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Structure of 1408168-76-2
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Potassium trifluoro(2-((tetrahydro-2H-pyran-2-yl)oxy)ethyl)borate delivers a stable, moisture-tolerant boron source for cross-coupling reactions. The tetrahydro-2H-pyran-2-yl protecting group ensures enhanced shelf life and ease of handling. This reagent integrates smoothly into palladium-catalyzed transformations, enabling efficient C–C bond formation under mild conditions.
Potassium trifluoro(2-((tetrahydro-2H-pyran-2-yl)oxy)ethyl)borate serves as a stable, bench-ready boron reagent enabling efficient Suzuki-Miyaura cross-coupling reactions. The tetrahydro-2H-pyran-2-yl ether protecting group ensures high functional group tolerance and compatibility with diverse substrates, facilitating selective C–C bond formation under mild conditions. Its robustness simplifies purification and handling, making it ideal for iterative 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-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: