2-[4-(dimethylamino)phenyl]-1H-benzo[de]isoquinoline-1,3(2H)-dione

The name of this compound is 2- [4- (dimethylamino) phenyl] -1H-benzo [de] isoquinoline-1,3 (2H) -dione. Its chemical structure is analyzed as follows:
First, "benzo [de] isoquinoline-1,3 (2H) -dione" is the core parent structure of this compound. Benzo isoquinoline compounds are formed by fusing the benzene ring with the isoquinoline ring. On this basis, two carbonyl groups (-CO-) at the 1,3 position form a dione structure.
And "2- [4- (dimethylamino) phenyl]" indicates that a phenyl group is connected at the No. 2 position of the benzo [de] isoquinoline-1,3 (2H) -diketone parent nuclear structure. And the 4 position of the phenyl group is replaced by dimethylamino (-N (CH
).
In general, this compound consists of a complex fused ring structure as the main body, and at the same time is connected with a phenyl group containing nitrogen substituents at a specific position. This structure endows the compound with unique physicochemical properties and possible biological activities, and may have certain research value and application potential in organic synthesis, medicinal chemistry and other fields.

2-% 5B4-% 28 dimethylamino% 29 phenyl% 5D-1H-benzo% 5Bde% 5D isoquinoline-1% 2C3% 282H% 29-dione, this is an organic compound with specific physical properties.
Looking at its properties, under normal temperature and pressure, it is mostly in solid form and has certain stability. When it encounters hot topics, open flames or strong oxidants, it may be dangerous. Its melting point and boiling point are key physical constants. The melting point refers to the temperature at which a substance changes from a solid state to a liquid state. The melting point of this compound is of great significance to its phase change under specific conditions, and is related to its existence form under different temperature environments. The boiling point is the temperature at which the liquid boils, which determines the timing of its transition from liquid to gaseous state during heating.
Solubility is also an important property. Its solubility in organic solvents varies, and it may have good solubility in some organic solvents such as dichloromethane, N, N-dimethylformamide, but its solubility in water may be very low. This difference in solubility affects its application in different solvent systems. For example, in organic synthesis reactions, the selection of a suitable solvent is crucial and needs to be determined according to its solubility characteristics.
In addition, the density of this compound reflects its mass per unit volume, which has an impact on its distribution and behavior in specific systems. Its density data can help to understand the physical state changes when it is mixed with other substances, such as when preparing solutions or suspensions, which can be used to predict its sedimentation or delamination.
Furthermore, its spectral properties, such as infrared spectroscopy, nuclear magnetic resonance spectroscopy, etc., can provide detailed information on the molecular structure. Infrared spectroscopy can reveal the vibration absorption peaks of different chemical bonds in a molecule, helping to determine the functional groups present in the molecule. Nuclear magnetic resonance spectroscopy can reveal the chemical environment and relationships of hydrogen atoms or other magnetic nuclei in a molecule, providing a key basis for accurate analysis of molecular structure.
The physical properties of this compound are complex and interrelated, and it has important research and application value in the fields of organic synthesis, drug development and materials science.

2-% 5B4-% 28 dimethylamino% 29 phenyl% 5D-1H-benzo% 5Bde% 5D isoquinoline-1% 2C3% 282H% 29-dione, this is an organic compound. It has a wide range of uses and has important applications in many fields.
In the field of medicinal chemistry, this compound is often used as a potential drug intermediate. Due to its specific chemical structure or unique biological activity, it can help researchers develop new drugs. After modifying and modifying its chemical structure, it may be possible to obtain drugs with therapeutic effects on specific diseases, such as anti-tumor and anti-virus. For example, through in-depth research and experiments, researchers have developed drugs with inhibitory effects on certain types of tumor cells through these compounds, opening up new avenues for tumor treatment.
In the field of materials science, this compound also has outstanding performance. Because it has certain optical and electrical properties, it may be used to prepare optoelectronic materials. For example, incorporating it into a specific material system may improve the optical properties of materials, such as luminous efficiency, fluorescence stability, etc., so that it can be applied to the fabrication of optoelectronic devices such as organic Light Emitting Diodes (OLEDs) to improve device performance and display effect.
In the field of organic synthetic chemistry, this compound can participate in the synthesis of many complex organic compounds as a key intermediate. Chemists can build more complex and functional organic molecular structures based on various organic reactions, expand the boundaries of organic synthesis chemistry, and provide a rich material foundation for the development of new materials and drugs.

To prepare 2 - [4- (dimethylamino) phenyl] -1H -benzo [de] isoquinoline-1,3 (2H) -dione, there are many methods for its synthesis. It usually follows the path of organic synthesis, starting from the starting material and going through a multi-step reaction to achieve the target product.
One method can first take an appropriate benzo isoquinoline compound as the starting point, which has a modifiable check point in its structure and can undergo nucleophilic substitution reaction with reagents containing 4- (dimethylamino) phenyl. Under suitable reaction conditions, if a suitable solvent is selected, such as dichloromethane, N, N-dimethylformamide, etc., the reaction temperature is controlled, or at room temperature, or heated to reflux, and an appropriate amount of alkali is added, such as potassium carbonate, triethylamine, etc., to promote the reaction. After this nucleophilic substitution, 4- (dimethylamino) phenyl can be introduced into the benzoisoquinoline skeleton.
Furthermore, for the obtained intermediate, oxidation or other functional group conversion reactions are required to construct the 1,3-dione structure. Appropriate oxidants, such as Jones reagent, Dice-Martin oxidant, etc., can be selected. According to the characteristics of the intermediate, the reaction conditions are precisely regulated to convert hydroxyl and other functional groups into carbonyl groups, and the final target is 2 - [4- (dimethylamino) phenyl] -1H -benzo [de] isoquinoline-1,3 (2H) -dione.
There are other methods, which can be started from the construction of benzoisoquinoline ring system. First, benzene series and nitrogen-containing heterocyclic precursors are condensed to form benzoisoquinoline parent nucleus. In the condensation process, it is necessary to finely adjust the ratio of reactants, reaction solvents and catalysts, such as acid or base as catalyst, so that the reaction proceeds in the desired direction. Then, 4 - (dimethylamino) phenyl is introduced and the diketone structure is modified. The reaction conditions are similar to the above, and the selectivity and yield of each step of the reaction need to be paid attention to. After multiple optimizations, a pure target product can be obtained.

Nowadays, there are 2 - [4 - (dimethylamino) phenyl] -1H - benzo [de] isoquinoline - 1,3 (2H) -dione. The market prospect of this compound is of great concern to everyone.
In the field of current pharmaceutical and chemical industry, this compound has great potential value. At the end of drug research and development, its unique structure may become a key raw material for the creation of new drugs. In terms of pharmacological exploration, the activity of its molecular structure has a checking point, which may be able to fit with specific biological targets, and is expected to lead to specific drugs for some difficult diseases. This is because there is a strong demand for high-efficiency and low-toxicity innovative drugs in the pharmaceutical market today, and such new compounds are just right for this need, so there may be opportunities for future drug development.
In the field of materials science, it may also have extraordinary performance. Due to its special chemical structure, it may endow materials with different physical and chemical properties. For example, in the field of optoelectronic materials, it can improve the optical properties of materials, such as luminous efficiency and photostability, and then be applied to cutting-edge technologies such as organic Light Emitting Diode (OLED), contributing to the development of this field.
However, its market prospects are not smooth. The process of synthesizing this compound may be complicated and costly. In order to achieve large-scale production, it is urgent to optimize the synthesis path and reduce costs. And the market competition is fierce, and there are many similar or alternative compounds. Only by continuously improving technology and highlighting its own advantages can we occupy a place in the market.
In summary, although 2- [4- (dimethylamino) phenyl] -1H-benzo [de] isoquinoline-1,3 (2H) -dione faces challenges, its potential applications in medicine, materials and other fields make it have broad market prospects. If it can be properly developed and utilized, it will be able to create considerable value.