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CS-W001157 4
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Fmoc-N-Me-HomoPhe-OH

  • CAS No. 1065076-30-3

  • Cat. No. CS-0372410
  • Purity≥97%
  • MDL No.None

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

Fmoc-N-Me-HomoPhe-OH|CS-0372410

Structure of 1065076-30-3

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General Information

  • CAS No. 1065076-30-3
  • Cat. No. CS-0372410
  • Purity ≥97%
  • MDL No. None
  • Storage 4°C, sealed storage, away from moisture
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₆H₂₅NO₄
  • Molecular Weight 415.48
  • Synonym(s) None
  • SMILES OC([C@H](CCC1=CC=CC=C1)N(C)C(OCC2C3=CC=CC=C3C4=CC=CC=C42)=O)=O

Description

Fmoc-N-Me-HomoPhe-OH is a sterically hindered, bench-stable amino acid derivative featuring a methoxy-substituted phenylalanine backbone. This N-methylated variant enhances membrane permeability and resistance to enzymatic degradation, making it ideal for solid-phase peptide synthesis of bioactive sequences requiring improved stability and lipophilicity.

Application

Fmoc-N-Me-HomoPhe-OH serves as a valuable building block in peptide synthesis, enabling the incorporation of N-methylated homophenylalanine residues with enhanced metabolic stability. The Fmoc group provides orthogonal protection for the α-amino function, while the N-methyl substitution reduces hydrogen-bonding capacity and improves membrane permeability. This derivative exhibits excellent bench stability, facilitates efficient coupling under standard conditions, and supports straightforward purification via flash chromatography.

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

Quality Control

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Computational Chemistry Data

  • TPSA   66.84
  • LogP   4.9533
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   7

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