Methyl (2,6-dimethoxyphenoxy)acetate

Base Information

Chemical Name:Methyl (2,6-dimethoxyphenoxy)acetate
CAS No.:116249-88-8
Molecular Formula:C11H14O5
Molecular Weight:226.229
Hs Code.:
DSSTox Substance ID:DTXSID90552200
Wikidata:Q82432280
Mol file:116249-88-8.mol

Synonyms:116249-88-8;Methyl (2,6-dimethoxyphenoxy)acetate;DTXSID90552200;AKOS009098021

Suppliers and Price of Methyl (2,6-dimethoxyphenoxy)acetate

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 1 raw suppliers

Chemical Property of Methyl (2,6-dimethoxyphenoxy)acetate

Chemical Property:

XLogP3:1.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:6
Exact Mass:226.08412354
Heavy Atom Count:16
Complexity:206

Purity/Quality:: 99.90% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=C(C(=CC=C1)OC)OCC(=O)OC

Technology Process of Methyl (2,6-dimethoxyphenoxy)acetate

There total 3 articles about Methyl (2,6-dimethoxyphenoxy)acetate 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%

: 95110-10-4
(2,6-dimethoxy-phenoxy)acetic acid

: 74-88-4
methyl iodide

: 116249-88-8
methyl (2,6-dimethoxyphenoxy)acetate

Guidance literature:: With sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate; In chloroform; for 0.5h;

Reference yield:

: 91-10-1
1,3-dimethoxy-2-hydroxy-benzene

: 116249-88-8
methyl (2,6-dimethoxyphenoxy)acetate

Guidance literature:: Multi-step reaction with 2 steps

2: 85 percent / tetrabutylammonium hydrogen sulfate, aq. NaOH / CHCl₃ / 0.5 h

With sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate; In chloroform;