3,5-Difluoro-4-(trifluoromethoxy)phenol is an organic compound characterized by its phenolic structure, which includes a hydroxyl group (-OH) attached to a benzene ring. The presence of two fluorine atoms at the 3 and 5 positions of the phenol ring enhances its electronegativity and alters its reactivity compared to non-fluorinated phenols. Additionally, the trifluoromethoxy group (-O-CF3) at the 4 position contributes to the compound's unique properties, including increased lipophilicity and potential for strong hydrogen bonding interactions. This compound is likely to exhibit high thermal stability and resistance to oxidation due to the presence of fluorine atoms. Its applications may span various fields, including pharmaceuticals, agrochemicals, and materials science, where fluorinated compounds are often valued for their unique chemical properties. Safety and handling considerations are essential, as fluorinated compounds can exhibit toxicity and environmental persistence. Overall, 3,5-Difluoro-4-(trifluoromethoxy)phenol represents a specialized class of fluorinated organic compounds with distinct characteristics and potential applications.

3,5-Difluoro-4-(trifluoromethoxy)phenol

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CAS 195206-85-0: 3,5-Difluoro-4-(trifluoromethoxy)phenol

3,5-Difluoro-4-(trifluoromethoxy)phenol

Ref: 3D-VHA20685

3,5-Difluoro-4-(trifluoromethoxy)phenol

Ref: 10-F244776

Phenol, 3,5-difluoro-4-(trifluoroMethoxy)-

Ref: IN-DA00AK3W