Ditelluride, bis(4-ethoxyphenyl)

Base Information

Chemical Name:Ditelluride, bis(4-ethoxyphenyl)
CAS No.:35684-38-9
Molecular Formula:C16H18O2Te2
Molecular Weight:497.518
Hs Code.:
DSSTox Substance ID:DTXSID00402823
Wikidata:Q82206326

Synonyms:Ditelluride, bis(4-ethoxyphenyl);35684-38-9;di(4-ethoxyphenyl) ditelluride;SCHEMBL6679509;DTXSID00402823;AKOS024434697

Suppliers and Price of Ditelluride, bis(4-ethoxyphenyl)

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemical Property of Ditelluride, bis(4-ethoxyphenyl)

Chemical Property:

Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:7
Exact Mass:499.941364
Heavy Atom Count:20
Complexity:221

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC1=CC=C(C=C1)[Te][Te]C2=CC=C(C=C2)OCC

Technology Process of Ditelluride, bis(4-ethoxyphenyl)

There total 14 articles about Ditelluride, bis(4-ethoxyphenyl) 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: 77.0%

: 36310-31-3
p-ethoxyphenyltellurium(IV) trichloride

: 35684-38-9
bis-(4-ethoxy-phenyl)-ditelluride

Guidance literature:: With sodium L-ascorbate; In methanol; water; acetone; for 5h;
DOI:10.1080/00397919308009800

Reference yield: 60.0%

: chromium sulfate

: 36310-31-3
p-ethoxyphenyltellurium(IV) trichloride

: 12516-72-2,52747-09-8
monochloropentaquochromium(III) sulfate

: 35684-38-9
bis-(4-ethoxy-phenyl)-ditelluride

Guidance literature:: In 1,4-dioxane; water; react. under N2 (deoxygenated solns.); addn. of CrSO4 in distd. H2O to a slight excess of Te-compd. in dioxane at room temp.; extn. of Te2R2 into diethyl ether, washing of green-coloured aq. layer with ether (several times), concn. under reduced pressure at 30°C until pptn. occurs, filtration, washing with H2O, drying over P2O5 in vac.; elem. anal.;
DOI:10.1016/S0020-1693(00)83092-3