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Structure of 1902154-93-1
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N-(Phenylsulfonyl)-N-((trifluoromethyl)thio)benzenesulfonamide features a dual sulfonamide architecture with orthogonal electron-withdrawing groups: a phenylsulfonyl moiety and a trifluoromethylthio substituent. This combination imparts high stability and enhanced electrophilicity, enabling efficient incorporation into complex molecular scaffolds under mild conditions. The molecule’s robustness facilitates use in iterative synthetic sequences without degradation.
N-(Phenylsulfonyl)-N-((trifluoromethyl)thio)benzenesulfonamide serves as a stable, bench-ready sulfonamide building block enabling selective C–H functionalization and heterocycle synthesis. Its dual sulfonamide architecture provides orthogonal reactivity for late-stage modifications, while the trifluoromethylthio group enhances metabolic stability and lipophilicity in medicinal chemistry applications. The molecule exhibits excellent functional group tolerance and facilitates efficient purification via crystallization or column chromatography.
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GHS Pictogram :
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GHS No : GHS02
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Signal Word : Danger
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UN#: 2920
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Class : 8
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Packing Group : Ⅱ
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Hazard Statements : H228-H314
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Precautionary Statements : P210-P233-P240-P241-P242-P243-P260-P264-P280-P301+P330+P331-P304+P340-P363-P370+P378-P405-P501
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Lot numbers can be found on the outside label of a product: