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Structure of 69807-92-7
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2,6-Dichlorophenylboronic acid pinacol ester offers enhanced stability and moisture tolerance compared to free boronic acids. This bench-stable reagent integrates readily into Suzuki-Miyaura coupling protocols, enabling efficient C–C bond formation under mild conditions. The electron-deficient aryl group facilitates selective reaction with palladium catalysts, while the pinacol protection minimizes protodeboronation.
2,6-Dichlorophenylboronic acid pinacol ester serves as a stable, bench-ready building block for Suzuki-Miyaura cross-coupling reactions. Its pinacol boronate ester functionality enhances air and moisture stability while enabling efficient C–C bond formation with aryl halides under standard catalytic conditions. The 2,6-dichloro substitution pattern provides orthogonal reactivity and facilitates downstream functionalization in the synthesis of biaryl scaffolds 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: