5 D Imidazole 2 5 1h 3h Dione 1 3 4 6 Tetraacetyltetrahydro Imidazo
quinoline thiophene imidazole thiazole

5-d]imidazole-2,5(1h,3h)-dione,1,3,4,6-tetraacetyltetrahydro-imidazo[

    Specifications

    HS Code

    401957

    Chemical Formula C12H14N2O8
    Molar Mass 314.25 g/mol
    Physical State Solid (presumably, based on common nature of such organic compounds)
    Solubility In Water Expected to be low due to non - polar acetyl groups
    Solubility In Organic Solvents Likely soluble in polar organic solvents like DMSO, acetone
    Acidity Basicity Weakly acidic due to the imidazole - dione structure
    Stability Stable under normal conditions, but may decompose on heating or in presence of strong acids/bases

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    Frequently Asked Questions

    As a leading 5-d]imidazole-2,5(1h,3h)-dione,1,3,4,6-tetraacetyltetrahydro-imidazo[ supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    5 - d] imidazole - 2,5 (1h, 3h) -dione, 1,3,4,6 - tetraacetyltetrahydro - imidazo [what is the chemical property of
    The chemical properties of 1,3,4,6-tetraacetyltetrahydro-5- (5-imidazole-2,5 (1H, 3H) -diketone) imidazole are as follows:
    This compound has certain stability and has certain solubility in common organic solvents such as ethanol and dichloromethane. Its structure contains multiple acetyl groups, and the acetyl group has a certain electron-giving effect, which affects the distribution of molecular electron clouds. This makes the compound unique in electrophilic substitution reactions. Due to its electron cloud density distribution, it is more likely to be substituted at specific locations.
    The imidazole ring structure within the molecule gives it alkalinity and can react with acids to form salts. The diketone structural part is also active and can participate in some carbonyl-related reactions, such as addition reactions with nucleophiles.
    In the presence of high temperature or specific catalysts, the acetyl group in the molecule may undergo reactions such as hydrolysis and alcoholysis, which may change the molecular structure and properties. And due to the large and complex structure of the molecule, intra-molecular rearrangement may occur under certain conditions to generate different isomers.
    In addition, there are interactions between multiple groups of the compound, which jointly determine its overall chemical properties. It can be used as an important intermediate in the field of organic synthesis to construct more complex and functionally specific organic molecules.
    5 - d] imidazole - 2,5 (1h, 3h) -dione, 1,3,4,6 - tetraacetyltetrahydro - what are the main uses of imidazo [
    1,3,4,6-Tetraacetyltetrahydro-5- (dihydro-1,3-dioxo-1H-imidazole-2-yl) -1H-imidazole-2,5 (3H, 4H) -dione This substance has a wide range of uses. In the field of medicine, it is often used as a key intermediate in the synthesis of specific drugs. Due to its unique chemical structure, it can participate in many chemical reactions, helping to construct complex molecular structures with specific physiological activities, which in turn provides an important basis for the development of drugs for the treatment of various diseases.
    In the field of materials science, or can be used as a modifier to incorporate specific materials. Through its interaction with material molecules, it changes the properties of materials such as mechanical properties and thermal stability, making materials more suitable and superior in aerospace, electronics and other fields.
    It is also an important chemical reagent in the level of scientific research and exploration. Researchers can conduct various reaction studies on it, deeply explore the mechanism and laws of chemical reactions, and contribute to the development of chemical theory and promote progress in organic synthetic chemistry and other related fields.
    In summary, 1,3,4,6-tetraacetyltetrahydro-5- (dihydro-1,3-dioxo-1H-imidazole-2-yl) -1H-imidazole-2,5 (3H, 4H) -diketone has non-negligible uses in medicine, materials and scientific research, and is a valuable chemical substance.
    5 - d] imidazole - 2,5 (1h, 3h) -dione, 1,3,4,6 - tetraacetyltetrahydro - imidazo [what is the synthesis method
    The method of preparing 5-dimethyl-imidazole-2,5 (1H, 3H) -diketone, 1, 3, 4, 6-tetraacetyl-tetrahydro-imidazole is the best way in ancient times.
    First take appropriate starting materials, such as nitrogen-containing compounds and carbonyl compounds with specific structures, and the two are matched in a certain proportion. In a clean kettle, place an appropriate amount of catalyst, which may be an acid or a base, depending on the nature of the reaction, and the amount needs to be precisely controlled. At least the reaction is slow, and at most it causes side reactions.
