N-alpha-Boc-L-tryptophan amide

99%

Reagent Code: #215387
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CAS Number 62549-92-2

science Other reagents with same CAS 62549-92-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 303.36 g/mol
Formula C₁₆H₂₁N₃O₃
badge Registry Numbers
MDL Number MFCD00270519
thermostat Physical Properties
Boiling Point 573.9 °C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used in peptide synthesis as a protected intermediate, particularly in the production of pharmaceutical peptides where the indole ring and amino group need selective protection. The Boc (tert-butoxycarbonyl) group stabilizes the alpha-amine during coupling reactions, while the amide at the C-terminus can serve as a mimic for peptide bonds or as a precursor to C-terminal modified peptides. Commonly applied in solid-phase peptide synthesis and in the development of bioactive peptides with enhanced metabolic stability. Also utilized in research settings for studying receptor-ligand interactions involving tryptophan-containing sequences.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿8,990.00
1g
10-20 days ฿15,000.00
N-alpha-Boc-L-tryptophan amide
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Used in peptide synthesis as a protected intermediate, particularly in the production of pharmaceutical peptides where the indole ring and amino group need selective protection. The Boc (tert-butoxycarbonyl) group stabilizes the alpha-amine during coupling reactions, while the amide at the C-terminus can serve as a mimic for peptide bonds or as a precursor to C-terminal modified peptides. Commonly applied in solid-phase peptide synthesis and in the development of bioactive peptides with enhanced metaboli

Used in peptide synthesis as a protected intermediate, particularly in the production of pharmaceutical peptides where the indole ring and amino group need selective protection. The Boc (tert-butoxycarbonyl) group stabilizes the alpha-amine during coupling reactions, while the amide at the C-terminus can serve as a mimic for peptide bonds or as a precursor to C-terminal modified peptides. Commonly applied in solid-phase peptide synthesis and in the development of bioactive peptides with enhanced metabolic stability. Also utilized in research settings for studying receptor-ligand interactions involving tryptophan-containing sequences.

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