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CAS 287196-80-9

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2,6-dichloro-4-(piperidin-1-ylcarbonyl)pyridine

Description:
2,6-Dichloro-4-(piperidin-1-ylcarbonyl)pyridine is a chemical compound characterized by its pyridine ring substituted with two chlorine atoms at the 2 and 6 positions and a piperidinylcarbonyl group at the 4 position. This structure contributes to its potential biological activity and makes it of interest in medicinal chemistry. The presence of the piperidine moiety may enhance its lipophilicity and ability to interact with biological targets, potentially influencing its pharmacological properties. The compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its synthesis often involves multi-step reactions, including halogenation and carbonylation processes. As with many chlorinated compounds, it is essential to handle this substance with care due to potential toxicity and environmental concerns. The compound's specific applications and efficacy would depend on ongoing research and development, particularly in the context of drug discovery and development.
Formula:C11H12Cl2N2O
InChI:InChI=1/C11H12Cl2N2O/c12-9-6-8(7-10(13)14-9)11(16)15-4-2-1-3-5-15/h6-7H,1-5H2
SMILES:C1CCN(CC1)C(=O)c1cc(Cl)nc(c1)Cl
Synonyms:
  • (2,6-Dichloropyridin-4-yl)(piperidin-1-yl)methanone
  • Methanone, (2,6-Dichloro-4-Pyridinyl)-1-Piperidinyl-
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