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Structure of 1217501-28-4
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This boronate moiety integrates a bromo-chloro substitution pattern on a phenyl ring, enabling selective cross-coupling reactions. The ortho-halogen arrangement supports efficient palladium-catalyzed transformations under standard conditions. Bench-stable and moisture-tolerant, it streamlines the synthesis of complex aryl architectures in medicinal chemistry and materials science workflows.
(4-Bromo-3-chlorophenyl)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. Its compatibility with diverse functional groups and bench-stable nature facilitate reliable synthesis of complex arylated scaffolds, including those found in pharmaceutical intermediates and advanced materials.
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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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P363-P501
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Lot numbers can be found on the outside label of a product: