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Structure of 1041642-13-0
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Potassium trifluoro(isopropyl)borate offers a bench-stable, moisture-tolerant source of the trifluoroborate moiety. This reagent integrates seamlessly into cross-coupling protocols, enabling efficient C–C bond formation under mild conditions. The isopropyl group enhances solubility in organic solvents while maintaining high functional group compatibility.
Potassium trifluoro(isopropyl)borate serves as a stable, bench-friendly boron source for palladium-catalyzed cross-coupling reactions. It enables efficient Suzuki-Miyaura coupling with aryl and vinyl halides, offering excellent functional group tolerance and predictable reactivity. The isopropyl group enhances solubility and minimizes protodeboronation, making it particularly useful in the synthesis of complex heterocycles 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: