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CS-W001157 4
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(R)-[1,3':1',1'':3'',1'''-Quaternaphthalene]-2',2''-diol

  • CAS No. 851615-07-1

  • Cat. No. CS-0086802
  • Purity≥97%
  • MDL No.None

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

(R)-[1,3':1',1'':3'',1'''-Quaternaphthalene]-2',2''-diol|CS-0086802

Structure of 851615-07-1

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General Information

  • CAS No. 851615-07-1
  • Cat. No. CS-0086802
  • 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 C₄₀H₂₆O₂
  • Molecular Weight 538.63
  • Synonym(s) None
  • SMILES OC1=C(C2=C(C=CC=C3)C3=CC(C4=C(C=CC=C5)C5=CC=C4)=C2O)C6=CC=CC=C6C=C1C7=CC=CC8=C7C=CC=C8

Description

This chiral quaternaphthalene diol features a rigid, multi-ring architecture with defined stereochemistry at the 2',2''-positions. The hydroxyl groups enable hydrogen bonding and solubility in polar solvents, while the extended aromatic system supports π-stacking interactions. This structure serves as a robust scaffold for asymmetric synthesis and molecular recognition applications.

Application

(R)-[1,3':1',1'':3'',1'''-Quaternaphthalene]-2',2''-diol serves as a chiral building block for the synthesis of complex polycyclic architectures, leveraging its rigid, sterically defined framework to control stereochemistry in asymmetric transformations. The vicinal diol functionality enables selective derivatization and coordination in catalytic systems, while the extended naphthalenic core provides enhanced planarity and π-stacking potential useful in supramolecular and materials chemistry applications.

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   10.7116
  • H_Acceptors   2
  • H_Donors   2
  • Rotatable_Bonds   3

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