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CAS 206446-49-3

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1,1-Dimethylethyl 4-(2-pyridinyl)-1-piperidinecarboxylate

Description:
1,1-Dimethylethyl 4-(2-pyridinyl)-1-piperidinecarboxylate, with the CAS number 206446-49-3, is a chemical compound characterized by its unique structure, which includes a piperidine ring and a pyridine moiety. This compound typically exhibits properties associated with both heterocyclic and aliphatic compounds, making it of interest in various chemical applications, particularly in medicinal chemistry. It is likely to be a solid at room temperature, with moderate solubility in organic solvents due to the presence of both polar and non-polar functional groups. The presence of the dimethyl group contributes to steric hindrance, which can influence its reactivity and interaction with biological targets. Additionally, the pyridine ring may impart basicity and potential for coordination with metal ions, enhancing its utility in coordination chemistry. Overall, this compound's structural features suggest potential applications in drug development and synthesis, particularly in the design of compounds targeting specific biological pathways.
Formula:C15H22N2O2
InChI:InChI=1S/C15H22N2O2/c1-15(2,3)19-14(18)17-10-7-12(8-11-17)13-6-4-5-9-16-13/h4-6,9,12H,7-8,10-11H2,1-3H3
InChI key:InChIKey=ZTQIVJVEVSAJMX-UHFFFAOYSA-N
SMILES:C(OC(C)(C)C)(=O)N1CCC(CC1)C2=CC=CC=N2
Synonyms:
  • 3′,4′,5′,6′-Tetrahydro-2′H-[2,4′]bipyridinyl-1′-carboxylic acid tert-butyl ester
  • 1-Piperidinecarboxylic acid, 4-(2-pyridinyl)-, 1,1-dimethylethyl ester
  • 1,1-Dimethylethyl 4-(2-pyridinyl)-1-piperidinecarboxylate
  • tert-Butyl 4-(pyridin-2-yl)piperidine-1-carboxylate
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