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CS-W001157 4
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(4S,4'S)-4,4'-Di((S)-sec-butyl)-4,4',5,5'-tetrahydro-2,2'-bioxazole

  • CAS No. 133463-89-5

  • Cat. No. CS-0163378
  • Purity≥95%
  • MDL No.None

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

(4S,4'S)-4,4'-Di((S)-sec-butyl)-4,4',5,5'-tetrahydro-2,2'-bioxazole|CS-0163378

Structure of 133463-89-5

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General Information

  • CAS No. 133463-89-5
  • Cat. No. CS-0163378
  • Purity ≥95%
  • MDL No. None
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₄H₂₄N₂O₂
  • Molecular Weight 252.35
  • Synonym(s) (4S,4'S)-4,4'-Di[(2S)-2-butanyl]-4,4',5,5'-tetrahydro-2,2'-bi-1,3-oxazole
  • SMILES CC[C@@H]([C@@H]1N=C(C2=N[C@@H]([C@@H](C)CC)CO2)OC1)C

Description

This chiral oxazole derivative features a rigid, asymmetric backbone with sterically hindered sec-butyl groups at the 4 and 4' positions, enhancing stability and selectivity. The (4S,4'S) configuration ensures precise stereochemical control in asymmetric synthesis. Designed for use in catalytic systems and as a ligand scaffold, it delivers high enantioselectivity under mild reaction conditions.

Application

(4S,4'S)-4,4'-Di((S)-sec-butyl)-4,4',5,5'-tetrahydro-2,2'-bioxazole serves as a robust chiral auxiliary in asymmetric synthesis, enabling stereoselective C–C bond formation through well-established oxazoline-directed enolization and metalation protocols. Its bench-stable, crystalline nature and excellent functional group tolerance facilitate straightforward purification and integration into multi-step sequences. The rigid, chiral framework supports high diastereoselectivity in key transformations, making it a practical choice for the construction of complex heterocyclic scaffolds and stereochemically defined intermediates in medicinal chemistry.

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   43.18
  • LogP   2.6732
  • H_Acceptors   4
  • H_Donors   0
  • Rotatable_Bonds   5

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