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What is the chemical structure of Sodium 1-Amino-9,10-Dioxo-4- [ (2,4,6-Trimethylphenyl) Amino] -9,10-Dihydroanthracene-2-Sulfonate
This is a compound of sodium and 1-amino-9,10-dioxo-4- [ (2,4,6-trimethylphenyl) amino] -9,10-dihydroanthracene-2-sulfonate. In its chemical structure, sodium is a metal cation, giving this compound the properties of a salt.
1-amino-9,10-dioxo-4- [ (2,4,6-trimethylphenyl) amino] -9,10-dihydroanthracene-2-sulfonate moiety, anthracycline is the core structure, with dioxo groups at positions 9 and 10, which endows the molecule with specific electron cloud distribution and reactivity. The 1-linked amino group can participate in many nucleophilic reactions. The 4-linked (2,4,6-trimethylphenyl) amino group, the methyl group on the phenyl group enhances its hydrophobicity and affects the solubility and steric resistance of the molecule. The sulfonic acid group at position 2 makes the molecule have certain hydrophilicity and ionization ability, which can enhance the solubility of the compound in polar solvents. The interaction of various parts of the overall structure of this compound jointly determines its physical and chemical properties, and may have specific applications in the fields of organic synthesis and materials science.
What are the physical properties of Sodium 1-Amino-9,10-Dioxo-4- [ (2,4,6-Trimethylphenyl) Amino] -9, 10-Dihydroanthracene-2-Sulfonate
This is a compound named "1-amino-9,10-dioxo-4- [ (2,4,6-trimethylphenyl) amino] -9,10-dihydroanthracene-2-sodium sulfonate". Its physical properties are rich and diverse, and it is closely related to its own structure.
Looking at its appearance, it usually takes a solid form. Due to the existence of various forces between molecules, the molecules are arranged in an orderly manner to form a solid structure.
In terms of solubility, because it contains a sodium sulfonate group, which is a hydrophilic group, it has a certain solubility in water. Water molecules can interact with sodium sulfonate groups, and the ion-dipole force makes the compound disperse in water. However, the molecule also contains large organic groups, such as anthracycline and trimethylphenyl and other hydrophobic parts, which limits its solubility in water to a certain extent, making its solubility not excellent.
Melting point is also one of the important physical properties. The molecular structure of the compound is complex, and the intermolecular forces are strong, including van der Waals force, hydrogen bond, etc. Many forces are intertwined, so that high energy is required to break the original arrangement between molecules, so the melting point is relatively high. The exact melting point value depends on the specific structure and purity of the molecule and other factors.
In addition, the compound may exhibit unique optical properties when irradiated with specific wavelengths of light. The intra-molecular conjugated system, such as the anthracycline structure, can absorb specific energy photons, initiate electron transitions, and thus exhibit corresponding color or fluorescence phenomena. This optical property lays the foundation for its application in optical materials and other fields.
In conclusion, the physical properties of 1-amino-9,10-dioxo-4- [ (2,4,6-trimethylphenyl) amino] -9,10-dihydroanthracene-2-sulfonate sodium are dominated by its structure, and these properties play a key role in different applications.
What is the main use of Sodium 1-Amino-9,10-Dioxo-4- [ (2,4,6-Trimethylphenyl) Amino] -9,10-Dihydroanthracene-2-Sulfonate
Sodium-1-amino-9,10-dioxo-4- [ (2,4,6-trimethylphenyl) amino] -9,10-dihydroanthracene-2-sulfonate This compound has a wide range of uses. In the field of printing and dyeing, it can be used as a reactive dye aid. Because of its special molecular structure, it can make the dye more stable in combination with fabric fibers, greatly improve the color fastness of dyeing, and the color is also brighter. With its help, the fabric can be used for a long time and the color is not easy to fade, which is of great significance in the textile printing and dyeing industry.
In the process of scientific research, it is often a key intermediate in organic synthesis. Chemists can create diverse and unique organic compounds through structural modification and derivatization reactions, paving the way for new materials research and development, drug synthesis and other fields. In terms of materials science, functional materials constructed on this basis may have excellent optical and electrical properties, or emerge in the field of catalysis, promoting the progress of cutting-edge research in materials science.
In industrial production, or applied to some special chemical manufacturing processes. By virtue of its unique chemical properties, it participates in specific chemical reactions and helps to synthesize industrial raw materials or products with special properties, making significant contributions to improving the quality and performance of industrial products. With its diverse functions, this substance plays an important role in many fields and is an indispensable chemical raw material.
What is the synthesis method of Sodium 1-Amino-9,10-Dioxo-4- [ (2,4,6-Trimethylphenyl) Amino] -9, 10-Dihydroanthracene-2-Sulfonate
To prepare this "1-amino-9,10-dioxo-4- [ (2,4,6-trimethylphenyl) amino] -9,10-dihydroanthracene-2-sodium sulfonate", the method is as follows:
First take an appropriate amount of anthraquinone and place it in a clean kettle. Dissolve it in an appropriate organic solvent, so that it is evenly dispersed. Then, carefully add an amino-containing reagent, which must be pure and accurate in proportion. When reacting, control its temperature and pressure to a suitable environment. If the temperature is too high, it is easy to produce side reactions; if it is too low, the reaction will be slow.
After the amino group is successfully connected to the specific position of anthraquinone, the corresponding amino anthraquinone derivative is generated. At this time, another reagent containing (2,4,6-trimethylphenyl) amino group is prepared and slowly added to the kettle. In this step, it is also necessary to carefully control the reaction conditions so that the (2,4,6-trimethylphenyl) amino group is successfully connected to the designated part of the amino anthraquinone derivative to obtain an anthraquinone intermediate containing a specific amino group.
Subsequently, transfer this intermediate into the sulfonation kettle. Add sulfonating reagents, such as concentrated sulfuric acid or fuming sulfuric acid. When sulfonating, pay attention to the reaction process, because the control of the degree of sulfonation is related to the quality of the product. Sulfonation is completed, and the system is neutralized with an appropriate alkali solution to make the system neutral or weakly basic.
Finally, after precipitation, filtration, washing, drying and other processes, impurities are removed to obtain a pure "1-amino-9,10-dioxo-4- [ (2,4,6-trimethylphenyl) amino] -9,10-dihydroanthracene-2-sodium sulfonate" product. Every step of operation needs to be careful and fine, and a slight difference will affect the purity and yield of the product.
What is the market outlook for Sodium 1-Amino-9,10-Dioxo-4- [ (2,4,6-Trimethylphenyl) Amino] -9,10-Dihydroanthracene-2-Sulfonate
Guanfu Sodium-1-Amino-9,10-dioxo-4- [ (2,4,6-trimethylphenyl) amino] -9,10-dihydroanthracene-2-sulfonate This compound is a common observation in the industry in terms of market prospects.
This compound has emerged in many fields and has a lot of development. In the field of materials science, due to its special molecular structure, it may be used to create new functional materials. For example, in the field of optoelectronic materials, it may endow materials with unique optical and electrical properties, and then be applied to Light Emitting Diode, solar cells and other devices, bringing new opportunities for energy and display fields.
In the field of chemical research, its complex structure also provides challenges and opportunities for organic synthesis chemists. Researchers can use this to explore novel synthesis paths and reaction mechanisms to promote the progress of organic synthesis chemistry.
In the field of biomedicine, although it has not been widely used, in view of the active groups contained in its structure, it may be reasonably modified and modified to become potential drug lead compounds, opening up new paths for the treatment of diseases.
However, its market prospects are not smooth sailing. The synthesis process may be cumbersome and harsh conditions, resulting in high production costs, which hinders the promotion and application. And the market acceptance of new materials and compounds takes time to prove their performance and reliability.
In summary, sodium-1-amino-9,10-dioxo-4- [ (2,4,6-trimethylphenyl) amino] -9,10-dihydroanthracene-2-sulfonate has a bright future, but it also needs to overcome the problems of cost and market recognition in order to make great progress in various fields. The prospect can be described as both opportunities and challenges.