6-(2-tetrahydropyranyloxy)hex-1-ene

Reagent Code: #238989
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CAS Number 77022-44-7

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 184.27 g/mol
Formula C₁₁H₂₀O₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of complex molecules where protection of hydroxyl groups is required. The tetrahydropyranyl (THP) group acts as a protecting group for alcohols, making this compound valuable in multi-step synthesis of pharmaceuticals and natural products. Its terminal alkene functionality allows for further chemical modifications, such as cross-metathesis or hydroformylation, enabling the introduction of diverse functional groups. Commonly employed in research settings for constructing carbon chains with controlled regiochemistry and in the development of bioactive compounds.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿19,950.00
6-(2-tetrahydropyranyloxy)hex-1-ene
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Used as a key intermediate in organic synthesis, particularly in the preparation of complex molecules where protection of hydroxyl groups is required. The tetrahydropyranyl (THP) group acts as a protecting group for alcohols, making this compound valuable in multi-step synthesis of pharmaceuticals and natural products. Its terminal alkene functionality allows for further chemical modifications, such as cross-metathesis or hydroformylation, enabling the introduction of diverse functional groups. Commonly

Used as a key intermediate in organic synthesis, particularly in the preparation of complex molecules where protection of hydroxyl groups is required. The tetrahydropyranyl (THP) group acts as a protecting group for alcohols, making this compound valuable in multi-step synthesis of pharmaceuticals and natural products. Its terminal alkene functionality allows for further chemical modifications, such as cross-metathesis or hydroformylation, enabling the introduction of diverse functional groups. Commonly employed in research settings for constructing carbon chains with controlled regiochemistry and in the development of bioactive compounds.

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