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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
Structure of N-ACETYLSULFANILYL CHLORIDE

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)

HIDE SMILES / InChI
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

PubMed

TitleDatePubMed
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
3-[4-(Acetamido)-benzene-sulfonamido]-benzoic acid.
2010 Dec 4
N-[4-(Benzyl-sulfamo-yl)phen-yl]acetamide.
2010 Jul 17
N-{4-[(4-Methyl-phen-yl)sulfamo-yl]phen-yl}acetamide.
2010 Jul 17
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
Patents
Name Type Language
N-ACETYLSULFANILYL CHLORIDE
MI  
Systematic Name English
N-ACETYLSULFANILYL CHLORIDE [MI]
Common Name English
BENZENESULFONYL CHLORIDE, 4-(ACETYLAMINO)-
Systematic Name English
NSC-127860
Code English
4-(ACETYLAMINO)BENZENESULFONYL CHLORIDE [HSDB]
Common Name English
ASC
Common Name English
ACETYLAMINOBENZENE SULFONYL CHLORIDE, P-
Common Name English
P-ACETAMIDOBENZENESULFONYL CHLORIDE
Common Name English
4-(ACETYLAMINO)BENZENESULFONYL CHLORIDE
HSDB  
Systematic Name English
ACETANILIDE-P-SULFONYL CHLORIDE
Common Name English
P-ACETAMINOBENZENESULFONYL CHLORIDE
Common Name English
SULFANILYL CHLORIDE, N-ACETYL-
Systematic Name English
Code System Code Type Description
CAS
121-60-8
Created by admin on Fri Dec 15 16:39:56 GMT 2023 , Edited by admin on Fri Dec 15 16:39:56 GMT 2023
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NSC
127860
Created by admin on Fri Dec 15 16:39:56 GMT 2023 , Edited by admin on Fri Dec 15 16:39:56 GMT 2023
PRIMARY
EPA CompTox
DTXSID8026981
Created by admin on Fri Dec 15 16:39:56 GMT 2023 , Edited by admin on Fri Dec 15 16:39:56 GMT 2023
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MERCK INDEX
m1365
Created by admin on Fri Dec 15 16:39:56 GMT 2023 , Edited by admin on Fri Dec 15 16:39:56 GMT 2023
PRIMARY Merck Index
PUBCHEM
8481
Created by admin on Fri Dec 15 16:39:56 GMT 2023 , Edited by admin on Fri Dec 15 16:39:56 GMT 2023
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HSDB
2712
Created by admin on Fri Dec 15 16:39:56 GMT 2023 , Edited by admin on Fri Dec 15 16:39:56 GMT 2023
PRIMARY
ECHA (EC/EINECS)
204-485-1
Created by admin on Fri Dec 15 16:39:56 GMT 2023 , Edited by admin on Fri Dec 15 16:39:56 GMT 2023
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DRUG BANK
DB12337
Created by admin on Fri Dec 15 16:39:56 GMT 2023 , Edited by admin on Fri Dec 15 16:39:56 GMT 2023
PRIMARY
FDA UNII
LIX4M9AIVM
Created by admin on Fri Dec 15 16:39:56 GMT 2023 , Edited by admin on Fri Dec 15 16:39:56 GMT 2023
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