5-Ethyl-2-methoxyacetophenone

Base Information

Chemical Name:5-Ethyl-2-methoxyacetophenone
CAS No.:29643-54-7
Molecular Formula:C11H14O2
Molecular Weight:178.231
Hs Code.:
European Community (EC) Number:673-637-0
DSSTox Substance ID:DTXSID40374530
Wikidata:Q82163149
Mol file:29643-54-7.mol

Synonyms:5-Ethyl-2-methoxyacetophenone;29643-54-7;1-(5-ethyl-2-methoxyphenyl)ethanone;1-(5-ethyl-2-methoxyphenyl)ethan-1-one;SCHEMBL18782458;5'-ethyl-2'-methoxyacetophenone;DTXSID40374530;AKOS006278117;FS-1573;CS-0335985;FT-0707328;J-017589

Suppliers and Price of 5-Ethyl-2-methoxyacetophenone

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

Crysdot
1-(5-Ethyl-2-methoxyphenyl)ethanone 97%
25g
$ 486.00

American Custom Chemicals Corporation
5-ETHYL-2-METHOXYACETOPHENONE 95.00%
5MG
$ 503.09

AHH
5-ETHYL-2-METHOXYACETOPHENONE 97%
1g
$ 100.00

Total 5 raw suppliers

Chemical Property of 5-Ethyl-2-methoxyacetophenone

Chemical Property:

PSA：26.30000
LogP:2.46020
XLogP3:2.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:178.099379685
Heavy Atom Count:13
Complexity:177

Purity/Quality:

99% ^*data from raw suppliers

1-(5-Ethyl-2-methoxyphenyl)ethanone 97% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCC1=CC(=C(C=C1)OC)C(=O)C

Technology Process of 5-Ethyl-2-methoxyacetophenone

There total 4 articles about 5-Ethyl-2-methoxyacetophenone 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: 90.0%

: 24539-92-2
3-ethyl-6-hydroxyacetophenone

: 74-88-4
methyl iodide

: 29643-54-7
1-(5-ethyl-2-methoxyphenyl)ethanone

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 18h;

Reference yield:

: 110457-64-2
2,4-diethylanisole

: 29643-54-7
1-(5-ethyl-2-methoxyphenyl)ethanone

: 29643-34-3
1-(3-ethyl-4-methoxyphenyl)ethan-1-one

Guidance literature:: With pyridine; N-hydroxyphthalimide; tetrabutylammonium tetrafluoroborate; oxygen; In 2,2,2-trifluoroethanol; acetonitrile; at 35 ℃; Overall yield = 82 percent; Electrolysis;
DOI:10.1007/s11426-021-1061-x

Reference yield:

: 3245-23-6,746657-65-8
p-ethylphenyl acetate

: 29643-54-7
1-(5-ethyl-2-methoxyphenyl)ethanone

Guidance literature:: Multi-step reaction with 2 steps

1: aluminum (III) chloride / 2 h / 130 °C

2: potassium carbonate / N,N-dimethyl-formamide / 18 h / 20 °C

With aluminum (III) chloride; potassium carbonate; In N,N-dimethyl-formamide;