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Structure of 885523-43-3
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4-Bromo-1H-indazole-6-carboxylic acid features a brominated indazole core with a carboxylic acid group at the 6-position, enabling direct coupling in medicinal chemistry applications. The electron-deficient aromatic system enhances reactivity in transition-metal-catalyzed transformations, while the bench-stable functionality supports reliable handling in synthetic workflows.
4-Bromo-1H-indazole-6-carboxylic acid serves as a versatile building block for the synthesis of indazole-based pharmaceuticals and agrochemicals. The carboxylic acid group enables direct coupling reactions, while the bromine substituent facilitates palladium-catalyzed cross-couplings, including Suzuki-Miyaura and Buchwald-Hartwig transformations. Its stability under standard reaction conditions and compatibility with diverse functional groups make it well-suited for iterative synthetic sequences in medicinal chemistry and process development.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H315-H319-H335
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Precautionary Statements : P264-P270-P330-P405-P501
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Lot numbers can be found on the outside label of a product: