Iodosylbenzol

Iodosobenzene Struktur
536-80-1
CAS-Nr.
536-80-1
Bezeichnung:
Iodosylbenzol
Englisch Name:
Iodosobenzene
Synonyma:
PhIO;iodoso-benzen;IODOSOBENZENE;iodosyl-benzen;Iodosobenzene>Benzene, iodosyl-;Iodosobenzene,>95%;Phenyloxoiodine(III);[Oxoiodo(III)]benzene;Phenyliodine(III) oxide
CBNumber:
CB6375166
Summenformel:
C6H5IO
Molgewicht:
220.01
MOL-Datei:
536-80-1.mol

Iodosylbenzol Eigenschaften

Schmelzpunkt:
210°C (rough estimate)
Dichte
1.8665 (estimate)
storage temp. 
Freezer
Wasserlöslichkeit
Slightly soluble in water
Löslichkeit
Methanol (Slightly), TFA (Slightly)
Aggregatzustand
powder to crystal
Farbe
White to Yellow to Green
Merck 
14,5044
InChI
InChI=1S/C6H5IO/c8-7-6-4-2-1-3-5-6/h1-5H
InChIKey
JYJVVHFRSFVEJM-UHFFFAOYSA-N
SMILES
C1(I=O)=CC=CC=C1
EPA chemische Informationen
Benzene, iodosyl- (536-80-1)
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
S-Sätze: 17-36/37/39
RIDADR  1479
RTECS-Nr. DA3500000
TSCA  TSCA listed
HazardClass  4.1
PackingGroup  II
HS Code  29039990
Bildanzeige (GHS) Flame (GHS02)Exclamation Mark (GHS07)
Alarmwort Achtung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H228 Entzündbarer Feststoff. Entzündbare Feststoffe Kategorie 1 Achtung
Warnung
P210, P240,P241, P280, P370+P378
H315 Verursacht Hautreizungen. Hautreizung Kategorie 2 Warnung P264, P280, P302+P352, P321,P332+P313, P362
H319 Verursacht schwere Augenreizung. Schwere Augenreizung Kategorie 2 Warnung P264, P280, P305+P351+P338,P337+P313P
Sicherheit
P210 Von Hitze, heißen Oberflächen, Funken, offenen Flammen und anderen Zündquellenarten fernhalten. Nicht rauchen.
P240 Behälter und zu befüllende Anlage erden.
P241 Explosionsgeschützte [elektrische/Lüftungs-/ Beleuchtungs-/...] Geräte verwenden.
P264 Nach Gebrauch gründlich waschen.
P264 Nach Gebrauch gründlich waschen.
P280 Schutzhandschuhe/Schutzkleidung/Augenschutz tragen.

Iodosylbenzol Chemische Eigenschaften,Einsatz,Produktion Methoden

S-Sätze Betriebsanweisung:

S17:Von brennbaren Stoffen fernhalten.
S36/37/39:Bei der Arbeit geeignete Schutzkleidung,Schutzhandschuhe und Schutzbrille/Gesichtsschutz tragen.

Chemische Eigenschaften

Iodosobenzene is an amorphous yellow substance; it explodes at 210℃, decomposing with the evolution of iodine vapour, and dissolves in hot water and alcohol. If acids do not oxidise C6H5IO, they give saline compounds in which iodosobenzene appears as a basic oxide of a diatomic metal, C6H5I. Thus, for instance, when an acetic acid solution of iodosobenzene is treated with a solution of nitric acid, it gives large monoclinic crystals of a nitric acid salt having the composition C6H5(NO3)2 [like Ca(NO3)2). Iodosobenzene displaces iodine from potassium iodide (in a solution acidulated with acetic or hydrochloric acid)-ie, it acts with its oxygen like HClO. The action of peroxide of hydrogen, chromic acid, and other similar oxidising agents gives C6H5IO2, which is a neutral substance-i.e, is incapable of giving salts with acids.
Iodosobenzene is one of the very first oxidants and remains in use because it has excellent oxygen-transfer behavior and mechanistic cleanliness (Hill & Schardt, 1980; Rezaeifard et al., 2007; Potowicz et al., 2006).
The Principles of Chemistry Volume 1

Verwenden

Oxygen transfer reagent for stiochiometric or catalytic cross-functionalization of alkenes, alcohols, sulfides, and organometallo Compounds.
Iodosobenzene is used as an oxidizing and acetoxylating agent in organic synthesis. It is actively involved in the preparation of (Z)-3,7-dimethyl-2,6-octadien-1-al(neral) from (Z)-3,7-dimethyl-2,6-octadien-1-ol (nerol) in presence of 2,2,6,6-tetramethylpiperidin-1-oxyl (TEMPO). It is a useful reagent for the synthesis of a wide variety of heterocyclic compounds. It is also used in the Pd-catalyzed 2-arylation of indoles.

Synthese

Iodosobenzene has been prepared by the action of sodium or potassium hydroxide solution on iodobenzene dichloride and by addition of water to the dichloride.
Synthesis of Iodosobenzene
Iodosobenzene is prepared from iodobenzene.It is prepared by first oxidizing iodobenzene by peracetic acid. Hydrolysis of resulting diacetate affords "PhIO":
C6H5I + CH3CO3H + CH3CO2H → C6H5I(O2CCH3)2 + H2O
C6H5I(O2CCH3)2 + H2O → C6H5IO + 2CH3CO2H
http://orgsyn.org

Iodosylbenzol Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Iodosylbenzol Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 129)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Beijing Taiya Jie Technology Development Co., Ltd. 021-33690831-8001 13552411790;18616022633
postmaster@tyjchem.cn China 1541 55
Huai Hua Binfengchem Co., Ltd 0745-2866851 17711757908
3907837691@qq.com China 4744 58
J & K SCIENTIFIC LTD. 18210857532 18210857532
jkinfo@jkchemical.com China 96815 76
PharmaBlock Sciences (Nanjing),Inc. 025-86918202 4000255188
sales@pharmablock.com China 5000 55
Meryer (Shanghai) Chemical Technology Co., Ltd. 4006356688 18621169109
market03@meryer.com China 40202 62
TCI (Shanghai) Development Co., Ltd. 021-67121386
Sales-CN@TCIchemicals.com China 24512 81
Energy Chemical 400-0056266
sales8178@energy-chemical.com China 44850 61
Sichuan Kulinan Technology Co., Ltd 400-1166-196 18981987031
cdhxsj@163.com China 11674 57
Tianjin heowns Biochemical Technology Co., Ltd. 400 638 7771
sales@heowns.com China 14412 57
Hunan Hui Bai Shi Biotechnology Co., Ltd. 0731-85526065 13308475853
ivy@hnhbsj.com China 7236 62

536-80-1(Iodosylbenzol)Verwandte Suche:


  • iodoso-benzen
  • iodosyl-benzen
  • IODOSOBENZENE
  • [Oxoiodo(III)]benzene
  • Phenyliodine(III) oxide
  • Phenyloxoiodine(III)
  • Benzene, iodosyl-
  • 4-05-00-00692 (Beilstein Handbook Reference)
  • Iodosobenzene>
  • Iodosobenzene,>95%
  • IODOSOBENZENE ISO 9001:2015 REACH
  • PhIO
  • 536-80-1
  • 5396-80-1
  • Hypervalent Iodine Compounds
  • Oxidation
  • Benzene derivatives
  • Hypervalent Iodine Compounds
  • Oxidation
  • Synthetic Organic Chemistry
Copyright 2019 © ChemicalBook. All rights reserved