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(2S,5R)-Ethyl 5-((benzyloxy)amino)piperidine-2-carboxylate oxalate

  • CAS No. 1416134-48-9

  • Cat. No. CS-M3476
  • Purity≥98%
  • MDL No.None

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

(2S,5R)-Ethyl 5-((benzyloxy)amino)piperidine-2-carboxylate oxalate|CS-M3476

Structure of 1416134-48-9

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General Information

  • CAS No. 1416134-48-9
  • Cat. No. CS-M3476
  • Purity ≥98%
  • MDL No. None
  • Storage 4°C, sealed storage, away from moisture
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₇H₂₄N₂O₇
  • Molecular Weight 368.38
  • Synonym(s) ethyl(2S,5R)-5-((benzyloxy)amino)piperdine-2-carboxylate oxalate
  • SMILES O=C(OCC)[C@@H](NC1)CC[C@H]1NOCC2=CC=CC=C2.OC(C(O)=O)=O

Description

This chiral piperidine derivative features a bench-stable oxalate salt form and a benzyloxyamino handle for orthogonal functionalization. The (2S,5R) stereochemistry enables precise control in asymmetric synthesis, while the ethyl ester facilitates downstream transformations.

Application

(2S,5R)-Ethyl 5-((benzyloxy)amino)piperidine-2-carboxylate oxalate serves as a stereochemically defined piperidine scaffold for medicinal chemistry applications. The benzyloxycarbonyl-protected amine enables orthogonal deprotection, while the ethyl ester facilitates downstream functionalization. Its oxalate salt enhances crystallinity and bench stability, simplifying purification and handling in multi-step syntheses.

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   134.19
  • LogP   0.5471
  • H_Acceptors   7
  • H_Donors   4
  • Rotatable_Bonds   6

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