2-AMINO-5-METHYLBENZOIC ACID

CC1=CC=C(N)C(=C1)C(O)=O

InChIKey=NBUUUJWWOARGNW-UHFFFAOYSA-N

InChI=1S/C8H9NO2/c1-5-2-3-7(9)6(4-5)8(10)11/h2-4H,9H2,1H3,(H,10,11)

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

PubMed

Title	Date	PubMed
Localized auxin biosynthesis and postembryonic root development in Arabidopsis.	2009-08	19820306
Synthesis and cytotoxicity screening of piperazine-1-carbodithioate derivatives of 2-substituted quinazolin-4(3H)-ones.	2009-03	19212984
Synthesis of substituted benzylamino- and heterocyclylmethylamino carbodithioate derivatives of 4-(3H)-quinazolinone and their cytotoxic activity.	2006-05	16619282
Toward a new genetic system with expanded dimensions: size-expanded analogues of deoxyadenosine and thymidine.	2004-02-04	14746479

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 19:14:36 GMT 2025` Edited by `admin` on `Mon Mar 31 19:14:36 GMT 2025`
Record UNII	418XAJ22V2
Record Status	`Validated (UNII)`
Record Version

Name

Type

Language

NSC-39154

Preferred Name

English

2-AMINO-5-METHYLBENZOIC ACID

Systematic Name

English

2-CARBOXY-4-METHYLANILINE

Systematic Name

English

NSC-50786

Code

English

BENZOIC ACID, 2-AMINO-5-METHYL-

Common Name

English

M-TOLUIC ACID, 6-AMINO-

Common Name

English

5-METHYL-2-AMINOBENZOIC ACID

Systematic Name

English

5-METHYLANTHRANILIC ACID

Systematic Name

English

Code System Code Type Description

NSC

50786