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CS-W001157 4
Total: USD 88.00

(1,10-Phenanthroline)(trifluoromethyl)(triphenylphosphine)copper(I)

  • CAS No. 1334890-93-5

  • Cat. No. CS-0460048
  • Purity≥98%
  • MDL No.MFCD28386111

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

(1,10-Phenanthroline)(trifluoromethyl)(triphenylphosphine)copper(I)|CS-0460048

Structure of 1334890-93-5

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General Information

  • CAS No. 1334890-93-5
  • Cat. No. CS-0460048
  • Purity ≥98%
  • MDL No. MFCD28386111
  • Storage 4°C, sealed storage, away from moisture
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₃₁H₂₃CuF₃N₂P
  • Molecular Weight 575.04
  • Synonym(s) None
  • SMILES F[C-](F)([Cu+]1([P](C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4)[N]5=C6C7=[N]1C=CC=C7C=CC6=CC=C5)F

Description

This copper(I) complex features a trifluoromethyl-substituted phenanthroline ligand paired with triphenylphosphine, delivering enhanced stability and solubility in organic media. The electron-deficient trifluoromethyl group modulates redox potential, enabling efficient catalysis in cross-coupling reactions. Bench-stable under inert atmosphere, it streamlines synthesis of functionalized aryl derivatives.

Application

This copper(I) complex serves as a highly effective catalyst for copper-mediated C–N and C–C cross-coupling reactions, enabling efficient construction of biaryl and heteroaryl scaffolds under mild conditions. The ligand framework provides enhanced stability and solubility in organic media, facilitating clean reactions with broad functional group tolerance. Its bench-stable nature simplifies handling and improves reproducibility in synthetic 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 : H315-H319
Precautionary Statements : P264-P280-P302+P352-P362

Quality Control

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Computational Chemistry Data

  • TPSA   N/A
  • LogP   N/A
  • H_Acceptors   N/A
  • H_Donors   N/A
  • Rotatable_Bonds   N/A

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