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Structure of 1408168-73-9
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Potassium (2-benzyloxyethyl)trifluoroborate delivers a stable, bench-ready boron source for Suzuki-Miyaura cross-coupling reactions. The benzyloxyethyl group enhances solubility and functional group tolerance, enabling efficient C–C bond formation under mild conditions. This reagent integrates seamlessly into synthetic workflows requiring precise boron delivery without protodeboronation.
Potassium (2-benzyloxyethyl)trifluoroborate serves as a stable, bench-ready boron building block for Suzuki-Miyaura cross-coupling reactions. Its trifluoroborate group enables efficient C–C bond formation under mild conditions, with the benzyloxyethyl protecting group offering orthogonal stability and convenient deprotection. This reagent facilitates the synthesis of functionalized alkylated arenes and heterocyclic scaffolds commonly encountered 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-H315-H319-H335
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Precautionary Statements : P261-P280-P302+P352
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Lot numbers can be found on the outside label of a product: