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CS-W001157 4
Total: USD 88.00

Sodium tetrakis(pentafluorophenyl)borate

  • CAS No. 149213-65-0

  • Cat. No. CS-W020657
  • Purity≥97%
  • MDL No.MFCD12545881

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

Sodium tetrakis(pentafluorophenyl)borate|CS-W020657

Structure of 149213-65-0

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General Information

  • CAS No. 149213-65-0
  • Cat. No. CS-W020657
  • Purity ≥97%
  • MDL No. MFCD12545881
  • Storage Store at room temperature, keep dry and cool
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₄BF₂₀Na
  • Molecular Weight 702.03
  • Synonym(s) Sodiumtetrakis(pentafluorophenyl)borate
  • SMILES FC1=C([B-](C2=C(F)C(F)=C(F)C(F)=C2F)(C3=C(F)C(F)=C(F)C(F)=C3F)C4=C(F)C(F)=C(F)C(F)=C4F)C(F)=C(F)C(F)=C1F.[Na+]

Description

Sodium tetrakis(pentafluorophenyl)borate delivers exceptional stability and solubility in nonpolar solvents, enabling efficient catalytic activation in transition metal systems. This bench-stable reagent features a highly electron-deficient boron center that enhances Lewis acidity, facilitating C–C and C–heteroatom bond formation under mild conditions. Its robust performance supports scalable synthesis and reproducible results across diverse reaction platforms.

Application

Sodium tetrakis(pentafluorophenyl)borate serves as a highly effective, bench-stable source of the tetrakis(pentafluorophenyl)borate anion, enabling robust Lewis acid catalysis and facilitating a broad range of transition metal-catalyzed transformations. Its exceptional functional group tolerance and solubility in organic media make it particularly valuable for cross-coupling reactions and C–H activation processes. The compound functions as a non-coordinating counterion in organometallic reagents, enhancing catalyst activity while simplifying purification.

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H315-H319-H335-H413
Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P405-P501

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Computational Chemistry Data

  • TPSA   0
  • LogP   2.85
  • H_Acceptors   0
  • H_Donors   0
  • Rotatable_Bonds   4

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