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Structure of 1494466-28-2
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Potassium trifluoro(4-fluorophenyl)methylboranuide delivers a stable, bench-ready boron source for cross-coupling reactions. The para-fluorophenyl group enhances electron-withdrawing character, enabling efficient palladium-catalyzed transformations. This reagent combines high functional group tolerance with moisture-resistant handling, streamlining synthesis in complex molecular architectures.
Potassium trifluoro[(4-fluorophenyl)methyl]boranuide serves as a stable, bench-ready boron source for Suzuki-Miyaura cross-coupling reactions. It exhibits high functional group tolerance and facilitates efficient C–C bond formation with aryl and heteroaryl halides under mild conditions. The fluorinated benzyl moiety enhances solubility and reactivity while maintaining compatibility with common reaction protocols. This reagent enables reliable access to biaryl architectures prevalent in pharmaceutical and agrochemical scaffolds.
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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-P270-P271-P280-P302+P352-P304+P340-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: