Boc-Glu(Obzl)-OMe

95%

Reagent Code: #38575
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CAS Number 59279-58-2

science Other reagents with same CAS 59279-58-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 351.39 g/mol
Formula C₁₈H₂₅NO₆
badge Registry Numbers
MDL Number MFCD00190792
thermostat Physical Properties
Boiling Point 471.2±40.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is widely used in peptide synthesis as a protecting group for glutamic acid. The Boc (tert-butoxycarbonyl) group safeguards the amino group, while the Obzl (benzyl) ester protects the carboxyl side chain, and the OMe (methyl) ester protects the C-terminal carboxyl group. It is particularly valuable in solid-phase peptide synthesis (SPPS) to ensure selective deprotection and coupling reactions. Its stability under acidic conditions makes it suitable for sequential peptide assembly. Additionally, it is employed in the preparation of peptide-based drugs, bioactive peptides, and research tools for studying protein interactions and enzyme mechanisms.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,053.00
inventory 5g
10-20 days ฿3,654.00
inventory 10g
10-20 days ฿7,173.00

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Boc-Glu(Obzl)-OMe
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This compound is widely used in peptide synthesis as a protecting group for glutamic acid. The Boc (tert-butoxycarbonyl) group safeguards the amino group, while the Obzl (benzyl) ester protects the carboxyl side chain, and the OMe (methyl) ester protects the C-terminal carboxyl group. It is particularly valuable in solid-phase peptide synthesis (SPPS) to ensure selective deprotection and coupling reactions. Its stability under acidic conditions makes it suitable for sequential peptide assembly. Additiona

This compound is widely used in peptide synthesis as a protecting group for glutamic acid. The Boc (tert-butoxycarbonyl) group safeguards the amino group, while the Obzl (benzyl) ester protects the carboxyl side chain, and the OMe (methyl) ester protects the C-terminal carboxyl group. It is particularly valuable in solid-phase peptide synthesis (SPPS) to ensure selective deprotection and coupling reactions. Its stability under acidic conditions makes it suitable for sequential peptide assembly. Additionally, it is employed in the preparation of peptide-based drugs, bioactive peptides, and research tools for studying protein interactions and enzyme mechanisms.

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