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1H-Benzimidazole-2-carboxylic acid, 1-methyl-, ethyl ester is a chemical compound with the molecular formula C12H12N2O2. It is an ethyl ester derivative of 1-methyl-1H-benzimidazole-2-carboxylic acid, known for its potential pharmacological properties and applications in the synthesis of biologically active molecules.
Used in Pharmaceutical Industry:
1H-Benzimidazole-2-carboxylic acid, 1-methyl-, ethyl ester is used as a building block for the synthesis of various biologically active molecules, contributing to the development of new drugs and therapeutic agents.
Used in Antimicrobial Applications:
1H-Benzimidazole-2-carboxylic acid, 1-methyl-, ethyl ester is used as an antimicrobial agent for its potential to combat infections caused by various microorganisms, providing a valuable tool in the fight against antibiotic-resistant strains.
Used in Antitumor Applications:
1H-Benzimidazole-2-carboxylic acid, 1-methyl-, ethyl ester is used as an antitumor agent for its potential to inhibit the growth and proliferation of cancer cells, offering a promising avenue for cancer treatment and research.

35342-97-3

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35342-97-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35342-97-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,3,4 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 35342-97:
(7*3)+(6*5)+(5*3)+(4*4)+(3*2)+(2*9)+(1*7)=113
113 % 10 = 3
So 35342-97-3 is a valid CAS Registry Number.

35342-97-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 1-methylbenzimidazole-2-carboxylate

1.2 Other means of identification

Product number -
Other names 1-methyl-1H-benzoimidazole-2-carboxylic acid ethyl ester

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:35342-97-3 SDS

35342-97-3Relevant academic research and scientific papers

ADENOSINE RECEPTOR BINDING COMPOUNDS

-

, (2020/02/06)

The present invention relates to pharmaceutical compounds and compositions of Formula (I) and methods of treatment using the compounds and compositions, especially for the treatment and/or prevention of a proliferation disorder, such as cancer. Compounds of Formula (I) as further described herein are shown modulators of the adenosine A2A receptor and exhibit antiproliferative activity. Accordingly, these compounds are useful to treat proliferative disorders such as cancer, and other adenosine receptor-related conditions including an inflammatory disease, renal disease, diabetes, vascular disease, lung disease, or an autoimmune disease.

REARRANGEMENTS OF AROMATIC CARBONYL ARYLHYDRAZONES OF BENZENE, NAPHTHALENE, AND AZULENE

Benincori, Tiziana,Pagani, Silvia Bradamante,Fusco, Raffaello,Sannicolo, Franco

, p. 2721 - 2728 (2007/10/02)

Aromatic carbonyl arylhydrazones have been shown to undergo two kinds of rearrangement in polyphosphoric acid both involving nitrogen-nitrogen bond cleavage.The first proceeds via insertion of the imine portion in the position ortho to the second nitrogen atom to give o-phenylenediamine intermediates: their evolution depends on the nature of the starting substrate.This reaction has been employed for synthesizing the quinoxalines (5) and the phenanthridines (11), and was demonstrated to be intramolecular.The second reaction path is a sigmatropic rearrangment exclusive to electron-rich aromatic carbonyl hydrazones.

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