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Details

Stereochemistry ACHIRAL
Molecular Formula C19H17NO4
Molecular Weight 323.3426
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of N-(2,5-Dimethoxyphenyl)-3-hydroxy-2-naphthalenecarboxamide

SMILES

COC1=CC=C(OC)C(NC(=O)C2=CC3=C(C=CC=C3)C=C2O)=C1

InChI

InChIKey=LAKNSQZHAUYJJM-UHFFFAOYSA-N
InChI=1S/C19H17NO4/c1-23-14-7-8-18(24-2)16(11-14)20-19(22)15-9-12-5-3-4-6-13(12)10-17(15)21/h3-11,21H,1-2H3,(H,20,22)

HIDE SMILES / InChI
Molecular Formula C19H17NO4
Molecular Weight 323.3426
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Unknown
149124
Substance Class Chemical
Created
by admin
on Tue Apr 01 20:21:43 GMT 2025
Edited
by admin
on Tue Apr 01 20:21:43 GMT 2025
Record UNII
3NV5QT373M
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-37618
Preferred Name English
N-(2,5-Dimethoxyphenyl)-3-hydroxy-2-naphthalenecarboxamide
Systematic Name English
Naphtol AS-BG
Common Name English
Naphtanilide BG Supra
Common Name English
C.I. 37545
Common Name English
Hiltonaphthol AS-BG
Common Name English
Naphthol AS-BG Supra
Common Name English
Brenthol FO
Common Name English
Cibanaphthol RDM
Common Name English
Acna Naphthol BG
Common Name English
Naphtol AS-BG Supra
Common Name English
Sanatol BG
Common Name English
Amanil Naphthol AS-BG
Common Name English
2-Naphthalenecarboxamide, N-(2,5-dimethoxyphenyl)-3-hydroxy-
Systematic Name English
Azoic Coupling Component 19
Common Name English
3-Hydroxy-2',5'-dimethoxynaphthanilide
Systematic Name English
Tulathol AS BG
Common Name English
C.I. Azoic Coupling Component 19
Common Name English
Naphtanilide BG
Common Name English
Naphthol AS-BG Dispersible
Common Name English
Daito Grounder BG
Common Name English
Naphtazol BJ
Common Name English
Solunaptol FOL
Common Name English
Naphthol AS-BG
Common Name English
Code System Code Type Description
NSC
37618
Created by admin on Tue Apr 01 20:21:43 GMT 2025 , Edited by admin on Tue Apr 01 20:21:43 GMT 2025
PRIMARY
CAS
92-73-9
Created by admin on Tue Apr 01 20:21:43 GMT 2025 , Edited by admin on Tue Apr 01 20:21:43 GMT 2025
PRIMARY
FDA UNII
3NV5QT373M
Created by admin on Tue Apr 01 20:21:43 GMT 2025 , Edited by admin on Tue Apr 01 20:21:43 GMT 2025
PRIMARY
ECHA (EC/EINECS)
202-183-4
Created by admin on Tue Apr 01 20:21:43 GMT 2025 , Edited by admin on Tue Apr 01 20:21:43 GMT 2025
PRIMARY
EPA CompTox
DTXSID7059062
Created by admin on Tue Apr 01 20:21:43 GMT 2025 , Edited by admin on Tue Apr 01 20:21:43 GMT 2025
PRIMARY
PUBCHEM
66715
Created by admin on Tue Apr 01 20:21:43 GMT 2025 , Edited by admin on Tue Apr 01 20:21:43 GMT 2025
PRIMARY
NIH
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