Ethanone, 1-(2,4-dihydroxy-5-iodophenyl)-

Base Information

Chemical Name:Ethanone, 1-(2,4-dihydroxy-5-iodophenyl)-
CAS No.:62069-33-4
Molecular Formula:C8H7IO3
Molecular Weight:278.046
Hs Code.:
DSSTox Substance ID:DTXSID10450193
Wikidata:Q82269795

Synonyms:62069-33-4;Ethanone, 1-(2,4-dihydroxy-5-iodophenyl)-;DTXSID10450193

Suppliers and Price of Ethanone, 1-(2,4-dihydroxy-5-iodophenyl)-

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of Ethanone, 1-(2,4-dihydroxy-5-iodophenyl)-

Chemical Property:

XLogP3:2.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:277.94399
Heavy Atom Count:12
Complexity:183

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)C1=CC(=C(C=C1O)O)I

Technology Process of Ethanone, 1-(2,4-dihydroxy-5-iodophenyl)-

There total 6 articles about Ethanone, 1-(2,4-dihydroxy-5-iodophenyl)- 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: 85.0%

: 89-84-9
2',4'-dihydroxy-4-acetophenone

: 62069-33-4
1-(2,4-dihydroxy-5-iodophenyl)ethanone

Guidance literature:: With iodine; iodic acid; In ethanol; water; for 0.0833333h; Reflux;
DOI:10.1080/00397910903457332

Reference yield: 60.0%

: 89-84-9
2',4'-dihydroxy-4-acetophenone

: 62069-33-4
1-(2,4-dihydroxy-5-iodophenyl)ethanone

: 62069-34-5
1-(2,4-dihydroxy-3,5-diiodophenyl)ethanone

Guidance literature:: With N-iodo-succinimide; toluene-4-sulfonic acid; In acetonitrile; at 0 - 20 ℃; for 14h; Reagent/catalyst; Temperature;
DOI:10.1055/s-0039-1690001