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Structure of 1310383-42-6
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This boronate moiety integrates readily into Suzuki-Miyaura cross-coupling reactions, enabling efficient access to functionalized indazolyl architectures. The methyl group enhances electron density at the aromatic core, improving reactivity and stability under standard conditions.
(5-Methyl-2H-indazol-6-yl)boronic acid serves as a versatile building block in Suzuki-Miyaura coupling reactions, enabling efficient C–C bond formation under mild conditions. The indazolyl scaffold provides inherent stability and ortho-directed functionalization potential, while the boronic acid group offers excellent bench stability and compatibility with diverse functional groups. Its utility spans medicinal chemistry and materials science, facilitating rapid access to substituted heterocycles and complex molecular architectures.
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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: