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Structure of 1226985-36-9
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6-Bromo-1-methyl-1H-indazol-3(2H)-one features a brominated indazolone core with a methyl group at the nitrogen, offering a reactive site for cross-coupling and a stable scaffold for medicinal chemistry. This bench-stable heterocycle integrates readily into bioactive molecules, enabling efficient access to functionalized analogs in drug discovery workflows.
6-Bromo-1-methyl-1H-indazol-3(2H)-one serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the C6 position via palladium-catalyzed cross-coupling reactions. The bromo group exhibits high reactivity in Suzuki, Stille, and Negishi couplings, while the 3(2H)-one carbonyl supports enolization and metal coordination. Its bench-stable crystalline form facilitates handling and purification, making it well-suited for iterative synthesis of indazole-based pharmaceutical scaffolds.
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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: