6407-74-5

Usage

Uses

Used in Industrial Applications:
CI Solvent Yellow 56 is utilized as a coloring agent in the industrial sector, specifically for coloring plastics, textiles, and various coatings. Its strong coloration properties make it an effective choice for enhancing the visual appeal of these materials.
Used in Research and Development:
4-[(2-chlorophenyl)azo]-2,4-dihydro-5-methyl-2-phenyl-3H-pyrazol-3-one has been studied for its potential antimicrobial and anticancer properties, indicating that it may have applications in the fields of medicine and pharmaceuticals. Further research is necessary to fully understand and harness these potential benefits.
Used in Analytical Chemistry:
Due to its distinctive color and solubility characteristics, CI Solvent Yellow 56 may also find use in analytical chemistry for purposes such as the identification and quantification of substances in various samples. Its unique properties could be leveraged to improve the accuracy and efficiency of certain analytical techniques.

InChI:InChI=1/C16H13ClN4O/c1-11-15(19-18-14-10-6-5-9-13(14)17)16(22)21(20-11)12-7-3-2-4-8-12/h2-10,15H,1H3

Upstream product

• 19735-89-8 3-methyl-1-phenylpyrazolin-5(4H)-one 
• 95-51-2 o-chloroaniline 
• 89-25-8 edaravone 

Relevant academic research and scientific papers

A quantitative one-pot synthesis method for industrial azo pigments with recyclable wastewater

Most industrial azo pigments are synthesized by diazotization in one pot and then coupling in another. This two-pot process has been transformed into a one-pot method by adding granular PTFE (polytetrafluoroethylene) to a mechanically agitated aqueous mixture of NaNO2, HCl, a diazo component and a coupling component. This method avoids the step of using a base or a surfactant to dissolve the coupling component. The reactions were fast and quantitative. The granular PTFE, wastewater and excess HCl were then reused 11 times without deteriorating the reaction rate and product purity. Altogether, 22 industrial pigments and 3 azo compounds were synthesized and the reaction can produce up to 22.7 g of product in the laboratory. Some reactions require less than 2 equiv. of HCl and a mechanism explaining this is proposed. In addition, an o-nitro group effect is advanced to explain the differences in coupling reaction rates for o-, m- and p-nitroaniline.

Method used for synthesizing azo compound using solid particle one kettle method

The invention relates to a method used for synthesizing an azo compound using solid particle one kettle method. The method comprises following steps: solid particles are introduced into a reaction container, an inorganic acid, an aromatic primary amine, sodium nitrite, water, and a coupling component are added, mechanism stirring is carried out, when the reaction is monitored to be finished, filtering and rinsing are carried out, and the obtained filter cake is a finished product; or the solid particles are introduced into the reaction container, the inorganic acid, the aromatic primary amine,sodium nitrite, and water are added, mechanical stirring is carried out, after complete conversion of the aromatic primary amine, the coupling component is added, mechanical stirring is carried out,when the reaction is monitored to be finished, filtering and rinsing are carried out, and the obtained filter cake is a finished product. The solid particles are preferably selected from polytetrafluoroethylene particles, haw seeds, or stainless steel sand. The solid particles are added into the reaction system to promote reaction, no pre-heating or alkali adding dissolving of diazo components orthe coupling component is needed; most reaction is finished in 1h; reaction time is short; product quality is high; and reaction filtrate and excess inorganic acid can be recycled for a plurality of times.