Lithium Tetrakis(pentafluorophenyl)borate - Ethyl Ether Complex - ≥70% , CAS No.155543-02-5

CAS: 155543-02-5 Cat. No.: L157763 EC Number: 678-588-9 PubChem CID: 23701484

GRADE & PURITY ≥70%

Synonyms

Lithium(1+), [1,1'-oxybis[ethane]]-, tetrakis(2,3,4,5,6-pentafluorophenyl)borate(1-) (1:1) | Tetrakis(pentafluorophenyl)boron lithium ethyl etherate | Lithium tetrakis(pentafluorophenyl)borate ethyl etherate | lithium diethyl ether tetrakis(pentafluorophe

Storage

Argon charged,Room temperature

Shipped In

Normal

Specifications

Synonyms

Lithium(1+), [1, 1'-oxybis[ethane]]-, tetrakis(2, 3, 4, 5, 6-pentafluorophenyl)borate(1-) (1:1) | Tetrakis(pentafluorophenyl)boron lithium ethyl etherate | Lithium tetrakis(pentafluorophenyl)borate ethyl etherate | lithium diethyl ether tetrakis(pentafluorophe

Specifications & Purity

≥70%

Storage

Argon charged, Room temperature

Shipped In

Normal

Purity

≥70%

Names and Identifiers

• Pubchem Sid: 488200584
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488200584
• Canonical Smiles: [Li+].[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.CCOCC
• IUPAC Name: lithium;ethoxyethane;tetrakis(2,3,4,5,6-pentafluorophenyl)boranuide
• InChIKey: KPLZKJQZPFREPG-UHFFFAOYSA-N
• INCHI: 1S/C24BF20.C4H10O.Li/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;1-3-5-4-2;/h;3-4H2,1-2H3;/q-1;;+1
• Isomeric SMILES: [Li+].[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.CCOCC
• PubChem CID: 23701484
• Reaxy-Rn: 17365414

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Class: Benzene and substituted derivatives
• Subclass: Halobenzenes
• Intermediate Tree Nodes: Not available
• Direct Parent: Fluorobenzenes
• Alternative Parents: Aryl fluorides Organic metalloid salts Organic metal halides Organic lithium salts Dialkyl ethers Organometalloid compounds Organofluorides Hydrocarbon derivatives Organic cations
• Molecular Framework: Not available
• Substituents: Fluorobenzene - Aryl fluoride - Aryl halide - Organic metal halide - Dialkyl ether - Ether - Organic lithium salt - Organic metalloid salt - Organic alkali metal salt - Organofluoride - Organic metalloid moeity - Organohalogen compound - Organooxygen compound - Organic salt - Organic oxygen compound - Hydrocarbon derivative - Organic cation - Aromatic homomonocyclic compound
• Description: 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

Chemical and Physical Properties

• Solubility: Soluble in Methanol
• Sensitivity: Moisture sensitive
• Molecular Weight: 760.100 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 22
• Rotatable Bond Count: 2
• Exact Mass: 760.067 Da
• Monoisotopic Mass: 760.067 Da
• Topological Polar Surface Area: 9.200 Ų
• Heavy Atom Count: 51
• Formal Charge: 0
• Complexity: 826.000
• 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: 3

XLogP3

References

1. Qidi Hu, Cheng Cao, Hanglin Li, Jian Xu, Sheng Han, Jiusheng Li.  (2025)  Phosphorus- and sulfur-incorporated chemical modification of metallocene poly-α-olefin for dual-functional base oils with enhanced antioxidant and antiwear performance.  EUROPEAN POLYMER JOURNAL,      [PMID:] [10.1016/j.eurpolymj.2025.114337]