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Structure of 956388-05-9
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This boronate ester integrates a tetrahydropyran-2-yl protected indazole core, enabling stable handling and orthogonal deprotection. The tetramethylboronate moiety facilitates efficient Suzuki-Miyaura coupling under mild conditions, delivering functionalized indazoles with high chemoselectivity.
1-(Tetrahydropyran-2-yl)-4-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)-1H-indazole serves as a stable, bench-ready boron building block for Suzuki-Miyaura coupling reactions. The tetrahydropyranyl group provides protection of the indazole nitrogen, enhancing solubility and stability while enabling orthogonal deprotection. The pinacol borane moiety facilitates efficient cross-coupling with aryl and vinyl halides under mild conditions, making it ideal for constructing complex heterocyclic scaffolds in medicinal chemistry and materials science 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: