Boc-N-Me-Glu(Obzl)-OH

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Reagent Code: #104828
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CAS Number 200615-91-4

science Other reagents with same CAS 200615-91-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 351.39 g/mol
Formula C₁₈H₂₅NO₆
badge Registry Numbers
MDL Number MFCD00038756
thermostat Physical Properties
Boiling Point 501 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

This chemical is widely used in peptide synthesis as a protected N-methyl-glutamic acid derivative. Its primary application is in the construction of peptides, where it serves as a building block to introduce N-methyl-glutamic acid residues with specific side-chain protections. The Boc (tert-butoxycarbonyl) group protects the N-methyl amino group, while the Obzl (benzyl ester) group protects the carboxyl side chain, ensuring selective reactivity during peptide elongation. It is particularly useful in solid-phase peptide synthesis (SPPS) and solution-phase methods, enabling the synthesis of complex peptides and proteins. Additionally, it finds use in the development of peptide-based drugs, biomaterials, and research tools, where precise control over amino acid incorporation is essential. Its stability and compatibility with various coupling reagents make it a valuable component in organic and medicinal chemistry workflows.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,698.00

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Boc-N-Me-Glu(Obzl)-OH
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This chemical is widely used in peptide synthesis as a protected N-methyl-glutamic acid derivative. Its primary application is in the construction of peptides, where it serves as a building block to introduce N-methyl-glutamic acid residues with specific side-chain protections. The Boc (tert-butoxycarbonyl) group protects the N-methyl amino group, while the Obzl (benzyl ester) group protects the carboxyl side chain, ensuring selective reactivity during peptide elongation. It is particularly useful in solid-
This chemical is widely used in peptide synthesis as a protected N-methyl-glutamic acid derivative. Its primary application is in the construction of peptides, where it serves as a building block to introduce N-methyl-glutamic acid residues with specific side-chain protections. The Boc (tert-butoxycarbonyl) group protects the N-methyl amino group, while the Obzl (benzyl ester) group protects the carboxyl side chain, ensuring selective reactivity during peptide elongation. It is particularly useful in solid-phase peptide synthesis (SPPS) and solution-phase methods, enabling the synthesis of complex peptides and proteins. Additionally, it finds use in the development of peptide-based drugs, biomaterials, and research tools, where precise control over amino acid incorporation is essential. Its stability and compatibility with various coupling reagents make it a valuable component in organic and medicinal chemistry workflows.
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