(3,5-Dichlorophenyl)-[4-(morpholinomethyl)phenyl]methanone, identified by its CAS number 898770-63-3, is a synthetic organic compound characterized by its complex structure, which includes a dichlorophenyl group and a morpholinomethyl substituent. This compound typically exhibits properties associated with both aromatic and aliphatic systems, contributing to its potential biological activity. The presence of the dichlorophenyl moiety suggests that it may possess significant lipophilicity, which can influence its solubility and permeability in biological systems. The morpholine ring adds to its pharmacological profile, potentially enhancing interactions with biological targets. As a ketone, it features a carbonyl group that can participate in various chemical reactions, including nucleophilic attacks. This compound may be of interest in medicinal chemistry for its potential applications in drug development, particularly in the fields of oncology or neurology, due to the structural motifs that are often associated with bioactive molecules. However, specific biological activity and safety profiles would require further investigation through empirical studies.

(3,5-dichlorophenyl)-[4-(morpholinomethyl)phenyl]methanone

898770-63-3: (3,5-Dichlorophenyl)-[4-(morpholinomethyl)phenyl]methanone, identified by its CAS number 898770-63-3, is a synthetic organic compound characterized by its complex structure, which includes a dichlorophenyl group and a morpholinomethyl substituent. This compound typically exhibits properties associated with both aromatic and aliphatic systems, contributing to its potential biological activity. The presence of the dichlorophenyl moiety suggests that it may possess significant lipophilicity, which can influence its solubility and permeability in biological systems. The morpholine ring adds to its pharmacological profile, potentially enhancing interactions with biological targets. As a ketone, it features a carbonyl group that can participate in various chemical reactions, including nucleophilic attacks. This compound may be of interest in medicinal chemistry for its potential applications in drug development, particularly in the fields of oncology or neurology, due to the structural motifs that are often associated with bioactive molecules. However, specific biological activity and safety profiles would require further investigation through empirical studies.

CAS 898770-63-3

(3,5-dichlorophenyl)-[4-(morpholinomethyl)phenyl]methanone

3,5-dichloro-4′-morpholinomethyl benzophenone

Ref: 10-F204242