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(9H-Fluoren-9-yl)MethOxy]Carbonyl L-4-Acetylphe

  • CAS No. 204716-07-4

  • Cat. No. CS-0179063
  • Purity≥96%
  • MDL No.MFCD01317022

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

(9H-Fluoren-9-yl)MethOxy]Carbonyl L-4-Acetylphe|CS-0179063

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General Information

  • CAS No. 204716-07-4
  • Cat. No. CS-0179063
  • Purity ≥96%
  • MDL No. MFCD01317022
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₆H₂₃NO₅
  • Molecular Weight 429.46
  • Synonym(s) Fmoc-4-Acetyl-DL-phenylalanine
  • SMILES CC(C1=CC=C(C[C@H](NC(OCC2C3=CC=CC=C3C4=CC=CC=C42)=O)C(O)=O)C=C1)=O

Description

Fmoc-L-4-acetylphe is a protected amino acid derivative featuring a fluorenylmethoxy carbonyl (Fmoc) group at the N-terminus and an acetyl-modified side chain on the phenylalanine moiety. This combination enables stable incorporation into peptide synthesis workflows, where the Fmoc group facilitates orthogonal deprotection under mild basic conditions. The acetyl substitution enhances metabolic stability in bioactive peptide sequences.

Application

L-4-Acetylphe-(9H-Fluoren-9-yl)methyl ester serves as a stable, bench-ready amino acid building block for peptide synthesis. The fluorenylmethoxycarbonyl (Fmoc) group enables efficient orthogonal protection, while the acetyl side chain provides modulated reactivity and enhanced solubility. This derivative facilitates smooth coupling reactions, minimizes racemization, and simplifies purification—ideal for iterative solid-phase and solution-phase methodologies 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 : H302-H315-H319-H335
Precautionary Statements : P261-P280-P302+P352

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Computational Chemistry Data

  • TPSA   92.7
  • LogP   4.4236
  • H_Acceptors   4
  • H_Donors   2
  • Rotatable_Bonds   7

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