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Structure of 913835-76-4
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This boronic acid features a chlorinated aryl ring with a formyl group at the para position relative to the boronate, enabling selective coupling in Suzuki-Miyaura reactions. The electron-withdrawing chlorine enhances electrophilicity of the adjacent carbonyl, facilitating downstream functionalization. Bench-stable under standard conditions, it integrates seamlessly into complex molecule synthesis workflows.
(4-Chloro-2-formylphenyl)boronic acid serves as a versatile building block in transition-metal-catalyzed cross-coupling reactions, enabling efficient construction of biaryl and heteroaryl scaffolds. The formyl group offers direct access to aldehyde functionality for downstream derivatization, while the boronic acid moiety ensures compatibility with Suzuki-Miyaura coupling protocols. Bench-stable and readily purified by recrystallization, it facilitates streamlined synthesis of complex aromatic systems relevant to pharmaceutical and agrochemical development.
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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: