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2-Fluoro-3-nitropyridine

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2-Fluoro-3-nitropyridine Basic information

Product Name:
2-Fluoro-3-nitropyridine
Synonyms:
  • 2-FLUORO-3-NITROPYRIDINE
  • 3-bromo-2-fluoro-5-trifluoromethyl ryridine
  • 2-Fluoro-3-nitropyri
  • 2-Fluoro-3-nitrylpyridine
  • 2-Fluoro-3-nitropyridine, 97+%
  • 2-Fluoro-3-nitropyridine>
  • uoro-3-nitropyridine
  • Pyridine, 2-fluoro-3-nitro-
CAS:
1480-87-1
MF:
C5H3FN2O2
MW:
142.09
EINECS:
675-588-0
Product Categories:
  • Pyridines
  • Pyridine
  • Fluorine series
  • Boronic Acid
Mol File:
1480-87-1.mol
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2-Fluoro-3-nitropyridine Chemical Properties

Melting point:
18℃
Boiling point:
110℃/10mm
Density 
1.439±0.06 g/cm3(Predicted)
refractive index 
1.5300 to 1.5340
storage temp. 
Inert atmosphere,Room Temperature
form 
Low Melting Solid
pka
-4.47±0.10(Predicted)
color 
Yellow
Water Solubility 
Slightly soluble in water.
CAS DataBase Reference
1480-87-1(CAS DataBase Reference)
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Safety Information

Hazard Codes 
T,Xi,C
Risk Statements 
20/21/22-36/37/38-34
Safety Statements 
26-36/37/39-45
Hazard Note 
Toxic
HazardClass 
IRRITANT
HS Code 
2933399990
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2-Fluoro-3-nitropyridine Usage And Synthesis

Uses

2-Fluoro-3-nitropyridine is used as a pharmaceutical intermediate.

Synthesis

5470-18-8

1480-87-1

General procedure for the synthesis of 2-fluoro-3-nitropyridine from 2-chloro-3-nitropyridine: 2-chloro-3-nitropyridine (1.00 g, 6.76 mmol) was dissolved in DMSO (33.8 ml) at room temperature, followed by addition of CsF (2.053 g, 13.51 mmol). The reaction mixture was stirred in air at 110°C for 20 hrs. After 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 concentrated under reduced pressure. Purification of the residue by column chromatography (silica gel as stationary phase and EtOAc/hexane as eluent) afforded 2-fluoro-3-nitropyridine (0.639 g, 4.86 mmol, 71.9% yield) as a colorless oil. Similarly, compounds 3B'-8B' can be prepared according to the synthesis of 2B' above.

References

[1] European Journal of Inorganic Chemistry, 2017, vol. 2017, # 2, p. 330 - 339
[2] Tetrahedron Letters, 2015, vol. 56, # 44, p. 6043 - 6046
[3] Heterocycles, 1986, vol. 24, # 11, p. 3213 - 3221
[4] Journal of Labelled Compounds and Radiopharmaceuticals, 2004, vol. 47, # 6, p. 373 - 383
[5] Tetrahedron, 2001, vol. 57, # 4, p. 739 - 750

2-Fluoro-3-nitropyridine Preparation Products And Raw materials

Raw materials

2-Fluoro-3-nitropyridineSupplier

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