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Structure of 501435-91-2
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This boronate moiety integrates seamlessly into Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation under standard conditions. The electron-deficient pyridine ring enhances reactivity, while the ortho-halogen substitution pattern supports selective functionalization. Bench-stable and moisture-tolerant, it streamlines synthesis in medicinal chemistry and materials science applications.
(5-Bromo-2-fluoropyridin-3-yl)boronic acid serves as a versatile building block in palladium-catalyzed cross-coupling reactions, enabling efficient construction of biaryl and heteroaryl architectures. The ortho-fluoro and bromo substituents provide complementary reactivity for sequential functionalization, while the boronic acid group offers excellent bench stability and compatibility with standard Suzuki-Miyaura coupling conditions. Its defined regiochemistry and predictable transformation profile make it ideal for targeted synthesis of pharmaceutical intermediates and agrochemical scaffolds.
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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: