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Details

Stereochemistry ACHIRAL
Molecular Formula C13H12N2O5S
Molecular Weight 308.31
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 4-SULFANILAMIDOSALICYLIC ACID

SMILES

NC1=CC=C(C=C1)S(=O)(=O)NC2=CC(O)=C(C=C2)C(O)=O

InChI

InChIKey=CDUAVAXMQCAYTC-UHFFFAOYSA-N
InChI=1S/C13H12N2O5S/c14-8-1-4-10(5-2-8)21(19,20)15-9-3-6-11(13(17)18)12(16)7-9/h1-7,15-16H,14H2,(H,17,18)

HIDE SMILES / InChI

Molecular Formula C13H12N2O5S
Molecular Weight 308.31
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Synthesis of sulfanilamido-naphthoquinones as potential antituberculous agents.
1983-01
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:42:25 GMT 2025
Edited
by admin
on Mon Mar 31 22:42:25 GMT 2025
Record UNII
EOV38X32HR
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
METRASIL
Preferred Name English
4-SULFANILAMIDOSALICYLIC ACID
MI  
Systematic Name English
BENZOIC ACID, 4-(((4-AMINOPHENYL)SULFONYL)AMINO)-2-HYDROXY-
Systematic Name English
4-SULFANILAMIDOSALICYLIC ACID [MI]
Common Name English
P-SULFANILAMIDOSALICYLIC ACID
Common Name English
Code System Code Type Description
CAS
6202-21-7
Created by admin on Mon Mar 31 22:42:25 GMT 2025 , Edited by admin on Mon Mar 31 22:42:25 GMT 2025
PRIMARY
MERCK INDEX
m942
Created by admin on Mon Mar 31 22:42:25 GMT 2025 , Edited by admin on Mon Mar 31 22:42:25 GMT 2025
PRIMARY Merck Index
FDA UNII
EOV38X32HR
Created by admin on Mon Mar 31 22:42:25 GMT 2025 , Edited by admin on Mon Mar 31 22:42:25 GMT 2025
PRIMARY
ECHA (EC/EINECS)
228-263-9
Created by admin on Mon Mar 31 22:42:25 GMT 2025 , Edited by admin on Mon Mar 31 22:42:25 GMT 2025
PRIMARY
EPA CompTox
DTXSID30977559
Created by admin on Mon Mar 31 22:42:25 GMT 2025 , Edited by admin on Mon Mar 31 22:42:25 GMT 2025
PRIMARY
PUBCHEM
80335
Created by admin on Mon Mar 31 22:42:25 GMT 2025 , Edited by admin on Mon Mar 31 22:42:25 GMT 2025
PRIMARY