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2-Iodo-4-acetylphenol

2-Iodo-4-acetylphenol Struktur
62615-24-1
CAS-Nr.
62615-24-1
Englisch Name:
2-Iodo-4-acetylphenol
Synonyma:
2-Iodo-4-acetylphenol;4-Acetyl-2-iodophenol;4'-Hydroxy-3'-iodoacetophenone;3'-Iodo-4'-hydroxyacetophenone;4'-Hydroxy-3'-iodoacetophenone 97%;1-(4-Hydroxy-3-iodo-phenyl)-ethanone;Ethanone, 1-(4-hydroxy-3-iodophenyl)-
CBNumber:
CB82367833
Summenformel:
C8H7IO2
Molgewicht:
262.04
MOL-Datei:
62615-24-1.mol

2-Iodo-4-acetylphenol Eigenschaften

Schmelzpunkt:
155-160°C
Sicherheit
  • Risiko- und Sicherheitserkl?rung
  • Gefahreninformationscode (GHS)
Kennzeichnung gef?hrlicher Xn
R-S?tze: 22-41
S-S?tze: 26-39
WGK Germany  1
Bildanzeige (GHS) GHS hazard pictogramsGHS hazard pictograms
Alarmwort Achtung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H302 Gesundheitssch?dlich bei Verschlucken. Akute Toxizit?t oral Kategorie 4 Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P264, P270, P301+P312, P330, P501
H318 Verursacht schwere Augensch?den. Schwere Augensch?digung Kategorie 1 Achtung GHS hazard pictogramssrc="/GHS05.jpg" width="20" height="20" /> P280, P305+P351+P338, P310
Sicherheit
P280 Schutzhandschuhe/Schutzkleidung/Augenschutz tragen.

2-Iodo-4-acetylphenol Chemische Eigenschaften,Einsatz,Produktion Methoden

Verwenden

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

synthetische

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

2-Iodo-4-acetylphenol Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte

3'-IODOACETOPHENONE 5-Acetyl-2-(1-hydroxy-1-methylethyl)benzofuran

2-Iodo-4-acetylphenol Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 11)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Shaanxi Dideu Medichem Co. Ltd 		+86-29-87569262 +86-15319487004
 1015@dideu.com China 3209 58
sgtlifesciences pvt ltd 		+8617013299288
 dj@sgtlifesciences.com China 12373 58
Aladdin Scientific 		+1-+1(833)-552-7181
sales@aladdinsci.com United States 52924 58
Sigma-Aldrich 021-61415566 800-8193336
 orderCN@merckgroup.com China 51456 80
SuZhou ShiYa Biopharmaceuticals, Inc. 0512-52358471 17715136450
 sales@shiyabiopharm.com China 13492 58
Shaanxi Dideu Medichem Co. Ltd 029-61856358 15229202216
 1020@dideu.com China 10011 58
Zhuhai Aobokai Biomedical Technology Co., Ltd. 400-0628126
sales-team@aobchem.com.cn China 9997 58
Suzhou Hosyn Pharm Ltd. 17621975170; 17621975170
 sales@hosynpharm.com China 432 58
Shanghai Aladdin Biochemical Technology Co.,Ltd. +86-18521732826
 market@aladdin-e.com China 48461 58
  • 2-Iodo-4-acetylphenol
  • 3'-Iodo-4'-hydroxyacetophenone
  • 4'-Hydroxy-3'-iodoacetophenone
  • 4'-Hydroxy-3'-iodoacetophenone 97%
  • 4-Acetyl-2-iodophenol
  • Ethanone, 1-(4-hydroxy-3-iodophenyl)-
  • 1-(4-Hydroxy-3-iodo-phenyl)-ethanone
  • 62615-24-1
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