(3,5-Difluorophenyl)(4-propylphenyl)methanone, with the CAS number 844885-12-7, is an organic compound characterized by its unique structure, which includes a ketone functional group attached to two distinct aromatic rings. The presence of fluorine atoms at the 3 and 5 positions of the phenyl ring contributes to its electronic properties, potentially enhancing its reactivity and influencing its interactions with biological targets. The propyl group on the other phenyl ring adds hydrophobic characteristics, which can affect the compound's solubility and permeability in biological systems. This compound may exhibit interesting pharmacological properties, making it a candidate for research in medicinal chemistry. Its molecular structure suggests potential applications in drug development, particularly in the design of compounds targeting specific biological pathways. Additionally, the presence of fluorine can improve metabolic stability and bioavailability. Overall, (3,5-difluorophenyl)(4-propylphenyl)methanone is a compound of interest in both synthetic and medicinal chemistry due to its distinctive features and potential applications.

(3,5-difluorophenyl)(4-propylphenyl)methanone

844885-12-7: (3,5-Difluorophenyl)(4-propylphenyl)methanone, with the CAS number 844885-12-7, is an organic compound characterized by its unique structure, which includes a ketone functional group attached to two distinct aromatic rings. The presence of fluorine atoms at the 3 and 5 positions of the phenyl ring contributes to its electronic properties, potentially enhancing its reactivity and influencing its interactions with biological targets. The propyl group on the other phenyl ring adds hydrophobic characteristics, which can affect the compound's solubility and permeability in biological systems. This compound may exhibit interesting pharmacological properties, making it a candidate for research in medicinal chemistry. Its molecular structure suggests potential applications in drug development, particularly in the design of compounds targeting specific biological pathways. Additionally, the presence of fluorine can improve metabolic stability and bioavailability. Overall, (3,5-difluorophenyl)(4-propylphenyl)methanone is a compound of interest in both synthetic and medicinal chemistry due to its distinctive features and potential applications.

CAS 844885-12-7

(3,5-difluorophenyl)(4-propylphenyl)methanone

3,5-Difluoro-4′-n-propylbenzophenone

Ref: 10-F022754