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Structure of 865352-01-8
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This sulfonyl chloride features a trifluoromethyl group at the para position and a difluoroethoxy substituent, delivering enhanced electron-withdrawing character and improved solubility. The combination enables efficient coupling in synthetic workflows, particularly for fluorinated aromatic systems requiring stable, reactive intermediates under standard conditions.
2-(2,2-Difluoroethoxy)-6-(trifluoromethyl)benzene-1-sulfonyl chloride serves as a versatile sulfonyl chloride building block for constructing sulfonamide derivatives. Its reactivity is enhanced by the electron-withdrawing trifluoromethyl and difluoroethoxy substituents, which improve electrophilicity at the sulfonyl center. The compound exhibits good bench stability and facilitates clean coupling with amines under mild conditions, enabling efficient access to fluorinated sulfonamides used in medicinal chemistry and agrochemical research.
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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#: 3261
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H314
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Precautionary Statements : P260-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: