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5-Bromonicotinonitrile

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5-Bromonicotinonitrile Basic information

Product Name:
5-Bromonicotinonitrile
Synonyms:
  • AKOS BBS-00003122
  • 3-Bromo-5-cyanopyridine 97%
  • 5-Bromo-3-cyanopyridine,97%
  • 5-Bromonicotinonitrile,98%
  • 3-Cyano-5-broMopyridine
  • 5-BroMo-3-pyridinecarbonitrile
  • 3-Bromo-5-cyanopyridine, 5-Bromopyridine-3-carbonitrile
  • 5-Bromonicotinonitrile 97%
CAS:
35590-37-5
MF:
C6H3BrN2
MW:
183.01
Product Categories:
  • Boronic Acid
  • C6Heterocyclic Building Blocks
  • Halogenated Heterocycles
  • Heterocyclic Building Blocks
  • Pyridine
  • Organohalides
  • Nucleotides and Nucleosides
  • Bases & Related Reagents
  • Nucleotides
  • blocks
  • Bromides
  • Carboxes
  • Pyridines
Mol File:
35590-37-5.mol
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5-Bromonicotinonitrile Chemical Properties

Melting point:
103-107 °C(lit.)
Boiling point:
228.8±20.0 °C(Predicted)
Density 
1.72±0.1 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
solubility 
Chloroform (Heated), Ethyl Acetate (Slightly), Methanol (Slightly)
form 
Solid
pka
-0.57±0.20(Predicted)
color 
Pale Yellow to Yellow
InChI
InChI=1S/C6H3BrN2/c7-6-1-5(2-8)3-9-4-6/h1,3-4H
InChIKey
FTFFHWWIPOQCBC-UHFFFAOYSA-N
SMILES
C1=NC=C(Br)C=C1C#N
CAS DataBase Reference
35590-37-5(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
36/37/38-20/21/22
Safety Statements 
26-36-36/37/39
RIDADR 
3276
WGK Germany 
3
Hazard Note 
Irritant
HazardClass 
6.1
PackingGroup 
III
HS Code 
29333990

MSDS

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5-Bromonicotinonitrile Usage And Synthesis

Chemical Properties

White crystalline powder

Synthesis

625-92-3

35590-37-5

General procedure for the synthesis of 3-cyano-5-bromopyridine from 3,5-dibromopyridine: iPrMgCl (2M in THF, 4.1 mL) and THF (5 mL) were added to a flask containing dry LiCl (0.35 g, 8.24 mmol) at 15 °C. After stirring for 15 min, a solution of 3-bromo-1-benzylnitrile (1.46 g, 8.03 mmol) in THF (1 mL) was slowly added to the reaction mixture and stirring was continued for 15 min. Subsequently, DMF (1.3 mL, 12 mmol) was added dropwise at 0 °C and the mixture was stirred for 2 hours. Upon completion of the reaction, aqueous NH3 (7 mL, 28-30%) and I2 (4.06 g, 16 mmol) were added to the mixture. After stirring for 2 h at room temperature, the reaction mixture was poured into saturated aqueous Na2SO3 solution and extracted with CHCl3 (3 x 30 mL). The organic layers were combined, dried with Na2SO4 and filtered. After removing the solvent under reduced pressure, the residue was purified by silica gel short column chromatography (eluent: hexane/ethyl acetate = 9:1, v/v) to afford pure 3-cyano-5-bromopyridine (0.73 g) in 71% yield. Most of the nitrile compounds involved in this study were commercially available and were identified by comparison with real samples.

References

[1] Tetrahedron, 2013, vol. 69, # 5, p. 1462 - 1469

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