36160-52-8

Upstream product

• 67-56-1 methanol 
• 4992-63-6 4-Nitro-1,2-diethoxybenzene 
• 64-67-5 diethyl sulfate 
• 636-93-1 5-nitroguaiacol 
• 75-03-6 ethyl iodide 
• 709-09-1 3,4-dimethoxynitrobenzene 
• 141-78-6 ethyl acetate 
• 613-70-7 2-methoxyphenyl acetate 
• 99-59-2 3-amino-4-methoxynitrobenzene 
• 861800-46-6 carbonic acid bis-(5-nitro-2-methoxy-phenyl ester) 
• 7260-32-4 2-ethoxy-5-nitro-phenol 
• 74-88-4 methyl iodide 

Downstream Products

• 122756-35-8 1-ethoxy-2-methoxy-4,5-dinitrobenzene 
• 40130-25-4 3-ethoxy-4-hydroxynitrobenzene 
• 477742-46-4 3-ethoxy-4-methoxy-aniline 
• 65383-57-5 3-ethoxy-4-methoxy phenol 
• 686742-27-8 4-ethoxy-2-hydroxy-5-methoxy-benzaldehyde 
• 873984-11-3 4-ethoxy-2,5-dimethoxy-benzaldehyde 
• 881204-74-6 C₁₉H₂₁N₃O₄ 
• 881204-45-1 C₁₈H₁₉N₃O₃ 
• 19871-39-7 N-methyl-2-methoxy-5-nitroaniline 

Relevant academic research and scientific papers

Isoindole-imide compounds and compositions comprising and methods of using the same

This invention relates to isoindole-imide compounds, and pharmaceutically acceptable salts, solvates, stereoisomers, and prodrugs thereof. Methods of use, and pharmaceutical compositions of these compounds are disclosed.

Cyclic nucleotide phosphodiesterase inhibitors, preparation and uses thereof

The invention concerns novel benzodiazepine derivatives and their uses in the field of therapeutics particularly for treating pathologies involving the activity of a cyclic nucleotide phosphodiesterase. It also concerns methods for preparing them and novel synthesis intermediates. The inventive compounds more particularly correspond to general formula (I):

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.