Grundinformationen
- Standard-SMILES
F[Si](F)(c1ccccc1)c1ccccc1- InChIKey
BOMPXIHODLVNMC-UHFFFAOYSA-N- Summenformel
- C12H10F2Si
- Durchschnittliche Molmasse
- 220,29 g/mol
- Monoisotopische Masse
- 220,05198329
Namen und Bezeichner
- Bevorzugter Name
- Difluorodiphenylsilane
- IUPAC
- difluoro(diphenyl)silane
- Lokaler Name
- Difluordiphenylsilan
- Englischer Name
- DIPHENYLDIFLUOROSILANE
- Summenformel
- C12H10F2Si
- Molmasse
- 220.29
Namen und Synonyme
Weitere Namen anzeigen
Datenbank-Bezeichner
- CAS
312-40-3- PubChem CID
- 67557
- DTXSID
DTXSID2059801- UNII
- V3Y7X7Y43C
- EC Number
- 206-226-8
- Nikkaji
- J130.544A
Eigenschaften
Berechnete Struktureigenschaften
- Polarare Oberfläche (TPSA)
- 0 Ų
- H-Brücken-Donoren
- 0
- H-Brücken-Akzeptoren
- 2
- Frei drehbare Bindungen
- 2
- Schwere Atome
- 15
- Formalladung
- 0
- Komplexität
- 174
Experimentelle und physikochemische Eigenschaften
Physikochemische Eigenschaften
- Siedepunkt
- 159 °C · 159°C 50mm
- Dichte
- 1.145 · 1.145
- Brechungsindex
- 1.522 · 1.522
- Flammpunkt
- 87 °C · 87°C
- storage temp.
- 2 · under inert gas (nitrogen or Argon) at 2-8°C
- Löslichkeit
- soluble in ether.
- Wichte
- 1.145 · 1.145
- CAS Datenbank
- 312 · 312-40-3(CAS DataBase Reference)
- EPA chemische Informationen
- Silane, difluorodiphenyl- (312-40-3)
Sicherheit und Regulatorisches
GHS-Klassifizierung
GHS Classification
Danger
H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P354+P338, P317, P319, P321, P332+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 38 reports by companies from 1 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Gefahrenhinweise
Toxikologische Informationen
Sicherheitsdaten
- tsca
- TSCA listed
- ridadr
- 1760
- hs_code
- 2931900090
- risk_code
- 34
- hazard_code
- C
- hazard_note
- Corrosive
- safety_code
- 26-36/37/39-45
Chemie und Industrie
Verwendung und Herstellung
Anwendungen
VerwendenA moisture insensitive equivalent of diphenyldichlorosilane that is more reactive toward nucleophiles. Source of phenyl group in the Hiyama coupling reaction. More stable to electrophilic aromatic substitution than diphenyldichlorosilane. Eaborn reported that fluorosilanes are more reactive toward organometallic reagents than the corresponding chlorosilanes, and therefore more suited for preparation of sterically hindered organosilanes.
Darstellung
synthetischecommercially available. Readily prepared by oxidation of diphenylsilane with CuF2, or by treatment of diphenyldichlorosilane with HF, ZnF2, NaBF4, or (NH4)2SiF6. Rate enhancements of the chlorine–fluorine exchange have been achieved with ultrasound and addition of water. Diethoxydiphenylsilane and related structures are converted to diphenyldifluorosilane with 48% HF(aq).
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