1-(2,6-Dimethylphenyl)-3-(3,4,5-trifluorophenyl)propan-1-one, with the CAS number 898778-06-8, is an organic compound characterized by its ketone functional group. This substance features a propanone backbone, where the carbonyl group is flanked by two distinct aromatic rings. The first ring is a dimethyl-substituted phenyl group, which contributes to the compound's hydrophobic characteristics and potential for π-π stacking interactions. The second ring is a trifluorophenyl group, which introduces significant electronegativity due to the presence of three fluorine atoms, enhancing the compound's reactivity and influencing its electronic properties. This compound may exhibit interesting biological activities and has potential applications in pharmaceuticals or as an intermediate in organic synthesis. Its molecular structure suggests that it could participate in various chemical reactions, including nucleophilic additions and substitutions, due to the presence of both electron-rich and electron-deficient regions. Overall, the unique combination of substituents on the aromatic rings makes this compound a subject of interest in both synthetic and medicinal chemistry.

1-(2,6-dimethylphenyl)-3-(3,4,5-trifluorophenyl)propan-1-one

898778-06-8: 1-(2,6-Dimethylphenyl)-3-(3,4,5-trifluorophenyl)propan-1-one, with the CAS number 898778-06-8, is an organic compound characterized by its ketone functional group. This substance features a propanone backbone, where the carbonyl group is flanked by two distinct aromatic rings. The first ring is a dimethyl-substituted phenyl group, which contributes to the compound's hydrophobic characteristics and potential for π-π stacking interactions. The second ring is a trifluorophenyl group, which introduces significant electronegativity due to the presence of three fluorine atoms, enhancing the compound's reactivity and influencing its electronic properties. This compound may exhibit interesting biological activities and has potential applications in pharmaceuticals or as an intermediate in organic synthesis. Its molecular structure suggests that it could participate in various chemical reactions, including nucleophilic additions and substitutions, due to the presence of both electron-rich and electron-deficient regions. Overall, the unique combination of substituents on the aromatic rings makes this compound a subject of interest in both synthetic and medicinal chemistry.

CAS 898778-06-8

1-(2,6-dimethylphenyl)-3-(3,4,5-trifluorophenyl)propan-1-one