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CS-W001157 4
Total: USD 88.00

Fmoc-Lys(Fmoc)-OH

  • CAS No. 78081-87-5

  • Cat. No. CS-W008386
  • Purity≥97%
  • MDL No.MFCD00080275

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

Fmoc-Lys(Fmoc)-OH|CS-W008386

Structure of 78081-87-5

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General Information

  • CAS No. 78081-87-5
  • Cat. No. CS-W008386
  • Purity ≥97%
  • MDL No. MFCD00080275
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₃₆H₃₄N₂O₆
  • Molecular Weight 590.66
  • Synonym(s) None
  • SMILES O=C(OCC1C2=C(C3=C1C=CC=C3)C=CC=C2)NCCCC[C@@H](C(O)=O)NC(OCC4C5=C(C6=C4C=CC=C6)C=CC=C5)=O

Description

Fmoc-Lys(Fmoc)-OH is a bifunctional amino acid derivative featuring two Fmoc groups flanking a lysine backbone, enabling efficient incorporation into solid-phase peptide synthesis. The dual protecting groups provide orthogonal deprotection capability, simplifying the construction of complex peptides with multiple lysine residues. This variant offers enhanced solubility and stability under standard bench conditions.

Application

Fmoc-Lys(Fmoc)-OH serves as a key building block in peptide synthesis, enabling the incorporation of lysine residues with orthogonal protection. The Fmoc group on the α-amino terminus allows for mild base-labile deprotection, while the side-chain Boc-like Fmoc protection ensures selective functionalization. This dual protection facilitates efficient coupling and stepwise assembly of complex peptides, offering excellent stability and ease of purification in solid-phase workflows.

Safety Information

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Computational Chemistry Data

  • TPSA   113.96
  • LogP   6.6873
  • H_Acceptors   5
  • H_Donors   3
  • Rotatable_Bonds   11

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