80521-10-4

Basic information

• Product Name: Ethanone, 1-(2-furanyl)-2-[[(4-methylphenyl)sulfonyl]oxy]-
• CAS NO: 80521-10-4
• Molecular Formula: C13H12O5S
• Molecular Weight: 280.301
• Mol File: 80521-10-4.mol
• Article Data: 19

Chemical Properties

• CAS DataBase Reference: Ethanone, 1-(2-furanyl)-2-[[(4-methylphenyl)sulfonyl]oxy]-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-(2-furanyl)-2-[[(4-methylphenyl)sulfonyl]oxy]-(80521-10-4)
• EPA Substance Registry System: Ethanone, 1-(2-furanyl)-2-[[(4-methylphenyl)sulfonyl]oxy]-(80521-10-4)

Safety Data

• Hazardous Substances Data: 80521-10-4(Hazardous Substances Data)

Upstream product

• 62889-08-1 1-(2-furyl)-1-(trimethylsilyloxy)ethylene 
• 27126-76-7 [hydroxy(tosyloxy)iodo]benzene 
• 1192-62-7 1-(2-furyl)-1-ethanone 
• 4208-64-4 1-(2-furyl)ethanol 
• 104-15-4 toluene-4-sulfonic acid 
• 440365-99-1 3,5-bis(trifluoromethyl)-1-[hydroxy(tosyloxy)iodo]benzene 

Downstream Products

• 28795-36-0 2-(furan-2-yl)imidazo[1,2-a]pyridine 
• 3194-15-8 2-propionylfuran 
• 120284-29-9 1-(furan-2-yl)cyclopropan-1-ol 
• 948047-91-4 (S)-2-(furan-2-yl)-2-hydroxyethyl 4-methylbenzenesulfonate 
• 494-21-3 2-furan-2-yl-quinoxaline 
• 1203835-87-3 4-(2-furyl)-N-phenethylthiazol-2-amine 
• 77588-51-3 1-(furan-2-yl)-4-phenylbutane-1,4-dione 
• 131496-20-3 (benzoyloxy)methyl 2-furyl ketone 
• 21036-63-5 4-(2-furyl)-2-phenylthiazole 
• 28989-52-8 2-amino-4-(2-furyl)thiazole 

Relevant articles and documents

An iodobenzene-catalysed domino route toward quinoxaline derivatives from simple ketones and o-phenylenediamines in one pot

An iodobenzene-catalysed domino route to quinoxalines from ketones and o-phenylenediamines in one pot has been developed. This transformation consisted of the generation of Koser's generation, α-tosyloxylation of ketones, nucleophilic substitution and intramolecular dehydration with o-phenylenediamines, and dehydrogenation. Website

Iodobenzene-catalyzed synthesis of α-azidoketones and α-thiocyanatoketones from aryl ketones with MCPBA as a cooxidant

Iodobenzene-catalyzed synthesis of α-azidoketones and α-thiocyanatoketones from aryl ketones with MCPBA as a cooxidant is described. The method is simple, rapid and practical, generating α-azidoketones and α-thiocyanatoketones from the aryl ketone without

M-iodosylbenzoic acid: Recyclable hypervalent iodine reagent for-tosyloxylation and-mesyloxylation of ketones

m-Iodosylbenzoic acid-mediated reactions of various carbonyl compounds provided-organosulfonyloxy carbonyl compounds in good yields. The final products could be easily isolated without any chromatographic purification by simple treatment of the crude mixt