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3-AMINO-6-BROMOPYRAZINE-2-CARBONITRILE

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3-AMINO-6-BROMOPYRAZINE-2-CARBONITRILE Basic information

Product Name:
3-AMINO-6-BROMOPYRAZINE-2-CARBONITRILE
Synonyms:
  • 2-AMINO-5-BROMO-3-CYANOPYRAZINE
  • 3-AMINO-6-BROMOPYRAZINE-2-CARBONITRILE
  • 3-AMINO-6-BROMOPYRAZINE-2-CARBONITRILE, 95+%
  • 3-Amino-6-bromopyrazine-2-carbonitrile 98%
  • 2-Amino-3-cyano-5-bromopyrazine
  • 2-Pyrazinecarbonitrile, 3-amino-6-bromo-
  • 3-AMINO-6-BROMOPYRAZINE-2-CARBONITRILE ISO 9001:2015 REACH
  • 3-Amino-6-bromopyrazinecarbonitrile
CAS:
17231-51-5
MF:
C5H3BrN4
MW:
199.01
Mol File:
17231-51-5.mol
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3-AMINO-6-BROMOPYRAZINE-2-CARBONITRILE Chemical Properties

Melting point:
183-184 °C(Solv: benzene (71-43-2))
Boiling point:
341.0±42.0 °C(Predicted)
Density 
1.94±0.1 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
-0.11±0.10(Predicted)
Appearance
Light yellow to yellow Solid
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22-41
Safety Statements 
26-39
HS Code 
2933998090
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3-AMINO-6-BROMOPYRAZINE-2-CARBONITRILE Usage And Synthesis

Synthesis

25911-65-3

17231-51-5

Bromine (0.95 mL, 19 mmol) was added slowly and dropwise to a solution of 3-aminopyrazine-2-carbonitrile (1.7 g, 14 mmol) in acetic acid (40 mL) at room temperature. The reaction mixture was heated to 60 °C and held for 30 min, followed by cooling to room temperature. The mixture was poured into ice water and the precipitated solid was collected by filtration. After sufficient washing with water, 3-amino-6-bromopyrazine-2-carbonitrile was obtained as a yellow solid (2.3 g, 83% yield). The product was characterized by 1H NMR (500 MHz, DMSO-d6): δ 8.44 (s, 1H), 7.60 (br s, 2H). Mass spectrum (ES+): m/z 199 (M+H)+.

References

[1] Journal of Organic Chemistry, 1987, vol. 52, # 18, p. 3997 - 4000
[2] Patent: US2007/259876, 2007, A1. Location in patent: Page/Page column 18

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