The chemical substance known as 5-(5,5-dimethyl-1,3-dioxan-2-yl)-1-[4-(trifluoromethyl)phenyl]pentan-1-one, with the CAS number 898786-71-5, is a synthetic organic compound characterized by its complex structure, which includes a dioxane ring and a trifluoromethyl-substituted phenyl group. This compound typically exhibits properties associated with ketones, such as being a polar solvent and having a relatively high boiling point due to the presence of multiple functional groups. The dioxane moiety contributes to its solubility in various organic solvents, while the trifluoromethyl group can enhance lipophilicity and influence biological activity. The presence of these functional groups suggests potential applications in pharmaceuticals or agrochemicals, where such structural features can impart specific reactivity or biological properties. Additionally, the compound's stability and reactivity may be influenced by the steric hindrance introduced by the dimethyl groups, making it an interesting subject for further research in synthetic chemistry and material science.

5-(5,5-dimethyl-1,3-dioxan-2-yl)-1-[4-(trifluoromethyl)phenyl]pentan-1-one

898786-71-5: The chemical substance known as 5-(5,5-dimethyl-1,3-dioxan-2-yl)-1-[4-(trifluoromethyl)phenyl]pentan-1-one, with the CAS number 898786-71-5, is a synthetic organic compound characterized by its complex structure, which includes a dioxane ring and a trifluoromethyl-substituted phenyl group. This compound typically exhibits properties associated with ketones, such as being a polar solvent and having a relatively high boiling point due to the presence of multiple functional groups. The dioxane moiety contributes to its solubility in various organic solvents, while the trifluoromethyl group can enhance lipophilicity and influence biological activity. The presence of these functional groups suggests potential applications in pharmaceuticals or agrochemicals, where such structural features can impart specific reactivity or biological properties. Additionally, the compound's stability and reactivity may be influenced by the steric hindrance introduced by the dimethyl groups, making it an interesting subject for further research in synthetic chemistry and material science.

CAS 898786-71-5

5-(5,5-dimethyl-1,3-dioxan-2-yl)-1-[4-(trifluoromethyl)phenyl]pentan-1-one

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

Ref: 10-F208347