Trivinyltin acetate

Base Information

Chemical Name:Trivinyltin acetate
CAS No.:28521-10-0
Molecular Formula:C₈H₁₂O₂Sn
Molecular Weight:258.892
Hs Code.:
DSSTox Substance ID:DTXSID40586696
NSC Number:173032
Wikidata:Q82478857
Mol file:28521-10-0.mol

Synonyms:28521-10-0;Trivinyltin acetate;(Acetyloxy)(triethenyl)stannane;Stannane, (acetyloxy)triethenyl-;DTXSID40586696;NSC173032;NSC-173032

Suppliers and Price of Trivinyltin acetate

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 3 raw suppliers

Chemical Property of Trivinyltin acetate

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
Density:g/cm³
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:5
Exact Mass:259.985932
Heavy Atom Count:11
Complexity:175

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)O[Sn](C=C)(C=C)C=C

Technology Process of Trivinyltin acetate

There total 3 articles about Trivinyltin acetate 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:

: 1112-56-7
tetravinyltin (IV)

: 28521-10-0
Trivinylzinnacetat

Guidance literature:: With sodium acetate; In methanol; Electrolysis; at room temp.;
DOI:10.1016/S0022-328X(00)80274-0

Reference yield:

: 563-63-3
silver(I) acetate

: 10008-90-9
trivinyltin(IV)chloride

: 28521-10-0
Trivinylzinnacetat

Guidance literature:: prepared according Abel, Brandy, J.Chem. Soc., 1192,1965; Barbieri, Bertazzi, J. Organaomet. Chem., 84, 39(1975); Naik, Curran, J. Organomet. Chem.,81,177(1074); Blake, Coates, Tate, J.Chem.Soc., 756(1061); Clark, Ruddephatt, Organomet. Compounds, 2,11; elem. anal.;
DOI:10.1016/S0020-1693(00)90612-1