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dithianitronium hexafluoroarsenate

Base Information Edit
  • Chemical Name:dithianitronium hexafluoroarsenate
  • CAS No.:80485-40-1
  • Molecular Formula:
  • Molecular Weight:267.051
  • Hs Code.:
  • Mol file:80485-40-1.mol
dithianitronium hexafluoroarsenate

Synonyms:dithianitronium hexafluoroarsenate

Suppliers and Price of dithianitronium hexafluoroarsenate
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of dithianitronium hexafluoroarsenate Edit
Chemical Property:
  • PSA:64.18000 
  • LogP:2.95620 
Purity/Quality:
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  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

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Technology Process of dithianitronium hexafluoroarsenate

There total 8 articles about dithianitronium hexafluoroarsenate 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 SnCl2; In sulfur dioxide; byproducts: SnCl4; (N2); stirring, 18 h; removing solvent, pumping to dryness, washing ppt. with ice-cold CH2Cl2; elem. anal.;
DOI:10.1039/DT9920003097
Guidance literature:
With bromine; In liquid sulphur dioxide; byproducts: AsF3; condensing SO2, AsF5 and trace of Br2 onto mixture of S8 and S4N4, stirring at room temp. for 12h, evapn., addn. of more S8 in SO2, stirring for 12h, influence of Br2 studied; filtration, recrystn. of SNSAsF6 from SO2 (4x), extn. with SO2/CCl3F, cooling to -78°C, filtration (5x), evapn. of solvent from residue (vac.);
DOI:10.1039/DT9920001343
Guidance literature:
With bromine; In liquid sulphur dioxide; byproducts: AsF3; an excess of AsF5 and a trace of Br2 were condensed onto frozen SO2 over a mixt. of S8 and S4N4; mixt. stirred for 20 h at room temp.; the volatiles (SO2, AsF3 and AsF5) were removed, SO2-soln. was filtered, crystals were washed with SO2 for several times; elem. anal.;
DOI:10.1021/ic00134a083
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