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CS-W001157 4
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(11bS)-4-Phenoxy-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin

  • CAS No. 256441-54-0

  • Cat. No. CS-0088062
  • Purity≥97%
  • MDL No.None

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

(11bS)-4-Phenoxy-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin|CS-0088062

Structure of 256441-54-0

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General Information

  • CAS No. 256441-54-0
  • Cat. No. CS-0088062
  • 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 C₂₆H₁₇O₃P
  • Molecular Weight 408.39
  • Synonym(s) S-4-phenoxy-Dinaphtho[2,1-d
  • SMILES C12=CC=CC=C1C=CC3=[C@]2[C@]4=C(C=CC=C5)C5=CC=C4OP(OC6=CC=CC=C6)O3

Description

This sterically encumbered phosphine features a rigid, electron-rich dioxaphosphepin core that enhances stability and reactivity in palladium-catalyzed cross-coupling processes. The (11bS) stereochemistry ensures predictable coordination geometry, while the phenoxy substituent improves solubility and resistance to oxidation under standard conditions.

Application

(11bS)-4-Phenoxy-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin serves as a stereochemically defined phosphorus heterocycle with established utility in asymmetric synthesis. The phenoxy substituent enhances solubility and stability, while the rigid dioxaphosphepin core facilitates controlled reactivity in transition-metal-catalyzed transformations. It functions as a versatile building block for phosphorus-containing scaffolds, enabling efficient access to chiral ligands and catalysts through well-documented functional group interconversions.

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
Precautionary Statements : P264-P280-P302+P352-P362

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Computational Chemistry Data

  • TPSA   35.51
  • LogP   8.4385
  • H_Acceptors   3
  • H_Donors   0
  • Rotatable_Bonds   2

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