SODIUM 3-AMINO-2-NAPHTHOATE

[Na+].NC1=CC2=CC=CC=C2C=C1C([O-])=O

InChIKey=OMUOAKZXHOYWDB-UHFFFAOYSA-M

InChI=1S/C11H9NO2.Na/c12-10-6-8-4-2-1-3-7(8)5-9(10)11(13)14;/h1-6H,12H2,(H,13,14);/q;+1/p-1

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

PubMed

Title	Date	PubMed
Direct formation of ring-fused 1,3-thiazine-2,4-dithiones from aromatic o-amino carboxylic acids: observation of a carbon disulfide mediated thionation.	2010-08-20	20666472
Synthesis and biological properties of benzo-annulated rutaecarpines.	2010	20930379
Prediction of genotoxicity of chemical compounds by statistical learning methods.	2005-06	15962942
A metabonomic investigation of the biochemical effects of mercuric chloride in the rat using 1H NMR and HPLC-TOF/MS: time dependent changes in the urinary profile of endogenous metabolites as a result of nephrotoxicity.	2004-06	15152332

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 21:44:04 GMT 2025` Edited by `admin` on `Mon Mar 31 21:44:04 GMT 2025`
Record UNII	2J94M2N0R0
Record Status	`Validated (UNII)`
Record Version

Name

Type

Language

3-AMINO-2-NAPHTHOIC ACID SODIUM SALT

Preferred Name

English

SODIUM 3-AMINO-2-NAPHTHOATE

Systematic Name

English

3-AMINO-2-NAPHTHOIC ACID SODIUM SALT [MI]

Common Name

English

2-NAPHTHOIC ACID, 3-AMINO-, MONOSODIUM SALT

Common Name

English

2-NAPHTHALENECARBOXYLIC ACID, 3-AMINO-, MONOSODIUM SALT

Common Name

English

2-NAPHTHALENECARBOXYLIC ACID, 3-AMINO-, SODIUM SALT (1:1)

Common Name

English

Code System Code Type Description

FDA UNII

2J94M2N0R0