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

95%

Reagent Code: #64934
fingerprint
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

This compound is a Boc-protected amine derivative, N-(tert-butoxycarbonyl)-2,2'-(ethylenedioxy)diethylamine, widely used as a building block in organic synthesis, particularly in peptide and pharmaceutical manufacturing. The tert-butoxycarbonyl (Boc) group protects one terminal amine, enabling selective functionalization of the other amine without side reactions. Following the desired synthetic transformations, the Boc group can be selectively deprotected under mild acidic conditions to liberate the free amine. This orthogonality makes it invaluable for assembling complex molecules, such as pharmaceuticals and bioactive compounds. The ethylenedioxy linker enhances solubility in aqueous media and provides structural flexibility and stability across diverse reaction conditions, rendering it a versatile reagent in synthetic chemistry.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance Colorless to yellow viscous liquid
Proton NMR Spectrum Conforms to Structure
Purity (HPLC) 94.5-100%
Refractive Index (N20D) 1.45-1.47
Specific Gravity (20°C) 1.04-1.05

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿350.00
inventory 5g
10-20 days ฿4,160.00
inventory 1g
10-20 days ฿1,080.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
N-(tert-Butoxycarbonyl)-2,2'-(ethylenedioxy)diethylamine
No image available

This compound is a Boc-protected amine derivative, N-(tert-butoxycarbonyl)-2,2'-(ethylenedioxy)diethylamine, widely used as a building block in organic synthesis, particularly in peptide and pharmaceutical manufacturing. The tert-butoxycarbonyl (Boc) group protects one terminal amine, enabling selective functionalization of the other amine without side reactions. Following the desired synthetic transformations, the Boc group can be selectively deprotected under mild acidic conditions to liberate the free

This compound is a Boc-protected amine derivative, N-(tert-butoxycarbonyl)-2,2'-(ethylenedioxy)diethylamine, widely used as a building block in organic synthesis, particularly in peptide and pharmaceutical manufacturing. The tert-butoxycarbonyl (Boc) group protects one terminal amine, enabling selective functionalization of the other amine without side reactions. Following the desired synthetic transformations, the Boc group can be selectively deprotected under mild acidic conditions to liberate the free amine. This orthogonality makes it invaluable for assembling complex molecules, such as pharmaceuticals and bioactive compounds. The ethylenedioxy linker enhances solubility in aqueous media and provides structural flexibility and stability across diverse reaction conditions, rendering it a versatile reagent in synthetic chemistry.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...