1-(3,5-Difluorophenyl)-3-(4-methylsulfanylphenyl)propan-1-one, with the CAS number 898781-81-2, is an organic compound characterized by its unique structure that includes a propanone backbone substituted with a difluorophenyl group and a methylsulfanylphenyl group. This compound typically exhibits properties associated with ketones, such as being a liquid or solid at room temperature, depending on its specific formulation and purity. The presence of fluorine atoms often enhances the compound's lipophilicity and may influence its reactivity and biological activity. The methylsulfanyl group can impart distinct electronic and steric effects, potentially affecting the compound's interactions in biological systems. Additionally, the compound may exhibit interesting pharmacological properties, making it of interest in medicinal chemistry. Its synthesis and characterization would involve standard organic chemistry techniques, including NMR, IR spectroscopy, and mass spectrometry, to confirm its structure and purity. Overall, this compound represents a class of substituted ketones that may have applications in various fields, including pharmaceuticals and agrochemicals.

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

898781-81-2: 1-(3,5-Difluorophenyl)-3-(4-methylsulfanylphenyl)propan-1-one, with the CAS number 898781-81-2, is an organic compound characterized by its unique structure that includes a propanone backbone substituted with a difluorophenyl group and a methylsulfanylphenyl group. This compound typically exhibits properties associated with ketones, such as being a liquid or solid at room temperature, depending on its specific formulation and purity. The presence of fluorine atoms often enhances the compound's lipophilicity and may influence its reactivity and biological activity. The methylsulfanyl group can impart distinct electronic and steric effects, potentially affecting the compound's interactions in biological systems. Additionally, the compound may exhibit interesting pharmacological properties, making it of interest in medicinal chemistry. Its synthesis and characterization would involve standard organic chemistry techniques, including NMR, IR spectroscopy, and mass spectrometry, to confirm its structure and purity. Overall, this compound represents a class of substituted ketones that may have applications in various fields, including pharmaceuticals and agrochemicals.

CAS 898781-81-2

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

3′,5′-difluoro-3-(4-thiomethylphenyl)propiophenone

Ref: 10-F206034