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Structure of 443956-08-9
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6-Bromo-2-nitropyridin-3-ol features a bromine substituent at the 6-position and a nitro group at the 2-position on a pyridin-3-ol scaffold. This electron-deficient heterocycle integrates readily into cross-coupling reactions, leveraging its dual functional handles for further derivatization. The phenolic hydroxyl enhances solubility and provides a site for direct functionalization or metal coordination.
6-Bromo-2-nitropyridin-3-ol serves as a versatile building block for heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its bromo group and nitro functionality. The phenolic hydroxyl group provides additional reactivity for derivatization, while the molecule exhibits good bench stability and compatibility with standard purification methods. It functions as a key intermediate in the construction of functionalized pyridine scaffolds relevant to medicinal chemistry and agrochemical research.
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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: