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7-Methyl-6(5H)-pteridinone is a chemical compound belonging to the pteridine family, characterized by a bicyclic structure with a pyrazine ring fused to a pyrimidine ring. This specific compound features a methyl group at the 7th position and a 5-membered ring at the 6th position, which is in a half-chair conformation. It is an important intermediate in the synthesis of various biologically active compounds, such as folic acid and its derivatives, which play crucial roles in one-carbon transfer reactions and nucleic acid synthesis. The compound is also used in the development of anti-cancer and anti-inflammatory drugs due to its potential therapeutic properties.

1128-60-5

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1128-60-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1128-60-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,2 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1128-60:
(6*1)+(5*1)+(4*2)+(3*8)+(2*6)+(1*0)=55
55 % 10 = 5
So 1128-60-5 is a valid CAS Registry Number.

1128-60-5Downstream Products

1128-60-5Relevant academic research and scientific papers

Kinetic Study on the Anelation of Heterocycles. 3. Pyrazinopyrimidine Derivatives Synthesized by the Hinsberg Reaction

Abasolo, Maria Ines,Fernandez, Beatriz M.,Magrini, Edgardo

, p. 1279 - 1283 (2007/10/02)

A kinetic study on the obtainment of pyrazinopyrimidine derivatives (pteridines) was performed.The regioselective synthesis of compounds 6-methylpyrazinopyrimidin-7(8H)-one (5a) and 7-methylpyrazinopyrimidin-6(5H)-one (5b), in good yields, was expected by the Hinsberg reaction because the synthesis of both isomers analytically pure was never reported to date.This Hinsberg reaction gave good results to obtain compound 5a, regioselectively and in good yields, either in pH 5 aqueous buffer solution or in methylene chloride, among several organic solvents.However, structural and solvation factors prevented the synthesis of the isomer 5b, which was regioselectively formed in very acid solutions (Ho = -0.89), but in very poor yield.

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