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Structure of 1001907-58-9
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This boronate moiety integrates readily into Suzuki-Miyaura couplings, delivering functionalized indazoles with high efficiency. The 2-methyl substitution enhances stability and solubility under standard conditions, enabling reliable use in synthetic sequences.
(2-Methyl-2H-indazol-7-yl)boronic acid serves as a versatile building block in Suzuki-Miyaura coupling reactions, enabling efficient C–C bond formation with aryl and vinyl halides. Its indazolyl core provides structural rigidity and metabolic stability, making it valuable for constructing bioactive heterocycles. The boronic acid functionality offers excellent bench stability, straightforward purification, and broad functional group tolerance, facilitating integration into complex molecule synthesis.
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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
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Precautionary Statements : P264-P270-P280-P302+P352-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: