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Structure of 191089-06-2
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4-Borono-2-methylbenzoic acid features a boronate moiety ortho to a carboxylic acid and flanked by a methyl group, enabling selective transformations in Suzuki-Miyaura coupling. This bench-stable, moisture-tolerant reagent integrates readily into bioconjugation and medicinal chemistry workflows.
4-Borono-2-methylbenzoic acid serves as a versatile building block for Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl scaffolds under mild conditions. The boronic acid group exhibits excellent bench stability and functional group tolerance, while the carboxylic acid facilitates downstream derivatization via amide formation or esterification. Its ortho-methyl substituent enhances regiochemical control in coupling processes and contributes to improved metabolic stability in medicinal chemistry 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 : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: