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Structure of 175676-42-3
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Trifluoromethyl 4-methylbenzenesulfonate serves as a potent trifluoromethylating agent in synthetic organic chemistry. This bench-stable reagent features a para-methyl-substituted arylsulfonate moiety that enhances reactivity and selectivity. It facilitates efficient C–CF₃ bond formation under mild conditions, enabling direct trifluoromethylation of nucleophiles without requiring transition metal catalysis.
Trifluoromethyl 4-methylbenzenesulfonate serves as a robust trifluoromethylating agent in transition-metal-catalyzed cross-coupling reactions. Its stable, bench-friendly nature and excellent functional group tolerance enable efficient C–CF₃ bond formation under mild conditions. Widely employed in the synthesis of fluorinated aromatic compounds and pharmaceutical intermediates, it facilitates direct introduction of the trifluoromethyl group with high chemoselectivity and reproducibility in standard organic workflows.
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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: