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Structure of 1310404-48-8
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This boronate moiety integrates seamlessly into Suzuki-Miyaura cross-coupling reactions, delivering functionalized indazoles with high efficiency. The dimethyl substitution enhances solubility and stability under standard conditions, enabling reliable use in synthetic workflows.
(1,3-Dimethyl-1H-indazol-5-yl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl architectures. The indazolyl scaffold provides enhanced metabolic stability and favorable physicochemical properties, making it valuable for medicinal chemistry applications. The boronic acid moiety offers excellent bench stability, compatibility with diverse reaction conditions, and straightforward purification via standard chromatographic or crystallization methods.
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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: