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Structure of 688810-12-0
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This boronic acid features a difluoromethoxy-substituted aryl group, enhancing electronic modulation and metabolic stability. It integrates readily into Suzuki-Miyaura cross-coupling reactions under standard conditions, delivering high yields with minimal decomposition. The electron-deficient phenyl moiety facilitates efficient coupling, while the bench-stable solid offers reliable handling in synthetic workflows.
(4-(Difluoromethoxy)phenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura coupling reactions, enabling efficient construction of biaryl scaffolds under mild conditions. The difluoromethoxy group imparts enhanced metabolic stability and modulates electronic properties, making this arylboronic acid valuable for medicinal chemistry applications. It exhibits good bench stability, ease of handling, and compatibility with diverse functional groups, facilitating straightforward purification and integration into complex molecular architectures.
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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: