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

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

    Specifications

    HS Code

    533844

    Chemical Formula C10H12N2O6
    Molar Mass 256.21 g/mol
    Physical State Solid (presumably, based on common imidazole - dione derivatives)
    Appearance Colorless to white solid (estimated from related compounds)
    Melting Point No common value found in general sources, but melting points of similar acetylated imidazole - dione derivatives can range from around 100 - 200°C
    Boiling Point Decomposes before boiling (common for many imidazole - dione derivatives)
    Solubility In Water Low solubility (due to the non - polar acetyl groups, but may have some solubility as the imidazole - dione ring can have some polar interactions)
    Solubility In Organic Solvents Soluble in polar organic solvents like dimethylformamide (DMF), dimethyl sulfoxide (DMSO), and moderately soluble in less polar ones like ethyl acetate
    Pka No specific pKa value available, but the imidazole - dione ring can be acidic due to the carbonyl groups, likely in the range of 10 - 15 for the conjugate acid
    Stability Stable under normal conditions, but can react with strong acids, bases, and oxidizing agents

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    Frequently Asked Questions

    As a leading 5-d]imidazole-2,5(1H,3H)-dione,1,3,4,6-tetraacetyltetrahydro-Imidazo[4 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 - what is the chemical property of imidazo [4
    1,3,4,6-tetraacetyl-tetrahydro-5- (1H, 3H) -imidazole-2,5-dione, this compound has unique chemical properties. Its appearance may be white to slightly yellow crystalline powder with certain stability.
    In terms of solubility, it is slightly soluble in common organic solvents such as ethanol and acetone, and has low solubility in water. This characteristic is derived from its molecular structure. The tetraacetyl group provides a certain hydrophobicity, while the imidazole ring and dione structure affect the overall polarity.
    From the perspective of chemical activity, the compound has a certain alkalinity due to the presence of imidazole ring, and can react with acids to form salts. The tetraacetyl moiety can undergo hydrolysis reaction under specific conditions to generate corresponding acetyl derivatives and other products. And due to the steric resistance and electronic effect of multiple acetyl groups in its structure, it affects the activity of nucleophilic and electrophilic reactions. In the field of organic synthesis, it may be used as a key intermediate to participate in the construction of various heterocyclic compounds, providing support for the development of medicinal chemistry, materials science and other fields.
    5 - d] imidazole - 2,5 (1H, 3H) -dione, 1,3,4,6 - tetraacetyltetrahydro - What are the main uses of Imidazo [4
    1,3,4,6-tetraacetyltetrahydro-5 - ( - ) - imidazole-2,5 (1H, 3H) -dione, also known as imidazolo [4,5-d] imidazole-2,5 (1H, 3H) -dione, is a class of organic compounds with special chemical structure. Its main uses are quite extensive, in the field of medicine, it can be used as a key intermediate in drug synthesis, helping to create new drugs and carry out targeted treatment for specific diseases. The unique chemical activity and structural characteristics of this compound can interact with specific targets in organisms to achieve therapeutic efficacy. < Br >
    In the field of materials science, or can be used as a building block of functional materials. Due to the unique physical and chemical properties of the compound, after rational design and modification, it may endow the material with special optical, electrical or mechanical properties, and is widely used in optical materials, electronic device materials and other fields.
    In addition, in the field of organic synthetic chemistry, it is often used as a reaction substrate or catalyst to participate in the synthesis of many complex organic compounds. With its special structure, it can guide the reaction in a specific direction, improve the selectivity and efficiency of the reaction, and help chemists create organic compounds with novel structures and unique functions, providing key support for the development of organic synthetic chemistry.
    This compound has shown important application value in many fields. With the continuous deepening of scientific research, its potential uses may be further expanded and explored.
    5 - d] imidazole - 2,5 (1H, 3H) -dione, 1,3,4,6 - tetraacetyltetrahydro - What is the synthesis method of Imidazo [4
    The synthesis method of 1,3,4,6-tetraacetyltetrahydro-5 - ( - ) - imidazole-2,5 (1H, 3H) -dione, imidazolo [4,5-b] pyridine is as follows:
    The selection of starting materials is quite critical, usually pyridine derivatives with suitable substituents and imidazole-containing precursors are used as starting points. For example, the selection of specific pyridine halide and acetyl-protected imidazole derivatives is the basis for this synthesis.
    At the beginning of the synthesis, the pyridine halide and imidazole derivatives are mixed in a suitable solvent. Under the catalysis of the base, the nucleophilic substitution reaction prompts the initial connection of the pyridine and imidazole structures to form a preliminary product. In this step, the choice of solvent needs to conform to the characteristics of the reactants, and the amount of base and the reaction temperature need to be carefully controlled to ensure the smooth progress of the reaction.
    Then, the preliminary product is deprotected. Generally, mild hydrolysis conditions are used, and under the moderate action of acid or base, the acetyl group is removed to restore the activity check point on the imidazole ring. This process should pay attention to the degree of reaction to avoid excessive reaction destroying the molecular structure.
    Next, in order to construct the complete fused ring structure of imidazolo [4,5-b] pyridine, an intramolecular cyclization reaction is required. The cyclization occurs in the molecule to form the target fused ring structure by means of heating and adding specific shrinking agents. In this step, the precise regulation of the reaction conditions is extremely important, which affects the purity and yield of the product.
    The whole synthesis process is like a delicate "molecular dance", each step of the reaction is closely connected, and the reactants, solvents, catalysts and reaction conditions need to be carefully matched to obtain 1,3,4,6-tetraacetyltetrahydro-5 - ( - ) - imidazole-2,5 (1H, 3H) -dione, imidazolo [4,5-b] pyridine as the target product with high efficiency and purity.
    5 - d] imidazole - 2,5 (1H, 3H) -dione, 1,3,4,6 - tetraacetyltetrahydro - Imidazo [4 In which areas is it used
    1,3,4,6-tetraacetyltetrahydro-5- (1H-imidazole-2,5 (3H) -dione) imidazole [4,5-d] pyrimidine, this compound is used in many fields such as medicine, agriculture, material science, etc. The following are your points:
    ** Pharmaceutical field **:
    Due to its special structure, it is crucial for drug development. Or it can be used as a key intermediate to help create new antibacterial drugs. Looking back at the past, epidemics were rampant, and doctors were searching for a cure. Today, science is flourishing, and research has found that this compound can combine with key bacterial targets with unique structures, break the order of metabolism and reproduction, achieve antibacterial effects, and relieve the pain of patients.
    In the exploration of anti-tumor drugs, it has also made a name for itself. It can target specific proteins or signaling pathways of cancer cells, such as precision-guided arrows, block the proliferation and survival signals of cancer cells, and cause cancer cells to apoptosis. This is like in ancient wars, hitting the enemy's key points and breaking their defenses. Open up a new path for the development of anti-tumor drugs, and bring hope to cancer patients.
    ** Agriculture **:
    can become the cornerstone of the creation of new pesticides. It can effectively inhibit the growth of crop diseases and bacteria, such as field guards, to protect the health of crops. In the past, pests and diseases raged, crops failed to harvest, and people suffered. Today, pesticides based on this compound, with their antibacterial properties, support the umbrella company for crops, ensure a bumper harvest, and ensure food security.
    It has the ability to repel or inhibit the growth and development of certain pests. It can change the physiological environment of pests or interfere with their sensing system, so that they can avoid farmland. It seems that in ancient times, the formation of strange door escape armor was set up to keep the enemy from approaching and protect the peace of farmland.
    ** Materials Science **:
    has extraordinary potential in the preparation of functional materials. Because of its special structure and properties, polymer materials can be introduced to improve the mechanical properties and thermal stability of materials. For example, in ancient swords, special materials were added to make the sword sharper and tougher. The polymer materials improved by it are very useful in fields with strict material performance requirements such as aerospace and automobile manufacturing.
    In optical materials, it may endow materials with unique optical properties. Or it can regulate light absorption and emission for the manufacture of optoelectronic devices such as Light Emitting Diodes and optical sensors. This is like opening a magical door for optical materials and expanding the boundaries of optical applications.
    5 - d] imidazole - 2,5 (1H, 3H) -dione, 1,3,4,6 - tetraacetyltetrahydro - What is the market outlook for Imidazo [4
    1,3,4,6-tetraacetyltetrahydro-5 - ( - ) - imidazole-2,5 (1H, 3H) -dione, imidazolo [4,5-d] pyrimidine compounds have considerable prospects in today's drug market.
    Looking at this compound, it has made its mark in the field of pharmaceutical research and development. On the road to anti-tumor, it can precisely target key pathways in tumor cells, or it can become the cornerstone of new anti-cancer drugs. As shown in some studies, it has a significant inhibitory effect on the proliferation of specific tumor cell lines, just like a good general in ancient times, attacking the enemy's key points and inhibiting the crazy growth of tumor cells.
    In the field of anti-virus, there is also potential. Viruses are raging, like foreign enemies invading, and this compound seems to have the ability to resist. After experimental investigation, it may interfere with the replication process of the virus, as if building a strong barrier, making it difficult for the virus to spread in the host.
    From a market perspective, with the increasing incidence of cancer and viral infections, the demand for related drugs is eager. Due to its unique structure and potential activity, this compound is like a jade waiting to be carved, attracting many pharmaceutical companies and scientific research institutions to compete for research.
    Many R & D projects are in full swing, all hoping to develop it into a clinically usable medicine. Over time, if the research and development goes smoothly and it is put on the market, it will surely be able to be a good recipe for the world, bring good news to many patients, and occupy an important position in the pharmaceutical market, like a shining star, illuminating the road to recovery for patients.