Ethyl 3-[4-(2,5-dihydropyrrol-1-ylmethyl)benzoyl]benzoate is a synthetic organic compound characterized by its complex structure, which includes an ethyl ester group, a benzoyl moiety, and a dihydropyrrole unit. This compound typically exhibits properties associated with both aromatic and aliphatic systems, contributing to its potential reactivity and solubility in organic solvents. The presence of the dihydropyrrole ring suggests it may participate in various chemical reactions, such as electrophilic substitutions or cycloadditions, due to the electron-rich nature of the nitrogen atom. Additionally, the ester functional group can undergo hydrolysis or transesterification under appropriate conditions. Ethyl 3-[4-(2,5-dihydropyrrol-1-ylmethyl)benzoyl]benzoate may also display biological activity, making it of interest in medicinal chemistry and drug development. Its specific applications and behavior in biological systems would depend on further studies, including pharmacokinetics and toxicity assessments. Overall, this compound represents a versatile structure with potential implications in various fields of chemistry and pharmacology.

ethyl 3-[4-(2,5-dihydropyrrol-1-ylmethyl)benzoyl]benzoate

898763-91-2: Ethyl 3-[4-(2,5-dihydropyrrol-1-ylmethyl)benzoyl]benzoate is a synthetic organic compound characterized by its complex structure, which includes an ethyl ester group, a benzoyl moiety, and a dihydropyrrole unit. This compound typically exhibits properties associated with both aromatic and aliphatic systems, contributing to its potential reactivity and solubility in organic solvents. The presence of the dihydropyrrole ring suggests it may participate in various chemical reactions, such as electrophilic substitutions or cycloadditions, due to the electron-rich nature of the nitrogen atom. Additionally, the ester functional group can undergo hydrolysis or transesterification under appropriate conditions. Ethyl 3-[4-(2,5-dihydropyrrol-1-ylmethyl)benzoyl]benzoate may also display biological activity, making it of interest in medicinal chemistry and drug development. Its specific applications and behavior in biological systems would depend on further studies, including pharmacokinetics and toxicity assessments. Overall, this compound represents a versatile structure with potential implications in various fields of chemistry and pharmacology.

CAS 898763-91-2

ethyl 3-[4-(2,5-dihydropyrrol-1-ylmethyl)benzoyl]benzoate

3-carboethoxy-4'-(3-pyrrolinomethyl) benzophenone

Ref: 10-F204609