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Structure of 1310383-98-2
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This boronate moiety integrates a 1,5-dimethyl-1H-indazol-6-yl scaffold, delivering enhanced stability and solubility in polar solvents. The electron-rich indazole core enables efficient coupling in Suzuki-Miyaura reactions under standard conditions. Bench-stable and moisture-tolerant, this reagent streamlines access to functionalized heteroaromatic architectures in medicinal chemistry and materials science.
(1,5-Dimethyl-1H-indazol-6-yl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl architectures. The indazolyl scaffold imparts enhanced metabolic stability and favorable physicochemical properties, making it valuable for medicinal chemistry campaigns. Its boronic acid functionality exhibits excellent bench stability, tolerates common functional groups, and facilitates straightforward purification—ideal for iterative synthesis and library generation in drug discovery workflows.
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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: