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89426-90-4

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89426-90-4 Usage

Structure

Benzimidazole derivative with a trifluoromethyl group at the 2-position and a hydroxyl group at the 6-position

Physical form

White solid

Solubility

Sparingly soluble in water

Uses

Building block in the synthesis of pharmaceuticals and agrochemicals

Potential applications

Drug design and discovery, research and development of new materials and products

Unique properties

Valuable tool for studying enzymatic and biochemical processes in biological systems

Check Digit Verification of cas no

The CAS Registry Mumber 89426-90-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,4,2 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 89426-90:
(7*8)+(6*9)+(5*4)+(4*2)+(3*6)+(2*9)+(1*0)=174
174 % 10 = 4
So 89426-90-4 is a valid CAS Registry Number.

89426-90-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(trifluoromethyl)-3H-benzimidazol-5-ol

1.2 Other means of identification

Product number -
Other names -

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:89426-90-4 SDS

89426-90-4Downstream Products

89426-90-4Relevant articles and documents

Rapid one-pot preparation of 2-substituted benzimidazoles from 2-nitroanilines using microwave conditions

VanVliet, David S.,Gillespie, Paul,Scicinski, Jan J.

, p. 6741 - 6743 (2005)

A high yielding one-pot procedure for the generation of 2-substituted benzimidazoles directly from 2-nitroanilines by in situ reduction and cyclization using a microwave procedure is described.

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