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Structure of 1035690-56-2
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This boronate ester features a difluoromethoxy-substituted phenyl group, enabling efficient cross-coupling in palladium-catalyzed reactions. The tetramethyl-1,3,2-dioxaborolane scaffold imparts excellent stability and solubility under standard conditions, facilitating reliable incorporation into complex molecular architectures.
2-[3-(Difluoromethoxy)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane serves as a stable, bench-ready boronate building block for Suzuki-Miyaura cross-coupling reactions. Its difluoromethoxy-substituted aryl group enables efficient C–C bond formation with diverse halides and pseudohalides, offering enhanced electronic modulation and metabolic stability in target scaffolds. The tetramethyl-substituted dioxaborolane core ensures excellent shelf life, minimal protodeboronation, and straightforward purification, making it ideal for high-throughput synthesis and medicinal chemistry campaigns.
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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-P271-P280-P302+P352-P304+P340-P362-P405-P501
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Lot numbers can be found on the outside label of a product: