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Structure of 1159511-90-6
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5-Bromo-2,6-dimethyl-2H-indazole features a sterically hindered indazole core with bromine and methyl groups at strategic positions, enabling selective functionalization in cross-coupling reactions. This bench-stable heterocycle integrates readily into pharmaceutical scaffolds and serves as a key building block for bioactive molecule synthesis under standard conditions.
5-Bromo-2,6-dimethyl-2H-indazole serves as a versatile building block in medicinal chemistry, enabling late-stage functionalization via palladium-catalyzed cross-coupling reactions. The bromine substituent facilitates efficient Suzuki, Stille, or Negishi couplings, while the methyl groups enhance solubility and metabolic stability. This scaffold exhibits excellent bench stability and compatibility with common protecting group strategies, making it well-suited for iterative synthesis of heterocyclic APIs and targeted compound libraries.
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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-H332-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P363-P405-P501
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Lot numbers can be found on the outside label of a product: