1-(4-Hydroxy-3-iodophenyl)ethanone

Base Information

Chemical Name:1-(4-Hydroxy-3-iodophenyl)ethanone
CAS No.:62615-24-1
Molecular Formula:C8H7IO2
Molecular Weight:262.047
Hs Code.:2914700090
European Community (EC) Number:687-274-0
DSSTox Substance ID:DTXSID60359985
Nikkaji Number:J323.509B
Wikidata:Q82141459

Synonyms:1-(4-hydroxy-3-iodophenyl)ethanone;62615-24-1;4'-hydroxy-3'-iodoacetophenone;2-Iodo-4-acetylphenol;1-(4-hydroxy-3-iodo-phenyl)-ethanone;4-hydroxy-3-iodoacetophenone;4-hydroxy-3-iodo acetophenone;SCHEMBL1644004;DTXSID60359985;SJRAJHOOMLHHQN-UHFFFAOYSA-N;4'-Hydroxy-3'-iodoacetophenone, 97%;1-(4-hydroxy-3-iodophenyl)ethan-1-one

Suppliers and Price of 1-(4-Hydroxy-3-iodophenyl)ethanone

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

Sigma-Aldrich
4′-Hydroxy-3′-iodoacetophenone 97%
5g
$ 112.00

Chemcia Scientific
1-(4-Hydroxy-3-iodo-phenyl)-ethanone 95%
0.5 G
$ 265.00

American Custom Chemicals Corporation
4'-HYDROXY-3'-IODOACETOPHENONE 95.00%
5G
$ 897.44

AK Scientific
4′-Hydroxy-3′-iodoacetophenone
5g
$ 190.00

Total 5 raw suppliers

Chemical Property of 1-(4-Hydroxy-3-iodophenyl)ethanone

Chemical Property:

Melting Point:155-160°C
PSA：37.30000
LogP:2.19940
XLogP3:1.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:261.94908
Heavy Atom Count:11
Complexity:158

Purity/Quality:

98%,99%, ^*data from raw suppliers

4′-Hydroxy-3′-iodoacetophenone 97% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:Xn
Statements: 22-41
Safety Statements: 26-39

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

Canonical SMILES:CC(=O)C1=CC(=C(C=C1)O)I
Uses Reactant for:Preparation of cyclopentene fused benzofurans and indoles via Pd-catalyzed tandem ring opening-ring closing reaction with diazabicyclic alkenesHighly regioselective synthesis of spirocyclic compounds by a palladium-catalyzed intermolecular tandem reactionRegioselective synthesis of indene derivatives via Pd/C-catalyzed cyclization reaction in airPreparation of carbazoles via cross-coupling with silylaryl triflates followed by palladium-catalyzed cyclizationStereoselective preparation of heteropolycyclic compounds via palladium-catalyzed stereoselective heteroannulation of with cyclic alkenesPreparation of disubstituted coumarins via palladium-catalyzed carbonylative annulation of internal alkynesPreparation of arylalkynes, benzofurans and indoles via Sonogashira coupling and cyclization on alumina

Technology Process of 1-(4-Hydroxy-3-iodophenyl)ethanone

There total 5 articles about 1-(4-Hydroxy-3-iodophenyl)ethanone 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: 94.0%