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Structure of 1245816-10-7
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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 group enhances solubility and stability, while the electron-deficient core enables selective reactivity. Ideal for constructing complex heterocyclic architectures in medicinal chemistry and materials science.
5-Methyl-1H-indazol-4-yl-4-boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl and heteroaryl architectures. The boronic acid moiety exhibits good bench stability and functional group tolerance, facilitating straightforward purification and integration into complex molecular frameworks. Its utility is well-established in the synthesis of pharmaceutical intermediates and functionalized heterocycles.
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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: