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4,5,6,7-tetrahydro-3-phenylbenzo[d]thiazole-2(3H)-thione is a complex organic compound with the molecular formula C14H13NS2. It is a derivative of benzothiazole, a heterocyclic compound consisting of a benzene ring fused to a thiazole ring. The compound is characterized by its unique structure, where the benzene ring is attached to a thiazole ring, and the thiazole ring contains a sulfur atom and a nitrogen atom. The 3-phenyl group in the compound refers to a phenyl ring attached to the third carbon of the thiazole ring. 4,5,6,7-tetrahydro-3-phenylbenzo[d]thiazole-2(3H)-thione is of interest in the field of organic chemistry and may have potential applications in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals due to its unique structure and properties.

1962-05-6

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1962-05-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1962-05-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,6 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1962-05:
(6*1)+(5*9)+(4*6)+(3*2)+(2*0)+(1*5)=86
86 % 10 = 6
So 1962-05-6 is a valid CAS Registry Number.

1962-05-6Relevant academic research and scientific papers

New approaches for the synthesis and ctytotoxicity of thiazoles derived from cyclohexanone

Abbas, Nermeen S.,Ahmed, Ebtsam A.

, p. 835 - 843 (2015/02/05)

A new class of substituted thiazole derivatives 6a-c which showed promising anticancer activity was synthesized via the reaction of cyclohexanone with phenylisothiocyanate with a good yield. The latter compounds reacted with benzendiazonium chloride to form corresponding 5-phenylazothiazole derivatives 8a and 8b, respectively. Moreover, the reaction of thiazole derivatives 6a-c with each of elemental sulfur and either of malononitrile or ethyl cyanoacetate gave the thiophene derivatives 10a-e, respectively. Compounds 10a-e were subjected to a series of heterocylclization reactions to give heterocyclic derivatives. Their cytotoxicity against four human tumor cells lines was measured and showed promising anticancer activity.

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