57309-29-2

Upstream product

• 57309-24-7 1-hydroxy-2,2-diphenyl-indolin-3-one 

Downstream Products

• 65817-75-6 1-oxy-2,2-diphenyl-2H-indole-3,7-dione 
• 83195-93-1 1-Oxy-2,2-diphenyl-2H-indole-3,5-dione 
• 85036-23-3 1-Methoxy-2,2-diphenyl-1,2-dihydro-indol-3-one 
• 113296-95-0 C₃₄H₂₇N₂O₄ 
• 74441-23-9 2,2-Diphenylindolin-1,3-diol 
• 66312-80-9 7-Benzoyloxy-3-oxo-2,2-diphenylindolin-1-oxyl 
• 66312-83-2 5-Benzoyloxy-3-oxo-2,2-diphenylindolin-1-oxyl 
• 77494-99-6 5,7-Dibenzoyloxy-3-oxo-2,2-diphenylindolin-1-oxyl 
• 113272-28-9 2,2-diphenyl-4-(p-methoxyphenylamino)-5-(p-methoxyphenylimino)indolin-3-one-N-oxide 
• 74441-26-2 3-Hydroxy-2,2-diphenylindolin-1-oxyl 
• 113272-26-7 1-Oxy-2,2-diphenyl-5-[(E)-phenylimino]-2,5-dihydro-indol-3-one 
• 113272-30-3 1-Oxy-2,2-diphenyl-4-phenylamino-5-[(E)-phenylimino]-2,5-dihydro-indol-3-one 
• 113272-19-8 C₃₂H₂₃N₂O₂ 
• 113272-27-8 5-[(E)-4-Chloro-phenylimino]-1-oxy-2,2-diphenyl-2,5-dihydro-indol-3-one 

Relevant academic research and scientific papers

Hydroxylamines as oxidation catalysts: Thermochemical and kinetic studies

Bond dissociation enthalpies (BDE) of hydroxylamines containing alkyl, aryl, vinyl, and carbonyl substituents at the nitrogen atom have been determined by using the EPR radical equilibration technique in order to study the effect of the substituents on th