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(S)-2,2'-Bis[bis(3,5-dimethylphenyl)phosphino]-4,4',6,6'-tetramethoxy)-1,1'-biphenyl

  • CAS No. 1365531-90-3

  • Cat. No. CS-0087305
  • Molecule weight754.87
  • Purity≥97%
  • MDL No.None

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

(S)-2,2'-Bis[bis(3,5-dimethylphenyl)phosphino]-4,4',6,6'-tetramethoxy)-1,1'-biphenyl|CS-0087305

Structure of 1365531-90-3

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General Information

  • CAS No. 1365531-90-3
  • Cat. No. CS-0087305
  • Purity ≥97%
  • MDL No. None
  • Storage 4°C, protect from light, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₄₈H₅₂O₄P₂
  • Molecular Weight 754.87
  • Synonym(s) (S)-2,2''-Bis[bis(3,5-dimethylphenyl)phosphino]-4,4'',6,6''-tetramethoxy)-1,1''-biphenyl
  • SMILES COC1=CC(OC)=CC([P]C2=CC(C)=CC(C)=C2)=[C@]1[C@]3=C(OC)C=C(OC)C=C3[P]C4=CC(C)=CC(C)=C4

Description

(S)-2,2'-Bis[bis(3,5-dimethylphenyl)phosphino]-4,4',6,6'-tetramethoxy-1,1'-biphenyl is a sterically hindered, electron-rich chiral ligand featuring four methoxy groups that enhance solubility and stability. This configuration enables efficient coordination in palladium-catalyzed cross-coupling reactions, delivering high selectivity and turnover under mild conditions.

Application

(S)-2,2'-Bis[bis(3,5-dimethylphenyl)phosphino]-4,4',6,6'-tetramethoxy-1,1'-biphenyl serves as a sterically encumbered, electron-rich phosphine ligand that enables efficient palladium-catalyzed cross-coupling reactions. Its orthogonal methoxy groups enhance solubility and stability, while the chiral backbone provides stereocontrol in asymmetric transformations. Functions effectively in Suzuki-Miyaura, Negishi, and Stille couplings under mild conditions, offering high yields and reproducibility in complex molecule synthesis.

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   36.92
  • LogP   5.88028
  • H_Acceptors   4
  • H_Donors   0
  • Rotatable_Bonds   9

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