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Structure of 885698-95-3
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2-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-indazole features a boronate ester group enabling reliable Suzuki-Miyaura cross-coupling reactions. The tetramethyl-substituted dioxaborolane moiety enhances stability and solubility in organic media. This indazole scaffold offers a rigid, electron-deficient platform for constructing complex heterocyclic architectures under standard conditions.
2-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-indazole serves as a versatile boronate building block for Suzuki-Miyaura cross-coupling reactions. The tetramethylboronate group enables efficient palladium-catalyzed coupling under mild conditions, while the indazole core provides a rigid, nitrogen-rich scaffold relevant to medicinal chemistry. Bench-stable and readily purified by flash chromatography, it functions effectively in late-stage functionalization and heterocycle diversification 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: