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Structure of 52378-64-0
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(3-Bromopyridin-2-yl)methanol features a brominated pyridine ring bearing a reactive benzyl alcohol functionality. This combination enables direct coupling in cross-coupling reactions and facilitates downstream derivatization. The molecule exhibits good stability under standard conditions, making it suitable for use in synthetic sequences requiring controlled reactivity.
(3-Bromopyridin-2-yl)methanol serves as a versatile building block for C–H functionalization and cross-coupling reactions, enabling efficient access to substituted pyridine scaffolds. Its bromo group facilitates palladium-catalyzed coupling, while the primary alcohol allows for oxidation, protection, or derivatization under standard conditions. The molecule exhibits good bench stability and compatibility with diverse reaction environments, making it well-suited for iterative synthetic sequences in medicinal chemistry and process development.
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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-P302+P352-P304+P340
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Lot numbers can be found on the outside label of a product: