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Structure of 361447-81-6
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1-Phenyl-1H-imidazole trifluoromethanesulfonate serves as a highly reactive electrophilic imidazolium source, enabling efficient C–H functionalization under mild conditions. The triflate counterion ensures excellent solubility and stability, facilitating its use in transition-metal-catalyzed coupling reactions and synthetic transformations requiring precise control over reactivity.
1-Phenyl-1H-imidazole trifluoromethanesulfonate serves as a reliable electrophilic imidazole source in palladium-catalyzed cross-coupling reactions. Its triflate leaving group enables efficient C–N bond formation under mild conditions, offering excellent functional group tolerance and bench stability. This reagent facilitates the synthesis of biologically relevant imidazole-containing scaffolds and is particularly useful in the construction of heterocyclic frameworks common in medicinal chemistry 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: