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CS-W001157 4
Total: USD 88.00

(R)-5,​5',​6,​6',​7,​7',​8,​8'-​Octahydro-​3,​3'-​diphenyl-[1,​1'-​binaphthalene]​-​2,​2'-​diol

  • CAS No. 396134-73-9

  • Cat. No. CS-0087583
  • Purity≥97%
  • MDL No.None

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

(R)-5,​5',​6,​6',​7,​7',​8,​8'-​Octahydro-​3,​3'-​diphenyl-[1,​1'-​binaphthalene]​-​2,​2'-​diol|CS-0087583

Structure of 396134-73-9

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General Information

  • CAS No. 396134-73-9
  • Cat. No. CS-0087583
  • 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 C₃₂H₃₀O₂
  • Molecular Weight 446.58
  • Synonym(s) R-5,5',6,6',7,7',8,8'-octahydro-3,3'-diphenyl-[1,1'-Binaphthalene]-2,2'-diol
  • SMILES OC(C(C1=CC=CC=C1)=C2)=C(C3=C(CCCC4)C4=CC(C5=CC=CC=C5)=C3O)C6=C2CCCC6

Description

This chiral diol features a rigid binaphthyl backbone with sterically encumbered hydroxyl groups, enabling high enantioselectivity in asymmetric synthesis. The octahydro-bridged framework imparts exceptional stability and solubility in organic media, facilitating its use in catalytic applications.

Application

(R)-5,5',6,6',7,7',8,8'-Octahydro-3,3'-diphenyl-[1,1'-binaphthalene]-2,2'-diol serves as a chiral scaffold for asymmetric synthesis, leveraging its rigid binaphthyl framework and diol functionality. The hydroxyl groups enable selective derivatization, while the stereochemistry supports enantioselective transformations. Bench-stable and compatible with standard purification methods, it functions effectively in ligand development and catalytic applications requiring defined spatial orientation.

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   40.46
  • LogP   7.8564
  • H_Acceptors   2
  • H_Donors   2
  • Rotatable_Bonds   3

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