What is the main field application of 2,9-bis [4- (phenylazo) phenyl] anthra [2,1,9-def: 6,5,10-d'e'f '] diisoquinoline-1,3,8,10 (2H, 9H) -tetrone

2% 2C9 - bis% 5B4 - (phenylazo) phenyl%5Danthra%5B2%2C1%2C9 - def: 6% 2C5% 2C10 - d'e'f '% 5Ddiisoquinoline - 1% 2C3% 2C8% 2C10 (2H% 2C9H) - tetrone is an organic compound with a wide range of main application fields.

In the field of materials science, this compound can be used as a key component of functional materials. Due to its unique chemical structure and physical properties, it can impart specific optical and electrical properties to materials. For example, with its unique response mechanism to light, it can be used to develop photochromic materials, which can change color under light irradiation, and have great application potential in smart windows, anti-counterfeiting labels, etc.; or because of its special electrical conductivity, it can participate in the construction of conductive materials, promoting the miniaturization and high performance of electronic devices.

In the field of chemical analysis, this compound may act as a chemical probe. After it interacts specifically with specific substances, its physical and chemical properties will change significantly, such as color, fluorescence intensity, etc. With this property, researchers can accurately detect and identify specific ions and molecules, and assist in the detection of harmful pollutants in environmental monitoring, or the detection of biomarkers in biomedical fields.

In the field of biomedicine, certain properties of this compound may make it potentially bioactive. It may be able to combine with specific targets in organisms to affect physiological and biochemical processes in organisms. For example, it may exhibit certain anti-cancer activity by interfering with specific metabolic pathways or signaling pathways of cancer cells, providing direction for the development of new anti-cancer drugs; or in drug delivery systems, as a modified component of carrier materials to improve drug targeting and efficacy.

In addition, in the dye industry, with its complex conjugated structure, this compound may be used as a high-performance dye. It can dye fabrics, leather and other materials with long-lasting and bright colors, while maintaining good stability under different environmental conditions, ensuring the quality and aesthetics of dyeing products.

What are the physical properties of 2,9-bis [4- (phenylazo) phenyl] anthra [2,1,9-def: 6,5,10-d'e'f '] diisoquinoline-1,3,8,10 (2H, 9H) -tetrone

2% 2C9 - bis% 5B4 - (phenylazo) phenyl%5Danthra%5B2%2C1%2C9 - def% 3A6% 2C5% 2C10 - d%27e%27f%27%5Ddiisoquinoline - 1% 2C3% 2C8% 2C10 (2H% 2C9H) - tetrone, this is an organic compound, often referred to as a specific anthraquinone dye. Its physical properties are as follows:
- ** Appearance **: mostly crystalline solid, with bright orange, red or purple color. Due to the presence of multiple conjugated systems in the molecule, it has strong absorption of visible light and is widely used in the field of dyes.
- ** Melting point **: The melting point is high, and the specific value varies depending on the purity and test conditions, but most are above 200 ° C. The higher melting point is due to strong intermolecular interactions, including van der Waals forces and possible hydrogen bonds, which make the molecules closely arranged and require more energy to destroy the lattice structure and cause it to melt.
- ** Solubility **: The solubility in water is very low, because the molecule has a large non-polar part, contains multiple benzene rings and conjugated structures, and the force between it and water molecules is weak. However, it is soluble in some organic solvents, such as dichloromethane, N, N-dimethylformamide (DMF), etc. Because these organic solvents can form similar interactions with the compound molecules, such as dispersion forces, to help it dissolve.
- ** Stability **: Under normal temperature, pressure and dark conditions, the chemical properties are relatively stable. However, under extreme conditions such as strong oxidizing agents, reducing agents or high temperature, light, etc., the molecular structure may change. If under light, it may be caused by photochemical reactions to break or rearrange chemical bonds in molecules, affecting its color and performance, so it needs to be protected from strong light and high temperature when storing.

What are the chemical properties of 2,9-bis [4- (phenylazo) phenyl] anthra [2,1,9-def: 6,5,10-d'e'f '] diisoquinoline-1,3,8,10 (2H, 9H) -tetrone

2% 2C9 - bis%5B4-%28phenylazo%29phenyl%5Danthra%5B2%2C1%2C9 - def% 3A6% 2C5% 2C10 - d%27e%27f%27%5Ddiisoquinoline - 1%2C3%2C8%2C10%282H%2C9H%29 - tetrone, this is an organic compound with unique chemical properties.

This compound contains a complex conjugated system, which is fused by anthracene and diisoquinoline structures, and the benzophenyl group is modified at a specific position. The conjugated system endows it with special electronic properties, which have a great impact on the optical and electrical properties. Or it has a significant color. Because the conjugated structure absorbs visible light of specific wavelengths, it is common in the field of dyes and is used for dyeing with its chromatic properties.

Furthermore, the electron cloud distribution of the compound varies due to the interaction of conjugation and substituents, which affects its chemical reactivity. The nitrogen and nitrogen double bonds of benzenazophenyl can participate in the coupling reaction for the construction of larger molecular structures. Molecular rigidity and planarity are enhanced by the structure of thick rings, or affect their aggregation behavior in solution and solid-state stacking. In materials science, its crystallinity and thin film formation ability are involved, which affects its application in organic electronic devices such as organic Light Emitting Diodes and field-effect transistors.

The carbonyl of this compound is electrophilic and can react with nucleophiles, such as reacting with alcohols to form esters and amines to form amides. It can be used to synthesize more complex functional molecules and expand its application potential in pharmaceutical chemistry, materials science and other fields.

What is the preparation method of 2,9-bis [4- (phenylazo) phenyl] anthra [2,1,9-def: 6,5,10-d'e'f '] diisoquinoline-1,3,8,10 (2H, 9H) -tetrone

To prepare 2,9-bis [4- (phenylazo) phenyl] anthracene [2,1,9-def: 6,5,10-d'e'f '] diisoquinoline-1,3,8,10 (2H, 9H) -tetraketone, you can follow the following method.

First take an appropriate amount of anthracene dianhydride and place it in a clean reactor. Prepare a certain amount of 4-aminoazobenzene, dissolve it in an appropriate organic solvent, and then slowly pour it into the reactor containing anthracene dianhydride. During this process, the reaction temperature should be strictly controlled, and the warm water bath should be maintained at a moderate warm state, about 40 to 50 degrees Celsius, and continue to stir to make the two fully blend and react.

During the reaction, the color state of the solution in the kettle can be observed to change gradually. After several hours of reaction, the reaction liquid is slowly poured into a large amount of ice water, and precipitation can be seen. This precipitation is the preliminary product.

Next, the precipitate is filtered and repeatedly washed with water to remove its impurities. Then the filtered solid is placed in an oven and dried at a moderate low temperature. The dried product still contains some impurities, which need to be further purified by column chromatography. Select a suitable silica gel as the fixed phase, and use a specific proportion of organic solvents such as petroleum ether and ethyl acetate as the mobile phase for column chromatography. Through this step, a pure 2,9-bis [4- (phenylazo) phenyl] anthracene [2,1,9-def: 6,5,10-d'e'f '] diisoquinoline-1,3,8,10 (2H, 9H) -tetraketone product can be obtained. The whole preparation process requires attention to temperature, solvent ratio and fine operation to obtain ideal results.

What is the price range of 2,9-bis [4- (phenylazo) phenyl] anthra [2,1,9-def: 6,5,10-d'e'f '] diisoquinoline-1,3,8,10 (2H, 9H) -tetrone in the market?

I haven't heard of "2,9 - bis [4- (phenylazo) phenyl] anthra [2,1,9 - def: 6,5,10 - d'e'f '] diisoquinoline - 1,3,8,10 (2H, 9H) - tetrone" on the market. This is a very professional chemical substance. Its name is long and complex, and it must be used for fine chemistry or special scientific research.

The chemical naming of the concept shows that its structure is exquisite and complex, and it is not an ordinary and common thing. In common sense, the price of such a special chemical should be determined by many factors. The first one is the difficulty of synthesis. If the synthesis of this substance requires complicated steps, rare raw materials, and harsh reaction conditions, the cost will be high, and the price will also rise.

Furthermore, its use is also critical. If it is used in cutting-edge scientific research, high-end material preparation, etc., although the demand is rarely important, the price may remain high. On the contrary, if the application area is narrow and there is no urgent demand, the price may be relatively easy.

However, I have searched all over the ancient books, but I have not been able to obtain the actual price. Market prices often fluctuate due to changes in time, place, supply and demand, etc. It is difficult to generalize. Or you can consult chemical reagent manufacturers and scientific research material suppliers to get the approximate price range. Or refer to the price of similar complex chemical substances, make a little guess, but in the end it is not accurate.