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Structure of 937049-58-6
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6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole integrates a stable boronate handle with a nitrogen-rich heterocyclic core, enabling efficient cross-coupling reactions under standard conditions. This bench-stable reagent facilitates rapid assembly of biologically relevant indazole scaffolds in late-stage functionalization workflows.
6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole serves as a versatile boronate building block for Suzuki-Miyaura cross-coupling reactions. The indazole core provides a rigid, bioactive scaffold commonly found in pharmaceuticals, while the stable, bench-ready boronate group enables efficient C–C bond formation under mild conditions. Excellent functional group tolerance and straightforward purification make it ideal for constructing complex heterocyclic architectures in medicinal chemistry and process R&D workflows.
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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-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: