(1S)-1-[4-(Trifluoromethyl)phenyl]ethanol, with the CAS number 99493-93-3, is an organic compound characterized by its chiral center, which imparts specific stereochemical properties. This compound features a trifluoromethyl group attached to a phenyl ring, enhancing its lipophilicity and potentially influencing its reactivity and biological activity. The presence of the hydroxyl (-OH) group in the ethanol moiety contributes to its polarity, making it soluble in polar solvents. The trifluoromethyl group is known for its electron-withdrawing properties, which can affect the acidity of the hydroxyl group and the overall reactivity of the compound. This substance may be utilized in various applications, including pharmaceuticals and agrochemicals, due to its unique electronic and steric properties. Additionally, the chiral nature of the compound may lead to different biological activities depending on the stereoisomer, making it of interest in medicinal chemistry and drug development. Overall, (1S)-1-[4-(trifluoromethyl)phenyl]ethanol exemplifies the interplay between structure and function in organic chemistry.

(1S)-1-[4-(trifluoromethyl)phenyl]ethanol

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(S)-1-[4-(Trifluoromethyl)phenyl]ethanol

(S)-1-(4-(Trifluoromethyl)phenyl)ethanol

(1S)-1-[4-(Trifluoromethyl)phenyl]ethan-1-ol

CAS 99493-93-3: (1S)-1-[4-(trifluoromethyl)phenyl]ethanol

(S)-1-[4-(Trifluoromethyl)phenyl]ethanol

Ref: 3D-FT103393

(S)-1-(4-(Trifluoromethyl)phenyl)ethanol

Ref: IN-DA006NQ7

(S)-1-(4-(Trifluoromethyl)phenyl)ethanol

Ref: 10-F334941

(1S)-1-[4-(Trifluoromethyl)phenyl]ethan-1-ol

Ref: 54-PC0595