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Structure of 1245816-07-2
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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 electron density at the heterocyclic core, improving reactivity and stability in synthetic workflows.
(7-Methyl-1H-indazol-5-yl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation under mild conditions. Its indazolyl scaffold provides robust stability and favorable solubility, while the boronic acid group exhibits excellent functional group tolerance and compatibility with diverse reaction partners. The methyl substituent enhances metabolic stability and modulates electronic properties, making it a practical choice for constructing biologically relevant heterocyclic architectures in medicinal chemistry and materials science applications.
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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: