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Structure of 385370-80-9
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2-Chloro-6-methoxyphenylboronic acid features a boronic acid group flanked by electron-withdrawing chlorine and electron-donating methoxy substituents, enabling efficient Suzuki-Miyaura coupling under mild conditions. This bench-stable reagent integrates readily into complex molecular architectures, particularly in pharmaceutical and agrochemical synthesis where regioselective C–C bond formation is critical.
2-Chloro-6-methoxyphenylboronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation under mild conditions. The ortho-chloro substituent provides compatibility with subsequent palladium-catalyzed transformations, while the methoxy group enhances solubility and electronic modulation. Bench-stable and readily purified by recrystallization, it facilitates the construction of substituted biaryl scaffolds relevant to pharmaceutical and agrochemical synthesis.
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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: