4,4,5,5-Tetramethyl-2-(3-methylbenzyl)-1,3,2-dioxaborolane
98%
Reagent
Code: #244388
CAS Number
365564-12-1
blur_circular Chemical Specifications
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Molecular Information
Weight
232.13 g/mol
Formula
C₁₄H₂₁BO₂
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Registry Numbers
MDL Number
MFCD23102598
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Storage & Handling
Storage
Room temperature, seal, dry
description Product Description
Used as a boronic ester reagent in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds in organic synthesis. It serves as a stable, lipophilic precursor for generating 3-methylbenzylboronic acid in situ, enabling the preparation of substituted aromatic and heteroaromatic compounds. Commonly applied in pharmaceutical and agrochemical research for constructing biaryl intermediates. Its tetramethyl-substituted dioxaborolane ring enhances stability and handling compared to more sensitive boronic acids.
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