2 Amino 3 Methyl 3h Imidazo 4 5 F Quinoline
quinoline thiophene imidazole thiazole

2-Amino-3-methyl-3H-imidazo[4,5-F]quinoline

    Specifications

    HS Code

    699619

    Chemical Formula C12H10N4
    Molecular Weight 210.24 g/mol
    Appearance Solid (color may vary)
    Solubility In Water Low (poorly soluble in water)
    Solubility In Organic Solvents Soluble in some organic solvents (e.g., DMSO)

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    General Information
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    Frequently Asked Questions

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    What are the main uses of 2-Amino-3-methyl-3H-imidazo [4,5-F] quinoline?
    2 - Amino - 3 - methyl - 3H - imidazo [4,5 - f] quinoline, Chinese name 2 - amino - 3 - methyl - 3H - imidazolo [4,5 - f] quinoline, the main use of this substance is general.
    In the field of research, it is often used as an active ingredient in the chemical. Due to its special chemical properties, it may have a therapeutic effect on certain diseases. For example, some studies on specific enzymes or receptors, exploring the interaction of 2-Amino-3-methyl-3H-imidazo [4,5-f] quinoline, are expected to generate novel compounds for the treatment of diseases such as tumors and inflammation.
    In terms of materials science, it can be used as a medium for synthesizing special functional materials. Using its chemical properties, it can be used to pass a series of reactions, and it can be introduced into polymer materials to give new properties of the materials, such as changing the optical properties and properties of the materials, making them useful in the fields of photonic devices, sensors, etc.
    In addition, in chemical analysis, it can be used for chemical analysis, for the determination or determination of specific compounds. Because of its ability to reverse the chemical properties of certain substances, it can generate observable images, such as chromatization, sedimentation, etc., and assist in chemical analysis and quantitative analysis of chemical compounds. In addition, 2-Amino-3-methyl-3H-imidazo [4,5-f] quinoline plays an important role in many important fields, and has a significant research and application value.
    What are the physical properties of 2-Amino-3-methyl-3H-imidazo [4,5-F] quinoline
    2-Amino-3-methyl-3H-imidazolo [4,5-f] quinoline, this is an organic compound. Its physical properties are unique and relevant to its application in many fields.
    Looking at its appearance, it is mostly solid at room temperature and pressure. The color of this compound is usually white to light yellow powder, delicate and uniform, like fine quicksand, gently twisted in the hand, smooth to the touch. This appearance feature provides an important basis for its identification and preliminary judgment.
    Melting point is also a key physical property. After precise determination, its melting point is in a specific temperature range, which is the inherent property of the compound. The determination of the melting point is like setting a precise temperature scale for it. Under this temperature, it is as stable as a rock and exists safely in a solid state; and when the temperature rises to the melting point range, that is, like ice and snow meeting warm sunlight, it gradually melts from a solid state to a liquid state, and the intermolecular forces change significantly in this process.
    In terms of solubility, it varies in common organic solvents. In some polar organic solvents, such as ethanol, it has a certain solubility, just like a fish entering water, and some molecules can interact with ethanol molecules and disperse them evenly; in non-polar organic solvents, such as n-hexane, the solubility is very small, just like oil and water, and it is difficult to blend. This difference in solubility has a profound impact on its reaction, separation and purification operations in different solvent systems.
    In addition, its density is also a specific value. Density represents the mass per unit volume of a substance, which is like a measure of its "compactness". This value is not only related to the physical state of the compound itself, but also has important significance in practical applications, such as the proportion of space to mass in the mixed system.
    The physical properties of 2-amino-3-methyl-3H-imidazolo [4,5-f] quinoline described above lay a solid foundation for in-depth understanding and rational application of this compound.
    What is the chemical synthesis method of 2-Amino-3-methyl-3H-imidazo [4,5-F] quinoline
    The synthesis of 2-amino-3-methyl-3H-imidazolo [4,5-f] quinoline is quite complicated and requires fine steps and ingenious skills to obtain it.
    The first to bear the brunt, the selection of raw materials is the key. It is often started with suitable quinoline derivatives, supplemented by specific reagents containing amino groups and methyl groups. For example, if a quinoline compound is selected, its structure needs to meet the requirements of the reaction mechanism and have a good reactivity check point. The compatible amino-containing reagents should be considered for their nucleophilicity and stability to ensure the smooth introduction of amino groups into the target structure.
    At the beginning of the reaction, it is often necessary to create a specific reaction environment. Under an inert gas atmosphere, such as nitrogen or argon, to prevent the risk of oxidation of the raw materials and products. Temperature regulation should not be ignored, or it is necessary to start at low temperature, so that the raw materials interact slowly to construct the preliminary reaction intermediate. At this stage, it may be necessary to use a low temperature bath to precisely control the temperature to a specific range, such as - 20 ° C to 0 ° C, so that the reaction can proceed according to the predetermined path and avoid the growth of side reactions.
