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Structure of 885518-77-4
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6-Bromo-1H-indazol-4-ol features a brominated indazolone core with a phenolic hydroxyl group, offering enhanced reactivity for cross-coupling and functionalization. This bench-stable compound integrates readily into synthetic pathways requiring halogenated heterocycles, enabling efficient access to bioactive scaffolds in medicinal chemistry and materials science.
6-Bromo-1H-indazol-4-ol serves as a versatile building block for the synthesis of biologically active heterocycles, enabling direct functionalization at the C4 position via palladium-catalyzed cross-coupling reactions. Its bromo group facilitates efficient derivatization, while the phenolic hydroxyl supports orthogonal protection strategies and enhances solubility. The compound exhibits excellent bench stability and is readily purified by flash chromatography or recrystallization, making it ideal for iterative medicinal chemistry campaigns and API scaffold elaboration.
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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: