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Structure of 66107-30-0
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4-Bromophenyl trifluoromethanesulfonate serves as a robust arylating agent in transition-metal-catalyzed cross-coupling reactions. The triflate group enables facile C–C bond formation under mild conditions, while the bromo substituent offers orthogonal reactivity for sequential functionalization. This bifunctional scaffold integrates seamlessly into complex molecular architectures.
4-Bromophenyl trifluoromethanesulfonate serves as a reliable aryl electrophile in palladium-catalyzed cross-coupling reactions, enabling efficient C–C bond formation under standard Suzuki, Stille, and Negishi conditions. Its triflate group provides high reactivity and stability, facilitating clean transformations with broad functional group tolerance. The molecule exhibits excellent bench stability and simplifies purification, making it well-suited for iterative synthesis workflows 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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362
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Lot numbers can be found on the outside label of a product: