| Weight | 151.062 g/mol |
|---|---|
| Formula | C5HF4N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
2,3,5,6-Tetrafluoropyridine (2875-18-5)
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- Synthesis of Tetrahydropyrido[2,3-b]pyrazine Scaffolds from 2,3,5,6-Tetrafluoropyridine Derivatives. (Tetrahedron, 2007)
- Survey of reactivity of some enolates with pentafluoropyridine and 4-phenylsulfonyl-2,3,5,6-tetrafluoropyridine (Journal of Fluorine Chemistry, 2013)
- Synthetic utility of 4-bromo-2,3,5,6-tetrafluoropyridine (Journal of Fluorine Chemistry, 2008)
- N-halogeno-compounds. Part 9 [1]. Azoxy- and azo-arenes derived from 4-(dichloroamino)tetrafluoropyridine; crystal structure of trans-2,3,5,6-tetrafluoro-4-(2,4,6-trimethylphenyl-onn-azoxy)pyridine (Journal of Fluorine Chemistry, 1985)
- Azo-coupling of 2,3,5,6-tetrafluoropyridine-4-diazonium fluoride with mesitylene and anisole (Journal of Fluorine Chemistry, 1983)
- Ribonucleic acid-protein crosslinking in Escherichia coli ribosomal 30S subunits by the use of two new heterobifunctional reagents: 4-azido-2,3,5,6-tetrafluoropyridine and 4-azido-3,5-dichloro-2,6-difluoropyridine. (Biochemical and Biophysical Research Communications, 1981)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=C(C(=NC(=C1F)F)F)F
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InChIKeyHWIPMBCMGVXOKN-UHFFFAOYSA-N
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