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Structure of 221006-71-9
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This boronate reagent features a strategically positioned bromine and methyl group on the phenyl ring, enabling selective cross-coupling reactions. The electron-rich aromatic system enhances reactivity in palladium-catalyzed transformations, while the bench-stable boronic acid functionality simplifies handling and integration into synthetic workflows.
(4-Bromo-2-methylphenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation under mild conditions. Its stability under ambient storage and compatibility with diverse functional groups make it ideal for constructing biaryl scaffolds in pharmaceutical and materials synthesis. The ortho-methyl group enhances regioselectivity in subsequent transformations, while the boronic acid moiety facilitates straightforward purification and handling.
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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-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: