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Structure of 1003711-43-0
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2-Bromo-5-hydroxy-3-methylpyridine features a regioselective substitution pattern enabling direct functionalization in late-stage synthesis. The hydroxy group supports hydrogen bonding and solubility enhancements, while the bromine serves as a high-reactivity handle for cross-coupling. This pyridine scaffold combines bench-stable handling with compatibility across diverse reaction conditions.
2-Bromo-5-hydroxy-3-methylpyridine serves as a versatile building block for the synthesis of functionalized pyridine derivatives. The bromo group enables palladium-catalyzed cross-coupling reactions, while the hydroxyl and methyl functionalities offer sites for selective derivatization. Its bench-stable nature and compatibility with standard protection/deprotection sequences facilitate efficient access to complex heterocyclic scaffolds in medicinal chemistry and agrochemical research.
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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: