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4-CHLORO-5-FLUORO-2-METHYL-PYRIMIDINE

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4-CHLORO-5-FLUORO-2-METHYL-PYRIMIDINE Basic information

Product Name:
4-CHLORO-5-FLUORO-2-METHYL-PYRIMIDINE
Synonyms:
  • 4-CHLORO-5-FLUORO-2-METHYL-PYRIMIDINE
  • Pyrimidine, 4-chloro-5-fluoro-2-methyl-
  • 4-CHLORO-5-FLUORO-2-METHYL-PYRIMIDINE ISO 9001:2015 REACH
CAS:
898044-50-3
MF:
C5H4ClFN2
MW:
146.55
Product Categories:
  • Fluorine series
Mol File:
898044-50-3.mol
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4-CHLORO-5-FLUORO-2-METHYL-PYRIMIDINE Chemical Properties

Boiling point:
176.9±20.0 °C(Predicted)
Density 
1.352±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Store in freezer, under -20°C
pka
-0.65±0.29(Predicted)
Appearance
Colorless to light yellow Solid-Liquid Mixture
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Safety Information

HS Code 
2933599590
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4-CHLORO-5-FLUORO-2-METHYL-PYRIMIDINE Usage And Synthesis

Uses

4-Chloro-5-fluoro-2-methylpyrimidine

Synthesis

1480-91-7

898044-50-3

General procedure for the synthesis of 4-chloro-5-fluoro-2-methylpyrimidine from 5-fluoro-2-methylpyrimidin-4(3H)-one: 5-fluoro-2-methylpyrimidin-4(3H)-one (1.04 g, 7.21 mmol) and N,N-dimethylaniline (1.80 mL) were dissolved in phosphorus trichloride and heated to a reaction temperature of 110 °C for 90 min. After the reaction was completed, it was cooled to room temperature and the reaction mixture was carefully poured into ice water. The product was extracted with diethyl ether, and the ether layer was washed sequentially with 2N hydrochloric acid, water and saturated saline, and then dried with anhydrous magnesium sulfate. The ether was removed by careful evaporation under reduced pressure to give the volatile liquid product 4-chloro-5-fluoro-2-methylpyrimidine (0.39 g, 34% yield), which could be used in subsequent reactions without further purification. Thin layer chromatography (TLC) Rf value was 0.26 (unfolding agent: 10% ethyl acetate/hexane).1H NMR (400 MHz, DMSO-d6): δ 3.91 (s, 3H), 8.79 (s, 1H).

References

[1] Patent: WO2008/96260, 2008, A1. Location in patent: Page/Page column 40

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