1,2,3,4,5-Pentafluoro-6-(prop-2-en-1-yloxy)benzene is a fluorinated aromatic compound characterized by the presence of five fluorine atoms attached to a benzene ring, which significantly influences its chemical properties. The fluorine substituents enhance the compound's electronegativity and stability, making it less reactive compared to non-fluorinated analogs. The presence of the prop-2-en-1-yloxy group introduces a reactive alkene functionality, allowing for potential polymerization or further chemical modifications. This compound is likely to exhibit low volatility and high thermal stability due to the strong C-F bonds. Its unique structure may impart specific properties such as hydrophobicity and resistance to solvents, making it useful in various applications, including materials science and organic synthesis. Additionally, the compound's fluorinated nature may contribute to its utility in specialized fields such as pharmaceuticals or agrochemicals, where fluorinated compounds often exhibit enhanced biological activity or improved performance characteristics. Safety and handling considerations should be taken into account due to the potential toxicity associated with fluorinated compounds.

1,2,3,4,5-pentafluoro-6-(prop-2-en-1-yloxy)benzene

33104-02-8: 1,2,3,4,5-Pentafluoro-6-(prop-2-en-1-yloxy)benzene is a fluorinated aromatic compound characterized by the presence of five fluorine atoms attached to a benzene ring, which significantly influences its chemical properties. The fluorine substituents enhance the compound's electronegativity and stability, making it less reactive compared to non-fluorinated analogs. The presence of the prop-2-en-1-yloxy group introduces a reactive alkene functionality, allowing for potential polymerization or further chemical modifications. This compound is likely to exhibit low volatility and high thermal stability due to the strong C-F bonds. Its unique structure may impart specific properties such as hydrophobicity and resistance to solvents, making it useful in various applications, including materials science and organic synthesis. Additionally, the compound's fluorinated nature may contribute to its utility in specialized fields such as pharmaceuticals or agrochemicals, where fluorinated compounds often exhibit enhanced biological activity or improved performance characteristics. Safety and handling considerations should be taken into account due to the potential toxicity associated with fluorinated compounds.

CAS 33104-02-8

1,2,3,4,5-pentafluoro-6-(prop-2-en-1-yloxy)benzene

Allyloxyperfluorobenzene

Ref: 54-PC6648