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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3-(1H-indol-3-yl)propanoic acid

  • CAS No. 112913-63-0

  • Cat. No. CS-0091374
  • Purity≥97%
  • MDL No.MFCD02682369

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

(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3-(1H-indol-3-yl)propanoic acid|CS-0091374

Structure of 112913-63-0

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General Information

  • CAS No. 112913-63-0
  • Cat. No. CS-0091374
  • Purity ≥97%
  • MDL No. MFCD02682369
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₇H₂₄N₂O₄
  • Molecular Weight 440.49
  • Synonym(s) FMOC-N-METHYL-L-TRYPTOPHAN
  • SMILES O=C(O)[C@H](CC1=CNC2=CC=CC=C12)N(C(OCC3C4=C(C5=C3C=CC=C5)C=CC=C4)=O)C

Application

(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3-(1H-indol-3-yl)propanoic acid serves as a robust chiral building block for peptide synthesis, enabling efficient incorporation of indole-containing side chains. The Fmoc-methylamine moiety provides excellent bench stability and facilitates straightforward deprotection under mild basic conditions. Its structure supports orthogonal functional group handling, making it ideal for constructing complex peptides and heterocyclic scaffolds in medicinal chemistry workflows.

Synthesis

  • Route1
    • null|null
      67-56-1
    • null|null
      28920-43-6
    • In-stock
      L-Trp-OH Amino acid impurity|CS-1733143
      73-22-3
    • ~%
    • In-stock
      (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3-(1H-indol-3-yl)propanoic acid|CS-0091374
      112913-63-0

    References

    • Tetrahedron Letters, , vol. 38, # 42 p. 7307 - 7310

Safety Information

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GHS Pictogram : N/A
GHS No : N/A
Signal Word : N/A
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Packing Group : N/A
Hazard Statements : N/A
Precautionary Statements : N/A

Quality Control

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Computational Chemistry Data

  • TPSA   82.63
  • LogP   5.0445
  • H_Acceptors   3
  • H_Donors   2
  • Rotatable_Bonds   6

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