Ethanone, 1-(4-ethyl-2,6-dihydroxyphenyl)-

Base Information

Chemical Name:Ethanone, 1-(4-ethyl-2,6-dihydroxyphenyl)-
CAS No.:209746-96-3
Molecular Formula:C10H12O3
Molecular Weight:180.203
Hs Code.:
DSSTox Substance ID:DTXSID70441688

Synonyms:Ethanone, 1-(4-ethyl-2,6-dihydroxyphenyl)-;209746-96-3;SCHEMBL3411046;DTXSID70441688

Suppliers and Price of Ethanone, 1-(4-ethyl-2,6-dihydroxyphenyl)-

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

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Chemical Property of Ethanone, 1-(4-ethyl-2,6-dihydroxyphenyl)-

Chemical Property:

XLogP3:2.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:180.078644241
Heavy Atom Count:13
Complexity:179

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

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

Technology Process of Ethanone, 1-(4-ethyl-2,6-dihydroxyphenyl)-

There total 3 articles about Ethanone, 1-(4-ethyl-2,6-dihydroxyphenyl)- 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:

: acetic acid 3-ethyl-5-hydroxy-phenyl ester

: 209746-96-3
4'-ethyl-2',6'-dihydroxyacetophenone

Guidance literature:: With aluminium trichloride; In chlorobenzene; at 90 ℃;
DOI:10.1016/j.bmcl.2004.07.082

Reference yield:

: 1026523-25-0
1-(3-acetyl-6-ethyl-2,4-dihydroxy-phenyl)-ethanone

: 209746-96-3
4'-ethyl-2',6'-dihydroxyacetophenone

Guidance literature:: With sulfuric acid; at 20 ℃; for 2h;
DOI:10.1021/jm990175n

Reference yield:

: 4299-72-3
5-ethylresorcinol

: 209746-96-3
4'-ethyl-2',6'-dihydroxyacetophenone

Guidance literature:: Multi-step reaction with 2 steps

1: pyridine

2: AlCl₃ / chlorobenzene / 90 °C

With pyridine; aluminium trichloride; In chlorobenzene; 2: Fries rearrangement;
DOI:10.1016/j.bmcl.2004.07.082