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4-Benzyl-1-methyl-5-phenyl-3,4-dihydropyrimidin-2(1H)-one is a complex organic compound belonging to the class of pyrimidines, which are heterocyclic aromatic compounds with the general formula C4H4N2. This specific compound features a dihydropyrimidin-2(1H)-one core structure, with a benzyl group attached at the 4-position, a methyl group at the 1-position, and a phenyl group at the 5-position. The compound is characterized by its unique molecular structure, which contributes to its potential applications in various fields, such as pharmaceuticals and agrochemicals, where it may serve as a building block for the synthesis of more complex molecules or as a potential bioactive compound itself.

4997-24-4

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4997-24-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4997-24-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,9 and 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4997-24:
(6*4)+(5*9)+(4*9)+(3*7)+(2*2)+(1*4)=134
134 % 10 = 4
So 4997-24-4 is a valid CAS Registry Number.

4997-24-4Downstream Products

4997-24-4Relevant academic research and scientific papers

A chemo- and regio-selective three-component dihydropyrimidinone synthesis

Bailey, Chris D.,Houlden, Chris E.,Bar, Gregory L. J.,Lloyd-Jones, Guy C.,Booker-Milburn, Kevin I.

, p. 2932 - 2934 (2007)

A selective three-component coupling, involving co-condensation of aldehyde pairs with substituted ureas under Lewis acid catalysis, provides rapid access to highly functionalised dihydropyrimidinones; sulfamides react analogously. The Royal Society of Ch

Efficient synthesis of dihydropyrimidinones via a three-component Biginelli-type reaction of urea, alkylaldehyde and arylaldehyde

Qu, Haijun,Li, Xuejian,Mo, Fan,Lin, Xufeng

supporting information, p. 2846 - 2851 (2014/01/06)

A one-pot three-component synthesis of dihydropyrimidinones via a molecular iodine-catalyzed tandem reaction of simple readily available mono-substituted urea, alkylaldehyde, and arylaldehyde has been developed. The reaction proceeds with high chemo- and

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