[Hydroxy(tosyloxy)iodo]benzene

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Products Intro: Product Name:[Hydroxy(tosyloxy)iodo]benzene
CAS:27126-76-7
Purity:98% Package:1kg;30USD
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CAS:27126-76-7
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CAS:27126-76-7
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CAS:27126-76-7
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[Hydroxy(tosyloxy)iodo]benzene manufacturers

[Hydroxy(tosyloxy)iodo]benzene Basic information
Product Name:[Hydroxy(tosyloxy)iodo]benzene
Synonyms:Iodine,hydroxy(4-Methylbenzenesulfonato-kO)phenyl-;[Hydroxy(tosyloxy)iodo]benzene 96%;[Hydroxy(4-toluenesulfonato)iodo]benzene;Hydroxy(phenyl)iodo tosylate;[Hydroxy(tosyloxy)iodo]benzene≥ 98%(Titration);Hydroxy{[(4-methylphenyl)sulfonyl]oxy} phenyliodine;Koser's Regent ,HTIB;Hydroxyl(toluenesulfonyloxygengeneration)iodobenzene
CAS:27126-76-7
MF:C13H13IO4S
MW:392.21
EINECS:629-501-8
Product Categories:Hypervalent Iodine Compounds;Oxidation;Synthetic Organic Chemistry;Phenyls & Phenyl-Het
Mol File:27126-76-7.mol
[Hydroxy(tosyloxy)iodo]benzene Structure
[Hydroxy(tosyloxy)iodo]benzene Chemical Properties
Melting point 131-137 °C (lit.)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
solubility soluble in Methanol
pka7.59±0.58(Predicted)
form Crystalline Powder
color Pale yellow
Sensitive Light Sensitive
Merck 14,5321
BRN 2150074
InChIKeyLRIUKPUCKCECPT-UHFFFAOYSA-N
CAS DataBase Reference27126-76-7(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/38
Safety Statements 26-36
WGK Germany 3
8
HazardClass IRRITANT
HS Code 29039990
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
[Hydroxy(tosyloxy)iodo]benzene Usage And Synthesis
Chemical PropertiesPale yellow crystalline powder
UsesReactant for:
  • Ligand-free palladium-catalyzed Heck-type coupling reactions
  • Preparation of carbodiimides via dehydrosulfurization of thioureas
  • Preparation of nitriles by oxidative conversion of alcohols, aldehydes, and amines
  • Preparation of substituted anilines via aromatic aldoxime reaction
  • Preparation of tetrahydrofurans by oxidative cyclization of homoallylic alcohols
  • Preparation of isoxazoline N-Oxides from ?-hydroxyketoximes via oxidative N-O coupling
  • Ring expansion in synthesis of aminopeptidase inhibitors
  • Oxidation and protonation reactions in acidic conditions
UsesVersatile synthetic reagent in phenyliodination and/or tosylation of a range of organic substrates; in oxidative transformations including oxidative rearrangements.
Purification MethodsPossible impurities are tosic acid (removed by washing with Me2CO) and acetic acid (removed by washing with Et2O). It is purified by dissolving in the minimum volume of MeOH, adding Et2O to cloud point and setting aside for the prisms to separate [Koser & Wettach J Org Chem 42 1476 1977, NMR: Koser et al. J Org Chem 41 3609 1976]. It has also been crystallised from CH2Cl2 (needles, m 140-142o) [Neiland & Karele J Org Chem, USSR (Engl Transl) 6 889 1970].
[Hydroxy(tosyloxy)iodo]benzene Preparation Products And Raw materials
Tag:[Hydroxy(tosyloxy)iodo]benzene(27126-76-7) Related Product Information
Butylated Hydroxytoluene Benzene Ethylbenzene Tosyl chloride Tosyl cyanide Allylbenzene p-Toluenesulfonamide Fipronil CHLOROPHOSPHONAZO III TOLBUTAMIDE Iodosobenzene 2-(4-Aminopentyl(ethyl)amino)ethanol HYDROXY ITRACONAZOLE Hydroxyacetic Acid Hydrazide Iodobenzene [Hydroxy(tosyloxy)iodo]benzene [HYDROXY(METHANESULFONYLOXY)IODO]BENZENE 1-[[(4-METHYLPHENYL)SULPHONYL]OXY]-1,2-BENZIODOXOL-3(1H)-ONE