36591-61-4

Basic information

• Product Name: 4(1H)-Pyrimidinone, 6-amino-5-hydroxy-2-methyl- (9CI)
• Synonyms: 4(1H)-Pyrimidinone, 6-amino-5-hydroxy-2-methyl- (9CI);4(1H)-PyriMidinone, 6-aMino-5-hydroxy-2-Methyl-;6-amino-5-hydroxy-2-methylpyrimidin-4(3H)-one;6-Amino-5-hydroxy-2-methyl-4(1H)-Pyrimidinone
• CAS NO: 36591-61-4
• Molecular Formula: C₅H₇N₃O₂
• Molecular Weight: 141.12798
• Product Categories: PYRIMIDINE
• Mol File: 36591-61-4.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 234°Cat760mmHg
• Flash Point: 95.3°C
• Appearance: /
• Density: 1.67g/cm³
• Vapor Pressure: 0.00998mmHg at 25°C
• Refractive Index: 1.7
• CAS DataBase Reference: 4(1H)-Pyrimidinone, 6-amino-5-hydroxy-2-methyl- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 4(1H)-Pyrimidinone, 6-amino-5-hydroxy-2-methyl- (9CI)(36591-61-4)
• EPA Substance Registry System: 4(1H)-Pyrimidinone, 6-amino-5-hydroxy-2-methyl- (9CI)(36591-61-4)

Safety Data

• Hazardous Substances Data: 36591-61-4(Hazardous Substances Data)

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 
• 767-16-8 4-amino-6-hydroxy-2-methylpyrimidine 
• 24614-14-0 5-hydroxy-2-methyl-(3H)-pyrimidin-4-one 
• 99170-32-8 2-methyl-5-(tetrahydro-2H-pyran-2-yloxy)pyrimidin-4(3H)-one 

Downstream Products

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

Relevant articles and documents

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.

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.