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(S)-3-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-fluorophenyl)propanoic acid

  • CAS No. 479064-89-6

  • Cat. No. CS-0062182
  • Purity≥97%
  • MDL No.None

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

(S)-3-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-fluorophenyl)propanoic acid|CS-0062182

Structure of 479064-89-6

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General Information

  • CAS No. 479064-89-6
  • Cat. No. CS-0062182
  • Purity ≥97%
  • MDL No. None
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₄H₂₀FNO₄
  • Molecular Weight 405.42
  • Synonym(s) Fmoc-S-3-Amino-3-(4-fluoro-phenyl)-propionic acid
  • SMILES O=C(O)C[C@@H](C1=CC=C(F)C=C1)NC(OCC2C3=CC=CC=C3C4=CC=CC=C42)=O

Description

This chiral fluorenonyl-protected amino acid derivative features a sterically hindered, electron-deficient aryl group and a bench-stable carbamate handle. It integrates seamlessly into solid-phase peptide synthesis workflows, enabling efficient incorporation of fluorinated phenylalanine analogs with high enantiocontrol.

Application

(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-fluorophenyl)propanoic acid serves as a robust chiral building block for the synthesis of biologically active peptides and pharmaceutical intermediates. The Fmoc-protected amino group enables efficient solid-phase peptide synthesis, while the 4-fluorophenyl side chain provides structural rigidity and favorable pharmacokinetic properties. Its bench-stable nature and compatibility with standard coupling conditions facilitate reliable purification and scalable processing 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-H312-H332
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P501

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Computational Chemistry Data

  • TPSA   75.63
  • LogP   4.8802
  • H_Acceptors   3
  • H_Donors   2
  • Rotatable_Bonds   6

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