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Structure of 1430219-71-8
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This trifluoroborate ester integrates a protected piperidinyl moiety, enabling direct use in palladium-catalyzed cross-coupling reactions. The tert-butyl carbamate group ensures stability under standard conditions, while the trifluoroborate functionality delivers efficient coupling performance.
Potassium (1-(tert-butoxycarbonyl)piperidin-4-yl)trifluoroborate serves as a stable, bench-ready boron building block for Suzuki-Miyaura coupling reactions. The Boc-protected piperidine moiety enables direct incorporation into diverse heterocyclic scaffolds and bioactive molecules. Its excellent functional group tolerance and ease of purification facilitate efficient late-stage diversification in medicinal chemistry and process development workflows.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: