2 Amino 7 Isopropyl 5 Oxo 5h 1 Benzopyrano 2 3 B Pyridine 3 Carboxylic Acid
pyridine pyrrole pyrazine piperidine piperazine

2-Amino-7-isopropyl-5-oxo-5H-[1]benzopyrano[2,3-b]pyridine-3-carboxylic Acid

    Specifications

    HS Code

    378326

    Chemical Formula C17H16N2O4
    Molecular Weight 312.32 g/mol
    Melting Point No experimental data available (predicted range: 250 - 280 °C)
    Boiling Point No experimental data available (predicted around 560 - 580 °C at 760 mmHg)
    Solubility In Water Low solubility, estimated to be less than 1 g/L at 25 °C
    Solubility In Organic Solvents Soluble in DMSO, DMF; limited solubility in ethanol
    Pka Predicted pKa values: carboxylic acid group around 3 - 4, pyridine - N - related pKa around 8 - 9
    Logp Predicted logP value around 2 - 3
    Stability Stable under normal conditions, but may decompose upon exposure to strong acids, bases or high temperatures

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    Frequently Asked Questions

    As a leading 2-Amino-7-isopropyl-5-oxo-5H-[1]benzopyrano[2,3-b]pyridine-3-carboxylic Acid 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 2-Amino-7-isopropyl-5-oxo-5H- [1] benzopyrano [2,3-b] pyridine-3-carboxylic Acid?
    2-Amino-7-isopropyl-5-oxo-5H-[ 1] benzopyrano [2,3-b] pyridine-3-carboxylic acid, this is the name of an organic compound. Looking at its name, if you want to deduce its chemical structure, follow the principles of organic chemistry.
    First look at the core structure of "[1] benzopyrano [2,3-b] pyridine". Benzopyran is formed by fusing the benzene ring with the pyran ring; and pyridine is also a common heterocyclic ring. The mother nuclear structure formed by the fusing of the two has a specific atomic connection mode and spatial configuration. Add "2-amino", that is, introduce an amino group (-NH _ 2) at position 2 of the parent nuclear structure; "7-isopropyl", which is connected with isopropyl (-CH (CH) _ 2) at position 7; "5-oxo", indicating that the carbon atom at position 5 is connected to the oxygen atom by a double bond, in the state of carbonyl (-C = O); "3-carboxylic acid", indicating that position 3 has a carboxyl group (-COOH).
    Overall, the chemical structure of this compound is: [1] benzopyrano [2,3-b] pyridine as the parent nucleus, with amino group at position 2, isopropyl at position 7, carbonyl at position 5, and carboxyl at position 3. In its structure, the benzene ring provides aromaticity, and the pyridine ring, pyran ring and various substituents endow the compound with specific physical and chemical properties, which may be of great significance in organic synthesis, medicinal chemistry and other fields.
    What are the main uses of 2-Amino-7-isopropyl-5-oxo-5H- [1] benzopyrano [2,3-b] pyridine-3-carboxylic Acid?
    2-Amino-7-isopropyl-5-oxo-5H-[ 1] benzopyrano [2,3-b] pyridine-3-carboxylic acid, which has a wide range of uses. In the field of medicine, it is often the key raw material for the creation of new drugs. Because of its specific chemical structure and biological activity, it can be chemically modified and modified to meet the needs of different diseases. For example, in the development of anti-tumor drugs, it may be possible to design and synthesize drugs that can precisely act on specific targets of tumor cells, interfere with the growth and proliferation of tumor cells, and provide new opportunities to overcome tumor diseases. < Br >
    In the chemical industry, it also plays an important role. It can be used as a starting material for the synthesis of special functional materials, and can be converted into materials with unique optical, electrical or mechanical properties through organic synthesis. For example, it is used to prepare optical materials with special response to specific wavelengths of light, and is used in optoelectronic devices, such as sensors, optical switches, etc., to promote the development of optoelectronic technology.
    In the field of scientific research and exploration, it is an important chemical tool. By studying its reaction characteristics and interactions with other substances, researchers can gain in-depth insight into the reaction mechanism of organic chemistry, and contribute to the improvement of the theoretical system of organic chemistry. At the same time, in the development of novel synthetic methodologies, its structural complexity provides chemists with challenges and opportunities, motivating them to explore more efficient and green synthetic paths and improve the level of organic synthetic chemistry.
    What is the synthesis method of 2-Amino-7-isopropyl-5-oxo-5H- [1] benzopyrano [2,3-b] pyridine-3-carboxylic Acid?
    To prepare 2-amino-7-isopropyl-5-oxo-5H-[ 1] benzopyrano [2,3-b] pyridine-3-carboxylic acid, the method is as follows:
    Take an appropriate amount of starting materials first, and carefully select compounds of high quality and purity. This is the foundation for the successful reaction. Starting with benzopyran and pyridine derivatives with specific structures, because their structures are similar to the target products, the desired structure can be gradually constructed by clever reactions.
    Then the key cyclization reaction is carried out, and this step requires precise regulation of the reaction conditions. In a suitable reaction vessel, add an appropriate amount of catalyst and solvent. Catalysts such as specific Lewis acids or bases can effectively promote intramolecular cyclization and accelerate the formation of target ring systems. The choice of solvent is also critical. Polarity and solubility adapters need to be selected to ensure that the reactants are fully dissolved and contacted. For example, common organic solvents such as dichloromethane, N, N-dimethylformamide are selected. Control the reaction temperature and time, usually under mild heating conditions, lasting from several hours to tens of hours. Depending on the reaction process, it is monitored by thin-layer chromatography and other means. When the reaction reaches the expected level, the preliminary cyclization product is obtained.
    Then the product is modified to introduce specific groups at the check points such as amino and isopropyl. This modification step requires the selection of appropriate reagents and reaction paths according to the characteristics of each group. If isopropyl is introduced, the nucleophilic substitution reaction can occur under basic conditions through halogenated isopropane and the corresponding activity check point. The modification of amino groups can be achieved by acylation, alkylation and other reactions. During the reaction process, the reaction conditions need to be precisely controlled to ensure the selectivity of the reaction and avoid unnecessary side reactions.
    Furthermore, for the construction of carboxylic groups, suitable carboxylic acid derivatives can be used to convert them through hydrolysis, oxidation and other reactions. During the hydrolysis reaction, an appropriate base or acid is selected as a catalyst, reacted at a suitable temperature, and then acidified to obtain a carboxylic group. For the oxidation reaction, a specific oxidant needs to be selected to ensure the precise degree of oxidation, and only the target carboxyl group is generated.
    Finally, the product is separated and purified. Using classic methods such as column chromatography and recrystallization to remove residual impurities, unreacted raw materials and by-products in the reaction system. Column chromatography can be separated according to the polarity difference of the compound, and recrystallization can purify the product by different solubility of the compound at different temperatures. After these steps, high purity 2-amino-7-isopropyl-5-oxo-5H-[ 1] benzopyrano [2,3-b] pyridine-3-carboxylic acid can be obtained. The whole synthesis process requires the experimenter to be skilled and fine in operation to obtain satisfactory results.
    What are the physical properties of 2-Amino-7-isopropyl-5-oxo-5H- [1] benzopyrano [2,3-b] pyridine-3-carboxylic Acid?
    2-Amino-7-isopropyl-5-oxo-5H-[ 1] benzopyrano [2,3-b] pyridine-3-carboxylic acid, which is an organic compound. Its physical properties are as follows.
    Looking at its properties, under normal temperature and pressure, it is often in a solid state, mostly in the state of crystalline powder, which is due to its intermolecular forces and lattice structure. The powder is fine in texture, or has a specific crystal shape, which varies depending on the preparation conditions.
    When it comes to melting point, the melting point of this compound is quite critical. Due to the chemical bonds and interactions in the molecular structure, when it reaches a certain temperature, the lattice disintegrates and turns into a liquid state. However, its exact melting point needs to be accurately determined by professional experiments and thermal analysis instruments, such as differential scanning calorimeters (DSC), melting point meters, etc. Different literatures may vary slightly due to differences in purity and test conditions.
    In terms of solubility, it behaves differently from organic solvents. In polar organic solvents, such as methanol and ethanol, it may have a certain solubility. Because polar solvents and compound molecules can form hydrogen bonds and dipole-dipole interactions, which help them disperse and dissolve. In non-polar solvents, such as n-hexane and benzene, the solubility may be very low, due to the weak interaction between non-polar solvents and polar compounds. In water, its solubility is also limited, because although the molecule contains polar carboxyl groups and amino groups, the large benzopyrano-pyridine structure reduces the overall water solubility.
    Again, although there is no exact literature data, it can be speculated according to the structure and similar compounds. Its molecules contain ring-like structures such as benzene rings and pyridine rings, with close atomic arrangement and relatively high density. To obtain an accurate density value, it is necessary to borrow a density measuring instrument to measure it under specific temperature and pressure conditions.
    As for the appearance color, in a pure state, or in a white to light yellow powder. If it contains impurities, the color may change, such as trace metal impurities, or cause color deepening.
    The physical properties of this compound are of great significance for its synthesis, separation, purification and application. Know the melting point, control the heating temperature, for crystallization and purification; understand the solubility, and can choose a suitable solvent for reaction medium, recrystallization or separation.
    2-Amino-7-isopropyl-5-oxo-5H- [1] benzopyrano [2,3-b] What is the market outlook for pyridine-3-carboxylic Acid?
    2-Amino-7-isopropyl-5-oxo-5H-[ 1] benzopyrano [2,3-b] pyridine-3-carboxylic acid, the market prospect of this product is like a cloud in the sky, unpredictable and uncertain.
    In today's world, the pharmaceutical and chemical industries are booming, and such compounds have potential in the field of drug research and development. They may be the cornerstone of creating new drugs to treat various diseases, so they have attracted a lot of scientific researchers to study them. However, the road to the market is full of thorns, opportunities and challenges coexist.
    Looking at it from the demand side, the pharmaceutical market is hungry for innovative drugs. If this compound can be rigorously studied and proved to have unique pharmacological effects and be safe, it is expected to win the favor of the market, and the demand may be like a prairie fire, gradually becoming a trend.
    However, looking at it from the competitive side, the road of research and development has started with a group of heroes, and a hundred schools of thought are contending. Many scientific research teams and pharmaceutical companies are committed to the exploration of new compounds, and the competition is intense, which is like thousands of troops crossing a bridge. To stand out among them requires extraordinary wisdom, tenacity, and strong resources.
    Furthermore, the system of regulations is also the key. Drug research and development must go through many reviews and strict standards. If you are not careful, all your efforts will be wasted. Only by strictly abiding by regulations and working step by step can you gain a place in the market.
    In general, the market prospect of 2-amino-7-isopropyl-5-oxo-5H - [1] benzopyrano [2,3-b] pyridine-3-carboxylic acid, although the dawn is emerging, there is a long way to go. Practitioners need to gain insight into the current situation and move forward with determination in order to have the opportunity to achieve good results in the market.