(4,4,4-Trifluorobut-1-yl)benzene, with the CAS number 104315-86-8, is an organic compound characterized by the presence of a benzene ring substituted with a trifluorobutyl group. This compound features a butyl chain that is fully fluorinated at the terminal carbon, which significantly influences its chemical properties, including increased hydrophobicity and altered reactivity. The trifluoromethyl group enhances the compound's stability and can affect its interaction with biological systems and other chemical species. Typically, such fluorinated compounds exhibit unique physical properties, such as higher boiling points and lower volatility compared to their non-fluorinated counterparts. They may also demonstrate distinct solubility profiles, often being soluble in organic solvents while exhibiting limited solubility in water. The presence of fluorine atoms can impart unique electronic characteristics, making these compounds of interest in various applications, including pharmaceuticals, agrochemicals, and materials science. Safety data sheets should be consulted for handling and toxicity information, as fluorinated compounds can pose specific health and environmental risks.

(4,4,4-TRIFLUOROBUT-1-YL)BENZENE 97

104315-86-8: (4,4,4-Trifluorobut-1-yl)benzene, with the CAS number 104315-86-8, is an organic compound characterized by the presence of a benzene ring substituted with a trifluorobutyl group. This compound features a butyl chain that is fully fluorinated at the terminal carbon, which significantly influences its chemical properties, including increased hydrophobicity and altered reactivity. The trifluoromethyl group enhances the compound's stability and can affect its interaction with biological systems and other chemical species. Typically, such fluorinated compounds exhibit unique physical properties, such as higher boiling points and lower volatility compared to their non-fluorinated counterparts. They may also demonstrate distinct solubility profiles, often being soluble in organic solvents while exhibiting limited solubility in water. The presence of fluorine atoms can impart unique electronic characteristics, making these compounds of interest in various applications, including pharmaceuticals, agrochemicals, and materials science. Safety data sheets should be consulted for handling and toxicity information, as fluorinated compounds can pose specific health and environmental risks.

CAS 104315-86-8

(4,4,4-TRIFLUOROBUT-1-YL)BENZENE 97

(4,4,4-Trifluorobut-1-yl)benzene

Ref: 54-PC4337