BOC-L-TYR(ALL)-OH

95%

Reagent Code: #104833
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CAS Number 127132-38-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 321.3682 g/mol
Formula C₁₇H₂₃NO₅
badge Registry Numbers
MDL Number MFCD00273424
thermostat Physical Properties
Melting Point 76-77 °C
Boiling Point 490.39 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.145 g/cm3
Storage 2-8°C

description Product Description

This compound is primarily used in peptide synthesis as a protected amino acid derivative. The BOC (tert-butoxycarbonyl) group serves as a protective group for the amine functionality, while the ALL (allyl) group protects the hydroxyl group of the tyrosine side chain. This dual protection allows for selective deprotection during peptide synthesis, enabling the controlled assembly of peptide chains. It is particularly useful in solid-phase peptide synthesis (SPPS) where sequential deprotection and coupling steps are required. The compound’s stability under various reaction conditions makes it a valuable reagent in the production of complex peptides and proteins for research, pharmaceuticals, and biotechnology applications.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,223.00
inventory 5g
10-20 days ฿8,334.00
BOC-L-TYR(ALL)-OH
This compound is primarily used in peptide synthesis as a protected amino acid derivative. The BOC (tert-butoxycarbonyl) group serves as a protective group for the amine functionality, while the ALL (allyl) group protects the hydroxyl group of the tyrosine side chain. This dual protection allows for selective deprotection during peptide synthesis, enabling the controlled assembly of peptide chains. It is particularly useful in solid-phase peptide synthesis (SPPS) where sequential deprotection and coupling steps are required. The compound’s stability under various reaction conditions makes it a valuable reagent in the production of complex peptides and proteins for research, pharmaceuticals, and biotechnology applications.
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