    Temperature control is crucial to promote the reaction. Initially, it is recommended to rise slowly, observe the state of the matter in the kettle, observe its changes, and wait for it to bloom, and then stabilize it at a suitable temperature. This temperature may be between tens and hundreds of degrees Celsius, depending on the raw material and the reaction mechanism. During the reaction, use a stirrer to homogenize the matter, so that the raw materials and catalysts blend seamlessly, so that the reaction is uniform.
    When the reaction is gradually completed, observe the change of its color and properties, and test it. After taking the obtained product, separate and purify it, or use distillation to remove the impurities of low boiling and high boiling; or apply recrystallization, and in an appropriate solvent, make the product pure and precipitated. Compound with analytical methods, such as chromatography and spectroscopy, to prove its purity and structure, 5-dimethyl-imidazole-2,5 (1H, 3H) -diketone, 1,3,4,6-tetraacetyl-tetrahydro-imidazole is obtained.
    5 - d] imidazole - 2,5 (1h, 3h) -dione, 1,3,4,6 - tetraacetyltetrahydro - imidazo [in which areas
    1,3,4,6-tetraacetyltetrahydro-5-imidazole-2,5 (1H, 3H) -dione, this substance has applications in medicine, materials science, organic synthesis and many other fields.
    In the field of medicine, it shows unique medicinal potential. Due to its structural properties, it can participate in specific biochemical reactions or act on key targets of certain diseases. For example, in the development of anti-tumor drugs, this substance can be used as a lead compound. After structural modification and optimization, it is expected to develop new anti-cancer drugs that can inhibit the growth and spread of tumor cells by interfering with the metabolic process or signal transduction pathway of tumor cells.
    In the field of materials science, this substance can be used as a key component of functional materials. Because of its specific chemical activity and structural characteristics, it can react with other materials to give new properties to the material. If this substance is introduced into polymer materials, it can improve the thermal stability, mechanical properties or biocompatibility of the material, so that the material can be applied in biomedical materials, high-performance engineering plastics, etc.
    In the field of organic synthesis, 1,3,4,6-tetraacetyltetrahydro-5-imidazole-2,5 (1H, 3H) -dione is an important intermediate. Its rich reaction check points can build complex organic molecular structures through various organic reactions. Chemists can use it to perform acylation, cyclization, and other reactions to synthesize organic compounds with special structures and functions, providing an important material foundation for the study of new organic materials and the total synthesis of natural products, and promoting the development of organic synthetic chemistry.
    5 - d] imidazole - 2,5 (1h, 3h) -dione, 1,3,4,6 - tetraacetyltetrahydro - what is the market outlook for imidazo [
    1,3,4,6-tetraacetyltetrahydro-5 - ( - ) - imidazole-2,5 (1H, 3H) -dione, the market prospects of this substance are as follows:
    In today's world, science and technology are new, and the pharmaceutical and chemical industries are booming. 1,3,4,6-tetraacetyltetrahydro-5 - ( - ) - imidazole-2,5 (1H, 3H) -dione is gradually becoming more and more important in the field of pharmaceutical synthesis. Because of its unique structure and specific reactivity, it can be a key intermediate for the creation of new drugs.
    The Guanfu pharmaceutical market is eager for new drugs with specific effects. Many pharmaceutical companies are working hard to develop new formulas. This compound has attracted the attention of many researchers and pharmaceutical manufacturers because it can participate in various organic reactions and help build complex drug molecular structures.
    In terms of chemical materials, it may contribute to the synthesis of new polymer materials. With the advancement of materials science, the need for materials with special properties is also increasing day by day. 1,3,4,6-tetraacetyltetrahydro-5 - ( - ) - imidazole-2,5 (1H, 3H) -dione may endow the material with different physical and chemical properties, such as enhanced stability and improved solubility, etc., and then expand its application in the field of high-end materials.
    However, its market prospect is not smooth. The complexity of the synthesis process and the control of cost are all problems to be solved. To make it widely available in the market, it is necessary to optimize the synthesis path, reduce costs and increase efficiency. However, over time, if technological breakthroughs are made, this compound will surely emerge in the pharmaceutical and chemical markets, create a new situation, become a strong driving force for the development of the industry, and contribute greatly to the well-being of people's livelihood and industrial progress.