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Structure of 876-88-0
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6-Bromocinnolin-4-ol features a brominated cinnolinone core with a phenolic hydroxyl group, enabling direct functionalization in cross-coupling reactions. The electron-deficient heteroaromatic scaffold supports robust reactivity in palladium-catalyzed transformations. This bench-stable compound integrates readily into pharmaceutical and agrochemical synthesis pathways.
6-Bromocinnolin-4-ol serves as a versatile building block for the synthesis of cinnolinone-based scaffolds, enabling direct functionalization at the C6 position via palladium-catalyzed cross-coupling. Its phenolic hydroxyl group provides site-specific reactivity for derivatization, while the bromine moiety offers high compatibility with standard coupling protocols. Bench-stable and readily purified by crystallization, it facilitates efficient access to biologically relevant heterocycles in medicinal chemistry and materials science 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
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Precautionary Statements : P261-P302+P352
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Lot numbers can be found on the outside label of a product: