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Structure of 220239-64-5
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2,4,6-Trifluorobenzene-1-sulfonyl chloride serves as a highly effective sulfonylating agent for the synthesis of sulfonamide derivatives. Its electron-deficient aromatic ring enhances reactivity while maintaining bench stability, enabling efficient coupling with amines under mild conditions. The trifluoromethyl group imparts excellent functional group tolerance and facilitates purification via crystallization or chromatography. This reagent functions reliably in the construction of bioactive scaffolds and pharmaceutical intermediates where enhanced metabolic stability is required.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3265
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Class : 8
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Packing Group : Ⅱ
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Hazard Statements : H314
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Precautionary Statements : P264-P280-P301+P330+P331-P304+P340-P363-P405-P501
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Lot numbers can be found on the outside label of a product: