23128-51-0

Usage

Uses

Used in Pharmaceutical Research:
3-(N,N-Diacetoxyethyl)amino-4-methoxyacetanilide is used as a research compound for its potential analgesic and anti-inflammatory properties due to its structural similarities with known drugs in these categories.
Used in Organic Chemistry:
In the field of organic chemistry, 3-(N,N-Diacetoxyethyl)amino-4-methoxyacetanilide serves as a reagent, facilitating various chemical reactions and synthesis processes.
Used in Drug Development:
3-(N,N-Diacetoxyethyl)amino-4-methoxyacetanilide is utilized in drug development studies, given its specific properties that make it a promising candidate for the creation of new pharmaceuticals, particularly in the areas of pain management and inflammation reduction.
Used in Chemical Synthesis:
3-(N,N-Diacetoxyethyl)amino-4-methoxyacetanilide is employed in chemical synthesis for the production of other organic compounds, leveraging its unique structural features to form new molecules with potential applications in various industries.

InChI:InChI=1/C17H24N2O6/c1-12(20)18-15-5-6-17(23-4)16(11-15)19(7-9-24-13(2)21)8-10-25-14(3)22/h5-6,11H,7-10H2,1-4H3,(H,18,20)

Upstream product

• 108-45-2 m-phenylenediamine 
• 24530-67-4 N-{3-[bis(2-hydroxyethyl)amino]-4-methoxyphenyl}acetamide 
• 6375-47-9 3-amino-4-methoxyacetanilide 
• 64-19-7 acetic acid 
• 108-24-7 acetic anhydride 

Downstream Products

• 87260-48-8 Acetic acid 2-{(2-acetoxy-ethyl)-[5-acetylamino-4-(2-bromo-6-cyano-4-nitro-phenylazo)-2-methoxy-phenyl]-amino}-ethyl ester 
• 3618-72-2 Disperse Blue 79 
• 3618-73-3 2,2'-({5-acetamido-4-[(2-chloro-4,6-dinitrophenyl)azo]-2-methoxyphenyl}imino)diethyl diacetate 
• 3618-66-4 C₂₃H₂₆N₆O₁₀ 
• 88167-23-1 Acetic acid 2-{(2-acetoxy-ethyl)-[5-acetylamino-4-(2-cyano-4,6-dinitro-phenylazo)-2-methoxy-phenyl]-amino}-ethyl ester 
• 105674-53-1 4-{2-Acetylamino-4-[bis-(2-acetoxy-ethyl)-amino]-5-methoxy-phenylazo}-3,5-dicyano-benzoic acid ethyl ester 
• 107829-00-5 Acetic acid 2-{(2-acetoxy-ethyl)-[5-acetylamino-4-(2,6-dicyano-4-nitro-phenylazo)-2-methoxy-phenyl]-amino}-ethyl ester 
• 76486-17-4 Acetic acid 2-{(2-acetoxy-ethyl)-[5-acetylamino-4-(2-cyano-4-nitro-naphthalen-1-ylazo)-2-methoxy-phenyl]-amino}-ethyl ester 
• 76486-27-6 Acetic acid 2-{(2-acetoxy-ethyl)-[5-acetylamino-4-(2-cyano-4-nitro-phenylazo)-2-methoxy-phenyl]-amino}-ethyl ester 

Relevant academic research and scientific papers

Preparation method of 2-methoxy-5-acetamido-N, N-diacetoxyethyl aniline

The invention provides a preparation method of 2-methoxy-5-acetamido-N, N-diacetoxyethyl aniline. The method comprises the following steps: (1) carrying out hydroxylation reaction on o-methoxy m-acetamido aniline and ethylene oxide to obtain a hydroxylate 2-methoxy-5-acetamido-N, N-dihydroxyethyl aniline; and step 2), carrying out an esterification reaction on the hydroxylate 2-methoxy-5-acetamido-N, N-dihydroxyethyl aniline and acetic anhydride and/or acetic acid, so as to obtain an esterified compound. The 2-methoxy-5-acetamido-N, N-diacetoxyethyl aniline prepared by the method disclosed by the invention is low in cost and simple in steps, and the obtained product is high in yield, high in purity and more suitable for workshop production.

Synthesis and Spectral Characterization of Blue Dyes of the Benzene Series

53 Donor-acceptor substituted azo dyes of the benzene series were prepared by diazonium-coupling reactions (1a-s) or halogen-cyanide exchange (->2a-x, 3a-j).Described are the preparation of the amines 4a-m and the coupling compounds 5a-t and the procedure of diazotizing and coupling.The colouristic and spectroscopic data show that compounds of the general formula 1 are excellent brilliant blue azo dyes usefull for dyeing polyester material.