2-(2-(Prop-2-yn-1-yloxy)ethoxy)tetrahydro-2H-pyran

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Reagent Code: #106983
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CAS Number 119096-95-6

science Other reagents with same CAS 119096-95-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 184.23 g/mol
Formula C₁₀H₁₆O₃
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This compound is a tetrahydropyranyl (THP)-protected propargyl ether, serving as a key intermediate in organic synthesis. The THP group acts as a protecting moiety for the primary alcohol, enabling selective reactions at the terminal alkyne moiety via copper-catalyzed azide-alkyne cycloaddition (CuAAC) click chemistry. This dual functionality is essential for constructing complex molecules in pharmaceutical development, bioconjugation, and the preparation of advanced materials like polymers and dendrimers. The protecting group can be efficiently deprotected under mild acidic conditions, providing versatility in multi-step synthetic workflows.

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inventory 100mg
10-20 days ฿14,400.00

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2-(2-(Prop-2-yn-1-yloxy)ethoxy)tetrahydro-2H-pyran
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This compound is a tetrahydropyranyl (THP)-protected propargyl ether, serving as a key intermediate in organic synthesis. The THP group acts as a protecting moiety for the primary alcohol, enabling selective reactions at the terminal alkyne moiety via copper-catalyzed azide-alkyne cycloaddition (CuAAC) click chemistry. This dual functionality is essential for constructing complex molecules in pharmaceutical development, bioconjugation, and the preparation of advanced materials like polymers and dendrimer

This compound is a tetrahydropyranyl (THP)-protected propargyl ether, serving as a key intermediate in organic synthesis. The THP group acts as a protecting moiety for the primary alcohol, enabling selective reactions at the terminal alkyne moiety via copper-catalyzed azide-alkyne cycloaddition (CuAAC) click chemistry. This dual functionality is essential for constructing complex molecules in pharmaceutical development, bioconjugation, and the preparation of advanced materials like polymers and dendrimers. The protecting group can be efficiently deprotected under mild acidic conditions, providing versatility in multi-step synthetic workflows.

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