Dimethyl [phenyl(trimethylsilyl)methyl]phosphonate

Base Information

Chemical Name:Dimethyl [phenyl(trimethylsilyl)methyl]phosphonate
CAS No.:86000-93-3
Molecular Formula:C12H21O3PSi
Molecular Weight:272.356
Hs Code.:
DSSTox Substance ID:DTXSID20516638

Synonyms:86000-93-3;Dimethyl [phenyl(trimethylsilyl)methyl]phosphonate;DTXSID20516638

Suppliers and Price of Dimethyl [phenyl(trimethylsilyl)methyl]phosphonate

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
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Total 1 raw suppliers

Chemical Property of Dimethyl [phenyl(trimethylsilyl)methyl]phosphonate

Chemical Property:

Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:272.09975806
Heavy Atom Count:17
Complexity:274

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COP(=O)(C(C1=CC=CC=C1)[Si](C)(C)C)OC

Technology Process of Dimethyl [phenyl(trimethylsilyl)methyl]phosphonate

There total 2 articles about Dimethyl [phenyl(trimethylsilyl)methyl]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: 92.0%

: 773-47-7
dimethyl benzylphosphonate

: 86000-93-3
dimethyl α-trimethylsilylbenzylphosphonate

Guidance literature:: 1.) lithiation; 2.) silylation;
DOI:10.1016/S0040-4039(00)81513-0

Reference yield:

: 100-52-7
benzaldehyde

: 86000-93-3
dimethyl α-trimethylsilylbenzylphosphonate

Guidance literature:: Multi-step reaction with 2 steps

1: CsF / tetrahydrofuran / Heating

2: 92 percent / 1.) lithiation; 2.) silylation

With cesium fluoride; In tetrahydrofuran;
DOI:10.1016/S0040-4039(00)81513-0