(Trifluorosilyl)benzene, with the CAS number 368-47-8, is an organosilicon compound characterized by the presence of a trifluorosilyl group attached to a benzene ring. This compound features a silicon atom bonded to three fluorine atoms and one phenyl group, which significantly influences its chemical properties. The trifluorosilyl group imparts unique reactivity and stability, making it useful in various applications, including as a precursor in the synthesis of silicon-containing materials and in surface modification processes. The presence of fluorine atoms enhances the compound's electronegativity and can affect its solubility and volatility. (Trifluorosilyl)benzene is typically a colorless to pale yellow liquid, exhibiting a relatively low boiling point compared to other organosilicon compounds. Its reactivity can be attributed to the silicon-fluorine bonds, which can participate in various chemical reactions, including nucleophilic substitutions and polymerization processes. Overall, (trifluorosilyl)benzene serves as an important compound in materials science and organic synthesis.

(Trifluorosilyl)benzene

368-47-8: (Trifluorosilyl)benzene, with the CAS number 368-47-8, is an organosilicon compound characterized by the presence of a trifluorosilyl group attached to a benzene ring. This compound features a silicon atom bonded to three fluorine atoms and one phenyl group, which significantly influences its chemical properties. The trifluorosilyl group imparts unique reactivity and stability, making it useful in various applications, including as a precursor in the synthesis of silicon-containing materials and in surface modification processes. The presence of fluorine atoms enhances the compound's electronegativity and can affect its solubility and volatility. (Trifluorosilyl)benzene is typically a colorless to pale yellow liquid, exhibiting a relatively low boiling point compared to other organosilicon compounds. Its reactivity can be attributed to the silicon-fluorine bonds, which can participate in various chemical reactions, including nucleophilic substitutions and polymerization processes. Overall, (trifluorosilyl)benzene serves as an important compound in materials science and organic synthesis.

CAS 368-47-8

(Trifluorosilyl)benzene

Phenyltrifluorosilane

Ref: 54-PC3873