The chemical substance known as (4-bromophenyl)-[2-(pyrrolidin-1-ylmethyl)phenyl]methanone, with the CAS number 898774-47-5, is a synthetic organic compound characterized by its complex structure, which includes a brominated phenyl group and a pyrrolidine moiety. This compound typically exhibits properties associated with both aromatic and aliphatic systems, contributing to its potential reactivity and interactions. The presence of the bromine atom enhances its electrophilic character, making it a candidate for various chemical reactions, including nucleophilic substitutions. The pyrrolidine ring introduces a degree of steric hindrance and can influence the compound's solubility and biological activity. Such compounds are often studied for their potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to their ability to interact with biological targets. Additionally, the compound's stability, melting point, and solubility characteristics would depend on the specific conditions under which it is synthesized and stored. Overall, this compound represents a class of molecules with diverse applications in chemical research and drug development.

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

898774-47-5: The chemical substance known as (4-bromophenyl)-[2-(pyrrolidin-1-ylmethyl)phenyl]methanone, with the CAS number 898774-47-5, is a synthetic organic compound characterized by its complex structure, which includes a brominated phenyl group and a pyrrolidine moiety. This compound typically exhibits properties associated with both aromatic and aliphatic systems, contributing to its potential reactivity and interactions. The presence of the bromine atom enhances its electrophilic character, making it a candidate for various chemical reactions, including nucleophilic substitutions. The pyrrolidine ring introduces a degree of steric hindrance and can influence the compound's solubility and biological activity. Such compounds are often studied for their potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to their ability to interact with biological targets. Additionally, the compound's stability, melting point, and solubility characteristics would depend on the specific conditions under which it is synthesized and stored. Overall, this compound represents a class of molecules with diverse applications in chemical research and drug development.

CAS 898774-47-5

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

4′-bromo-2-pyrrolidinomethyl benzophenone

Ref: 10-F205239