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Dichlorobis(triphenylphosphin)palladium
Pd(PPh3)2Cl2 · PdCl2(PPh3)2 · Pd(PPh3)Cl2 · DICHLOROBIS(TRIPHENYLPHOSPHINE)PALLADIUM · BIS(TRIPHENYLPHOSPHINE)PALLADIUM(II) DICHLORIDE · (PPh3)2PdCl2 · DICHLOROBIS(TRIPHENYLPHOSPHINE)PALLADIUM(II) · BIS(TRIPHENYLPHOSPHINE)PALLADIUM CHLORIDE
Identifikatoren & physikalische Daten
| CAS No. | 13965-03-2 |
|---|---|
| Summenformel | C36H30Cl2P2Pd |
| Durchschnittliche Molmasse | 701,9 g/mol |
| Monoisotopische Masse | 700,02346 g/mol |
| SMILES | [Cl-].[Cl-].[Pd+2].c1ccc(P(c2ccccc2)c2ccccc2)cc1.c1ccc(P(c2ccccc2)c2ccccc2)cc1 |
| InChIKey | YNHIGQDRGKUECZ-UHFFFAOYSA-L |
| PubChem CID | 84124 |
| Lokaler Name | Dichlorobis(triphenylphosphin)palladium |
Chemische & physikalische Eigenschaften
| Polarare Oberfläche (TPSA) | 0 |
|---|---|
| H-Brücken-Donoren | 0 |
| H-Brücken-Akzeptoren | 2 |
| Frei drehbare Bindungen | 6 |
| Schwere Atome | 41 |
| Formalladung | 0 |
| Komplexität | 202 |
| Schmelzpunkt | 260°C |
| Dampfdruck | 0Pa at 25℃ |
| Lagerbedingungen | Store below +30°C. |
| Löslichkeit | Chloroform (Slightly), Dichloromethane (Slightly, Heated), Methanol (Slightly,Insoluble in water. Soluble in benzene, and toluene. |
| Aggregatzustand | Powder |
| Farbe | Yellow |
| BRN | 4935975 |
| InChI | InChI=1S/2C18H15P.2ClH.Pd/c2*1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18/h2*1-15H2*1H/q+2/p-2 |
| InChIKey | ILBDOZRDKNIJBS-UHFFFAOYSA-N |
| SMILES | P(C1C=CC=CC=1)(C1=CC=CC=C1)C1C=CC=CC=1.P(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.[Pd](Cl)Cl |
| LogP (Verteilungskoeffizient) | 5.69 at 20℃ |
| CAS Datenbank | 13965-03-2(CAS DataBase Reference) |
Sicherheit & Vorschriften
| F | 3-10-21 |
|---|---|
| Wassergefährdungsklasse (WGK) | 3 |
| TSCA-Inventar-Status | No |
| Zollcode | 28439090 |
| R-Sätze (R) | 36/37/38-22-40-19 |
| Gefahrensymbole | Xn |
| Sicherheitshinweise (S) | 37/39-26-36/37 |
| Lagerklasse | 11 - Combustible Solids |
| Gefahrenklasse | Aquatic Chronic 4Skin Sens. 1A |
Anwendungen & Verwendung
Verwenden
Bis(triphenylphosphine)palladium(II) chloride is used primarily in organometallic catalytic reactions due to the palladium content of the compound. It is also involved in crystalized structures of me tallacyclic complexes which show antiinflammatory and antifungal properties.