The chemical substance known as (4-fluorophenyl)-[3-(pyrrolidin-1-ylmethyl)phenyl]methanone, with the CAS number 898770-31-5, is a synthetic organic compound characterized by its complex structure that includes a fluorinated phenyl group and a pyrrolidine moiety. This compound typically exhibits properties associated with both aromatic and aliphatic systems, which can influence its solubility, stability, and reactivity. The presence of the fluorine atom may enhance lipophilicity and alter the electronic properties of the molecule, potentially affecting its biological activity. The pyrrolidine ring contributes to the compound's steric and electronic characteristics, which can be significant in pharmacological contexts. Such compounds are often studied for their potential applications in medicinal chemistry, particularly in the development of pharmaceuticals targeting various biological pathways. Additionally, the compound's molecular interactions, including hydrogen bonding and π-π stacking, can play a crucial role in its behavior in biological systems and its overall efficacy as a therapeutic agent.

(4-fluorophenyl)-[3-(pyrrolidin-1-ylmethyl)phenyl]methanone

898770-31-5: The chemical substance known as (4-fluorophenyl)-[3-(pyrrolidin-1-ylmethyl)phenyl]methanone, with the CAS number 898770-31-5, is a synthetic organic compound characterized by its complex structure that includes a fluorinated phenyl group and a pyrrolidine moiety. This compound typically exhibits properties associated with both aromatic and aliphatic systems, which can influence its solubility, stability, and reactivity. The presence of the fluorine atom may enhance lipophilicity and alter the electronic properties of the molecule, potentially affecting its biological activity. The pyrrolidine ring contributes to the compound's steric and electronic characteristics, which can be significant in pharmacological contexts. Such compounds are often studied for their potential applications in medicinal chemistry, particularly in the development of pharmaceuticals targeting various biological pathways. Additionally, the compound's molecular interactions, including hydrogen bonding and π-π stacking, can play a crucial role in its behavior in biological systems and its overall efficacy as a therapeutic agent.

CAS 898770-31-5

(4-fluorophenyl)-[3-(pyrrolidin-1-ylmethyl)phenyl]methanone

4′-fluoro-3-pyrrolidinomethyl benzophenone

Ref: 10-F204788