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Cobaltocen
COBALTOCENE · BIS(CYCLOPENTADIENYL)COBALT(II) · Bis(cyclopentadienyl)cobalt(II),min.98%(Cobaltocene) · tocene · Kobaltocen · Cobaltocene,98% · Ferrocene cobalt · cobaltocene(1277-43-6)

Identifikatoren & physikalische Daten
| CAS No. | 1277-43-6 |
|---|---|
| Summenformel | C10H10Co |
| Durchschnittliche Molmasse | 189,12 g/mol |
| Monoisotopische Masse | 189,011444 g/mol |
| SMILES | [Co+2].c1cc[cH-]c1.c1cc[cH-]c1 |
| InChIKey | ILZSSCVGGYJLOG-UHFFFAOYSA-N |
| PubChem CID | 92884 |
| EC No. | 215-061-0 |
| Lokaler Name | Cobaltocen |
Chemische & physikalische Eigenschaften
| Polarare Oberfläche (TPSA) | 0 |
|---|---|
| H-Brücken-Donoren | 0 |
| H-Brücken-Akzeptoren | 2 |
| Frei drehbare Bindungen | 0 |
| Schwere Atome | 11 |
| Formalladung | 0 |
| Komplexität | 11 |
| Löslichkeit | less than 1 mg/mL at 70.7 °F (NTP, 1992)Insoluble in water. |
| Schmelzpunkt | 343 to 345 °F (NTP, 1992)176-180 °C (dec.)(lit.) |
| Physical Description | Cobaltocene appears as black-purple crystals or black solid. Sublimes at 104 °F and 0.1 mmHg. (NTP, 1992)Black-purple or black solidInsoluble in water[CAMEO] Black-violet crystals[Acros Organics MSDS] |
| Siedepunkt | 173℃ [CRC10] |
| Lagerbedingungen | 2-8°C |
| Aggregatzustand | crystal |
| Farbe | purplish-black |
| Stabilität | Stable, but very reactive and air and moisture sensitive - store under inert gas. Incompatible with strong oxidizing agents. Highly flammable. |
| InChI | InChI=1S/2C5H5.Co/c2*1-2-4-5-3-1/h2*1-5H |
| InChIKey | PXFGMRZPRDJDEK-UHFFFAOYSA-N |
| SMILES | [CH]1[CH][CH][CH][CH]1.[CH]1[CH][CH][CH][CH]1.[Co] |^1:0,1,2,3,4,5,6,7,8,9| |
| CAS Datenbank | 1277-43-6(CAS DataBase Reference) |
| EPA chemische Informationen | Cobaltocene (1277-43-6) |
Sicherheit & Vorschriften
| GHS-Einstufung | DangerH228 (100%): Flammable solid [Danger Flammable solids]H317 (29.5%): May cause an allergic skin reaction [Warning Sensitization, Skin]H334 (26.8%): May cause allergy or asthma symptoms or breathing difficulties if inhaled [Danger Sensitization, respiratory]H341 (29.5%): Suspected of causing genetic defects [Warning Germ cell mutagenicity]H351 (26.8%): Suspected of causing cancer [Warning Carcinogenicity]P203, P210, P233, P240, P241, P260, P261, P271, P272, P280, P284, P302+P352, P304+P340, P318, P321, P333+P317, P342+P316, P362+P364, P370+P378, P403, P405, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 149 reports by companies from 4 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.Information may vary between notifications depending on impurities, additives, and other factors. The percentage value in parenthesis indicates the notified classification ratio from companies that provide hazard codes. Only hazard codes with percentage values above 10% are shown. For more detailed information, please visit ECHA C&L website. |
|---|---|
| DOT-Kennzeichnung | Flammable Solid |
| Brandgefahren | Vendor information indicates that this chemical is flammable. (NTP, 1992) |
| Gesundheitsgefahren | ACUTE/CHRONIC HAZARDS: This compound is toxic by ingestion. (NTP, 1992) |
| Gefahrenübersicht | Intraperitoneal LD50 (mouse) = 80 mg/kg[RTECS] A strong reducing agentReadily oxidized by air and waterSensitive to air and light exposure[CAMEO] Highly reactiveToxic by ingestion[NTP] An irritantIngestion may cause CNS depression[Acros Organics MSDS] See Cobalt. |
| Reaktive Gruppe | Hydrocarbons, AromaticOrganometallics |
| Reactivity Alerts | Highly FlammableStrong Reducing AgentWater-ReactiveAir-Reactive |
Anwendungen & Verwendung
Verwenden
Bis(cyclopentadienyl)cobalt is used to catalyze the preparation of pyridines from alkynes and nitriles. It acts as a polymerization inhibitor of olefins. It is a common one-electron reducing agent in the laboratory. It reacts with carbon monoxide to prepare cobalt(I) derivative, cyclopentadienylcobalt dicarbonyl. It also serves as an internal standard in cyclic voltametry. Further, it finds use in Diels-Alder reactions. In addition to this, it is used as a paint drier and as an oxygen stripping agent.