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5-Pyrimidinecarboxylic acid, 6-ethyl-1,2,3,4-tetrahydro-4-(3-methylphenyl)-2-thioxo-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

330825-17-7

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330825-17-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 330825-17-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,0,8,2 and 5 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 330825-17:
(8*3)+(7*3)+(6*0)+(5*8)+(4*2)+(3*5)+(2*1)+(1*7)=117
117 % 10 = 7
So 330825-17-7 is a valid CAS Registry Number.

330825-17-7Downstream Products

330825-17-7Relevant academic research and scientific papers

Studies on synthesis, chromatographic resolution, and antiinflammatory activities of some 2-thioxo-1,2,3,4-tetrahydropyrimidines and their condensed derivatives

Tozkoparan, Birsen,Yarim, Mine,Sarac, Selma,Ertan, Mevluet,Kelicen, Pelin,Altinok, Guelcin,Demirdamar, Ruemeysa

, p. 415 - 420 (2000)

In this study, the synthesis of some new 2-thioxo-1,2,3,4-tetrahydropyrimidines and their condensed derivatives, thiazolo[3,2-a]pyrimidines, are described. The structures of the compounds were confirmed by IR, 1H-NMR, 13C-NMR, and mass spectroscopy. The direct high-performance liquid chromatographic separation of the compounds on derivatized cellulose chiral stationary phases such as cellulose tris(3,5-dimethylphenylcarbamate) (OD), cellulose tris(4-methylphenylcarbamate) (OG), and cellulose tris(4-methylbenzoate) (OJ) was studied. All of the compounds were screened for their antiinflammatory activity and also investigated histopathologically. Compounds 3 and 1a were found to be the most promising antiinflammatory agents in this group.

Synthesis of 4-aryl-3,4-dihydropyrimidin-2(1H)-thione derivatives as potential calcium channel blockers

Zorkun, Inci Selin,Sarac, Selma,Celebi, Semra,Erol, Kevser

, p. 8582 - 8589 (2008/02/07)

Biginelli reaction which involves condensation of methyl 3-oxopentanoate, aromatic aldehydes and thiourea with a catalytic amount of HCl at reflux temperature has been used for the synthesis of 4-aryl-6-ethyl-5-(methoxycarbonyl)-3,4-dihydropyrimidin-2(1H)

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