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Structure of 1001907-57-8
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This boronate moiety integrates seamlessly into Suzuki-Miyaura cross-coupling reactions, enabling efficient access to biologically active indazolyl scaffolds. The methyl group enhances stability and modulates electronic properties, while the pendant boronic acid facilitates reliable functionalization under standard conditions.
(2-Methyl-2H-indazol-6-yl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl scaffolds prevalent in medicinal chemistry. The boronic acid moiety exhibits good bench stability and tolerates a range of functional groups, facilitating direct incorporation into complex heterocyclic frameworks. Its utility is enhanced by predictable reactivity and straightforward purification, making it well-suited 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: