2-(But-3-yn-1-Yloxy)Tetrahydropyran

95%

Reagent Code: #149459
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CAS Number 40365-61-5

science Other reagents with same CAS 40365-61-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 154.21 g/mol
Formula C₉H₁₄O₂
badge Registry Numbers
MDL Number MFCD00012352
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of complex natural products and pharmaceuticals. Its alkyne functionality allows for participation in click chemistry reactions, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), making it valuable in drug discovery and bioconjugation. The tetrahydropyranyl group acts as a protecting group for alcohols, enabling selective protection and deprotection during multi-step syntheses. Its stability under various reaction conditions enhances its utility in building molecular complexity.

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Test Parameter Specification
Appearance Colorless to Yellow Liquid
Purity 94.5-100%
Mass Spectrum Conforms to Structure
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿480.00
inventory 1g
10-20 days ฿880.00
inventory 5g
10-20 days ฿2,990.00
inventory 25g
10-20 days ฿10,990.00

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2-(But-3-yn-1-Yloxy)Tetrahydropyran
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Used as a key intermediate in organic synthesis, particularly in the preparation of complex natural products and pharmaceuticals. Its alkyne functionality allows for participation in click chemistry reactions, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), making it valuable in drug discovery and bioconjugation. The tetrahydropyranyl group acts as a protecting group for alcohols, enabling selective protection and deprotection during multi-step syntheses. Its stability under various reaction

Used as a key intermediate in organic synthesis, particularly in the preparation of complex natural products and pharmaceuticals. Its alkyne functionality allows for participation in click chemistry reactions, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), making it valuable in drug discovery and bioconjugation. The tetrahydropyranyl group acts as a protecting group for alcohols, enabling selective protection and deprotection during multi-step syntheses. Its stability under various reaction conditions enhances its utility in building molecular complexity.

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