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Arsine, 1,6-hexanediylbis[diphenyl-

Base Information
  • Chemical Name:Arsine, 1,6-hexanediylbis[diphenyl-
  • CAS No.:82195-43-5
  • Molecular Formula:C30H32As2
  • Molecular Weight:542.427
  • Hs Code.:
Arsine, 1,6-hexanediylbis[diphenyl-

Synonyms:

Suppliers and Price of Arsine, 1,6-hexanediylbis[diphenyl-
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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Total 1 raw suppliers
Chemical Property of Arsine, 1,6-hexanediylbis[diphenyl-
Chemical Property:
Purity/Quality:

85.0-99.8% *data from raw suppliers

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

SDS file from LookChem

Useful:
Technology Process of Arsine, 1,6-hexanediylbis[diphenyl-

There total 1 articles about Arsine, 1,6-hexanediylbis[diphenyl- 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:

Guidance literature:
C6H5-AsBr-6-AsBr-C6H5, BrMg-C6H5, Ae.;
Guidance literature:
With phthalic acid dimethyl ester; In ethanol; byproducts: KCl; Pt-compd. and the ligand (in molar ratio 1:1) were placed in a round bottom flask, then abs. EtOH and DMP were added and the mixt. refluxed for24 h;; the mixt. was filtered and washed with water (3 portions), ethanol (2 portions), ether (2 portions) and dried under vacuum; elem.anal.;;
DOI:10.1016/S0020-1693(00)81399-7
Guidance literature:
In acetone; toluene; byproducts: KCl; Pt-compd. was dissolved in dry acetone and placed in a flat bottomed flask; the ligand (in molar ratio 1:1) dissolved in toluene was then added dropwise to a stirred salt soln. over a period of 30 min at room temp.;; the mixt. was filtered and the ppt. washed with toluene (3 portions); the acetone-toluene filtrate was then evapd. to dryness and the solid redissolved in toluene and filtered again to remove KCl; the soln. was evapd. to dryness ; the ppt. was dried;;
DOI:10.1016/S0020-1693(00)81399-7
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