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

95%

Reagent Code: #242083
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CAS Number 2223002-73-9

science Other reagents with same CAS 2223002-73-9

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Weight 264.12514 g/mol
Formula C₁₄H₂₁BO₄
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic synthesis. Its boron-containing structure allows efficient coupling with aryl or vinyl halides under palladium catalysis, making it valuable in pharmaceutical and agrochemical research for constructing biaryl systems. The presence of a tetrahydrofuran ring enhances solubility and can influence stereoselectivity in certain transformations. Commonly employed in late-stage functionalization due to its stability and reactivity profile.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿33,840.00
inventory 25mg
10-20 days ฿99,800.00

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4,4,5,5-tetramethyl-2-(4-(tetrahydrofuran-3-yl)furan-2-yl)-1,3,2-dioxaborolane
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Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic synthesis. Its boron-containing structure allows efficient coupling with aryl or vinyl halides under palladium catalysis, making it valuable in pharmaceutical and agrochemical research for constructing biaryl systems. The presence of a tetrahydrofuran ring enhances solubility and can influence stereoselectivity in certain transformations. Commonly employed in late-stage funct

Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic synthesis. Its boron-containing structure allows efficient coupling with aryl or vinyl halides under palladium catalysis, making it valuable in pharmaceutical and agrochemical research for constructing biaryl systems. The presence of a tetrahydrofuran ring enhances solubility and can influence stereoselectivity in certain transformations. Commonly employed in late-stage functionalization due to its stability and reactivity profile.

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