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4-(4-chlorophenyl)-N-(naphthalen-1-yl)thiazol-2-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

284668-45-7

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284668-45-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 284668-45-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,4,6,6 and 8 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 284668-45:
(8*2)+(7*8)+(6*4)+(5*6)+(4*6)+(3*8)+(2*4)+(1*5)=187
187 % 10 = 7
So 284668-45-7 is a valid CAS Registry Number.

284668-45-7Downstream Products

284668-45-7Relevant academic research and scientific papers

Aryliodoazide synthons: A different approach for diversified synthesis of 2-aminothiazole, 1,3-thiazole, and 1,3-selenazole scaffolds

Majnooni, Sahar,Duffield, Joseph,Price, Jessica,Khosropour, Ahmad Reza,Zali-Boeini, Hassan,Beyzavi, M. Hassan

supporting information, p. 516 - 521 (2019/08/01)

Several straightforward and practical processes have been established for the construction of 2-aminothiazoles, 1,3-thiazoles and 1,3-selenazoles from aryliodoazides. These strategies successfully proceed with a wide spectrum of substituted thioamides and its derivatives producing the resulting five-membered heterocycles obtained in satisfactory yields. The unique features of these protocols are operational simplicity and highly functional group tolerance, which make them convenient and practical routes for the preparation of various libraries of 2-aminothiazoles, 1,3-thiazoles, and 1,3-selenazoles.

Synthesis and biological activity of 2-aminothiazoles as novel inhibitors of PGE2 production in cells

Smith, Breland,Chang, Hui-Hua,Medda, Federico,Gokhale, Vijay,Dietrich, Justin,Davis, Angela,Meuillet, Emmanuelle J.,Hulme, Christopher

experimental part, p. 3567 - 3570 (2012/07/03)

This Letter presents the synthesis and biological evaluation of a collection of 2-aminothiazoles as a novel class of compounds with the capability to reduce the production of PGE2 in HCA-7 human adenocarcinoma cells. A total of 36 analogs were

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