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iodo-triphenylphosphoranylidene-cobalt, oxoazanide

Base Information
  • Chemical Name:iodo-triphenylphosphoranylidene-cobalt, oxoazanide
  • CAS No.:14318-98-0
  • Molecular Formula:C18H15 Co I N2 O2 P
  • Molecular Weight:0
  • Hs Code.:
  • Mol file:14318-98-0.mol
iodo-triphenylphosphoranylidene-cobalt, oxoazanide

Synonyms:Cobalt,iododinitrosyl(triphenylphosphine)- (7CI,8CI);Iododinitrosyl(triphenylphosphine)cobalt

Suppliers and Price of iodo-triphenylphosphoranylidene-cobalt, oxoazanide
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
Total 2 raw suppliers
Chemical Property of iodo-triphenylphosphoranylidene-cobalt, oxoazanide
Chemical Property:
  • PSA:47.73000 
  • LogP:1.09320 
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of iodo-triphenylphosphoranylidene-cobalt, oxoazanide

There total 3 articles about iodo-triphenylphosphoranylidene-cobalt, oxoazanide 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:
With triphenylphosphine; In acetone; under N2, soln. of Co-compd. and PPh3 in acetone refluxed for 1 h; according to Heiber, W.; Heinecke, K. Z. Anorg. Allg. Chem. 1962, 316, 305; filtered, abs. EtOH added, vol. reduced by rotary evapn., stood for about 1 h, filtered, hexane added to mother liquor, coold to 0°C (second crop); elem. anal.;
Guidance literature:
In tetrahydrofuran; N2-atmosphere; refluxing for 2 h; filtration, evapn., recrystn. (hot hexane); elem. anal.;
DOI:10.1039/DT9770002085
Guidance literature:
Multi-step reaction with 2 steps
1: methanol; benzene
2: dichloromethane
In methanol; dichloromethane; benzene;
DOI:10.1039/DT9770002085
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