N-Fmoc-5-methoxy-L-tryptophan

98%

Reagent Code: #219262
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CAS Number 460751-69-3

science Other reagents with same CAS 460751-69-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 456.49 g/mol
Formula C₂₇H₂₄N₂O₅
badge Registry Numbers
MDL Number MFCD28166522
thermostat Physical Properties
Melting Point 82-85 °C
Boiling Point 734.2±60.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.343±0.06 g/cm3(Predicted)
Storage 2-8°C, away from light, dry

description Product Description

Used in solid-phase peptide synthesis, particularly for constructing peptides containing modified tryptophan residues. The 5-methoxy group enhances stability and modulates the electronic properties of the indole ring, which can improve peptide solubility and influence biological activity. The Fmoc protection allows for orthogonal protection strategies, enabling stepwise assembly of complex peptides under mild basic conditions. Commonly employed in the synthesis of bioactive peptides and peptide-based pharmaceuticals where tryptophan modifications affect receptor binding or metabolic stability.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,950.00
inventory 250mg
10-20 days ฿4,750.00
inventory 1g
10-20 days ฿12,150.00
inventory 5g
10-20 days ฿37,260.00
N-Fmoc-5-methoxy-L-tryptophan
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Used in solid-phase peptide synthesis, particularly for constructing peptides containing modified tryptophan residues. The 5-methoxy group enhances stability and modulates the electronic properties of the indole ring, which can improve peptide solubility and influence biological activity. The Fmoc protection allows for orthogonal protection strategies, enabling stepwise assembly of complex peptides under mild basic conditions. Commonly employed in the synthesis of bioactive peptides and peptide-based pha

Used in solid-phase peptide synthesis, particularly for constructing peptides containing modified tryptophan residues. The 5-methoxy group enhances stability and modulates the electronic properties of the indole ring, which can improve peptide solubility and influence biological activity. The Fmoc protection allows for orthogonal protection strategies, enabling stepwise assembly of complex peptides under mild basic conditions. Commonly employed in the synthesis of bioactive peptides and peptide-based pharmaceuticals where tryptophan modifications affect receptor binding or metabolic stability.

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