What is the chemical structure of 2,9-bis (4-chlorophenyl) anthra [2,1,9-def: 6,5,10-d'e'f '] diisoquinoline-1,3,8,10 (2H, 9H) -tetrone?

This is a compound of 2,9-bis (4-chlorophenyl) anthrano [2,1,9-def: 6,5,10-d'e'f '] diisoquinoline-1,3,8,10 (2H, 9H) -tetraketone. Looking at its name, it can be inferred that its structure is very complex.

This compound contains the core structure of anthro-diisoquinoline, and at positions 2 and 9, there are two 4-chlorophenyl groups connected. In its ring system, the anthracycline and the diisoquinoline ring are cleverly conjugated to form a unique fused ring system. At positions 1, 3, 8, and 10, each is connected to a carbonyl group, resulting in significant chemical activity.

The properties of this structure make it potentially useful in the fields of materials science, medicinal chemistry, etc. For example, in the field of materials, its fused ring conjugated system may endow materials with special optical and electrical properties; in medicinal chemistry, carbonyl and chlorophenyl may interact specifically with biological targets and have pharmacological activities.

In short, the structure of 2,9-bis (4-chlorophenyl) anthraco [2,1,9-def: 6,5,10-d'e'f '] diisoquinoline-1,3,8,10 (2H, 9H) -tetraketone brings infinite possibilities for multi-field research due to its uniqueness, and it needs to be further explored by scholars to uncover more mysteries.

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

2%2C9-bis%284-chlorophenyl%29anthra%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 physical properties.

Looking at its appearance, it often takes the form of a powder, which is related to intermolecular interactions and crystallization habits. Powdered substances usually indicate that the molecular arrangement does not form a regular bulk crystal structure, and intermolecular forces promote its existence in the form of fine particles under specific conditions.

In terms of solubility, in common organic solvents such as dichloromethane and chloroform, the compound exhibits a certain solubility. This is due to the specific interactions between the molecules of the organic solvent and the compound molecules, such as van der Waals forces, dipole-dipole interactions, etc. These forces can overcome the interactions between the molecules of the compound themselves and make it uniformly dispersed in the solvent. However, in water, its solubility is minimal. Water is a highly polar solvent, and the molecular structure of this compound makes its polarity relatively weak, and it is difficult to form effective interactions with water molecules, so it is difficult to dissolve in water.

Melting point is also an important physical property. After determination, the melting point of the compound is in a specific temperature range. The melting point depends on the strength of the intermolecular forces. There are various chemical bonds and functional groups in its molecular structure. These factors work together to form intermolecular forces of specific strength, thus determining the melting point value. When the external temperature reaches the melting point, the molecule obtains enough energy to overcome the intermolecular forces and transform from a solid state to a liquid state.

In addition, the compound has a certain stability. Under normal environmental conditions, its chemical structure is not prone to significant changes. This is due to the stability of chemical bonds in the molecular structure and the balance of interactions between functional groups. However, under specific conditions, such as high temperature and strong acid-base environment, its stability may be affected, and the molecular structure may change, resulting in corresponding changes in physical properties.

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

2% 2C9 - bis% 284 - chlorophenyl%29anthra%5B2%2C1%2C9 - def% 3A6% 2C5% 2C10 - d%27e%27f%27%5Ddiisoquinoline - 1%2C3%2C8%2C10%282H%2C9H%29 - tetrone, a complex organic compound commonly referred to as dichloroanthraquinone (DCA). It has a wide range of uses and plays an important role in both industrial and scientific research fields.

In the dye industry, dichloroanthraquinone is a key intermediate. With its unique molecular structure, it can be converted into a variety of colorful and high-performance anthraquinone dyes through a series of chemical reactions. These dyes are widely used in the textile industry to give fabrics rich color, and have good light resistance and washable fastness, making fabrics last for a long time.

In the field of pharmaceutical research, dichloroanthraquinone has also shown potential value. Scientists have found that it has certain inhibitory activity on specific cancer cells, and may become an important lead compound for the development of anti-cancer drugs. Through structural modification and optimization, it is expected to develop new anti-cancer drugs with better efficacy and fewer side effects, which will bring hope for solving cancer problems.

In addition, in the field of materials science, dichloroanthraquinone has emerged in the preparation of organic semiconductor materials due to its special photoelectric properties. After rational design and synthesis, organic materials with specific electrical and optical properties can be prepared, which can be used in cutting-edge fields such as organic Light Emitting Diode (OLED) and organic solar cells to promote the development of related technologies.

In summary, 2% 2C9 - bis% 284 - chlorophenyl%29anthra%5B2%2C1%2C9 - def% 3A6% 2C5% 2C10 - d%27e%27f%27%5Ddiisoquinoline - 1%2C3%2C8%2C10%282H%2C9H%29 - tetrone plays an important role in many fields such as dyes, medicine and materials science, and is of great significance to the development of various industries.

What are the methods for preparing 2,9-bis (4-chlorophenyl) anthra [2,1,9-def: 6,5,10-d'e'f '] diisoquinoline-1,3,8,10 (2H, 9H) -tetrone?

2% 2C9 - bis% 284 - chlorophenyl%29anthra%5B2%2C1%2C9 - def% 3A6% 2C5% 2C10 - d%27e%27f%27%5Ddiisoquinoline - 1%2C3%2C8%2C10%282H%2C9H%29 - tetrone, this is the scientific name of an organic compound, and most people call it by its common name or trade name. The method of preparing this compound is quite complicated, and it requires proficiency in organic synthetic chemistry, and corresponding experimental conditions and skills. The following are common preparation methods:

Starting materials, compounds containing specific functional groups are often selected, and the construction of target molecules is achieved through multi-step organic reactions. First, compounds containing chlorophenyl groups and anthraquinone derivatives can be used as starting materials. Under suitable reaction conditions, through nucleophilic substitution, cyclization and other reaction steps, the skeleton of the target molecule can be gradually built. During the reaction process, the choice of temperature, solvent, and catalyst is crucial, which can significantly affect the reaction rate and product purity.

Furthermore, transition metal catalysis can be used as a reaction strategy. For example, palladium-catalyzed cross-coupling reactions can effectively connect different fragments to accurately construct complex molecular structures. This method requires careful selection of suitable ligands and reaction conditions to improve the selectivity and efficiency of the reaction.

When preparing, the reaction process needs to be closely monitored. Commonly used methods, such as thin-layer chromatography (TLC) and high-performance liquid chromatography (HPLC), can help determine whether the reaction is completed and the purity of the product. After the reaction, the separation and purification of the product are also key steps. Column chromatography, recrystallization and other means are often used to obtain high-purity target products.

However, it should be noted that organic synthesis reactions are dangerous. Many raw materials and reagents are toxic, corrosive or flammable and explosive. When operating, be sure to strictly follow safety procedures, work in a well-ventilated environment, and wear appropriate protective equipment to ensure the safety and health of experimental personnel.

In what fields is 2,9-bis (4-chlorophenyl) anthra [2,1,9-def: 6,5,10-d'e'f '] diisoquinoline-1,3,8,10 (2H, 9H) -tetrone used?

2% 2C9 - bis% 284 - chlorophenyl%29anthra%5B2%2C1%2C9 - def% 3A6% 2C5% 2C10 - d%27e%27f%27%5Ddiisoquinoline - 1%2C3%2C8%2C10%282H%2C9H%29 - tetrone, which is the name of an organic compound. According to its structure and characteristics, it has applications in many fields.

In the field of materials science, it may have unique optical and electrical properties, and can be used to manufacture optoelectronic devices such as organic Light Emitting Diodes (OLEDs). Due to its structure, it can affect the intramolecular charge transfer and luminous efficiency. Therefore, with appropriate modification, the brightness and stability of OLEDs may be improved, making the display device clearer and longer lasting.

In the field of medicinal chemistry, it may have potential biological activity. After research, it has been found that compounds with such structures may interact with specific biological targets, such as certain enzymes or receptors. After rational design and modification, they may be developed into new drugs for the treatment of specific diseases, such as cancer or inflammation-related diseases.

In the field of analytical chemistry, due to its unique structure and spectral properties, it can be used as an analytical reagent. Through its specific interaction with target substances, spectroscopic analysis and other means, highly sensitive detection and analysis of specific components in complex samples can be achieved, which can assist environmental monitoring, food safety testing, etc.

In the field of material protection, it may endow materials with specific protective properties. Adding to coatings, plastics and other materials may enhance the oxidation and corrosion resistance of materials, prolong the service life of materials, and have application potential in construction, automotive and other industries.

In summary, 2% 2C9 - bis% 284 - chlorophenyl%29anthra%5B2%2C1%2C9 - def% 3A6% 2C5% 2C10 - d%27e%27f%27%5Ddiisoquinoline - 1%2C3%2C8%2C10%282H%2C9H%29 - tetrone has shown important application value in many fields such as materials, drugs, analysis and protection, providing new opportunities for technological development and innovation in various fields.