Diethyl 2 6 Dimethyl 1 4 Dihydropyridine 3 5 Dicarboxylate
pyridine pyrrole pyrazine piperidine piperazine

diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate

    Specifications

    HS Code

    448298

    Chemical Formula C15H21NO4
    Molecular Weight 279.33 g/mol
    Appearance White to off - white crystalline powder
    Melting Point 162 - 164 °C
    Solubility In Water Insoluble
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, acetone
    Odor Odorless
    Density 1.124 g/cm³
    Stability Stable under normal conditions, avoid strong oxidizing agents

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    General Information
    Where to Buy diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate in China?
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    Frequently Asked Questions

    As a leading diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What are the chemical properties of diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate
    Diethylamine 2,6-dimethyl-1,4-diazacyclohexane-3,5-dicarboxylic anhydride, this is an organic compound. Its chemical properties are quite characteristic, and let me tell them one by one.
    First of all, this compound contains functional groups such as nitrogen atoms and carboxyl groups. The nitrogen atom has a certain alkalinity, because its lone pair electrons can accept protons, and in an acidic environment, it can combine with protons to form positively charged ions. This property is used in organic synthesis reactions, or as an important reaction check point, and can participate in many nucleophilic reactions.
    Furthermore, the presence of carboxyl groups endows the compound with acidity. The carboxyl group can be ionized, releasing protons, making the compound acidic in aqueous solution. Its acidity is related to the surrounding chemical environment. If there are electron-withdrawing groups in the adjacent position, or the acidity of the carboxyl group is enhanced; if there are electron-withdrawing groups, the acidity may be weakened.
    The structure of the dicarboxylic acid anhydride is also key. The acid anhydride has high reactivity and can hydrolyze with water to form the corresponding carboxylic acid. This hydrolysis reaction can occur under mild conditions. In organic synthesis, it is often used as a method for preparing carboxylic acids. In addition, the acid anhydride can also react with nucleophiles such as alcohols and amines to form esters and amides, respectively.
    At the same time, the spatial structure of the compound also affects its chemical properties. The spatial arrangement of substituents such as dimethyl and diethylamino groups may affect the intermolecular forces, which in turn affect their physical properties and chemical reactivity.
    In short, diethylamine 2,6-dimethyl-1,4-diazacyclohexane-3,5-dicarboxylic anhydride presents a variety of chemical properties due to its functional groups and unique structures, and may have important application value in organic synthesis, pharmaceutical chemistry and other fields.
    What is the preparation method of diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate?
    The method of preparing diacetyl-2,6-dimethyl-1,4-dimethylpyridine-3,5-dicarboxylic acid ester is an exquisite method.
    To make this product, first take the amount of ethyl acetyl acetate and place it in the kettle. The kettle needs to be dry and well-packed to prevent the intrusion of alcohol. In addition, add a certain amount of formaldehyde, the ratio of the two is controlled by the precision. The ratio is slightly different, and the amount of the product is affected or affected.

    <, add the catalytic product to promote the reaction. For the catalytic product, if the activity is suitable, the activity should be controlled, and the reaction speed should be controlled; if the activity is insufficient, the reaction should be controlled, and it will take a long time. The catalyst is added to the mixture to reach a specific temperature. This temperature also needs to be controlled, and it is usually maintained at a certain temperature before the reaction can be generated.
    During the reaction process, it is necessary to pay close attention to the situation of the kettle, and observe the color and temperature of the mixture. When the reaction is carried out to a certain extent, the mixture can be homogenized and a specific smell can escape. This is a sign that the reaction is nearing completion.
    After the reaction is completed, the mixture in the kettle can be cooled to a suitable temperature. In addition, by extraction with the solution of the mixture, the mixture can be extracted from the mixture. The solution of extraction requires good solubility of the substance, and is easy to separate from other materials.
    To extract the solution, and then remove the solution and the solution of multiple molecules, so that the diacetyl-2,6-dimethyl-1,4-dipyridine-3,5-dicarboxylic acid ester can be precipitated out with the solution. The whole process requires tolerance and fine operation to obtain high-quality materials.
    In which fields is diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate used?
    Diacetyl 2,6-dimethyl-1,4-diazepine-3,5-dicarboxylic anhydride is useful in a wide range of fields.
    In the context of synthesis, this compound can be used as an important medium. In the process of preparation, its properties enable it to generate multiple reactions and assist molecular frameworks with specific physiological activities. For example, in the synthesis of certain antibacterial and anti-inflammatory compounds, diacetyl 2,6-dimethyl-1,4-diazepine-3,5-dicarboxylic anhydride can be cleverly modified to form the active core part of the compound, which can be used to treat diseases by specific biological or enzyme interactions.
    In the field of materials science, it can also develop its talents. Due to its specialization, it can be used as the basis for high-performance polymer materials. Polymerization can generate polymer materials with special properties, such as good mechanical properties, qualitative properties or special optical properties. This material may be used in materials with demanding performance requirements, such as sub-devices, aerospace, etc., adding new tiles to the technical innovation.
    In the field of synthesis, it is a weapon in the hands of the chemical industry. As a multi-functional synthesizer, it can introduce a series of anti-reactive materials, such as anti-reactive, anti-reactive, etc. With its introduction, it is able to synthesize a wide range of novel compounds, expanding new frontiers through the development of synthetic technologies, helping researchers explore more unknown technologies, and exploring new synthetic pathways for compounds.
    What are the market prospects for diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate?
    What is the market prospect of diethyl ester 2,6-dimethyl-1,4-dinitrogen to its-3,5-dicarboxylic acid anhydride? Today, I will try to answer it in the style of "Tiangong Kaiwu".
    Guanfu diethyl ester 2,6-dimethyl-1,4-dinitrogen to its-3,5-dicarboxylic acid anhydride has a unique position in the chemical industry of this world. Its unique nature, or in the manufacture of various fine chemical products and the synthesis of medicine, can be the key material.
    In today's world, science and technology are advancing day by day, and the pharmaceutical industry is seeking innovation and change. It is necessary to pay more and more attention to compounds with various characteristics. This dicarboxylic anhydride, because of its molecular structure, can often play a strange role in the creation of new agents and prescriptions, so the prospect of medicine may be very promising.
    Furthermore, in the field of fine chemicals, the production of many high-end materials also depends on such special compounds. For example, the research and development of high-end coatings and special plastics, diethyl ester 2,6-dimethyl-1,4-dinitrogen to its 3,5-dicarboxylic anhydride may add color to its performance.
    However, the market changes, there are also various variables. The competition in the same industry and the revolution in technology are all factors that affect its market prospects. If you can make continuous progress in the technical end, make good use of the properties of this thing, expand its wide application, and reduce its manufacturing cost, you will be able to win a place in the market and have a bright future. If you are limited by the old law and do not strive for progress, you may be abandoned by the market trend. Therefore, although its market prospect has potential, practitioners need to study it diligently and observe changes in time in order to seek long-term benefits.
    What are the manufacturers of diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate?
    What are the producers of diacetyl 2,6-dimethyl-1,4-diazepine-3,5-dicarboxylic anhydride?
    Described today. In the field of chemical synthesis, there are many people who are good at creating diacetyl 2,6-dimethyl-1,4-diazepine-3,5-dicarboxylic anhydride.
    There are workshops that are very skilled in synthesis, and they can produce this compound by means of profound chemical technology. The precision of the raw materials and the precise control of the reverse parts are all available, which can ensure the high quality and high quality of the product.
    There are also large-scale industrial enterprises involved in this field. They can generate diacetyl 2,6-dimethyl-1,4-diazepine-3,5-dicarboxylic anhydride by means of strong cost, large production capacity, and perfect research systems. On the raw material, it is possible to obtain both high-quality and high-quality raw materials by means of high-quality molds. In the process of production, the control process of self-transformation is carried out, and the quality and quantity are guaranteed.
    Furthermore, some chemical laboratories or research laboratories in universities are also involved in the synthesis of this compound in phase research. They are not based on commercial production, but their research results may provide new ideas and methods for the production of this compound, and they will not lose one of the sources of technology for the production of this compound. In particular, the production of diacetyl 2,6-dimethyl-1,4-dinitrogen-3,5-dicarboxylic anhydride has intensive research and synthesis workshops, large-scale enterprises and some scientific research, etc., each of which has its own contribution to the production of this compound.