Ethyl 6 4 Aminophenyl 1 4 Methoxyphenyl 7 Oxo 4 5 6 7 Tetrahydro 1h Pyrazolo 3 4 C Pyridine 3 Carboxylate
pyridine pyrrole pyrazine piperidine piperazine

ethyl 6-(4-aminophenyl)-1-(4-methoxyphenyl)-7-oxo-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridine-3-carboxylate

    Specifications

    HS Code

    972925

    Chemical Name ethyl 6-(4-aminophenyl)-1-(4-methoxyphenyl)-7-oxo-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridine-3-carboxylate
    Molecular Formula C23H23N3O4
    Molecular Weight 405.45 g/mol
    Appearance Solid (predicted, based on similar structures)
    Solubility In Water Low (due to non - polar aromatic groups)
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform (aromatic and polar - aprotic solvents)
    Logp High (hydrophobic due to aromatic rings, predicted logP > 3)

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    Frequently Asked Questions

    As a leading ethyl 6-(4-aminophenyl)-1-(4-methoxyphenyl)-7-oxo-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridine-3-carboxylate supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What is the chemical structure of ethyl 6- (4-aminophenyl) -1- (4-methoxyphenyl) -7-oxo-4,5,6,7-tetrahydro-1H-pyrazolo [3,4-c] pyridine-3-carboxylate
    This is the chemical structure analysis of "ethyl 6- (4-aminophenyl) -1- (4-methoxyphenyl) -7-oxo-4,5,6,7-tetrahydro-1H-pyrazolo [3,4-c] pyridine-3-carboxylate". According to its name, this compound is an organic molecule with a complex structure.
    First examine its main structure, which is composed of "1H-pyrazolo [3,4-c] pyridine". This is the parent nuclear structure of pyrazolo-pyridine, which is like the cornerstone of a building and lays the basic outline of the molecule. On the parent nucleus, there are many substituents at specific positions. < Br >
    At the 6th position, there is " (4-aminophenyl) ", that is, 4-aminophenyl group. In this substituent, the benzene ring is a stable hexavalent aromatic ring structure, and the amino group is a group with certain reactivity, or can participate in many chemical reactions, which affects the properties of the molecule. At the 1st position, there is " (4-methoxyphenyl) ", 4-methoxyphenyl, and the presence of methoxy groups changes the electron cloud density of the benzene ring, which in turn affects the electronic properties and steric resistance of the whole molecule. < Br >
    At position 7 is "7-oxo", that is, carbonyl. Carbonyl groups have strong polarity and have significant effects on the physical and chemical properties of molecules, such as boiling point, solubility and chemical reactivity. At position 3, there is "carboxylate", which is a carboxylate group, and its existence endows the molecule with specific chemical activity and physical properties.
    In addition, "4,5,6,7-tetrahydro" indicates that the double bonds at positions 4, 5, 6, and 7 of the parent nucleus are hydrogenated to become saturated single bonds. This structural change also plays an important role in the stability and reactivity of the molecule.
    In summary, this compound is composed of a specific parent nucleus and a combination of many different substituents, and each part interacts to jointly determine the unique chemical properties and potential applications of the molecule.
    What are the physical properties of ethyl 6- (4-aminophenyl) -1- (4-methoxyphenyl) -7-oxo-4,5,6,7-tetrahydro-1H-pyrazolo [3,4-c] pyridine-3-carboxylate
    Ethyl 6- (4-aminophenyl) -1- (4-methoxyphenyl) -7-oxo-4,5,6,7-tetrahydro-1H-pyrazolo [3,4-c] pyridine-3-carboxylate is an organic compound. Its physical properties are as follows:
    - ** Appearance **: It is often in powder form, which is convenient for the storage and transportation of compounds, and the large specific surface area of the powder is conducive to its full contact with other substances in chemical reactions and accelerates the reaction rate.
    - ** Solubility **: It has certain solubility in organic solvents such as dichloromethane, N, N -dimethylformamide (DMF). Dichloromethane, as a commonly used organic solvent, has good solubility and can dissolve many organic compounds. The compound can form a homogeneous solution in it, which provides convenience for related reactions or analysis; DMF is famous for its strong polarity and high solubility to various organic compounds, which helps the compound to disperse uniformly and participate in various reactions. However, its poor solubility in water is mainly due to the large proportion of hydrophobic groups in the compound molecule, and it is difficult to form effective interactions between water molecules and compound molecules.
    - ** Melting point **: The compound has a specific melting point, and the melting point is one of the key indicators for identifying the purity and characteristics of organic compounds. The specific molecular structure and intermolecular forces determine its melting point. By accurately measuring the melting point, the purity of the compound can be judged. If the melting point range is narrow, it indicates that the purity of the compound is high; conversely, a wide melting point range may mean that it contains impurities.
    - ** Stability **: Relatively stable under conventional environmental conditions, but should avoid contact with strong oxidants, strong acids, strong bases and other substances. Strong oxidants have the ability to seize electrons and may oxidize with the compound molecule, changing its chemical structure and properties; hydrogen ions or hydroxide ions in strong acids and strong bases easily react with some functional groups in the compound molecule, resulting in the destruction of the compound structure or the change of its properties. Therefore, suitable conditions need to be selected during storage to ensure its stability and maintain its chemical properties unchanged.
    What is the synthesis method of ethyl 6- (4-aminophenyl) -1- (4-methoxyphenyl) -7-oxo-4,5,6,7-tetrahydro-1H-pyrazolo [3,4-c] pyridine-3-carboxylate
    The method of preparing ethyl 6- (4-aminophenyl) -1- (4-methoxyphenyl) -7-oxo-4,5,6,7-tetrahydro-1H-pyrazolo [3,4-c] pyridine-3-carboxylate can be carried out according to the following steps.
    First, appropriate starting materials are taken, one of which is a compound containing 4-aminophenyl, and the other is a substance containing 4-methoxyphenyl, and related raw materials capable of constructing a pyrazolopyridine structure.
    At the beginning of the reaction, the above raw materials can be placed in a suitable reaction solvent, which needs to be able to dissolve the reactants well without adverse interference to the reaction, such as dichloromethane, N, N-dimethylformamide and the like.
    Then, add an appropriate amount of catalyst. This catalyst should promote the chemical reaction between the raw materials and accelerate the formation of the target product. For example, some Lewis acid catalysts can effectively catalyze the related cyclization reaction and the condensation reaction between functional groups.
    It is essential to control the reaction temperature and time. At the beginning of the reaction, the reactants can be initially mixed and interacted at a lower temperature, and then gradually heated to a suitable reaction temperature to promote the smooth progress of the reaction. Too high or too low temperature may lead to an increase in side reactions or a slow reaction rate. Generally speaking, the temperature can be controlled between 50 and 100 degrees Celsius, and the reaction time depends on the monitoring of the reaction process, which may take several hours or even tens of hours.
    During the reaction process, the progress of the reaction can be monitored by means of thin-layer chromatography (TLC) to clarify the consumption of raw materials and the formation of products. When the reaction is generally completed, that is, when the raw materials are exhausted and the amount of product formation does not increase significantly, the reaction is terminated.
    After that, the reaction mixture is post-processed. First, the target product is extracted with an appropriate organic solvent, and the target product is separated from the reaction system to remove impurities. The product is further purified by means of column chromatography to obtain high-purity ethyl 6- (4-aminophenyl) -1- (4-methoxyphenyl) -7-oxo-4,5,6,7-tetrahydro-1H-pyrazolo [3,4-c] pyridine-3-carboxylate. < Br >
    After this series of steps, the desired product can be obtained. However, in actual operation, depending on the specific experimental conditions and raw material characteristics, the reaction parameters and steps should be appropriately adjusted and optimized to achieve the best reaction effect.
    What are the application fields of ethyl 6- (4-aminophenyl) -1- (4-methoxyphenyl) -7-oxo-4,5,6,7-tetrahydro-1H-pyrazolo [3,4-c] pyridine-3-carboxylate
    Ethyl 6 - (4 - aminophenyl) - 1 - (4 - methoxyphenyl) - 7 - oxo - 4,5,6,7 - tetrahydro - 1H - pyrazolo [3,4 - c] pyridine - 3 - carboxylic acid ester, this is an organic compound. Its application field is quite wide, in the field of pharmaceutical research and development, often used as a key intermediate for the creation of new drugs.
    Guanfu Pharmaceutical Chemistry, the unique structure of this compound makes it have specific biological activity, which can be modified and modified to meet the needs of different diseases. For example, it may be able to target specific targets of tumor cells through precise design for certain tumor diseases, and then develop high-efficiency and low-toxicity anti-cancer drugs.
    In the field of materials science, it may also have outstanding performance. Due to its specific chemical structure and properties, it may be used to prepare materials with unique functions. For example, through rational design and synthesis, adsorbent materials with high selectivity for specific substances can be prepared, which is useful in environmental monitoring, separation and purification of substances, etc.
    Furthermore, in the field of organic synthetic chemistry, it is also an important cornerstone. Chemists can use this as a starting material to construct more complex and novel organic molecules through various organic reactions, expand the types and properties of organic compounds, and contribute to the progress of chemical science.
    In short, ethyl 6- (4-aminophenyl) -1- (4-methoxyphenyl) -7-oxo-4,5,6,7-tetrahydro-1H-pyrazolo [3,4-c] pyridine-3-carboxylic acid esters have great application potential in many fields such as medicine, materials, and organic synthesis, and are expected to bring new opportunities and breakthroughs for the development of various fields.
    Ethyl 6- (4-aminophenyl) -1- (4-methoxyphenyl) -7-oxo-4,5,6,7-tetrahydro-1H-pyrazolo [3,4-c] pyridine-3-carboxylate
    "Tiangong Kaiwu" focuses on the objective explanation of things in the classical Chinese style. The following is a similar style to "ethyl 6- (4-aminophenyl) -1- (4-methoxyphenyl) -7-oxo-4,5,6,7-tetrahydro-1H-pyrazolo [3,4-c] What is the market prospect of pyridine-3-carboxylate":
    Today there is a name ethyl 6- (4-aminophenyl) -1- (4-methoxyphenyl) -7-oxo-4,5,6,7-tetrahydro-1H-pyrazolo [3,4-c] pyridine-3-carboxylate, this is an organic compound. Looking at its market prospects, the first look at the field of medicine. In the field of pharmaceuticals, it may be the key raw material for the creation of new drugs. If it can understand pharmacology, adapt properly with other drugs, or become a cure for diseases, it will occupy a place in the pharmaceutical market and have a promising prospect.
    Furthermore, in the field of scientific research, such compounds have unique structures and can be the cornerstone of organic synthesis research. Scientists use their characteristics to explore new synthesis paths and reaction mechanisms. If there is a breakthrough, it can attract the attention of the academic community, and then promote its market demand.
    However, the market is also uncertain. The difficulty of synthesis and the level of cost are all constraints. If the synthesis process is complicated and the cost is high, it will be difficult for marketing activities. And the competition in the same industry is fierce. If other similar compounds take the lead and take the lead, their market expansion will also be hindered.
    Overall, ethyl 6- (4-aminophenyl) -1- (4-methoxyphenyl) -7-oxo-4,5,6,7-tetrahydro-1H-pyrazolo [3,4-c] pyridine-3-carboxylate The market prospect has both opportunities and challenges. If you can overcome the difficulty of synthesis, control the rise in costs, and take the innovation of medicine and scientific research as the wing, you may soar in the market and harvest good results; otherwise, you are afraid of the ups and downs in the market torrent.