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Structure of 1206968-92-4
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This boronate moiety integrates a bromo-fluoro pyridine scaffold with a reactive alcohol group, enabling direct functionalization in cross-coupling reactions. The ortho-halo substitution pattern enhances electrophilicity for palladium-catalyzed transformations, while the hydroxyl terminus offers a handle for derivatization or conjugation under standard conditions.
(5-Bromo-3-fluoropyridin-2-yl)methanol serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the pyridine ring via palladium-catalyzed cross-coupling reactions. The bromo and fluoro groups provide orthogonal reactivity for sequential derivatization, while the benzylic alcohol facilitates oxidation to aldehyde or carboxylic acid, or conversion to esters and ethers. Its bench-stable nature and compatibility with standard protecting group strategies make it a practical choice for modular synthesis of heterocyclic scaffolds and API intermediates.
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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: