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Structure of 850623-71-1
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Potassium trifluoro(4-nitrophenyl)borate delivers a stabilized, electron-deficient boronate moiety for cross-coupling reactions. The para-nitro group enhances reactivity while improving solubility in polar solvents. This bench-stable reagent enables efficient Suzuki-Miyaura coupling under mild conditions, streamlining synthesis of functionalized aryl compounds.
Potassium trifluoro(4-nitrophenyl)borate serves as a stable, bench-ready boron source for Suzuki-Miyaura cross-coupling reactions. Its trifluoroborate moiety enables efficient palladium-catalyzed coupling with aryl halides and pseudohalides, offering high functional group tolerance and predictable reactivity. The 4-nitrophenyl group enhances solubility and facilitates purification, making it ideal for iterative synthesis of complex biaryls and pharmaceutical intermediates.
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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: