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Structure of 852212-89-6
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This trifluoromethanesulfonamide derivative features a chiral diphenylethyl amine scaffold, offering enhanced stability and solubility in organic media. The electron-withdrawing trifluoromethylsulfonyl group imparts strong electrophilicity, enabling efficient coupling reactions. Designed for use in asymmetric synthesis, it serves as a robust chiral auxiliary in enantioselective transformations.
N-[(1R,2R)-2-Amino-1,2-diphenylethyl]-1,1,1-trifluoromethanesulfonamide serves as a versatile chiral auxiliary in asymmetric synthesis, enabling stereoselective transformations through its well-defined stereochemistry and stable trifluoromethylsulfonyl group. The molecule exhibits bench stability, facilitates efficient purification, and functions effectively in amide bond formation and enantioselective functionalization reactions. Its orthogonality to common protecting groups supports complex molecule assembly in medicinal chemistry workflows.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362
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Lot numbers can be found on the outside label of a product: