(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(6-methyl-1H-indol-3-yl)propanoic acid

95%

Reagent Code: #237055
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CAS Number 908846-99-1

science Other reagents with same CAS 908846-99-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 440.49 g/mol
Formula C₂₇H₂₄N₂O₄
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Widely used in peptide synthesis, this compound serves as a protected amino acid derivative, specifically for incorporating tryptophan analogs into peptide chains. The Fmoc group provides orthogonal protection, allowing selective deprotection under mild basic conditions while maintaining stability during solid-phase synthesis. Its indole side chain enables the study of peptide interactions involving aromatic and hydrophobic residues. Commonly applied in the production of bioactive peptides, enzyme substrates, and pharmaceutical intermediates, especially in research targeting receptor ligands and signaling molecules. The stereochemistry ensures correct chiral configuration in the final peptide product, critical for biological activity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,090.00
inventory 250mg
10-20 days ฿16,730.00
inventory 1g
10-20 days ฿41,050.00
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(6-methyl-1H-indol-3-yl)propanoic acid
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Widely used in peptide synthesis, this compound serves as a protected amino acid derivative, specifically for incorporating tryptophan analogs into peptide chains. The Fmoc group provides orthogonal protection, allowing selective deprotection under mild basic conditions while maintaining stability during solid-phase synthesis. Its indole side chain enables the study of peptide interactions involving aromatic and hydrophobic residues. Commonly applied in the production of bioactive peptides, enzyme substr

Widely used in peptide synthesis, this compound serves as a protected amino acid derivative, specifically for incorporating tryptophan analogs into peptide chains. The Fmoc group provides orthogonal protection, allowing selective deprotection under mild basic conditions while maintaining stability during solid-phase synthesis. Its indole side chain enables the study of peptide interactions involving aromatic and hydrophobic residues. Commonly applied in the production of bioactive peptides, enzyme substrates, and pharmaceutical intermediates, especially in research targeting receptor ligands and signaling molecules. The stereochemistry ensures correct chiral configuration in the final peptide product, critical for biological activity.

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