4 Oxo 1 4 Dihydropyridine 2 6 Dicarboxylic Acid
pyridine pyrrole pyrazine piperidine piperazine

4-oxo-1,4-dihydropyridine-2,6-dicarboxylic acid

    Specifications

    HS Code

    474904

    Chemical Formula C7H5NO5
    Molar Mass 183.12 g/mol
    Appearance Solid
    Melting Point Decomposes
    Solubility In Water Slightly soluble
    Solubility In Organic Solvents Soluble in some polar organic solvents
    Acidity Dicarboxylic acid, acidic
    Structural Feature Contains pyridine ring with oxo and carboxyl groups
    Odor Odorless
    Stability Stable under normal conditions but may decompose on heating

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    General Information
    Where to Buy 4-oxo-1,4-dihydropyridine-2,6-dicarboxylic acid in China?
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    Frequently Asked Questions

    As a leading 4-oxo-1,4-dihydropyridine-2,6-dicarboxylic 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 4-oxo-1,4-dihydropyridine-2,6-dicarboxylic acid?
    In the case of 4-oxo-1,4-dihydropyridine-2,6-dicarboxylic acid, its chemical composition is also a compound containing pyridine. The pyridine of this compound has a dimethyl group at the 1,4 position, and a dimethyl group at the 4-oxo position, and a monocarboxylic group at the 2,6 position.
    Its basic framework is pyridine, but the sum of the 1,4 positions forms a binary form, so that the molecular composition and chemical properties of pyridine are similar to those of typical pyridine. The oxygen atom at the 4-position exists in the form of carbonyl groups, that is, C = O, and the carbonyl group has properties. The physical and chemical properties of the molecule are greatly affected, such as the molecular properties, boiling properties, and anti-reactive sites.
    2,6 bis carboxyl groups (-COOH) are also important functional groups. The carboxyl group is acidic and can be solved to produce molecules. And the carboxyl group can be esterified, acylated, etc. to reverse the reaction of other functional groups. This reaction is used in the synthesis of chemicals to build more molecules. The integrity of this compound makes it specific, active and physical, and may have important uses in the fields of chemical synthesis, materials science, etc.
    What are the common physical properties of 4-oxo-1,4-dihydropyridine-2,6-dicarboxylic acid?
    4-Oxo-1,4-dihydropyridine-2,6-dicarboxylic acid, often has various physical properties. In terms of color, it is mostly white to light yellow crystalline powder. Viewed in sunlight, it can be seen that its texture is delicate, like the purity of the first snow in winter. The melting point of this substance is quite critical, about 290-300 ° C. When the temperature gradually rises near the melting point, its solid structure begins to gradually change, just like ice and snow melting in the warm sun.
    Solubility is also an important property. In water, its solubility is very small, just like a drop of ink falling on Wang Yang, and its insoluble state is obvious; however, in organic solvents such as dimethyl sulfoxide (DMSO), N, N-dimethylformamide (DMF), it can be well dissolved, just like fish getting water, and can be fused with the solvent.
    In terms of stability, in a dry environment at room temperature and pressure, this substance is quite stable and can maintain its own structure and properties for a long time; however, if exposed to high temperature, high humidity or strong acid and alkali environment, its structure is easily damaged, just like a delicate flower in a violent wind and rain, it is difficult to maintain its original state. Although there is no exact precise value for its density, it is about the same as the density of common organic crystals. Placing it on the balance, a relative value can be obtained, which is also one of the characteristics of its physical properties. In general, the various physical properties are interrelated and together outline the characteristics of 4-oxo-1,4-dihydropyridine-2,6-dicarboxylic acid.
    Where is 4-oxo-1,4-dihydropyridine-2,6-dicarboxylic acid used?
    4-Oxo-1,4-dihydropyridine-2,6-dicarboxylic acid, namely 4-oxo-1,4-dihydropyridine-2,6-dicarboxylic acid, has wonderful uses in many fields such as medicine and chemical industry.
    In the field of medicine, this compound is a key raw material for the development of cardiovascular drugs. Its unique chemical structure can be closely combined with specific biological targets in the human body, thereby regulating the physiological function of the cardiovascular system. For example, it may act on calcium ion channels, regulate the flow of calcium ions across membranes, and affect myocardial contractility and vascular tension, thus providing a potential effective strategy for the treatment of cardiovascular diseases such as hypertension and arrhythmia.
    In the chemical industry, 4-oxo-1,4-dihydropyridine-2,6-dicarboxylic acid also plays an important role. Because of its good reactivity, it is often used as an intermediate in organic synthesis. Through a series of chemical reactions, it can be converted into organic compounds with more complex structures and more specific functions, which are widely used in materials science, fine chemical product preparation, etc. For example, in some high-performance polymer synthesis, the introduction of this compound structure unit may endow the polymer with unique physical and chemical properties, such as improved thermal stability and improved mechanical properties.
    Furthermore, in the field of biochemical research, this substance can also be used as a tool molecule to help researchers delve deeper into specific biochemical reaction mechanisms in organisms and contribute to basic research in life sciences. Its diverse applications in different fields demonstrate the important value and broad application prospects of this compound.
    What are the synthesis methods of 4-oxo-1,4-dihydropyridine-2,6-dicarboxylic acid
    In the synthesis of 4-oxo-1,4-dihydropyridine-2,6-dicarboxylic acid, there are many paths to follow.
    First, it can be condensed from ethyl acetoacetate and urea under suitable reaction conditions. In this process, ethyl acetoacetate and urea are condensed in a specific solvent with the help of a catalyst, through careful regulation of temperature and reaction time, and the condensation reaction occurs, and the molecular structure of 4-oxo-1,4-dihydropyridine-2,6-dicarboxylic acid is gradually constructed.
    Second, diethyl malonate is used as the starting material and reacts with related nitrogen-containing compounds. First, diethyl malonate and a suitable nitrogen-containing reagent, under the action of a base catalyst, in a specific solvent, after specific reaction steps and conditions, the prototype of the target product is gradually derived, and then after subsequent modification and transformation, the final 4-oxo-1,4-dihydropyridine-2,6-dicarboxylic acid is obtained.
    Third, it is also prepared by the oxidation reaction of pyridine compounds. Select a specific pyridine derivative, in the presence of a suitable oxidant, in a suitable reaction system, control the reaction temperature, time and other conditions to promote the oxidative modification of the pyridine ring, and realize the transition to 4-oxo-1,4-dihydropyridine-2,6-dicarboxylic acid.
    All synthesis methods have their own advantages and disadvantages. The cost of the starting material, the difficulty of obtaining it, the severity of the reaction conditions, and the yield and purity of the product are all key factors to consider. In actual synthesis, it is necessary to carefully weigh and choose the most suitable synthesis path according to specific needs and conditions, so as to achieve the purpose of efficient, economical and high-quality synthesis of 4-oxo-1,4-dihydropyridine-2,6-dicarboxylic acid.
    What is the market outlook for 4-oxo-1,4-dihydropyridine-2,6-dicarboxylic acid?
    4-Oxo-1,4-dihydropyridine-2,6-dicarboxylic acid, which has great prospects in the field of pharmaceuticals and organic synthesis, is widely used.
    In the field of pharmaceutical chemistry, it is a key building block for the construction of many active compounds. Due to its unique structure containing pyridine ring, carboxyl group and carbonyl group, many derivatives with pharmacological activity can be derived through various chemical reactions. For example, after modification, it can be used to develop drugs for cardiovascular diseases. Many studies have focused on exploring its potential in the creation of calcium channel blockers, hoping to use its structural properties to optimize the effect of drugs on calcium channels, improve efficacy and reduce side effects.
    In the field of organic synthesis, it is also an important intermediate. By reacting with various reagents, complex organic molecular structures can be constructed. Chemists often use it to participate in cyclization reactions, condensation reactions, etc., to expand the molecular skeleton and synthesize novel structural compounds. This not only enriches organic synthesis strategies, but also provides possibilities for the development of new materials and the total synthesis of natural products.
    Furthermore, at the level of biological activity research, many experiments have investigated its effect on specific enzymes or receptors in organisms. Preliminary studies suggest that it may interact with certain protein targets and affect cell signaling pathways. This provides important clues for the discovery and development of new drugs.
    To sum up, 4-oxo-1,4-dihydropyridine-2,6-dicarboxylic acids have a bright future. With the deepening of scientific research and technological advancement, or in many fields such as medicine and materials, it will bloom more brilliance, give birth to more innovative achievements, and benefit human society.