99069-17-7

Basic information

• Product Name: 4-Acetylamino-1,2-dimethoxy-5-nitrobenzene
• Synonyms: 4-Acetylamino-1,2-dimethoxy-5-nitrobenzene
• CAS NO: 99069-17-7
• Molecular Weight: 240.216
• Mol File: 99069-17-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 4-Acetylamino-1,2-dimethoxy-5-nitrobenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Acetylamino-1,2-dimethoxy-5-nitrobenzene(99069-17-7)
• EPA Substance Registry System: 4-Acetylamino-1,2-dimethoxy-5-nitrobenzene(99069-17-7)

Safety Data

• Hazardous Substances Data: 99069-17-7(Hazardous Substances Data)

Upstream product

• 30710-17-9 3,4-dimethoxy-2-nitroaniline 
• 3535-37-3 3,4-dimethoxybenzoic acid chloride 
• 116495-88-6 2,2'-diamino-3,3',4,4'-tetramethoxybenzophenone 
• 5385-65-9 4,5,4',5'-tetramethoxy-2,2'-dinitro-benzophenone 
• 4131-03-7 bis(3,4-dimethoxyphenyl)methanone 
• 1131-62-0 1-(3,4-dimethoxyphenyl)ethanone 
• 4101-30-8 2-amino-4,5-dimethoxyacetophenone 
• 4101-32-0 4',5'-dimethoxy-2'-nitroacetophenone 
• 3395-03-7 4,5-dimethoxy-1,2-dinitrobenzene 
• 709-09-1 3,4-dimethoxynitrobenzene 
• 861307-23-5 2,2'-bis-acetylamino-4,5,4',5'-tetramethoxy-benzophenone 
• 7697-37-2 nitric acid 
• 64-19-7 acetic acid 
• 148842-95-9 acetic acid-(2-acetyl-4,5-dimethoxy-anilide) 

Downstream Products

• 7595-31-5 4-amino-5-nitroveratrol 
• 6938-02-9 8-amino-5,6-dimethoxyquinoline 
• 27841-33-4 4,5-dimethoxybenzene-1,2-diamine 
• 92848-29-8 2-acetamido-4,5-dimethoxyacetanilide 
• 113475-71-1 C₂₂H₂₆N₄O₁₂S 
• 113475-70-0 C₂₃H₂₈N₄O₁₂ 
• 113475-67-5 4,5-Dimethoxy-2-nitrophenyl Isocyanate 
• 5333-02-8 5,6-dimethoxy-8-nitroquinoline 

Relevant articles and documents

Electrochemical Nitration with Nitrite

Aromatic nitration has tremendous importance in organic chemistry as nitroaromatic compounds serve as versatile building blocks. This study represents the electrochemical aromatic nitration with NBu4NO2, which serves a dual role as supporting electrolyte and as a safe, readily available, and easy-to-handle nitro source. Stoichiometric amounts of 1,1,1-3,3,3-hexafluoroisopropan-2-ol (HFIP) in MeCN significantly increase the yield by solvent control. The reaction mechanism is based on electrochemical oxidation of nitrite to NO2, which initiates the nitration reaction in a divided electrolysis cell with inexpensive graphite electrodes. Overall, the reaction is demonstrated for 20 examples with yields of up to 88 %. Scalability is demonstrated by a 13-fold scale-up.