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Structure of 148355-75-3
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This boronic acid features a methylsulfonamido group positioned ortho to the boronic acid moiety, enhancing solubility and metabolic stability. The electron-deficient aryl ring facilitates efficient Suzuki-Miyaura coupling under mild conditions. Ideal for constructing biologically active scaffolds in medicinal chemistry and materials science.
(3-(Methylsulfonamido)phenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl scaffolds under mild conditions. Its methylsulfonamide group provides enhanced solubility and metabolic stability, while the boronic acid functionality offers excellent bench stability and compatibility with diverse functional groups. This reagent facilitates rapid access to pharmacologically relevant heterocyclic systems and is particularly valuable in medicinal chemistry for lead optimization and macrocyclic scaffold synthesis.
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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-H319
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Precautionary Statements : P264-P270-P280
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Lot numbers can be found on the outside label of a product: