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1673-62-7

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1673-62-7 Usage

Derivative of

benzimidazole

Usage

production of pharmaceuticals, polymer and rubber industries

Properties

antimicrobial, antifungal

Applications

formulation of antiseptics and disinfectants, building block for the synthesis of organic compounds

Versatility

wide range of applications in different industries

Check Digit Verification of cas no

The CAS Registry Mumber 1673-62-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,7 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1673-62:
(6*1)+(5*6)+(4*7)+(3*3)+(2*6)+(1*2)=87
87 % 10 = 7
So 1673-62-7 is a valid CAS Registry Number.

1673-62-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Methyl-1-vinyl-1H-benzimidazole

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:1673-62-7 SDS

1673-62-7Downstream Products

1673-62-7Relevant articles and documents

-

Hopff et al.

, p. 135,138 (1960)

-

Synthesis of annelated imidazoles and benzimidazoles

McClure, James R.,Custer, John H.,Schwarz, H. Dean,Lill, Deborah A.

, p. 710 - 712 (2007/10/03)

A variety of fused ring imidazole or benzimidazole derivatives were prepared through two successive condensations of a dihalide with 4,5- diphenylimidazole or benzimidazole. The 2-methyl substituted derivatives of 4,5-diphenylimidazole or benzimidazole were also used. The size of the annelated ring, which is dependent on the dihalide used, can be varied from five to seven atoms. Initially, N-alkylhalo derivatives were prepared by condensation of the heterocyclic starting materials with a dihalide. Ring closure was then effected through intramolecular condensation of a carbanion derived from the 2-position or the 2-methyl group of the parent heterocyclic ring with the N-alkylhalo moiety.

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