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152126-31-3

152126-31-3 Structure

152126-31-3 Structure
IdentificationMore
[Name]

3-FLUOROPYRIDINE-2-CARBOXYLIC ACID
[CAS]

152126-31-3
[Synonyms]

3-FLUOROPICOLINIC ACID
3-FLUOROPYRIDINE-2-CARBOXYLIC 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
[Molecular Formula]

C6H4FNO2
[MDL Number]

MFCD04114108
[Molecular Weight]

141.1
[MOL File]

152126-31-3.mol
Chemical PropertiesBack Directory
[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
[form ]

powder
[pka]

2.71±0.10(Predicted)
[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)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P280a-P304+P340-P305+P351+P338-P405-P501a
[Hazard Codes ]

Xi,Xn
[Hazard Note ]

Irritant
[HazardClass ]

IRRITANT
[HS Code ]

2933399990
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Hydrochloric acid-->Acetic acid-->n-Butyllithium-->Nitrogen-->Copper (II) acetate monohydrate-->Triethylenediamine-->3-Fluoropyridine-->Ferrous sulfide-->Carbon dioxide-->Diethyl ether
[Preparation Products]

3-Fluoro-pyridine-2-carboxylic acid methyl ester
Hazard InformationBack Directory
[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]

3-Fluoropyridine

372-47-4

Carbon dioxide

124-38-9

3-Fluoropyridine-2-carboxylic acid

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
Spectrum DetailBack Directory
[Spectrum Detail]

3-FLUOROPYRIDINE-2-CARBOXYLIC ACID(152126-31-3)1HNMR
3-FLUOROPYRIDINE-2-CARBOXYLIC ACID(152126-31-3)FT-IR
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