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[Hydroxy(tosyloxy)iodo]benzene_Molecular_structure_CAS_27126-76-7)
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[Hydroxy(tosyloxy)iodo]benzene

Catalog No. 301035 Name Sigma Aldrich
CAS Number 27126-76-7 Website http://www.sigmaaldrich.com
M. F. C13H13IO4S Telephone 1-800-521-8956
M. W. 392.20939 Fax
Purity 96% Email
Storage Chembase ID: 32051

SYNONYMS

Title
羟基甲苯磺酰碘苯
IUPAC name
hydroxy phenyl 4-methylbenzene-1-sulfonoperoxoyl iodide
IUPAC Traditional name
hydroxy phenyl 4-methylbenzenesulfonoperoxoyl iodide
Synonyms
Koser’s reagent
Koser 试剂
Hydroxy(phenyl)iodo tosylate
[Hydroxy(4-toluenesulfonato)iodo]benzene
Iodosobenzene-I-mono-p-toluenesulfonate
HTIB
NSC 294176
Phenyliodosyl hydroxide tosylate
Hydroxy(4-methylbenzenesulfonato-O)phenyliodine
羟基(甲苯磺酰氧代)碘苯

DATABASE IDS

PubChem SID 24858159
CAS Number 27126-76-7
MDL Number MFCD00011547
Beilstein Number 2150074

PROPERTIES

Linear Formula CH3C6H4SO3I(OH)C6H5
Purity 96%
Melting Point 131-137 °C(lit.)
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H315-H319
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Gloves
GHS Precautionary statements P305 + P351 + P338
Risk Statements 36/38
Safety Statements 26-36
German water hazard class 3

DETAILS

Description (English)
Application
Widely used oxidant in the synthesis of various organic compounds.9
Reactant for:
• Ligand-free palladium-catalyzed Heck-type coupling reactions1
• Preparation of carbodiimides via dehydrosulfurization of thioureas2
• Preparation of nitriles by oxidative conversion of alcohols, aldehydes, and amines3
• Preparation of substituted anilines via aromatic aldoxime reaction4
• Preparation of tetrahydrofurans by oxidative cyclization of homoallylic alcohols5
• Preparation of isoxazoline N-Oxides from β-hydroxyketoximes via oxidative N-O coupling6
• Ring expansion in synthesis of aminopeptidase inhibitors7
• Oxidation and protonation reactions in acidic conditions8
Packaging
5, 25 g in glass bottle
Description (简体中文)
Application
广泛用于合成各种有机化合物的氧化剂。9
Reactant for:
• Ligand-free palladium-catalyzed Heck-type coupling reactions1
• Preparation of carbodiimides via dehydrosulfurization of thioureas2
• Preparation of nitriles by oxidative conversion of alcohols, aldehydes, and amines3
• Preparation of substituted anilines via aromatic aldoxime reaction4
• Preparation of tetrahydrofurans by oxidative cyclization of homoallylic alcohols5
• Preparation of isoxazoline N-Oxides from β-hydroxyketoximes via oxidative N-O coupling6
• Ring expansion in synthesis of aminopeptidase inhibitors7
• Oxidation and protonation reactions in acidic conditions8
包装
5, 25 g in glass bottle

REFERENCES