Potassium tetrakis(pentafluorophenyl)borate - ≥97% , CAS No.89171-23-3

CAS: 89171-23-3 Cat. No.: P304843 Peso molecular: 718.13 PubChem CID: 23693577

GRADE & PURITY ≥97%

Synonyms

E76344 | Potassium tetrakis(perfluorophenyl)borate | Tetrakis-(pentafluorophenyl)-potassium borate | SCHEMBL134248 | potassium tetrakis(pentafluorophenyl)borate | potassium tetrakis(pentafluorophe-nyl)borate | potassium;tetrakis(2,3,4,5,6-pentafluoropheny

Storage

Room temperature

Shipped In

Normal

Descripción general

Product Application：

Potassium tetrakis(pentafluorophenyl)borate is used as a biochemical reagent, a catalyst and a pharmaceutical intermediate.

Specifications

Sinónimos

E76344 | Potassium tetrakis(perfluorophenyl)borate | Tetrakis-(pentafluorophenyl)-potassium borate | SCHEMBL134248 | potassium tetrakis(pentafluorophenyl)borate | potassium tetrakis(pentafluorophe-nyl)borate | potassium;tetrakis(2, 3, 4, 5, 6-pentafluoropheny

Especificaciones y pureza

≥97%

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Pureza

≥97%

Nombres e identificadores

• Pubchem Sid: 504769682
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504769682
• Sonrisas canónicas: [B-](C1=C(C(=C(C(=C1F)F)F)F)F)(C2=C(C(=C(C(=C2F)F)F)F)F)(C3=C(C(=C(C(=C3F)F)F)F)F)C4=C(C(=C(C(=C4F)F)F)F)F.[K+]
• IUPAC Name: potassium;tetrakis(2,3,4,5,6-pentafluorophenyl)boranuide
• InChIKey: GYBHRIJOPWTIKA-UHFFFAOYSA-N
• INCHI: 1S/C24BF20.K/c26-5-1(6(27)14(35)21(42)13(5)34)25(2-7(28)15(36)22(43)16(37)8(2)29,3-9(30)17(38)23(44)18(39)10(3)31)4-11(32)19(40)24(45)20(41)12(4)33;/q-1;+1
• Isómeros SMILES: [B-](C1=C(C(=C(C(=C1F)F)F)F)F)(C2=C(C(=C(C(=C2F)F)F)F)F)(C3=C(C(=C(C(=C3F)F)F)F)F)C4=C(C(=C(C(=C4F)F)F)F)F.[K+]
• PubChem CID: 23693577
• Peso molecular: 718.13

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Clase Benzene and substituted derivatives
      • Subclass Halobenzenes

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: Benzene and substituted derivatives
• Subclass: Halobenzenes
• Intermediate Tree Nodes: Not available
• Direct Parent: Fluorobenzenes
• Alternative Parents: Aryl fluorides Organic metalloid salts Organic metal halides Organometalloid compounds Organofluorides Organic potassium salts Hydrocarbon derivatives Organic cations
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Fluorobenzene - Aryl halide - Aryl fluoride - Organic metal halide - Organic alkali metal salt - Organic metalloid salt - Hydrocarbon derivative - Organic potassium salt - Organic salt - Organofluoride - Organic metalloid moeity - Organohalogen compound - Organic cation - Aromatic homomonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as fluorobenzenes. These are compounds containing one or more fluorine atoms attached to a benzene ring.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Propiedades químicas y físicas

• Punto de fusión (°C): >300°C
• Peso molecular: 718.100 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 21
• Rotatable Bond Count: 0
• Exact Mass: 717.941 Da
• Monoisotopic Mass: 717.941 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 46
• Formal Charge: 0
• Complexity: 815.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 2

XLogP3

Referencias

1. Long Xia, Liu Xiao-Chi, Yang Yan-Yi, Dai Jia-Qing, Cao Jue-Xian, Hu Yong.  (2025)  Solvent-induced conformation gating of single-molecule charge transport in valinomycin and valinomycin-K+ junctions.  RARE METALS,      [PMID:] [10.1007/s12598-024-03123-8]

2. Zijun Yi, Long Zhang, Fang Ding, Xuehong Ren.  (2025)  A novel dopant replacing LiTFSI and TBP in Spiro-OMeTAD for high-performance perovskite solar cells.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2025.168527]