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Structure of 731817-89-3
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This boronate moiety features a strategically positioned bromine and fluorine substituent on the benzene ring, enabling selective cross-coupling reactions. The ortho-halogen arrangement enhances reaction control in Suzuki-Miyaura protocols, while the bench-stable boronic acid functionality simplifies handling and integration into complex molecular architectures.
2-Bromo-3-fluorobenzeneboronic 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 fluorine substituents provide orthogonal reactivity for sequential functionalization, while the boronic acid group ensures good bench stability and ease of purification. Its compatibility with diverse reaction partners makes it ideal for constructing complex aromatic scaffolds in medicinal chemistry and materials synthesis.
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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: