Keywords

• in bulk supply Cobalt 10210-68-1
• Cobalt top purity 10210-68-1
• Hot Sale di-m-carbonylhexacarbonyldi-

Quick Details

• ProName: in bulk supply Cobalt 10210-68-1 Cobal...
• CasNo: 10210-68-1
• Molecular Formula: C8Co2 O8
• Appearance: Powder
• Application: Used in Pharmaceutical, health food, c...
• DeliveryTime: 3-10days
• PackAge: 100g/pack,1kg/pack,25kg/drum
• Port: Shanghai Port
• ProductionCapacity: 10000 Metric Ton/Month
• Purity: 98%,99%
• Storage: Storage in a dry, ventilated place und...
• Transportation: By Air,EMS,FEDEX,UPS and Special Line
• LimitNum: 1 Kilogram
• Grade: Pharma Grade
• Related Substances: qualified
• Residue on Ignition: qualified
• Heavy Metal: qualified
• Valid Period: 2years
• Batch: 20210720

Superiority

in bulk supply Cobalt 10210-68-1 Cobalt top purity 10210-68-1 Hot Sale di-m-carbonylhexacarbonyldi-

Dicobalt octacarbonyl is the organometallic compound with composition Co₂(CO)₈. This metal carbonyl is used as a reagent and catalyst in organometallic chemistry and organic synthesis, and is central to much known organocobalt chemistry. It is the precursor to a hydroformylation catalyst, cobalt tetracarbonyl hydride. Each molecule consists of two cobalt atoms bound to eight carbon monoxide ligands, though multiple distinct structural arrangements are known. Some of the carbonyl ligands are highly labile. The compound 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 reactionand the Pauson–Khand reaction

1. Reagent for the Pauson-Khand conversion of an olefin, an alkyne and carbon monoxide into a cyclopentenone.
2. Precatalyst in combination with triphenylphosphite for the cataytic Pauson-Khand reaction.
3. Catalyzes the rearrangement of 1-alkynylcyclopropanols to cyclopentenones.
4. Catalyzes the conversion of aziridines to β-lactams.
5. Catalyzes the conversion of diallylanilines and aryliminies to quinolines.
6. Reagent for the selective cleavage of benzyl ethers.
7. Domino Nicholas and Pauson-Khand process induced by nitroarene reduction.

Details