(2,4-Difluorophenyl)-[2-(pyrrolidin-1-ylmethyl)phenyl]methanone, identified by its CAS number 898775-03-6, is a synthetic organic compound characterized by its complex structure, which includes a difluorophenyl group and a pyrrolidinylmethyl substituent. This compound typically exhibits properties associated with both aromatic and aliphatic systems, contributing to its potential biological activity. The presence of fluorine atoms enhances lipophilicity and can influence the compound's interaction with biological targets, potentially affecting its pharmacokinetic and pharmacodynamic profiles. The pyrrolidine moiety may impart additional steric and electronic effects, which can be crucial for its reactivity and binding affinity in medicinal chemistry applications. As a ketone, it may also participate in various chemical reactions, including nucleophilic additions and reductions. Overall, this compound's unique structural features suggest potential utility in drug discovery and development, particularly in the context of targeting specific biological pathways or receptors. However, detailed studies would be necessary to fully elucidate its properties and potential applications.

(2,4-difluorophenyl)-[2-(pyrrolidin-1-ylmethyl)phenyl]methanone

898775-03-6: (2,4-Difluorophenyl)-[2-(pyrrolidin-1-ylmethyl)phenyl]methanone, identified by its CAS number 898775-03-6, is a synthetic organic compound characterized by its complex structure, which includes a difluorophenyl group and a pyrrolidinylmethyl substituent. This compound typically exhibits properties associated with both aromatic and aliphatic systems, contributing to its potential biological activity. The presence of fluorine atoms enhances lipophilicity and can influence the compound's interaction with biological targets, potentially affecting its pharmacokinetic and pharmacodynamic profiles. The pyrrolidine moiety may impart additional steric and electronic effects, which can be crucial for its reactivity and binding affinity in medicinal chemistry applications. As a ketone, it may also participate in various chemical reactions, including nucleophilic additions and reductions. Overall, this compound's unique structural features suggest potential utility in drug discovery and development, particularly in the context of targeting specific biological pathways or receptors. However, detailed studies would be necessary to fully elucidate its properties and potential applications.

CAS 898775-03-6

(2,4-difluorophenyl)-[2-(pyrrolidin-1-ylmethyl)phenyl]methanone

2,4-difluoro-2′-pyrrolidinomethyl benzophenone

Ref: 10-F205267