23128-51-0

Basic information

• Product Name: 3-(N,N-Diacetoxyethyl)amino-4-methoxyacetanilide
• Synonyms: N-[3-[bis[2-(acetyloxy)ethyl]amino]-4-methoxyphenyl]-Acetamide;2-(N,N-DIACETOXYETHYL)-AMINO-4-ACETAMINOANISOLE;3-DIACETOXYETHYLAMINO-4-METHOXY ACETANILIDE;3-(N,N-DIACETOXYETHYL)AMINO-4-METHOXY ACETANILIDE;2,2'-[[5-acetamido-2-methoxyphenyl]imino]diethyl diacetate;acetamide,N-[3-[bis[2-(acetyloxy)ethyl]amino]-4-methoxyphenyl]-;3-(N,N-Diacetoxylethyl)amino-4-methoxylacetanilide;3''-[N,N-Bis-(2-acetoxyethyl)-amino]-4''-methoxyacetanilide
• CAS NO: 23128-51-0
• Molecular Formula: C₁₇H₂₄N₂O₆
• Molecular Weight: 352.38
• EINECS: 245-441-1
• Product Categories: Intermediates of Dyes and Pigments
• Mol File: 23128-51-0.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 526.783 °C at 760 mmHg
• Flash Point: 272.389 °C
• Appearance: /
• Density: 1.213 g/cm³
• Vapor Pressure: 3.46E-11mmHg at 25°C
• Refractive Index: 1.552
• PKA: 14.29±0.70(Predicted)
• CAS DataBase Reference: 3-(N,N-Diacetoxyethyl)amino-4-methoxyacetanilide(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(N,N-Diacetoxyethyl)amino-4-methoxyacetanilide(23128-51-0)
• EPA Substance Registry System: 3-(N,N-Diacetoxyethyl)amino-4-methoxyacetanilide(23128-51-0)

Safety Data

• Hazardous Substances Data: 23128-51-0(Hazardous Substances Data)

Usage

General Description

The chemical compound 3-(N,N-Diacetoxyethyl)amino-4-methoxyacetanilide, also known as acetoxydihydroxypropylaminopara-methoxyacetanilide, is an organic compound belonging to the acetanilide class of chemicals. It is derived from acetoxyethylamine and 4-methoxyacetanilide, and is commonly used as a reagent in organic chemistry and pharmaceutical research. The compound has potential pharmaceutical applications due to its structural similarities to known analgesic and anti-inflammatory drugs. Its chemical structure consists of an acetanilide moiety with an amine and an acetoxyethyl group attached to the para position of the phenyl ring. 3-(N,N-Diacetoxyethyl)amino-4-methoxyacetanilide's specific properties and potential uses make it a subject of interest for further studies in drug development and chemical synthesis.

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

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

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 
• 107829-00-5 Acetic acid 2-{(2-acetoxy-ethyl)-[5-acetylamino-4-(2,6-dicyano-4-nitro-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 
• 88167-23-1 Acetic acid 2-{(2-acetoxy-ethyl)-[5-acetylamino-4-(2-cyano-4,6-dinitro-phenylazo)-2-methoxy-phenyl]-amino}-ethyl ester 
• 3618-66-4 C₂₃H₂₆N₆O₁₀ 
• 3618-73-3 2,2'-({5-acetamido-4-[(2-chloro-4,6-dinitrophenyl)azo]-2-methoxyphenyl}imino)diethyl diacetate 
• 3618-72-2 Disperse Blue 79 
• 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 articles and documents

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.