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ChemicalBook >  Product Catalog >  Pharmaceutical intermediates >  Heterocyclic compound >  Pyridine compound >  Fluoropyridine >  2,3,5,6-TETRAFLUORO-4-PYRIDINE-CARBONITRILE

2,3,5,6-TETRAFLUORO-4-PYRIDINE-CARBONITRILE

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2,3,5,6-TETRAFLUORO-4-PYRIDINE-CARBONITRILE Basic information

Product Name:
2,3,5,6-TETRAFLUORO-4-PYRIDINE-CARBONITRILE
Synonyms:
  • 4-CYANO-2,3,4,5,6-TETRAFLUOROFLUOROPYRIDINE
  • 2,3,5,6-Tetrafluoropyridine-4-carbonitrile
  • 2,3,5,6-TETRAFLUORO-4-PYRIDINE- CARBONITRILE 99%
  • 2,3,5,6-Tetrafluoropyridine-4-carbonitrile, 4-Cyano-2,3,5,6-tetrafluoropyridine
  • 2,3,5,6-TETRAFLUORO-4-PYRIDINE-CARBONITRILE
  • 4-CYANO-2,3,5,6-TETRAFLUOROPYRIDINE
  • 2,3,5,6-Tetrafluoropyridine-4-carbonitrile, 4-Cyano-2,3,5,6-tetraf
  • 4-Pyridinecarbonitrile, 2,3,5,6-tetrafluoro-
CAS:
16297-07-7
MF:
C6F4N2
MW:
176.07
Product Categories:
  • C6
  • Heterocyclic Building Blocks
  • Heterocyclic Compounds
  • Pyridines
Mol File:
16297-07-7.mol
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2,3,5,6-TETRAFLUORO-4-PYRIDINE-CARBONITRILE Chemical Properties

Melting point:
66-68 °C (lit.)
Boiling point:
166.1±35.0 °C(Predicted)
Density 
1.56±0.1 g/cm3(Predicted)
pka
-14.32±0.28(Predicted)
form 
crystalline powder
color 
White
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Safety Information

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

MSDS

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2,3,5,6-TETRAFLUORO-4-PYRIDINE-CARBONITRILE Usage And Synthesis

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.

2,3,5,6-TETRAFLUORO-4-PYRIDINE-CARBONITRILESupplier

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