1-Ethoxy-2,4-dimethylbenzene

Base Information

Chemical Name:1-Ethoxy-2,4-dimethylbenzene
CAS No.:35338-30-8
Molecular Formula:C10H14O
Molecular Weight:150.221
Hs Code.:
DSSTox Substance ID:DTXSID10490236
Nikkaji Number:J284.035I
Wikidata:Q82333917
Mol file:35338-30-8.mol

Synonyms:1-ethoxy-2,4-dimethylbenzene;35338-30-8;2,4-dimethylphenetole;SCHEMBL144438;DTXSID10490236;AKOS006241760

Suppliers and Price of 1-Ethoxy-2,4-dimethylbenzene

Supply Marketing:

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

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Chemical Property of 1-Ethoxy-2,4-dimethylbenzene

Chemical Property:

Vapor Pressure:0.297mmHg at 25°C
XLogP3:3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:150.104465066
Heavy Atom Count:11
Complexity:111

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC1=C(C=C(C=C1)C)C

Technology Process of 1-Ethoxy-2,4-dimethylbenzene

There total 4 articles about 1-Ethoxy-2,4-dimethylbenzene 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: 40.0%

: 64-17-5
ethanol

: 87241-52-9
2,4-dimethylphenyl trifluoromethanesulfonate

: 35338-30-8
1-ethoxy-2,4-dimethylbenzene

Guidance literature:: With Trimethyl borate; acetone; trifluoroacetic acid; at 15 ℃; UV-irradiation; Inert atmosphere;
DOI:10.1021/jacs.9b02684

Reference yield:

: 64-67-5
diethyl sulfate

: 104-93-8
p-methylanizole

: 622-60-6
1-ethoxy-4-methylbenzene

: 1585-06-4
1-ethoxy-4-ethylbenzene

: 35338-30-8
1-ethoxy-2,4-dimethylbenzene

Guidance literature:: With n-butyllithium; hexane; potassium tert-butylate; Yield given. Multistep reaction. Yields of byproduct given; 1) heptane, reflux, 4.5 h, 2) THF;
DOI:10.1021/jo00291a044

Reference yield:

: 64-17-5
ethanol

: 95-66-9
2,4-dimethylchlorobenzene

: 35338-30-8
1-ethoxy-2,4-dimethylbenzene

: 108-38-3,104809-90-7
m-xylene

Guidance literature:: With 5-(di-tert-butylphosphino)-1′, 3′, 5′-triphenyl-1′H-[1,4′]bipyrazole; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; potassium hydroxide; at 0.1 ℃; for 3h; Inert atmosphere;
DOI:10.1021/op7002858