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84445-91-0

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84445-91-0 Usage

Structure

Bicyclic organic compound, derivative of benzimidazole

Usage

Synthesis of pharmaceuticals and agrochemicals

Biological activities

Antifungal and antiviral properties

Potential

Building block for new compounds for medicinal and industrial purposes

Research

Shown promise for various applications and research purposes

Check Digit Verification of cas no

The CAS Registry Mumber 84445-91-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,4,4 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 84445-91:
(7*8)+(6*4)+(5*4)+(4*4)+(3*5)+(2*9)+(1*1)=150
150 % 10 = 0
So 84445-91-0 is a valid CAS Registry Number.

84445-91-0SDS

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 1-acetyl-7-methylbenzimidazole

1.2 Other means of identification

Product number -
Other names 1-(7-Methyl-benzoimidazol-1-yl)-ethanone

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:84445-91-0 SDS

84445-91-0Downstream Products

84445-91-0Relevant articles and documents

Synthesis of N-Acetylbenzimidazole Derivatives

Tanaka, Kenjiro,Shimazaki, Michiko,Murakami, Yasuoki

, p. 2714 - 2722 (2007/10/02)

For the structure determination of thiazolobenzimidazol-3(2H)-one derivatives (2 or 3) they were converted to the corresponding 1-acetylbenzimidazoles (4) by desulfurization.The latter compounds (4) were alternatively prepared by the cyclization of 2-aminoacetanilide derivatives (5) with CS2 in dimethylformamide (DMF), followed by desulfurization with Raney Ni.However, the reactions of 5 with ethyl orthoformate/H2SO4 in DMF gave a mixture of 4 and its acetyl-rearranged product (7).Keywords-acetyl group; rearrangement; thiazolobenzimidazol-3(2H)-one; N-acetylbenzimidazoles; ethyl orthoformate; carbon disulfide; desulfurization

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