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Structure of 130115-85-4
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5-Bromo-6-chloropyridin-3-ol features a pyridinol core functionalized with bromo and chloro substituents at the 5- and 6-positions, respectively. This electron-deficient heterocycle integrates readily into cross-coupling reactions, serving as a robust building block for pharmaceutical intermediates and agrochemicals. The hydroxyl group enables direct derivatization or coordination in catalytic systems.
5-Bromo-6-chloropyridin-3-ol serves as a versatile building block for the synthesis of heterocyclic scaffolds in medicinal chemistry and agrochemical research. Its orthogonal halogenation pattern enables selective cross-coupling reactions, while the phenolic hydroxyl group offers opportunities for derivatization or metal complexation. The compound exhibits good bench stability and facilitates straightforward purification, making it well-suited for iterative synthetic sequences and scale-up applications.
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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-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: