{[(2-Methoxyethoxy)methoxy]methyl}benzene

Base Information

Chemical Name:{[(2-Methoxyethoxy)methoxy]methyl}benzene
CAS No.:88738-41-4
Molecular Formula:C11H16O3
Molecular Weight:196.246
Hs Code.:
DSSTox Substance ID:DTXSID30519039
Nikkaji Number:J464.638J
Wikidata:Q82381955

Synonyms:88738-41-4;{[(2-METHOXYETHOXY)METHOXY]METHYL}BENZENE;DTXSID30519039

Suppliers and Price of {[(2-Methoxyethoxy)methoxy]methyl}benzene

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 {[(2-Methoxyethoxy)methoxy]methyl}benzene

Chemical Property:

XLogP3:1.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:7
Exact Mass:196.109944368
Heavy Atom Count:14
Complexity:122

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COCCOCOCC1=CC=CC=C1

Technology Process of {[(2-Methoxyethoxy)methoxy]methyl}benzene

There total 2 articles about {[(2-Methoxyethoxy)methoxy]methyl}benzene 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: 100.0%

: 3970-21-6
2-Methoxyethoxymethyl chloride

: 100-51-6,185532-71-2
benzyl alcohol

: 88738-41-4
<<(methoxyethoxy)methoxy>methyl>benzene

Guidance literature:: DOI:10.1021/jo00034a057

Reference yield:

: 53172-91-1
(benzyloxy)(tert-butyl)dimethylsilane

: 88738-41-4
<<(methoxyethoxy)methoxy>methyl>benzene

Guidance literature:: Multi-step reaction with 2 steps

1: H₂SiF₆ / H₂O; acetonitrile / 8 h / 0 °C / competition reaction with Bn-O-TIPS; other times; in the presence of Et₃N; selective deprotection of trialkylsilyl ethers

2: 100 percent

With fluorosilicic acid; In water; acetonitrile;
DOI:10.1021/jo00034a057

Reference yield: 98.0%

: 88738-41-4
<<(methoxyethoxy)methoxy>methyl>benzene

: 100-51-6,185532-71-2
benzyl alcohol

Guidance literature:: With cerium(III) chloride; In acetonitrile; for 3h; Further Variations:; Reaction partners; Product distribution; Heating;
DOI:10.1021/ol015585w