Tris[4-(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl)phenyl]phosphane is a phosphane compound characterized by its unique structure, which includes a phosphorus atom bonded to three bulky, fluorinated phenyl groups. The presence of the heptadecafluorodecyl substituents imparts significant hydrophobic and lipophobic properties, making the compound highly nonpolar and resistant to chemical interactions with water and other polar solvents. This fluorinated nature also contributes to its thermal stability and potential applications in various fields, including materials science and nanotechnology. The compound's large molecular size and complex structure may influence its solubility and reactivity, making it suitable for specialized applications such as surfactants or in the development of advanced coatings. Additionally, the presence of multiple fluorine atoms enhances its chemical inertness, which can be advantageous in environments where chemical stability is paramount. Overall, this compound exemplifies the unique properties of fluorinated organic compounds, particularly in terms of their physical and chemical behavior.

tris[4-(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl)phenyl]phosphane

325459-92-5: Tris[4-(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl)phenyl]phosphane is a phosphane compound characterized by its unique structure, which includes a phosphorus atom bonded to three bulky, fluorinated phenyl groups. The presence of the heptadecafluorodecyl substituents imparts significant hydrophobic and lipophobic properties, making the compound highly nonpolar and resistant to chemical interactions with water and other polar solvents. This fluorinated nature also contributes to its thermal stability and potential applications in various fields, including materials science and nanotechnology. The compound's large molecular size and complex structure may influence its solubility and reactivity, making it suitable for specialized applications such as surfactants or in the development of advanced coatings. Additionally, the presence of multiple fluorine atoms enhances its chemical inertness, which can be advantageous in environments where chemical stability is paramount. Overall, this compound exemplifies the unique properties of fluorinated organic compounds, particularly in terms of their physical and chemical behavior.

CAS 325459-92-5

tris[4-(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl)phenyl]phosphane