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CS-W001157 4
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(1S,2S)-N1,N2-Dimethyl-1,2-bis(3-(trifluoromethyl)phenyl)ethane-1,2-diamine

  • CAS No. 205873-26-3

  • Cat. No. CS-0182502
  • Purity≥98%
  • MDL No.None

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

(1S,2S)-N1,N2-Dimethyl-1,2-bis(3-(trifluoromethyl)phenyl)ethane-1,2-diamine|CS-0182502

Structure of 205873-26-3

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General Information

  • CAS No. 205873-26-3
  • Cat. No. CS-0182502
  • Purity ≥98%
  • MDL No. None
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₈H₁₈F₆N₂
  • Molecular Weight 376.34
  • Synonym(s) (1S,2S)-(-)-N,N'-Dimethyl-1,2-bis[3-(trifluoromethyl)phenyl]ethylenediamine
  • SMILES CN[C@H]([C@@H](NC)C1=CC(C(F)(F)F)=CC=C1)C2=CC(C(F)(F)F)=CC=C2

Description

This chiral diamine features two trifluoromethylphenyl groups flanking a dimethyl-substituted ethane backbone, delivering enhanced electron-withdrawing character and steric bulk. The (1S,2S) stereochemistry ensures high enantioselectivity in asymmetric catalysis, enabling precise control in transition metal complexation. Bench-stable and moisture-tolerant, it integrates seamlessly into synthetic workflows requiring robust chiral ligands.

Application

(1S,2S)-N1,N2-Dimethyl-1,2-bis(3-(trifluoromethyl)phenyl)ethane-1,2-diamine serves as a chiral diamine ligand in transition metal catalysis, enabling asymmetric transformations through well-defined coordination geometry. Its sterically congested bis(aryl) backbone and trifluoromethyl groups enhance electronic modulation and stability under reaction conditions. The molecule exhibits bench stability, facilitates efficient metal complexation, and supports high enantioselectivity in established coupling and reduction processes.

Safety Information

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GHS Pictogram :
GHS No : GHS09
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H410
Precautionary Statements : P273-P391-P501

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Computational Chemistry Data

  • TPSA   24.06
  • LogP   4.9454
  • H_Acceptors   2
  • H_Donors   2
  • Rotatable_Bonds   5

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