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CS-W001157 4
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(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-phenylpropanoic acid

  • CAS No. 209252-15-3

  • Cat. No. CS-W011741
  • Purity≥98%
  • MDL No.MFCD01311759

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

(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-phenylpropanoic acid|CS-W011741

Structure of 209252-15-3

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General Information

  • CAS No. 209252-15-3
  • Cat. No. CS-W011741
  • Purity ≥98%
  • MDL No. MFCD01311759
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₄H₂₁NO₄
  • Molecular Weight 387.43
  • Synonym(s) Fmoc-S-3-Amino-3-phenylpropionic acid
  • SMILES O=C(C[C@@H](C1=CC=CC=C1)NC(OCC2C3=CC=CC=C3C4=CC=CC=C24)=O)O

Description

This fluorenylmethoxycarbonyl-protected amino acid derivative features a chiral benzylic center and a phenyl-substituted propanoic acid side chain, enabling selective incorporation into peptide sequences. The Cbz group provides robust protection under standard deprotection conditions while maintaining stability during synthetic manipulations.

Application

(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-phenylpropanoic acid serves as a robust chiral building block for peptide synthesis, enabling efficient incorporation of β-arylalanine motifs. The Fmoc group provides excellent stability under basic conditions and facilitates straightforward deprotection. Its bench-stable nature and compatibility with standard coupling protocols make it ideal for both manual and automated synthesis workflows in medicinal chemistry and peptide library development.

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

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Computational Chemistry Data

  • TPSA   75.63
  • LogP   4.7411
  • H_Acceptors   3
  • H_Donors   2
  • Rotatable_Bonds   6

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