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Structure of 2121511-91-7
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3-Chloro-6-fluoro-2-methoxyphenylboronic acid features a boronate moiety integrated into a halogenated aromatic scaffold, enabling efficient cross-coupling under standard conditions. The electron-deficient ring enhances reactivity in Suzuki-Miyaura transformations, while the methoxy group improves solubility and stability. This bench-stable reagent streamlines access to functionalized biaryl architectures in medicinal chemistry and materials synthesis.
3-Chloro-6-fluoro-2-methoxyphenylboronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl architectures. Its ortho-halogenated and methoxy-substituted aryl framework provides predictable regiochemistry and enhanced stability under standard reaction conditions. The boronic acid functionality facilitates mild coupling with aryl halides and pseudohalides, offering excellent functional group tolerance and straightforward purification, making it a practical choice for 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-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: