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Structure of 910251-10-4
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Potassium (tert-butoxymethyl)trifluoroborate serves as a stable, bench-friendly boronate source for Suzuki-Miyaura cross-coupling reactions. The tert-butoxymethyl group enhances solubility and minimizes protodeboronation, enabling efficient coupling under mild conditions. This reagent integrates seamlessly into synthetic workflows requiring selective C–C bond formation.
Potassium (tert-butoxymethyl)trifluoroborate serves as a stable, bench-friendly boron building block for Suzuki-Miyaura cross-coupling reactions. Its trifluoroborate group enables efficient C–C bond formation under mild conditions, with excellent functional group tolerance and compatibility with diverse substrates. The tert-butoxymethyl protecting group enhances stability and simplifies purification, making it a practical choice for the synthesis of complex molecular architectures in medicinal chemistry and materials science applications.
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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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: