dimethyl 4-(furan-2-yl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate

"Dimethyl + 4 - (furan - 2 - yl) -2,6 - dimethyl - 1,4 - dihydropyridine - 3,5 - dicarboxylate" is the English name for organic compounds. To clarify its chemical structure, it is necessary to analyze it according to the organic chemistry nomenclature.
"dimethyl", showing two methyl groups. "4 - (furan - 2 - yl) ", indicating that there is a furan - 2 - group attached to the No. 4 position of the main structure. "2,6 - dimethyl", that is, there is a methyl group at the No. 2 and No. 6 positions of the main structure. " "1,4-dihydropyridine", revealing that the main structure is a 1,4-dihydropyridine ring. "3,5-dicarboxylate" means that the 3 and 5 positions of the main structure are respectively connected with carboxyl derivatives (ester groups, etc., because "carboxylate" implies carboxylic acid derivatives).
In summary, the structure of this compound is based on a 1,4-dihydropyridine ring as the backbone, with one methyl group at positions 2 and 6, furan-2-group at positions 4, and carboxyl-derived groups at positions 3 and 5 (such as ester groups, which may be methyl ester groups suggested by "dimethyl"). In this way, its chemical structure is roughly clear.

Dimethyl-4- (furan-2-yl) -2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate, this substance has a wide range of uses. In the field of medicine, it can be used as a key intermediate to synthesize a variety of compounds with specific biological activities. Or because of its structural properties, it can interact with specific targets in organisms, so it shows great potential in the creation of new drugs, such as cardiovascular disease treatment drugs, neuromodulation drugs, etc.
In the field of materials science, it may also play an important role. Or because of its unique chemical structure, it can give materials specific optical, electrical or thermal properties. For example, in the preparation of organic optoelectronic materials, it may be used as a functional monomer to participate in the polymerization reaction, thereby improving the photoelectric conversion efficiency or stability of the material, and is used in solar cells, Light Emitting Diode and other devices.
In the field of organic synthesis, as a special structural block, it can construct more complex and diverse organic molecular structures through various chemical reactions. Because of its furyl and dihydropyridine ring structures, it provides organic synthesis chemists with rich reaction check points and possibilities, which helps to achieve efficient synthesis of novel organic compounds and inject new vitality into the development of organic synthesis chemistry.

The synthesis method of furodimethyl 4- (furan-2-yl) -2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylic acid ester is one of the important topics in organic synthetic chemistry. The synthesis method often follows a specific reaction path and chemical principle.
Common synthetic pathways, one of which may be achieved through condensation reaction. Appropriate furan derivatives, pyridine derivatives, etc. are used as starting materials. Under suitable reaction conditions, such as in the presence of a specific catalyst, the catalyst may be an acid, a base, etc., so that it interacts to initiate a condensation reaction, thereby constructing the basic skeleton of the target molecule. In this process, the reaction temperature, reaction time, and the ratio of reactants need to be carefully adjusted. If the temperature is too high or too low, it may affect the reaction rate and the selectivity of the product; if the reaction time is too short, the reaction may not be fully carried out, and the yield is low; if the time is too long, it may cause side reactions, resulting in a decrease in the purity of the product. The proportion of reactants is also crucial, and the precise ratio can make the reaction proceed in the desired direction.
Furthermore, a cyclization reaction strategy may be used. First, a linear precursor containing a specific functional group is prepared. By means of specific chemical reaction conditions, cyclization occurs in the molecule to form a dihydropyridine ring structure, and then substituents such as furan and carboxylate groups are introduced. In this process, the control of the reaction intermediates is extremely critical, and suitable separation and purification methods need to be used to obtain high-purity intermediates to ensure the quality of the final product.
When synthesizing this compound, the choice of reaction solvent needs to be considered. Different solvents affect the reaction rate, selectivity and product solubility. The choice of polar solvent or non-polar solvent depends on the characteristics of the reaction and the properties of the reactants. And in the entire synthesis process, analysis and detection methods are indispensable, such as monitoring the reaction process by chromatography to determine the purity of the product; using spectroscopy, such as nuclear magnetic resonance spectroscopy, infrared spectroscopy, etc., to identify the structure of the product and ensure that the resulting product is the target, dimethyl 4- (furan-2-yl) -2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate.

Dimethyl 4- (furan-2-yl) -2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylic acid ester, this is an organic compound. Its physical properties are quite critical, and it is widely used in chemical, pharmaceutical and other fields. Knowing its physical properties is of great benefit to related research and applications.
First talk about the appearance. At room temperature and pressure, this compound is mostly in the state of white to light yellow crystalline powder. The texture is fine and uniform, and it has no impurities to the naked eye. It can be seen under light with fine crystalline luster.
And the melting point, which has been experimentally determined, is about 130-135 ° C. The melting point is an important physical constant of a substance. This temperature range can help identify its purity. If it contains impurities, the melting point tends to decrease and the melting range becomes wider.
In terms of boiling point, due to its structural characteristics, under specific pressure conditions, the boiling point is roughly 350-370 ° C. The boiling point reflects the energy required for a substance to change from a liquid state to a gaseous state, which is of great significance for its separation and purification.
Solubility is also an important property. The compound is slightly soluble in water, because water is a polar solvent, and the molecular polarity of this compound is relatively weak, and the interaction between the two is not strong. But it is soluble in common organic solvents, such as ethanol, chloroform, dichloromethane, etc. In ethanol, under appropriate temperature and stirring conditions, it can be better dissolved to form a clear solution. This property provides convenience for its application in organic synthesis and drug preparation, because many reactions are carried out in organic solvents.
The density is about 1.25 - 1.30 g/cm ³, and the density reflects the mass per unit volume of the substance, which has reference value in solution preparation, reaction system design, etc.
In addition, the chemical properties of this compound are relatively stable at room temperature. When encountering specific chemicals such as strong oxidants, strong acids, and strong bases, chemical reactions may occur and change its structure and properties. Therefore, such substances should be avoided when storing, and stored in a cool, dry, and well-ventilated place to prevent deterioration.

Dimethyl 4- (furan-2-yl) -2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate, this compound has great potential in the chemical and pharmaceutical fields.
In today's market, in the field of chemical raw materials, with the booming fine chemical industry, the demand for many new materials and special chemicals is increasing. As a key organic synthesis intermediate, this dihydropyridine compound can be used to construct a multi-component complex organic molecular structure, and may play an important role in the synthesis of materials with specific functions, such as photochromic materials, conductive polymers, etc., so there is room for expansion in the chemical raw materials market.
In the field of pharmaceutical research and development, many studies have revealed that dihydropyridine compounds have a variety of biological activities, such as calcium channel blockade, antioxidation, etc. The dimethyl 4- (furan-2-yl) -2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate with this specific structure, after reasonable modification and optimization, may be developed into new cardiovascular disease treatment drugs, or emerge as neuroprotective drugs. With the advancement of medical science and technology, the exploration of novel active compounds continues to deepen, and there are many opportunities in the front-end field of pharmaceutical research and development.
However, there are also challenges. The synthesis process needs to be further optimized to improve yield, reduce costs, and enhance market competitiveness. At the same time, drug development has to go through rigorous clinical trials and verification, with a long cycle and huge investment. But overall, the market prospect of dimethyl 4- (furan-2-yl) -2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate is promising, and it may shine in the chemical and pharmaceutical markets over time.