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1-(4-Trifluoromethylpyrimidin-2-yl)piperazine

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1-(4-Trifluoromethylpyrimidin-2-yl)piperazine Basic information

Product Name:
1-(4-Trifluoromethylpyrimidin-2-yl)piperazine
Synonyms:
  • 1-[4-(Trifluoromethyl)pyrimid-2-yl]piperazine ,97%
  • 1-(4-Trifluoromethylpyrimidin-2-yl)piperazine
  • 2-(Piperazin-1-yl)-4-(trifluoromethyl)pyrimidine
  • 2-PIPERAZIN-YL-4-(TRIFLUOROMETHYL)PYRIMIDINE
  • 1-[4-(TrifluoroMethyl)-2-pyriMidinyl]piperazine, 97%
  • Pyrimidine, 2-(1-piperazinyl)-4-(trifluoromethyl)-
  • 1-(4-Trifluoromethylpyrimidin-2-yl)piperazine ISO 9001:2015 REACH
  • 2-(1-Piperazinyl)-4-(trifluoromethyl)pyrimidine
CAS:
179756-91-3
MF:
C9H11F3N4
MW:
232.21
Product Categories:
  • pharmacetical
Mol File:
179756-91-3.mol
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1-(4-Trifluoromethylpyrimidin-2-yl)piperazine Chemical Properties

Melting point:
50-52°C
Boiling point:
331.3±52.0 °C(Predicted)
Density 
1.306±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
8.56±0.10(Predicted)
Appearance
White to off-white Solid
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Safety Information

Hazard Codes 
Xi
HS Code 
29335990
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1-(4-Trifluoromethylpyrimidin-2-yl)piperazine Usage And Synthesis

Chemical Properties

Gray solid

Synthesis

110-85-0

33034-67-2

179756-91-3

2-Chloro-4-trifluoromethylpyrimidine (2.0 g, 11 mmol) and piperazine (2.8 g, 33 mmol) were dissolved in DMF (10 mL) and triethylamine (3.0 mL, 22 mmol) was added as base. The reaction mixture was placed in a sealed tube and the reaction was stirred at 100 °C overnight. After completion of the reaction, most of the solvent was removed under reduced pressure. The crude product was purified by silica gel column chromatography with EtOAc to EtOAc/MeOH/NEt3 (9:1:0.5) as eluent to afford 1-(4-trifluoromethylpyrimidin-2-yl)piperazine (1.48 g, 56% yield). Mass spectrometry analysis: the calculated value (M+H) of C9H11F3N4 was 233 and the measured value was 233.1.

References

[1] Patent: US2006/4018, 2006, A1. Location in patent: Page/Page column 37

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