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CS-W001157 4
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(3aS,8aR)-2-(Quinolin-2-yl)-3a,8a-dihydro-8H-indeno[1,2-d]oxazole

  • CAS No. 2055935-90-3

  • Cat. No. CS-0096801
  • Molecule weight286.33
  • Purity≥97%
  • MDL No.None

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

(3aS,8aR)-2-(Quinolin-2-yl)-3a,8a-dihydro-8H-indeno[1,2-d]oxazole|CS-0096801

Structure of 2055935-90-3

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General Information

  • CAS No. 2055935-90-3
  • Cat. No. CS-0096801
  • Purity ≥97%
  • MDL No. None
  • Storage 4°C, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₉H₁₄N₂O
  • Molecular Weight 286.33
  • Synonym(s) (3aS,8aR)-2-(2-Quinolinyl)-8,8a-dihydro-3aH-indeno[1,2-d][1,3]oxazole
  • SMILES C1(C=CC=C2)=C2N=C(C3=N[C@@H](C(C=CC=C4)=C4C5)[C@@H]5O3)C=C1

Description

(S,R)-In-Quinox delivers a stereochemically defined quinoxaline scaffold with enhanced solubility and stability under standard handling conditions. This chiral heterocycle integrates seamlessly into medicinal chemistry campaigns, offering precise spatial control for target engagement in kinase inhibition and receptor modulation studies.

Application

(S,R)-In-Quinox serves as a versatile chiral building block in synthetic organic chemistry, enabling the construction of quinoxaline-based scaffolds with defined stereochemistry. Its stability under standard reaction conditions and compatibility with diverse functional groups facilitate efficient synthesis of bioactive heterocycles. The compound functions effectively in coupling reactions and transition-metal-catalyzed transformations, supporting scalable access to complex molecular architectures relevant to medicinal chemistry research.

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   3.6776
  • H_Acceptors   3
  • H_Donors   0
  • Rotatable_Bonds   1

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