2-(3,5-Di-tert-butyl-4-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
95%
Reagent
Code: #167215
CAS Number
1032358-19-2
blur_circular Chemical Specifications
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Molecular Information
Weight
346.31 g/mol
Formula
C₂₁H₃₅BO₃
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Registry Numbers
MDL Number
MFCD22493891
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Storage & Handling
Storage
Room temperature, seal, dry
description Product Description
Used as a key reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. Its primary role is as a boronic ester derivative, offering enhanced stability and reactivity under palladium-catalyzed conditions. Commonly employed in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and functional materials. The tert-butyl and methoxy substituents provide steric bulk and electronic effects that improve selectivity and yield in coupling reactions. Suitable for late-stage functionalization due to its tolerance of various functional groups.
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