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Structure of 898747-24-5
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Methyl 5-bromo-1H-indazole-7-carboxylate features a brominated indazole core with a methyl ester at the C7 position, enabling direct functionalization in cross-coupling reactions. The electron-deficient heterocycle pairs well with palladium catalysts, while the ester group offers versatility in downstream derivatization. This bench-stable reagent facilitates rapid access to bioactive indazole scaffolds.
Methyl 5-bromo-1H-indazole-7-carboxylate serves as a versatile building block for the synthesis of indazole-based pharmaceuticals and agrochemicals. The bromo group enables palladium-catalyzed cross-coupling reactions, while the ester functionality supports subsequent transformations such as hydrolysis or reduction. Its bench-stable nature and compatibility with diverse reaction conditions make it well-suited for iterative synthetic strategies 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: