[3-(Morpholinomethyl)phenyl]-(m-tolyl)methanone, identified by its CAS number 898765-01-0, is a chemical compound that features a phenyl ring substituted with a morpholinomethyl group and a methanone moiety. This compound typically exhibits characteristics common to ketones, such as a carbonyl functional group that contributes to its reactivity and potential for forming hydrogen bonds. The presence of the morpholine ring suggests that it may possess basic properties, allowing it to interact with various biological targets. Additionally, the presence of the m-tolyl group indicates potential hydrophobic interactions, which can influence its solubility and bioavailability. The compound may be of interest in medicinal chemistry due to its structural features, which could be relevant for developing pharmaceuticals or other biologically active agents. Overall, its unique combination of functional groups may confer specific chemical reactivity and biological activity, making it a subject of interest in research and development.

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

898765-01-0: [3-(Morpholinomethyl)phenyl]-(m-tolyl)methanone, identified by its CAS number 898765-01-0, is a chemical compound that features a phenyl ring substituted with a morpholinomethyl group and a methanone moiety. This compound typically exhibits characteristics common to ketones, such as a carbonyl functional group that contributes to its reactivity and potential for forming hydrogen bonds. The presence of the morpholine ring suggests that it may possess basic properties, allowing it to interact with various biological targets. Additionally, the presence of the m-tolyl group indicates potential hydrophobic interactions, which can influence its solubility and bioavailability. The compound may be of interest in medicinal chemistry due to its structural features, which could be relevant for developing pharmaceuticals or other biologically active agents. Overall, its unique combination of functional groups may confer specific chemical reactivity and biological activity, making it a subject of interest in research and development.

CAS 898765-01-0

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

3-methyl-3′-morpholinomethyl benzophenone

Ref: 10-F204656