Diethyl [2-(benzenesulfinyl)ethyl]phosphonate

Base Information

Chemical Name:Diethyl [2-(benzenesulfinyl)ethyl]phosphonate
CAS No.:86517-46-6
Molecular Formula:C12H19O4PS
Molecular Weight:290.32
Hs Code.:
DSSTox Substance ID:DTXSID90513917

Synonyms:86517-46-6;Diethyl [2-(benzenesulfinyl)ethyl]phosphonate;DTXSID90513917

Suppliers and Price of Diethyl [2-(benzenesulfinyl)ethyl]phosphonate

Supply Marketing:

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

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Chemical Property of Diethyl [2-(benzenesulfinyl)ethyl]phosphonate

Chemical Property:

XLogP3:1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:8
Exact Mass:290.07416725
Heavy Atom Count:18
Complexity:293

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOP(=O)(CCS(=O)C1=CC=CC=C1)OCC

Technology Process of Diethyl [2-(benzenesulfinyl)ethyl]phosphonate

There total 3 articles about Diethyl [2-(benzenesulfinyl)ethyl]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: 88.0%

: 86517-43-3
ethyl 2-phenylthioethylphosphonate

: 86517-46-6
(2-Benzenesulfinyl-ethyl)-phosphonic acid diethyl ester

Guidance literature:: With bromine; potassium hydrogencarbonate; In dichloromethane; water;
DOI:10.1016/S0040-4020(01)91883-6

Reference yield:

: 5324-30-1
diethyl 2-bromoethylphosphonate

: 86517-46-6
(2-Benzenesulfinyl-ethyl)-phosphonic acid diethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 90 percent / diethyl ether; 1,2-dimethoxy-ethane / several hours

2: 88 percent / Br₂, KHCO₃ / CH₂Cl₂; H₂O

With bromine; potassium hydrogencarbonate; In 1,2-dimethoxyethane; diethyl ether; dichloromethane; water;
DOI:10.1016/S0040-4020(01)91883-6

Reference yield:

: 930-69-8
sodium thiophenolate

: 86517-46-6
(2-Benzenesulfinyl-ethyl)-phosphonic acid diethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 90 percent / diethyl ether; 1,2-dimethoxy-ethane / several hours

2: 88 percent / Br₂, KHCO₃ / CH₂Cl₂; H₂O

With bromine; potassium hydrogencarbonate; In 1,2-dimethoxyethane; diethyl ether; dichloromethane; water;
DOI:10.1016/S0040-4020(01)91883-6