N-Boc-2,2-dimethyl-1,3-diaminopropane

97%

Reagent Code: #217819
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CAS Number 292606-35-0

science Other reagents with same CAS 292606-35-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 202.3 g/mol
Formula C₁₀H₂₂N₂O₂
badge Registry Numbers
MDL Number MFCD01076212
thermostat Physical Properties
Melting Point 74°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and biologically active compounds, particularly in the development of protease inhibitors and other therapeutic agents. Its protected amine functionality allows for selective reactions in multi-step organic syntheses. Commonly employed in medicinal chemistry for constructing complex amine-containing molecules, especially in the preparation of peptidomimetics and drug candidates where controlled nitrogen reactivity is required. The Boc-protected group enables easy deprotection under mild acidic conditions, making it ideal for solid-phase and solution-phase peptide synthesis. Also utilized in the production of specialty polymers and ligands for catalysis.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿2,240.00
5g
10-20 days ฿10,100.00
N-Boc-2,2-dimethyl-1,3-diaminopropane
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Used as a key intermediate in the synthesis of pharmaceuticals and biologically active compounds, particularly in the development of protease inhibitors and other therapeutic agents. Its protected amine functionality allows for selective reactions in multi-step organic syntheses. Commonly employed in medicinal chemistry for constructing complex amine-containing molecules, especially in the preparation of peptidomimetics and drug candidates where controlled nitrogen reactivity is required. The Boc-protect

Used as a key intermediate in the synthesis of pharmaceuticals and biologically active compounds, particularly in the development of protease inhibitors and other therapeutic agents. Its protected amine functionality allows for selective reactions in multi-step organic syntheses. Commonly employed in medicinal chemistry for constructing complex amine-containing molecules, especially in the preparation of peptidomimetics and drug candidates where controlled nitrogen reactivity is required. The Boc-protected group enables easy deprotection under mild acidic conditions, making it ideal for solid-phase and solution-phase peptide synthesis. Also utilized in the production of specialty polymers and ligands for catalysis.

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