36160-52-8

Basic information

• Product Name: Benzene, 2-ethoxy-1-methoxy-4-nitro-
• CAS NO: 36160-52-8
• Molecular Formula: C9H11NO4
• Molecular Weight: 197.191
• Mol File: 36160-52-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzene, 2-ethoxy-1-methoxy-4-nitro-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 2-ethoxy-1-methoxy-4-nitro-(36160-52-8)
• EPA Substance Registry System: Benzene, 2-ethoxy-1-methoxy-4-nitro-(36160-52-8)

Safety Data

• Hazardous Substances Data: 36160-52-8(Hazardous Substances Data)

Upstream product

• 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 
• 861800-46-6 carbonic acid bis-(5-nitro-2-methoxy-phenyl ester) 
• 99-59-2 3-amino-4-methoxynitrobenzene 
• 613-70-7 2-methoxyphenyl acetate 
• 7260-32-4 2-ethoxy-5-nitro-phenol 
• 74-88-4 methyl iodide 
• 67-56-1 methanol 
• 4992-63-6 4-Nitro-1,2-diethoxybenzene 

Downstream Products

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

Relevant articles and documents

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.

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.