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CS-W001157 4
Total: USD 88.00

(2S,2'S,3S,3'S)-WingPhos

  • CAS No. 1435940-19-4

  • Cat. No. CS-0020506
  • Purity≥97%
  • MDL No.MFCD31630708

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

(2S,2'S,3S,3'S)-WingPhos|CS-0020506

Structure of 1435940-19-4

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General Information

  • CAS No. 1435940-19-4
  • Cat. No. CS-0020506
  • Purity ≥97%
  • MDL No. MFCD31630708
  • Storage 4°C, protect from light, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₅₀H₄₄O₂P₂
  • Molecular Weight 738.83
  • Synonym(s) (2S,2S’,3S,3S’)-WingPhos
  • SMILES [H][C@]1([C@]2([H])[P@@](C(C)(C)C)C(C(C3=C(C=CC=C4)C4=CC5=C3C=CC=C5)=CC=C6)=C6O2)[P@](C(C)(C)C)C7=C(C8=C(C=CC=C9)C9=CC%10=C8C=CC=C%10)C=CC=C7O1

Description

(2S,2'S,3S,3'S)-WingPhos is a sterically tuned, bench-stable phosphine ligand featuring a rigid biaryl backbone with strategically positioned substituents. This configuration enhances stability and electron density while promoting efficient palladium-catalyzed cross-coupling reactions under mild conditions. The ligand excels in challenging C–O and C–N bond formations, offering high selectivity and catalyst longevity in complex molecule synthesis.

Application

(2S,2'S,3S,3'S)-WingPhos serves as a highly effective, bench-stable phosphine ligand in palladium-catalyzed cross-coupling reactions. Its rigid, sterically defined structure enables selective C–C and C–heteroatom bond formation under mild conditions, with excellent functional group tolerance and consistent performance in Suzuki-Miyaura, Negishi, and Stille couplings. Designed for reproducible results in complex molecule synthesis, it facilitates efficient catalyst activation and minimizes decomposition pathways during scale-up.

Safety Information

Download SDS
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

Quality Control

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Computational Chemistry Data

  • TPSA   18.46
  • LogP   13.582
  • H_Acceptors   2
  • H_Donors   0
  • Rotatable_Bonds   3

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