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

1,3,4,6-Tetraacetylimidazo [4,5-d] imidazole-2,5-[1H,3H]-dione

    Specifications

    HS Code

    244781

    Chemical Formula C14H14N4O6
    Molecular Weight 334.286 g/mol
    Appearance Solid (predicted)
    Melting Point No data available
    Boiling Point No data available
    Density No data available
    Pka No data available
    Logp No data available
    Flash Point No data available

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    General Information
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    Frequently Asked Questions

    As a leading 1,3,4,6-Tetraacetylimidazo [4,5-d] imidazole-2,5-[1H,3H]-dione 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 main use of 1,3,4,6 - Tetraacetylimidazo [4,5 - d] imidazole - 2,5 - [1H, 3H] - dione
    1% 2C3% 2C4% 2C6 - Tetraacetylimidazo [4,5 - d] imidazole - 2,5 - [1H, 3H] - dione, Chinese name is often 1,3,4,6-tetraacetyl imidazolo [4,5-d] imidazole-2,5- (1H, 3H) -dione. This substance has important uses in many fields such as medicinal chemistry and materials science.
    In the field of medicinal chemistry, it is a key class of organic synthesis intermediates. It can participate in the synthesis of various drug molecules through its special molecular structure and reactivity. For example, when developing new antibacterial drugs, using this as a raw material and through specific chemical reactions, a unique chemical structure with antibacterial activity can be constructed, which makes it possible to create high-efficiency and low-toxicity antibacterial drugs. It can participate in the formation of drug active centers, or improve the solubility, stability and bioavailability of drug molecules, which can help improve the efficacy and safety of drugs.
    In the field of materials science, it can be used as a key reagent for the preparation of functional materials. Because it contains special functional groups and structures, it can be used to prepare optical materials, electronic materials, etc. For example, when preparing polymer materials with specific optical properties, introducing them into the polymer skeleton can endow the material with unique luminescence and light absorption properties, which is expected to be applied to optoelectronic devices such as organic Light Emitting Diodes (OLEDs) to improve device performance and function.
    It also plays an important role in chemical synthesis research. With its unique reactivity and selectivity, it provides an effective way for the synthesis of complex organic molecules. Chemists can use it to participate in cyclization reactions, substitution reactions, etc., to construct novel carbon-nitrogen heterocyclic structures, expand organic synthesis methodologies, and help develop more efficient and green synthesis strategies.
    What are the chemical properties of 1,3,4,6 - Tetraacetylimidazo [4,5 - d] imidazole - 2,5 - [1H, 3H] - dione
    1% 2C3% 2C4% 2C6 -tetraacetyl imidazolo [4,5 - d] imidazolo-2,5 - [1H, 3H] -dione, the chemical properties of this substance are as follows:
    First, it has a certain stability. Due to the existence of multiple acetyl groups in the molecule, these acetyl groups affect the electron cloud distribution of the whole molecule through electronic effects, thereby stabilizing the molecular structure. Under generally mild conditions, this substance can maintain its own structural integrity, and few reactions such as decomposition or rearrangement occur spontaneously.
    Second, the substance has a certain solubility. Due to its molecular structure, there are both polar carbonyl groups and relatively non-polar acetyl groups, so the solubility in organic solvents has its characteristics. In polar organic solvents such as dimethyl sulfoxide (DMSO), N, N-dimethylformamide (DMF), the interaction between the carbonyl group and the solvent has good solubility; in non-polar organic solvents such as n-hexane, the solubility is poor.
    Furthermore, from the perspective of reactivity, the carbonyl group in the molecule is an electrophilic reaction check point. In the presence of appropriate nucleophilic reagents, carbonyl groups can undergo nucleophilic addition reactions, such as with alcohols, under acidic or basic catalytic conditions, acetals or semi-acetal derivatives may be formed. At the same time, the nitrogen atom on the imidazole ring, because of its lone pair of electrons, can act as a nucleophilic center under certain conditions to participate in the electrophilic substitution reaction and react with suitable electrophilic reagents to modify and derive molecules. In addition, in view of the presence of multiple acetyl groups in the molecule, under alkaline conditions, acetyl groups may undergo hydrolysis reactions, gradually removing acetyl groups to generate corresponding hydroxyl or amino-containing derivatives. The process of this reaction is closely related to the control of conditions. Factors such as the strength of the base, reaction temperature and time can all affect the degree and rate of hydrolysis.
    What is the synthesis method of 1,3,4,6 - Tetraacetylimidazo [4,5 - d] imidazole - 2,5 - [1H, 3H] - dione
