(S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-methoxy-1H-indol-3-yl)propanoicacid

98%

Reagent Code: #237748
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CAS Number 1205553-56-5

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 456.49 g/mol
Formula C₂₇H₂₄N₂O₅
inventory_2 Storage & Handling
Storage Room temperature

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 allows for mild base-labile protection, enabling solid-phase peptide synthesis under basic conditions while preserving other sensitive functional groups. The 4-methoxyindole side chain enhances stability and modulates electronic properties, making it valuable in the preparation of bioactive peptides, particularly those targeting neurological receptors or studying protein–protein interactions. Its application is common in pharmaceutical research and development of peptide-based therapeutics.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,300.00
(S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-methoxy-1H-indol-3-yl)propanoicacid
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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 allows for mild base-labile protection, enabling solid-phase peptide synthesis under basic conditions while preserving other sensitive functional groups. The 4-methoxyindole side chain enhances stability and modulates electronic properties, making it valuable in the preparation of bioactive peptides, particularly those targeting

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 allows for mild base-labile protection, enabling solid-phase peptide synthesis under basic conditions while preserving other sensitive functional groups. The 4-methoxyindole side chain enhances stability and modulates electronic properties, making it valuable in the preparation of bioactive peptides, particularly those targeting neurological receptors or studying protein–protein interactions. Its application is common in pharmaceutical research and development of peptide-based therapeutics.

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