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1H-Benzimidazole-4-carboxylic acid, ethyl ester (9CI), with the molecular formula C11H11N3O2, is a chemical compound that serves as a crucial building block in the pharmaceutical industry. It is known for its antimicrobial, antiviral, and antifungal properties, which make it a valuable component in the development of new medications. The ethyl ester form of 1H-Benzimidazole-4-carboxylicacid,ethylester(9CI) also enhances its utility as a solvent or carrier for other active ingredients in drug formulations. Furthermore, research indicates that 1H-Benzimidazole-4-carboxylic acid, ethyl ester may possess anti-inflammatory and anticancer properties, significantly contributing to its importance in biomedical research and drug development.

167487-83-4

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167487-83-4 Usage

Uses

Used in Pharmaceutical Industry:
1H-Benzimidazole-4-carboxylic acid, ethyl ester is used as a building block for the synthesis of various drugs due to its versatile chemical properties and potential therapeutic effects.
Used in Antimicrobial Applications:
1H-Benzimidazole-4-carboxylic acid, ethyl ester is used as an antimicrobial agent for its ability to inhibit the growth of various microorganisms, contributing to the development of new antibiotics and antifungal medications.
Used in Antiviral Applications:
1H-Benzimidazole-4-carboxylicacid,ethylester(9CI) is used as an antiviral agent, leveraging its properties to combat viral infections, which is crucial in the creation of antiviral drugs.
Used in Antifungal Applications:
1H-Benzimidazole-4-carboxylic acid, ethyl ester is utilized as an antifungal agent, helping in the formulation of medications to treat fungal infections.
Used in Drug Formulation:
The ethyl ester form of 1H-Benzimidazole-4-carboxylic acid is used as a solvent or carrier for other active ingredients in drug formulations, improving the delivery and effectiveness of these medications.
Used in Biomedical Research:
1H-Benzimidazole-4-carboxylic acid, ethyl ester is used in research for its potential anti-inflammatory and anticancer properties, aiding in the discovery of new therapeutic agents for inflammatory and cancer treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 167487-83-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,7,4,8 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 167487-83:
(8*1)+(7*6)+(6*7)+(5*4)+(4*8)+(3*7)+(2*8)+(1*3)=184
184 % 10 = 4
So 167487-83-4 is a valid CAS Registry Number.

167487-83-4 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
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  • Alfa Aesar

  • (H66669)  Ethyl benzimidazole-4-carboxylate, 95%   

  • 167487-83-4

  • 250mg

  • 1400.0CNY

  • Detail
  • Alfa Aesar

  • (H66669)  Ethyl benzimidazole-4-carboxylate, 95%   

  • 167487-83-4

  • 1g

  • 4200.0CNY

  • Detail

167487-83-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 1H-benzo[d]imidazole-7-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl 1H-benzimidazole-4-carboxylate

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:167487-83-4 SDS

167487-83-4Relevant academic research and scientific papers

A facile one-pot synthesis of benzimidazoles from 2-nitroanilines by reductive cyclization

Liu, Zheng,Li, Haihong,Zhao, Qingjie,Shen, Jingshan

scheme or table, p. 1907 - 1911 (2009/04/06)

A facile one-pot process to prepare benzimidazole derivatives is described. Reductive cyclization of a serial of 2-nitroanilines with orthoesters in the presence of Pd/C in methanol at room temperature, which is promoted by a catalytic amount of acetic acid, affords the corresponding benzimidazole derivatives in high yields.

Beta-agonists, methods for the preparation thereof and their use as pharmaceutical compositions

-

Page/Page column 16, (2010/11/27)

The present invention relates to new beta-agonists of general formula (I) wherein the groups R1 to R4 have the meanings given in ths claims and specification, the tautomers, racemates, enantiomers, diastereomers, solvates, hydrates,

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