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Structure of 143381-72-0
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This boronate moiety integrates readily into Suzuki-Miyaura cross-coupling reactions under standard conditions, delivering functionalized aryl products with high efficiency. The methyl substituent enhances electron density at the coupling site while maintaining bench-stable handling properties.
(5-Methylbenzofuran-2-yl)boronic acid serves as a versatile building block in Suzuki-Miyaura coupling reactions, enabling efficient C–C bond formation with aryl and vinyl halides. Its benzofuran scaffold provides structural relevance to bioactive molecules and pharmaceutical intermediates. The boronic acid moiety offers excellent bench stability, compatibility with diverse functional groups, and straightforward purification via crystallization or flash chromatography, making it ideal for iterative synthesis in medicinal chemistry and process development workflows.
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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: