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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
Wasserl?slichkeit
Slightly soluble in water
L?slichkeit
Methanol (Slightly), TFA (Slightly)
Aggregatzustand
powder to crystal
Farbe
White to Yellow to Green
Merck 
14,5044
InChIKey
JYJVVHFRSFVEJM-UHFFFAOYSA-N
EPA chemische Informationen
Benzene, iodosyl- (536-80-1)
Sicherheit
  • Risiko- und Sicherheitserkl?rung
  • Gefahreninformationscode (GHS)
S-S?tze: 17-36/37/39
RIDADR  1479
RTECS-Nr. DA3500000
HazardClass  4.1
PackingGroup  II
HS Code  29039990
Bildanzeige (GHS) GHS hazard pictogramsGHS hazard pictograms
Alarmwort Achtung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H228 Entzündbarer Feststoff. Entzündbare Feststoffe Kategorie 1 Achtung
Warnung
GHS hazard pictogramssrc="/GHS02.jpg" width="20" height="20" /> P210, P240,P241, P280, P370+P378
H315 Verursacht Hautreizungen. Hautreizung Kategorie 2 Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P264, P280, P302+P352, P321,P332+P313, P362
H319 Verursacht schwere Augenreizung. Schwere Augenreizung Kategorie 2 Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P264, P280, P305+P351+P338,P337+P313P
Sicherheit
P210 Von Hitze, hei?en Oberfl?chen, Funken, offenen Flammen und anderen Zündquellenarten fernhalten. Nicht rauchen.
P240 Beh?lter und zu befüllende Anlage erden.
P241 Explosionsgeschützte [elektrische/Lüftungs-/ Beleuchtungs-/...] Ger?te verwenden.
P264 Nach Gebrauch gründlich waschen.
P264 Nach Gebrauch gründlich waschen.
P280 Schutzhandschuhe/Schutzkleidung/Augenschutz tragen.

Iodosylbenzol Chemische Eigenschaften,Einsatz,Produktion Methoden

S-S?tze 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; Po?towicz 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 H?ndler.

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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
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