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Structure of 956283-09-3
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This boronic acid features a methylsulfamoyl group at the ortho position, enhancing solubility and metabolic stability. The pendant boronate moiety enables efficient Suzuki-Miyaura cross-coupling under standard conditions, delivering arylated scaffolds with high functional group tolerance.
(2-(N-Methylsulfamoyl)phenyl)boronic acid serves as a versatile boron building block for Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl scaffolds under mild conditions. Its stability in air and moisture facilitates handling and purification, while the sulfonamide group provides enhanced solubility and functional group tolerance. This reagent functions effectively in late-stage diversification and the synthesis of medicinally relevant heterocyclic systems.
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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: