124761-89-3

Upstream product

• 59570-09-1 1-hydroxy-5,5-dimethyl-4-phenyl-3-imidazoline 3-oxide 
• 104406-65-7 5,5-dimethyl-2,2-dimethoxy-4-phenyl-3-imidazoline 3-oxide-1-oxyl 
• 60-34-4 methylhydrazine 

Relevant academic research and scientific papers

Reduction of α,α-dialkoxy-substituted nitroxides: the synthesis of α-alkoxynitrones and acetals of N-hydroxyamides

Reduction of stable nitroxides derived from tetrahydrooxazole, tetrahydroimidazole, 2,5-dihydroimidazole, and 2,5-dihydroimidazole 3-oxide containing alkoxy groups in α-position to the nitroxyl group affords α-alkoxynitrones, acetals of N-hydroxyamides, or their equilibrium mixtures.