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Structure of 352535-98-9
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(3-Bromo-2-chlorophenyl)boronic acid features a sterically accessible boronate moiety flanked by bromo and chloro substituents, enabling efficient cross-coupling in palladium-catalyzed transformations. This bench-stable reagent integrates seamlessly into synthetic workflows requiring halogen-directed functionalization, delivering high chemoselectivity under standard conditions.
(3-Bromo-2-chlorophenyl)boronic acid serves as a versatile building block in palladium-catalyzed cross-coupling reactions, enabling efficient C–C bond formation with aryl halides and triflates. The molecule exhibits excellent bench stability, tolerates diverse functional groups, and facilitates straightforward purification via crystallization or standard chromatography. Its dual halogenation pattern supports sequential functionalization strategies in the synthesis of complex biaryl architectures and heterocyclic scaffolds relevant to medicinal chemistry and materials science.
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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: