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CAS 1246471-48-6

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Ethyl 1-(6-chloro-3-pyridazinyl)-4-piperidineacetate

Description:
Ethyl 1-(6-chloro-3-pyridazinyl)-4-piperidineacetate is a chemical compound characterized by its unique structure, which includes an ethyl ester functional group and a piperidine ring. The presence of a pyridazine moiety, specifically a 6-chloro substitution, contributes to its potential biological activity. This compound is typically classified as an organic heterocyclic compound due to the incorporation of nitrogen atoms in its ring structures. Its molecular formula reflects a combination of carbon, hydrogen, chlorine, and nitrogen, indicating a moderate level of complexity. Ethyl 1-(6-chloro-3-pyridazinyl)-4-piperidineacetate may exhibit properties such as solubility in organic solvents and potential reactivity with various nucleophiles, making it of interest in medicinal chemistry and drug development. The specific characteristics, including melting point, boiling point, and spectral data, would require empirical determination or reference to specialized databases for precise values. Overall, this compound's structural features suggest it could be investigated for pharmacological applications, particularly in the context of neuroactive or anti-inflammatory agents.
Formula:C13H18ClN3O2
InChI:InChI=1S/C13H18ClN3O2/c1-2-19-13(18)9-10-5-7-17(8-6-10)12-4-3-11(14)15-16-12/h3-4,10H,2,5-9H2,1H3
InChI key:InChIKey=OJTDRIHFGFJLBA-UHFFFAOYSA-N
SMILES:C(C(OCC)=O)C1CCN(CC1)C2=CC=C(Cl)N=N2
Synonyms:
  • 4-Piperidineacetic acid, 1-(6-chloro-3-pyridazinyl)-, ethyl ester
  • Ethyl 1-(6-chloro-3-pyridazinyl)-4-piperidineacetate
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