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5-bromo-3-methylpicolinonitrile

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5-bromo-3-methylpicolinonitrile Basic information

Product Name:
5-bromo-3-methylpicolinonitrile
Synonyms:
  • 5-bromo-3-methylpicolinonitrile
  • 5-Bromo-2-cyano-3-methylpyridine, 5-Bromo-3-methylpicolinonitrile
  • 5-BroMo-2-cyano-3-Methylpyridine
  • 2-Pyridinecarbonitrile,5-bromo-3-methyl-
  • 5-bromo-3-methyl-2-pyridinecarbonitrile
  • 5-Bromo-3-methylpicolinonitrile/5-bromo-3-methylpyridine-2-carbonitrile
  • 5- Bromo-2-Cyano-3-methyl picolinonitrile
  • 5-Bromo-3-methyl-2-pyridinitrile
CAS:
156072-86-5
MF:
C7H5BrN2
MW:
197.03
Mol File:
156072-86-5.mol
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5-bromo-3-methylpicolinonitrile Chemical Properties

Boiling point:
283.6±35.0 °C(Predicted)
Density 
1.61±0.1 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
pka
-2.38±0.20(Predicted)
Appearance
White to yellow Solid
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Safety Information

RIDADR 
2811
HazardClass 
6.1
PackingGroup 
HS Code 
2933399990
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5-bromo-3-methylpicolinonitrile Usage And Synthesis

Synthesis

3430-18-0

544-92-3

156072-86-5

Example 9.1: Synthesis of 5-bromo-3-methylpyridine-2-carbonitrile. To a solution of 2,5-dibromo-3-methylpyridine (2.5 g, 9.96 mmol) in dimethylformamide (10 mL) was added cuprous cyanide (892 mg, 9.96 mmol), and the reaction mixture was stirred for 12 hours at 120 °C. Upon completion of the reaction, the reaction mixture was partitioned between ethyl acetate and water. The organic layer was separated, washed with saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate, filtered and concentrated. Purification by column chromatography gave a white solid product (970 mg, 57.6% yield). Product characterization data: 1H NMR (300 MHz, CDCl3): δ 8.55 (s, 1H), 7.64 (t, 1H), 2.54 (s, 3H).

References

[1] Patent: WO2008/100715, 2008, A1. Location in patent: Page/Page column 33
[2] Patent: US2006/199817, 2006, A1. Location in patent: Page/Page column 27

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