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1-(6-methyl-1,2-diphenyl-4-thioxo-1,4-dihydropyrimidin-5-yl)ethan-1-one is a complex organic compound belonging to the class of pyrimidines, characterized by a unique molecular structure. 1-(6-methyl-1,2-diphenyl-4-thioxo-1,4-dihydropyrimidin-5-yl)ethan-1-one features a 1,4-dihydropyrimidin-5-yl core, which is substituted with a methyl group at the 6th position and two phenyl rings at the 1st and 2nd positions. The 4th position is occupied by a thioxo group, while the 1st position is connected to an ethan-1-one moiety, which contributes to the compound's ketone functionality. This chemical structure endows the molecule with potential applications in various fields, such as pharmaceuticals and materials science, due to its diverse chemical properties and reactivity.

2228-13-9

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2228-13-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2228-13-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,2 and 8 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2228-13:
(6*2)+(5*2)+(4*2)+(3*8)+(2*1)+(1*3)=59
59 % 10 = 9
So 2228-13-9 is a valid CAS Registry Number.

2228-13-9Downstream Products

2228-13-9Relevant academic research and scientific papers

Design and chemical behavior of novel pyrimidine derivatives and their evaluation of cytotoxicity

Assy, Mohamed G.,ELasaad, Youssra S.,Sakr, Alaa R.

, (2020)

Diphenyl-4-thioxo-1,4-dihydropyrimidin-5-yl)ethan-1-one 4 was obtained upon the reaction of (phenylamino)but-2-enethioyl)benzamide 3 with sodium hydroxide. The reactions of 4 with several active species such as benzaldehyde, urea, malononitrile, ethyl cyanoacetate, hydrazine, and carbon disulfide were studied. The antitumor activities of some selective compounds were examined against two cell lines: Mammalian cell lines: A-549 cells (human lung cancer cell line) and MRC-5 cells (normal human lung fibroblast cell line); some of the compounds were highly efficient; compound 13 has the most effective anticancer activity.

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