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3-Bromo-2-fluoropyridine

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3-Bromo-2-fluoropyridine Basic information

Product Name:
3-Bromo-2-fluoropyridine
Synonyms:
  • 2-fluoro-3-bromopyridine
  • broMo-3 fluoro-2 pyridine
  • 2--3-pyridyl broMidefluoride
  • 2-fluoro -3-pyridyl broMide
  • 3-BROMO-2-FLUOROPYRIDINE
  • 3-Bromo-3-Fluoropyridine
  • 3-Bromo-2-fluoropyridine >
  • 3-Bromo-2-fL
CAS:
36178-05-9
MF:
C5H3BrFN
MW:
175.99
EINECS:
672-944-7
Product Categories:
  • blocks
  • Bromides
  • FluoroCompounds
  • Pyridines
  • Pyridine
  • Pyridine series
  • Fluorine series
  • Halides
  • Variety of halogenated heterocyclic series
  • Fluorin-contained pyridine series
Mol File:
36178-05-9.mol
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3-Bromo-2-fluoropyridine Chemical Properties

Boiling point:
76°C
Density 
1.729
refractive index 
1.5370-1.5410
Flash point:
54℃
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
form 
clear liquid
pka
-2.79±0.10(Predicted)
color 
Colorless to Light yellow
CAS DataBase Reference
36178-05-9(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
22-37/38-41
Safety Statements 
26-39
RIDADR 
2810
HazardClass 
6.1
HazardClass 
IRRITANT
PackingGroup 
HS Code 
29333990
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3-Bromo-2-fluoropyridine Usage And Synthesis

Chemical Properties

Light yellow liquid

Synthesis

52200-48-3

36178-05-9

GENERAL METHOD: 2,3-Dichloropyridine (1.00 g, 6.76 mmol) was dissolved in DMSO (33.8 mL) at room temperature, followed by the addition of CsF (2.053 g, 13.51 mmol). The reaction mixture was stirred at 110 °C for 20 h in air. Upon completion of the reaction, the reaction mixture was quenched with ice water and extracted with EtOAc. The organic layer was separated, washed sequentially with water and brine, dried over anhydrous Na2SO4 and subsequently concentrated under reduced pressure. Purification of the residue by column chromatography (silica gel as stationary phase and EtOAc in hexane as eluent) afforded 3-chloro-2-fluoropyridine (0.639 g, 4.86 mmol, 71.9% yield) as a colorless oil. Compounds 3B'-8B' were prepared by a method similar to the synthetic procedure described above for 2B'.

References

[1] Tetrahedron Letters, 2015, vol. 56, # 44, p. 6043 - 6046

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