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(R)-Methyl piperidine-3-carboxylate hydrochloride

  • CAS No. 1255651-12-7

  • Cat. No. CS-0040391
  • Molecule weight179.64
  • Purity≥97%
  • MDL No.MFCD08274539

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

(R)-Methyl piperidine-3-carboxylate hydrochloride|CS-0040391

Structure of 1255651-12-7

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General Information

  • CAS No. 1255651-12-7
  • Cat. No. CS-0040391
  • Purity ≥97%
  • MDL No. MFCD08274539
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₁₄ClNO₂
  • Molecular Weight 179.64
  • Synonym(s) Methyl (R)-Piperidine-3-carboxylate Hydrochloride
  • SMILES O=C([C@H]1CNCCC1)OC.[H]Cl

Description

(R)-Methyl piperidine-3-carboxylate hydrochloride is a chiral building block featuring a stereochemically defined piperidine core with a methyl ester group at the 3-position. This bench-stable salt form enhances solubility and handling in synthetic workflows, enabling efficient incorporation into complex molecular architectures.

Application

(R)-Methyl piperidine-3-carboxylate hydrochloride serves as a chiral building block for the synthesis of bioactive molecules, particularly in medicinal chemistry and asymmetric catalysis. The piperidine core provides structural rigidity and favorable pharmacokinetic properties, while the methyl ester offers a versatile handle for further derivatization. Bench-stable and readily purified, it functions effectively in standard coupling reactions and reductive amination protocols, enabling efficient access to complex heterocyclic scaffolds.

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

  • TPSA   38.33
  • LogP   0.5808
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   1

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