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Structure of 68716-49-4
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2-(4-Bromophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a bench-stable boronate reagent featuring a para-brominated aryl group. This electrophilically active moiety integrates seamlessly into Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation under standard conditions. The sterically shielded dioxaborolane core enhances stability and minimizes protodeboronation.
2-(4-Bromophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane serves as a stable, bench-ready boron reagent for palladium-catalyzed cross-coupling reactions. Its aryl bromide functionality enables efficient Suzuki-Miyaura coupling with a wide range of boronic acids and halides, offering high functional group tolerance and predictable regiochemistry. The tetramethyl-substituted dioxaborolane ring enhances air and moisture stability, simplifying handling and purification in routine synthetic 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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: