4,4,5,5-Tetramethyl-2-(tetrahydrofuran-3-yl)-1,3,2-dioxaborolane

97%

Reagent Code: #240856
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CAS Number 331958-90-8

science Other reagents with same CAS 331958-90-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 198.07 g/mol
Formula C₁₀H₁₉BO₃
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a boronic ester reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in organic synthesis. Its tetrahydrofuran ring provides structural rigidity and can influence stereoselectivity in certain transformations. Commonly employed in pharmaceutical and agrochemical research for constructing complex molecules, especially where functional group tolerance and mild reaction conditions are required. The compound is valued for its stability and reactivity profile in palladium-catalyzed reactions.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿168.00
inventory 250mg
10-20 days ฿516.00
inventory 1g
10-20 days ฿2,880.00
inventory 10g
10-20 days ฿22,360.00
inventory 25g
10-20 days ฿44,710.00
inventory 5g
10-20 days ฿14,340.00
4,4,5,5-Tetramethyl-2-(tetrahydrofuran-3-yl)-1,3,2-dioxaborolane
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Used as a boronic ester reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in organic synthesis. Its tetrahydrofuran ring provides structural rigidity and can influence stereoselectivity in certain transformations. Commonly employed in pharmaceutical and agrochemical research for constructing complex molecules, especially where functional group tolerance and mild reaction conditions are required. The compound is valued for its stability and reactivity profil

Used as a boronic ester reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in organic synthesis. Its tetrahydrofuran ring provides structural rigidity and can influence stereoselectivity in certain transformations. Commonly employed in pharmaceutical and agrochemical research for constructing complex molecules, especially where functional group tolerance and mild reaction conditions are required. The compound is valued for its stability and reactivity profile in palladium-catalyzed reactions.

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