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CS-W001157 4
Total: USD 88.00

Fmoc-Phe-OSu

  • CAS No. 101214-43-1

  • Cat. No. CS-0149751
  • Purity≥95%
  • MDL No.MFCD00062204

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

Fmoc-Phe-OSu|CS-0149751

Structure of 101214-43-1

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General Information

  • CAS No. 101214-43-1
  • Cat. No. CS-0149751
  • Purity ≥95%
  • MDL No. MFCD00062204
  • Storage -20°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₈H₂₄N₂O₆
  • Molecular Weight 484.50
  • Synonym(s) None
  • SMILES O=C(ON1C(CCC1=O)=O)[C@@H](NC(OCC2C3=CC=CC=C3C4=CC=CC=C42)=O)CC5=CC=CC=C5

Description

Fmoc-Phe-OSu delivers a protected phenylalanine residue with high reactivity for peptide coupling. The Fmoc group enables efficient orthogonal deprotection, while the OSu ester facilitates rapid amide bond formation under mild conditions. This reagent integrates seamlessly into solid-phase synthesis workflows, offering reliable incorporation with minimal racemization.

Application

Fmoc-Phe-OSu serves as a robust amino acid derivative for solid-phase peptide synthesis, enabling efficient coupling of phenylalanine residues under mild conditions. The Fmoc group provides orthogonal protection, while the OSu (N-hydroxysuccinimide ester) moiety ensures high reactivity with primary amines. Its stability in storage and ease of purification make it ideal for routine use in peptide assembly workflows.

Synthesis

  • Route1

    References

    • Bioorganic and Medicinal Chemistry Letters, , vol. 18, # 20 p. 5559 - 5562
  • Route2

    References

    • Journal of Pharmaceutical Sciences, , vol. 83, # 7 p. 999 - 1005

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-P280-P302+P352

Quality Control

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Computational Chemistry Data

  • TPSA   102.01
  • LogP   3.7436
  • H_Acceptors   6
  • H_Donors   1
  • Rotatable_Bonds   7

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