13532-81-5

Basic information

• Product Name: glyoxime-N_.N'-diphenyl ether
• Synonyms: glyoxime-N_.N'-diphenyl ether
• CAS NO: 13532-81-5
• Molecular Weight: 240.261
• Mol File: 13532-81-5.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: glyoxime-N_.N'-diphenyl ether(CAS DataBase Reference)
• NIST Chemistry Reference: glyoxime-N_.N'-diphenyl ether(13532-81-5)
• EPA Substance Registry System: glyoxime-N_.N'-diphenyl ether(13532-81-5)

Safety Data

• Hazardous Substances Data: 13532-81-5(Hazardous Substances Data)

Upstream product

• 186581-53-3 diazomethane 
• 60-29-7 diethyl ether 
• 586-96-9 Nitrosobenzene 
• 64-17-5 ethanol 
• 35225-46-8 N,N'-dihydroxy-N,N'-diphenyl-methanediyldiamine 
• 108-24-7 acetic anhydride 
• 50-00-0 formaldehyd 
• 100-65-2 N-Phenylhydroxylamine 
• 92-87-5 p,p'-diaminobiphenyl 
• 7020-80-6 acetaldehyde N-tert-butylimine 
• 4432-77-3 N-t-butylethylamine 
• 5459-93-8 N-ethyl-cyclohexanamine 
• 113832-57-8 N-ethylidenecyclohexylamine 
• 109-89-7 diethylamine 

Downstream Products

• 620-81-5 N,N'-Diphenyloxamid 
• 20915-45-1 glyoxal bis(N-methyl-N-phenylhydrazone) 
• 100-65-2 N-Phenylhydroxylamine 
• 1534-21-0 glyoxal bis(phenylhydrazone) 
• 116626-13-2 glyoxal-bis-(4-bromo-phenylhydrazone) 
• 62-53-3 aniline 
• 20972-43-4 trans-azoxybenzene 
• 586-96-9 Nitrosobenzene 
• 131543-46-9 Glyoxal 
• 495-48-7 azoxybenzene 
• 407636-62-8 Rh(CO)2Cl[N_.N-diphenyldinitrone] 

Relevant articles and documents

Semi-synthesis of a novel hybrid isoxazolidino withaferin via chemoselective and diastereoselective 1,3-dipolar nitrone cycloaddition reaction

A facile, atom-economic synthesis of isoxazilidino withaferin, a novel hybrid of withaferin A, has been accomplished via two-step reaction of nitrone synthesis followed by nitrone 1,3-dipolar cycloaddition. The reaction is highly chemoselective (preferent

Synthesis of some novel class of bisisoxazolidine derivatives via 1,3-dipolar cycloaddition reactions in water

Simultaneous double 1,3-dipolar cycloaddition reactions of glyoxal derived bisnitrones have been described in water. Significant rate acceleration and improved yields of exclusively diastereoselective and regioselective novel bisisoxazolidines in water ha

Nitroxides as reaction intermediates

Vinyl nitroxides 4 are obtained by oxidation of the nitrones 3, as was shown by esr studies by esr and by identification of the reaction products.The formation of 4d-f is even observed in oxidation of the hydroxylamines 1d-f, nitroxides 2d-f and nitrones