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CAS 306937-22-4

:

ethyl 1-(3-aminobenzyl)piperidine-4-carboxylate

Description:
Ethyl 1-(3-aminobenzyl)piperidine-4-carboxylate is a chemical compound characterized by its piperidine core, which is a six-membered ring containing one nitrogen atom. This compound features an ethyl ester functional group, contributing to its solubility and reactivity. The presence of a 3-aminobenzyl substituent indicates that there is an amino group attached to a benzyl group at the third position of the piperidine ring, which can influence its biological activity and interactions. The carboxylate group is typically involved in various chemical reactions, including esterification and amidation. This compound may exhibit properties such as moderate polarity, making it soluble in organic solvents, and it may participate in hydrogen bonding due to the amino and carboxylate groups. Its structural features suggest potential applications in medicinal chemistry, particularly in the development of pharmaceuticals targeting neurological or psychiatric conditions. However, specific biological activities and safety profiles would require further investigation through empirical studies.
Formula:C15H22N2O2
InChI:InChI=1/C15H22N2O2/c1-2-19-15(18)13-6-8-17(9-7-13)11-12-4-3-5-14(16)10-12/h3-5,10,13H,2,6-9,11,16H2,1H3
SMILES:CCOC(=O)C1CCN(CC1)Cc1cccc(c1)N
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