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Nonafluorbutansulfonylfluorid, 90+ %, Thermo Scientific Chemicals
Beschreibung
Benzynes were generated from o-(trimethylsilyl) phenols using nonafluorobutanesulfonyl fluoride (NfF) by a domino process.Nonafluorobutanesulfonyl fluoride (nonaflyl fluoride, C 4 F 9 SO 2 F, NfF) is the most widely used commercially available reagent for the synthesis of nonaflates.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Arine wurden aus O-(trimethylsilyl-)phenolen erzeugt, wobei Nonafluorbutansulfonylfluorid (NfF) durch einen Dominoprozess verwendet wurde. Nonafluorbutansulfonylfluorid (Nonaflylfluorid, C4F9SO2F, NfF) ist das am häufigsten verwendete kommerziell erhältliche Reagenz für die Synthese von Nonaflaten.
Löslichkeit
Hydrolysiert in Wasser.
Hinweise
Kühl lagern. Behälter an einem trockenen und gut belüfteten Ort dicht verschlossen halten. Getrennt von starken Oxidationsmitteln, Feuchtigkeit, Basen lagern.
Spezifikation
Specifications
| Chemischer Name oder Material | Nonafluorobutanesulfonyl fluoride |
| Schmelzpunkt | -110°C |
| Dichte | 1.75 |
| Siedepunkt | 65°C to 66°C |
| Flammpunkt | None |
| Brechungsindex | 1.281 |
| Menge | 100 g |
| UN-Nummer | UN3265 |
| Beilstein | 1813589 |
| Empfindlichkeit | Moisture sensitive |
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RUO – Research Use Only
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