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CS-W001157 4
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(S)-4-(tert-Butyl)-2-(quinolin-2-yl)-4,5-dihydrooxazole

  • CAS No. 226387-12-8

  • Cat. No. CS-0088303
  • Purity≥95%
  • MDL No.MFCD28963788

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

(S)-4-(tert-Butyl)-2-(quinolin-2-yl)-4,5-dihydrooxazole|CS-0088303

Structure of 226387-12-8

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General Information

  • CAS No. 226387-12-8
  • Cat. No. CS-0088303
  • Purity ≥95%
  • MDL No. MFCD28963788
  • Storage 4°C, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₆H₁₈N₂O
  • Molecular Weight 254.33
  • Synonym(s) Quinoline, 2-[(4S)-4-(1,1-dimethylethyl)-4,5-dihydro-2-oxazolyl]-
  • SMILES CC(C)(C)[C@@H](CO1)N=C1C2=NC3=CC=CC=C3C=C2

Description

(S)-tBu-Quinox is a chiral, bench-stable quinoxaline derivative featuring a tert-butyl group at the 3-position. This steric shield enhances stability and solubility while preserving reactivity in asymmetric synthesis. The (S)-configuration enables precise stereocontrol in transition-metal-catalyzed couplings and C–H functionalization processes.

Application

(S)-tBu-Quinox serves as a robust chiral auxiliary in asymmetric synthesis, enabling stereoselective construction of quinoxaline-based scaffolds. Its tert-butyl group enhances bench stability and facilitates purification, while the chiral backbone provides high diastereoselectivity in C–H functionalization and cycloaddition reactions. Functions effectively in standard organic transformations with excellent functional group tolerance.

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 : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501

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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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