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22223-49-0

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22223-49-0 Usage

Description

Methyl 2-amino-3-methylbenzoate, also known as 2-Amino-3-methylbenzoic Acid Methyl Ester, is a methyl ester derivative of 2-Amino-3-methylbenzoic Acid (A612150). It is a metabolite of Lidocaine (L397800) and has potential herbicidal activity. Additionally, it serves as a starting material in the synthesis of N-(2-Methoxyacetate)-N-(2-carboxy-6-methylphenyl)-alanine (M260810), a metabolite of Metalaxyl (M258740), which is an agricultural fungicide.

Uses

Used in Agriculture:
Methyl 2-amino-3-methylbenzoate is used as a herbicide for its potential herbicidal activity, helping to control the growth of unwanted plants and improve crop yields.
Used in Pharmaceutical Synthesis:
Methyl 2-amino-3-methylbenzoate is used as a starting material in the synthesis of N-(2-Methoxyacetate)-N-(2-carboxy-6-methylphenyl)-alanine (M260810), which is a metabolite of Metalaxyl (M258740). Metalaxyl is an agricultural fungicide, indicating that Methyl 2-amino-3-methylbenzoate plays a crucial role in the development of fungicides to protect crops from fungal infections.

Check Digit Verification of cas no

The CAS Registry Mumber 22223-49-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,2,2 and 3 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 22223-49:
(7*2)+(6*2)+(5*2)+(4*2)+(3*3)+(2*4)+(1*9)=70
70 % 10 = 0
So 22223-49-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H11NO2/c1-6-3-4-7(8(10)5-6)9(11)12-2/h3-5H,10H2,1-2H3

22223-49-0 Well-known Company Product Price

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  • Alfa Aesar

  • (H61448)  Methyl 2-amino-3-methylbenzoate, 98%   

  • 22223-49-0

  • 25g

  • 762.0CNY

  • Detail
  • Alfa Aesar

  • (H61448)  Methyl 2-amino-3-methylbenzoate, 98%   

  • 22223-49-0

  • 100g

  • 2029.0CNY

  • Detail

22223-49-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-amino-3-methylbenzoate

1.2 Other means of identification

Product number -
Other names Methyl 3-Methylanthranilate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:22223-49-0 SDS

22223-49-0Relevant articles and documents

Tunable Electrosynthesis of Anthranilic Acid Derivatives via a C-C Bond Cleavage of Isatins

Qian, Peng,Liu, Jiaojiao,Zhang, Yan,Wang, Zhiyong

, p. 16008 - 16015 (2021/07/31)

A facile and direct electrocatalytic C-C bond cleavage/functionalization reaction of isatins was developed. With isatins as the amino-attached C1 sources, a variety of aminobenzoates, and aminobenzamides were synthesized in moderate to good yields under mild conditions.

PARP INHIBITORS FOR TREATING CANCER AND ASTHMA

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Page/Page column 21; 23; 24, (2020/03/23)

Provided are substituted 8-methylquinazolin-4(3H)-one compounds useful as PARP inhibitors for the treatment of cancer and asthma, as well as pharmaceutical compositions comprising them and methods for their synthesis.

A Potent and Selective PARP11 Inhibitor Suggests Coupling between Cellular Localization and Catalytic Activity

Kirby, Ilsa T.,Schultz, Carsten,Cohen, Michael S.,Arnold, Moriah R.,Vermehren-Schmaedick, Anke,Sreenivasan, Raashi,Kojic, Ana,Thorsell, Ann-Gerd,Karlberg, Tobias,Schüler, Herwig

, p. 1547 - 1553 (2019/01/24)

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