Ethyl 3-[3-(2,5-dihydropyrrol-1-ylmethyl)benzoyl]benzoate, identified by its CAS number 898789-84-9, is an organic compound characterized by its complex structure, which includes an ethyl ester functional group and a benzoyl moiety. This compound features a dihydropyrrole ring, contributing to its potential biological activity and interactions. The presence of multiple aromatic rings suggests that it may exhibit interesting electronic properties, potentially influencing its reactivity and solubility. Ethyl esters are generally known for their pleasant odors and are often used in flavor and fragrance applications. Additionally, the dihydropyrrole component may impart unique pharmacological properties, making this compound of interest in medicinal chemistry. Its synthesis and characterization would typically involve standard organic reactions, including esterification and possibly cyclization processes. Overall, the compound's structural features suggest potential applications in pharmaceuticals or as a synthetic intermediate in organic synthesis. However, specific biological activities or applications would require further investigation through empirical studies.

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

898789-84-9: Ethyl 3-[3-(2,5-dihydropyrrol-1-ylmethyl)benzoyl]benzoate, identified by its CAS number 898789-84-9, is an organic compound characterized by its complex structure, which includes an ethyl ester functional group and a benzoyl moiety. This compound features a dihydropyrrole ring, contributing to its potential biological activity and interactions. The presence of multiple aromatic rings suggests that it may exhibit interesting electronic properties, potentially influencing its reactivity and solubility. Ethyl esters are generally known for their pleasant odors and are often used in flavor and fragrance applications. Additionally, the dihydropyrrole component may impart unique pharmacological properties, making this compound of interest in medicinal chemistry. Its synthesis and characterization would typically involve standard organic reactions, including esterification and possibly cyclization processes. Overall, the compound's structural features suggest potential applications in pharmaceuticals or as a synthetic intermediate in organic synthesis. However, specific biological activities or applications would require further investigation through empirical studies.

CAS 898789-84-9

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

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

Ref: 10-F205065