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Structure of 913835-80-0
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This boronate reagent features a strategically positioned bromine and fluorine substituent on the phenyl ring, enabling selective cross-coupling reactions. The electron-withdrawing fluorine enhances stability while the bromine serves as a reactive handle for palladium-catalyzed transformations under standard conditions.
(2-Bromo-6-fluorophenyl)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 dual halogen functionality offers orthogonal reactivity for sequential transformations, while the boronic acid group provides excellent bench stability and compatibility with diverse functional groups. Ideal for constructing substituted biaryls and heterocyclic scaffolds in medicinal chemistry and materials science applications.
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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: