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CS-W001157 4
Total: USD 88.00

Fmoc-Oic-OH

  • CAS No. 130309-37-4

  • Cat. No. CS-W022729
  • Purity≥98%
  • MDL No.MFCD09750487

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

Fmoc-Oic-OH|CS-W022729

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General Information

  • CAS No. 130309-37-4
  • Cat. No. CS-W022729
  • Purity ≥98%
  • MDL No. MFCD09750487
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₄H₂₅NO₄
  • Molecular Weight 391.47
  • Synonym(s) None
  • SMILES O=C(O)[C@H]1N([C@]2(CCCC[C@]2(C1)[H])[H])C(OCC3C4=C(C=CC=C4)C5=C3C=CC=C5)=O

Description

Fmoc-Oic-OH is a protected amino acid derivative featuring a fluorinated indole side chain, designed for efficient incorporation into peptide sequences. This scaffold enhances backbone stability and provides unique steric and electronic profiles beneficial in bioactive peptide design. The Fmoc group enables straightforward solid-phase synthesis under standard conditions.

Application

Fmoc-Oic-OH serves as a valuable building block in peptide synthesis, enabling the incorporation of ortho-iodophenylalanine residues with high fidelity. The Fmoc group provides excellent protection for the amine, allowing for efficient stepwise elongation under standard coupling conditions. The ortho-iodinated aromatic side chain offers a versatile handle for subsequent palladium-catalyzed transformations, facilitating site-specific modifications in complex peptide architectures. Its bench stability and compatibility with common purification methods make it a practical choice for synthetic applications requiring functionalized amino acid units.

Safety Information

Download SDS
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

Quality Control

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Computational Chemistry Data

  • TPSA   66.84
  • LogP   4.6532
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   3

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