ChemicalBook--->CAS DataBase List--->16297-07-7

16297-07-7

16297-07-7 Structure

16297-07-7 Structure
IdentificationBack Directory
[Name]

2,3,5,6-TETRAFLUORO-4-PYRIDINE-CARBONITRILE
[CAS]

16297-07-7
[Synonyms]

4-CYANO-2,3,5,6-TETRAFLUOROPYRIDINE
2,3,5,6-Tetrafluoropyridine-4-carbonitrile
4-CYANO-2,3,4,5,6-TETRAFLUOROFLUOROPYRIDINE
2,3,5,6-TETRAFLUORO-4-PYRIDINE-CARBONITRILE
4-Pyridinecarbonitrile, 2,3,5,6-tetrafluoro-
2,3,5,6-TETRAFLUORO-4-PYRIDINE- CARBONITRILE 99%
2,3,5,6-TETRAFLUORO-4-PYRIDINE-CARBONITRILE ISO 9001:2015 REACH
2,3,5,6-Tetrafluoropyridine-4-carbonitrile, 4-Cyano-2,3,5,6-tetraf
2,3,5,6-Tetrafluoropyridine-4-carbonitrile, 4-Cyano-2,3,5,6-tetrafluoropyridine
[Molecular Formula]

C6F4N2
[MDL Number]

MFCD00075302
[MOL File]

16297-07-7.mol
[Molecular Weight]

176.07
Chemical PropertiesBack Directory
[Melting point ]

66-68 °C (lit.)
[Boiling point ]

166.1±35.0 °C(Predicted)
[density ]

1.56±0.1 g/cm3(Predicted)
[storage temp. ]

Storage temp. 2-8°C
[form ]

crystalline powder
[pka]

-14.32±0.28(Predicted)
[color ]

White
[InChI]

1S/C6F4N2/c7-3-2(1-11)4(8)6(10)12-5(3)9
[InChIKey]

JXISJBVJNUKKBK-UHFFFAOYSA-N
[SMILES]

Fc1nc(F)c(F)c(C#N)c1F
Safety DataBack Directory
[Hazard Codes ]

Xn,Xi
[Risk Statements ]

20/21/22-36/37/38
[Safety Statements ]

26-37/39
[WGK Germany ]

3
[Hazard Note ]

Irritant
[HS Code ]

2933399990
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Dermal
Acute Tox. 4 Inhalation
Acute Tox. 4 Oral
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Hazard InformationBack Directory
[Uses]

2,3,5,6-Tetrafluoro-4-pyridinecarbonitrile may be used in the preparation of 2-anilino-3,5,6-trifluoroisonicotinonitrile.
[General Description]

2,3,5,6-Tetrafluoro-4-pyridinecarbonitrile is a perfluorinated heteroaromatic compound. 2,3,5,6-Tetrafluoro-4-pyridinecarbonitrile (tetrafluoro-4-cyanopyridine) reacts with 1,3-dicarbonyl systems to yield the corresponding [5,6]-ring fused furo derivatives. 2,3,5,6-Tetrafluoro-4-pyridinecarbonitrile (4-cyanotetrafluoropyridine) reacts with amidines to yield [6,6]-fused pyrimidinopyridine system via nucleophilic substitution at the C-3 position of the pyridine ring followed by intramolecular cyclization onto the pendant cyano group. Reaction of 2,3,5,6-tetrafluoro-4-pyridinecarbonitrile (4-cyanotetrafluoropyridine) with sulfur centred nucleophiles has been reported.
Spectrum DetailBack Directory
[Spectrum Detail]

2,3,5,6-TETRAFLUORO-4-PYRIDINE-CARBONITRILE(16297-07-7)1HNMR
2,3,5,6-TETRAFLUORO-4-PYRIDINE-CARBONITRILE(16297-07-7)FT-IR
2,3,5,6-TETRAFLUORO-4-PYRIDINE-CARBONITRILE(16297-07-7)IR
2,3,5,6-TETRAFLUORO-4-PYRIDINE-CARBONITRILE(16297-07-7)Raman
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