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Structure of 774608-13-8
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This boronate moiety features a strategically positioned bromine and methyl group, enabling selective cross-coupling reactions under standard conditions. The electron-deficient aryl ring enhances reactivity in Suzuki-Miyaura transformations, while the bench-stable nature simplifies handling and storage.
(5-Bromo-2-methylphenyl)boronic acid serves as a versatile building block in palladium-catalyzed cross-coupling reactions, enabling efficient C–C bond formation under standard Suzuki-Miyaura conditions. The ortho-bromine and methyl groups provide predictable regiochemistry and enhanced stability for bench storage. Its compatibility with diverse functional groups facilitates streamlined synthesis of substituted biaryls, heterocycles, and advanced intermediates 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-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: