2-5H,1H3,(H,10,11)
N-Acetylsulfanilyl chloride is a benzenesulfonyl chloride derivative used as intermediate in the synthesis of various pharmaceuticals and organic compounds. N-Acetylsulfanilyl chloride is also used in the synthesis of N,N-dimethylsulfanilamide as the internal standard in the reaction. The reaction is used to determine tramadol and its O-demethylated metabolite in blood plasma.
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| 3-[4-(Acetamido)-benzene-sulfonamido]-benzoic acid. | 2010-12-04 |
|
| N-{4-[(3,4-Dimethyl-phen-yl)sulfamo-yl]phen-yl}acetamide. | 2010-07-31 |
|
| N-[4-(Benzyl-sulfamo-yl)phen-yl]acetamide. | 2010-07-17 |
|
| N-{4-[(4-Methyl-phen-yl)sulfamo-yl]phen-yl}acetamide. | 2010-07-17 |
|
| 2-(4-Acetamido-benzene-sulfonamido)-3-methyl-butanoic acid. | 2010-05-08 |
|
| Synthesis and antifungal properties of sulfanilamide derivatives of chitosan. | 2007-11-26 |
|
| The preparation and antioxidant activity of the sulfanilamide derivatives of chitosan and chitosan sulfates. | 2007-06-01 |
|
| Carbonic anhydrase inhibitors: synthesis and inhibition of cytosolic/tumor-associated carbonic anhydrase isozymes I, II, and IX with sulfonamides incorporating thioureido-sulfanilyl scaffolds. | 2005-05-02 |
|
| Expression of a novel carbonic anhydrase, CA XIII, in normal and neoplastic colorectal mucosa. | 2005-04-18 |
|
| A novel kind of antitumour drugs using sulfonamide as parent compound. | 2002-01-05 |
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SUBSTANCE RECORD
