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1H-Benzimidazole, 5-chloro-2-(4-methoxyphenyl)-1-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53703-85-8

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53703-85-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53703-85-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,7,0 and 3 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 53703-85:
(7*5)+(6*3)+(5*7)+(4*0)+(3*3)+(2*8)+(1*5)=118
118 % 10 = 8
So 53703-85-8 is a valid CAS Registry Number.

53703-85-8SDS

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-benzyl-5-chloro-2-(4-methoxyphenyl)benzimidazole

1.2 Other means of identification

Product number -
Other names 1-benzyl-5-chloro-2-(4-methoxy-phenyl)-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:53703-85-8 SDS

53703-85-8Downstream Products

53703-85-8Relevant academic research and scientific papers

Synthesis of fused imidazoles and benzothiazoles from (hetero)aromatic ortho-diamines or ortho-aminothiophenol and aldehydes promoted by chlorotrimethylsilane

Ryabukhin, Sergey V.,Plaskon, Andrey S.,Volochnyuk, Dmitriy M.,Tolmachev, Andrey A.

, p. 3715 - 3726 (2006)

New convenient conditions for benzimidazole and benzothiazole syntheses are described. A set of benzimidazoles, 3H-imidazo[4,5-b]pyridines, purines, xanthines and benzothiazoles was readily prepared from (hetero)aromatic ortho-diamines or ortho-aminothiop

Pyrolysis of N1,N3-Disubstituted 5-Methyl- and 5-Chlorobenzimidazolines

Chalapathi Rao, C. V.,Kondal Reddy, K.,Rao, N. V. Subba

, p. 967 - 969 (2007/10/02)

The pyrolysis of 2-aryl-1-benzyl-3,5-dimethyl(I)-, 5-chloro-3-methyl(II)-, 3-substituted-benzyl-5-methyl(III)- and 3-substituted-benzyl-5-chloro-(IV)-benzimidazolines has been carried out to study the orientation of their elimination reactions.The benzyl group is eliminated in preference to methyl in benzimidazolines of the types (I) and (II) irrespective of the nature of the substituent in phenylene and aryl moieties.The course of the elimination reaction in compounds of the types (III) and (IV) appears to be determined by the relative stabilities of benzyl and substituted benzyl radicals.The structures of the pyrolysis products have been established on the basis of spectral and chemical evidences.

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