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Structure of 1403767-25-8
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6-Bromo-2-methyl-2H-indazol-5-ol features a brominated indazolone core with a methyl group at the 2-position and a hydroxyl substituent at C5, enabling direct functionalization in cross-coupling reactions. This bench-stable scaffold integrates readily into bioactive molecule design, particularly in kinase inhibitor and medicinal chemistry applications.
6-Bromo-2-methyl-2H-indazol-5-ol serves as a versatile building block for the synthesis of bioactive heterocycles, enabling direct functionalization at C5 via palladium-catalyzed cross-coupling. The phenolic hydroxyl group provides a handle for derivatization, while the bromide facilitates further diversification through standard coupling reactions. Bench-stable and compatible with common protecting group strategies, it functions effectively in medicinal chemistry campaigns targeting kinase inhibitors and CNS-active compounds.
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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-H320-H335
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Precautionary Statements : P261-P280-P302+P352
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Lot numbers can be found on the outside label of a product: