Learn More
Fluoruro de nonafluorobutanosulfonilo, +90 %, Thermo Scientific Chemicals
Description
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.
Los bencinos se generaron a partir de fenoles de o-(trimetilsililo) con fluoruro de nonafluorobutanosulfonilo (NfF) mediante un proceso de dominó. El fluoruro de nonafluorobutanosulfonilo (fluoruro de nonaflilo, C 4 F 9 SO 2 F, NfF) es el reactivo más utilizado comercialmente disponible para la síntesis de nonaflatos.
Solubilidad
Se hidroliza en agua.
Notas
Almacenar en un lugar fresco. Mantenga el recipiente bien cerrado en un lugar seco y bien ventilado. Almacenar lejos de agentes oxidantes fuertes, humedad y bases.
Specifications
Specifications
| Nombre del producto químico o material | Nonafluorobutanesulfonyl fluoride |
| Punto de fusión | -110°C |
| Densidad | 1.75 |
| Punto de ebullición | 65°C to 66°C |
| Temperatura de inflamación | None |
| Índice de refracción | 1.281 |
| Cantidad | 100 g |
| Número UN | UN3265 |
| Beilstein | 1813589 |
| Sensibilidad | Moisture sensitive |
| Show More |
RUO – Research Use Only
By clicking Submit, you acknowledge that you may be contacted by Fisher Scientific in regards to the feedback you have provided in this form. We will not share your information for any other purposes. All contact information provided shall also be maintained in accordance with our Privacy Policy.