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Atomfair Pentafluorobenzonitrile C7F5N
Description Pentafluorobenzonitrile (CAS 773-82-0) is a high-purity fluorinated aromatic nitrile compound with the molecular formula C7F5N . This specialty chemical, also known as 2,3,4,5,6-pentafluorobenzonitrile, features a benzene ring fully substituted with fluorine atoms and a cyano functional group, making it a valuable building block in organic synthesis and material science. Its unique electronic properties and chemical stability under harsh conditions make it ideal for advanced applications in pharmaceuticals, agrochemicals, and liquid crystal materials. Available in >98% purity, this compound is rigorously tested via GC-MS, NMR, and HPLC to ensure consistency for research and industrial use. Proper handling under inert conditions…
Description
Description
Pentafluorobenzonitrile (CAS 773-82-0) is a high-purity fluorinated aromatic nitrile compound with the molecular formula C7F5N. This specialty chemical, also known as 2,3,4,5,6-pentafluorobenzonitrile, features a benzene ring fully substituted with fluorine atoms and a cyano functional group, making it a valuable building block in organic synthesis and material science. Its unique electronic properties and chemical stability under harsh conditions make it ideal for advanced applications in pharmaceuticals, agrochemicals, and liquid crystal materials. Available in >98% purity, this compound is rigorously tested via GC-MS, NMR, and HPLC to ensure consistency for research and industrial use. Proper handling under inert conditions is recommended due to its moisture sensitivity.
- CAS No: 773-82-0
- Molecular Formula: C7F5N
- Molecular Weight: 193.07
- Exact Mass: 192.99508981
- Monoisotopic Mass: 192.99508981
- IUPAC Name: 2,3,4,5,6-pentafluorobenzonitrile
- SMILES: C(#N)C1=C(C(=C(C(=C1F)F)F)F)F
- Synonyms: Pentafluorobenzonitrile, 773-82-0, 2,3,4,5,6-Pentafluorobenzonitrile, Benzonitrile, pentafluoro-, Perfluorobenzonitrile
Application
Pentafluorobenzonitrile is widely used as a precursor in the synthesis of fluorinated pharmaceuticals and agrochemicals due to its electron-withdrawing properties. It serves as a key intermediate in the development of liquid crystal materials for display technologies. Researchers also utilize it in cross-coupling reactions to create complex fluorinated aromatic systems for advanced material applications.
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