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What is the chemical structure of dimethyl 2,6-dimethyl-4- (2-nitrophenyl) -1,4-dihydropyridine-3,5-dicarboxylate?
This is a compound named dimethyl 2,6-dimethyl-4- (2-nitrophenyl) -1,4-dihydropyridine-3,5-dicarboxylate. Looking at its name, it can be seen that its structure contains dimethyl groups, with one methyl group at the 2nd and 6th positions of the pyridine ring; 2-nitrophenyl group at the 4th position of the pyridine ring; and one carboxylic acid ester group at the 3rd and 5th positions, both of which are esterified with dimethyl.
In terms of structure, the pyridine ring is the core structure, and the structure of 1,4-dihydropyridine gives it special chemical activity. The methyl group at the 2,6 position affects the reactivity and physical properties of the molecule due to its steric resistance and electronic effects. The 2-nitrophenyl group at the 4 position is a strong electron-absorbing group, which changes the electron cloud density distribution of the pyridine ring and makes the pyridine ring more prone to nucleophilic substitution and other reactions. The 3-5 bis carboxylic acid ester group not only affects the molecular polarity, but also participates in many esterification, hydrolysis and other reactions. The interaction of various groups in the structure of this compound makes it have unique chemical properties and potential application value.
What are the main uses of dimethyl 2,6-dimethyl-4- (2-nitrophenyl) -1,4-dihydropyridine-3,5-dicarboxylate
Dimethyl ester 2,6-dimethyl-4- (2-nitrophenyl) -1,4-dihydropyridine-3,5-dicarboxylate, an organic compound. Its main uses are quite extensive. In the field of medicine, it is often used as a key intermediate of calcium channel blockers. Calcium channel blockers can regulate the flow of calcium ions inside and outside the cells, and have a significant effect on the prevention and treatment of cardiovascular system diseases. Such diseases as hypertension, angina pectoris and arrhythmia can be improved by these drugs.
In the field of chemical synthesis, this compound can be used as an important synthetic block for the preparation of more complex nitrogen-containing heterocyclic compounds due to its unique chemical structure. Many substances with biological activity or special properties can only be obtained by using them as starting materials through a series of chemical reactions.
In the field of materials science, after appropriate chemical modification or polymerization, it can be prepared with special optical and electrical properties. It may have potential application value in optoelectronic devices, sensors, etc.
This compound plays an important role in the fields of medicine, chemical synthesis and materials science, providing a key material basis for the research and development of related fields.
What are the physical properties of dimethyl 2,6-dimethyl-4- (2-nitrophenyl) -1,4-dihydropyridine-3,5-dicarboxylate
Dimethyl-2,6-dimethyl-4- (2-nitrophenyl) -1,4-dihydropyridine-3,5-dicarboxylate, an organic compound. Looking at its physical properties, it is mostly in a solid state at room temperature and pressure. The color of this compound is usually white or almost white powder, uniform and delicate.
The melting point is about a specific range of values. This value is the critical temperature for its conversion from solid to liquid, which is crucial for the identification and purification of this compound. As for solubility, it exhibits certain solubility properties in some organic solvents. For example, in common organic solvents such as ethanol and acetone, it can be moderately dissolved. This is because there are specific interaction forces between the molecular structure of the compound and the molecules of these organic solvents, such as van der Waals forces, hydrogen bonds, etc., which promote the dissolution process to occur.
However, in water, its solubility is poor. This is because water is a highly polar solvent, while the polarity of the compound is relatively weak. According to the principle of "similar miscibility", the polarity difference is significant, making it difficult to disperse and dissolve in large quantities in water.
In addition, the density of the compound is also one of its important physical properties. The value of its density reflects the mass of the substance per unit volume, and has important reference value for the measurement and ratio of materials in related chemical production and experimental operations. At the same time, this compound will undergo corresponding physical changes under heating and other conditions, such as sublimation at specific high temperatures, which are its unique physical properties.
What are the synthesis methods of dimethyl 2,6-dimethyl-4- (2-nitrophenyl) -1,4-dihydropyridine-3,5-dicarboxylate
To prepare dimethyl 2,6-dimethyl-4- (2-nitrophenyl) -1,4-dihydropyridine-3,5-dicarboxylic acid ester, there are three methods.
One is the classical Hantzsch synthesis method. This is the use of ethyl acetoacetate, formaldehyde and 2-nitrobenzaldehyde as raw materials, in ethanol, with glacial acetic acid as the catalyst, heated and refluxed. The reason is that the reactants are condensed to form the prototype of the dihydropyridine ring first, and then cyclized within the molecule, and finally obtain the target product. In this process, the catalytic activity of glacial acetic acid is moderate, which can make the reaction proceed smoothly. However, the reaction takes a long time and the yield is not very high, about 50% - 60%.
The second is the microwave-assisted synthesis method. This is to place the above raw materials and an appropriate amount of catalyst in a microwave reactor with methanol as the solvent. Under microwave radiation, the molecular vibration intensifies and the reaction rate increases greatly. Compared with traditional heating, the reaction time is greatly shortened, only tens of minutes, and the yield can be increased to 70% - 80%. Due to the unique heating method of microwave, the reaction system is heated evenly, and the collision frequency and effective collision probability between molecules are increased, thus promoting the reaction. < Br >
The third is the solid-phase synthesis method. The reactants are supported on a solid support without solvent and catalyzed by a small amount of catalyst. The reaction occurs under grinding or heating conditions. This advantage is that it is green and environmentally friendly, the post-treatment is simple, and the product is easy to separate and purify. However, it requires high requirements on the carrier and reaction conditions, and requires fine regulation, with a yield of about 60% - 70%.
What is the market outlook for dimethyl 2,6-dimethyl-4- (2-nitrophenyl) -1,4-dihydropyridine-3,5-dicarboxylate?
Dimethyl ester 2,6-dimethyl-4- (2-nitrophenyl) -1,4-dihydropyridine-3,5-dicarboxylate is an attractive organic compound in the field of chemical synthesis. Looking at its market prospects, it really contains many opportunities and challenges.
From its chemical structure analysis, the unique structure of this compound gives it a variety of potential applications. In the field of pharmaceutical research and development, it may become a key intermediate to help create new drugs. Today, the pharmaceutical industry has an increasing demand for efficient and novel drugs. If this compound can emerge in the drug synthesis process, it will surely open up new avenues for the treatment of many diseases, so it is expected to find a wide range of fields in the pharmaceutical market.
Looking at the field of materials science, with the rapid development of science and technology, the demand for special performance materials is also rising. Dimethyl ester 2,6-dimethyl-4- (2-nitrophenyl) -1,4-dihydropyridine-3,5-dicarboxylate may contribute to the synthesis of high-performance materials by virtue of its special chemical properties, such as in optoelectronic materials, polymer materials, etc., all have potential application value. If successfully developed and utilized, a new material market will be opened up.
However, its marketing activities are not smooth sailing. First, the complexity and cost of the synthesis process need to be solved urgently. The complex synthesis steps may cause high production costs, thus affecting the competitiveness of the product market. Secondly, safety and environmental impact cannot be ignored. In the production and application process, it is necessary to ensure that it is environmentally friendly and harmless to human health, which is also a necessary consideration for entering the market.
In summary, the market prospect of dimethyl ester 2,6-dimethyl-4- (2-nitrophenyl) -1,4-dihydropyridine-3,5-dicarboxylate is promising, but it also needs to overcome many difficulties in order to occupy a place in the market and inject strong impetus into the development of related industries.