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Structure of 1189042-70-3
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This boronate ester features a fluorinated nitroaryl group enabling direct C–H functionalization in cross-coupling reactions. The tetramethyl-substituted dioxaborolane ring enhances stability and solubility, facilitating handling under standard conditions. Ideal for Suzuki-Miyaura couplings requiring electron-deficient aryl partners.
2-(2-Fluoro-3-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane serves as a stable, bench-ready boronate building block for palladium-catalyzed cross-coupling reactions. Its fluorinated nitroaryl motif enables efficient Suzuki-Miyaura coupling with diverse partners, offering high functional group tolerance and predictable regiochemistry. The tetramethyl-substituted dioxaborolane enhances stability and simplifies purification, making it ideal for constructing complex heterocycles and pharmaceutical scaffolds in iterative synthesis 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 : 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: