Ethyl 4-[3-(morpholinomethyl)benzoyl]benzoate, identified by its CAS number 898765-26-9, is an organic compound characterized by its ester functional group, which is derived from benzoic acid and ethanol. This compound features a morpholinomethyl substituent, indicating the presence of a morpholine ring, which contributes to its potential biological activity and solubility properties. The structure includes two aromatic rings, enhancing its stability and possibly influencing its interactions in biological systems. Ethyl 4-[3-(morpholinomethyl)benzoyl]benzoate may exhibit properties such as moderate lipophilicity, making it suitable for various applications in medicinal chemistry and drug design. Its unique combination of functional groups suggests potential uses in pharmaceuticals, particularly in the development of compounds targeting specific biological pathways. Additionally, the presence of the morpholine moiety may impart favorable pharmacokinetic properties, such as improved membrane permeability. As with many organic compounds, its reactivity and stability can be influenced by environmental factors such as pH and temperature.

ethyl 4-[3-(morpholinomethyl)benzoyl]benzoate

898765-26-9: Ethyl 4-[3-(morpholinomethyl)benzoyl]benzoate, identified by its CAS number 898765-26-9, is an organic compound characterized by its ester functional group, which is derived from benzoic acid and ethanol. This compound features a morpholinomethyl substituent, indicating the presence of a morpholine ring, which contributes to its potential biological activity and solubility properties. The structure includes two aromatic rings, enhancing its stability and possibly influencing its interactions in biological systems. Ethyl 4-[3-(morpholinomethyl)benzoyl]benzoate may exhibit properties such as moderate lipophilicity, making it suitable for various applications in medicinal chemistry and drug design. Its unique combination of functional groups suggests potential uses in pharmaceuticals, particularly in the development of compounds targeting specific biological pathways. Additionally, the presence of the morpholine moiety may impart favorable pharmacokinetic properties, such as improved membrane permeability. As with many organic compounds, its reactivity and stability can be influenced by environmental factors such as pH and temperature.

CAS 898765-26-9

ethyl 4-[3-(morpholinomethyl)benzoyl]benzoate

4′-carboethoxy-3-morpholinomethyl benzophenone

Ref: 10-F204666