N N 6 Trimethyl 2 4 Methylphenyl Imidazo 1 2 A Pyridine 3 Acetamide
pyridine pyrrole pyrazine piperidine piperazine

N,N,6-Trimethyl-2-(4-methylphenyl)imidazo[1,2-a]pyridine-3-acetamide

    Specifications

    HS Code

    374255

    Chemical Formula C20H23N3O
    Molar Mass 321.42 g/mol
    Physical State At Standard Conditions Solid (usually)
    Appearance Off - white to pale yellow solid
    Melting Point Data specific to pure sample needed
    Boiling Point Data specific to pure sample needed
    Solubility In Water Low solubility, likely sparingly soluble
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
    Density Data specific to pure sample needed
    Pka Value Data specific to functional groups in the molecule needed

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    General Information
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    Frequently Asked Questions

    As a leading N,N,6-Trimethyl-2-(4-methylphenyl)imidazo[1,2-a]pyridine-3-acetamide 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 N, N, 6-Trimethyl-2- (4-methylphenyl) imidazo [1,2-a] pyridine-3-acetamide?
    This is an organic compound, and its name is N, 2, N, 6-tetramethyl-2 - (4-methylphenyl) imidazolo [1,2-a] pyridine-3-acetamide. To clarify its chemical structure, it is necessary to analyze its naming in detail.
    View "N, 2, N, 6-tetramethyl", which shows that in the molecular structure of the compound, each has a methyl group (-CH 🥰) connected to the nitrogen atom (N) and the 2,6 positions. "2 - (4-methylphenyl) " was observed again, indicating that there is a phenyl group attached to the 2 position, and the 4 position of the phenyl group has methyl substitution. "Imidazolo [1,2-a] pyridine", this shows that the core of the compound is formed by fusing the imidazole ring with the pyridine ring, and the fusing method is [1,2-a]. As for "-3-acetamide", it means that at the 3 position of the imidazolo-pyridine ring, the acetamide group (-CH -2 CONH -) is connected.
    In summary, the chemical structure of this compound is based on imidazolo [1,2-a] pyridine as the core structure, with methyl at the N, 2, and 6 positions, 4-methylphenyl at the 2 position, and acetamido at the 3 position. In this way, the approximate morphology of its chemical structure can be deduced.
    What are the main uses of N, N, 6-Trimethyl-2- (4-methylphenyl) imidazo [1,2-a] pyridine-3-acetamide?
    N, 2, N, 6-tetramethyl-2- (4-methylphenyl) imidazolo [1,2-a] pyridine-3-acetamide is useful in the fields of medicine and chemical industry.
    In the field of medicine, it may be involved in drug research and development. The molecular structure of this compound is unique, or it can be used as a lead compound. It has been carefully carved by pharmacists and researchers to modify its structure in order to obtain new drugs with specific pharmacological activities. For example, by chemically modifying it, or enabling it to bind to specific targets, such as receptors or enzymes associated with certain diseases, it can regulate physiological processes and potentially treat diseases such as inflammation and tumors.
    In the field of chemical industry, it may be used as a key intermediate in organic synthesis. Organic synthesis craftsmen can use it as a starting material to use various organic reactions, such as substitution reactions, addition reactions, etc., to construct more complex organic molecules to produce materials with special properties, such as organic materials with special optical and electrical properties, or for the improvement of chemical products such as coatings and plastics, to improve their quality and performance.
    Furthermore, this compound may be emerging in materials science research. Researchers may explore its properties in material self-assembly, molecular recognition, etc., providing an opportunity to create new smart materials, such as preparing smart materials that can respond to specific environmental factors to meet various practical needs.
    What are the physical properties of N, N, 6-Trimethyl-2- (4-methylphenyl) imidazo [1,2-a] pyridine-3-acetamide?
    N, 2, N, 6-tetramethyl-2- (4-methylphenyl) imidazolo [1,2-a] pyridine-3-acetamide This substance has unique physical properties. In terms of its color state, it is often white to white crystalline powder. It is delicate and uniform in appearance, and shimmering under light can be seen, just like the first fall of fine snow, which is pure. Its melting point is quite high, about 160-165 ° C. It requires a higher temperature to cause it to melt, just like the strength of a rock, and it is difficult to change its shape without high temperature.
    In terms of solubility, in organic solvents, such as dichloromethane, N, N-dimethylformamide, it exhibits good solubility, just like fish entering a river and dissolving freely; however, in water, the solubility is very small, just like oil floating on the water surface, and it is difficult to miscible. This difference in solubility is due to its molecular structure characteristics, which are mostly lipophilic groups in the molecule, resulting in weak hydrophilicity.
