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1225223-42-6

1225223-42-6 Structure

1225223-42-6 Structure
IdentificationBack Directory
[Name]

2-Methyl-5-acetylpyriMidine
[CAS]

1225223-42-6
[Synonyms]

2-Methl-5-acetylpyrimidine
2-Methyl-5-acetylpyriMidine
1-(2-Methyl-5-pyriMidyl)ethanone
1-(2-MethylpyriMidin-5-yl)ethanone
1-(2-methylpyrimidin-5-yl)ethan-1-one
Ethanone, 1-(2-methyl-5-pyrimidinyl)-
[Molecular Formula]

C7H8N2O
[MDL Number]

MFCD18073349
[MOL File]

1225223-42-6.mol
[Molecular Weight]

136.15
Chemical PropertiesBack Directory
[Boiling point ]

219.9±13.0 °C(Predicted)
[density ]

1.100±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

0.02±0.22(Predicted)
[Appearance]

White to light yellow Solid
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

2-Methyl-5-acetylpyriMidine(1225223-42-6)1HNMR
Hazard InformationBack Directory
[Synthesis]

5-(1-ethoxyethenyl)-2-methylpyrimidine

1421922-89-5

2-Methyl-5-acetylpyriMidine

1225223-42-6

General procedure for the synthesis of 1-(2-methyl-5-pyrimidinyl)ethanone from the compound (CAS: 1421922-89-5): the compound (0.47 g) obtained in Reference Example 38-1 was dissolved in acetone (8.0 mL), 1.0 mol/L aqueous hydrochloric acid (2.0 mL) was added, and the reaction was stirred for 24 hours at room temperature. After completion of the reaction, water and saturated aqueous sodium bicarbonate solution were added to the reaction mixture, stirred and extracted using chloroform. The organic layer was separated by a phase separator and the solvent was subsequently removed by distillation under reduced pressure to afford 1-(2-methyl-5-pyrimidinyl)ethanone (0.40 g), the product was a pale yellow solid.1H NMR (600 MHz, chloroform-d) δ ppm: 2.63 (3H, s), 2.80-2.84 (3H, m), 9.13 (2H, s).

[References]

[1] Patent: US2014/155597, 2014, A1. Location in patent: Paragraph 0373; 0374; 0375
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