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Structure of 1219741-94-2
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This boronate ester features a cyclopropyl-substituted aryl group, enabling efficient cross-coupling in Suzuki-Miyaura reactions. The tetramethyl-substituted dioxaborolane ring enhances stability and shelf life under standard conditions. Ideal for constructing biaryl architectures in medicinal chemistry and materials synthesis.
2-(4-Cyclopropylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane serves as a stable, bench-ready boron building block for Suzuki-Miyaura cross-coupling reactions. Its cyclopropyl-substituted aryl group enables efficient incorporation into biaryl scaffolds common in pharmaceutical and agrochemical development. The tetramethyl-substituted dioxaborolane moiety offers enhanced stability, mild reaction conditions, and compatibility with diverse functional groups, facilitating reliable coupling across standard synthetic workflows.
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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 : P260-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: