4-Trifluoromethylstyrene is an organic compound characterized by the presence of a trifluoromethyl group (-CF3) attached to the para position of a styrene molecule, which consists of a vinyl group (–CH=CH2) bonded to a phenyl ring. This compound is notable for its unique electronic properties due to the electronegative fluorine atoms, which can influence reactivity and stability. It is typically a colorless to pale yellow liquid with a distinct odor. 4-Trifluoromethylstyrene is used in various applications, including as a monomer in polymer synthesis, particularly in the production of specialty polymers with enhanced thermal and chemical resistance. The presence of the trifluoromethyl group can also impart unique properties to the resulting polymers, such as increased hydrophobicity and improved mechanical strength. Additionally, this compound may exhibit interesting behavior in reactions such as polymerization and electrophilic aromatic substitution due to the electron-withdrawing nature of the trifluoromethyl group. Safety precautions should be taken when handling this substance, as it may pose health and environmental risks.

4-Trifluoromethylstyrene

55186-75-9: 4-Trifluoromethylstyrene is an organic compound characterized by the presence of a trifluoromethyl group (-CF3) attached to the para position of a styrene molecule, which consists of a vinyl group (–CH=CH2) bonded to a phenyl ring. This compound is notable for its unique electronic properties due to the electronegative fluorine atoms, which can influence reactivity and stability. It is typically a colorless to pale yellow liquid with a distinct odor. 4-Trifluoromethylstyrene is used in various applications, including as a monomer in polymer synthesis, particularly in the production of specialty polymers with enhanced thermal and chemical resistance. The presence of the trifluoromethyl group can also impart unique properties to the resulting polymers, such as increased hydrophobicity and improved mechanical strength. Additionally, this compound may exhibit interesting behavior in reactions such as polymerization and electrophilic aromatic substitution due to the electron-withdrawing nature of the trifluoromethyl group. Safety precautions should be taken when handling this substance, as it may pose health and environmental risks.

CAS 55186-75-9

4-Trifluoromethylstyrene

1-Isopropenyl-4-trifluoromethyl-benzene

Ref: 10-F033002