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 |
---|---|---|
Carbonic anhydrase inhibitors: synthesis and inhibition of cytosolic/tumor-associated carbonic anhydrase isozymes I, II, and IX with sulfonamides incorporating thioureido-sulfanilyl scaffolds. | 2005 May 2 |
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3-[4-(Acetamido)-benzene-sulfonamido]-benzoic acid. | 2010 Dec 4 |
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N-[4-(Benzyl-sulfamo-yl)phen-yl]acetamide. | 2010 Jul 17 |
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N-{4-[(4-Methyl-phen-yl)sulfamo-yl]phen-yl}acetamide. | 2010 Jul 17 |
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N-{4-[(3,4-Dimethyl-phen-yl)sulfamo-yl]phen-yl}acetamide. | 2010 Jul 31 |
|
2-(4-Acetamido-benzene-sulfonamido)-3-methyl-butanoic acid. | 2010 May 8 |
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SUBSTANCE RECORD