Methanone, specifically the compound known as [4-(1,3-dioxolan-2-yl)phenyl][4-(trifluoromethyl)phenyl]-, is an organic compound characterized by its complex structure that includes a methanone functional group and two distinct aromatic substituents. The presence of a 1,3-dioxolane ring contributes to its potential reactivity and solubility properties, while the trifluoromethyl group enhances its electronic characteristics, often increasing lipophilicity and altering its interaction with biological systems. This compound may exhibit interesting pharmacological properties due to the combination of these functional groups, making it a candidate for various applications in medicinal chemistry. Its molecular structure suggests potential for hydrogen bonding and dipole interactions, which can influence its behavior in different solvents. Additionally, the trifluoromethyl group is known for imparting unique properties such as increased metabolic stability and altered binding affinity in drug design. Overall, the characteristics of this compound make it a subject of interest in both synthetic and applied chemistry contexts.

Methanone, [4-(1,3-dioxolan-2-yl)phenyl][4-(trifluoromethyl)phenyl]-

898760-55-9: Methanone, specifically the compound known as [4-(1,3-dioxolan-2-yl)phenyl][4-(trifluoromethyl)phenyl]-, is an organic compound characterized by its complex structure that includes a methanone functional group and two distinct aromatic substituents. The presence of a 1,3-dioxolane ring contributes to its potential reactivity and solubility properties, while the trifluoromethyl group enhances its electronic characteristics, often increasing lipophilicity and altering its interaction with biological systems. This compound may exhibit interesting pharmacological properties due to the combination of these functional groups, making it a candidate for various applications in medicinal chemistry. Its molecular structure suggests potential for hydrogen bonding and dipole interactions, which can influence its behavior in different solvents. Additionally, the trifluoromethyl group is known for imparting unique properties such as increased metabolic stability and altered binding affinity in drug design. Overall, the characteristics of this compound make it a subject of interest in both synthetic and applied chemistry contexts.

CAS 898760-55-9

Methanone, [4-(1,3-dioxolan-2-yl)phenyl][4-(trifluoromethyl)phenyl]-

4-(1,3-dioxolan-2-yl)-4′-trifluoromethylbenzophenone

Ref: 10-F206878