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N-[(1R,2R)-2-Amino-1,2-diphenylethyl]-1,1,1-trifluoromethanesulfonamide

  • CAS No. 852212-89-6

  • Cat. No. CS-0093736
  • Purity≥98%
  • MDL No.None

*For research and further manufacturing use only, not for direct human use.

N-[(1R,2R)-2-Amino-1,2-diphenylethyl]-1,1,1-trifluoromethanesulfonamide|CS-0093736

Structure of 852212-89-6

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General Information

  • CAS No. 852212-89-6
  • Cat. No. CS-0093736
  • Purity ≥98%
  • MDL No. None
  • Storage 4°C, protect from light, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₅H₁₅F₃N₂O₂S
  • Molecular Weight 344.35
  • Synonym(s) N-[(1R,2R)-2-aMino-1,2-diphenylethyl]-1,1,1-trifluoro-MethanesulfonaMide
  • SMILES N[C@@H]([C@H](NS(=O)(C(F)(F)F)=O)C1=CC=CC=C1)C2=CC=CC=C2

Description

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.

Application

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.

Safety Information

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GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H315-H319
Precautionary Statements : P264-P280-P302+P352-P362

Quality Control

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Computational Chemistry Data

  • TPSA   72.19
  • LogP   2.8669
  • H_Acceptors   3
  • H_Donors   2
  • Rotatable_Bonds   5

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