(3,4-Difluorophenyl)(3-fluoro-4-methoxyphenyl)methanone, identified by its CAS number 845781-11-5, is an organic compound characterized by its complex aromatic structure. This substance features two phenyl rings, one of which is substituted with two fluorine atoms and the other with a fluorine atom and a methoxy group. The presence of these substituents significantly influences its chemical properties, including its reactivity and polarity. The fluorine atoms enhance the compound's electronegativity, potentially affecting its interactions with other molecules, while the methoxy group can provide additional steric and electronic effects. This compound may exhibit interesting biological activities, making it of interest in pharmaceutical research. Its synthesis typically involves multi-step organic reactions, and it may be analyzed using techniques such as NMR spectroscopy or mass spectrometry to confirm its structure and purity. As with many fluorinated compounds, it may also exhibit unique physical properties, such as altered solubility and stability compared to non-fluorinated analogs.

(3,4-difluorophenyl)(3-fluoro-4-methoxyphenyl)methanone

845781-11-5: (3,4-Difluorophenyl)(3-fluoro-4-methoxyphenyl)methanone, identified by its CAS number 845781-11-5, is an organic compound characterized by its complex aromatic structure. This substance features two phenyl rings, one of which is substituted with two fluorine atoms and the other with a fluorine atom and a methoxy group. The presence of these substituents significantly influences its chemical properties, including its reactivity and polarity. The fluorine atoms enhance the compound's electronegativity, potentially affecting its interactions with other molecules, while the methoxy group can provide additional steric and electronic effects. This compound may exhibit interesting biological activities, making it of interest in pharmaceutical research. Its synthesis typically involves multi-step organic reactions, and it may be analyzed using techniques such as NMR spectroscopy or mass spectrometry to confirm its structure and purity. As with many fluorinated compounds, it may also exhibit unique physical properties, such as altered solubility and stability compared to non-fluorinated analogs.

CAS 845781-11-5

(3,4-difluorophenyl)(3-fluoro-4-methoxyphenyl)methanone

4-Methoxy-3,3′,4′-trifluorobenzophenone

Ref: 10-F022805