2-(Allyloxy)-1,2-oxaborolane

95%

Reagent Code: #138658
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CAS Number 79363-73-8

science Other reagents with same CAS 79363-73-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 125.96 g/mol
Formula C₆H₁₁BO₂
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of boron-containing compounds for pharmaceuticals and agrochemicals. Its allyloxy group enables further functionalization through cross-coupling reactions or olefin transformations, making it valuable in building complex molecules. Commonly employed in Suzuki-Miyaura coupling reactions due to the presence of the borolane ring, which provides a reactive boron species for carbon-carbon bond formation. Also utilized in the development of novel boronic acid derivatives for use in medicinal chemistry and materials science.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,460.00
inventory 1g
10-20 days ฿4,230.00
inventory 5g
10-20 days ฿18,340.00
2-(Allyloxy)-1,2-oxaborolane
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Used as a key intermediate in organic synthesis, particularly in the preparation of boron-containing compounds for pharmaceuticals and agrochemicals. Its allyloxy group enables further functionalization through cross-coupling reactions or olefin transformations, making it valuable in building complex molecules. Commonly employed in Suzuki-Miyaura coupling reactions due to the presence of the borolane ring, which provides a reactive boron species for carbon-carbon bond formation. Also utilized in the deve

Used as a key intermediate in organic synthesis, particularly in the preparation of boron-containing compounds for pharmaceuticals and agrochemicals. Its allyloxy group enables further functionalization through cross-coupling reactions or olefin transformations, making it valuable in building complex molecules. Commonly employed in Suzuki-Miyaura coupling reactions due to the presence of the borolane ring, which provides a reactive boron species for carbon-carbon bond formation. Also utilized in the development of novel boronic acid derivatives for use in medicinal chemistry and materials science.

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