[(2-Ethoxyethoxy)methyl]benzene

Base Information

Chemical Name:[(2-Ethoxyethoxy)methyl]benzene
CAS No.:61911-33-9
Molecular Formula:C11H16O2
Molecular Weight:180.247
Hs Code.:
DSSTox Substance ID:DTXSID40597949
Nikkaji Number:J1.405.438C
Wikidata:Q82493613

Synonyms:61911-33-9;[(2-ETHOXYETHOXY)METHYL]BENZENE;SCHEMBL13226430;DTXSID40597949

Suppliers and Price of [(2-Ethoxyethoxy)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
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price

Total 0 raw suppliers

Chemical Property of [(2-Ethoxyethoxy)methyl]benzene

Chemical Property:

XLogP3:1.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:6
Exact Mass:180.115029749
Heavy Atom Count:13
Complexity:109

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOCCOCC1=CC=CC=C1

Technology Process of [(2-Ethoxyethoxy)methyl]benzene

There total 4 articles about [(2-Ethoxyethoxy)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:

: 74-96-4
ethyl bromide

: 622-08-2,1201808-31-2
2-Benzyloxyethanol

: 61911-33-9
benzyl cellosolve

Guidance literature:: 2-Benzyloxyethanol; With sodium hydride; In tetrahydrofuran; at 50 ℃; for 4h;

ethyl bromide; In tetrahydrofuran; at 20 ℃; for 12h;
DOI:10.1016/j.chemphyslip.2003.08.002

Reference yield:

: 110-80-5
2-ethoxy-ethanol

: 100-44-7
benzyl chloride

: 61911-33-9
benzyl cellosolve

Guidance literature:: With potassium hydroxide;
DOI:10.1021/ja01162a534

Reference yield:

: 100-44-7
benzyl chloride

: 61911-33-9
benzyl cellosolve

Guidance literature:: Multi-step reaction with 2 steps

1.1: NaH / dimethylformamide / 10 h / 50 °C

1.2: dimethylformamide / 20 °C

2.1: NaH / tetrahydrofuran / 4 h / 50 °C

2.2: tetrahydrofuran / 12 h / 20 °C

With sodium hydride; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1016/j.chemphyslip.2003.08.002