| Identification | Back Directory | [Name]
2-Iodo-4-acetylphenol | [CAS]
62615-24-1 | [Synonyms]
2-Iodo-4-acetylphenol
4-Acetyl-2-iodophenol
3'-Iodo-4'-hydroxyacetophenone
4'-Hydroxy-3'-iodoacetophenone
4'-Hydroxy-3'-iodoacetophenone 97%
1-(4-Hydroxy-3-iodo-phenyl)-ethanone
Ethanone, 1-(4-hydroxy-3-iodophenyl)- | [Molecular Formula]
C8H7IO2 | [MDL Number]
MFCD06200221 | [MOL File]
62615-24-1.mol | [Molecular Weight]
262.04 |
| Hazard Information | Back Directory | [Uses]
Reactant for:
- Preparation of cyclopentene fused benzofurans and indoles via Pd-catalyzed tandem ring opening-ring closing reaction with diazabicyclic alkenes
- Highly regioselective synthesis of spirocyclic compounds by a palladium-catalyzed intermolecular tandem reaction
- Regioselective synthesis of indene derivatives via Pd/C-catalyzed cyclization reaction in air
- Preparation of carbazoles via cross-coupling with silylaryl triflates followed by palladium-catalyzed cyclization
- Stereoselective preparation of heteropolycyclic compounds via palladium-catalyzed stereoselective heteroannulation of with cyclic alkenes
- Preparation of disubstituted coumarins via palladium-catalyzed carbonylative annulation of internal alkynes
- Preparation of arylalkynes, benzofurans and indoles via Sonogashira coupling and cyclization on alumina
| [Preparation]
Preparation by reaction of iodine and potassium iodide on 4-hydroxyacetophenone in aqueous ammonium hydroxide at r.t. (54–57%). | [Synthesis Reference(s)]
Journal of Medicinal Chemistry, 23, p. 738, 1980 DOI: 10.1021/jm00181a008 |
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Sigma-Aldrich
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https://www.sigmaaldrich.cn |
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Merck KGaA
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www.sigmaaldrich.cn |
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