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CS-W001157 4
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(4S)-4,5-Dihydro-2-[2-[(S)-(4-methylphenyl)sulfinyl]phenyl]-4-phenyloxazole

  • CAS No. 402755-64-0

  • Cat. No. CS-0610813
  • Purity≥98%
  • MDL No.None

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

(4S)-4,5-Dihydro-2-[2-[(S)-(4-methylphenyl)sulfinyl]phenyl]-4-phenyloxazole|CS-0610813

Structure of 402755-64-0

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General Information

  • CAS No. 402755-64-0
  • Cat. No. CS-0610813
  • Purity ≥98%
  • MDL No. None
  • Storage 4°C, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₂H₁₉NO₂S
  • Molecular Weight 361.46
  • Synonym(s) None
  • SMILES O=[S@](C1=CC=CC=C1C2=N[C@@H](C3=CC=CC=C3)CO2)C4=CC=C(C)C=C4

Description

This chiral oxazole scaffold features a strategically positioned (S)-p-tolylsulfinyl group, enabling stereocontrolled synthesis in asymmetric catalysis. The phenyl and dihydrooxazole moieties combine for enhanced stability and predictable reactivity under standard bench conditions.

Application

(R)-4-Phenyl-2-(2-((S)-p-tolylsulfinyl)phenyl)-4,5-dihydrooxazole serves as a chiral building block for asymmetric synthesis, leveraging its stable oxazole core and defined stereocenters to facilitate enantioselective transformations. The (S)-p-tolylsulfinyl group provides a removable, stereocontrolling auxiliary, enabling predictable diastereoselective reactions in medicinal chemistry workflows. Its bench-stable nature and compatibility with standard functional group manipulations make it a practical choice for constructing complex heterocyclic scaffolds.

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   38.66
  • LogP   4.67982
  • H_Acceptors   3
  • H_Donors   0
  • Rotatable_Bonds   4

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