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CS-W001157 4
Total: USD 88.00

(S)-Bn-iQuinox

  • CAS No. 2058236-52-3

  • Cat. No. CS-0145102
  • Molecule weight288.34
  • Purity≥97%
  • MDL No.None

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

(S)-Bn-iQuinox|CS-0145102

Structure of 2058236-52-3

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General Information

  • CAS No. 2058236-52-3
  • Cat. No. CS-0145102
  • Purity ≥97%
  • MDL No. None
  • Storage -20°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₉H₁₆N₂O
  • Molecular Weight 288.34
  • Synonym(s) (S)-4-Benzyl-2-(isoquinolin-1-yl)-4,5-dihydrooxazole
  • SMILES [C@@H]1(COC(C2=NC=CC3=CC=CC=C23)=N1)CC4=CC=CC=C4

Description

(S)-Bn-iQuinox delivers a chiral, bench-stable scaffold for asymmetric synthesis, featuring a protected amino group and a quinoxaline core that enables efficient coupling reactions. This rigid, electron-deficient heterocycle facilitates stereocontrolled transformations in medicinal chemistry and materials science applications.

Application

(S)-Bn-iQuinox serves as a chiral building block for the synthesis of quinoline-based pharmaceutical intermediates, enabling efficient access to bioactive heterocycles through Pd-catalyzed cross-coupling and C–H functionalization reactions. Its benzyl-protected indole moiety offers enhanced bench stability and facilitates straightforward purification, while the (S)-configuration ensures stereochemical fidelity in asymmetric synthesis.

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-P280-P302+P352

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Computational Chemistry Data

  • TPSA   34.48
  • LogP   3.6229
  • H_Acceptors   3
  • H_Donors   0
  • Rotatable_Bonds   3

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