Welcome to LookChem.com Sign In|Join Free

CAS

  • or

55671-58-4

Post Buying Request

55671-58-4 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

55671-58-4 Usage

Structure

benzimidazole derivative with a chloro substituent attached to the phenylmethyl group

Usage

used in scientific research as a building block in the synthesis of various organic compounds

Biological activities

potential as pharmaceutical agents, including anticancer, antiviral, and antimicrobial properties

Potential for further investigation

structural features make it a potentially interesting candidate for further investigation in the development of new drugs or as a research tool in chemical and biomedical research.

Check Digit Verification of cas no

The CAS Registry Mumber 55671-58-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,6,7 and 1 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 55671-58:
(7*5)+(6*5)+(5*6)+(4*7)+(3*1)+(2*5)+(1*8)=144
144 % 10 = 4
So 55671-58-4 is a valid CAS Registry Number.

55671-58-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[chloro(phenyl)methyl]-1H-benzimidazole

1.2 Other means of identification

Product number -
Other names 2-(chloro-phenyl-methyl)-1H-benzoimidazole

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:55671-58-4 SDS

55671-58-4Relevant articles and documents

Synthesis and in vitro antifungal evaluation of benzoimidazolyl-piperazinyl-phenylmethanone derivatives

Kankate, Rani S.,Gide, Parag S.,Belsare, Deepak P.

, p. 1855 - 1863 (2015/04/22)

Benzimidazole and piperazines are the important pharmacophores in the structures of many antifungal compounds. Further, the phenylmethanone are also a unique class of compounds whose antifungal profile is not much exploited. So to exploit their antifungal potential we have selected these three combinations and framed the novel parent structure for our research work. In this study a novel series of benzimidazoles derivatives was synthesized by microwave irradiation and characterized by 1H NMR, 13C NMR, Infra Red (IR), and Mass Spectroscopy (MS), and by elemental analysis. The screening of compound for in vitro (turbidimetric method) antifungal activity against C.albicans revealed activity in many of the compounds as comparable to that of ketoconazole.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 55671-58-4