ChemicalBook > Product Catalog >Organic Chemistry >Hydrocarbons and derivatives >Aromatic hydrocarbons >Iodosobenzene

Iodosobenzene

Iodosobenzene Structure
CAS No.
536-80-1
Chemical Name:
Iodosobenzene
Synonyms
PhIO;iodoso-benzen;IODOSOBENZENE;iodosyl-benzen;Iodosobenzene>Benzene, iodosyl-;Iodosobenzene,>95%;Phenyloxoiodine(III);[Oxoiodo(III)]benzene;Phenyliodine(III) oxide
CBNumber:
CB6375166
Molecular Formula:
C6H5IO
Molecular Weight:
220.01
MOL File:
536-80-1.mol
Modify Date:
2023/6/8 17:06:38

Iodosobenzene Properties

Melting point 210°C (rough estimate)
Density 1.8665 (estimate)
storage temp. Freezer
Water Solubility Slightly soluble in water
solubility Methanol (Slightly), TFA (Slightly)
form powder to crystal
color White to Yellow to Green
Merck 14,5044
InChIKey JYJVVHFRSFVEJM-UHFFFAOYSA-N
EPA Substance Registry System Benzene, iodosyl- (536-80-1)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS02,GHS07
Signal word  Danger
Hazard statements  H228-H315-H319
Precautionary statements  P210-P240-P241-P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
Safety Statements  17-36/37/39
RIDADR  1479
RTECS  DA3500000
HazardClass  4.1
PackingGroup  II
HS Code  29039990
NFPA 704
1
2 0

Iodosobenzene Chemical Properties,Uses,Production

Chemical Properties

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

Uses

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.

Synthesis

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

Iodosobenzene Preparation Products And Raw materials

Raw materials

Preparation Products

Iodosobenzene Suppliers

Global( 117)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
VGS SYNTHESIS PRIVATE LIMITED +91-9866975588 +91-9866975588 Hyderabad, India 1818 58 Inquiry
Riddhesh Pharmachem +91-9106014993 +91-9106014993 Gujarat, India 126 58 Inquiry
Innovative Labs +91-9885794886 +91-9885794886 Telangana, India 219 58 Inquiry
ABINTIO BIOSCIENCES +91-6302904517 +91-7386106841 Hyderabad, India 301 58 Inquiry
CHEMSWORTH +91-261-2397244 New Delhi, India 6707 30 Inquiry
Laksh Finechem Private Limited +91-8048600905 Gujarat, India 195 58 Inquiry
Henan Tianfu Chemical Co.,Ltd. +86-0371-55170693 +86-19937530512 China 21676 55 Inquiry
CONIER CHEM AND PHARMA LIMITED +8618523575427 China 49391 58 Inquiry
career henan chemical co +86-0371-86658258 +8613203830695 China 29826 58 Inquiry
Hefei TNJ Chemical Industry Co.,Ltd. 0551-65418671 China 34571 58 Inquiry
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