1-(3,5-Difluorophenyl)-3-(3,4-dimethylphenyl)propan-1-one, identified by its CAS number 898779-89-0, is an organic compound characterized by its ketone functional group. This substance features a propanone backbone with two distinct aromatic substituents: a 3,5-difluorophenyl group and a 3,4-dimethylphenyl group. The presence of fluorine atoms in the phenyl ring can influence the compound's electronic properties, potentially enhancing its reactivity and lipophilicity. The dimethyl substitution on the second phenyl ring contributes to steric hindrance, which may affect the compound's interaction with biological targets. This compound is likely to be a solid at room temperature, with potential applications in medicinal chemistry, particularly in the development of pharmaceuticals or agrochemicals. Its unique structure may also make it a candidate for studies in material science or as a synthetic intermediate in organic synthesis. As with many organic compounds, safety and handling precautions should be observed due to potential toxicity or reactivity.

1-(3,5-difluorophenyl)-3-(3,4-dimethylphenyl)propan-1-one

898779-89-0: 1-(3,5-Difluorophenyl)-3-(3,4-dimethylphenyl)propan-1-one, identified by its CAS number 898779-89-0, is an organic compound characterized by its ketone functional group. This substance features a propanone backbone with two distinct aromatic substituents: a 3,5-difluorophenyl group and a 3,4-dimethylphenyl group. The presence of fluorine atoms in the phenyl ring can influence the compound's electronic properties, potentially enhancing its reactivity and lipophilicity. The dimethyl substitution on the second phenyl ring contributes to steric hindrance, which may affect the compound's interaction with biological targets. This compound is likely to be a solid at room temperature, with potential applications in medicinal chemistry, particularly in the development of pharmaceuticals or agrochemicals. Its unique structure may also make it a candidate for studies in material science or as a synthetic intermediate in organic synthesis. As with many organic compounds, safety and handling precautions should be observed due to potential toxicity or reactivity.

CAS 898779-89-0

1-(3,5-difluorophenyl)-3-(3,4-dimethylphenyl)propan-1-one