Diethyl {1-[(trimethylsilyl)oxy]ethenyl}phosphonate

Base Information

Chemical Name:Diethyl {1-[(trimethylsilyl)oxy]ethenyl}phosphonate
CAS No.:31675-42-0
Molecular Formula:C9H21O4PSi
Molecular Weight:252.323
Hs Code.:
DSSTox Substance ID:DTXSID60508456
Wikidata:Q82365386
Mol file:31675-42-0.mol

Synonyms:31675-42-0;Diethyl {1-[(trimethylsilyl)oxy]ethenyl}phosphonate;DTXSID60508456

Suppliers and Price of Diethyl {1-[(trimethylsilyl)oxy]ethenyl}phosphonate

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 Diethyl {1-[(trimethylsilyl)oxy]ethenyl}phosphonate

Chemical Property:

Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:7
Exact Mass:252.09467268
Heavy Atom Count:15
Complexity:249

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOP(=O)(C(=C)O[Si](C)(C)C)OCC

Technology Process of Diethyl {1-[(trimethylsilyl)oxy]ethenyl}phosphonate

There total 1 articles about Diethyl {1-[(trimethylsilyl)oxy]ethenyl}phosphonate 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:

: 4071-85-6
trimetylsilylketene

: 762-04-9
phosphonic acid diethyl ester

: 31675-42-0
diethyl <1-(trimethylsiloxy)vinyl>phosphonate

Guidance literature:

Reference yield:

: 64-17-5
ethanol

: 31675-42-0
diethyl <1-(trimethylsiloxy)vinyl>phosphonate

: 100-52-7
benzaldehyde

: 103-36-6
ethyl 3-phenyl-2-propenoate

Guidance literature:: With titanium tetrachloride; toluene-4-sulfonic acid; Yield given. Multistep reaction; 1.) CH₂Cl₂, reflux, 1 h, 2.) reflux, 1 h;
DOI:10.1246/cl.1981.1087