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Details

Stereochemistry ACHIRAL
Molecular Formula C14H16N2
Molecular Weight 212.2902
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of N-BENZYL-4-METHYL-O-PHENYLENEDIAMINE

SMILES

CC1=CC(N)=C(NCC2=CC=CC=C2)C=C1

InChI

InChIKey=BXKFJRIHXLNJPC-UHFFFAOYSA-N
InChI=1S/C14H16N2/c1-11-7-8-14(13(15)9-11)16-10-12-5-3-2-4-6-12/h2-9,16H,10,15H2,1H3

HIDE SMILES / InChI

Molecular Formula C14H16N2
Molecular Weight 212.2902
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Suppressive effect of novel aromatic diamine compound on nuclear factor-kappaB-dependent expression of inducible nitric oxide synthase in macrophages.
2005-10-03
Anti-inflammatory benzene diamine compound inhibited toll-like receptor 4-mediated inducible nitric oxide synthase expression and nuclear factor-kappa B activation.
2005-05
Anti-inflammatory effects of N1-benzyl-4-methylbenzene-1,2-diamine (JSH-21) analogs on nitric oxide production and nuclear factor-kappa B transcriptional activity in lipopolysaccharide-stimulated macrophages RAW 264.7.
2004-10
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 23:40:50 GMT 2025
Edited
by admin
on Mon Mar 31 23:40:50 GMT 2025
Record UNII
1JB5C96T8S
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CLAROMINE
Preferred Name English
N-BENZYL-4-METHYL-O-PHENYLENEDIAMINE
INCI  
INCI  
Official Name English
1,2-BENZENEDIAMINE, 4-METHYL-N1-(PHENYLMETHYL)-
Systematic Name English
N-BENZYL-4-METHYLBENZENE-1,2-DIAMINE
Systematic Name English
JSH-21
Code English
JSH 21
Code English
Code System Code Type Description
FDA UNII
1JB5C96T8S
Created by admin on Mon Mar 31 23:40:50 GMT 2025 , Edited by admin on Mon Mar 31 23:40:50 GMT 2025
PRIMARY
PUBCHEM
10727275
Created by admin on Mon Mar 31 23:40:50 GMT 2025 , Edited by admin on Mon Mar 31 23:40:50 GMT 2025
PRIMARY
CAS
39235-93-3
Created by admin on Mon Mar 31 23:40:50 GMT 2025 , Edited by admin on Mon Mar 31 23:40:50 GMT 2025
PRIMARY
EPA CompTox
DTXSID501254833
Created by admin on Mon Mar 31 23:40:50 GMT 2025 , Edited by admin on Mon Mar 31 23:40:50 GMT 2025
PRIMARY