Z-Trp-OMe

≥95%

Reagent Code: #38062
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CAS Number 2717-76-2

science Other reagents with same CAS 2717-76-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 352.38 g/mol
Formula C₂₀H₂₀N₂O₄
badge Registry Numbers
MDL Number MFCD06658545
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

Z-Trp-OMe is widely used in peptide synthesis as a protecting group for tryptophan. The Z group (benzyloxycarbonyl) safeguards the amino group during the coupling reactions, while the methyl ester protects the carboxyl group, ensuring selective reactions in peptide chain assembly. It is particularly valuable in solid-phase peptide synthesis (SPPS) and solution-phase methods, where controlled deprotection steps are crucial. Additionally, it finds application in the preparation of modified peptides and peptidomimetics for drug discovery and biochemical research, enabling the study of peptide structure-activity relationships. Its stability under various reaction conditions makes it a reliable choice in complex synthetic pathways.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿315.00
inventory 5g
10-20 days ฿1,656.00
inventory 1g
10-20 days ฿621.00

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Z-Trp-OMe
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Z-Trp-OMe is widely used in peptide synthesis as a protecting group for tryptophan. The Z group (benzyloxycarbonyl) safeguards the amino group during the coupling reactions, while the methyl ester protects the carboxyl group, ensuring selective reactions in peptide chain assembly. It is particularly valuable in solid-phase peptide synthesis (SPPS) and solution-phase methods, where controlled deprotection steps are crucial. Additionally, it finds application in the preparation of modified peptides and pep

Z-Trp-OMe is widely used in peptide synthesis as a protecting group for tryptophan. The Z group (benzyloxycarbonyl) safeguards the amino group during the coupling reactions, while the methyl ester protects the carboxyl group, ensuring selective reactions in peptide chain assembly. It is particularly valuable in solid-phase peptide synthesis (SPPS) and solution-phase methods, where controlled deprotection steps are crucial. Additionally, it finds application in the preparation of modified peptides and peptidomimetics for drug discovery and biochemical research, enabling the study of peptide structure-activity relationships. Its stability under various reaction conditions makes it a reliable choice in complex synthetic pathways.

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