427659
3-Chloro-2,4,5,6-tetrafluoropyridine
98%
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About This Item
Empirical Formula (Hill Notation):
C5ClF4N
CAS Number:
Molecular Weight:
185.51
UNSPSC Code:
12352100
PubChem Substance ID:
MDL number:
Assay:
98%
Form:
liquid
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InChI
1S/C5ClF4N/c6-1-2(7)3(8)5(10)11-4(1)9
SMILES string
Fc1nc(F)c(Cl)c(F)c1F
InChI key
UXUZMYHSICIOQT-UHFFFAOYSA-N
assay
98%
form
liquid
refractive index
n20/D 1.436 (lit.)
bp
118-121 °C (lit.)
density
1.609 g/mL at 25 °C (lit.)
General description
3-Chloro-2,4,5,6-tetrafluoropyridine (3-chlorotetrafluoropyridine) is a fluoropyridine derivative. Its quantum mechanical calculations of energies, geometries and vibrational wave numbers have been performed by DFT level of theory. The interpretation of its FT-IR and FT-Raman spectra have been reported.[1] It forms corresponding organo-zinc compound by reacting with zinc.[2] 3-Chlorotetrafluoropyridine reacts with tris(diethylamino)phosphine (P(NEt)3) in the presence of a proton donor to form product with fluorine replaced by hydrogen at position 4.[3]
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Reactions of polyfluoroaromatic compounds with electrophilic agents in the presence of tris(dialkylamino)phosphines.
Bardin VV.
Russian Chemical Bulletin, 46(8), 1434-1436 (1997)
3-Fluoropyridyl nickel complexes as useful tools for the selective synthesis of new 2,4,5,6-tetrafluoropyridines: a route complementing the established methods to access fluorinated pyridines.
Sladek MI, et al.
New. J. Chem., 27(2), 313-318 (2003)
Reactions of polyfluoroarenes with zinc: hydrogenolysis and synthesis of polyfluoroaromatic organozinc compounds.
Krasnov VI and Platonov VE.
Journal of Fluorine Chemistry, 58(2), 247-247 (1992)
Photochemical reaction of ethylene with 3-chlorotetrafluoropyridine: a novel insertion into a C-Cl bond.
Barlow MG, et al.
Journal of the Chemical Society. Chemical Communications, 14, 608-609 (1979)
Heterocyclic polyfluoro-compounds. Part XII. Synthesis and some reactions of 2,3,5,6-tetrafluoro-4-iodopyridine.
Banks RE, et al.
J. Chem. Soc. Sect. C, 2091-2095 (1967)
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