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Structure of 192182-54-0
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Reactant for:Palladium-catalyzed coupling reactionsPreparation of benzopyranone derivatives as positive GABAA receptor modulatorsPreparation of aryl alkenes via three-component coupling catalyzed by palladiumSuzuki-Miyaura couplingRhodium catalyzed cyanation with N-cyano-N-phenyl-p-methylbenzenesulfonamidePreparation of bisphosphonate inhibitors of human farnesyl pyrophosphate synthase
3,5-Dimethoxyphenylboronic acid serves as a reliable building block for Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl scaffolds under mild conditions. Its ortho-dimethoxy substitution enhances stability and solubility while maintaining compatibility with diverse functional groups. The boronic acid moiety facilitates straightforward purification and is well-suited for scalable synthesis in medicinal chemistry and materials science applications.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: