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CS-W001157 4
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Sodium 1-(prop-2-enoyl)piperidine-4-carboxylate

  • CAS No. 1423031-89-3

  • Cat. No. CS-0198932
  • Molecule weight205.19
  • Purity≥97%
  • MDL No.MFCD22421872

*For research and further manufacturing use only, not for direct human use.

Sodium 1-(prop-2-enoyl)piperidine-4-carboxylate|CS-0198932

Structure of 1423031-89-3

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General Information

  • CAS No. 1423031-89-3
  • Cat. No. CS-0198932
  • Purity ≥97%
  • MDL No. MFCD22421872
  • Storage 4°C, sealed storage, away from moisture
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₉H₁₂NNaO₃
  • Molecular Weight 205.19
  • Synonym(s) None
  • SMILES O=C(O[Na])C1CCN(CC1)C(C=C)=O

Description

Sodium 1-(prop-2-enoyl)piperidine-4-carboxylate features a conjugated enamide system linked to a piperidine scaffold, enabling efficient Michael addition reactions. The carboxylate counterion enhances solubility in polar solvents, facilitating use in aqueous or mixed solvent systems. This stable, bench-ready reagent integrates readily into synthetic sequences requiring nucleophilic attack at α,β-unsaturated carbonyls.

Application

Sodium 1-(prop-2-enoyl)piperidine-4-carboxylate serves as a versatile building block in synthetic organic chemistry, enabling efficient construction of bioactive heterocycles and peptide-like scaffolds. Its conjugated enamide functionality facilitates Michael additions, cycloadditions, and palladium-catalyzed couplings under mild conditions. The carboxylate counterion enhances solubility and stability, simplifying purification and handling in aqueous or mixed solvent systems. This reagent is particularly valuable for late-stage functionalization and scaffold diversification in medicinal chemistry workflows.

Safety Information

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Computational Chemistry Data

  • TPSA   46.61
  • LogP   0.0377
  • H_Acceptors   3
  • H_Donors   0
  • Rotatable_Bonds   2

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