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Structure of 1256811-26-3
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4-Bromo-6-methylpyridin-3-ol features a pyridinol core with bromine and methyl substituents at meta and para positions, respectively. This electron-deficient heterocycle integrates readily into cross-coupling reactions, offering stable access to functionalized pyridine scaffolds under standard conditions.
4-Bromo-6-methylpyridin-3-ol serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its bromo substituent and electron-rich pyridine core. The phenolic hydroxyl group provides a handle for derivatization, while the methyl group enhances regioselectivity in subsequent functionalizations. This compound exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for iterative 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 : H302-H315-H319
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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: