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Iodosobenzene

Product Name
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
Formula Weight
220.01
MOL File
536-80-1.mol
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Iodosobenzene Property

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)
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Safety

Safety Statements 
17-36/37/39
RIDADR 
1479
RTECS 
DA3500000
HazardClass 
4.1
PackingGroup 
II
HS Code 
29039990
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H228Flammable solid

H315Causes skin irritation

H319Causes serious eye irritation

Precautionary statements

P210Keep away from heat/sparks/open flames/hot surfaces. — No smoking.

P240Ground/bond container and receiving equipment.

P241Use explosion-proof electrical/ventilating/lighting/…/equipment.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P280Wear protective gloves/protective clothing/eye protection/face protection.

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N-Bromosuccinimide Price

TCI Chemical
Product number
I0072
Product name
Iodosobenzene
Purity
>95.0%(T)
Packaging
5g
Price
$209
Updated
2024/03/01
TCI Chemical
Product number
I0072
Product name
Iodosobenzene
Packaging
25G
Price
$609
Updated
2024/03/01
TRC
Product number
I737195
Product name
Iodosobenzene
Packaging
100mg
Price
$60
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
HCH0352769
Product name
IODOSOBENZENE
Purity
95.00%
Packaging
5G
Price
$919.33
Updated
2021/12/16
Matrix Scientific
Product number
128409
Product name
Iodosobenzene
Purity
97%
Packaging
1g
Price
$451
Updated
2021/12/16
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Iodosobenzene Chemical Properties,Usage,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.

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

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Iodosobenzene Suppliers

Beijing Taiya Jie Technology Development Co., Ltd.
Tel
021-33690831-8001 13552411790
Fax
021-33690831
Email
postmaster@tyjchem.cn
Country
China
ProdList
1541
Advantage
55
J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
94657
Advantage
76
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
021-61259108 18621169109
Fax
86-21-61259102
Email
market03@meryer.com
Country
China
ProdList
40228
Advantage
62
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Fax
021-67121385
Email
Sales-CN@TCIchemicals.com
Country
China
ProdList
24529
Advantage
81
Energy Chemical
Tel
021-021-58432009 400-005-6266
Fax
021-58436166
Email
sales8178@energy-chemical.com
Country
China
ProdList
44688
Advantage
61
Sichuan Kulinan Technology Co., Ltd
Tel
400-1166-196 18981987031
Fax
028-84555506 800101999
Email
cdhxsj@163.com
Country
China
ProdList
11707
Advantage
57
Tianjin heowns Biochemical Technology Co., Ltd.
Tel
400 638 7771
Email
sales@heowns.com
Country
China
ProdList
14435
Advantage
57
Hunan Hui Bai Shi Biotechnology Co., Ltd.
Tel
0731-85526065 13308475853
Email
ivy@hnhbsj.com
Country
China
ProdList
4554
Advantage
62
TOKYO CHEMICAL INDUSTRY CO., LTD.
Tel
03-36680489
Fax
03-3668-0520
Email
Sales-JP@TCIchemicals.com
Country
Japan
ProdList
28387
Advantage
80
TCI AMERICA
Tel
800-4238616
Fax
+1-888-520-1075 / +1-503-283-1987
Email
sales@tciamerica.com
Country
Americas
ProdList
23653
Advantage
75
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View Lastest Price from Iodosobenzene manufacturers

Career Henan Chemical Co
Product
IODOSOBENZENE 536-80-1
Price
US $1.00/KG
Min. Order
1KG
Purity
95-99%
Supply Ability
1ton
Release date
2020-01-02

536-80-1, IodosobenzeneRelated Search:


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