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Structure of 374564-36-0
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Potassium trifluoro(4-formylphenyl)borate delivers a reactive boronate handle paired with an electron-deficient aryl group, enabling efficient Suzuki-Miyaura coupling under mild conditions. This bench-stable reagent integrates seamlessly into synthetic workflows requiring precise C–C bond formation.
Potassium trifluoro(4-formylphenyl)borate serves as a stable, bench-ready boron reagent enabling efficient Suzuki-Miyaura cross-coupling reactions. Its formyl group provides orthogonal functionality for downstream derivatization, while the trifluoroborate moiety ensures high chemoselectivity and compatibility with diverse functional groups. This reagent facilitates reliable C–C bond formation under mild conditions, making it ideal for constructing complex aryl scaffolds in medicinal chemistry and materials synthesis.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: