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Structure of 915411-02-8
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7-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole features a boronate ester group enabling reliable Suzuki-Miyaura cross-coupling reactions. The tetramethyl-substituted dioxaborolane enhances stability and solubility in organic media. This bench-stable reagent integrates readily into diverse synthetic sequences for constructing biaryl architectures in medicinal chemistry and materials science.
7-(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. Its stability under ambient conditions and compatibility with diverse functional groups enable efficient construction of biaryl architectures. The indazole core provides a pharmacophoric scaffold relevant to medicinal chemistry, while the pinacol boronate moiety facilitates mild, palladium-catalyzed coupling with aryl halides and triflates, offering reliable access to complex heterocyclic frameworks in drug discovery and materials science.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: