4397-12-0

Upstream product

• 22596-43-6 N-(2-hydroxy-2-phenylethyl)-α-phenylnitrone 
• 32256-40-9 N-(2-oxo-2-phenylethyl)-α-phenylnitrone 
• 141377-54-0 2-nitro-1-phenylethan-1-ol 

Downstream Products

• 22596-43-6 N-(2-hydroxy-2-phenylethyl)-C-phenylnitrone 
• 63829-54-9 C₁₆H₁₇NO₃ 
• 63830-35-3 C₁₀H₁₃NO₂ 
• 63830-41-1 2-methyl-5-phenyl-oxazolidin-3-ol 
• 84966-15-4 N-Furfuryliden-2-hydroxy-2-phenylethanamin-N-oxid 
• 31890-28-5 2-Hydroxy-N-(5-nitrofurfuryliden)-2-phenylethanamin-N-oxid 
• 84966-21-2 2-Hydroxy-2-phenyl-N-(5-piperidinofurfuryliden)ethanamin-N-oxid 
• 28369-66-6 N-Isopropyliden(2-hydroxy-2-phenylethyl)amin-N-oxid 
• 83502-01-6 3-Hydroxy-2,2-dimethyl-5-phenyl-1,3-oxazolidin 
• 22596-43-6 N-(2-hydroxy-2-phenylethyl)-α-phenylnitrone 
• 84966-32-5 2-(2-Furyl)-3-(4-nitrobenzoyloxy)-5-phenyl-1,3-oxazolidin 
• 84966-53-0 N-Furfuryliden-2-phenyl-2-(phenylcarbamoyloxy)ethanamin-N-oxid 
• 63829-72-1 C₁₅H₁₄N₂O₄ 

Relevant academic research and scientific papers

SYNTHESIS OF STABLE OXAZOLIDINE NITROXYL RADICALS WITH METHOXY GROUPS AT THE α-CARBON ATOMS TO THE RADICAL SITE

The condensation of α-hydroxyaminoalcohols with aldehydes and acetone gave 3-hydroxyoxazolidines and tautomeric N-(2-hydroxyethyl)-α-arylnitrones, whose oxidation by PbO2 in methanol leads to stable oxazolidine nitroxyl radicals with methoxy groups at Cs