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3-(N,N-Diacetoxyethyl)amino-4-methoxyacetanilide, also known as acetoxydihydroxypropylaminopara-methoxyacetanilide, is an organic compound within the acetanilide class. It is synthesized from acetoxyethylamine and 4-methoxyacetanilide and features an acetanilide moiety with an amine and an acetoxyethyl group at the para position of the phenyl ring. 3-(N,N-Diacetoxyethyl)amino-4-methoxyacetanilide is recognized for its potential pharmaceutical applications, owing to its structural resemblance to established analgesic and anti-inflammatory drugs, and is a valuable reagent in organic chemistry and pharmaceutical research.

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  • dark blue esterification solution 3-(N,N-Diacetoxyethyl)amino-4-methoxyacetanilide

    Cas No: 23128-51-0

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  • 23128-51-0 Structure
  • Basic information

    1. Product Name: 3-(N,N-Diacetoxyethyl)amino-4-methoxyacetanilide
    2. 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
    3. CAS NO:23128-51-0
    4. Molecular Formula: C17H24N2O6
    5. Molecular Weight: 352.38
    6. EINECS: 245-441-1
    7. Product Categories: Intermediates of Dyes and Pigments
    8. Mol File: 23128-51-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 526.783 °C at 760 mmHg
    3. Flash Point: 272.389 °C
    4. Appearance: /
    5. Density: 1.213 g/cm3
    6. Vapor Pressure: 3.46E-11mmHg at 25°C
    7. Refractive Index: 1.552
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 14.29±0.70(Predicted)
    11. CAS DataBase Reference: 3-(N,N-Diacetoxyethyl)amino-4-methoxyacetanilide(CAS DataBase Reference)
    12. NIST Chemistry Reference: 3-(N,N-Diacetoxyethyl)amino-4-methoxyacetanilide(23128-51-0)
    13. EPA Substance Registry System: 3-(N,N-Diacetoxyethyl)amino-4-methoxyacetanilide(23128-51-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 23128-51-0(Hazardous Substances Data)

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.

Check Digit Verification of cas no

The CAS Registry Mumber 23128-51-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,1,2 and 8 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 23128-51:
(7*2)+(6*3)+(5*1)+(4*2)+(3*8)+(2*5)+(1*1)=80
80 % 10 = 0
So 23128-51-0 is a valid CAS Registry Number.
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)

23128-51-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(N,N-Diacetoxyethyl)amino-4-methoxyacetanilide

1.2 Other means of identification

Product number -
Other names 3-N,N-bis-

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:23128-51-0 SDS

23128-51-0Relevant articles and documents

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

-

Paragraph 0055; 0057-0058; 0060-0061; 0063; 0067; 0069; ..., (2021/10/27)

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

Thiel, W.,Mayer, R.,Jauer, E.-A.,Modrow, H.,Dost, H.

, p. 497 - 514 (2007/10/02)

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.

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