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Structure of 219735-99-6
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2-Chloro-4-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-4-methoxyphenylboronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl scaffolds. The chloro group provides orthogonal reactivity for subsequent functionalization, while the methoxy substituent enhances solubility and modulates electronic properties. Bench-stable and readily purified by recrystallization, it functions reliably in diverse synthetic workflows requiring precise control over regiochemistry and functional group compatibility.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352
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Lot numbers can be found on the outside label of a product: