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2,2'-[[5-acetamido-4-[(2-chloro-4,6-dinitrophenyl)azo]-2-methoxyphenyl]imino]diethyl diacetate is a complex, synthetic chemical compound characterized by a diverse array of chemical groups. It features an azo group (-N=N-), which is known for imparting color to compounds, making it a potential candidate for dye production. The molecule also contains acetate and nitro groups, along with a single chloro group. Derived from phenol, specifically a dinitrophenyl derivative, it also includes the functional group of an imino. While its specific applications may vary, it is likely to be utilized in industrial or laboratory processes.

3618-73-3

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3618-73-3 Usage

Uses

Used in Dye Production:
2,2'-[[5-acetamido-4-[(2-chloro-4,6-dinitrophenyl)azo]-2-methoxyphenyl]imino]diethyl diacetate is used as a colorant in dye production due to the presence of the azo group, which contributes to the compound's colorful properties.
Used in Industrial Processes:
2,2'-[[5-acetamido-4-[(2-chloro-4,6-dinitrophenyl)azo]-2-methoxyphenyl]imino]diethyl diacetate is used as a chemical intermediate in various industrial processes, taking advantage of its complex structure and functional groups.
Used in Laboratory Research:
2,2'-[[5-acetamido-4-[(2-chloro-4,6-dinitrophenyl)azo]-2-methoxyphenyl]imino]diethyl diacetate is used as a research compound in laboratory settings, where its unique properties can be explored for potential applications in chemical synthesis or as a model for studying the behavior of similar compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 3618-73-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,1 and 8 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3618-73:
(6*3)+(5*6)+(4*1)+(3*8)+(2*7)+(1*3)=93
93 % 10 = 3
So 3618-73-3 is a valid CAS Registry Number.

3618-73-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[5-acetamido-N-(2-acetyloxyethyl)-4-[(2-chloro-4,6-dinitrophenyl)diazenyl]-2-methoxyanilino]ethyl acetate

1.2 Other means of identification

Product number -
Other names ({5-(acetylamino)-4-[(e)-(2-chloro-4,6-dinitrophenyl)diazenyl]-2-methoxyphenyl}imino)diethane-2,1-diyl diacetate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Dyes
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:3618-73-3 SDS

3618-73-3Downstream Products

3618-73-3Relevant academic research and scientific papers

Diazotization method of wet nitroaniline

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Paragraph 0024-0027, (2019/01/05)

The invention provides a diazotization method of wet nitroaniline, and relates to the field of dye synthesis. The diazotization method comprises following steps: step one, evenly stirring sulfuric acid (98%) and nitrosyl sulfuric acid (40%) in a diazotization reactor; and step two, adding wet nitroaniline into the diazotization reactor at a controlled temperature of -10 to 40 DEG C to obtain diazotization salts, wherein the mole ratio of sulfuric acid to nitrosyl sulfuric acid to diazotization component is 1.0-6: 1.02-1.1: 1. The quality of the provided wet dye is the same as that of a dry product, the diazotization component does not need to be dried, and the provided dye is energy saving and environmentally friendly.

Preparation method of ester group-containing azo disperse dye

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Paragraph 0050; 0051; 0052; 0053, (2016/10/10)

The invention discloses a preparation method of an ester group-containing azo disperse dye. The method comprises the following steps: carrying out a coupling reaction on a diazo salt and a coupling component, adding an alkali to the above obtained azo compound material system after the coupling reaction is completed in order to adjust the pH value of the system to 5-7, carrying out heating crystal transformation, and post-processing to obtain a dye filter cake. The pH value of the system is adjusted to 5-7 after the coupling reaction and before the crystal transformation, so hydrolysis of ester groups in the dye product is avoided, the yield of the dye product is improved, and the content of organic matters in wastewater is reduced, thereby the wastewater post-treatment difficulty is reduced.

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