3-(2-((tert-Butoxycarbonyl)amino)ethoxy)propanoic acid

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Reagent Code: #44221
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CAS Number 1260092-44-1

science Other reagents with same CAS 1260092-44-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.26 g/mol
Formula C₁₀H₁₉NO₅
badge Registry Numbers
MDL Number MFCD22574796
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This chemical is primarily used in organic synthesis as a building block for more complex molecules. It is often employed in peptide chemistry, where it serves as a protected intermediate for the introduction of aminoethoxy groups. The tert-butoxycarbonyl (Boc) group acts as a protective moiety for amines, allowing selective reactions to occur without interference. It is also utilized in the development of pharmaceuticals, particularly in the synthesis of drug candidates that require specific functionalization or conjugation. Additionally, it finds application in the preparation of linkers for bioconjugation, enabling the attachment of biomolecules to various substrates for research or therapeutic purposes.

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Test Parameter Specification
Appearance Colorless to Light yellow clear liquid
Purity (%) 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿540.00
inventory 5g
10-20 days ฿6,435.00
inventory 1g
10-20 days ฿1,674.00

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3-(2-((tert-Butoxycarbonyl)amino)ethoxy)propanoic acid
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This chemical is primarily used in organic synthesis as a building block for more complex molecules. It is often employed in peptide chemistry, where it serves as a protected intermediate for the introduction of aminoethoxy groups. The tert-butoxycarbonyl (Boc) group acts as a protective moiety for amines, allowing selective reactions to occur without interference. It is also utilized in the development of pharmaceuticals, particularly in the synthesis of drug candidates that require specific functionali

This chemical is primarily used in organic synthesis as a building block for more complex molecules. It is often employed in peptide chemistry, where it serves as a protected intermediate for the introduction of aminoethoxy groups. The tert-butoxycarbonyl (Boc) group acts as a protective moiety for amines, allowing selective reactions to occur without interference. It is also utilized in the development of pharmaceuticals, particularly in the synthesis of drug candidates that require specific functionalization or conjugation. Additionally, it finds application in the preparation of linkers for bioconjugation, enabling the attachment of biomolecules to various substrates for research or therapeutic purposes.

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