Boc-D-Tyr(Bzl)-OH

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Reagent Code: #50469
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CAS Number 63769-58-4

science Other reagents with same CAS 63769-58-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 371.43 g/mol
Formula C₂₁H₂₅NO₅
badge Registry Numbers
MDL Number MFCD00038249
thermostat Physical Properties
Boiling Point 552.4°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This chemical is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for creating complex peptides, ensuring the tyrosine residue remains unaffected during the reaction process. Its application is crucial in pharmaceutical research, particularly in developing peptide-based drugs and therapeutic agents. The Boc (tert-butoxycarbonyl) group provides stability, while the Bzl (benzyl) group protects the hydroxyl function of tyrosine, allowing selective deprotection and modification in subsequent steps. This compound is especially valuable in solid-phase peptide synthesis, enabling the production of high-purity peptides for biological studies and drug development.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿495.00
inventory 25g
10-20 days ฿8,136.00
inventory 5g
10-20 days ฿1,998.00
inventory 10g
10-20 days ฿3,744.00

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Boc-D-Tyr(Bzl)-OH
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This chemical is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for creating complex peptides, ensuring the tyrosine residue remains unaffected during the reaction process. Its application is crucial in pharmaceutical research, particularly in developing peptide-based drugs and therapeutic agents. The Boc (tert-butoxycarbonyl) group provides stability, while the Bzl (benzyl) group protects the hydroxyl function of tyrosine, allowing selective deprotec
This chemical is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for creating complex peptides, ensuring the tyrosine residue remains unaffected during the reaction process. Its application is crucial in pharmaceutical research, particularly in developing peptide-based drugs and therapeutic agents. The Boc (tert-butoxycarbonyl) group provides stability, while the Bzl (benzyl) group protects the hydroxyl function of tyrosine, allowing selective deprotection and modification in subsequent steps. This compound is especially valuable in solid-phase peptide synthesis, enabling the production of high-purity peptides for biological studies and drug development.
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