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22223-49-0

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22223-49-0 Usage

Uses

2-Amino-3-methylbenzoic Acid Methyl Ester is the methyl ester derivative of 2-Amino-3-methylbenzoic Acid (A612150); a metabolite of Lidocaine (L397800) with potential herbicidal activity. 2-Amino-3-methylbenzoic Acid Methyl Ester is also used as the 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.

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

Rational design of selective inhibitors of PARP4

Cohen, Michael,Kirby, Ilsa T.,Person, Ashley

, p. 1950 - 1957 (2021/12/24)

PARPs (PARP1-16 in humans) are a large family of ADP-ribosyltransferases (ARTs) that have diverse roles in cellular physiology and pathophysiology. Most PARP family members mediate mono-ADP-ribosylation (MARylation) of targets. The function of PARP-mediated MARylation in cells is poorly characterized, due in large part to the paucity of selective small molecule inhibitors of the catalytic activity of individual PARP enzymes. Herein we describe the rational design of selective small molecule inhibitors of PARP4 (also known as vPARP). These inhibitors are based on a quinazolin-4(3H)-one scaffold, and contain substituents at the C-8 position designed to exploit a unique threonine (Thr484, human PARP4 numbering) in the PARP4 nicotinamide sub-pocket. Our most potent analog, AEP07, which contains an iodine at the C-8 position, is at least 12-fold selective over other PARP family members. AEP07 will serve as a useful lead compound for the further development of PARP4 inhibitors that can be used to probe the cellular functions of PARP4 catalytic activity. This journal is

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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