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CS-W001157 4
Total: USD 88.00

(S)-3-3'-Bis(3,5-dimethylphenyl)-1,1'-bi-2-naphthol

  • CAS No. 435327-17-6

  • Cat. No. CS-0086796
  • Purity≥98%
  • MDL No.None

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

(S)-3-3'-Bis(3,5-dimethylphenyl)-1,1'-bi-2-naphthol|CS-0086796

Structure of 435327-17-6

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General Information

  • CAS No. 435327-17-6
  • Cat. No. CS-0086796
  • Purity ≥98%
  • MDL No. None
  • Storage 4°C, protect from light, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₃₆H₃₀O₂
  • Molecular Weight 494.62
  • Synonym(s) S-3-3'-Bis(3,5-bis(methyl)phenyl)-1,1'-bi-2-naphthol
  • SMILES OC1=[C@]([C@]2=C(C=CC=C3)C3=CC(C4=CC(C)=CC(C)=C4)=C2O)C5=CC=CC=C5C=C1C6=CC(C)=CC(C)=C6

Description

(S)-3,3'-Bis(3,5-dimethylphenyl)-1,1'-bi-2-naphthol is a chiral biaryl scaffold featuring sterically hindered aryl groups that enhance stability and define its asymmetric environment. This configuration enables precise stereocontrol in transition-metal catalysis, particularly in asymmetric synthesis applications requiring high enantioselectivity. The electron-rich naphthalene core facilitates metal coordination, while the bulky substituents minimize unwanted side reactions.

Application

(S)-3,3'-Bis(3,5-dimethylphenyl)-1,1'-bi-2-naphthol serves as a chiral ligand in asymmetric catalysis, enabling enantioselective transformations through well-established coordination modes. Its sterically shielded naphthalene framework enhances stereocontrol in transition metal-catalyzed reactions. The molecule exhibits high bench stability and facilitates efficient purification, making it suitable for reproducible synthesis of enantiomerically enriched compounds in medicinal chemistry and process development workflows.

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-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501

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Computational Chemistry Data

  • TPSA   40.46
  • LogP   9.63888
  • H_Acceptors   2
  • H_Donors   2
  • Rotatable_Bonds   3

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