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Structure of 456-64-4
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1,1,1-Trifluoro-N-phenylmethanesulfonamide features a trifluoromethyl group linked to a sulfonamide nitrogen, delivering enhanced stability and lipophilicity. This configuration supports efficient incorporation into bioactive scaffolds, particularly in medicinal chemistry where electron-withdrawing character and metabolic resistance are advantageous. The phenyl ring provides a rigid aromatic handle for further derivatization.
1,1,1-Trifluoro-N-phenylmethanesulfonamide serves as a stable, bench-ready trifluoromethylating agent that facilitates the introduction of CF₃ groups under mild conditions. Its robust functional group tolerance enables selective trifluoromethylation in complex molecule synthesis, particularly valuable in medicinal chemistry and agrochemical development. The compound functions as a reliable source of the trifluoromethyl anion equivalent and is compatible with standard reaction protocols requiring minimal purification.
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H315-H319
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Precautionary Statements : P264-P270-P280-P302+P352-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: