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405314-01-4

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405314-01-4 Usage

Structure

A hydroxy derivative of benzimidazole with a nitro group and a methyl group attached to the benzene ring

Usage

Building block in the synthesis of pharmaceuticals and agrochemicals

Biological activity

Exhibits antimicrobial and antifungal properties

Potential use

Investigation for treatment of various diseases and as a potential candidate for drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 405314-01-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,5,3,1 and 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 405314-01:
(8*4)+(7*0)+(6*5)+(5*3)+(4*1)+(3*4)+(2*0)+(1*1)=94
94 % 10 = 4
So 405314-01-4 is a valid CAS Registry Number.

405314-01-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-Benzimidazole,1-hydroxy-2-methyl-6-nitro-(9CI)

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:405314-01-4 SDS

405314-01-4Downstream Products

405314-01-4Relevant articles and documents

Reductive cyclization with baker's yeast of 4-alkyl-2-nitro-acetanilides to 6-alkylbenzimidazoles and 1-hydroxy-2-methyl-6-alkylbenzimidazoles

Navarro-Ocana,Olguin,Luna,Jimenez-Estrada,Barzana

, p. 2754 - 2756 (2007/10/03)

Reduction of 4-substituted 2-nitroacetanilides by baker's yeast in acid media effected cyclization, resulting in the formation of n-substituted 2-methylbenzimidazoles and 6-substituted 1-hydroxy-2-methylbenzimidazole via the chemo- and regioselective reduction of the 2-nitro aromatic group to amine or hydroxylamine.

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