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(R,S)-Bn-BisPh-Sabox

  • CAS No. 897942-79-9

  • Cat. No. CS-0145074
  • Purity≥95%
  • MDL No.None

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

(R,S)-Bn-BisPh-Sabox|CS-0145074

Structure of 897942-79-9

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General Information

  • CAS No. 897942-79-9
  • Cat. No. CS-0145074
  • Purity ≥95%
  • MDL No. None
  • Storage -20°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₄₅H₃₈N₂O₂
  • Molecular Weight 638.80
  • Synonym(s) Oxazole, 2,2'-[2-phenyl-1-(phenylmethyl)ethylidene]bis[4,5-dihydro-4,5-diphenyl-, (4R,4'R,5S,5'S)- (9CI)
  • SMILES C1(C(CC2=CC=CC=C2)(CC3=CC=CC=C3)C4=N[C@H](C5=CC=CC=C5)[C@H](C6=CC=CC=C6)O4)=N[C@H](C7=CC=CC=C7)[C@H](C8=CC=CC=C8)O1

Description

(R,S)-Bn-BisPh-Sabox delivers a chiral bisphosphine scaffold with benzyl-protected phosphorus centers, enabling robust coordination in asymmetric catalysis. The stereochemically defined backbone supports high enantioselectivity in transition-metal-catalyzed transformations, particularly in cross-coupling and hydrogenation processes. This bench-stable ligand features enhanced solubility in organic media and tolerates air during handling, streamlining synthetic workflows.

Application

(R,S)-Bn-BisPh-Sabox serves as a robust chiral ligand for asymmetric catalysis, enabling high enantioselectivity in transition-metal-catalyzed transformations. Its benzyl-protected bisphosphine architecture offers excellent bench stability and functional group tolerance, facilitating efficient synthesis of enantiomerically enriched intermediates. Widely applicable in cross-coupling and hydrogenation protocols, it functions reliably across diverse reaction conditions, making it a practical choice for industrial and academic R&D workflows.

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-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

  • TPSA   43.18
  • LogP   10.2808
  • H_Acceptors   4
  • H_Donors   0
  • Rotatable_Bonds   10

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