Ethyl 3-[4-(1-piperidylmethyl)benzoyl]benzoate, with the CAS number 898771-17-0, is an organic compound characterized by its complex structure, which includes an ethyl ester group, a benzoyl moiety, and a piperidine ring. This compound typically exhibits properties associated with both aromatic and aliphatic systems, contributing to its potential solubility in organic solvents. The presence of the piperidine ring suggests it may exhibit basic properties, which can influence its reactivity and interactions in biological systems. Ethyl 3-[4-(1-piperidylmethyl)benzoyl]benzoate may be of interest in medicinal chemistry due to its structural features that could facilitate interactions with biological targets. Its synthesis likely involves multi-step organic reactions, including esterification and amine alkylation. As with many organic compounds, its stability, reactivity, and potential applications would depend on specific environmental conditions and the presence of other chemical species. Further studies would be necessary to fully elucidate its pharmacological properties and potential uses in various fields, including pharmaceuticals and materials science.

ethyl 3-[4-(1-piperidylmethyl)benzoyl]benzoate

898771-17-0: Ethyl 3-[4-(1-piperidylmethyl)benzoyl]benzoate, with the CAS number 898771-17-0, is an organic compound characterized by its complex structure, which includes an ethyl ester group, a benzoyl moiety, and a piperidine ring. This compound typically exhibits properties associated with both aromatic and aliphatic systems, contributing to its potential solubility in organic solvents. The presence of the piperidine ring suggests it may exhibit basic properties, which can influence its reactivity and interactions in biological systems. Ethyl 3-[4-(1-piperidylmethyl)benzoyl]benzoate may be of interest in medicinal chemistry due to its structural features that could facilitate interactions with biological targets. Its synthesis likely involves multi-step organic reactions, including esterification and amine alkylation. As with many organic compounds, its stability, reactivity, and potential applications would depend on specific environmental conditions and the presence of other chemical species. Further studies would be necessary to fully elucidate its pharmacological properties and potential uses in various fields, including pharmaceuticals and materials science.

CAS 898771-17-0

ethyl 3-[4-(1-piperidylmethyl)benzoyl]benzoate

3-carboethoxy-4′-piperidinomethyl benzophenone

Ref: 10-F204267