2-Cyano-1,4-dihydro-6-methyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic Acid 3-Methyl 5-(1-Methylethyl) Ester

This is the name of an organic compound, which is analyzed in modern chemical terms. It contains many functional groups and structural characteristics. To clarify its chemical structure, it is necessary to start with the parts of the name.
"2 - Cyano - 1,4 - dihydro - 6 - methyl - 4 - (3 - nitrophenyl) - 3,5 - pyridinedicarboxylic Acid", this part reveals the existence of the pyridine ring. The pyridine ring is a six-membered nitrogen-containing heterocycle, and 1,4 - dihydro indicates that the 1,4 positions of the pyridine ring are dihydro structures. 2-Cyano refers to the presence of a cyano group (-CN) at the 2nd position of the pyridine ring, 6-methyl means that there is a methyl group (-CH 🥰) at the 6th position, 4- (3-nitrophenyl) means that there is a 3-nitrophenyl group at the 4th position (-C H NO ³, nitro is attached to the interposition of the benzene ring), and the 3,5-position is a pyridinedicarboxylic acid structure.
"3-Methyl 5- (1 - Methylethyl) Ester", which is the ester structure of pyridinedicarboxylic acid. 3-Methyl, that is, 3-carboxyl group forms methyl esters (- COOCH (CH
), and 5- (1-Methylethyl) indicates that 5-carboxyl group forms isopropyl ester (- COOCH (CH <)
In summary, the structure of this compound is 1, 4-dihydro-6-methyl-4 - (3-nitrophenyl) -pyridine-3,5-dicarboxylic acid as the core skeleton, 2-cyano group, 3-carboxyl group forms methyl ester, and 5-carboxyl group forms isopropyl ester. Although there is no visual illustration, through the analysis of this text, the approximate chemical structure has been clearly presented, and the delicacy of organic chemistry is evident in the correspondence between structure and naming.

2-Cyano-1,4-dihydro-6-methyl-4- (3-nitrophenyl) -3,5-pyridinedicarboxylic acid 3-methyl-5- (1-methyl ethyl) ester, which is widely used.
In the field of pharmaceutical chemistry, or as a key intermediate for the creation of new drugs. Its structure is unique, or it can be chemically modified to develop compounds with specific pharmacological activities. Taking the development of antimalarial drugs as an example, many drugs in the past were modified based on specific heterocyclic structures. The pyridyl dicarboxylate structure of this compound may provide novel ideas for the creation of new antimalarial drugs.
In the field of materials science, or can participate in the preparation of functional materials. Because it contains functional groups such as cyanide groups and nitro groups, it may endow materials with special photoelectric properties. In ancient times, materials with unique optical properties were prepared by using specific chemical substances. Today, this compound can be used as a raw material to prepare new functional materials that can be used in optical displays and optoelectronic devices.
In the field of organic synthesis, it is an important synthetic building block, which can build more complex organic molecular structures through various organic reactions. Just as ancient craftsmen built exquisite buildings with basic components, today's chemists can use it to use reactions such as esterification and substitution to synthesize fine chemicals with higher added value for flavors, pesticides and other industries. In short, it has potential application value in many fields and needs to be further studied and developed.

The synthesis method of 2-cyano-1,4-dihydro-6-methyl-4- (3-nitrophenyl) -3,5-pyridinedicarboxylic acid 3-methyl-5- (1-methylethyl) ester, although the ancient books do not have the details of this modern chemical synthesis, it can be logically deduced by imitating the ancient method.
At the beginning of the synthesis, it is necessary to find a suitable starting material. Pyridine derivatives with corresponding substituents can be selected as the basis for the construction of the target molecule pyridine ring. If the pyridine compound containing methyl, nitrophenyl and other groups is used as the starting point, just like the ancient method of alchemy, the selection of materials is the key.
Then, the cyano group is introduced. It can be used for nucleophilic substitution or addition reaction to connect the cyano group to the specific position of the pyridine ring. This step is similar to the ancient method of processing, and requires precise control of the reaction conditions, such as temperature and solvent. If the temperature is too high, it may cause side reactions, such as excessive reaction of cyanyl groups or structural damage of the pyridine ring; if the temperature is too low, the reaction will be delayed or the expected transformation will not be achieved.
As for the construction of the dihydropyridine ring, a suitable reduction reaction may be used to partially hydrogenate the pyridine ring. This process also requires caution. Due to improper hydrogenation, it will also affect the structure of the product. Just like the ancient method of making medicine, the choice of heat is crucial to success or failure.
Synthetic ester-based moiety can be obtained by esterification of the corresponding carboxylic acid and alcohol in the presence of a catalyst. Select an appropriate catalyst to control the reaction time and temperature to ensure the efficient generation of ester groups. This is like the ancient method of preparing a drug, the ratio and timing need to be just right.
In addition, the reaction process needs to be monitored at all times during the reaction process to ensure that every step meets expectations. Modern analytical methods can be used, analogous to the observation and judgment of ancient methods, and the reaction parameters can be adjusted in time. In this way, 2-cyano-1,4-dihydro-6-methyl-4- (3-nitrophenyl) -3,5-pyridinedicarboxylic acid 3-methyl-5- (1-methylethyl) ester can be obtained through delicate operation in multiple steps.

2-Cyano-1,4-dihydro-6-methyl-4- (3-nitrophenyl) -3,5-pyridinedicarboxylic acid 3-methyl-5- (1-methylethyl) ester, the physical properties of this substance are critical to its many applications.
Looking at its morphology, it is often in a solid state, and the color may be white to light yellow. This color and morphological characteristics are the basis for the initial identification of this substance. Its melting point is also an important physical property, but the specific value needs to be determined by precise experiments. The melting point plays a huge role in the identification of the purity of substances and the study of phase transformation.
When it comes to solubility, this substance behaves differently in common organic solvents. In polar organic solvents, such as methanol and ethanol, it may have a certain solubility. This property makes the substance can participate in reactions as a solute in organic synthesis, drug preparation and other fields. In non-polar solvents, such as n-hexane and cyclohexane, the solubility may be low. This difference in solubility is due to the difference between the molecular structure of the substance and the interaction between the solvent molecules.
Furthermore, its density is also an important part of physical properties. Although the exact density value needs to be precisely measured experimentally, the density is related to the distribution state of the substance in the mixture, which is of great significance for industrial production, product separation and other links.
In addition, the stability of the substance cannot be ignored. Under normal temperature and pressure conditions, it may have certain stability. In case of extreme conditions such as high temperature, strong acid, and strong base, the molecular structure may change, resulting in changes in chemical properties. This stability characteristic determines the conditions for storage and transportation of substances.
In summary, the morphology, melting point, solubility, density and stability of 2-cyano-1,4-dihydro-6-methyl-4- (3-nitrophenyl) -3,5-pyridinedicarboxylic acid 3-methyl-5- (1-methylethyl) ester are of great significance for its application in chemical and pharmaceutical fields.

There are currently 2-cyano-1,4-dihydro-6-methyl-4- (3-nitrophenyl) -3,5-pyridinedicarboxylic acid 3-methyl-5- (1-methyl ethyl) ester, and its market prospects are many.
This compound may have potential utility in the field of pharmaceutical research and development. For example, in the creation of innovative drugs, its unique chemical structure may become the key to conquering specific disease targets. With today's medical development trend, the demand for novel and targeted drugs is on the rise. If this compound can be studied in depth and demonstrate significant efficacy for certain diseases, it will definitely gain a place in the pharmaceutical market.
In terms of chemical materials, its properties may endow materials with special properties. In today's material field, the pursuit of high-performance, multi-functional materials is the general trend. If this compound can be used as an additive to improve the stability and durability of materials, chemical companies may increase its demand, thus opening up a broad market space.
However, its market prospects also pose challenges. If the process of synthesizing this compound is complex and costly, its large-scale production and application will be limited. And the market competition is fierce, and similar or alternative products will also share the share. Only by continuously optimizing the synthesis process, reducing costs, and exploring its unique advantages can we stand out in the market and seek long-term development.