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CS-W001157 4
Total: USD 88.00

Fmoc-D-Phe(2-F)-OH

  • CAS No. 198545-46-9

  • Cat. No. CS-W011690
  • Purity≥95%
  • MDL No.MFCD00672553

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

Fmoc-D-Phe(2-F)-OH|CS-W011690

Structure of 198545-46-9

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General Information

  • CAS No. 198545-46-9
  • Cat. No. CS-W011690
  • Purity ≥95%
  • MDL No. MFCD00672553
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₄H₂₀FNO₄
  • Molecular Weight 405.42
  • Synonym(s) None
  • SMILES O=C([C@H](NC(OCC1C2=CC=CC=C2C3=CC=CC=C13)=O)CC4=CC=CC=C4F)O

Description

Fmoc-D-Phe(2-F)-OH features a fluorinated phenyl ring at the ortho position, enhancing electron-withdrawing character and metabolic stability. This D-amino acid derivative integrates seamlessly into peptide sequences, offering improved proteolytic resistance and structural rigidity in synthetic applications.

Application

Fmoc-D-Phe(2-F)-OH serves as a valuable building block in peptide synthesis, offering enhanced metabolic stability and modulated hydrophobicity through the 2-fluorophenyl substitution. The Fmoc group enables efficient solution-phase and solid-phase coupling with minimal epimerization, while the D-configured amino acid provides stereochemical control. This derivative facilitates the incorporation of fluorinated aromatic residues into bioactive peptides, supporting structural diversification in medicinal chemistry campaigns.

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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

Quality Control

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Computational Chemistry Data

  • TPSA   75.63
  • LogP   4.3601
  • H_Acceptors   3
  • H_Donors   2
  • Rotatable_Bonds   6

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