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Structure of 1227563-78-1
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(6-Bromo-2-fluoropyridin-3-yl)methanol features a pyridine core functionalized with bromo and fluoro substituents at the 6- and 2-positions, respectively, and a reactive methanol group at the 3-position. This configuration enables direct incorporation into cross-coupling reactions and facilitates downstream derivatization in medicinal chemistry applications. The molecule exhibits good stability under standard handling conditions and serves as a key intermediate in the synthesis of bioactive heterocycles.
(6-Bromo-2-fluoropyridin-3-yl)methanol serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the pyridine C3 position via the aldehyde group. Its bromo and fluoro substituents provide orthogonal reactivity for cross-coupling and nucleophilic substitution, respectively. The compound exhibits good bench stability and facilitates efficient synthesis of heterocyclic scaffolds and API intermediates through standard coupling protocols.
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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: