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Structure of 174671-89-7
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6-Fluorobenzo[c][1,2]oxaborol-1(3H)-ol features a boronate moiety fused to a fluorinated benzene ring, combining enhanced stability with high reactivity in cross-coupling processes. The electron-withdrawing fluorine substituent modulates boron electrophilicity, enabling efficient palladium-catalyzed transformations under mild conditions. This bench-stable scaffold integrates readily into complex molecular architectures.
6-Fluorobenzo[c][1,2]oxaborol-1(3H)-ol serves as a stable, bench-ready boron building block for Suzuki-Miyaura cross-coupling reactions. Its fluorinated aryl core enhances metabolic stability and modulates electronic properties, enabling efficient C–C bond formation under mild conditions. The oxaborolone scaffold exhibits excellent functional group tolerance and compatibility with diverse reaction partners, facilitating the synthesis of complex biaryl architectures relevant to pharmaceutical 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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362
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Lot numbers can be found on the outside label of a product: