This product Ethyl 6- (4-iodophenyl) -1- (4-methoxyphenyl) -7-oxo-4,5,6, 7-tetrahydro-1h-pyrazolo [3,4-c] What is the main use of pyridine-3-carboxylate

Ethyl 6- (4-iodophenyl) -1- (4-methoxyphenyl) -7-oxo-4,5,6,7-tetrahydro-1H-pyrazolo [3,4-c] pyridine-3-carboxylate This compound is a key intermediate in the field of organic synthesis. It shines brightly in the field of medicinal chemistry.

In the research and development of medicine, the creation of many drug molecules needs to be based on such compounds containing specific heterocyclic structures. The unique structure of this compound can precisely fit with specific targets in the body, just like the tenon and tenon, thus showing significant pharmacological activity. For example, in the exploration of anti-cancer drugs, it may participate in the construction of molecular architectures with the ability to inhibit the proliferation of cancer cells; in the development of drugs for the treatment of neurological diseases, it may also play a key role in regulating neurotransmitter transmission or repairing nerve cell function.

In the field of materials science, it has also emerged. The development of organic optoelectronic materials is changing rapidly, and these compounds may become the cornerstone of the preparation of high-performance optoelectronic materials due to their special electronic properties. It may optimize the performance of organic Light Emitting Diodes (OLEDs) to improve their luminous efficiency and stability; it may also play an important role in organic solar cell materials to improve the efficiency of light energy conversion.

In short, Ethyl 6- (4-iodophenyl) -1- (4-methoxyphenyl) -7-oxo-4,5,6,7-tetrahydro-1H-pyrazolo [3,4-c] pyridine-3-carboxylate in the field of medicine and materials science, like a shining star, for the progress of related fields, providing unlimited possibilities and opportunities.

What are the synthesis methods of Ethyl 6- (4-iodophenyl) -1- (4-methoxyphenyl) -7-oxo-4,5,6,7-tetrahydro-1h-pyrazolo [3,4-c] pyridine-3-carboxylate

Ethyl 6- (4 - iodophenyl) -1- (4 - methoxyphenyl) -7 - oxo - 4,5,6,7 - tetrahydro - 1H - pyrazolo [3,4 - c] pyridine - 3 - carboxylate is an organic compound, and its synthesis method is quite complicated. Let me explain in detail for you.

To synthesize this compound, pyridine or pyrazole compounds containing corresponding substituents are often used as the starting materials. The first step may require a nucleophilic substitution reaction to make specific halogenated aromatics interact with nitrogen-containing heterocyclic compounds. In this process, the halogen atom acts as the leaving group, and the nitrogen atom launches a nucleophilic attack with its lone pair of electrons to form a new carbon-nitrogen bond.

Afterwards, oxidation or reduction reactions may be required to adjust the oxidation state of some functional groups in the molecule. For example, a specific alcohol hydroxyl group can be oxidized to a carbonyl group by using a suitable oxidant, or an unsaturated bond can be reduced with a reducing agent to achieve the structural requirements of the target molecule.

Furthermore, the cyclization reaction is also a key step. The dense ring structure of pyrazolopyridine can be constructed through nucleophilic addition or elimination reactions in the molecule. This process requires precise control of reaction conditions, such as temperature, solvent and catalyst.

In addition, during the reaction process, the separation and purification of the reaction intermediates are also crucial. Column chromatography, recrystallization and other means are often used to ensure the purity of the intermediate, thereby improving the quality of the final product.

In addition, the design of the synthesis route needs to take into account the availability of starting materials, the simplicity of the reaction steps and the yield. In this way, through the careful design and operation of multiple steps, it is expected that Ethyl 6- (4-iodophenyl) -1- (4-methoxyphenyl) -7-oxo-4,5,6,7-tetrahydro-1H-pyrazolo [3,4-c] pyridine-3-carboxylate can be successfully synthesized.

What are the physical and chemical properties of Ethyl 6- (4-iodophenyl) -1- (4-methoxyphenyl) -7-oxo-4,5,6,7-tetrahydro-1h-pyrazolo [3,4-c] pyridine-3-carboxylate

Ethyl 6- (4-iodophenyl) -1- (4-methoxyphenyl) -7-oxo-4,5,6,7-tetrahydro-1H-pyrazolo [3,4-c] pyridine-3-carboxylate is an organic compound. Its physical and chemical properties are as follows:

Looking at its appearance, it often takes a solid state. Due to the intermolecular force, it has a relatively orderly arrangement at room temperature and pressure. Melting point is a key physical property, but the specific value needs to be accurately determined by experiment, and it fluctuates due to different purity and experimental conditions or melting point. Generally speaking, the melting point of organic solids depends on the molecular structure and interaction. The compound contains aromatic rings, heterocycles and carbonyl groups, etc. The intermolecular force is complex, or the melting point is within a certain range.

In terms of solubility, it is more soluble in organic solvents or better than water. Due to its molecular structure containing more hydrophobic groups, such as aromatic rings, its interaction with water is weak. Common organic solvents such as dichloromethane, chloroform, N, N-dimethylformamide (DMF), etc., or due to the formation of van der Waals force and dipole-dipole interaction with compound molecules, it has good solubility. In dichloromethane, due to its moderate polarity and certain lipid solubility, it matches the structure of the compound and may be well miscible.

When it comes to chemical properties, iodine atoms have high reactivity on 4-iodophenyl groups and can participate in a variety of organic reactions. If under the action of an appropriate catalyst, a coupling reaction can occur, and a new carbon-carbon bond can be formed by reacting with other organometallic reagents, providing the possibility for the construction of complex organic structures. Carbonyl (7-oxo) is electrophilic and can react with nucleophilic reagents such as alcohols and amines, such as reacting with alcohols or forming acetals, reacting with amines or forming imines. These reactions are important pathways for the derivatization and functionalization of the compound. Although methoxy (4-methoxyphenyl) is relatively stable, under certain conditions, such as strongly acidic or basic environments, or demethylation reactions, the molecular structure and properties are changed. In addition, the heterocyclic structure endows compounds with unique electron cloud distribution and reactivity, which can participate in cyclization, ring opening and other reactions, enriching their chemical transformation paths.

Ethyl 6- (4-iodophenyl) -1- (4-methoxyphenyl) -7-oxo-4,5,6,7-tetrahydro-1h-pyrazolo [3,4-c] pyridine-3-carboxylate What is the price range in the market?

Ethyl 6- (4 - iodophenyl) -1- (4 - methoxyphenyl) -7 - oxo - 4,5,6,7 - tetrahydro - 1H - pyrazolo [3,4 - c] pyridine - 3 - carboxylate is a more complex organic compound. However, on the market, its price range is quite difficult to specify. Due to many factors, its price will be affected.

First, the purity of this compound has a huge impact on the price. If the purity is very high, it is almost up to the standard for high-end scientific research or specific pharmaceutical production, and the price is often expensive. If the purity is slightly lower, it is only for general research or industrial preliminary application, and the price will be reduced.

Second, the market supply and demand relationship is also the key. If for a while, many scientific research institutions or enterprises have strong demand for this compound, but the supply is limited, the price will rise; conversely, if the market demand is low, and there are many manufacturers and sufficient supply, the price will fall.

Third, the cost of producing this compound also affects its price. The cost of raw materials, the complexity of the synthesis process, and the equipment and manpower required in the production process are all components of the cost. If the raw materials are scarce and expensive, the synthesis process is cumbersome, and the cost will naturally increase, the price will also increase accordingly.

In general, without more detailed market survey and analysis, it is difficult to determine the exact price range of Ethyl 6- (4 - iodophenyl) -1- (4 - methoxyphenyl) -7 - oxo - 4,5,6,7 - tetrahydro - 1H - pyrazolo [3,4 - c] pyridine - 3 - carboxylate. However, it can be roughly speculated that in the scientific research reagent market, the price per gram may range from tens of yuan to thousands of yuan depending on different purity. In the industrial application field, due to the large demand, in kilograms, the price may fluctuate between hundreds of yuan and tens of thousands of yuan per kilogram according to the above factors.

Ethyl 6- (4-iodophenyl) -1- (4-methoxyphenyl) -7-oxo-4,5,6,7-tetrahydro-1h-pyrazolo [3,4-c] What are the storage conditions pyridine-3-carboxylate

Ethyl 6- (4-iodophenyl) -1- (4-methoxyphenyl) -7-oxo-4,5,6,7-tetrahydro-1H-pyrazolo [3,4-c] pyridine-3-carboxylate is an organic compound. To properly store this compound, many conditions need to be paid attention to.

First, it should be placed in a cool place. This is because the temperature is too high, or the molecular activity of the compound is enhanced, triggering a chemical reaction, causing its structure to be damaged and its properties to be changed. If it is hot on a summer day, the sun is like fire, if the compound is exposed to a high temperature environment, it may deteriorate rapidly.

Second, be sure to keep it dry. Moisture or water vapor can cause the compound to undergo reactions such as hydrolysis. If the storage place is humid and the water vapor is lingering, it is easy to cause the composition of the compound to change, reducing the purity and quality.

Third, it needs to be stored in dark conditions. Light or providing energy prompts the compound to undergo photochemical reactions, which in turn changes its chemical structure and properties. Just as direct sunlight accelerates the aging and deterioration of many substances, this compound is no exception.

Fourth, ensure that it is sealed and stored. Sealing can avoid contact with gases such as oxygen and carbon dioxide in the air. Oxygen or compounds cause oxidation, and carbon dioxide may participate in chemical reactions, affecting their stability and quality. When storing Ethyl 6- (4-iodophenyl) -1- (4-methoxyphenyl) -7-oxo-4,5,6,7-tetrahydro-1H-pyrazolo [3,4-c] pyridine-3-carboxylate, a cool, dry, dark and sealed environment is critical to maintain its chemical stability and ensure quality and purity.