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124530-70-7

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124530-70-7 Usage

Also known as

1-methyl-1H-benzimidazole-2-thiol or 1-methyl-2-mercaptobenzimidazole

Structure

Benzimidazole derivative with a thioether functional group

Potential applications

Pharmaceutical and agrochemical industries

Biological activities

Unknown, but may have potential in the development of new drugs or crop protection products

Safety

Handle with caution and follow proper safety protocols in laboratory or industrial settings.

Check Digit Verification of cas no

The CAS Registry Mumber 124530-70-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,5,3 and 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 124530-70:
(8*1)+(7*2)+(6*4)+(5*5)+(4*3)+(3*0)+(2*7)+(1*0)=97
97 % 10 = 7
So 124530-70-7 is a valid CAS Registry Number.

124530-70-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-propan-2-ylsulfanyl-1H-benzimidazole

1.2 Other means of identification

Product number -
Other names 2-(methylethylthio)benzimidazole

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:124530-70-7 SDS

124530-70-7Relevant articles and documents

Synthesis and preliminary evaluation of benzimidazole derivatives as antimicrobial agents

Klimesova, Vera,Koci, Jan,Pour, Milan,Stachel, Jiri,Waisser, Karel,Kaustova, Jarmila

, p. 409 - 418 (2007/10/03)

A series of 2-alkylsulphanylbenzimidazoles was synthesised and the compounds were evaluated for their in vitro antimicrobial activity. The structures of the compounds were confirmed by 1H-NMR and IR data, and their purity by elemental analysis. Antimycobacterial activities against Mycobacterium tuberculosis and non-tuberculous mycobacteria as well as antifungal activities against Candida albicans, Candida tropicalis, Candida krusei, Candida glabrata, Trichosporon beigelii, Trichophyton mentagrophytes and Aspergillus fumigatus were expressed as the corresponding MIC values. The substances exhibited appreciable antimycobacterial activity, in particular, against non-tuberculous mycobacteria. The activity of the most active compound in the set, 3,5-dinitro derivative 4t, exceeded that of the standard isoniazide against M. kansasii and M. avium. The antifungal activities of the compounds were relatively low. A weak antifungal effect was observed against the dermatophyte Trichophyton mentagrophytes. None of the compounds showed significant inhibitory activity against yeasts.

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