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Structure of 1015484-22-6
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Potassium trifluoro((4-methylpiperazin-1-yl)methyl)borate delivers a stable, moisture-tolerant boron source featuring a sterically hindered piperazinylmethyl scaffold. This reagent integrates readily into cross-coupling protocols, enabling efficient C–B bond formation under mild conditions. The electron-rich piperazine moiety enhances reactivity while maintaining bench stability and ease of handling in synthetic workflows.
Potassium trifluoro((4-methylpiperazin-1-yl)methyl)borate serves as a stable, bench-friendly boron reagent enabling efficient Suzuki-Miyaura cross-coupling reactions. Its trifluoroborate moiety exhibits high functional group tolerance and compatibility with diverse aryl and heteroaryl electrophiles. The 4-methylpiperazine side chain enhances solubility and stability, facilitating straightforward purification and reproducible coupling outcomes in medicinal chemistry and process synthesis 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: