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(R)-1-((Benzyloxy)carbonyl)piperidine-2-carboxylic acid

  • CAS No. 28697-09-8

  • Cat. No. CS-0199076
  • Purity≥98%
  • MDL No.None

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

(R)-1-((Benzyloxy)carbonyl)piperidine-2-carboxylic acid|CS-0199076

Structure of 28697-09-8

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General Information

  • CAS No. 28697-09-8
  • Cat. No. CS-0199076
  • Purity ≥98%
  • MDL No. None
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₄H₁₇NO₄
  • Molecular Weight 263.29
  • Synonym(s) 1,2-piperidinedicarboxylic acid, 1-(phenylmethyl) ester, (2R)-
  • SMILES C1=CC=C(C=C1)COC(=O)N2CCCC[C@@H]2C(=O)O

Description

This chiral piperidine derivative features a benzyl-protected carboxylic acid group, enabling straightforward deprotection and functionalization. The (R)-configuration ensures stereochemical fidelity in asymmetric synthesis, while the benzyloxycarbonyl moiety provides stability and compatibility with standard peptide coupling protocols.

Application

(R)-1-((Benzyloxy)carbonyl)piperidine-2-carboxylic acid serves as a valuable chiral building block in medicinal chemistry, enabling the synthesis of bioactive heterocycles and peptidomimetics. Its bench-stable Boc-like protecting group facilitates orthogonal deprotection strategies, while the piperidine core supports diverse functionalization. The molecule exhibits excellent compatibility with standard coupling reactions and is well-suited for iterative synthesis workflows in API development.

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   66.84
  • LogP   2.2623
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   3

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