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Structure of 913836-14-3
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This boronate reagent features a chloro-substituted aromatic ring paired with a methyl group, enabling selective cross-coupling in palladium-catalyzed reactions. The electron-deficient aryl framework enhances reactivity while maintaining bench-stable handling under standard conditions.
(3-Chloro-5-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. Its ortho-chloro and meta-methyl substituents provide predictable regiochemical control and enhanced stability during storage and handling. The boronic acid functionality exhibits excellent functional group tolerance and facilitates straightforward purification, making it well-suited for the synthesis of substituted biaryls and complex heterocyclic scaffolds in medicinal chemistry and materials science applications.
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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: