N-Me-Asp(OtBu)-OMe·HCl

97%

Reagent Code: #219440
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CAS Number 1070867-71-8

science Other reagents with same CAS 1070867-71-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 253.726 g/mol
Formula C₁₀H₂₀ClNO₄
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

N-Methyl-aspartic acid derivative used in peptide synthesis as a protected building block for incorporating N-methylated residues. The tert-butyl group protects the carboxylic acid side chain, while the methyl ester masks the C-terminus, and the N-methylation on the alpha-amino group enables selective coupling reactions without side-chain interference or unwanted reactivity at the nitrogen. This allows stepwise assembly of complex peptides with modified backbone properties. Commonly employed in solid-phase synthesis and pharmaceutical research for developing bioactive peptides with improved stability, specificity, and pharmacological profiles.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿23,010.00
N-Me-Asp(OtBu)-OMe·HCl
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N-Methyl-aspartic acid derivative used in peptide synthesis as a protected building block for incorporating N-methylated residues. The tert-butyl group protects the carboxylic acid side chain, while the methyl ester masks the C-terminus, and the N-methylation on the alpha-amino group enables selective coupling reactions without side-chain interference or unwanted reactivity at the nitrogen. This allows stepwise assembly of complex peptides with modified backbone properties. Commonly employed in solid-pha

N-Methyl-aspartic acid derivative used in peptide synthesis as a protected building block for incorporating N-methylated residues. The tert-butyl group protects the carboxylic acid side chain, while the methyl ester masks the C-terminus, and the N-methylation on the alpha-amino group enables selective coupling reactions without side-chain interference or unwanted reactivity at the nitrogen. This allows stepwise assembly of complex peptides with modified backbone properties. Commonly employed in solid-phase synthesis and pharmaceutical research for developing bioactive peptides with improved stability, specificity, and pharmacological profiles.

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