N-(tert-Butoxycarbonyl)-2,2'-(ethylenedioxy)diethylamine

≥97.0%(HPLC)

Reagent Code: #64933
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CAS Number 153086-78-3

science Other reagents with same CAS 153086-78-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 248.32 g/mol
Formula C₁₁H₂₄N₂O₄
badge Registry Numbers
MDL Number MFCD03788155
inventory_2 Storage & Handling
Density 1.04g/mL
Storage room temperature, dry

description Product Description

N-(tert-Butoxycarbonyl)-2,2'-(ethylenedioxy)diethylamine is a selectively protected diamine derivative used as a building block in organic synthesis, particularly in peptide chemistry and pharmaceutical manufacturing. The Boc (tert-butoxycarbonyl) group protects one amine, enabling selective functionalization of the free amine and preventing side reactions during multi-step assembly of complex molecules. Its stability across diverse conditions supports applications in bioactive molecule synthesis, drug delivery systems, and polymer chemistry.

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Test Parameter Specification
Appearance Colorless to light yellow Liquid
Purity (%) 97-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿14,760.00
inventory 1g
10-20 days ฿1,080.00
inventory 5g
10-20 days ฿4,167.00

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N-(tert-Butoxycarbonyl)-2,2'-(ethylenedioxy)diethylamine
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N-(tert-Butoxycarbonyl)-2,2'-(ethylenedioxy)diethylamine is a selectively protected diamine derivative used as a building block in organic synthesis, particularly in peptide chemistry and pharmaceutical manufacturing. The Boc (tert-butoxycarbonyl) group protects one amine, enabling selective functionalization of the free amine and preventing side reactions during multi-step assembly of complex molecules. Its stability across diverse conditions supports applications in bioactive molecule synthesis, drug d

N-(tert-Butoxycarbonyl)-2,2'-(ethylenedioxy)diethylamine is a selectively protected diamine derivative used as a building block in organic synthesis, particularly in peptide chemistry and pharmaceutical manufacturing. The Boc (tert-butoxycarbonyl) group protects one amine, enabling selective functionalization of the free amine and preventing side reactions during multi-step assembly of complex molecules. Its stability across diverse conditions supports applications in bioactive molecule synthesis, drug delivery systems, and polymer chemistry.

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