    In terms of stability, it is quite stable in a dry environment at room temperature, and can maintain its own structure and properties for a long time, such as the foundation of an old house, which is as stable as Mount Tai; in the event of strong acids and alkalis, or high temperature and high humidity, the structure is easily damaged and its properties change, as if the building is shaken by a strong earthquake. In addition, it is also more sensitive to light. Under strong light, it may decompose and deteriorate, just like a delicate flower seeing the hot sun, gradually losing its fragrance. These physical properties are of great significance in their synthesis, storage and application, and are related to their efficacy and quality.
    What is the synthesis method of N, N, 6-Trimethyl-2- (4-methylphenyl) imidazo [1,2-a] pyridine-3-acetamide?
    To prepare N% 2CN% 2C6-trimethyl-2- (4-methylphenyl) imidazolo [1,2-a] pyridine-3-acetamide, the synthesis method is quite complicated. First, appropriate starting materials, such as pyridine and imidazole derivatives containing specific substituents, need to be taken.
    At the outset, when the pyridine derivative is reacted with a reagent containing a suitable substituent in a fine way to introduce the desired substituent on the pyridine ring. This step requires precise control of the reaction conditions, such as temperature, reaction duration, and the proportion of reactants, so that the reaction proceeds in the desired direction.
    Then, the imidazole derivative is combined with the treated pyridine intermediate. The reaction of this binding also requires careful operation or the help of suitable catalysts to promote its efficient reaction. In this process, the choice of solvent is also crucial, as it affects the rate and selectivity of the reaction.
    After the construction of the imidazole pyridine skeleton is completed, the acetamide group is introduced at a specific location. This step requires the use of suitable acylating reagents to achieve precise acylation of the target location under appropriate reaction conditions.
    The whole synthesis process requires strict control of each step. After multiple processes such as separation and purification, impurities can be removed to obtain pure N% 2CN% 2C6-trimethyl-2 - (4-methylphenyl) imidazolo [1,2-a] pyridine-3-acetamide. The road of synthesis is like carving beautiful jade, which requires careful steps, and it is difficult to achieve the expected target product with a slight error.
    What is the market outlook for N, N, 6-Trimethyl-2- (4-methylphenyl) imidazo [1,2-a] pyridine-3-acetamide?
    N, 2, N, 6-tetramethyl-2- (4-methylphenyl) imidazolo [1,2-a] pyridine-3-acetamide is a rather special organic compound. In today's market prospects, it has something to explore.
    This compound may have potential uses in the field of pharmaceutical research and development. Covering today's pharmaceutical industry, the demand for new specific drugs is eager, and many pharmaceutical companies and scientific research institutions are all working hard to explore new compounds with unique therapeutic effects. This N, 2, N, 6 -tetramethyl-2 - (4-methylphenyl) imidazolo [1,2-a] pyridine-3-acetamide, if further studied, may exhibit unique pharmacological activities, such as on the therapeutic target of certain diseases, can play a precise role, and then is expected to become the lead compound of innovative drugs. In this way, its market potential is huge, and once it is successfully developed and put into the market, it will be able to obtain considerable benefits.
    Furthermore, in the field of materials science, it may also be promising. Today, the field of materials pursues high-performance, multi-functional new materials, and the special structure of this compound may give it unique physical and chemical properties. For example, in optoelectronic materials, it may affect the electronic transmission and luminescence properties of materials. If it can be applied rationally to develop new optoelectronic materials, it will definitely open up new market space in electronic display, lighting and other industries.
    However, its market prospects are not entirely bright. The process of synthesizing this compound may be complicated and costly. If the synthesis process cannot be effectively optimized and production costs reduced, it will be difficult to have a price advantage in the market competition. And the road of new drug research and development is long and full of thorns. Many links of clinical trials require a lot of manpower, material resources and time. If you are not careful, all previous efforts will be wasted. The research and development of material applications also needs to face competition with existing materials. To gain market recognition, it is necessary to demonstrate significant advantages.
    In summary, the market prospects, opportunities and challenges of N, 2, N, 6-tetramethyl-2 - (4-methylphenyl) imidazolo [1,2-a] pyridine-3-acetamide coexist. It is up to people of insight to explore its potential with wisdom and hard work and open up new opportunities.