A Methyl 5h 1 Benzopyrano 2 3 B Pyridine 7 Acetic Acid
pyridine pyrrole pyrazine piperidine piperazine

a-Methyl-5H-[1]benzopyrano[2,3-b]pyridine-7-acetic Acid

    Specifications

    HS Code

    407076

    Chemical Formula C17H15NO4
    Molar Mass 297.306 g/mol
    Physical State Solid (usually)
    Appearance Colorless to white crystalline powder
    Solubility In Water Low solubility
    Solubility In Organic Solvents Soluble in some organic solvents like DMSO, methanol
    Melting Point Data needed for exact value
    Boiling Point Data needed for exact value
    Pka Value Data needed for exact value
    Logp Value Data needed for exact value

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    General Information
    Where to Buy a-Methyl-5H-[1]benzopyrano[2,3-b]pyridine-7-acetic Acid in China?
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    Frequently Asked Questions

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    What is the chemical structure of a-Methyl-5H- [1] benzopyrano [2,3-b] pyridine-7-acetic Acid
    Alas! Now I want to talk about the chemical structure of "a - Methyl - 5H - [1] benzopyrano [2,3 - b] pyridine - 7 - acetic Acid". This is the name of an organic compound. To clarify its structure, we need to analyze its name in detail.
    "a - Methyl" is shown to be connected to a methyl group at a specific location. " 5H - [1] benzopyrano [2,3 - b] pyridine "In this part, [1] benzopyrano shows the basic structure of benzopyran, the number 5H indicates the specific positional relationship of its unsaturated bond and ring system, while [2,3 - b] pyridine shows that the pyridine ring is fused with the benzopyran ring in a specific way, that is, the pyridine ring is connected to the benzopyran ring in a b-type manner at the 2,3 position.
    As for" -7-acetic Acid ", it indicates that there is an acetate group attached at the 7th position of the entire fused ring system.
    Overall, the chemical structure of this compound is based on the fused ring system of benzopyran and pyridine, with methyl at the a position and acetic acid at the 7 position. Its structure is complex and delicate, reflecting the precise description of complex molecular structures by organic chemical nomenclature. The characteristics and properties of this structure may affect its chemical activity, physical properties and behavior in various chemical reactions and biological processes.
    What are the main uses of a-Methyl-5H- [1] benzopyrano [2,3-b] pyridine-7-acetic Acid
    A-methyl-5H-[ 1] benzopyrano [2,3-b] pyridine-7-acetic acid has a wide range of uses. In the field of medicine, it can be used as an active ingredient to create new drugs. Due to its unique structure and specific pharmacological activity, it may act on specific targets in the human body, bringing hope for the treatment of certain diseases, such as the treatment of specific diseases, it can use its special chemical properties to regulate human physiology and hope to improve the condition.
    In the field of chemical research, it is an important intermediate in organic synthesis. Chemists can use it to build more complex compounds, expand the variety of organic compounds through various chemical reactions, such as substitution, addition, etc., and assist in the development of new drugs and materials science exploration.
    In the field of materials science, it may have potential applications. Because of its unique chemical structure, or endowing materials with special properties, such as optical and electrical properties, it provides the possibility for the creation of new materials, such as for the development of polymer materials with special functions.
    In conclusion, a-methyl-5H- [1] benzopyrano [2,3-b] pyridine-7-acetic acid has shown important application value in many fields such as medicine, chemical research, and materials science. With the deepening of research, more potential uses may be explored.
    What are the physical properties of a-Methyl-5H- [1] benzopyrano [2,3-b] pyridine-7-acetic Acid
    A-methyl-5H-[ 1] benzopyrano [2,3-b] pyridine-7-acetic acid, this is an organic compound. Its physical properties are quite critical and related to applications in many fields.
    First of all, its appearance is often white to light yellow crystalline powder, delicate and uniform, and it is pure in appearance. This form has advantages in storage and transportation, and it can maintain its stability.
    When it comes to melting point, it has been accurately determined to be in a specific temperature range. Melting point is an important marker of compounds, which can help identify purity. If the purity is high, the melting point range is narrow and close to the theoretical value; if it contains impurities, the melting point is reduced and the range is wider.
    Solubility is also a key property. In common organic solvents, such as ethanol, dichloromethane, etc., it exhibits a certain solubility. In ethanol, with the increase of temperature, the solubility gradually increases. This characteristic can be used in synthesis and purification processes to achieve separation and purification of compounds by temperature regulation.
    In water, the solubility is relatively limited. This characteristic makes the compound need special consideration when applying in aqueous systems, either with the help of surfactants or with the selection of suitable co-solvents to increase solubility, to meet specific experimental or production needs.
    Furthermore, its density also has corresponding values. Density is related to the degree of material accumulation. In the preparation, preparation and other operations, accurate knowledge of density can accurately control the dosage to ensure uniform and stable product quality. < Br >
    Its stability is good at room temperature and pressure, but when exposed to high temperature, strong light or a specific chemical environment, the structure may change. Under strong light irradiation, the electrons in the molecule transition, or cause chemical reactions to cause structural changes. Therefore, it is necessary to avoid light and control temperature during storage to ensure its quality and activity.
    What are the synthesis methods of a-Methyl-5H- [1] benzopyrano [2,3-b] pyridine-7-acetic Acid
    To prepare α-methyl-5H- [1] benzopyrano [2,3-b] pyridine-7-acetic acid, there are many methods, which are described in detail below.
    Take an appropriate amount of starting materials first, and choose those with similar structures and easy conversion. If benzopyran and pyridine derivatives with appropriate substituents are used as bases, the structures of these two are similar to the parent core part of the target product, which can lay the foundation for the reaction.
    In the reaction kettle, add the selected raw materials and mix them in a certain proportion. Adding an appropriate amount of catalyst is the key to the choice of catalyst, which can accelerate the reaction process and change the rate and direction of the chemical reaction. For example, a specific metal salt or organic base catalyst is selected, and its interaction with the reactant molecules promotes the fracture and recombination of chemical bonds.
    regulates the temperature and pressure of the reaction. Temperature needs to be precisely controlled, because the reaction rate and product selectivity vary at different temperatures. Generally speaking, moderate heating can accelerate the reaction rate, but excessive temperature or increase side reactions. Pressure also needs to be adapted, either under normal pressure or in a moderate pressurized environment, depending on the specific needs of the reaction.
    During the reaction process, close monitoring is required. The consumption of reactants and the formation of products can be detected by means of thin-layer chromatography, liquid chromatography and other analytical methods. When the reaction reaches the expected level, the reaction is terminated.
    Subsequent separation and purification are also indispensable. After extraction and column chromatography, impurities in the reaction system are removed to obtain pure α-methyl-5H- [1] benzopyrano [2,3-b] pyridine-7-acetic acid products. During extraction, an appropriate organic solvent is selected to separate the product and impurities in different solvent phases. Column chromatography achieves the purpose of purification according to the difference in adsorption and elution characteristics of the product and impurities.
    A-Methyl-5H- [1] benzopyrano [2,3-b] pyridine-7-acetic Acid
    A-methyl-5H-[ 1] benzopyrano [2,3-b] pyridine-7-acetic acid, this substance is a matter of safety and should not be ignored. Its nature is unknown, or it has potential risks.
    When taking it, you must be cautious. Check the classics carefully first to know its physical and chemical properties, such as the point of melting and boiling, the dissolution, and the degree of acid and alkali, to understand the changes in contact with other things, to prevent accidents. The place of operation must be clean and bright, and the ventilation must be good, so as to prevent it from gathering gas and causing danger.
    The person who manages it should also be well protected. Dress in special clothes, wear a tough cover on your hands, cover your face with eye-protecting mirrors, and cover your mouth and nose to avoid it from entering your body. If you accidentally touch it, rinse it with water as soon as possible, and in severe cases, seek medical treatment for medicine.
    When storing, choose a cool and dry place, away from the source of fire heat, and separate it from other objects to prevent it from reacting. The logo is clear, so that people can know the risk at a glance.
    When handling, handle it with care, do not collide, and prevent it from leaking. If there is a leak, take measures quickly, contain and clean it up, and do not spread. This is all about the importance of safety, and must not be forgotten. You must always keep it in mind to keep it safe.