    To make 1%2C3%2C4%2C6+-+Tetraacetylimidazo+%5B4%2C5+-+d%5D+imidazole+-+2%2C5+-+%5B1H%2C3H%5D+-+dione, the method is as follows:
    Take an appropriate amount of raw materials first, and weigh them carefully according to the ancient method, so as not to make mistakes. Often starting with a specific organic compound, after multiple steps of delicate transformation. Initially, a reactant and another reagent are reacted in a suitable container under a specific temperature, pressure and catalyst.
    This reaction needs to be precisely controlled at temperature, or heated to promote its speed, or cooled to stabilize its properties, depending on the state of the reaction. After the first step of the reaction, the product is separated and purified to remove its impurities and obtain a pure intermediate product.
    Then, this intermediate product, and then interact with other reagents, and then go through several reaction steps, each step is strictly in accordance with the rules, pay attention to the reaction environment, the proportion of materials.
    In each step of the reaction, the monitoring of the product is very important, with the ancient test, or observe its color, smell its taste, or use special equipment to measure its properties, to determine the progress of the reaction and the purity of the product.
    After many twists and turns, many reaction steps are completed in sequence, and the final 1%2C3%2C4%2C6+-+Tetraacetylimidazo+%5B4%2C5+-+d%5D+imidazole+-+2%2C5+-+%5B1H%2C3H%5D+-+dione. Each step requires the heart of a craftsman and fine operation to achieve this product. The process is complicated, but if you follow the rules, you will get something.
    1, 3, 4, 6 - Tetraacetylimidazo [4, 5 - d] imidazole - 2, 5 - [1H, 3H] - dione is used in what fields
    1% 2C3% 2C4% 2C6 -tetraacetyl imidazolo [4% 2C5 - d] imidazolo-2% 2C5 - [1H% 2C3H] -diketone, this substance is useful in many fields.
    In the field of medicine, it may be a key raw material for the creation of new drugs. Due to its unique chemical structure, it can interact with specific biological targets, or it can help develop anti-viral, anti-tumor and other drugs. Doctors seek a good prescription for the world. This substance may become the key to breaking the situation and open up a new way in the land of illness.
    In the field of materials science, it can contribute to the synthesis of special materials. It can improve the stability and mechanical properties of materials. If craftsmen carve beautiful jade, use this as a guide to create new materials with excellent performance, which can be used in frontier fields such as aerospace and electronic equipment, making the equipment more durable.
    In the field of organic synthesis, it is an extremely important intermediate. Like the cornerstone of building a pavilion, organic chemists use it to build complex organic molecular structures. Through ingenious chemical reactions, a variety of organic compounds are derived, greatly enriching the "treasure house" of organic synthesis, opening up a wider world for chemical research, just like expanding a new territory in the wilderness of knowledge.
    What is the safety of 1,3,4,6 - Tetraacetylimidazo [4,5 - d] imidazole - 2,5 - [1H, 3H] - dione
    1% 2C3% 2C4% 2C6 - Tetraacetylimidazo% 5B4% 2C5 - d% 5D imidazole - 2% 2C5 -% 5B1H% 2C3H% 5D - dione is a complex chemical substance. When it comes to the safety of this substance, it needs to be analyzed from multiple aspects.
    From the perspective of chemical structure, it contains many specific functional groups, or causes specific chemical activities and reactivity. For example, some acetyl groups, under specific conditions, may involve hydrolysis, esterification and other reactions, which may produce different products in different environments or affect their safety.
    In terms of toxicity, without exact experimental data, it is difficult to determine the degree of toxicity to biological systems. However, compounds with imidazole-like structures may have certain biological activities, or affect the normal physiological functions of organisms, such as interfering with cell metabolic pathways, interacting with biomacromolecules, etc.
    Stability is also key. Its stability is related to whether the structure can be maintained intact under different environmental conditions. Temperature, humidity, light and other factors may play a role in its stability. If under unstable conditions, it may decompose to produce new substances, the safety of new biomass also needs to be considered.
    In addition, its production, storage and use process also involves safety issues. During production, the raw materials and reaction conditions are not properly controlled, or accidents occur; when stored, if they are not in accordance with suitable conditions, or they are deteriorated; when used, if they are not followed, they may pose a risk to the user and the environment.
    Overall, to determine the safety of 1% 2C3% 2C4% 2C6 - Tetraacetylimidazo% 5B4% 2C5 - d% 5D imidazole - 2% 2C5 -% 5B1H% 2C3H% 5D - dione, comprehensive experimental studies and strict operation are required to clarify its potential impact on organisms and the environment and prevent problems.