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Structure of 870238-67-8
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This boronate ester features a cyano-fluorophenyl moiety with enhanced stability and compatibility in cross-coupling reactions. The tetramethyl-substituted dioxaborolane ring resists protodeboronation and enables reliable Suzuki-Miyaura coupling under standard conditions. Designed for efficient integration into complex molecular architectures, this reagent delivers high functional group tolerance and predictable reactivity.
2-(4-Cyano-3-fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane serves as a stable, bench-ready boronate building block for Suzuki-Miyaura cross-coupling reactions. Its ortho-fluoro and cyano substituents enable selective functionalization in complex molecule synthesis, with excellent tolerance to diverse reaction conditions. The tetramethyl-substituted dioxaborolane enhances stability and simplifies purification, making it ideal for constructing biaryl and heterocyclic scaffolds in medicinal chemistry and materials science applications.
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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: