3,5-Bis(trifluoromethoxy)benzyl alcohol is an organic compound characterized by its aromatic structure, featuring a benzyl alcohol moiety substituted with two trifluoromethoxy groups at the 3 and 5 positions of the benzene ring. This compound is notable for its high electronegativity due to the presence of trifluoromethoxy groups, which can significantly influence its chemical reactivity and physical properties. The trifluoromethoxy groups enhance the compound's lipophilicity and may impart unique solubility characteristics in various solvents. Additionally, the presence of the hydroxyl (-OH) group in the benzyl alcohol structure contributes to its potential as a hydrogen bond donor, affecting its interactions in biological systems and chemical reactions. The compound may exhibit interesting properties such as antimicrobial activity or serve as a building block in the synthesis of more complex molecules. Its applications could extend to pharmaceuticals, agrochemicals, or materials science, depending on its reactivity and functionalization potential. Safety and handling precautions should be observed due to the presence of fluorinated groups, which can pose environmental and health risks.

3,5-Bis(Trifluoromethoxy)benzyl alcohol

1121586-22-8: 3,5-Bis(trifluoromethoxy)benzyl alcohol is an organic compound characterized by its aromatic structure, featuring a benzyl alcohol moiety substituted with two trifluoromethoxy groups at the 3 and 5 positions of the benzene ring. This compound is notable for its high electronegativity due to the presence of trifluoromethoxy groups, which can significantly influence its chemical reactivity and physical properties. The trifluoromethoxy groups enhance the compound's lipophilicity and may impart unique solubility characteristics in various solvents. Additionally, the presence of the hydroxyl (-OH) group in the benzyl alcohol structure contributes to its potential as a hydrogen bond donor, affecting its interactions in biological systems and chemical reactions. The compound may exhibit interesting properties such as antimicrobial activity or serve as a building block in the synthesis of more complex molecules. Its applications could extend to pharmaceuticals, agrochemicals, or materials science, depending on its reactivity and functionalization potential. Safety and handling precautions should be observed due to the presence of fluorinated groups, which can pose environmental and health risks.

CAS 1121586-22-8

3,5-Bis(Trifluoromethoxy)benzyl alcohol

(3,5-Bis(trifluoromethoxy)phenyl)methanol

Ref: IN-DA0083BE

(3,5-Bis(trifluoromethoxy)phenyl)methanol

Ref: 54-PC110637

(3,5-Bis(trifluoromethoxy)phenyl)methanol

Ref: 10-F633504