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Structure of 952319-71-0
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This boronate moiety integrates readily into Suzuki-Miyaura cross-coupling reactions under standard conditions, delivering functionalized indazoles with high efficiency. The methyl substituent enhances stability and solubility, enabling straightforward handling and reliable performance in synthetic workflows involving nitrogen heterocycles.
(2-Methyl-2H-indazol-5-yl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl and heteroaryl architectures. Its boronic acid functionality exhibits excellent bench stability, tolerates common functional groups, and facilitates straightforward purification. This compound is particularly valuable for the synthesis of indazole-based pharmaceutical scaffolds and advanced materials, offering reliable reactivity under standard coupling conditions.
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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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: