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CS-W001157 4
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(R)-3,3'-Dibromo-5,5',6,6',7,7',8,8'-octahydro-[1,1'-binaphthalene]-2,2'-diol

  • CAS No. 65355-08-0

  • Cat. No. CS-W009650
  • Purity≥97%
  • MDL No.None

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

(R)-3,3'-Dibromo-5,5',6,6',7,7',8,8'-octahydro-[1,1'-binaphthalene]-2,2'-diol|CS-W009650

Structure of 65355-08-0

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General Information

  • CAS No. 65355-08-0
  • Cat. No. CS-W009650
  • 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 C₂₀H₂₀Br₂O₂
  • Molecular Weight 452.18
  • Synonym(s) (R)-(+)-3,3'-Dibromo-5,5',6,6',7,7',8,8'-octahydro-2,2'-dihydroxy-1,1'-binaphthyl
  • SMILES BrC1=CC2=C(C(C3=C(CCCC4)C4=CC(Br)=C3O)=C1O)CCCC2

Description

(R)-3,3'-Dibromo-5,5',6,6',7,7',8,8'-octahydro-[1,1'-binaphthalene]-2,2'-diol features a chiral binaphthyl backbone with brominated and hydroxylated substituents, enabling its use in asymmetric synthesis. This bench-stable derivative integrates readily into catalytic systems requiring rigid, electron-rich scaffolds for stereocontrol.

Application

(R)-3,3'-Dibromo-5,5',6,6',7,7',8,8'-octahydro-[1,1'-binaphthalene]-2,2'-diol serves as a stereochemically defined chiral building block for asymmetric synthesis. The dibromo functionality enables subsequent palladium-catalyzed cross-coupling reactions, while the diol moiety offers orthogonal handle for protection or metal complexation. Its bench-stable solid form and established utility in constructing enantioselective ligands make it valuable for medicinal chemistry and catalytic system development.

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 : H315-H319-H335
Precautionary Statements : P261-P264-P271-P280-P302+P352

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Computational Chemistry Data

  • TPSA   40.46
  • LogP   6.0474
  • H_Acceptors   2
  • H_Donors   2
  • Rotatable_Bonds   1

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