N-(Diphenylmethylene)Glycine Benzyl Ester

98%

Reagent Code: #121466
label
Alias Benzyl Dibenzylidene Glycine; DPM-GLY-OBZL, Benzyl N-Diphenylmethylene Glycine; Benzyl N-(Diphenylmethylene) Glycine
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CAS Number 81477-91-0

science Other reagents with same CAS 81477-91-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 329.39 g/mol
Formula C₂₂H₁₉NO₂
badge Registry Numbers
MDL Number MFCD08062206
inventory_2 Storage & Handling
Density 1.064 g/cm3
Storage 2~8℃

description Product Description

This compound is primarily utilized in organic synthesis as a protective group for amino acids, particularly glycine. It is often employed in peptide synthesis to shield the amino group during reactions, allowing selective modification of other functional groups. The benzyl ester moiety provides additional protection for the carboxyl group, ensuring stability under various reaction conditions. Its application is significant in the development of pharmaceuticals and bioactive peptides, where precise control over amino acid reactivity is crucial. Additionally, it serves as an intermediate in the preparation of complex organic molecules, contributing to advancements in medicinal chemistry and drug discovery.

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Test Parameter Specification
Melting Point 88-90
Purity (%) 98-100%
Loss on Drying 0-0.5
Appearance White To Off-White Powder Or Crystals

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿320.00
inventory 100g
10-20 days ฿11,890.00
inventory 5g
10-20 days ฿890.00
inventory 25g
10-20 days ฿3,390.00

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N-(Diphenylmethylene)Glycine Benzyl Ester
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This compound is primarily utilized in organic synthesis as a protective group for amino acids, particularly glycine. It is often employed in peptide synthesis to shield the amino group during reactions, allowing selective modification of other functional groups. The benzyl ester moiety provides additional protection for the carboxyl group, ensuring stability under various reaction conditions. Its application is significant in the development of pharmaceuticals and bioactive peptides, where precise contr

This compound is primarily utilized in organic synthesis as a protective group for amino acids, particularly glycine. It is often employed in peptide synthesis to shield the amino group during reactions, allowing selective modification of other functional groups. The benzyl ester moiety provides additional protection for the carboxyl group, ensuring stability under various reaction conditions. Its application is significant in the development of pharmaceuticals and bioactive peptides, where precise control over amino acid reactivity is crucial. Additionally, it serves as an intermediate in the preparation of complex organic molecules, contributing to advancements in medicinal chemistry and drug discovery.

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