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CS-W001157 4
Total: USD 88.00

(S,S)-tBu-Dbfox

  • CAS No. 2067322-25-0

  • Cat. No. CS-0145081
  • Purity≥97%
  • MDL No.None

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

(S,S)-tBu-Dbfox|CS-0145081

Structure of 2067322-25-0

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General Information

  • CAS No. 2067322-25-0
  • Cat. No. CS-0145081
  • Purity ≥97%
  • MDL No. None
  • Storage -20°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₆H₃₀N₂O₃
  • Molecular Weight 418.53
  • Synonym(s) (4S,4'S)-2,2'-Dibenzo[b,d]furan-4,6-diylbis[4-(2-methyl-2-propanyl)-4,5-dihydro-1,3-oxazole]
  • SMILES CC(C)(C)[C@H]1COC(C2=CC=CC3=C2OC4=C3C=CC=C4C5=N[C@@H](C(C)(C)C)CO5)=N1

Description

(S,S)-tBu-Dbfox is a bench-stable, chiral bis(oxazoline) ligand featuring a tert-butyl-substituted dihydroxybenzene core. This sterically hindered architecture enhances enantioselectivity in transition-metal-catalyzed asymmetric reactions, particularly in copper-mediated transformations. The ligand's robustness under standard conditions enables reliable performance in process development workflows.

Application

(S,S)-tBu-Dbfox serves as a highly effective chiral ligand in asymmetric transition metal catalysis, enabling enantioselective transformations such as allylic alkylation and conjugate addition. Its robust tert-butyl substituents enhance steric control and bench stability, while the dibenzofuran scaffold provides rigidity and favorable electronic properties. The ligand demonstrates excellent functional group tolerance and reproducible enantioselectivity in established synthetic protocols, making it a practical choice for scalable asymmetric synthesis.

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P302+P352

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Computational Chemistry Data

  • TPSA   56.32
  • LogP   5.969
  • H_Acceptors   5
  • H_Donors   0
  • Rotatable_Bonds   2

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