tert-Butyl (2-(2-aminoethoxy)ethyl)carbamate

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Reagent Code: #146596
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CAS Number 127828-22-2

science Other reagents with same CAS 127828-22-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 204.27 g/mol
Formula C₉H₂₀N₂O₃
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a protected amine building block in organic synthesis, particularly in pharmaceutical and peptide chemistry. The tert-butoxycarbonyl (Boc) group provides stability under various reaction conditions while allowing selective deprotection under mild acidic conditions. The ethylene glycol linker with a terminal amino group enables conjugation to other molecules, making it valuable in the development of drug delivery systems, bifunctional reagents, and functionalized polymers. Its hydrophilic spacer arm improves solubility in aqueous and mixed solvent systems, facilitating reactions in biological and medicinal chemistry contexts.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿530.00
inventory 1g
10-20 days ฿660.00
inventory 25g
10-20 days ฿11,260.00
inventory 5g
10-20 days ฿2,300.00

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tert-Butyl (2-(2-aminoethoxy)ethyl)carbamate
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Used as a protected amine building block in organic synthesis, particularly in pharmaceutical and peptide chemistry. The tert-butoxycarbonyl (Boc) group provides stability under various reaction conditions while allowing selective deprotection under mild acidic conditions. The ethylene glycol linker with a terminal amino group enables conjugation to other molecules, making it valuable in the development of drug delivery systems, bifunctional reagents, and functionalized polymers. Its hydrophilic spacer a

Used as a protected amine building block in organic synthesis, particularly in pharmaceutical and peptide chemistry. The tert-butoxycarbonyl (Boc) group provides stability under various reaction conditions while allowing selective deprotection under mild acidic conditions. The ethylene glycol linker with a terminal amino group enables conjugation to other molecules, making it valuable in the development of drug delivery systems, bifunctional reagents, and functionalized polymers. Its hydrophilic spacer arm improves solubility in aqueous and mixed solvent systems, facilitating reactions in biological and medicinal chemistry contexts.

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