82209-17-4

Upstream product

• 872266-60-9 4,5-dimethoxy-3-methyl-2-nitro-aniline 
• 75-52-5 nitromethane 
• 82209-15-2 C₈H₁₁O₃⁽¹⁺⁾*FO₃S^(1-) 
• 860749-16-2 2,3-dimethoxy-4,6-dinitro-toluene 
• 148-53-8 3-methoxy-2-hydroxybenzaldehyde 
• 872266-63-2 2,3-dimethoxy-5,6-dinitro-toluene 
• 78312-28-4 5-nitro-2,3-dimethoxytoluene 
• 2896-67-5 2-methyl-6-methoxyphenol 
• 4463-33-6 1,2-dimethoxy-3-methylbenzene 
• 18102-31-3 2-methoxy-3-methylphenol 
• 709-09-1 3,4-dimethoxynitrobenzene 
• 67-68-5 dimethyl sulfoxide 
• 77-78-1 dimethyl sulfate 

Downstream Products

• 72517-26-1 2,3-dimethoxy-6-nitrobenzoic acid 

Relevant academic research and scientific papers

Effects of superoxide anion generated from aromatic radical anions produced in nucleophilic aromatic photosubstitution reactions

Superoxide anion is generated from aromatic radical anions produced in nucleophilic aromatic photosubstitutions when the reactions are carried out in non-deoxygenated solutions of polar aprotic solvents. Superoxide anion thus generated displaces cyanide anion from acetonitrile and benzyl cyanide, ethoxide anion from ethyl acetate, and methanesulfenate anion from dimethyl sulfoxide. Hence, non-deoxygenated polar aprotic solvents should be avoided in nucleophilic aromatic photosubstitution reactions.