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Structure of 221290-14-8
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This boronic acid features a tert-butylsulfamoyl group at the meta position, enhancing solubility and stability. The phenylboronic moiety enables efficient Suzuki-Miyaura coupling under standard conditions. Designed for synthetic flexibility in medicinal chemistry and materials science applications.
(3-(N-(tert-Butyl)sulfamoyl)phenyl)boronic acid serves as a stable, bench-ready building block for Suzuki-Miyaura cross-coupling reactions. The ortho-sulfamoyl group imparts enhanced solubility and metabolic stability, while the boronic acid functionality enables reliable coupling with aryl halides and pseudohalides under standard conditions. Its compatibility with diverse functional groups makes it particularly valuable for constructing biologically relevant heterocyclic scaffolds and pharmaceutical intermediates.
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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: