1-(2,3-Dichlorophenyl)-5-(5,5-dimethyl-1,3-dioxan-2-yl)pentan-1-one, with the CAS number 898756-85-9, is a synthetic organic compound characterized by its complex structure, which includes a pentanone backbone and a dichlorophenyl group. This compound features a dioxane moiety, contributing to its potential solubility and reactivity. The presence of the dichlorophenyl group suggests that it may exhibit significant biological activity, possibly influencing its interaction with various biological targets. The dimethyl substitution on the dioxane ring may enhance its lipophilicity, affecting its pharmacokinetic properties. As a ketone, it may participate in various chemical reactions, including nucleophilic additions and reductions. The compound's unique structure may also impart specific physical properties, such as melting and boiling points, which are influenced by intermolecular forces like van der Waals interactions and dipole-dipole interactions. Overall, this compound's characteristics make it of interest in fields such as medicinal chemistry and materials science, although specific applications would depend on further research and analysis.

1-(2,3-dichlorophenyl)-5-(5,5-dimethyl-1,3-dioxan-2-yl)pentan-1-one

898756-85-9: 1-(2,3-Dichlorophenyl)-5-(5,5-dimethyl-1,3-dioxan-2-yl)pentan-1-one, with the CAS number 898756-85-9, is a synthetic organic compound characterized by its complex structure, which includes a pentanone backbone and a dichlorophenyl group. This compound features a dioxane moiety, contributing to its potential solubility and reactivity. The presence of the dichlorophenyl group suggests that it may exhibit significant biological activity, possibly influencing its interaction with various biological targets. The dimethyl substitution on the dioxane ring may enhance its lipophilicity, affecting its pharmacokinetic properties. As a ketone, it may participate in various chemical reactions, including nucleophilic additions and reductions. The compound's unique structure may also impart specific physical properties, such as melting and boiling points, which are influenced by intermolecular forces like van der Waals interactions and dipole-dipole interactions. Overall, this compound's characteristics make it of interest in fields such as medicinal chemistry and materials science, although specific applications would depend on further research and analysis.

CAS 898756-85-9

1-(2,3-dichlorophenyl)-5-(5,5-dimethyl-1,3-dioxan-2-yl)pentan-1-one

2′,3′-dichloro-5-(5,5-dimethyl-1,3-dioxan-2-yl)valerophenone

Ref: 10-F208446