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5-ethyldihydro-1-methyl-5-phenyl-4,6(1H,5H)-pyrimidinedione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69243-48-7

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69243-48-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69243-48-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,2,4 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 69243-48:
(7*6)+(6*9)+(5*2)+(4*4)+(3*3)+(2*4)+(1*8)=147
147 % 10 = 7
So 69243-48-7 is a valid CAS Registry Number.

69243-48-7Downstream Products

69243-48-7Relevant academic research and scientific papers

Methylation of 5-ethyl-5-phenyl-2-thioxo-4,6(1H,3H,5H)-pyrimidinedione

Kubaszek, M.,Paluchowska, M.,Chmiel, E.,Bojarski, J.

, p. 117 - 124 (2007/10/02)

Methylation of the title compound (2-thiophenobarbital) under different conditions yielded two pairs of isomeric N-, and S--monomethyl and N,N'- and N,S-dimethyl derivatives.Spectral data confirm their structure and allow to identify the methyl substitution.Preliminary results of irradiation of N-CH3 substituted compounds are also presented. Key words: pyrimidines, sulfur compounds, 2-thiobarbiturate

N-Alkyl barbiturates. A series of compounds for the study of metabolic structure-activity relationships

Treston,Hooper

, p. 1627 - 1629 (2007/10/02)

Many therapeutic agents are metabolised along multiple pathways, but up to now there have been few investigations addressing the question of which chemical features of drugs govern the participation in, and quantitative significance of, different biotransformation pathways. To assess the influence of variations of the chemical structure upon metabolim, a series of novel barbiturate analogues has been synthesized. The N1-monoalkylated and N1,N2-dialkylated phenobarbitones and 2-desoxyphenobarbitones have been synthesized via condensation of ethylphenylmalonic acid derivatives with different N-alkylated ureas or thioureas, and/or by base-catalyzed N-alkylation of different barbituric acids.

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