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ChemicalBook--->CAS DataBase List--->393-53-3

393-53-3

393-53-3 Structure

393-53-3 Structure
IdentificationMore
[Name]

3-Fluoropyridine-4-carboxylic acid
[CAS]

393-53-3
[Synonyms]

3-FLUORO-4-PYRIDINECARBOXYLIC ACID
3-FLUOROISONICOTINIC ACID
3-FLUOROPYRIDINE-4-CARBOXYLIC ACID
3-Fluoropyridine-4-carboxylic acid mono hydrate
3-Fluoroisonicotinic
3-FLUORONICOTINIC ACID
3-FLUOROISONICOTINIC ACID MONO HYDRATE
[EINECS(EC#)]

639-266-3
[Molecular Formula]

C6H4FNO2
[MDL Number]

MFCD03789251
[Molecular Weight]

141.1
[MOL File]

393-53-3.mol
Chemical PropertiesBack Directory
[Melting point ]

251-254°C (dec.)
[Boiling point ]

360.0±22.0 °C(Predicted)
[density ]

1.419±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Sealed in dry,Room Temperature
[form ]

solid
[pka]

2.85±0.10(Predicted)
[color ]

White to off-white
[BRN ]

383678
[InChIKey]

POLXLLIQWDBJMD-UHFFFAOYSA-N
[CAS DataBase Reference]

393-53-3(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi,F
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
R10:Flammable.
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
S16:Keep away from sources of ignition-No smoking .
[WGK Germany ]

3
[Hazard Note ]

Irritant
[HazardClass ]

IRRITANT
[HS Code ]

2933399990
Spectrum DetailBack Directory
[Spectrum Detail]

3-Fluoropyridine-4-carboxylic acid(393-53-3)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

3-Fluoropyridine-4-carboxylic acid, 97%(393-53-3)
[Sigma Aldrich]

393-53-3(sigmaaldrich)
Hazard InformationBack Directory
[Synthesis]

Carbon dioxide

124-38-9

3-Fluoropyridine-4-carboxylic acid

393-53-3

3-Fluoropyridine (25 g, 257 mmol) was slowly added dropwise to a solution of tetrahydrofuran (600 mL) containing butyl lithium (270 mmol) and diisopropylamine (27.4 g, 271 mmol) at -78 °C. The reaction mixture was stirred continuously at this temperature for 1 hour. Subsequently, crushed dry ice was added to the reaction system and gradually warmed to room temperature over 1 hour. Upon completion of the reaction, the pH of the reaction solution was adjusted to 5 with an aqueous solution of hydrogen chloride and acidified. The resulting precipitate was collected by filtration and dried. The final 3-fluoroisonicotinic acid (25.2 g, 179 mmol, 70% yield) was obtained as colorless crystals.

[References]

[1] Patent: WO2006/36015, 2006, A2. Location in patent: Page/Page column 121-122
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