Diethyl (cyclobutanecarbonyl)phosphonate

Base Information

Chemical Name:Diethyl (cyclobutanecarbonyl)phosphonate
CAS No.:1490-08-0
Molecular Formula:C₉H₁₇O₄P
Molecular Weight:220.205
Hs Code.:
NSC Number:82845
DSSTox Substance ID:DTXSID60933522
Wikidata:Q82909343
Mol file:1490-08-0.mol

Synonyms:1490-08-0;NSC82845;Diethyl (cyclobutanecarbonyl)phosphonate;NCIOpen2_004652;DTXSID60933522;NSC-82845

Suppliers and Price of Diethyl (cyclobutanecarbonyl)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
Packaging
price

Total 3 raw suppliers

Chemical Property of Diethyl (cyclobutanecarbonyl)phosphonate

Chemical Property:

Vapor Pressure:0.00436mmHg at 25°C
Boiling Point:278°C at 760 mmHg
Flash Point:135.9°C
Density:1.167g/cm³
XLogP3:1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:6
Exact Mass:220.08644602
Heavy Atom Count:14
Complexity:237

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOP(=O)(C(=O)C1CCC1)OCC

Technology Process of Diethyl (cyclobutanecarbonyl)phosphonate

There total 2 articles about Diethyl (cyclobutanecarbonyl)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:

: 3721-95-7
Cyclobutanecarboxylic acid

: 1490-08-0
Diaethyl-cyclobutylcarbonyl-phosphonat

Guidance literature:: Multi-step reaction with 2 steps

1: 100 percent / thionyl chloride / toluene / Heating

2: toluene

With thionyl chloride; In toluene;
DOI:10.1016/j.ejmech.2005.02.011