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Ms.NancyCAS NO.10210-68-1
99%(1-10000)Kilogram
Hot Sale 10210-68-1 supplier Cobalt good producer di-m-carbonylhexacarbonyldi-
Solid phase reaction complexing agent, catalyst, can be used for hydroformylation reaction, hydrogenation reaction, hydrosilylation reaction, isomerization reaction, carboxylation reaction, carbonylation reaction, and can also be used as a catalyst for olefin polymerization to replace three Titanium chloride. Gasoline antiknock agent. Preparation of high purity cobalt salt.
As a catalyst in organic synthesis and organometallic chemistry, Cobalt Carbonyl is a versatile reagent. It is commonly used as a catalyst in the hydroformylation (oxo reaction) of alkenes. It can also be used as a catalyst in the carboxylation of alkenes into corresponding esters and acids. Cobalt Carbonyl is a key precursor in the preparation of cobalt sulfide, cobalt platinum, and cobalt selenide nanocrystals.
Dicobalt octacarbonyl is the inorganic compound Co2(CO)8. This metal carbonyl is a reagent and catalyst in organometallic chemistry and organic synthesis. It is used as a catalyst for hydroformylation, the conversion of alkenes into aldehydes. It is highly reactive towards alkynes, and is sometimes used as an alkyne protecting group. As the cobalt-alkyne complex, it plays a role in promoting both the Nicholas reaction and the Pauson–Khand reaction.
| Catalogue number: | PA 27 0020083 |
| Chemical name: | Cobalt carbonyl |
CAS Number: |
10210-68-1 |
| Category: | miscellaneous compounds |
| Synonyms: |
Cobalt octacarbonyl (co2(co)8); cobalt tetracarbonyl dimer; di-μ-carbonylhexacarbonyldicobalt; dicobalt carbonyl; dicobalt octacarbonyl; octacarbonyldicobalt; |
| Molecular form: | C8Co2O8 |
| Appearance: | Red to Brown Solid |
| Mol. Weight: | 341.95 |
| Storage: | 2-8°C Refrigerator |
| Shipping Conditions: | Ambient |
| Applications: | Cobalt Carbonyl is a metal carbonyl used as a reagent and catalyst in organometallic chemistry and organic synthesis. Cobalt Carbonyl is commonly used as a hydroformylation catalyst for the conversion of alkenes to aldehydes. |