2-Ethyl-4,6-dimethylphenol

Base Information

Chemical Name:2-Ethyl-4,6-dimethylphenol
CAS No.:2219-79-6
Molecular Formula:C10H14O
Molecular Weight:150.221
Hs Code.:
UNII:FH36J57LG1
DSSTox Substance ID:DTXSID601311606
Nikkaji Number:J1.243.547I

Synonyms:2-Ethyl-4,6-dimethylphenol;2,4-Xylenol, 6-ethyl-;2219-79-6;4,6-Dimethyl-2-ethyl-phenol;FH36J57LG1;Phenol, 4,6-dimethyl-2-ethyl-;UNII-FH36J57LG1;SCHEMBL1021767;MXHAHSBTOVFDBK-UHFFFAOYSA-N;DTXSID601311606

Suppliers and Price of 2-Ethyl-4,6-dimethylphenol

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-Ethyl-4,6-dimethylphenol

Chemical Property:

XLogP3:3.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:150.104465066
Heavy Atom Count:11
Complexity:122

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCC1=CC(=CC(=C1O)C)C

Technology Process of 2-Ethyl-4,6-dimethylphenol

There total 7 articles about 2-Ethyl-4,6-dimethylphenol 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:

: triethyl-(2-ethyl-4,6-dimethyl-phenoxy)-silane

: 2219-79-6
2-ethyl-4,6-dimethyl-phenol

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 20 ℃;
DOI:10.1021/ja0586790

Reference yield:

: 4028-66-4
2,4,6-trimethylanisole

: 2219-79-6
2-ethyl-4,6-dimethyl-phenol

Guidance literature:: Multi-step reaction with 2 steps

1.1: benzene / 60 °C

1.2: H₂ / cyclohexane / 115 °C / 3040 Torr

2.1: tetrabutylammonium fluoride / tetrahydrofuran / 20 °C

With tetrabutyl ammonium fluoride; In tetrahydrofuran; benzene;
DOI:10.1021/ja0586790