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Structure of 1396762-16-5
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6-Bromo-1H-indazole-5-carboxylic acid methyl ester features a brominated indazole core with a carboxylate ester at the 5-position, enabling direct incorporation into Suzuki-Miyaura coupling workflows. The electron-deficient aryl bromide facilitates efficient cross-coupling, while the methyl ester offers stability and compatibility under standard bench conditions. This scaffold serves as a key intermediate for bioactive molecule synthesis.
6-Bromo-1H-indazole-5-carboxylic acid methyl ester 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 methyl ester facilitates further functionalization via hydrolysis or nucleophilic substitution. Its bench-stable nature and compatibility with diverse reaction conditions make it well-suited for iterative synthetic workflows in medicinal chemistry and process development.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: