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Structure of 881302-73-4
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5-Boronoisophthalic acid features a rigid aromatic core with strategically positioned boronic acid and carboxylic acid groups, enabling efficient conjugation in Suzuki coupling reactions. This dual-functional scaffold integrates seamlessly into bioconjugation workflows and materials synthesis under standard conditions.
5-Boronoisophthalic acid serves as a versatile building block in transition-metal-catalyzed coupling reactions, particularly Suzuki-Miyaura cross-couplings. Its ortho-dicarboxylic acid motif provides enhanced solubility and facilitates purification, while the boronic acid group enables reliable C–C bond formation under mild conditions. The molecule exhibits good bench stability and functional group tolerance, making it well-suited for modular synthesis of complex aromatic systems and biologically relevant scaffolds.
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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: