4,4,4-Trifluoro-3-hydroxy-1-phenyl-3-(trifluoromethyl)butan-1-one, with CAS number 731-00-0, is a synthetic organic compound characterized by its unique trifluoromethyl and hydroxy functional groups. This compound features a phenyl group attached to a butanone backbone, which contributes to its chemical reactivity and potential applications in various fields, including pharmaceuticals and agrochemicals. The presence of multiple fluorine atoms enhances its lipophilicity and stability, making it resistant to degradation. Additionally, the hydroxy group can participate in hydrogen bonding, influencing its solubility and interaction with biological systems. The compound's structure suggests potential use as an intermediate in the synthesis of more complex molecules or as a reagent in organic reactions. Its properties, such as boiling point, melting point, and solubility, are influenced by the fluorinated groups, which can alter the physical characteristics compared to non-fluorinated analogs. Overall, this compound exemplifies the significance of fluorinated organic compounds in modern chemistry.

4,4,4-trifluoro-3-hydroxy-1-phenyl-3-(trifluoromethyl)butan-1-one

731-00-0: 4,4,4-Trifluoro-3-hydroxy-1-phenyl-3-(trifluoromethyl)butan-1-one, with CAS number 731-00-0, is a synthetic organic compound characterized by its unique trifluoromethyl and hydroxy functional groups. This compound features a phenyl group attached to a butanone backbone, which contributes to its chemical reactivity and potential applications in various fields, including pharmaceuticals and agrochemicals. The presence of multiple fluorine atoms enhances its lipophilicity and stability, making it resistant to degradation. Additionally, the hydroxy group can participate in hydrogen bonding, influencing its solubility and interaction with biological systems. The compound's structure suggests potential use as an intermediate in the synthesis of more complex molecules or as a reagent in organic reactions. Its properties, such as boiling point, melting point, and solubility, are influenced by the fluorinated groups, which can alter the physical characteristics compared to non-fluorinated analogs. Overall, this compound exemplifies the significance of fluorinated organic compounds in modern chemistry.

<p>3-Hydroxy-1-phenyl-4,4,4-trifluoro-3-(trifluoromethyl)butan-1-one</p>

CAS 731-00-0

4,4,4-trifluoro-3-hydroxy-1-phenyl-3-(trifluoromethyl)butan-1-one

3-Hydroxy-1-phenyl-4,4,4-trifluoro-3-(trifluoromethyl)butan-1-one

Ref: 54-PC2899