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CS-W001157 4
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Bis(2-((S)-4-isopropyl-4,5-dihydrooxazol-2-yl)phenyl)amine

  • CAS No. 485394-20-5

  • Cat. No. CS-0145094
  • Molecule weight391.51
  • Purity≥95%
  • MDL No.None

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

Bis(2-((S)-4-isopropyl-4,5-dihydrooxazol-2-yl)phenyl)amine|CS-0145094

Structure of 485394-20-5

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General Information

  • CAS No. 485394-20-5
  • Cat. No. CS-0145094
  • Purity ≥95%
  • MDL No. None
  • Storage -20°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₄H₂₉N₃O₂
  • Molecular Weight 391.51
  • Synonym(s) Bis[2-((4S)-4,5-dihydro-4-isopropyloxazol-2-yl)phenyl]amine
  • SMILES CC(C)[C@H]1COC(C2=CC=CC=C2NC3=CC=CC=C3C4=N[C@@H](C(C)C)CO4)=N1

Description

Bis(2-((S)-4-isopropyl-4,5-dihydrooxazol-2-yl)phenyl)amine features a chiral oxazoline scaffold flanked by aryl amine units, delivering enhanced stereochemical control in asymmetric catalysis. The isopropyl-substituted dihydrooxazoline ring imparts steric rigidity and moisture tolerance, enabling robust performance under standard bench conditions. This configuration supports efficient metal coordination and selective transformation pathways in transition-metal-catalyzed reactions.

Application

Bis(2-((S)-4-isopropyl-4,5-dihydrooxazol-2-yl)phenyl)amine serves as a versatile chiral ligand scaffold in transition metal catalysis, enabling asymmetric transformations through well-established coordination modes. The dihydrooxazoline moiety provides robust steric and electronic control, while the aryl amine framework offers stability and compatibility with common synthetic protocols. Its bench-stable nature and functional group tolerance facilitate efficient use in palladium- and copper-catalyzed cross-coupling reactions, particularly in the construction of enantioenriched biaryl and heterocyclic architectures.

Safety Information

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GHS Pictogram :
GHS No : GHS09
Signal Word : Warning
UN#: 3077
Class : 9
Packing Group : Ⅲ
Hazard Statements : H410
Precautionary Statements : P273-P391-P501

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Computational Chemistry Data

  • TPSA   55.21
  • LogP   5.033
  • H_Acceptors   5
  • H_Donors   1
  • Rotatable_Bonds   6

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