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CAS 1272756-00-9

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1-(1,1-Dimethylethyl) 3-ethyl 5-hydroxy-1,3-piperidinedicarboxylate

Description:
1-(1,1-Dimethylethyl) 3-ethyl 5-hydroxy-1,3-piperidinedicarboxylate, identified by its CAS number 1272756-00-9, is a chemical compound characterized by its piperidine structure, which includes two carboxylate groups and a hydroxyl group. This compound features a tert-butyl group (1,1-dimethylethyl) and an ethyl group, contributing to its hydrophobic characteristics. The presence of the hydroxyl group suggests potential for hydrogen bonding, which may influence its solubility and reactivity. The piperidine ring structure typically imparts basic properties, making it a potential candidate for various chemical reactions, including nucleophilic substitutions. Its unique combination of functional groups may also suggest applications in medicinal chemistry, particularly in the development of pharmaceuticals. However, specific physical properties such as melting point, boiling point, and solubility would require empirical data for precise characterization. Overall, this compound's structural features indicate a versatile chemical behavior, suitable for further exploration in synthetic and medicinal chemistry contexts.
Formula:C13H23NO5
InChI:InChI=1S/C13H23NO5/c1-5-18-11(16)9-6-10(15)8-14(7-9)12(17)19-13(2,3)4/h9-10,15H,5-8H2,1-4H3
InChI key:InChIKey=JZPKVZMVVCCMSR-UHFFFAOYSA-N
SMILES:C(OC(C)(C)C)(=O)N1CC(C(OCC)=O)CC(O)C1
Synonyms:
  • 1,3-Piperidinedicarboxylic acid, 5-hydroxy-, 1-(1,1-dimethylethyl) 3-ethyl ester
  • 1-(1,1-Dimethylethyl) 3-ethyl 5-hydroxy-1,3-piperidinedicarboxylate
  • 1-tert-Butyl 3-ethyl 5-hydroxypiperidine-1,3-dicarboxylate
  • 1-tert-butyl 3-ethyl 5-Hydroxypiperidine-1,3-dicarboxylic acid
  • Ethyl N-Boc-5-hydroxypiperidine-3-carboxylate
  • Ethyl N-tert-butoxycarbonyl-5-hydroxypiperidine-3-carboxylate
  • 5-Hydroxy-1,3-piperidinedicarboxylic acid 1-(1,1-dimethylethyl) 3-ethyl ester
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