97794-07-5

Usage

Uses

Used in Pharmaceutical Industry:
(2Z)-2-[[2-chloro-4-[3-chloro-4-[(2Z)-2-[2-oxo-1-(phenylcarbamoyl)propylidene]hydrazinyl]phenyl]phenyl]hydrazinylidene]-3-oxo-N-phenyl-butanamide is used as a pharmaceutical agent for its potential biological activities. (2Z)-2-[[2-chloro-4-[3-chloro-4-[(2Z)-2-[2-oxo-1-(phenylcarbamoyl)propylidene]hydrazinyl]phenyl]phenyl]hydrazinylidene]-3-oxo-N-phenyl-butanamide's complex structure and multiple functional groups may contribute to its efficacy in targeting specific biological pathways or receptors, making it a candidate for the development of new drugs or therapeutic agents.
Used in Chemical Research:
In the field of chemical research, (2Z)-2-[[2-chloro-4-[3-chloro-4-[(2Z)-2-[2-oxo-1-(phenylcarbamoyl)propylidene]hydrazinyl]phenyl]phenyl]hydrazinylidene]-3-oxo-N-phenyl-butanamide serves as a subject for studying the synthesis, reactivity, and properties of complex organic molecules. Its unique structure allows researchers to explore new methods of chemical bonding, functional group interactions, and the compound's behavior under various conditions.
Used in Material Science:
(2Z)-2-[[2-chloro-4-[3-chloro-4-[(2Z)-2-[2-oxo-1-(phenylcarbamoyl)propylidene]hydrazinyl]phenyl]phenyl]hydrazinylidene]-3-oxo-N-phenyl-butanamide may also find applications in material science, where its complex structure and functional groups could be leveraged to develop new materials with specific properties. These materials could have uses in various industries, such as in the creation of advanced coatings, sensors, or other high-tech applications.

Upstream product

• 102-01-2 N-phenylacetoacetamide 
• 91-94-1 3,3'-dichlorobenzidine 
• 56766-13-3 4-(3-oxobutanamido)benzamide 
• 35354-86-0 2-acetoacetylamino benzoic acid 
• 49744-39-0 3,3'-dichloro-biphenyl-4,4'-bisdiazonium; chloride 

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.

Preparation method of C.I. pigment yellow 12

The invention provides a preparation method of C.I. pigment yellow 12. The preparation method comprises the following steps: carrying out diazotization by the use of nitrosyl sulfuric acid, reacting in a microreactor and reacting in a coupling vessel for coupling so as to finally prepare the C.I. pigment yellow 12. The product has advantages of uniform particle size, soft particle, excellent brightness, strong tinting strength, good light resistance and good transparency and covering power.

Production process and system for insoluble azo pigments

An insoluble azo pigment is produced by ejecting a diazo solution and a grounding solution continuously into an ejector such that within the ejector, the diazo solution and grounding solution are mixed with each other and are subjected to a coupling reaction. A production system for the insoluble azo pigment includes the following units (1) to (4): (1) a first feed tank (2) for a first fluid selected from the diazo solution or grounding solution, a first flow path (a) for feeding the first fluid to nozzles of an ejector (1), and a pump (d) for feeding the first fluid through the first flow path; (2) the ejector (1) provided with the nozzles, a suction chamber, a diffuser, and a temperature control device (g); (3) a second feed tank (3) for a second fluid, a second flow path (b) for guiding the second fluid into the suction chamber, and a flow control device (e) for controlling a flow rate of the second fluid through the second flowpath (b); and (4) a heat treatment tank (5) for subjecting to heat treatment a suspension of the insoluble azo pigment formed by a reaction between the first fluid and the second fluid, and a third flow path (a′) for guiding the suspension from the diffuser to the heat treatment tank.