2-Iodo-4-acetylphenol

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

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Eigenschaften Sicherheit Verwendungswort Produktionsfirma 9

2-Iodo-4-acetylphenol Eigenschaften

Schmelzpunkt:: 155-160°C

Sicherheit

Risiko- und Sicherheitserklärung
Gefahreninformationscode (GHS)

Kennzeichnung gefährlicher	Xn
R-Sätze:	22-41
S-Sätze:	26-39
WGK Germany	1

Bildanzeige (GHS)

Alarmwort

Achtung

Gefahrenhinweise

Code	Gefahrenhinweise	Gefahrenklasse	Abteilung	Alarmwort	Symbol	P-Code
H302	Gesundheitsschädlich bei Verschlucken.	Akute Toxizität oral	Kategorie 4	Warnung	src="/GHS07.jpg" width="20" height="20" />	P264, P270, P301+P312, P330, P501
H318	Verursacht schwere Augenschäden.	Schwere Augenschädigung	Kategorie 1	Achtung	src="/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 Händler.

Global( 9)Lieferanten

Firmenname	Telefon	E-Mail	Land	Produktkatalog	Edge Rate
sgtlifesciences pvt ltd	+8617013299288	dj@sgtlifesciences.com	China	12382	58
Aladdin Scientific	+1-833-552-7181	sales@aladdinsci.com	United States	52927	58
Sigma-Aldrich	021-61415566 800-8193336	orderCN@merckgroup.com	China	51471	80
SuZhou ShiYa Biopharmaceuticals, Inc.	0512-52358471 17715136450	sales@shiyabiopharm.com	China	13502	58
Zhuhai Aobokai Biomedical Technology Co., Ltd.	400-0628126 15697568815;	sales-team@aobchem.com.cn	China	20186	58
Shaanxi Dideu Medichem Co. Ltd	029-81124267 15229202216	1073@dideu.com	China	10011	58
Shanghai Aladdin Biochemical Technology Co.,Ltd.	+86-18521732826	market@aladdin-e.com	China	48617	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