tert-butyl [N'-(2-aminoethyl)-N-(tert-butoxycarbonyl)carbamimidoyl]carbamate (non-preferred name)

≥95%

Reagent Code: #41351
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CAS Number 203258-44-0

science Other reagents with same CAS 203258-44-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 302.3699 g/mol
Formula C₁₃H₂₆N₄O₄
badge Registry Numbers
MDL Number MFCD04974571
thermostat Physical Properties
Melting Point 95-98℃
inventory_2 Storage & Handling
Density 1.137g/cm3
Storage −20°C, inert gas

description Product Description

This compound is a selectively protected derivative of N-(2-aminoethyl)guanidine, featuring a free primary amine and two tert-butoxycarbonyl (Boc) groups protecting the guanidine moiety. It serves as a building block in organic synthesis, particularly peptide synthesis and pharmaceutical intermediate preparation. The Boc groups prevent unwanted reactions of the guanidine during complex processes, provide stability under various conditions for multi-step syntheses, and allow deprotection under mild acidic conditions to reveal the guanidine functionality with precision.

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Test Parameter Specification
Appearance White to yellow powder
Purity 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿17,550.00
inventory 250mg
10-20 days ฿6,500.00

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tert-butyl [N'-(2-aminoethyl)-N-(tert-butoxycarbonyl)carbamimidoyl]carbamate (non-preferred name)
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This compound is a selectively protected derivative of N-(2-aminoethyl)guanidine, featuring a free primary amine and two tert-butoxycarbonyl (Boc) groups protecting the guanidine moiety. It serves as a building block in organic synthesis, particularly peptide synthesis and pharmaceutical intermediate preparation. The Boc groups prevent unwanted reactions of the guanidine during complex processes, provide stability under various conditions for multi-step syntheses, and allow deprotection under mild acidic

This compound is a selectively protected derivative of N-(2-aminoethyl)guanidine, featuring a free primary amine and two tert-butoxycarbonyl (Boc) groups protecting the guanidine moiety. It serves as a building block in organic synthesis, particularly peptide synthesis and pharmaceutical intermediate preparation. The Boc groups prevent unwanted reactions of the guanidine during complex processes, provide stability under various conditions for multi-step syntheses, and allow deprotection under mild acidic conditions to reveal the guanidine functionality with precision.

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