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*For research and further manufacturing use only, not for direct human use.
Structure of 226396-31-2
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This boronic acid features a methylsulfamoyl group at the para position, enhancing solubility and metabolic stability. The boronate moiety enables efficient Suzuki-Miyaura coupling under standard conditions, delivering arylated products with high fidelity. Designed for robust performance in medicinal chemistry applications.
(4-(N-Methylsulfamoyl)phenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl scaffolds with enhanced solubility and metabolic stability. The N-methylsulfamoyl group imparts favorable functional group tolerance and bench stability, facilitating straightforward purification and integration into complex molecular architectures relevant to medicinal chemistry and process development.
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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: