Pentafluoroethyl phenyl ketone, with the CAS number 394-52-5, is an organic compound characterized by the presence of a phenyl group attached to a ketone functional group, along with a pentafluoroethyl substituent. This compound is notable for its high fluorine content, which imparts unique properties such as increased lipophilicity and thermal stability. The presence of multiple fluorine atoms enhances its chemical resistance and alters its reactivity compared to non-fluorinated analogs. Pentafluoroethyl phenyl ketone is typically used in specialized applications, including as a reagent in organic synthesis and in the development of fluorinated materials. Its physical properties, such as boiling point and solubility, are influenced by the fluorinated ethyl group, which can affect its behavior in various chemical environments. Additionally, the compound's structure may contribute to its utility in pharmaceuticals and agrochemicals, where fluorinated compounds often exhibit enhanced biological activity. Safety precautions should be observed when handling this substance due to its potential toxicity and environmental impact.

pentafluoroethyl phenyl ketone

394-52-5: Pentafluoroethyl phenyl ketone, with the CAS number 394-52-5, is an organic compound characterized by the presence of a phenyl group attached to a ketone functional group, along with a pentafluoroethyl substituent. This compound is notable for its high fluorine content, which imparts unique properties such as increased lipophilicity and thermal stability. The presence of multiple fluorine atoms enhances its chemical resistance and alters its reactivity compared to non-fluorinated analogs. Pentafluoroethyl phenyl ketone is typically used in specialized applications, including as a reagent in organic synthesis and in the development of fluorinated materials. Its physical properties, such as boiling point and solubility, are influenced by the fluorinated ethyl group, which can affect its behavior in various chemical environments. Additionally, the compound's structure may contribute to its utility in pharmaceuticals and agrochemicals, where fluorinated compounds often exhibit enhanced biological activity. Safety precautions should be observed when handling this substance due to its potential toxicity and environmental impact.

CAS 394-52-5

pentafluoroethyl phenyl ketone

1-Propanone, 2,2,3,3,3-pentafluoro-1-phenyl-

Ref: IN-DA00I7RA

2,2,3,3,3-Pentafluoropropiophenone

Ref: 54-PC5605