N-tert-butoxycarbonyl-N-(1-phenylethyl)-N-(prop-2-yn-1-yl)amine

Reagent Code: #216079
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CAS Number 951128-39-5

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 259.348 g/mol
Formula C₁₆H₂₁NO₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive molecules. Its structure supports selective protection of amine functionalities during multi-step reactions, especially in peptide synthesis and medicinal chemistry. The propargyl and chiral benzylic components make it valuable in asymmetric synthesis and click chemistry applications. Commonly employed in the development of enzyme inhibitors and receptor ligands due to its stability and reactivity profile under various coupling and deprotection conditions.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿22,800.00
N-tert-butoxycarbonyl-N-(1-phenylethyl)-N-(prop-2-yn-1-yl)amine
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive molecules. Its structure supports selective protection of amine functionalities during multi-step reactions, especially in peptide synthesis and medicinal chemistry. The propargyl and chiral benzylic components make it valuable in asymmetric synthesis and click chemistry applications. Commonly employed in the development of enzyme inhibitors and receptor ligands due to its stability and reactivi

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive molecules. Its structure supports selective protection of amine functionalities during multi-step reactions, especially in peptide synthesis and medicinal chemistry. The propargyl and chiral benzylic components make it valuable in asymmetric synthesis and click chemistry applications. Commonly employed in the development of enzyme inhibitors and receptor ligands due to its stability and reactivity profile under various coupling and deprotection conditions.

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