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Details

Stereochemistry ACHIRAL
Molecular Formula C17H14N2O
Molecular Weight 262.3059
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of 1-(4-TOLYLAZO)-2-NAPHTHOL

SMILES

CC1=CC=C(C=C1)\N=N\C2=C(O)C=CC3=CC=CC=C23

InChI

InChIKey=JCZUIEHTNMQCRK-VHEBQXMUSA-N
InChI=1S/C17H14N2O/c1-12-6-9-14(10-7-12)18-19-17-15-5-3-2-4-13(15)8-11-16(17)20/h2-11,20H,1H3/b19-18+

HIDE SMILES / InChI

Molecular Formula C17H14N2O
Molecular Weight 262.3059
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

Approval Year

Substance Class Chemical
Created
by admin
on Mon Mar 31 18:52:58 GMT 2025
Edited
by admin
on Mon Mar 31 18:52:58 GMT 2025
Record UNII
35H0V3D0KK
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
COLOR RELATED COMPOUND 007
USP-RS  
Preferred Name English
1-(4-TOLYLAZO)-2-NAPHTHOL
Systematic Name English
1-((4-METHYLPHENYL)AZO)-2-NAPHTHOL
Systematic Name English
NSC-106296
Code English
1-P-TOLYLAZO-2-NAPHTHOL
Common Name English
2-NAPHTHALENOL, 1-((4-METHYLPHENYL)AZO)-
Systematic Name English
2-NAPHTHOL, 1-(P-TOLYLAZO)-
Common Name English
2-NAPHTHALENOL, 1-(2-(4-METHYLPHENYL)DIAZENYL)-
Systematic Name English
COLOR RELATED COMPOUND 007 [USP-RS]
Common Name English
1-((4-METHYLPHENYL)AZO)-2-NAPHTHALENOL
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID501031796
Created by admin on Mon Mar 31 18:52:58 GMT 2025 , Edited by admin on Mon Mar 31 18:52:58 GMT 2025
PRIMARY
NSC
106296
Created by admin on Mon Mar 31 18:52:58 GMT 2025 , Edited by admin on Mon Mar 31 18:52:58 GMT 2025
PRIMARY
CAS
6756-41-8
Created by admin on Mon Mar 31 18:52:58 GMT 2025 , Edited by admin on Mon Mar 31 18:52:58 GMT 2025
PRIMARY
FDA UNII
35H0V3D0KK
Created by admin on Mon Mar 31 18:52:58 GMT 2025 , Edited by admin on Mon Mar 31 18:52:58 GMT 2025
PRIMARY
RS_ITEM_NUM
1148250
Created by admin on Mon Mar 31 18:52:58 GMT 2025 , Edited by admin on Mon Mar 31 18:52:58 GMT 2025
PRIMARY