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CAS 1218790-81-8

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3-Ethyl 1-(3-boronobenzoyl)-3-piperidinecarboxylate

Description:
3-Ethyl 1-(3-boronobenzoyl)-3-piperidinecarboxylate is a chemical compound characterized by its unique structure, which includes a piperidine ring, an ethyl group, and a boron-containing benzoyl moiety. The presence of the boron atom suggests potential applications in medicinal chemistry, particularly in drug design and development, as boron compounds can enhance biological activity and selectivity. The piperidine ring contributes to the compound's basicity and potential interactions with biological targets. This compound may exhibit properties such as solubility in organic solvents, and its reactivity can be influenced by the functional groups present. Additionally, the presence of the carboxylate group indicates that it can participate in various chemical reactions, including esterification and nucleophilic substitution. Overall, 3-Ethyl 1-(3-boronobenzoyl)-3-piperidinecarboxylate is of interest in the field of organic synthesis and medicinal chemistry, where its structural features may be leveraged for the development of novel therapeutic agents.
Formula:C15H20BNO5
InChI:InChI=1S/C15H20BNO5/c1-2-22-15(19)12-6-4-8-17(10-12)14(18)11-5-3-7-13(9-11)16(20)21/h3,5,7,9,12,20-21H,2,4,6,8,10H2,1H3
InChI key:InChIKey=ADLXIBSCIGGNHP-UHFFFAOYSA-N
SMILES:C(=O)(N1CC(C(OCC)=O)CCC1)C2=CC(B(O)O)=CC=C2
Synonyms:
  • 3-Ethyl 1-(3-boronobenzoyl)-3-piperidinecarboxylate
  • (3-(3-(Ethoxycarbonyl)piperidine-1-carbonyl)phenyl)boronicacid
  • (3-(3-(Ethoxycarbonyl)piperidine-1-carbonyl)phenyl)boronic acid
  • 3-Piperidinecarboxylic acid, 1-(3-boronobenzoyl)-, 3-ethyl ester
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