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Structure of 1451391-45-9
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4-Bromo-3,5-dimethylphenylboronic acid features a sterically hindered boronic acid group flanked by two methyl substituents and a bromine atom, enabling selective cross-coupling in Suzuki-Miyaura reactions. The electron-rich aromatic core enhances reactivity under mild conditions, while the bench-stable nature simplifies handling and storage. This structure facilitates efficient incorporation into complex molecular architectures.
4-Bromo-3,5-dimethylphenylboronic acid serves as a versatile building block in Suzuki-Miyaura coupling reactions, enabling efficient C–C bond formation under mild conditions. Its ortho-dimethyl substitution enhances bench stability and reduces protodeboronation, while the bromine handle permits downstream functionalization via cross-coupling or palladium-catalyzed transformations. Ideal for constructing substituted biaryls and heterocyclic scaffolds in medicinal chemistry and materials science.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319
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Precautionary Statements : P264-P270-P280-P302+P352-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: