1-(2,4-Difluorophenyl)-4-(5,5-dimethyl-1,3-dioxan-2-yl)butan-1-one, with the CAS number 898786-83-9, is a synthetic organic compound characterized by its complex structure, which includes a butanone moiety and a dioxane ring. The presence of the difluorophenyl group suggests that it may exhibit unique electronic properties, potentially influencing its reactivity and interaction with biological targets. The dioxane component contributes to the compound's stability and solubility in various solvents. This compound may be of interest in medicinal chemistry, particularly in the development of pharmaceuticals, due to its potential biological activity. Its molecular structure indicates that it could participate in various chemical reactions, including nucleophilic substitutions and electrophilic additions, depending on the functional groups present. Additionally, the presence of fluorine atoms often enhances lipophilicity, which can affect the compound's pharmacokinetics and bioavailability. Overall, this compound represents a class of molecules that may have significant applications in drug discovery and development.

1-(2,4-difluorophenyl)-4-(5,5-dimethyl-1,3-dioxan-2-yl)butan-1-one

898786-83-9: 1-(2,4-Difluorophenyl)-4-(5,5-dimethyl-1,3-dioxan-2-yl)butan-1-one, with the CAS number 898786-83-9, is a synthetic organic compound characterized by its complex structure, which includes a butanone moiety and a dioxane ring. The presence of the difluorophenyl group suggests that it may exhibit unique electronic properties, potentially influencing its reactivity and interaction with biological targets. The dioxane component contributes to the compound's stability and solubility in various solvents. This compound may be of interest in medicinal chemistry, particularly in the development of pharmaceuticals, due to its potential biological activity. Its molecular structure indicates that it could participate in various chemical reactions, including nucleophilic substitutions and electrophilic additions, depending on the functional groups present. Additionally, the presence of fluorine atoms often enhances lipophilicity, which can affect the compound's pharmacokinetics and bioavailability. Overall, this compound represents a class of molecules that may have significant applications in drug discovery and development.

CAS 898786-83-9

1-(2,4-difluorophenyl)-4-(5,5-dimethyl-1,3-dioxan-2-yl)butan-1-one

2′,4′-difluoro-4-(5,5-dimethyl-1,3-dioxan-2-yl)butyrophenone

Ref: 10-F208355