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2-(4-amidinophenyl)benzothiazole hydrochloride is a chemical compound with the molecular formula C14H10ClN3S. It is a derivative of benzothiazole, a heterocyclic compound consisting of a benzene ring fused to a thiazole ring. The compound features an amidinophenyl group attached to the benzothiazole core, which is further substituted with a hydrochloride group. This chemical is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as a building block for the development of new compounds with biological activity. Its unique structure allows for the exploration of its properties in different chemical reactions and its potential use in the creation of new drugs or chemical intermediates.

76284-94-1

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76284-94-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76284-94-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,2,8 and 4 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 76284-94:
(7*7)+(6*6)+(5*2)+(4*8)+(3*4)+(2*9)+(1*4)=161
161 % 10 = 1
So 76284-94-1 is a valid CAS Registry Number.

76284-94-1Downstream Products

76284-94-1Relevant academic research and scientific papers

Synthesis and antiproliferative activity of cyano and amidino substituted 2-phenylbenzothiazoles

Racane, Livio,Tralic-Kulenovic, Vesna,Kitson, Richard P.,Karminski-Zamola, Grace

, p. 1571 - 1577 (2006)

Series of cyano, dicyano, amidino, and diamidino substituted 2-phenylbenzothiazoles were prepared. Mono- and dicyano substituted benzothiazoles were obtained by condensation of appropriate substituted benzaldehydes with 2-aminothiophenol or 4-amino-3-mercaptobenzonitrile. The appropriate amidines or diamidines were prepared by Pinner reaction. The compounds were tested against breast, prostate, and lung cancer cell lines in a 72∈h cytotoxicity assay. Many of the compounds had at 10∈μM activity equivalent to 2-(4-aminophenyl)benzothiazole, while four compounds had significantly better activity, particularly in the breast cancer model. Springer-Verlag 2006.

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