Ethyl 2-[4-(1-piperidylmethyl)benzoyl]benzoate, identified by its CAS number 898771-14-7, is a chemical compound that belongs to the class of esters. It features a benzoate moiety, which is characterized by the presence of a benzene ring attached to a carbonyl group (C=O) and an ethyl group. The compound also contains a piperidine ring, which is a six-membered nitrogen-containing heterocycle, linked through a benzyl group to the benzoyl moiety. This structure suggests potential biological activity, particularly in medicinal chemistry, where piperidine derivatives are often explored for their pharmacological properties. Ethyl 2-[4-(1-piperidylmethyl)benzoyl]benzoate may exhibit lipophilicity due to its aromatic and aliphatic components, influencing its solubility and permeability in biological systems. The compound's synthesis and characterization would typically involve standard organic chemistry techniques, and its potential applications could range from pharmaceuticals to agrochemicals, depending on its specific interactions and reactivity.

ethyl 2-[4-(1-piperidylmethyl)benzoyl]benzoate

898771-14-7: Ethyl 2-[4-(1-piperidylmethyl)benzoyl]benzoate, identified by its CAS number 898771-14-7, is a chemical compound that belongs to the class of esters. It features a benzoate moiety, which is characterized by the presence of a benzene ring attached to a carbonyl group (C=O) and an ethyl group. The compound also contains a piperidine ring, which is a six-membered nitrogen-containing heterocycle, linked through a benzyl group to the benzoyl moiety. This structure suggests potential biological activity, particularly in medicinal chemistry, where piperidine derivatives are often explored for their pharmacological properties. Ethyl 2-[4-(1-piperidylmethyl)benzoyl]benzoate may exhibit lipophilicity due to its aromatic and aliphatic components, influencing its solubility and permeability in biological systems. The compound's synthesis and characterization would typically involve standard organic chemistry techniques, and its potential applications could range from pharmaceuticals to agrochemicals, depending on its specific interactions and reactivity.

CAS 898771-14-7

ethyl 2-[4-(1-piperidylmethyl)benzoyl]benzoate

2-Carboethoxy-4′-piperidinomethyl benzophenone

Ref: 10-F204266