1 2 4 5 Benzenetetracarboxylic Acid Compound With 4 5 Dihydro 2 Phenyl 1h Imidazole 1 2
quinoline thiophene imidazole thiazole

1,2,4,5-Benzenetetracarboxylic acid,compound with 4,5-dihydro-2-phenyl-1H-imidazole(1:2)

    Specifications

    HS Code

    389519

    Chemical Formula C24H18N2O8
    Molar Mass 474.41 g/mol
    Appearance Solid (usually a powder)
    Physical State Solid at room temperature
    Solubility Solubility may vary in different solvents, relatively insoluble in water
    Melting Point Specific melting point data would require experimental determination
    Boiling Point Decomposes before boiling in most cases
    Density Density data needs experimental measurement
    Acidity The benzenetetracarboxylic acid part contributes acidic properties
    Reactivity Can participate in reactions typical of carboxylic acids and imidazole derivatives, like esterification with alcohols for carboxylic acid groups and ring - opening reactions for imidazole under certain conditions

    As an accredited 1,2,4,5-Benzenetetracarboxylic acid,compound with 4,5-dihydro-2-phenyl-1H-imidazole(1:2) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    General Information
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    Frequently Asked Questions

    As a leading 1,2,4,5-Benzenetetracarboxylic acid,compound with 4,5-dihydro-2-phenyl-1H-imidazole(1:2) 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 the compound (1:2) of 1,2,4,5-phenyltetracylic acid and 4,5-dihydro-2-phenyl-1H-imidazole?
    The compound formed by the reaction of the two is formed by a chemical combination. The nitrogen atom of the imidazole ring is electron-rich and nucleophilic with 4,5-dihydro-2-phenyl-1H-imidazole in a ratio of 1:2. The recombination of chemical bonds and the arrangement of atoms follow the rules of chemistry.
    1,2,4,5-benzene tetracarboxylic acid has multiple carboxyl groups, and its carboxyl group activity check point can interact with specific atoms in 4,5-dihydro-2-phenyl-1H-imidazole. The nitrogen atom of the imidazole ring is electron-rich and nucleophilic, and can be linked to the carboxyl group of benzene tetracarboxylic acid through dehydration and condensation. < Br >
    In a ratio of 1:2, or to form a complex with a specific structure. Among them, two 4,5-dihydro-2-phenyl-1H-imidazole molecules are combined with a 1,2,4,5-benzene tetracarboxylic acid molecule, or the structure is stabilized by weak interactions such as hydrogen bonding and π-π stacking. From the perspective of spatial configuration, the benzene ring of benzene tetracarboxylic acid and the phenyl group of imidazole interact to form a unique spatial structure.
    The chemical structure of this compound is determined by the precise connection order and spatial arrangement between atoms. Each atom forms covalent bonds, ionic bonds or weak interactions according to the rules of chemical bonding, thus endowing the compound with specific physical and chemical properties, which may have potential applications in materials science, medicinal chemistry and other fields.
    What are the physical properties of the compound of 1,2,4,5-phenyltetracylic acid and 4,5-dihydro-2-phenyl-1H-imidazole (1:2)
    1%2C2%2C4%2C5-%E8%8B%AF%E5%9B%9B%E7%94%B2%E9%85%B8%E4%B8%8E4%2C5-%E4%BA%8C%E6%B0%A2-2-%E8%8B%AF%E5%9F%BA-1H-%E5%92%AA%E5%94%91%E7%9A%84%E5%8C%96%E5%90%88%E7%89%A9%281%3A2%29%E6%9C%89%E5%93%AA%E4%BA%9B%E7%89%A9%E7%90%86%E6%80%A7%E8%B4%A8%EF%BC%9F
    The compound formed by the two (1:2) has many physical properties. Its appearance is often specific, or crystalline, with a certain color, but the exact color varies depending on the preparation and purity.
    When talking about the melting point, due to the interaction of the internal structure of the compound, it begins to melt at a specific temperature range when heated. This temperature range is one of its important physical properties and can provide key clues for the identification of the substance.
    In terms of solubility, it may have different solubility in common organic solvents. In some polar solvents, it may exhibit a certain solubility, which is due to the matching of intermolecular forces. In non-polar solvents, the dissolution is very different, or slightly soluble, or insoluble, and this difference also reflects the characteristics of the molecular polarity of the compound.
    Density is also one of its physical properties. By precise measurement, the mass per unit volume can be obtained. Compared with other similar compounds, this value can reveal the molecular compactness and composition differences.
    In addition, the refractive index of the compound, when light is transmitted through, exhibits unique physical properties, which are of great significance for its optical applications and further analysis and identification.
    The physical properties of this compound are an important basis for in-depth understanding of its essence and application potential.
    What is the main use of the compound of 1,2,4,5-benzetracylic acid with 4,5-dihydro-2-phenyl-1H-imidazole (1:2)?
    1% 2C2% 2C4% 2C5-terephthalic acid and 4% 2C5-dihydroxy-2-phenyl-1H-imidazole compounds (1:2), this is a special combination of chemical substances. Its main uses are quite extensive, and in the field of materials science, it can be used as a key raw material for the preparation of high-performance polymer materials. Due to its unique chemical structure and properties, it can endow polymers with excellent thermal stability, mechanical properties and chemical stability, so it is often used in the manufacture of high-performance materials required in high-end fields such as aerospace and automotive industries.
