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5-Amino-2-fluoropyridine

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5-Amino-2-fluoropyridine Basic information

Product Name:
5-Amino-2-fluoropyridine
Synonyms:
  • 2-FLUORO-5-AMINO PYRIDINE
  • 6-FLUORO-3-PYRIDINAMINE
  • 6-FLUOROPYRIDIN-3-AMINE
  • 6-FLUORO-PYRIDIN-3-YLAMINE
  • 5-AMINO-2-FLUOROPYRIDINE
  • 2-FLUOROPYRIDIN-5-AMINE
  • 5-Amino-2-fluoropyridine 98%
  • 5-Amino-2-fluoropyridine98%
CAS:
1827-27-6
MF:
C5H5FN2
MW:
112.11
EINECS:
675-011-2
Product Categories:
  • Pyridine
  • pharmacetical
  • Pyridine series
  • Pyridines
  • Boronic Acid
  • Fluorin-contained pyridine series
  • Fluorine series
  • Building Blocks
  • C5
  • C5 to C6
  • Chemical Synthesis
  • Fluorinated Building Blocks
  • Halogenated Heterocycles
  • Heterocyclic Building Blocks
  • Heterocyclic Fluorinated Building Blocks
  • Other Fluorinated Heterocycles
Mol File:
1827-27-6.mol
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5-Amino-2-fluoropyridine Chemical Properties

Melting point:
86-87°C
Boiling point:
264.0±20.0 °C(Predicted)
Density 
1.257±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
pka
2?+-.0.10(Predicted)
form 
powder to crystal
color 
Purple to Dark purple to Dark red
CAS DataBase Reference
1827-27-6(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38-41-37/38
Safety Statements 
26-36/37/39
WGK Germany 
3
Hazard Note 
Irritant
HazardClass 
6.1
HS Code 
29333990
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5-Amino-2-fluoropyridine Usage And Synthesis

Chemical Properties

Light yellow Cryst

Uses

5-Amino-2-fluoropyridine is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

Synthesis

456-24-6

1827-27-6

General procedure for the synthesis of 2-fluoro-5-aminopyridine from 2-fluoro-5-nitropyridine: 50 mL of toluene and 50 mmol of 2-fluoro-5-nitropyridine were added to a 100 mL round-bottomed flask, followed by 0.282 g of 5% Pd/C catalyst and 10 mmol of anhydrous sodium sulfate. The reaction system was placed under hydrogen atmosphere, heated and stirred for 15 hours. Upon completion of the reaction, the mixture was cooled to room temperature, the catalyst was removed by filtration and the filtrate was concentrated by rotary evaporation. The resulting crude product was purified by recrystallization and finally dried under vacuum to give 1.6806 g of 2-fluoro-5-aminopyridine solid in 75% yield.

References

[1] Journal of the Chemical Society - Perkin Transactions 1, 1996, # 18, p. 2221 - 2226
[2] Patent: CN103755744, 2016, B. Location in patent: Paragraph 0065; 0066
[3] Bioorganic and Medicinal Chemistry Letters, 2004, vol. 14, # 6, p. 1411 - 1416
[4] Patent: US6355636, 2002, B1. Location in patent: Page column 64
[5] Patent: EP1171440, 2004, B1. Location in patent: Page 53

5-Amino-2-fluoropyridine Preparation Products And Raw materials

Preparation Products

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