1-Ethenyl-4-(trifluoromethoxy)benzene, also known by its CAS number 1736-08-9, is an organic compound characterized by the presence of a vinyl group (ethenyl) and a trifluoromethoxy substituent on a benzene ring. This compound features a trifluoromethoxy group, which is a strong electron-withdrawing moiety, enhancing its reactivity in various chemical reactions. The presence of the vinyl group suggests that it can participate in polymerization processes, making it useful in the synthesis of more complex organic materials. The trifluoromethoxy group also contributes to the compound's unique physical properties, such as increased lipophilicity and potential volatility. In terms of applications, compounds with similar structures are often explored in fields such as materials science, pharmaceuticals, and agrochemicals due to their distinctive electronic properties and reactivity. Safety data should be consulted for handling and usage, as the trifluoromethoxy group may impart specific hazards associated with fluorinated compounds.

1-Ethenyl-4-(trifluoromethoxy)benzene

1736-08-9: Anisole, α,α,α-trifluoro-p-vinyl-, 1-(Trifluoromethoxy)-4-vinylbenzene, Benzene, 1-ethenyl-4-(trifluoromethoxy)-, 1-Ethenyl-4-(trifluoromethoxy)benzene, 4-(Trifluoromethoxy)styrene

CAS 1736-08-9: 1-Ethenyl-4-(trifluoromethoxy)benzene

4-(Trifluoromethoxy)styrene

Ref: 54-PC500744

4-(Trifluoromethoxy)styrene

Ref: 3D-BAA73608