2-(3,4,5-Trimethoxyphenyl)oxirane

Base Information

Chemical Name:2-(3,4,5-Trimethoxyphenyl)oxirane
CAS No.:54767-81-6
Molecular Formula:C11H14O4
Molecular Weight:210.23
Hs Code.:
DSSTox Substance ID:DTXSID90449661
Nikkaji Number:J2.650.978E
Mol file:54767-81-6.mol

Synonyms:2-(3,4,5-trimethoxyphenyl)oxirane;54767-81-6;Oxirane, (3,4,5-trimethoxyphenyl)-;SCHEMBL6822928;DTXSID90449661;AKOS012069025;EN300-1839298

Suppliers and Price of 2-(3,4,5-Trimethoxyphenyl)oxirane

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 4 raw suppliers

Chemical Property of 2-(3,4,5-Trimethoxyphenyl)oxirane

Chemical Property:

Melting Point:54-55 °C
Boiling Point:127-129 °C(Press: 4-5 Torr)
PSA：40.22000
Density:1.164±0.06 g/cm3(Predicted)
LogP:1.78370
XLogP3:0.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:210.08920892
Heavy Atom Count:15
Complexity:195

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC(=CC(=C1OC)OC)C2CO2

Technology Process of 2-(3,4,5-Trimethoxyphenyl)oxirane

There total 10 articles about 2-(3,4,5-Trimethoxyphenyl)oxirane 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: 95.0%

: 2181-42-2
trimethylsulphonium iodide

: 86-81-7
3,4,5-trimethoxy-benzaldehyde

: 13443-56-6
β-hydroxy-3,4-dimethoxy phenethyl alcohol

: 54767-81-6
5-(epoxyethyl)-1,2,3-tris(methoxy)benzene

Guidance literature:: With sodium hydroxide; tetrabutylammomium bromide; In dichloromethane; at 50 ℃; for 96h;
DOI:10.1002/jhet.5570220326

Reference yield: 91.0%

: (carboxymethyl)methylphenylsulfonium trifluoromethanesulfonate

: 86-81-7
3,4,5-trimethoxy-benzaldehyde

: 54767-81-6
5-(epoxyethyl)-1,2,3-tris(methoxy)benzene

Guidance literature:: With caesium carbonate; In tetrahydrofuran; at 80 ℃; for 12h;
DOI:10.1016/j.tet.2008.10.019

Reference yield: 84.0%

: 2181-42-2
trimethylsulphonium iodide

: 86-81-7
3,4,5-trimethoxy-benzaldehyde

: 54767-81-6
5-(epoxyethyl)-1,2,3-tris(methoxy)benzene

Guidance literature:: trimethylsulphonium iodide; With sodium hydride; In tetrahydrofuran; dimethyl sulfoxide; mineral oil; at 20 ℃; for 0.5h; Inert atmosphere;

3,4,5-trimethoxy-benzaldehyde; In tetrahydrofuran; dimethyl sulfoxide; mineral oil; Inert atmosphere;
DOI:10.1021/acs.joc.5b01776