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CAS 72738-09-1

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4-Piperidinecarboxylic acid, 3-oxo-, ethyl ester, hydrochloride (1:1)

Description:
4-Piperidinecarboxylic acid, 3-oxo-, ethyl ester, hydrochloride (1:1) is a chemical compound characterized by its piperidine ring structure, which contributes to its basicity and potential biological activity. The presence of a carboxylic acid group and an ester functional group indicates that it can participate in various chemical reactions, such as esterification and hydrolysis. The hydrochloride salt form enhances its solubility in water, making it more accessible for biological and chemical applications. This compound may exhibit properties typical of piperidine derivatives, including potential use in pharmaceuticals, particularly as intermediates in the synthesis of biologically active molecules. Its molecular structure suggests it could interact with biological systems, possibly influencing neurotransmitter pathways or serving as a scaffold for drug development. Safety and handling precautions should be observed, as with all chemical substances, due to potential toxicity or reactivity. Further studies would be necessary to fully elucidate its pharmacological properties and applications.
Formula:C8H13NO3·ClH
InChI:InChI=1S/C8H13NO3.ClH/c1-2-12-8(11)6-3-4-9-5-7(6)10;/h6,9H,2-5H2,1H3;1H
InChI key:InChIKey=VMVUBCKFICINHZ-UHFFFAOYSA-N
SMILES:C(OCC)(=O)C1C(=O)CNCC1.Cl
Synonyms:
  • 4-(Ethoxycarbonyl)-3-oxopiperidinium chloride
  • 4-Piperidinecarboxylic acid, 3-oxo-, ethyl ester, hydrochloride
  • 4-Piperidinecarboxylic acid, 3-oxo-, ethyl ester, hydrochloride (1:1)
  • Ethyl 3-oxopiperidine-4-carboxylate HCl
  • 3-Oxo-4-piperidinecarboxylic acid ethyl ester hydrochloride
  • 4-Piperidinecarboxylicacid, 3-oxo-, ethyl ester
  • ethyl 3-oxopiperidin-1-ium-4-carboxylate
  • ethyl 3-oxopiperidine-4-carboxylate hydrochloride
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