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CS-W001157 4
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Fmoc-hLys(Alloc)-OH

  • CAS No. 281655-70-7

  • Cat. No. CS-0439416
  • Purity≥97%
  • MDL No.MFCD01860682

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

Fmoc-hLys(Alloc)-OH|CS-0439416

Structure of 281655-70-7

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General Information

  • CAS No. 281655-70-7
  • Cat. No. CS-0439416
  • Purity ≥97%
  • MDL No. MFCD01860682
  • Storage 4°C, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₆H₃₀N₂O₆
  • Molecular Weight 466.53
  • Synonym(s) None
  • SMILES C(OC(N[C@@H](CCCCCNC(OCC=C)=O)C(O)=O)=O)C1C=2C(C=3C1=CC=CC3)=CC=CC2

Description

Fmoc-hLys(Alloc)-OH is a protected lysine derivative designed for solid-phase peptide synthesis. The Fmoc group enables orthogonal Nα-deprotection, while the Alloc moiety provides a stable, removable side-chain protection. This combination supports efficient coupling and selective deprotection under palladium-catalyzed conditions, streamlining complex peptide assembly.

Application

Fmoc-hLys(Alloc)-OH serves as a protected lysine building block for solid-phase peptide synthesis, enabling site-selective incorporation of lysine residues with orthogonal functionality. The Fmoc group provides efficient N-terminal protection compatible with standard deprotection conditions, while the Alloc (allyloxycarbonyl) side chain protection allows for mild, palladium-catalyzed removal under neutral conditions. This orthogonal strategy facilitates selective modification during late-stage diversification, supporting the synthesis of complex peptides and peptidomimetics with high fidelity and minimal side reactions.

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-P330-P362+P364-P405-P501

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Computational Chemistry Data

  • TPSA   113.96
  • LogP   4.4509
  • H_Acceptors   5
  • H_Donors   3
  • Rotatable_Bonds   12

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