2-Phenyl-1-[2-(trifluoromethyl)phenyl]ethanone, with the CAS number 898783-80-7, is an organic compound characterized by its ketone functional group and the presence of both phenyl and trifluoromethyl substituents. This compound typically exhibits a white to off-white crystalline appearance and is soluble in organic solvents such as dichloromethane and acetone, but may have limited solubility in water due to its hydrophobic nature. The trifluoromethyl group enhances the compound's lipophilicity and can influence its reactivity and biological activity. As a ketone, it may participate in various chemical reactions, including nucleophilic additions and reductions. The presence of the phenyl groups contributes to its stability and can affect its electronic properties, making it of interest in fields such as medicinal chemistry and materials science. Additionally, the compound's unique structure may impart specific pharmacological properties, making it a candidate for further research in drug development or as a synthetic intermediate in organic synthesis.

2-phenyl-1-[2-(trifluoromethyl)phenyl]ethanone

898783-80-7: 2-Phenyl-1-[2-(trifluoromethyl)phenyl]ethanone, with the CAS number 898783-80-7, is an organic compound characterized by its ketone functional group and the presence of both phenyl and trifluoromethyl substituents. This compound typically exhibits a white to off-white crystalline appearance and is soluble in organic solvents such as dichloromethane and acetone, but may have limited solubility in water due to its hydrophobic nature. The trifluoromethyl group enhances the compound's lipophilicity and can influence its reactivity and biological activity. As a ketone, it may participate in various chemical reactions, including nucleophilic additions and reductions. The presence of the phenyl groups contributes to its stability and can affect its electronic properties, making it of interest in fields such as medicinal chemistry and materials science. Additionally, the compound's unique structure may impart specific pharmacological properties, making it a candidate for further research in drug development or as a synthetic intermediate in organic synthesis.

CAS 898783-80-7

2-phenyl-1-[2-(trifluoromethyl)phenyl]ethanone

2-phenyl-2′-trifluoromethylacetophenone

Ref: 10-F203750