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5-BROMOPYRAZINE-2-CARBONITRILE

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5-BROMOPYRAZINE-2-CARBONITRILE Basic information

Product Name:
5-BROMOPYRAZINE-2-CARBONITRILE
Synonyms:
  • 2-Pyrazinecarbonitrile, 5-bromo- Pyrazinecarbonitrile, 5-bromo- (9CI)
  • 2-BROMO-5-CYANOPYRAZINE
  • 5-BROMOPYRAZINE-2-CARBONITRILE
  • 2-Pyrazinecarbonitrile, 5-broMo-
  • 2-Bromo-5-cyanopyrazine, 2-Bromo-5-cyano-1,4-diazine
  • 5-BROMOPYRAZINE-2-CARBONITRILE ISO 9001:2015 REACH
  • 5-Bromo-2-pyrazinecarbonitrile
  • 2-BROMO-5-CYANOPYRAZIN
CAS:
221295-04-1
MF:
C5H2BrN3
MW:
183.99
Product Categories:
  • Building Blocks
  • Pyrazine
Mol File:
221295-04-1.mol
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5-BROMOPYRAZINE-2-CARBONITRILE Chemical Properties

Boiling point:
264.7±35.0 °C(Predicted)
Density 
1.86±0.1 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
-5.41±0.10(Predicted)
form 
crystalline solid
color 
Faint peach
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Safety Information

HS Code 
2933998090
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5-BROMOPYRAZINE-2-CARBONITRILE Usage And Synthesis

Synthesis

113305-94-5

221295-04-1

ii) 5-Aminopyrazine-2-carbonitrile (0.208 mmol) was dissolved in acetonitrile (1 mL) and added slowly and dropwise to a stirred solution of copper (II) bromide (0.25 mmol) and tert-butyl nitrite (0.31 mmol) in acetonitrile (2 mL). The reaction mixture was stirred at a constant temperature at 60 °C for 1 hour. After completion of the reaction, the reaction solution was diluted with ethyl acetate (15 mL) and washed twice with 1N aqueous hydrochloric acid. The organic phase was dried over anhydrous sodium sulfate and purified by silica gel column chromatography (eluent: hexane/ethyl acetate) to afford the target compound 2-bromo-5-cyanopyrazine in 49% yield.1H NMR (CDCl3) δ (ppm): 8.83 (s, 1H); 8.71 (s, 1H).

References

[1] Patent: US2007/37820, 2007, A1. Location in patent: Page/Page column 15

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