N-tert-Butoxycarbonyl-D-glutamic acid gamma-methyl ester

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Reagent Code: #218285
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CAS Number 76379-01-6

science Other reagents with same CAS 76379-01-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 261.27 g/mol
Formula C₁₁H₁₉NO₆
badge Registry Numbers
MDL Number MFCD00136803
thermostat Physical Properties
Boiling Point 428.4±40.0 °C
inventory_2 Storage & Handling
Density 1.182±0.06 g/cm3
Storage 2-8°C, dry

description Product Description

Used as a protected amino acid derivative in peptide synthesis, particularly in the preparation of complex peptides where selective protection of functional groups is required. The Boc (tert-butoxycarbonyl) group provides temporary protection of the alpha-amino group, while the gamma-methyl ester masks the side chain carboxylic acid of glutamic acid, allowing stepwise assembly of peptides without unwanted side reactions. Its D-configuration makes it suitable for synthesizing peptides with specific stereochemical requirements, such as those used in medicinal chemistry and biochemical research. Commonly employed in solid-phase and solution-phase peptide coupling strategies.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿720.00
25g
10-20 days ฿3,070.00
100g
10-20 days ฿9,620.00
N-tert-Butoxycarbonyl-D-glutamic acid gamma-methyl ester
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Used as a protected amino acid derivative in peptide synthesis, particularly in the preparation of complex peptides where selective protection of functional groups is required. The Boc (tert-butoxycarbonyl) group provides temporary protection of the alpha-amino group, while the gamma-methyl ester masks the side chain carboxylic acid of glutamic acid, allowing stepwise assembly of peptides without unwanted side reactions. Its D-configuration makes it suitable for synthesizing peptides with specific stereo

Used as a protected amino acid derivative in peptide synthesis, particularly in the preparation of complex peptides where selective protection of functional groups is required. The Boc (tert-butoxycarbonyl) group provides temporary protection of the alpha-amino group, while the gamma-methyl ester masks the side chain carboxylic acid of glutamic acid, allowing stepwise assembly of peptides without unwanted side reactions. Its D-configuration makes it suitable for synthesizing peptides with specific stereochemical requirements, such as those used in medicinal chemistry and biochemical research. Commonly employed in solid-phase and solution-phase peptide coupling strategies.

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