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Structure of 910251-11-5
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Potassium trifluoro(methoxymethyl)borate delivers a highly stable, moisture-tolerant boron source for C–C bond formation. This bench-stable reagent integrates seamlessly into Suzuki-Miyaura coupling protocols, enabling efficient cross-coupling under mild conditions. The methoxymethyl group enhances solubility and functional group compatibility, while the trifluoroborate moiety ensures predictable reactivity.
Potassium trifluoro(methoxymethyl)borate serves as a stable, bench-ready boron reagent enabling efficient Suzuki-Miyaura cross-coupling reactions. It functions as a reliable source of the trifluoromethyl-containing methoxymethyl group, offering excellent functional group tolerance and compatibility with diverse aryl, heteroaryl, and vinyl electrophiles. Its low toxicity and ease of handling make it ideal for scalable synthesis of fluorinated building blocks in medicinal chemistry and materials science.
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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: