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Structure of 269410-06-2
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This boronate moiety integrates a brominated aryl group within a stable, sterically shielded dioxaborolane framework. Designed for efficient cross-coupling reactions, it enables direct functionalization of complex heterocycles under standard conditions. The para-bromophenyl substitution enhances reactivity in palladium-catalyzed transformations while maintaining bench-stability and moisture tolerance.
2-(2-Bromophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane serves as a stable, bench-ready boron building block for palladium-catalyzed cross-coupling reactions. Its aryl bromide functionality enables efficient Suzuki-Miyaura coupling with diverse boronic acids and electrophiles, facilitating the construction of biaryl scaffolds. The tetramethyl-substituted dioxaborolane ring enhances shelf stability and minimizes protodeboronation, while the ortho-bromine substitution allows for selective functionalization in complex molecule synthesis.
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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-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: