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

95%

Reagent Code: #242064
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CAS Number 2223005-99-8

science Other reagents with same CAS 2223005-99-8

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Weight 280.19074 g/mol
Formula C₁₄H₂₁BO₃S
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 organic synthesis. Its boron-containing structure allows it to couple with aryl or heteroaryl halides under palladium catalysis, making it valuable in the preparation of complex organic molecules, particularly in pharmaceutical and agrochemical research. The tetrahydrofuran and thiophene moieties enhance solubility and electronic properties, improving reaction efficiency in heterocyclic systems. Commonly employed in late-stage functionalization due to its stability and reactivity profile.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿53,110.00
inventory 100mg
10-20 days ฿159,320.00

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4,4,5,5-tetramethyl-2-(5-(tetrahydrofuran-2-yl)thiophen-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 organic synthesis. Its boron-containing structure allows it to couple with aryl or heteroaryl halides under palladium catalysis, making it valuable in the preparation of complex organic molecules, particularly in pharmaceutical and agrochemical research. The tetrahydrofuran and thiophene moieties enhance solubility and electronic properties, improving reaction efficiency in heterocyclic syst

Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in organic synthesis. Its boron-containing structure allows it to couple with aryl or heteroaryl halides under palladium catalysis, making it valuable in the preparation of complex organic molecules, particularly in pharmaceutical and agrochemical research. The tetrahydrofuran and thiophene moieties enhance solubility and electronic properties, improving reaction efficiency in heterocyclic systems. Commonly employed in late-stage functionalization due to its stability and reactivity profile.

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