Ethyl phenyl methylphosphonate

Base Information

Chemical Name:Ethyl phenyl methylphosphonate
CAS No.:38074-88-3
Molecular Formula:C9H13O3P
Molecular Weight:200.174
Hs Code.:
DSSTox Substance ID:DTXSID40508479
Nikkaji Number:J2.259.725F
Mol file:38074-88-3.mol

Synonyms:Ethyl phenyl methylphosphonate;38074-88-3;SCHEMBL10885712;DTXSID40508479

Suppliers and Price of Ethyl phenyl methylphosphonate

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 Ethyl phenyl methylphosphonate

Chemical Property:

XLogP3:1.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:200.06023127
Heavy Atom Count:13
Complexity:187

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOP(=O)(C)OC1=CC=CC=C1

Technology Process of Ethyl phenyl methylphosphonate

There total 3 articles about Ethyl phenyl methylphosphonate 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: 85.0%

: diphenyl(trifluoromethanesulfonato)-λ³-iodane

: 683-08-9
Diethyl methylphosphonate

: 38074-88-3
O-ethyl O-phenyl methylphosphonate

Guidance literature:: With 2,6-di-tert-butyl-pyridine; copper(l) chloride; In dichloromethane; at 40 ℃; Schlenk technique; Inert atmosphere;
DOI:10.1021/ja505281v

Reference yield: 85.0%

: 683-08-9
Diethyl methylphosphonate

: 108-95-2,27073-41-2
phenol

: 38074-88-3
O-ethyl O-phenyl methylphosphonate

Guidance literature:: Diethyl methylphosphonate; With pyridine; trifluoromethylsulfonic anhydride; In dichloromethane; at 20 ℃; for 0.166667h; Sealed tube;

phenol; In dichloromethane; at 20 ℃; for 0.5h; Sealed tube;
DOI:10.1002/anie.201802082