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CS-W001157 4
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Fmoc-L-Trp(5-Me)-OH

  • CAS No. 460751-68-2

  • Cat. No. CS-0798723
  • Purity≥98%
  • MDL No.None

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

Fmoc-L-Trp(5-Me)-OH|CS-0798723

Structure of 460751-68-2

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General Information

  • CAS No. 460751-68-2
  • Cat. No. CS-0798723
  • Purity ≥98%
  • MDL No. None
  • Storage 4°C, sealed storage, away from moisture
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₇H₂₄N₂O₄
  • Molecular Weight 440.49
  • Synonym(s) None
  • SMILES C(OC(N[C@@H](CC=1C=2C(NC1)=CC=C(C)C2)C(O)=O)=O)C3C=4C(C=5C3=CC=CC5)=CC=CC4

Description

Fmoc-L-Trp(5-Me)-OH features a methoxy-substituted indole ring, enhancing electron density and stability in solid-phase peptide synthesis. This bench-stable derivative simplifies incorporation of modified tryptophan residues, offering improved solubility and reduced side reactions during coupling steps.

Application

Fmoc-L-Trp(5-Me)-OH serves as a key building block in peptide synthesis, enabling the incorporation of 5-methyltryptophan into polypeptide chains. The Fmoc group provides orthogonal protection for the α-amino function, facilitating efficient stepwise elongation under standard solid-phase conditions. The 5-methyl substitution enhances metabolic stability and modulates electronic properties, offering utility in bioactive peptide design and structural probing studies. The compound exhibits excellent bench stability and compatibility with common coupling reagents.

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
Precautionary Statements : P264-P270-P280-P302+P352-P305+P351+P338-P330-P362+P364-P501

Quality Control

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Computational Chemistry Data

  • TPSA   91.42
  • LogP   5.01072
  • H_Acceptors   3
  • H_Donors   3
  • Rotatable_Bonds   6

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