(E)-4,4,5,5-Tetramethyl-2-(3-methylbut-1-en-1-yl)-1,3,2-dioxaborolane
97%
Reagent
Code: #180531
CAS Number
177949-92-7
blur_circular Chemical Specifications
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Molecular Information
Weight
196.09 g/mol
Formula
C₁₁H₂₁BO₂
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Registry Numbers
MDL Number
MFCD16996225
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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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