1,3-Dichlor-2-fluor-5-nitrobenzol
1,3-dichloro-2-fluoro-5-nitrobenzene · uoro-1-nitrob · 3,5-Dichloro-4-fluoro-1-nitrob · 5-Dichloro-4-fluoronitrobenzene · 3,5-DICHLORO-4-FLUORONITROBENZENE · 2,6-DICHLORO-P-NITROFLUOROBENZENE · 4-Fluoro-3,5-dichloronitrobenzene · 3,5 dichloro 4-Fluoro Nirto Benzene
Identifikatoren & physikalische Daten
| CAS No. | 3107-19-5 |
|---|---|
| Summenformel | C6H2Cl2FNO2 |
| Durchschnittliche Molmasse | 209,99 g/mol |
| Monoisotopische Masse | 208,94466188 g/mol |
| SMILES | O=[N+]([O-])c1cc(Cl)c(F)c(Cl)c1 |
| InChIKey | VMAATSFMXSMKPG-UHFFFAOYSA-N |
| PubChem CID | 76554 |
| EC No. | 221-466-3 |
| DTXSID | DTXSID00185023 |
| Lokaler Name | 1,3-Dichlor-2-fluor-5-nitrobenzol |
Chemische & physikalische Eigenschaften
| XLogP | 3,4 |
|---|---|
| Polarare Oberfläche (TPSA) | 45,8 |
| H-Brücken-Donoren | 0 |
| H-Brücken-Akzeptoren | 3 |
| Frei drehbare Bindungen | 0 |
| Schwere Atome | 12 |
| Formalladung | 0 |
| Komplexität | 175 |
| Schmelzpunkt | 44 °C |
| Siedepunkt | 259.3±35.0 °C(Predicted) |
| Dichte | 1.622±0.06 g/cm3(Predicted) |
| Lagerbedingungen | Sealed in dry,Room Temperature |
| Aggregatzustand | Powder |
| Farbe | White |
| CAS Datenbank | 3107-19-5(CAS DataBase Reference) |
Sicherheit & Vorschriften
| GHS-Einstufung | WarningH315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]P264, P264+P265, P280, P302+P352, P305+P351+P338, P321, P332+P317, P337+P317, and P362+P364 (click each P-code to see the statement)Aggregated GHS information provided per 5 reports by companies from 1 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies. |
|---|---|
| Regulatorische Informationen | Status: Active Update: 31-03-2023 https://echa.europa.eu/registration-dossier/-/registered-dossier/34697 |
| Hazard Classes and Categories | Skin Irrit. 2 (100%) |
| Zollcode | 2904990090 |
| Gefahrensymbole | Xi |
| hazard_note | Irritant |
Anwendungen & Verwendung
Verwenden
3,5-Dichloro-4-fluoronitrobenzene is an important synthetic chemical raw material for the synthesis of other compounds. It is commonly used in chemical factories and laboratory research.
Herstellung & Synthese
synthetische
3,5-Dichloro-4-fluoronitrobenzene can be produced by reacting persulfate with ammonium nitrate to form a phosphine salt. The phosphine salt reacts with 3,5-Dichloro-4-fluorobenzene in the presence of hydrogen peroxide to form the desired product. The reaction occurs on a large scale to produce 3,5-dichloro-4-fluoronitrobenzene in high yield.