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CS-W001157 4
Total: USD 88.00

(S)-tBu-iQuinox

  • CAS No. 1402851-52-8

  • Cat. No. CS-0087918
  • Purity≥98%
  • MDL No.MFCD32201195

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

(S)-tBu-iQuinox|CS-0087918

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General Information

  • CAS No. 1402851-52-8
  • Cat. No. CS-0087918
  • Purity ≥98%
  • MDL No. MFCD32201195
  • Storage -20°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₆H₁₈N₂O
  • Molecular Weight None
  • Synonym(s) 1-[(4S)-4-tert-Butyl-4,5-dihydro-2-oxazolyl]isoquinoline
  • SMILES CC(C)([C@H]1COC(C2=NC=CC3=CC=CC=C23)=N1)C

Description

(S)-tBu-iQuinox is a bench-stable, sterically hindered chiral auxiliary designed for asymmetric synthesis. This quinoxaline-based scaffold integrates seamlessly into enantioselective transformations, offering high diastereoselectivity in C–C bond formation. The (S)-configuration and tert-butyl substitution enhance stereocontrol and stability under standard reaction conditions.

Application

(S)-tBu-iQuinox serves as a robust chiral auxiliary in asymmetric synthesis, enabling stereoselective construction of quinoline and isoquinoline scaffolds. Its tert-butyl group confers enhanced bench stability and facilitates straightforward purification, while the rigid bicyclic framework provides high diastereoselectivity in electrophilic functionalization and coupling reactions. Functions effectively in standard amine- or metal-catalyzed transformations, offering reliable access to enantioenriched heterocyclic building blocks for medicinal chemistry applications.

Safety Information

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Computational Chemistry Data

  • TPSA   34.48
  • LogP   3.4263
  • H_Acceptors   3
  • H_Donors   0
  • Rotatable_Bonds   1

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