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Structure of 351003-43-5
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3,4,5-Trifluorobenzenesulfonyl chloride features a highly electron-deficient aromatic ring that enhances reactivity in sulfonylation processes. This bench-stable reagent facilitates efficient introduction of sulfonate groups into nucleophilic substrates under mild conditions, offering superior selectivity and yield in synthetic applications.
3,4,5-Trifluorobenzenesulfonyl chloride serves as a highly reactive sulfonylating agent for the efficient introduction of trifluoromethyl-substituted sulfonamide groups. Its electron-deficient aromatic ring enhances electrophilicity, enabling rapid reaction with amines and alcohols under mild conditions. The compound exhibits excellent bench stability and facilitates clean, high-yielding transformations, making it ideal for constructing fluorinated sulfonamide building blocks in medicinal chemistry and agrochemical synthesis.
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GHS Pictogram :
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GHS No : GHS02,GHS05
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Signal Word : Danger
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UN#: 2924
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Class : 3,8
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Packing Group : Ⅲ
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Hazard Statements : H225-H314
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Precautionary Statements : P210-P240-P241-P280-P370+P378
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Lot numbers can be found on the outside label of a product: