1-Bromo-4-{2-[2-(2-methoxyethoxy)ethoxy]ethoxy}benzene

Base Information

Chemical Name:1-Bromo-4-{2-[2-(2-methoxyethoxy)ethoxy]ethoxy}benzene
CAS No.:125808-05-1
Molecular Formula:C₁₃H₁₉BrO₄
Molecular Weight:319.195
Hs Code.:
European Community (EC) Number:818-105-2
Nikkaji Number:J2.965.742D

Synonyms:1-bromo-4-{2-[2-(2-methoxyethoxy)ethoxy]ethoxy}benzene;125808-05-1;1-bromo-4-[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]benzene;SCHEMBL9811777;AKOS034047216;SB67186;EN300-1608371;Z1665350344

Suppliers and Price of 1-Bromo-4-{2-[2-(2-methoxyethoxy)ethoxy]ethoxy}benzene

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemicals and raw materials
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Total 1 raw suppliers

Chemical Property of 1-Bromo-4-{2-[2-(2-methoxyethoxy)ethoxy]ethoxy}benzene

Chemical Property:

XLogP3:1.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:10
Exact Mass:318.04667
Heavy Atom Count:18
Complexity:184

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COCCOCCOCCOC1=CC=C(C=C1)Br

Technology Process of 1-Bromo-4-{2-[2-(2-methoxyethoxy)ethoxy]ethoxy}benzene

There total 7 articles about 1-Bromo-4-{2-[2-(2-methoxyethoxy)ethoxy]ethoxy}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%

: 106-41-2
4-bromo-phenol

: 62921-74-8,518012-62-9,58320-73-3
2-(2-(2-methoxyethoxy)ethoxy)ethyl p-toluenesulfonate

: 125808-05-1
1-bromo-4-(2-(2-(2-methoxyethoxy)ethoxy)ethoxy)benzene

Guidance literature:: With potassium carbonate; In acetonitrile; for 16h; Reflux;
DOI:10.1021/ol2020175

Reference yield:

: 112-35-6,95507-80-5
triethylene glucol monomethyl ether

: 125808-05-1
1-bromo-4-(2-(2-(2-methoxyethoxy)ethoxy)ethoxy)benzene

Guidance literature:: Multi-step reaction with 2 steps

1: trimethylamine hydrochloride; triethylamine / acetonitrile / 3.5 h / 0 - 20 °C

2: potassium carbonate / acetonitrile / 16 h / Reflux

With trimethylamine hydrochloride; potassium carbonate; triethylamine; In acetonitrile;
DOI:10.1021/ol2020175