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

CAS: 20083-34-5 Cat. No.: T162306 Formula: C₁₂H₁₅F₅O₃Si Peso molecolare: 330.33 Numero EC: 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

Sinonimi

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-

Specifiche e purezza

≥95%(GC)

Condizioni di conservazione di stoccaggio

Store at 2-8°C,Argon charged

Spedito in

Wet ice

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Purezza

≥95%(GC)

Nomi e identificatori

• Pubchem Sid: 508811446
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/508811446
• Sorrisi canonici: 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
• Isomeri SMILES: CCO[Si](C1=C(C(=C(C(=C1F)F)F)F)F)(OCC)OCC
• WGK Germania: 3
• PubChem CID: 2782625
• Peso molecolare: 330.33

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organometallic compounds
    • Classe Organometalloid compounds
      • Subclass Organosilicon compounds
        • Level5 Alkoxysilanes
          • Level6 Trialkoxysilanes

• Kingdom: Organic compounds
• Superclass: Organometallic compounds
• Classe: 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
• Descrizione: 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

Proprietà chimiche e fisiche

• Sensibilità: Moisture & heat sensitive
• Indice di rifrazione: 1.42
• Punto di infiammabilità (°F): 219.2 °F
• Punto di infiammabilità (°C): 104 °C
• Punto di ebollizione (°C): 238 °C
• Peso molecolare: 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

Riferimenti

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]