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1H-Benzimidazole,1-chloro-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

348619-94-3

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348619-94-3 Usage

Structure

Chlorinated derivative of benzimidazole with a benzene ring fused to an imidazole ring

Usage

Building block for the synthesis of various organic compounds in the pharmaceutical industry and research laboratories

Potential

Identified as a potential scaffold for the development of new drugs due to its diverse biological activities

Biological activities

Studied for its antifungal, antibacterial, and antiviral properties, making it valuable for a wide range of applications.

Check Digit Verification of cas no

The CAS Registry Mumber 348619-94-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,8,6,1 and 9 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 348619-94:
(8*3)+(7*4)+(6*8)+(5*6)+(4*1)+(3*9)+(2*9)+(1*4)=183
183 % 10 = 3
So 348619-94-3 is a valid CAS Registry Number.

348619-94-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-chlorobenzimidazole

1.2 Other means of identification

Product number -
Other names 1H-Benzimidazole,1-chloro

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:348619-94-3 SDS

348619-94-3Upstream product

348619-94-3Downstream Products

348619-94-3Relevant academic research and scientific papers

Kinetics and Mechanism of Oxidation of Aliphatic Primary Alcohols with 1-Chlorobenzimidazole in Aqueous Acetic Acid Medium

Rukmangathan, Muthusamy,Santhoshkumar, Vetrivel,Ramkumar, Balasubramanian

, p. 1139 - 1152 (2016)

The kinetics of oxidation of a few aliphatic primary alcohols with 1-chlorobenzimidazole (CBI) was studied in aqueous acetic acid medium. The reactions were found to be first order each with respect to the concentrations of CBI and alcohol. The added HClO4 increases the rate and the order in HClO4 was found to be fractional. The reactions were catalyzed by NaCl and fractional order dependence was observed. The ionic strength had negligible influence on the rate. The reaction rates increase with decrease in dielectric constant of acetic acid. Addition of benzimidazole, one of the products does not affect the rate. Effect of temperature on the reaction rates was studied at different temperatures and the various activation and thermodynamic parameters were evaluated. The rate constants show good correlation with Taft-Pavelich Dual substituent parameter model (DSP). Product analysis shows the formation of aldehydes as major products of oxidation of aliphatic primary alcohols. CBIH+ has been postulated as the reactive oxidizing species. A mechanism involving a proton transfer by water molecule has been proposed.

Chlorotropy of 1-chlorobenzimidazole

De Rosa, Michael,Canudas, Nieves,Arnold, David,Yennawar, Hemant

, p. 7264 - 7267 (2013)

The chlorotropy observed by NMR in this study occurred by the rapid intermolecular transfer of a chloro group between 1-chlorobenzimidazole and benzimidazole in CCl4/CH3OH/K2CO3 solution.

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