ChemicalBook--->CAS DataBase List--->1480-64-4

1480-64-4

1480-64-4 Structure

1480-64-4 Structure
IdentificationMore
[Name]

3-Chloro-2-fluoro-pyridine
[CAS]

1480-64-4
[Synonyms]

3-CHLORO-2-FLUOROPYRIDINE
2-Fluoro-3-chloro pyridine
[Molecular Formula]

C5H3ClFN
[MDL Number]

MFCD04114144
[Molecular Weight]

131.54
[MOL File]

1480-64-4.mol
Chemical PropertiesBack Directory
[Boiling point ]

162℃
[density ]

1.33
[Fp ]

52°(126°F)
[refractive index ]

1.5030
[storage temp. ]

Inert atmosphere,2-8°C
[form ]

clear liquid
[pka]

-2.71±0.10(Predicted)
[color ]

Colorless to Almost colorless
[InChI]

InChI=1S/C5H3ClFN/c6-4-2-1-3-8-5(4)7/h1-3H
[InChIKey]

IHGMHTQDGNVKTA-UHFFFAOYSA-N
[SMILES]

C1(F)=NC=CC=C1Cl
[CAS DataBase Reference]

1480-64-4(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Flame (GHS02)Exclamation Mark (GHS07)Corrosion (GHS05)
GHS02,GHS07,GHS05
[Signal word ]

Warning
[Hazard statements ]

H226-H302+H312+H332-H315-H319-H302-H312-H314-H318-H332
[Precautionary statements ]

P303+P361+P353-P305+P351+P338-P310-P210-P233-P240-P241+P242+P243-P261-P264-P270-P271-P280-P301+P312+P330-P302+P352+P312+P362+P364-P304+P340+P312-P305+P351+P338+P337+P313-P403+P235-P501
[Hazard Codes ]

T
[Risk Statements ]

22-37/38-41-34-20/21/22-10
[Safety Statements ]

26-39-45-36/37/39
[RIDADR ]

2924
[HazardClass ]

3
[PackingGroup ]

III
[HS Code ]

29333990
Hazard InformationBack Directory
[Uses]

3-Chloro-2-fluoropyridine is used as a reactant in the synthesis of several compounds with therapeutic potential.
[Synthesis]

2,3-Dichloropyridine

2402-77-9

3-Chloro-2-fluoro-pyridine

1480-64-4

GENERAL METHOD: To a solution of 2,3-dichloropyridine (1.00 g, 6.76 mmol) in dimethyl sulfoxide (DMSO, 33.8 mL) was added cesium fluoride (CsF, 2.053 g, 13.51 mmol) at room temperature. The reaction mixture was stirred in air at 110 °C for 20 hours. After completion of the reaction, the reaction mixture was quenched with ice water and extracted with ethyl acetate (EtOAc). The organic layer was separated, washed sequentially with water and saturated brine, dried over anhydrous sodium sulfate (Na2SO4) and concentrated under reduced pressure. The residue was purified by silica gel column chromatography using ethyl acetate (EtOAc) in hexane as eluent to afford 3-chloro-2-fluoropyridine (0.639 g, 4.86 mmol, 71.9% yield) as a colorless oil. Compounds 3B'-8B' were prepared by a method similar to the synthetic procedure for compound 2B'.

[References]

[1] Tetrahedron Letters, 2015, vol. 56, # 44, p. 6043 - 6046
[2] Angewandte Chemie - International Edition, 2006, vol. 45, # 17, p. 2720 - 2725
[3] Patent: EP1595867, 2005, A1. Location in patent: Page/Page column 33-34
[4] Organic Letters, 2015, vol. 17, # 8, p. 1866 - 1869
[5] Patent: EP1726590, 2006, A1. Location in patent: Page/Page column 56
Spectrum DetailBack Directory
[Spectrum Detail]

3-Chloro-2-fluoro-pyridine(1480-64-4)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

3-Chloro-2-fluoropyridine, 95%(1480-64-4)
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