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(11aS)-(-)-10,11,12,13-Tetrahydrodiindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin-5-phenoxy

  • CAS No. 885701-71-3

  • Cat. No. CS-0037008
  • Purity≥97%
  • MDL No.None

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

(11aS)-(-)-10,11,12,13-Tetrahydrodiindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin-5-phenoxy|CS-0037008

Structure of 885701-71-3

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General Information

  • CAS No. 885701-71-3
  • Cat. No. CS-0037008
  • 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 C₂₃H₁₉O₃P
  • Molecular Weight 374.37
  • Synonym(s) None
  • SMILES C1(C(OP(OC2=CC=CC=C2)O3)=CC=C4)=C4CCC15CCC6=C5C3=CC=C6

Description

This chiral phosphocin derivative features a rigid, electron-rich diindeno scaffold that enables selective coordination in asymmetric catalysis. The phenoxy substituent enhances solubility and modulates steric profile, while the tetrahydrocyclohexene core provides conformational stability under standard conditions.

Application

(11aS)-(-)-10,11,12,13-Tetrahydrodiindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin-5-phenoxy serves as a chiral phosphorus-containing building block with defined stereochemistry at the 11a position. Its rigid fused-ring architecture provides excellent configurational stability and facilitates stereoselective transformations. The phenoxy substituent enhances solubility and enables further functionalization via electrophilic or transition-metal-catalyzed coupling reactions. This compound functions effectively in asymmetric synthesis applications requiring robust, bench-stable phosphorus scaffolds for catalytic systems or molecular probe 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 : 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   27.69
  • LogP   5.9422
  • H_Acceptors   3
  • H_Donors   0
  • Rotatable_Bonds   2

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