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(S)-3-(3-(Allyloxy)phenyl)-2-((tert-butoxycarbonyl)amino)propanoic acid,97%(stabilized with TBC)

  • CAS No. 1175919-93-3

  • Cat. No. CS-0157973
  • Purity97%(stabilized with TBC)
  • MDL No.None

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

(S)-3-(3-(Allyloxy)phenyl)-2-((tert-butoxycarbonyl)amino)propanoic acid,97%(stabilized with TBC)|CS-0157973

Structure of 1175919-93-3

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General Information

  • CAS No. 1175919-93-3
  • Cat. No. CS-0157973
  • Purity 97%(stabilized with TBC)
  • MDL No. None
  • Storage 4°C, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₇H₂₃NO₅
  • Molecular Weight 321.37
  • Synonym(s) 4-Allyloxy-N-Boc-L-phenylalanine
  • SMILES C=CCOC1=CC=CC(C[C@H](NC(OC(C)(C)C)=O)C(O)=O)=C1

Description

(S)-3-(3-(Allyloxy)phenyl)-2-((tert-butoxycarbonyl)amino)propanoic acid features a chiral center and a protected amine, enabling direct incorporation into peptide synthesis. The allyloxy group provides a handle for orthogonal functionalization, while the tert-butoxycarbonyl moiety ensures stability during handling and storage under standard conditions.

Application

(S)-3-(3-(Allyloxy)phenyl)-2-((tert-butoxycarbonyl)amino)propanoic acid serves as a valuable chiral building block for the synthesis of bioactive heterocycles and peptide-like scaffolds. The allyloxy group enables efficient post-functionalization via click chemistry or transition-metal-catalyzed coupling, while the Boc-protected amine offers orthogonal handling and stability during multi-step syntheses. Bench-stable and readily purified, this compound facilitates scalable access to complex molecular architectures in medicinal chemistry and process development workflows.

Safety Information

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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   84.86
  • LogP   2.7718
  • H_Acceptors   4
  • H_Donors   2
  • Rotatable_Bonds   7

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