(E)-{2,2-Dimethyl-1-[(trimethylsilyl)oxy]propylidene}(phenyl)phosphane

Base Information

Chemical Name:(E)-{2,2-Dimethyl-1-[(trimethylsilyl)oxy]propylidene}(phenyl)phosphane
CAS No.:60820-29-3
Molecular Formula:C₁₄H₂₃OPSi
Molecular Weight:266.395
Hs Code.:
DSSTox Substance ID:DTXSID70516769
Wikidata:Q82378333

Synonyms:60820-29-3;DTXSID70516769;(E)-{2,2-Dimethyl-1-[(trimethylsilyl)oxy]propylidene}(phenyl)phosphane

Suppliers and Price of (E)-{2,2-Dimethyl-1-[(trimethylsilyl)oxy]propylidene}(phenyl)phosphane

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of (E)-{2,2-Dimethyl-1-[(trimethylsilyl)oxy]propylidene}(phenyl)phosphane

Chemical Property:

PSA：43.37000
LogP:4.28560
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:4
Exact Mass:266.12557889
Heavy Atom Count:17
Complexity:267

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)C(=PC1=CC=CC=C1)O[Si](C)(C)C

Technology Process of (E)-{2,2-Dimethyl-1-[(trimethylsilyl)oxy]propylidene}(phenyl)phosphane

There total 3 articles about (E)-{2,2-Dimethyl-1-[(trimethylsilyl)oxy]propylidene}(phenyl)phosphane 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:

: 78114-26-8,114091-61-1,63853-15-6
(2,2-dimethyl-1-(trimethylsiloxy)propylidene)-trimethylsilylphosphine

: 60820-29-3,119179-89-4
[2,2-Dimethyl-1-trimethylsilanyloxy-prop-(Z)-ylidene]-phenyl-phosphane

Guidance literature:: Multi-step reaction with 2 steps

1: 65 percent / C₂Cl₆ / toluene / 2.5 h / Heating

2: 0.25 h / 0 °C

With hexachloroethane; In toluene;