36591-61-4

Usage

InChI:InChI=1/C5H7N3O2/c1-2-7-4(6)3(9)5(10)8-2/h9H,1H3,(H3,6,7,8,10)

Upstream product

• 38953-40-1 6-amino-2-methyl-4-oxo-1,4-dihydropyrimidin-5-yl hydrogen sulfate 
• 99170-32-8 2-methyl-5-(tetrahydro-2H-pyran-2-yloxy)pyrimidin-4(3H)-one 
• 24614-14-0 5-hydroxy-2-methyl-(3H)-pyrimidin-4-one 
• 767-16-8 4-amino-6-hydroxy-2-methylpyrimidine 

Downstream Products

• 127535-93-7 N-phenyl-N'-(2-methyl-6,7-dihydro-1,4-dioxino<2,3-d>pyrimidin-4-yl)urea 
• 20783-19-1 4-amino-5-hydroxy-2-methylpyrimidine 
• 38953-43-4 4-amino-6-chloro-5-hydroxy-2-methylpyrimidine 

Relevant academic research and scientific papers

SUBSTITUTED PYRIMIDINES, PROCESS FOR THEIR PRODUCTION AND THEIR USE AS EFFECTIVE ABSORBENTS OF UV IRRADIATION

The present invention discloses substituted pyrimidines, processes for their synthesis and their use as effective sun-protecting agents either alone or in combination with other known sun-protecting agents.

An autoxidation study of C2 substituted pyrimidine amino reductones

Three pyrimidine derivatives (8a-c), differing from isouramil and divicine at C2, have been synthesized and their autoxidation rates measured spectrophotometrically. The autoxidation rates of all five pyrimidines (8a-c, isouramil and divicine) were correl

Application of the Elbs Persulfate Oxidation to the Preparation of 5-Hydroxypyrimidines

The use of potassium persulfate in cold sodium hydroxide solution has been shown to give the pyrimidin-5-yl hydrogen sulfates in cases where the pyrimidine has at least two electron-releasing groups in the 2, 4 or 6 positions.However, the reaction has been unsuccessful in a number of cases.The pyrimidin-5-yl hydrogen sulfates are hydrolysed to the corresponding 5-hydroxypyrimidines by hydrochloric acid.