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CS-W001157 4
Total: USD 88.00

Fmoc-L-Phe(3-NH2)-OH

  • CAS No. 223581-75-7

  • Cat. No. CS-0439326
  • Purity≥95%
  • MDL No.None

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

Fmoc-L-Phe(3-NH2)-OH|CS-0439326

Structure of 223581-75-7

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General Information

  • CAS No. 223581-75-7
  • Cat. No. CS-0439326
  • Purity ≥95%
  • MDL No. None
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₄H₂₂N₂O₄
  • Molecular Weight 402.44
  • Synonym(s) (S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-(3-aminoph
  • SMILES C(OC(N[C@@H](CC1=CC(N)=CC=C1)C(O)=O)=O)C2C=3C(C=4C2=CC=CC4)=CC=CC3

Description

Fmoc-L-Phe(3-NH2)-OH features a para-amino-substituted phenylalanine residue with an Fmoc protecting group, enabling efficient solid-phase peptide synthesis. The electron-rich aromatic ring and amine-functionalized side chain facilitate coupling reactions while maintaining stability under standard conditions.

Application

Fmoc-L-Phe(3-NH2)-OH serves as a key building block for the synthesis of peptide conjugates and peptidomimetics, leveraging the ortho-amino functionality for site-specific derivatization. The Fmoc group enables efficient solid-phase peptide synthesis, while the 3-aminophenyl side chain provides a versatile handle for bioconjugation and heterocycle formation. This derivative exhibits excellent bench stability, facilitates straightforward purification, and is compatible with standard coupling protocols in medicinal chemistry workflows.

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 : H315-H319-H335
Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501

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Computational Chemistry Data

  • TPSA   101.65
  • LogP   3.8032
  • H_Acceptors   4
  • H_Donors   3
  • Rotatable_Bonds   6

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