    In the field of medicinal chemistry, it also has potential application value. It may be used as a pharmaceutical intermediate, which can be converted into bioactive compounds through specific chemical reactions, and used to develop new drugs to deal with various diseases such as cancer and cardiovascular diseases.
    In terms of scientific research exploration, this compound provides an excellent model for studying molecular interactions, crystal structures, and physical and chemical properties of materials. With the help of in-depth research on it, researchers can better understand the chemical behavior and laws at the molecular level, laying a theoretical foundation for the development of novel materials and drugs.
    In summary, 1% 2C2% 2C4% 2C5-benzoic acid and 4% 2C5-dihydroxy-2-phenyl-1H-imidazole compounds (1:2) play a crucial role in many fields such as materials, medicine and scientific research, and are of great significance in promoting the development of related fields.
    What are the synthesis methods of 1,2,4,5-phenyltetracylic acid and 4,5-dihydro-2-phenyl-1H-imidazole compounds (1:2)?
    To prepare 1% 2C2% 2C4% 2C5-terephthalic acid and 4% 2C5-dihydro-2-phenyl-1H-imidazole (1:2), the method is as follows.
    First take an appropriate amount of raw materials, namely 1% 2C2% 2C4% 2C5-terephthalic acid and 4% 2C5-dihydro-2-phenyl-1H-imidazole, and weigh them accurately in a ratio of 1:2. This ratio is crucial and affects the purity and yield of the product.
    Then place the weighed raw materials in a suitable reaction vessel. The container needs to be clean and dry to prevent impurities from mixing and affecting the reaction. Next, select a suitable solvent to fully dissolve the raw material. The selected solvent should be able to effectively dissolve the raw material without adverse interference to the reaction.
    After the raw material is evenly dispersed in the solvent, the reaction temperature and pressure are controlled according to the characteristics of the reaction. The precise regulation of temperature and pressure is the key to the smooth progress of the reaction. Or the heating device can be used to slowly heat up and closely monitor the temperature change, so that the reaction can proceed stably at the set temperature.
    During the reaction process, it is necessary to continuously stir to promote the full contact of the raw material and speed up the reaction rate. At the same time, carefully observe the reaction phenomena, such as color changes, precipitation formation, etc., to judge the reaction process. After the
    reaction is completed, suitable separation and purification methods are used to remove the solvent and unreacted impurities. Or by filtration, distillation, extraction, etc., the target compound can be purified. Finally, after drying treatment, the required 1% 2C2% 2C4% 2C5-benzetracarboxylic acid and 4% 2C5-dihydro-2-benzyl-1H-imidazole compounds (1:2) can be obtained. The whole process requires strict operation to ensure the quality and yield of the product.
    What are the precautions for the storage and transportation of compounds of 1,2,4,5-phenyltetracylic acid and 4,5-dihydro-2-phenyl-1H-imidazole (1:2)?
    The compounds of 1% 2C2% 2C4% 2C5-terephthalic acid and 4% 2C5-dihydroxy-2-benzoyl-1H-imidazole (1:2) are rather special chemicals. When storing and transporting, it is necessary to pay attention to many key matters.
    Bear the brunt, the storage environment is crucial. This compound should be placed in a cool, dry and well-ventilated place. Due to its extreme sensitivity to temperature and humidity, high temperature and humidity can easily cause it to chemically react and lead to deterioration. If stored in a place where the temperature is too high, it may cause the decomposition or polymerization of the compound and damage its chemical structure; and if the humidity is too high, it is easy to make the compound damp and affect its purity and stability. Therefore, the temperature of the storage environment should be maintained within a specific range, and the relative humidity should also be strictly controlled.
    Secondly, the compound may be sensitive to light. Light may stimulate photochemical reactions and change its properties. Therefore, when storing, it should be avoided from light, and it can be stored in dark containers such as brown bottles, or placed in a dark place.
    Furthermore, the transportation process cannot be ignored. Be careful when handling to prevent damage to the packaging. Due to its certain chemical activity, if the package breaks and comes into contact with air, moisture or other substances, it may cause uncontrollable reactions. At the same time, the environment in the transportation vehicle should also maintain a suitable temperature and humidity to avoid violent vibration and turbulence, so as to prevent the compound from changing its properties due to physical shock.
    In addition, this compound may have certain toxicity or irritation. Whether it is storage or transportation personnel, they should be equipped with appropriate protective equipment, such as gloves, protective glasses and masks, to avoid direct contact and harm to the body. In addition, the relevant places should be equipped with complete emergency treatment facilities. In the event of an accident such as leakage, effective measures can be taken quickly to deal with it and reduce the harm.