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Triphenyl{bis[(trifluoroacetyl)oxy]}-lambda~5~-stibane

Base Information
  • Chemical Name:Triphenyl{bis[(trifluoroacetyl)oxy]}-lambda~5~-stibane
  • CAS No.:36971-66-1
  • Molecular Formula:C22H15 F6 O4 Sb
  • Molecular Weight:579.099
  • Hs Code.:
  • DSSTox Substance ID:DTXSID80586791
  • NSC Number:171098
  • Wikidata:Q82478995
  • Mol file:36971-66-1.mol
Triphenyl{bis[(trifluoroacetyl)oxy]}-lambda~5~-stibane

Synonyms:36971-66-1;Triphenyl{bis[(trifluoroacetyl)oxy]}-lambda~5~-stibane;DTXSID80586791;NSC171098;NSC-171098;triphenyl-antimony bis(trifluoroacetate);Antimony, triphenylbis[(2,2,2-trifluoroacetyl)oxy]-

Suppliers and Price of Triphenyl{bis[(trifluoroacetyl)oxy]}-lambda~5~-stibane
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 5 raw suppliers
Chemical Property of Triphenyl{bis[(trifluoroacetyl)oxy]}-lambda~5~-stibane
Chemical Property:
  • Boiling Point:°Cat760mmHg 
  • Flash Point:°C 
  • Density:g/cm3 
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:10
  • Rotatable Bond Count:7
  • Exact Mass:577.99126
  • Heavy Atom Count:33
  • Complexity:624
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)[Sb](C2=CC=CC=C2)(C3=CC=CC=C3)(OC(=O)C(F)(F)F)OC(=O)C(F)(F)F
Technology Process of Triphenyl{bis[(trifluoroacetyl)oxy]}-lambda~5~-stibane

There total 3 articles about Triphenyl{bis[(trifluoroacetyl)oxy]}-lambda~5~-stibane 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:
In methanol; acetonitrile; Electrolysis; N2 atmosphere, ambient temp.; constant current electrolysis (Pt plate and wire electrodes); extraction (ethyl acetate), washing of extracts (water, brine), drying (MgSO4), solvent removal, recrystn. (ethanol);
DOI:10.1016/S0013-4686(97)85470-9
Guidance literature:
With tert.-butylhydroperoxide; In diethyl ether; byproducts: t-BuOH, H2O; t-BuOOH was added dropwise to stirred cold (5-10°C) soln. of Sb-compound and acid in Et2O, kept in the dark for 24 h at room temp.; solvent was distilled off under reduced pressure, recrystd. from CHCl3/hexane;
DOI:10.1016/S0022-328X(02)02179-4
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