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84445-81-8

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84445-81-8 Usage

General Description

1H-Benzimidazole, 1-acetyl-4-methyl-(9CI) is a chemical compound with the molecular formula C11H11N3O. It is a derivative of benzimidazole and is used in various pharmaceutical applications. 1H-Benzimidazole,1-acetyl-4-methyl-(9CI) is known for its antimicrobial, antifungal, antitumor, and anti-inflammatory properties. It is also being researched for its potential use in the treatment of neurological disorders and as a potential anticancer agent. Additionally, it has been studied for its potential as an inhibitor of a specific enzyme involved in cancer progression. Its chemical structure and properties make it a valuable compound for further research and development in the pharmaceutical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 84445-81-8 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, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 84445-81:
(7*8)+(6*4)+(5*4)+(4*4)+(3*5)+(2*8)+(1*1)=148
148 % 10 = 8
So 84445-81-8 is a valid CAS Registry Number.

84445-81-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-acetyl-4-methylbenzimidazole

1.2 Other means of identification

Product number -
Other names 1-(4-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:84445-81-8 SDS

84445-81-8Downstream Products

84445-81-8Relevant 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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