(E)-4,4,5,5-Tetramethyl-2-(3-methylbut-1-en-1-yl)-1,3,2-dioxaborolane

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Reagent Code: #180531
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CAS Number 177949-92-7

science Other reagents with same CAS 177949-92-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 196.09 g/mol
Formula C₁₁H₂₁BO₂
badge Registry Numbers
MDL Number MFCD16996225
inventory_2 Storage & Handling
Storage Room temperature, seal, 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 structure supports efficient transmetalation, making it valuable for constructing aryl alkenes in pharmaceuticals, agrochemicals, and advanced materials. The (E)-alkenylboronate functionality provides high stereoselectivity and stability, allowing for selective coupling under mild conditions. Commonly employed in late-stage functionalization where functional group tolerance is essential.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,620.00
inventory 1g
10-20 days ฿15,150.00
inventory 5g
10-20 days ฿52,940.00

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(E)-4,4,5,5-Tetramethyl-2-(3-methylbut-1-en-1-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 structure supports efficient transmetalation, making it valuable for constructing aryl alkenes in pharmaceuticals, agrochemicals, and advanced materials. The (E)-alkenylboronate functionality provides high stereoselectivity and stability, allowing for selective coupling under mild conditions. Commonly employed in late-stage functionalization where functional group tole

Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in organic synthesis. Its structure supports efficient transmetalation, making it valuable for constructing aryl alkenes in pharmaceuticals, agrochemicals, and advanced materials. The (E)-alkenylboronate functionality provides high stereoselectivity and stability, allowing for selective coupling under mild conditions. Commonly employed in late-stage functionalization where functional group tolerance is essential.

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