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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-(pyridin-3-yl)phenyl)propanoic acid

  • CAS No. 352525-25-8

  • Cat. No. CS-0169354
  • Purity≥97%
  • MDL No.None

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

(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-(pyridin-3-yl)phenyl)propanoic acid|CS-0169354

Structure of 352525-25-8

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General Information

  • CAS No. 352525-25-8
  • Cat. No. CS-0169354
  • Purity ≥97%
  • MDL No. None
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₉H₂₄N₂O₄
  • Molecular Weight 464.51
  • Synonym(s) N-Fmoc-4-(3-pyridinyl)-L-phenylalanine
  • SMILES O=C(O)[C@H](CC1=CC=C(C2=CC=CN=C2)C=C1)NC(OCC3C4=C(C5=C3C=CC=C5)C=CC=C4)=O

Description

(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-(pyridin-3-yl)phenyl)propanoic acid features a chiral α-amino acid core with a fluorenylmethoxycarbonyl (Fmoc) protecting group, enabling direct use in solid-phase peptide synthesis. The para-pyridinyl-substituted aryl side chain imparts enhanced solubility and stability under standard coupling conditions. This derivative integrates seamlessly into peptide chains with minimal epimerization risk.

Application

(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-(pyridin-3-yl)phenyl)propanoic acid serves as a valuable chiral building block in peptide synthesis and medicinal chemistry. The Fmoc group enables efficient solid-phase peptide coupling, while the phenylpyridine side chain provides a rigid, polar scaffold for drug discovery applications. Its bench-stable nature and compatibility with standard deprotection protocols facilitate reliable incorporation into complex molecular architectures.

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-P330-P362+P364-P405-P501

Quality Control

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Computational Chemistry Data

  • TPSA   88.52
  • LogP   5.283
  • H_Acceptors   4
  • H_Donors   2
  • Rotatable_Bonds   7

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