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Structure of 832695-88-2
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This boronic acid features a methylcarbamoyl group at the meta position, enhancing solubility and stability. The para-boronate moiety enables efficient Suzuki-Miyaura coupling under standard conditions, facilitating rapid access to functionalized biaryl scaffolds in medicinal chemistry and materials synthesis.
3-(Methylcarbamoyl)benzeneboronic acid serves as a versatile building block in Suzuki-Miyaura coupling reactions, enabling efficient construction of biaryl scaffolds with retained functional group compatibility. The methylcarbamoyl group provides enhanced solubility and stability compared to unsubstituted analogs, while the boronic acid moiety facilitates reliable cross-coupling under standard conditions. This compound functions effectively in the synthesis of pharmaceutical intermediates and heterocyclic architectures requiring orthogonal reactivity.
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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: