Ethyl 5-oxo-5-[4-(pyrrolidin-1-ylmethyl)phenyl]pentanoate, identified by its CAS number 898777-10-1, is a synthetic organic compound characterized by its complex structure, which includes an ester functional group and a ketone moiety. The presence of the pyrrolidine ring indicates potential for biological activity, as pyrrolidine derivatives are often explored in medicinal chemistry for their pharmacological properties. This compound features a pentanoate backbone, which contributes to its lipophilicity, potentially influencing its solubility and permeability in biological systems. The aromatic phenyl group, substituted with a pyrrolidinylmethyl group, suggests that it may engage in π-π stacking interactions, which can be relevant in drug design and molecular recognition. Ethyl 5-oxo-5-[4-(pyrrolidin-1-ylmethyl)phenyl]pentanoate may exhibit interesting reactivity due to the presence of both the carbonyl and ester functionalities, making it a candidate for further chemical transformations or as a precursor in the synthesis of more complex molecules. Its specific applications and biological activities would require further investigation through experimental studies.

ethyl 5-oxo-5-[4-(pyrrolidin-1-ylmethyl)phenyl]pentanoate

898777-10-1: Ethyl 5-oxo-5-[4-(pyrrolidin-1-ylmethyl)phenyl]pentanoate, identified by its CAS number 898777-10-1, is a synthetic organic compound characterized by its complex structure, which includes an ester functional group and a ketone moiety. The presence of the pyrrolidine ring indicates potential for biological activity, as pyrrolidine derivatives are often explored in medicinal chemistry for their pharmacological properties. This compound features a pentanoate backbone, which contributes to its lipophilicity, potentially influencing its solubility and permeability in biological systems. The aromatic phenyl group, substituted with a pyrrolidinylmethyl group, suggests that it may engage in π-π stacking interactions, which can be relevant in drug design and molecular recognition. Ethyl 5-oxo-5-[4-(pyrrolidin-1-ylmethyl)phenyl]pentanoate may exhibit interesting reactivity due to the presence of both the carbonyl and ester functionalities, making it a candidate for further chemical transformations or as a precursor in the synthesis of more complex molecules. Its specific applications and biological activities would require further investigation through experimental studies.

CAS 898777-10-1

ethyl 5-oxo-5-[4-(pyrrolidin-1-ylmethyl)phenyl]pentanoate

ethyl 5-oxo-5-[(4-pyrrolidinomthyl)phenyl]valerate

Ref: 10-F204366