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hexacarbonylvanadium

Base Information
  • Chemical Name:hexacarbonylvanadium
  • CAS No.:14024-00-1
  • Molecular Formula:C6O6 V
  • Molecular Weight:219.004
  • Hs Code.:
  • European Community (EC) Number:237-849-3
  • UNII:WA8Q7FLK2X
  • Wikipedia:Vanadium_hexacarbonyl
  • Wikidata:Q419078
  • Mol file:14024-00-1.mol
hexacarbonylvanadium

Synonyms:Hexacarbonylvanadium;Vanadium hexacarbonyl

Suppliers and Price of hexacarbonylvanadium
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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  • Chemicals and raw materials
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Total 35 raw suppliers
Chemical Property of hexacarbonylvanadium
Chemical Property:
  • PSA:0.00000 
  • LogP:-1.24800 
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:0
  • Exact Mass:218.913445
  • Heavy Atom Count:13
  • Complexity:10
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Chemical Classes:Metals -> Metals, Organic Compounds
  • Canonical SMILES:[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[V]
  • Uses Hexacarbonylvanadium is used as a catalyst in isomerization andhydrogenation reactions.
Technology Process of hexacarbonylvanadium

There total 22 articles about hexacarbonylvanadium which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
Heating of starting compd. (40°C, 1E-2 Torr) for 3 h, during which green color of solid turns gray.; Spect. (IR) identification of blue-black resulted solid as V(CO)6 and anal. and spect. (IR) identification of org. residue.;
DOI:10.1021/om00095a011
Guidance literature:
With H3PO4; under N2 slow stirring while mixt. heated to 40-45°C for 12 h;
Guidance literature:
With hydrogenchloride; In pentane; under N2 or Ar, treated with HCl at -70°C with stirring, temp. raised to 20°C within 1 h; filtered, cooled to dry-ice temp., filtered, dried under reduced pressure;
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