2-Phenyl-3-((4-(2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)ethyl)phenyl)amino)inden-1-one is a complex organic compound characterized by its unique molecular structure, which includes an indene core, multiple aromatic rings, and trifluoromethyl groups. The presence of trifluoromethyl groups contributes to its lipophilicity and potential biological activity, making it of interest in medicinal chemistry. The compound features a phenyl group and an amino substituent, which can influence its reactivity and interactions with biological targets. Its molecular weight, solubility, and stability are influenced by the trifluoromethyl and hydroxyl functionalities, which can also affect its pharmacokinetic properties. This compound may exhibit specific optical properties due to its conjugated system, and its synthesis typically involves multi-step organic reactions. As with many fluorinated compounds, it may possess unique characteristics such as increased metabolic stability and altered binding affinities in biological systems. Further studies would be necessary to fully elucidate its potential applications and mechanisms of action.

2-PHENYL-3-((4-(2,2,2-TRIFLUORO-1-HYDROXY-1-(TRIFLUOROMETHYL)ETHYL)PHENYL)AMINO)INDEN-1-ONE

1024213-52-2: 2-Phenyl-3-((4-(2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)ethyl)phenyl)amino)inden-1-one is a complex organic compound characterized by its unique molecular structure, which includes an indene core, multiple aromatic rings, and trifluoromethyl groups. The presence of trifluoromethyl groups contributes to its lipophilicity and potential biological activity, making it of interest in medicinal chemistry. The compound features a phenyl group and an amino substituent, which can influence its reactivity and interactions with biological targets. Its molecular weight, solubility, and stability are influenced by the trifluoromethyl and hydroxyl functionalities, which can also affect its pharmacokinetic properties. This compound may exhibit specific optical properties due to its conjugated system, and its synthesis typically involves multi-step organic reactions. As with many fluorinated compounds, it may possess unique characteristics such as increased metabolic stability and altered binding affinities in biological systems. Further studies would be necessary to fully elucidate its potential applications and mechanisms of action.

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CAS 1024213-52-2

2-PHENYL-3-((4-(2,2,2-TRIFLUORO-1-HYDROXY-1-(TRIFLUOROMETHYL)ETHYL)PHENYL)AMINO)INDEN-1-ONE

2-phenyl-3-((4-(2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)ethyl)phenyl)amino)inden-1-one

Ref: 3D-ZQB21352