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Structure of 1092533-91-9
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This boronate moiety enables direct coupling in Suzuki-Miyaura reactions, delivering arylated products with high fidelity. The para-fluorine and ortho-bromo substituents provide complementary reactivity for sequential functionalization, while the bench-stable nature simplifies handling under standard conditions.
(3-Bromo-4-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. The molecule combines ortho-halogen substitution with a stable boronic acid group, offering predictable reactivity and compatibility with diverse functional groups. Its bench-stable nature and ease of purification make it well-suited for iterative synthesis 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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: