Chemical Formula | C21H18N2O2 |
Appearance | Solid (usually powder or crystal) |
Physical State | Solid at room temperature |
Melting Point | Needs experimental determination |
Boiling Point | Needs experimental determination |
Solubility | Solubility varies with solvents, e.g., may be sparingly soluble in water, more soluble in organic solvents like DMSO |
Pka | Needs experimental determination |
Logp | Needs experimental determination |
Density | Needs experimental determination |
What is the chemical structure of 6-amino-2- (2,4-dimethylphenyl) -1H-benz [de] isoquinoline-1,3 (2H) -dione
This is the question of 6-amino-2- (2,4-dimethylphenyl) -1H-benzo [de] isoquinoline-1,3 (2H) -dione. To clarify its chemical structure, let me tell you in detail.
This compound, according to its name, has a core structure of benzo [de] isoquinoline-1,3 (2H) -dione. In this core structure, the benzene ring and the isoquinoline ring are fused, just like the two rings are closely dependent and integrated. At the 1H position and the 3 (2H) position, each is connected to a carbonyl group. The carbonyl group is a functional group formed by the double bond of carbon and oxygen. Its reactivity has a great influence on the properties of the compound.
Furthermore, at the 2 position there is (2,4-dimethylphenyl). Above this phenyl group, there is a methyl group at the 2 and 4 positions. Methyl, an alkyl group composed of hydrocarbon atoms, is added to the phenyl group, which may affect the spatial configuration of the molecule and the distribution of electron clouds, and then affect the physical and chemical properties of the compound.
There is an amino group at the 6 position. The amino group is a functional group composed of nitrogen and hydrogen, which is basic and can react with acidic substances. It is attached to the core structure and also gives the compound a unique chemical activity.
In summary, the chemical structure of 6-amino-2- (2,4-dimethylphenyl) -1H-benzo [de] isoquinoline-1,3 (2H) -dione is composed of the core benzo [de] isoquinoline-1,3 (2H) -dione, together with the 2-position (2,4-dimethylphenyl) and the 6-position amino group, and each part affects each other, giving this compound unique properties.
What are the physical properties of 6-amino-2- (2,4-dimethylphenyl) -1H-benz [de] isoquinoline-1,3 (2H) -dione
6-Amino-2- (2,4-dimethylphenyl) -1H-benz [de] isoquinoline-1,3 (2H) -dione, which is an organic compound. Its physical properties are quite important and related to its application in many fields.
When it comes to appearance, it is often crystalline, mesoscopic, and the crystals are regular and orderly, like a natural miniature building. The color may be white to light yellow, like the first snow in winter or the shimmer at dusk, pure and soft.
Melting point is one of the key physical properties. After experimental determination, its melting point is within a certain range, which is similar to the "body temperature critical value" of this compound. At this temperature, its solid-state structure begins to change, and the intermolecular forces are rearranged, gradually melting from the solid state to the liquid state. This melting point range gives it the characteristics of stable existence under a specific temperature environment.
Solubility cannot be ignored either. In organic solvents, such as some alcohols and ether solvents, their solubility varies. In specific alcohols, it may be moderately soluble, just like snowflakes blending into warm water, and the molecules are evenly dispersed to form a uniform system. In water, its solubility is poor, like unmeltable ice, most of which remain in solid form, which is closely related to the role of hydrophobic groups in its molecular structure.
In addition, the density of the compound, like its "weight mark", determines its position in the mixture. Its density value is specific, and when mixed with other substances, it either rises or sinks according to the density difference, which affects the physical state of the mixed system.
The physical properties of this compound are interrelated, forming its unique "physical profile", which lays the foundation for its application in chemical synthesis, drug discovery and other fields.
What is the main use of 6-amino-2- (2,4-dimethylphenyl) -1H-benz [de] isoquinoline-1,3 (2H) -dione
6 - amino - 2 - (2,4 - dimethylphenyl) - 1H - benz [de] isoquinoline - 1,3 (2H) - dione is an organic compound with a wide range of uses.
In the field of medicine, this compound may have unique pharmacological activities. The structure of benzoisoquinoline dione is often found in many bioactive molecules, or it can interact with specific biological targets, such as binding to key enzymes or receptors in cells, showing potential medicinal value. It may participate in the regulation of cell signaling pathways and have an impact on certain disease processes, or it is expected to be developed as a drug for the treatment of specific diseases, such as anti-tumor, anti-inflammatory, neuroprotective and other drugs, but further pharmacological experiments and studies are needed to determine its exact efficacy and safety.
In the field of materials science, the compound may have unique optical, electrical or thermal properties due to its special molecular structure. Or it can be used to prepare functional materials, such as certain groups in its structure or imparting specific light absorption and emission characteristics to the material, which can be applied to the field of fluorescent materials for making fluorescent probes to achieve high sensitivity detection of specific substances or biomolecules; or its electrical properties can play a role in organic electronic devices such as organic Light Emitting Diodes (OLEDs), organic field effect transistors (OFETs), etc., helping to optimize device performance.
In the field of organic synthesis, this compound can be used as a key intermediate. Its complex and unique structure can further derive more compounds with novel structures and specific functions by means of organic synthesis. Based on this compound, chemists can modify its substituents to carry out diverse chemical reactions, build more complex and huge molecular systems, expand the library of organic compounds, and provide a rich material foundation for new drug development and material innovation.
What are the synthesis methods of 6-amino-2- (2,4-dimethylphenyl) -1H-benz [de] isoquinoline-1,3 (2H) -dione
The synthesis method of 6-amino-2- (2,4-dimethylphenyl) -1H-benzo [de] isoquinoline-1,3 (2H) -dione has been known since ancient times, and is described in detail as follows.
First, 2,4-dimethylbenzoic acid is used. After the method of acylation, oxalyl chloride or dichlorosulfoxide is used to form 2,4-dimethylbenzoyl chloride under suitable reaction conditions, such as heating or the presence of a catalyst.
times, with o-phenylenediamine and the obtained 2,4-dimethylbenzoyl chloride. In organic solvents such as toluene and dichloromethane, the temperature and reaction time can be controlled, and the condensation reaction can occur to obtain 2 - (2,4 - dimethylphenyl) benzo [de] isoquinoline - 1,3 (2H) -dione.
Then, the resulting product is aminized. Often an ammonia source, such as ammonia gas, ammonia water or amine compounds, is used in an appropriate reaction system, or with the help of catalysts, such as metal catalysts and their ligand combinations, through nucleophilic substitution and other reaction pathways, the amino group is introduced at the target position, and the final product is 6-amino-2- (2,4-dimethylphenyl) -1H-benzo [de] isoquinoline-1,3 (2H) -dione.
Or, there is a method of starting with other raw materials and going through a multi-step reaction. If a specific aromatic derivative is first functionalized, the relevant substituent is introduced, and then many steps such as cyclization and functional group transformation, the synthesis of this target product can also be achieved. However, no matter what method is used, the conditions of each step of the reaction need to be carefully considered, such as temperature, solvent, catalyst selection, and the proportion of reactants, etc., in order to smooth the synthesis path and obtain high-purity products.
What is the market outlook for 6-amino-2- (2,4-dimethylphenyl) -1H-benz [de] isoquinoline-1,3 (2H) -dione?
Today there are 6 - amino - 2 - (2,4 - dimethylphenyl) - 1H - benz [de] isoquinoline - 1,3 - (2H) - dione. Its market prospects are related to many aspects. Let me tell you in detail.
This product may have considerable prospects in the field of pharmaceutical research and development. Due to the way of medicine, it is often necessary to explore new compounds in order to find a cure for diseases and save people. The unique structure of this compound may be combined with specific targets in the human body, and then exert pharmacological effects, such as anti-cancer, anti-inflammatory, etc. Today's world is suffering from various diseases, and the demand for anti-disease drugs is eager. If this compound can demonstrate good efficacy and safety through in-depth research and development, it will be able to gain a place in the pharmaceutical market and benefit all people.
Furthermore, it is also of great value in the process of scientific research and exploration. Scientists often use novel compounds as tools to explore the mysteries of biochemistry and analyze the mechanism of life processes. 6-amino-2- (2,4-dimethylphenyl) -1H-benz [de] isoquinoline-1,3- (2H) -dione can provide new perspectives and paths for scientific research, and promote the expansion and deepening of knowledge in related fields.
However, its market prospects are not smooth. The difficulty of synthesis and the high cost are all obstacles. To achieve large-scale production, it is necessary to overcome many technical difficulties and find an efficient and economical synthesis method. And the road to new drug research and development is long and difficult, the strict screening of clinical trials, and the restrictions of regulations and policies may all hinder the research and development process.
Overall, 6-amino-2- (2,4-dimethylphenyl) -1H-benz [de] isoquinoline-1,3- (2H) -dione has a bright future, but it is also full of thorns. If we can gather the strength of everyone and break through the difficulties, it is expected to bloom and succeed in the market.