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Details

Stereochemistry ACHIRAL
Molecular Formula C13H10ClNO2
Molecular Weight 247.677
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CHLOROSALICYLANILIDE

SMILES

OC1=CC=C(Cl)C=C1C(=O)NC2=CC=CC=C2

InChI

InChIKey=KGYNGVVNFRUOOZ-UHFFFAOYSA-N
InChI=1S/C13H10ClNO2/c14-9-6-7-12(16)11(8-9)13(17)15-10-4-2-1-3-5-10/h1-8,16H,(H,15,17)

HIDE SMILES / InChI

Molecular Formula C13H10ClNO2
Molecular Weight 247.677
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Antimycobacterial assessment of Salicylanilide benzoates including multidrug-resistant tuberculosis strains.
2012-10-31
Salicylanilide derivatives block Mycobacterium tuberculosis through inhibition of isocitrate lyase and methionine aminopeptidase.
2012-09
Relationship between the structure and antimycobacterial activity of substituted salicylanilides.
2003-03
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 17:49:52 GMT 2025
Edited
by admin
on Mon Mar 31 17:49:52 GMT 2025
Record UNII
QI22Q9QE3I
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CHLOROSALICYLANILIDE
Systematic Name English
NSC-402600
Preferred Name English
5-CHLORO-2-HYDROXY-N-PHENYL-BENZAMIDE
Systematic Name English
WR-13084
Code English
BENZAMIDE, 5-CHLORO-2-HYDROXY-N-PHENYL-
Systematic Name English
5-CHLOROSALICYLANILIDE
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID9037749
Created by admin on Mon Mar 31 17:49:52 GMT 2025 , Edited by admin on Mon Mar 31 17:49:52 GMT 2025
PRIMARY
NSC
402600
Created by admin on Mon Mar 31 17:49:52 GMT 2025 , Edited by admin on Mon Mar 31 17:49:52 GMT 2025
PRIMARY
FDA UNII
QI22Q9QE3I
Created by admin on Mon Mar 31 17:49:52 GMT 2025 , Edited by admin on Mon Mar 31 17:49:52 GMT 2025
PRIMARY
ECHA (EC/EINECS)
225-065-4
Created by admin on Mon Mar 31 17:49:52 GMT 2025 , Edited by admin on Mon Mar 31 17:49:52 GMT 2025
PRIMARY
CAS
4638-48-6
Created by admin on Mon Mar 31 17:49:52 GMT 2025 , Edited by admin on Mon Mar 31 17:49:52 GMT 2025
PRIMARY
PUBCHEM
14869
Created by admin on Mon Mar 31 17:49:52 GMT 2025 , Edited by admin on Mon Mar 31 17:49:52 GMT 2025
PRIMARY