| Identification | Back Directory | [Name]
CHLOROTRIS(TRIPHENYLPHOSPHINE)COBALT(I) | [CAS]
26305-75-9 | [Synonyms]
CoCl(Ph3P)3
Cobalt,triphenylphosphane,chloride
Chlorotris(triphenylphosphine)cobalt
Tris(triphenylphosphine)cobalt chloride
CHLOROTRIS(TRIPHENYLPHOSPHINE)COBALT(I)
cobalt(I) tris(triphenylphosphine) chloride
Chlorotris(triphenylphosphine)cobalt(I)
Chlorotris(triphenylphosphine)cobalt(I),Min.98%
Chlorotris(triphenylphosphine)cobalt(I), min. 98%
Chlorotris(triphenylphosphine)cobalt(I),98% (PPh3)3CoCl | [Molecular Formula]
C54H45ClCoP3 | [MDL Number]
MFCD00015864 | [MOL File]
26305-75-9.mol | [Molecular Weight]
881.24 |
| Chemical Properties | Back Directory | [Melting point ]
135-139 °C (dec.)(lit.)
| [storage temp. ]
Inert atmosphere,Room Temperature | [form ]
Powder | [color ]
brown | [Water Solubility ]
Insoluble in water. | [Sensitive ]
Air & Moisture Sensitive |
| Questions And Answer | Back Directory | [Reaction]
- Cobalt(I)-catalyzed, steroselective olefination of alkylzinc reagents with aryl aldehydes.
- Reagent for the reductive radical dimerization of 3-haloindoline derivatives.
- Cobalt-catalyzed, asymmetric addition of silylacetylene to 1,1-disubstituted allenes.
|
| Hazard Information | Back Directory | [Uses]
A stoichiometric reducing agent employed in the radical dimerization of halogenated organic molecules. | [Uses]
A stoichiometric reducing agent that is used in the radical dimerization of halogenated organic molecules. |
|
|