882-32-6

Usage

Uses

Used in Chemical Synthesis:
[(E)-(4-chlorophenyl)diazenyl]propanedinitrile is used as a precursor in the chemical synthesis industry for producing a range of organic compounds. Its unique structure allows it to serve as a building block for more complex molecules, contributing to the development of new materials and products.
Used in Dyes and Pigments Industry:
In the dyes and pigments industry, [(E)-(4-chlorophenyl)diazenyl]propanedinitrile is utilized as a key component in the synthesis of various dyes and pigments. Its ability to impart color and stability to these products makes it a valuable asset in this field.
Used in Organic Semiconductor Materials:
[(E)-(4-chlorophenyl)diazenyl]propanedinitrile has also been studied for its potential applications in the field of organic semiconductor materials. Its properties make it a candidate for use in the development of advanced electronic devices and components.
Safety Precautions:
It is crucial to handle [(E)-(4-chlorophenyl)diazenyl]propanedinitrile with care, as it may cause skin and eye irritation. Proper safety protocols should be followed during its storage and use to minimize potential health risks.

Upstream product

• 106-47-8 4-chloro-aniline 
• 109-77-3 malononitrile 

Downstream Products

• 114299-65-9 3-[3,5-Diamino-4-(4-chloro-phenylazo)-pyrazol-1-yl]-propionitrile 
• 1261067-95-1 C₂₅H₁₄ClN₇O₅ 
• 1316194-40-7 C₂₀H₁₃ClN₄OS 
• 1316194-31-6 C₂₅H₁₆N₄O₂S 
• 114275-56-8 2,5-Diamino-3-(4-chloro-phenylazo)-7-(4-methoxy-phenyl)-pyrazolo[1,5-a]pyrimidine-6-carbonitrile 
• 114275-53-5 2,5-Diamino-7-(4-chloro-phenyl)-3-(4-chloro-phenylazo)-pyrazolo[1,5-a]pyrimidine-6-carbonitrile 
• 114275-50-2 2,5-Diamino-3-(4-chloro-phenylazo)-7-phenyl-pyrazolo[1,5-a]pyrimidine-6-carbonitrile 
• 114275-78-4 7-(4-Chloro-phenylazo)-1,3-diphenyl-1H-pyrazolo[5,1-c][1,2,4]triazol-6-ylamine 
• 114275-72-8 7-Amino-8-(4-chloro-phenylazo)-4-phenyl-pyrazolo[5,1-c][1,2,4]triazine-3-carbonitrile 
• 114275-75-1 7-Amino-8-(4-chloro-phenylazo)-4-methyl-pyrazolo[5,1-c][1,2,4]triazine-3-carboxylic acid ethyl ester 
• 114275-47-7 7-Amino-9-(4-chloro-phenylazo)-1,3,4,5-tetrahydro-1,4a,4b,8-tetraaza-fluoren-2-one 
• 114275-70-6 4,7-Diamino-8-(4-chloro-phenylazo)-pyrazolo[5,1-c][1,2,4]triazine-3-carbonitrile 
• 114275-62-6 2-Amino-3-(4-chloro-phenylazo)-7-oxo-4,7-dihydro-pyrazolo[1,5-a]pyrimidine-6-carbonitrile 
• 114275-59-1 2,7-Diamino-3-(4-chloro-phenylazo)-pyrazolo[1,5-a]pyrimidine-6-carbonitrile 

Relevant academic research and scientific papers

Nano-CuFe2O4-supported sulfonic acid as a novel and recyclable nanomagnetic acid for diazotization of aromatic amines: efficient synthesis of various azo dyes

Abstract: A novel heterogeneous sulfonic acid functionalized nanomagnetic CuFe2O4 was successfully prepared and characterized by analyzing different obtained data including Fourier transform infrared spectroscopy, X-ray powder diffraction, field emission scanning electron microscopy, energy-dispersive X-ray spectroscopy, thermogravimetric analysis, dynamic light scattering and vibrating sample magnetometer. Then the novel acidic reagent was examined in synthesis of various azo-containing compounds from coupling of aryl diazonium ferrite sulfate salts with aromatic and non-aromatic compounds. The procedure starts by diazotization of aromatic amines with NaNO2 and wet CuFe2O4–SO3H and then coupling reaction of aryl diazonium ferrite sulfate salts with appropriate reagent. The prepared nano-solid acid showed high activity in synthesis of variety of aryl diazonium salts. In addition the as-prepared aryl diazonium ferrite sulfate salts are stable at room temperature for many hours and reacted efficiently in coupling reactions of aryl diazonium salts. All the azo dyes are synthesized in high yields and simple reaction conditions at room temperature. Moreover, the nanomagnetic solid acid was easily recovered from the reaction mixture and reused five runs without significant loss of activity. Graphical Abstract: [Figure not available: see fulltext.]