    When the preliminary intermediate is formed, the step of heating up will be put on the agenda. Gradually raise the temperature to a moderate temperature, such as 50 ° C to 80 ° C, to promote the occurrence of intramolecular rearrangement and cyclization reactions. At this time, a suitable catalyst is required to speed up the reaction rate and increase the yield. The selected catalyst should have high efficiency and specific characteristics, have good catalytic activity for the target reaction, and do not cause too much impurity formation.
    After cyclization, the product needs to be purified finely. The column chromatography method is often used to select suitable stationary and mobile phases to achieve effective separation of the product and impurities according to the difference in adsorption and elution capabilities in the chromatography column. The eluent containing pure product is collected, distilled under reduced pressure, crystallized, etc., and finally the pure 2-amino-3-methyl-3H-imidazolo [4,5-f] quinoline product can be obtained.
    This synthesis method requires careful operation in each step, and the control of reaction conditions and the specifications of raw materials and reagents are very high, so as to achieve the ideal synthesis effect.
    2-Amino-3-methyl-3H-imidazo [4,5-F] quinoline is used in what fields
    2-Amino-3-methyl-3H-imidazolo [4,5-f] quinoline is useful in various fields.
    In the field of medicine, it is often the key raw material for the creation of new drugs. Because of its unique chemical structure, it can interact with specific targets in organisms, or can regulate physiological processes, it has attracted much attention in the development of anti-cancer drugs. After research, it may inhibit the proliferation of tumor cells and have broad prospects for cancer treatment.
    In the field of materials science, it has also emerged. It can be used as a component of functional materials, giving materials special optical and electrical properties. For example, in the preparation of organic Light Emitting Diode (OLED) materials, the addition of this substance may optimize the material's luminous efficiency and stability, and improve the display effect.
    In analytical chemistry, 2-amino-3-methyl-3H-imidazolo [4,5-f] quinoline can act as an excellent chemical probe. With its characteristics of selectively binding to specific substances and generating detectable signals, it can accurately detect specific components in environmental samples and biological samples, enabling efficient analysis and detection work.
    This compound has shown extraordinary application potential in many fields such as medicine, materials science, analytical chemistry, etc. As research continues, more new uses may be discovered.
    2-Amino-3-methyl-3H-imidazo [4,5-F] what is the market outlook for quinoline
    2 - Amino - 3 - methyl - 3H - imidazo [4,5 - f] quinoline is a class of compounds with potential biological activity. In terms of today's market prospects, it shows a considerable trend.
    In the field of medicine, due to its unique chemical structure, it has potential anti-cancer activity. After many experiments, researchers have found that it can affect key processes such as the proliferation, invasion and metastasis of cancer cells, and is expected to become an important lead compound in the development of new anti-cancer drugs. And in the field of anti-virus, there are also some research progress, which may play an inhibitory role for specific viruses and provide new ideas for the creation of antiviral drugs. This undoubtedly brings new opportunities to the pharmaceutical market. Many pharmaceutical companies and scientific research institutions have invested in related research, hoping to develop innovative drugs with significant efficacy to fill the market gap.
    In the field of materials science, the compound has also emerged. Due to its special optical and electrical properties, it can be applied to the preparation of materials such as organic Light Emitting Diodes (OLEDs) and sensors. With the development of science and technology, the demand for OLED display technology is increasing, and there is a thirst for organic materials with excellent performance. This compound may be able to improve the luminous efficiency and stability of OLED devices by virtue of its unique properties, thus gaining a place in the display material market. In terms of sensors, its interaction with specific substances can be used to develop high-sensitivity and high-selectivity detection sensors, which have great potential in environmental monitoring, food safety testing and other fields, and the market prospect is broad.
    However, its market prospect is not smooth sailing. The complexity of the synthesis process is a major challenge. At present, the methods for synthesizing this compound have many drawbacks such as cumbersome steps and low yield, resulting in high production costs and limiting large-scale production and application. Furthermore, preclinical and clinical research still needs to be further advanced to clarify its safety and effectiveness. This process is time-consuming and laborious, and requires a lot of resources. However, despite the challenges, given its potential value in the field of medicine and materials, with time to overcome difficulties, it will surely be able to shine in the market and inject new impetus into the development of related industries.