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19875-04-8

19875-04-8 Structure

19875-04-8 Structure
IdentificationBack Directory
[Name]

4(1H)-Pyrimidinone, 2-methyl- (8CI,9CI)
[CAS]

19875-04-8
[Synonyms]

2-Methyl-4-pyrimidinol
2-Methylpyrimidine-4-ol
2-Methyl-4(3H)-pyrimidinone
2-Methylpyrimidin-4(1H)-one
2-methylpyrimidin-4(3H)-one
2-methyl-1H-pyrimidin-6-one
4(3H)-Pyrimidinone,2-methyl-
2-Methyl-4-hydroxypyriMidine
2-Methylpyrimidine-4(3H)-one
2-Methyl-4-hydroxy-pyriMidine
2-Methylpyrimidin-4(3H)-one ,≥96%
4(1H)-Pyrimidinone, 2-methyl- (8CI,9CI)
2-METHYLPYRIMIDIN-4(3H)-ONE,PURITY:95% MIN(HPLC)
4(1H)-Pyrimidinone, 2-methyl- (8CI,9CI) ISO 9001:2015 REACH
[Molecular Formula]

C5H6N2O
[MDL Number]

MFCD05864425
[MOL File]

19875-04-8.mol
[Molecular Weight]

110.11
Chemical PropertiesBack Directory
[Melting point ]

214 °C
[density ]

1.22±0.1 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

9.43±0.40(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Raw materials And Preparation ProductsBack Directory
Hazard InformationBack Directory
[Uses]

4-Hydroxy-2-methylpyrimidine is a useful synthetic intermediate. It is an intermediate used to synthesize 2-Methyl-4-pyrimidinyl-boronic Acid (M328125) which is used to synthesize indazole-derived S-adenosyl homocysteine/methylthioadenosine nucleosidase inhibitors with antimicrobial activities.
[Synthesis Reference(s)]

Synthesis, p. 286, 1974 DOI: 10.1055/s-1974-23295
Spectrum DetailBack Directory
[Spectrum Detail]

4(1H)-Pyrimidinone, 2-methyl- (8CI,9CI)(19875-04-8)MS
4(1H)-Pyrimidinone, 2-methyl- (8CI,9CI)(19875-04-8)IR1
4(1H)-Pyrimidinone, 2-methyl- (8CI,9CI)(19875-04-8)IR2
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