[2-(Morpholinomethyl)phenyl]-(m-tolyl)methanone, identified by its CAS number 898749-90-1, is a chemical compound characterized by its complex structure that includes a phenyl ring, a morpholine group, and a ketone functional group. This compound typically exhibits properties associated with both aromatic and aliphatic systems, which can influence its reactivity and solubility. Morpholine, a cyclic amine, contributes to the compound's potential as a nucleophile, while the ketone group may participate in various chemical reactions, such as nucleophilic addition or condensation. The presence of the m-tolyl group suggests that the compound may have hydrophobic characteristics, affecting its solubility in polar versus non-polar solvents. Additionally, the compound may exhibit biological activity, making it of interest in pharmaceutical research. Its specific applications and behavior in chemical reactions would depend on the context of use, including the presence of other reagents and the reaction conditions. Overall, this compound represents a unique combination of functional groups that can lead to diverse chemical properties and potential applications.

[2-(morpholinomethyl)phenyl]-(m-tolyl)methanone

898749-90-1: [2-(Morpholinomethyl)phenyl]-(m-tolyl)methanone, identified by its CAS number 898749-90-1, is a chemical compound characterized by its complex structure that includes a phenyl ring, a morpholine group, and a ketone functional group. This compound typically exhibits properties associated with both aromatic and aliphatic systems, which can influence its reactivity and solubility. Morpholine, a cyclic amine, contributes to the compound's potential as a nucleophile, while the ketone group may participate in various chemical reactions, such as nucleophilic addition or condensation. The presence of the m-tolyl group suggests that the compound may have hydrophobic characteristics, affecting its solubility in polar versus non-polar solvents. Additionally, the compound may exhibit biological activity, making it of interest in pharmaceutical research. Its specific applications and behavior in chemical reactions would depend on the context of use, including the presence of other reagents and the reaction conditions. Overall, this compound represents a unique combination of functional groups that can lead to diverse chemical properties and potential applications.

CAS 898749-90-1

[2-(morpholinomethyl)phenyl]-(m-tolyl)methanone

3′-Methyl-2-morpholinomethyl benzophenone

Ref: 10-F205113