Triethoxy(pentafluorophenyl)silane - ≥95%(GC) , CAS No.20083-34-5

CAS: 20083-34-5 Cat. No.: T162306 Summenformel: C₁₂H₁₅F₅O₃Si Molekulargewicht: 330.33 EG-Nummer: 806-774-3 PubChem CID: 2782625

GRADE & PURITY ≥95%(GC)

Synonyms

Benzene, 1,2,3,4,5-pentafluoro-6-(triethoxysilyl)- | FS-4681 | (Pentafluorophenyl)triethoxysilane | triethoxy(pentafluorophenyl)silane | MFCD03411257 | PENTAFLUOROPHENYLTRIETHOXYSILANE | Triethoxy-(2,3,4,5,6-pentafluorophenyl)silane | TRIETHOXY(2,3,4,5,6-

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Specifications

Synonyme

Benzene, 1,2,3,4,5-pentafluoro-6-(triethoxysilyl)- | FS-4681 | (Pentafluorophenyl)triethoxysilane | triethoxy(pentafluorophenyl)silane | MFCD03411257 | PENTAFLUOROPHENYLTRIETHOXYSILANE | Triethoxy-(2,3,4,5,6-pentafluorophenyl)silane | TRIETHOXY(2,3,4,5,6-

Spezifikationen & Reinheit

≥95%(GC)

Storage

Store at 2-8°C,Argon charged

Verschickt in

Wet ice

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Reinheit

≥95%(GC)

Namen und Kennungen

• Pubchem Sid: 508811446
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/508811446
• Kanonisches Lächeln: CCO[Si](C1=C(C(=C(C(=C1F)F)F)F)F)(OCC)OCC
• IUPAC Name: triethoxy-(2,3,4,5,6-pentafluorophenyl)silane
• InChIKey: QALDFNLNVLQDSP-UHFFFAOYSA-N
• INCHI: 1S/C12H15F5O3Si/c1-4-18-21(19-5-2,20-6-3)12-10(16)8(14)7(13)9(15)11(12)17/h4-6H2,1-3H3
• Isomere SMILES: CCO[Si](C1=C(C(=C(C(=C1F)F)F)F)F)(OCC)OCC
• WGK Deutschland: 3
• PubChem CID: 2782625
• Molekulargewicht: 330.33

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organometallic compounds
    • Klasse Organometalloid compounds
      • Subclass Organosilicon compounds
        • Ebene5 Alkoxysilanes
          • Ebene6 Trialkoxysilanes

• Kingdom: Organic compounds
• Superclass: Organometallic compounds
• Klasse: Organometalloid compounds
• Subclass: Organosilicon compounds
• Intermediate Tree Nodes: Alkoxysilanes
• Direct Parent: Trialkoxysilanes
• Alternative Parents: Fluorobenzenes Aryl fluorides Silyl ethers Organoheterosilanes Organic metalloid salts Organooxygen compounds Organofluorides Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Trialkoxysilane - Fluorobenzene - Halobenzene - Aryl fluoride - Aryl halide - Monocyclic benzene moiety - Benzenoid - Silyl ether - Organoheterosilane - Organic metalloid salt - Organic oxygen compound - Organohalogen compound - Organofluoride - Organooxygen compound - Organic salt - Hydrocarbon derivative - Aromatic homomonocyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as trialkoxysilanes. These are organosilicon compounds with the general formula RO[Si](R')(OR'')OR''' (R-R''' = aliphatic organyl group).
• 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

Chemische und physikalische Eigenschaften

• Empfindlichkeit: Moisture & heat sensitive
• Brechungsindex: 1.42
• Flammpunkt (°F): 219.2 °F
• Flammpunkt (°C): 104 °C
• Siedepunkt (°C): 238 °C
• Molekulargewicht: 330.320 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 8
• Rotatable Bond Count: 7
• Exact Mass: 330.071 Da
• Monoisotopic Mass: 330.071 Da
• Topological Polar Surface Area: 27.700 Ų
• Heavy Atom Count: 21
• Formal Charge: 0
• Complexity: 292.000
• 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: 1

XLogP3

Referenzen

1. Xue Chen, Chengfeng Li, Shuai Chen, Xinzi Shi, Changyong Mo, Youhao Liao, Weishan Li.  (2026)  Fluorobenzosilane additive derived low-impedance SEI enables high-rate capacity of graphite anode.  ELECTROCHIMICA ACTA,      [PMID:] [10.1016/j.electacta.2026.149446]