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Structure of 458532-97-3
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This boronate moiety integrates a fluorinated pyridine scaffold, offering enhanced stability and predictable reactivity in cross-coupling transformations. The electron-deficient heteroaryl system facilitates efficient palladium-catalyzed coupling under standard conditions, enabling rapid access to bioactive arylated derivatives with improved metabolic resilience.
(3-Fluoropyridin-4-yl)boronic acid serves as a versatile building block in cross-coupling reactions, enabling efficient C–C bond formation under Suzuki-Miyaura conditions. Its fluorinated pyridine core offers enhanced metabolic stability and tunable electronic properties, making it valuable for constructing bioactive heterocycles. The boronic acid functionality provides excellent bench stability, straightforward purification, and compatibility with diverse functional groups, facilitating its integration into complex molecule 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 : H315-H319-H335
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Precautionary Statements : P260-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: