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Structure of 912350-00-6
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Potassium 4-iodophenyltrifluoroborate delivers a stable, bench-ready boronate handle for Suzuki-Miyaura cross-coupling. The para-iodo substituent enables selective activation, while the trifluoroborate moiety resists hydrolysis and tolerates diverse reaction conditions. This reagent integrates seamlessly into complex molecular architectures with minimal decomposition.
Potassium 4-iodophenyltrifluoroborate serves as a stable, bench-ready boron source for Suzuki-Miyaura cross-coupling reactions. It functions reliably with aryl iodides under standard catalytic conditions, enabling efficient C–C bond formation with high functional group tolerance. The trifluoroborate moiety enhances stability and solubility, simplifying purification and facilitating scalable synthesis of biaryl architectures common in pharmaceutical and agrochemical development.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: