Triphenylmethylium Tetrakis(pentafluorophenyl)borate - ≥98% , CAS No.136040-19-2

CAS: 136040-19-2 Cat. No.: T162785 Peso molecular: 922.37 Número EC: 685-485-2 PubChem CID: 9832824

GRADE & PURITY ≥98%

Synonyms

Triphenylmethylium tetrakis(perfluorophenyl)borate | Trityl tetrakis(pentafluorophenyl)borate | Triphenylmethylium Tetrakis(pentafluorophenyl)borate | Tritylium Tetrakis(pentafluorophenyl)borate | diphenylmethylbenzene;tetrakis(2,3,4,5,6-pentafluorophenyl

Storage

Argon charged,Room temperature

Shipped In

Normal

Specifications

Sinónimos

Triphenylmethylium tetrakis(perfluorophenyl)borate | Trityl tetrakis(pentafluorophenyl)borate | Triphenylmethylium Tetrakis(pentafluorophenyl)borate | Tritylium Tetrakis(pentafluorophenyl)borate | diphenylmethylbenzene;tetrakis(2, 3, 4, 5, 6-pentafluorophenyl

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Argon charged, Room temperature

Enviado en

Normal

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 504764929
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504764929
• 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.C1=CC=C(C=C1)[C+](C2=CC=CC=C2)C3=CC=CC=C3
• IUPAC Name: diphenylmethylbenzene;tetrakis(2,3,4,5,6-pentafluorophenyl)boranuide
• InChIKey: TZOSNOQHGGONMD-UHFFFAOYSA-N
• INCHI: 1S/C24BF20.C19H15/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;1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18/h;1-15H/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.C1=CC=C(C=C1)[C+](C2=CC=CC=C2)C3=CC=CC=C3
• PubChem CID: 9832824
• Peso molecular: 922.37
• Reaxy-Rn: 7985568

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 Aromatic hydrocarbons Organic metalloid salts Unsaturated hydrocarbons Organometalloid compounds Organofluorides Hydrocarbon derivatives Organic cations
• Molecular Framework: Not available
• Substituents: Fluorobenzene - Aryl halide - Aryl fluoride - Aromatic hydrocarbon - Organic metalloid salt - Unsaturated hydrocarbon - Hydrocarbon derivative - Organofluoride - Organic metalloid moeity - Organohalogen compound - Organic cation - Hydrocarbon - 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

• Solubilidad: Soluble in Methanol
• Sensibilidad: Moisture sensitive.
• Punto de fusión (°C): 183 °C
• Peso molecular: 922.400 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 21
• Rotatable Bond Count: 7
• Exact Mass: 922.095 Da
• Monoisotopic Mass: 922.095 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 64
• Formal Charge: 0
• Complexity: 1000.000
• 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. 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]

2. Junjie Liu, Jianmin Wu, Qiwen Sun, Jiancheng Wang, Yan Sun, Hengxuan Zhang.  (2025)  High-viscosity poly-alpha-olefin production from Fischer-Tropsch mixed α-olefins: Synthesis, kinetics and mechanism.  FUEL,      [PMID:] [10.1016/j.fuel.2025.136421]