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(S,R)-BisPh-Pybox

  • CAS No. 292625-77-5

  • Cat. No. CS-0090906
  • Purity≥95%
  • MDL No.MFCD32640806

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

(S,R)-BisPh-Pybox|CS-0090906

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General Information

  • CAS No. 292625-77-5
  • Cat. No. CS-0090906
  • Purity ≥95%
  • MDL No. MFCD32640806
  • Storage 4°C, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₃₅H₂₇N₃O₂
  • Molecular Weight 521.61
  • Synonym(s) 2,6-bis[(4S,5R)-4,5-dihydro-4,5-diphenyl-2-oxazolyl]-Pyridine
  • SMILES C1(C2=N[C@@H](C3=CC=CC=C3)[C@@H](C4=CC=CC=C4)O2)=CC=CC(C5=N[C@@H](C6=CC=CC=C6)[C@@H](C7=CC=CC=C7)O5)=N1

Description

This chiral bisphosphine ligand features a Pybox backbone with (S,R) stereochemistry, delivering high enantioselectivity in transition metal catalysis. The rigid, electron-rich framework enhances coordination stability and facilitates asymmetric transformations under mild conditions.

Application

(S,R)-BisPh-Pybox serves as a highly effective chiral ligand in transition metal-catalyzed asymmetric synthesis, particularly for enantioselective transformations involving palladium and copper complexes. Its rigid, bidentate architecture with phenyl-substituted pyridine and oxazoline moieties enables high stereocontrol in C–C and C–heteroatom bond-forming reactions. The ligand exhibits excellent bench stability, ease of handling, and compatibility with diverse functional groups, making it a practical choice for scalable asymmetric catalysis in medicinal chemistry and fine chemical synthesis.

Safety Information

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Computational Chemistry Data

  • TPSA   56.07
  • LogP   7.6004
  • H_Acceptors   5
  • H_Donors   0
  • Rotatable_Bonds   6

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