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Structure of 1192025-01-6
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This boronate ester features a 3-chloro-2-fluorophenyl group attached to a tetramethyl-1,3,2-dioxaborolane scaffold, delivering enhanced stability and reactivity in cross-coupling applications. The electron-deficient aryl moiety enables efficient palladium-catalyzed coupling under standard conditions. Bench-stable and moisture-tolerant, it streamlines synthesis of functionalized biaryl architectures.
2-(3-Chloro-2-fluorophenyl)-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 ortho-heteroaryl substitution enables efficient construction of biaryl scaffolds with retained halogen functionality for downstream functionalization. The tetramethyl-substituted dioxaborolane core ensures excellent shelf stability and compatibility with diverse reaction conditions.
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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: