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Iodosobenzene

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
MDL Number:
MFCD00039507
MOL File:
536-80-1.mol
Last updated:2023-06-08 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
FDA UNII TWW7V7Q50P
EPA Substance Registry System Benzene, iodosyl- (536-80-1)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
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 price More Price(7)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TCI Chemical I0072 Iodosobenzene >95.0%(T) 536-80-1 5g $209 2024-03-01 Buy
TCI Chemical I0072 Iodosobenzene 536-80-1 25G $609 2024-03-01 Buy
TRC I737195 Iodosobenzene 536-80-1 100mg $60 2021-12-16 Buy
American Custom Chemicals Corporation HCH0352769 IODOSOBENZENE 95.00% 536-80-1 5G $919.33 2021-12-16 Buy
Matrix Scientific 128409 Iodosobenzene 97% 536-80-1 1g $451 2021-12-16 Buy
Product number Packaging Price Buy
I0072 5g $209 Buy
I0072 25G $609 Buy
I737195 100mg $60 Buy
HCH0352769 5G $919.33 Buy
128409 1g $451 Buy

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.

Uses

lodosobenzene is a relatively new, selective oxidizing agent which is particularly useful for the preparation of sulfoxides from unsaturated or otherwise sensitive sulfides. The preparation of diallyl, di-2-hydroxyethyl and phenyl 2-chloroethyl sulfoxides illustrates its use.
Iodosobenzene diacetate behaves similarly and oxidizes diphenyl and 4-nitro-phenyl 4'-carboxyphenyl sulfide exclusively to the sulfoxides. This reagent failed, however, to oxidize bis(2-nitro-4-trifuoromethylphenyl) sulfide and in the case of bis(2-aminophenyl) sulfide it gave complex products. Iodosobenzene diacetate caused diacetoxylation of the heterocycle of 2,5-diphenyl-1 ,4-dithiadiene rather than oxidation of the sulfide function, and with 2,5-diphenylI-1 ,4-dithiadiene-1-oxide unexpected results were obtained, as discussed in section C-4.
Organic Sulfur Compounds

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( 114)Suppliers
Supplier Tel Email Country ProdList Advantage
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21691 55
Hubei xin bonus chemical co. LTD
86-13657291602 linda@hubeijusheng.com CHINA 22968 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 47465 58
career henan chemical co
+86-0371-86658258 15093356674; factory@coreychem.com China 29826 58
Shaanxi Dideu Medichem Co. Ltd
+86-029-81148696 +8615536356810 1047@dideu.com China 3459 58
Hefei TNJ Chemical Industry Co.,Ltd.
0551-65418671 sales@tnjchem.com China 34572 58
Shaanxi Dideu Medichem Co. Ltd
+86-029-89586680 +86-18192503167 1026@dideu.com China 9358 58
Dayang Chem (Hangzhou) Co.,Ltd.
571-88938639 +8617705817739 info@dycnchem.com CHINA 52867 58
sgtlifesciences pvt ltd
+8617013299288 dj@sgtlifesciences.com China 12382 58
Nanjing Doge Biomedical Technology Co., Ltd
+86-25-58227606 +86-15305155328 sales@dogechemical.com China 4128 58

View Lastest Price from Iodosobenzene manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Iodosobenzene pictures 2020-01-13 Iodosobenzene
536-80-1
US $0.10 / KG 1KG 99.0% 1000 tons Shaanxi Dideu Medichem Co. Ltd
IODOSOBENZENE pictures 2020-01-03 IODOSOBENZENE
536-80-1
US $1.00 / KG 1KG 95-99% 1ton Career Henan Chemical Co
  • Iodosobenzene pictures
  • Iodosobenzene
    536-80-1
  • US $0.10 / KG
  • 99.0%
  • Shaanxi Dideu Medichem Co. Ltd
  • IODOSOBENZENE pictures
  • IODOSOBENZENE
    536-80-1
  • US $1.00 / KG
  • 95-99%
  • Career Henan Chemical Co
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