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Structure of 1027642-25-6
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Potassium ((benzyloxy)methyl)trifluoroborate delivers a stable, bench-ready boronate handle for Suzuki-Miyaura cross-coupling. The benzyloxy-methyl group enables selective protection and orthogonal reactivity, while the trifluoroborate moiety ensures high functional group tolerance and ease of handling under standard conditions.
Potassium ((benzyloxy)methyl)trifluoroborate serves as a stable, bench-ready boron source for Suzuki-Miyaura cross-coupling reactions. It enables efficient formation of biaryl and heteroaryl scaffolds with excellent functional group tolerance. The benzyloxymethyl group enhances solubility and stability, while the trifluoroborate moiety facilitates reliable C–C bond formation under standard catalytic conditions. Ideal for late-stage functionalization 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-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: