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1H-Benzimidazole, 2-[[(3-methylphenyl)methyl]thio]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

253168-40-0

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253168-40-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 253168-40-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,3,1,6 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 253168-40:
(8*2)+(7*5)+(6*3)+(5*1)+(4*6)+(3*8)+(2*4)+(1*0)=130
130 % 10 = 0
So 253168-40-0 is a valid CAS Registry Number.

253168-40-0Downstream Products

253168-40-0Relevant articles and documents

Synthesis and spectral characterization of 2-mercaptobenzimidazole derivatives using a new active phase transfer reagent under PTC conditions

Jayachandran, J. Paul,Wang, Maw-Ling

, p. 4087 - 4099 (1999)

The phase transfer catalyzed synthesis of 2-Mercaptobenzimidazole derivatives using the new active phase transfer reagent namely, 2- benzilidine-N,N,N,N',N',N'-hexaethyl propane-1,3-diammonium dibromide (Dq-Br) have been described. The structures of all the fifteen compounds have been established by spectroscopic means.

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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