Dichlorobis(3-(diphenylphosphino)propylamine)ruthenium(II), 97%

Base Information

Chemical Name:Dichlorobis(3-(diphenylphosphino)propylamine)ruthenium(II), 97%
CAS No.:911128-25-1
Molecular Formula:C₃₀H₃₆Cl₂N₂P₂Ru
Molecular Weight:658.553
Hs Code.:28439090
Mol file:911128-25-1.mol

Synonyms:Dichlorobis(3-(diphenylphosphino)propylamine)ruthenium(II), 97%

Suppliers and Price of Dichlorobis(3-(diphenylphosphino)propylamine)ruthenium(II), 97%

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
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price

Sigma-Aldrich
Dichlorobis(3-(diphenylphosphino)propylamine)ruthenium(II) 97%
250mg
$ 68.40

Total 5 raw suppliers

Chemical Property of Dichlorobis(3-(diphenylphosphino)propylamine)ruthenium(II), 97%

Chemical Property:

Melting Point:290 °C (dec.)
PSA：51.24000
LogP:6.62780

Purity/Quality:

99% ^*data from raw suppliers

Dichlorobis(3-(diphenylphosphino)propylamine)ruthenium(II) 97% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of Dichlorobis(3-(diphenylphosphino)propylamine)ruthenium(II), 97%

There total 1 articles about Dichlorobis(3-(diphenylphosphino)propylamine)ruthenium(II), 97% 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:

Reference yield: 86.0%

: 50982-12-2
cyclooctadiene ruthenium(II) dichloride

: 16605-03-1
(3-aminopropyl)diphenylphosphine

: 1196467-26-1,911128-25-1
trans-RuCl₂(Ph₂P(CH₂)3NH₂)2

Guidance literature:: In toluene; a mixt. of complex and aminophosphine was refluxed in toluene under Ar for 4 h, the mixt. was cooled to room temp.; ether was added, suspn. was stirred for 30 min, filtered, washed with ether and dried under vac.; elem. anal.;
DOI:10.1039/b911459a