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CS-W001157 4
Total: USD 88.00

2,6-Bis((S)-4-((S)-sec-butyl)-4,5-dihydrooxazol-2-yl)pyridine

  • CAS No. 118949-62-5

  • Cat. No. CS-0064045
  • Purity≥95%
  • MDL No.None

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

2,6-Bis((S)-4-((S)-sec-butyl)-4,5-dihydrooxazol-2-yl)pyridine|CS-0064045

Structure of 118949-62-5

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General Information

  • CAS No. 118949-62-5
  • Cat. No. CS-0064045
  • Purity ≥95%
  • MDL No. None
  • Storage -20°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₉H₂₇N₃O₂
  • Molecular Weight 329.44
  • Synonym(s) (S)-sBu-Pybox
  • SMILES C[C@@H](CC)[C@H]1COC(C2=CC=CC(C3=N[C@@H]([C@@H](C)CC)CO3)=N2)=N1

Description

This chiral pyridine scaffold features two sterically encumbered oxazoline groups at the 2,6-positions, enabling precise coordination in asymmetric catalysis. The (S)-sec-butyl substituents enhance rigidity and enantioselectivity, while the dihydrooxazol-2-yl moieties offer stable, electron-rich binding sites. Ideal for transition metal complexation in stereoselective transformations under ambient conditions.

Application

2,6-Bis((S)-4-((S)-sec-butyl)-4,5-dihydrooxazol-2-yl)pyridine serves as a chiral, sterically hindered ligand scaffold enabling efficient asymmetric catalysis in transition-metal-catalyzed transformations. Its oxazoline moieties provide robust coordination to palladium and copper centers, while the (S)-sec-butyl groups enforce defined stereochemical control. The pyridine core offers strong π-basicity and stability under standard reaction conditions. This structure facilitates enantioselective C–C bond formation with high functional group tolerance and ease of purification, making it suitable for iterative synthesis in medicinal chemistry workflows.

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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

  • TPSA   56.07
  • LogP   3.4646
  • H_Acceptors   5
  • H_Donors   0
  • Rotatable_Bonds   6

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