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3-Fluoropyridine-2-carboxylic acid

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3-Fluoropyridine-2-carboxylic acid Basic information

Product Name:
3-Fluoropyridine-2-carboxylic acid
Synonyms:
  • 3-FLUOROPYRIDINE-2-CARBOXYLIC ACID
  • 3-FLUOROPICOLINIC ACID
  • 3-Fluoropyridine-2-carboxylicacid98%
  • 2-Pyridinecarboxylicacid,3-fluoro-(9CI)
  • 3-fluropyridine-2-carboxylic acid
  • 3-FLUOROPICOLINIC ACID / 3-FLUOROPYRIDINE-2-CARBOXYLIC ACID
  • 3-FLUOROPYRIDINE-2-CARBOXYLIC ACID HYDROCHLORIDE
  • 3-Fluoro-2-pyridinecarboxylic acid
CAS:
152126-31-3
MF:
C6H4FNO2
MW:
141.1
Product Categories:
  • Pyridines
  • Building Blocks
  • Carboxy
  • CARBOXYLICACID
  • PYRIDINE
Mol File:
152126-31-3.mol
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3-Fluoropyridine-2-carboxylic acid Chemical Properties

Melting point:
154°C
Boiling point:
265.2±20.0 °C(Predicted)
Density 
1.419±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,2-8°C
pka
2.71±0.10(Predicted)
form 
powder
color 
White
InChI
InChI=1S/C6H4FNO2/c7-4-2-1-3-8-5(4)6(9)10/h1-3H,(H,9,10)
InChIKey
IRERRSXDWUCFIY-UHFFFAOYSA-N
SMILES
C1(C(O)=O)=NC=CC=C1F
CAS DataBase Reference
152126-31-3(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi,Xn
HazardClass 
IRRITANT
HS Code 
2933399990
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3-Fluoropyridine-2-carboxylic acid Usage And Synthesis

Uses

3-Fluoropyridine-2-carboxylic acid is mainly used as an intermediate in organic synthesis and medicinal chemistry. It is a synthetic intermediate of tridentate nitrogen ligands in pesticide molecules and transition metal catalytic reactions.

Synthesis

372-47-4

124-38-9

152126-31-3

To a diethyl ether (50 ml) solution of 1,4-diazabicyclo[2.2.2]octane (1.15 g, 10.3 mmol) was slowly added n-butyllithium (2.6 M hexane solution, 3.95 ml, 10.3 mmol) dropwise at -78 °C. The reaction mixture was stirred at -20°C for 1 hr, then a diethyl ether (30 ml) solution of 3-fluoropyridine (1.00 g, 10.29 mmol) was added dropwise at -78°C. The resulting yellow suspension was stirred at -60°C for 1 hr and subsequently cooled to -78°C and an excess of dry ice was added. The reaction solution was slowly warmed to -10°C over a period of 20 min. The precipitate was collected by filtration and the residue was washed with ether to give pure 3-fluoropyridine-2-carboxylic acid (1.20 g, 8.51 mmol, 83% yield).

References

[1] Tetrahedron, 1998, vol. 54, # 42, p. 12859 - 12886
[2] Patent: WO2014/82737, 2014, A1. Location in patent: Page/Page column 38

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