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Structure of 1150655-02-9
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Potassium trifluoro(neopentyl)borate delivers a sterically shielded, bench-stable boronate handle ideal for cross-coupling reactions. The neopentyl group confers exceptional resistance to protodeboronation, while the trifluoroborate moiety enables efficient transmetalation under mild conditions. This reagent integrates seamlessly into Suzuki-Miyaura protocols, offering high functional group tolerance and predictable reactivity in complex molecule synthesis.
Potassium trifluoro(neopentyl)borate serves as a stable, bench-friendly boron source for Suzuki-Miyaura cross-coupling reactions. Its neopentyl group enhances hydrolytic stability and minimizes protodeboronation, enabling reliable coupling with aryl and heteroaryl halides under mild conditions. The trifluoroborate moiety facilitates efficient transmetalation, offering excellent functional group tolerance and predictable reactivity in complex molecule 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-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: