Welcome to LookChem.com Sign In|Join Free
  • or

Encyclopedia

1,3,4,5-tetraphenyl-1,3-diphospholene 2,2-dimethyl thioacetal

Base Information Edit
  • Chemical Name:1,3,4,5-tetraphenyl-1,3-diphospholene 2,2-dimethyl thioacetal
  • CAS No.:126134-65-4
  • Molecular Formula:C29H26P2S2
  • Molecular Weight:500.605
  • Hs Code.:
  • Mol file:126134-65-4.mol
1,3,4,5-tetraphenyl-1,3-diphospholene 2,2-dimethyl thioacetal

Synonyms:

Suppliers and Price of 1,3,4,5-tetraphenyl-1,3-diphospholene 2,2-dimethyl thioacetal
Supply Marketing:Edit
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 0 raw suppliers
Chemical Property of 1,3,4,5-tetraphenyl-1,3-diphospholene 2,2-dimethyl thioacetal Edit
Chemical Property:
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 1,3,4,5-tetraphenyl-1,3-diphospholene 2,2-dimethyl thioacetal

There total 1 articles about 1,3,4,5-tetraphenyl-1,3-diphospholene 2,2-dimethyl thioacetal 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:
1,3,4,5-tetraphenyl-1,3-diphospholene 2,2-dimethyl thioacetal; With dicyclopentadienyltitanium(II) bis(trimethyl phosphite) complex; In tetrahydrofuran; at 20 ℃;
With water; In tetrahydrofuran; at 20 ℃; for 12h;
DOI:10.1039/b403436h
Guidance literature:
With Li; tert-butylchloride; In tetrahydrofuran; A soln. of the starting compd. in THF is stirred at room temp. for 24 h with Li (Ar). To the intermediate tBuCl is added and the mixt. should stand for 24 h. The resulting compd. reacts with the ferrocene compd. at room temp. for 4 h.; Filtn. over silicagel (CH2Cl2), removing of solvent in vacuo, chromy. (silicagel, hexane/CH2Cl2), sublimation (120°C, 1E-1 Torr) or recrystn. from toluene/CH3OH.;
Post RFQ for Price