Triphenylsulfonium Bromide

Triphenylsulfonium Bromide  Struktur
3353-89-7
CAS-Nr.
3353-89-7
Englisch Name:
Triphenylsulfonium Bromide
Synonyma:
riphenylsulfanium,bromide;Triphenylsulfonium Bromid;TRIPHENYLSULFONIUM BROMIDE;Triphenyl sulphonium bromide
CBNumber:
CB1705979
Summenformel:
C18H15BrS
Molgewicht:
343.28
MOL-Datei:
3353-89-7.mol

Triphenylsulfonium Bromide Eigenschaften

Schmelzpunkt:
293 °C
Aggregatzustand
powder to crystal
Farbe
White to Almost white
CAS Datenbank
3353-89-7
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
HS Code  2930.90.2900
Bildanzeige (GHS) GHS hazard pictograms
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H315 Verursacht Hautreizungen. Hautreizung Kategorie 2 Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P264, P280, P302+P352, P321,P332+P313, P362
H319 Verursacht schwere Augenreizung. Schwere Augenreizung Kategorie 2 Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P264, P280, P305+P351+P338,P337+P313P
Sicherheit
P264 Nach Gebrauch gründlich waschen.
P264 Nach Gebrauch gründlich waschen.
P280 Schutzhandschuhe/Schutzkleidung/Augenschutz tragen.

Triphenylsulfonium Bromide Chemische Eigenschaften,Einsatz,Produktion Methoden

Verwenden

Triphenylsulfonium Bromide is used in the preparation of sulfonium salt photoacid generator for deep-UV microlithography.

synthetische

Triphenylsulfonium bromide synthesis: A 3.0 M solution of phenylmagnesium bromide in diethyl ether (50 ml, 0.15 mole) was distilled under vacuum with slow heating from 20° to 80°C. Benzene (40 ml) was added, followed by n-heptane (300 ml). The resulting mixture was stirred and a solution of diphenylsulfoxide 10.1 g, (0.050 mol), in benzene (60 ml) was added during 1 hour at 80°C. The mixture was stirred for 3 hours and cooled to room temperature. An 25% aqueous hydrobromic acid solution (180 ml) was slowly added to the reaction mixture (exotherm-). The layers were separated and the organic layer was extracted twice with 5% aqueous hydrobromic acid (2 x 30 ml). The combined aqueous extracts were extracted three times with dichloromethane (3×250 ml). The dichloromethane extracts were dried over magnesium sulfate, filtered and the organic solvent evaporated to leave triphenylsulfonium bromide (10.2 g, 60%), which was crystallized from dichloromethane/diethyl ether. M.p. 285-7°C.

Triphenylsulfonium Bromide Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Triphenylsulfonium Bromide Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 57)Lieferanten
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3353-89-7()Verwandte Suche:


  • TRIPHENYLSULFONIUM BROMIDE
  • Triphenyl sulphonium bromide
  • Triphenylsulfonium Bromid
  • riphenylsulfanium,bromide
  • 3353-89-7
  • C18H15BrS
  • Sulfonium Compounds
  • Iodonium Sulfonium & Oxonium Compounds
  • Iodonium Sulfonium & Oxonium Compounds
  • Sulfonium Compounds
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