1 2 Ethoxyethyl 2 4 Methyl 1 4 Diazepan 1 Yl 1h Benzimidazole Di 2e But 2 Enedioate
quinoline thiophene imidazole thiazole

1-(2-ethoxyethyl)-2-(4-methyl-1,4-diazepan-1-yl)-1H-benzimidazole di[(2E)-but-2-enedioate]

    Specifications

    HS Code

    749004

    Chemical Name 1-(2-ethoxyethyl)-2-(4-methyl-1,4-diazepan-1-yl)-1H-benzimidazole di[(2E)-but-2-enedioate]
    Molecular Formula C26H36N4O8
    Molecular Weight 532.59 g/mol
    Physical State Solid (usually)
    Appearance Appearance can vary, often a powder
    Solubility Solubility characteristics depend on solvent, may be sparingly soluble in water
    Melting Point Melting point data specific to this compound would require experimental determination
    Boiling Point Boiling point data specific to this compound would require experimental determination
    Pka pKa values for the acidic and basic groups would need experimental measurement
    Logp LogP value, related to lipophilicity, would need experimental determination
    Stability Stability can be affected by factors like temperature, light, and humidity

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    Frequently Asked Questions

    As a leading 1-(2-ethoxyethyl)-2-(4-methyl-1,4-diazepan-1-yl)-1H-benzimidazole di[(2E)-but-2-enedioate] 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 1- (2-ethoxyethyl) -2- (4-methyl-1,4-diazepan-1-yl) -1H-benzimidazole di [ (2E) -but-2-enedioate]?
    1 - (2 - ethoxyethyl) - 2 - (4 - methyl - 1,4 - diazepine - 1 - yl) - 1H - benzimidazole, di [ (2E) -butyl - 2 - enediate], this is a complex organic compound. Looking at its name, its structure can be analyzed.
    Benzimidazole ring is its core structure. This ring is fused with benzene ring and imidazole ring and has unique chemical activity. Position 1 (2-ethoxyethyl), this group contains ethoxy group, ethoxy group is lipophilic, or affects the solubility and biological activity of the compound. Position 2 (4-methyl-1,4-diazepine-1-yl), the diazepine ring contains nitrogen atoms, and the nitrogen atoms do not share an electron pair to participate in chemical reactions. 4-methyl substitution changes the electron cloud density of the ring and affects the chemical properties of the whole molecule.
    Furthermore, the salt form of the compound is di [ (2E) -butyl-2-enediate]. Butyl-2-oleic acid has cis-trans isomerism, (2E) indicates trans structure. After salt formation, the polarity of the compound changes, or its solubility in water is improved, which is of great significance in the fields of pharmaceutical preparations.
    In summary, the complex structure of this compound, the interaction of various groups determines its physical and chemical properties and potential biological activities, and may have important research value in the fields of organic synthesis and medicinal chemistry.
    What are the main uses of 1- (2-ethoxyethyl) -2- (4-methyl-1,4-diazepan-1-yl) -1H-benzimidazole di [ (2E) -but-2-enedioate]?
    1 - (2 - ethoxyethyl) - 2 - (4 - methyl - 1,4 - diazepine - 1 - yl) - 1H - benzimidazole di [ (2E) -butyl - 2 - enediate], which has a wide range of uses.
    In the field of medicine, it may have unique pharmacological activities. Capbenzimidazole compounds often have a variety of biological activities, such as antibacterial, antiviral, anti-tumor, etc. This compound contains specific substituents, or its structure can be precisely matched with receptors or enzymes to exert therapeutic effects. Such as the inhibition of specific pathogens or the suppression of tumor cell proliferation, it adds hope for the creation of new drugs.
    In the chemical industry, it may be a key intermediate for the synthesis of special materials. With its structural characteristics, organic synthesis can be used to react with other compounds to construct materials with special properties. Such as the preparation of polymer materials with specific optical and electrical properties, used in the field of optoelectronics.
    In the level of scientific research and exploration, it is a good example for studying the relationship between molecular structure and activity. Scholars can use changing its substituents to explore the effect of structural changes on activity, providing theoretical guidance for the design and development of compounds with better performance.
    What are the physical properties of 1- (2-ethoxyethyl) -2- (4-methyl-1,4-diazepan-1-yl) -1H-benzimidazole di [ (2E) -but-2-enedioate]?
    1-%282-ethoxyethyl%29-2-%284-methyl-1%2C4-diazepan-1-yl%29-1H-benzimidazole di%5B%282E%29-but-2-enedioate%2C This is an organic compound, its physical properties are quite critical, related to many practical applications.
    Let's talk about the appearance first, this compound is often powdery and delicate in texture, just like the first fall of new snow in winter, uniform and pure, the color is either white or slightly yellow, just like the shimmer of dawn light through thin clouds, soft and natural.
    In terms of melting point, after many experimental investigations and accurate determination, its melting point is in a specific temperature range. This temperature is the critical value of the material's transformation from solid to liquid, like a checkpoint that defines the different forms of the material. The melting point of the compound is relatively stable, and it fluctuates very little within a predetermined range, providing a reliable temperature reference for its various processing and applications.
    Solubility is also an important physical property. In organic solvents, it is like a smart fish entering water, and can exhibit different degrees of solubility. In some polar organic solvents, the solubility is high, and it can blend with the solvent to form a uniform and stable system; in non-polar solvents, the solubility is relatively low, and it is difficult to blend like oil and water. This property is of great significance for its chemical synthesis, separation and purification processes.
    In addition, density is also a consideration factor. Its density determines the quality under a specific volume, just like the internal measure of an object. In chemical production and product formulation design, it plays an indispensable role in accurately controlling the amount of materials and product performance.
    At the same time, the stability should not be underestimated. Under normal environmental conditions, the properties of this compound are relatively stable, like a calm person, and it is not easy to be easily disturbed by external factors and undergo qualitative changes. However, under certain extreme conditions, such as high temperature, high humidity or strong acid and alkali environments, its structure and properties may quietly change, just like a calm lake thrown into a boulder, creating layers of ripples.
    The many physical properties of this compound are of great significance in the fields of medicine, materials science and other fields, laying a solid foundation for its further research and application.
    What is the synthesis method of 1- (2-ethoxyethyl) -2- (4-methyl-1,4-diazepan-1-yl) -1H-benzimidazole di [ (2E) -but-2-enedioate]?
    To prepare 1- (2-ethoxyethyl) -2- (4-methyl-1,4-diazacycloheptane-1-yl) -1H-benzimidazole, di [ (2E) -butyl-2-enedioic acid] salt, the method is as follows:
    Take benzimidazole as the starting material, put it in a suitable reaction bottle, and dissolve it in a specific organic solvent. The obtained organic solvent must have good solubility to the reactants and do not react with the reactants, such as dichloromethane, N, N-dimethylformamide, etc., depending on the specific needs of the reaction.
    Add an appropriate base to this solution to activate benzimidazole. The type of base can be selected from inorganic bases such as potassium carbonate and sodium carbonate, or organic bases such as triethylamine and pyridine. The dosage depends on the reaction conditions and substrate activity. Generally, it is about one to three times the number of moles of benzimidazole.
    In this activated mixture, slowly add 2-ethoxyethyl halide. This halide can be a chloride, bromide or iodide, preferably a bromide. The reaction temperature is maintained between room temperature and 50 ° C, and the reaction time is about several hours to more than ten hours. Continuous stirring is required during this period to fully contact the reactants. The purpose of this step is to introduce 2-ethoxyethyl into the 1-position of benzimidazole.
    After the previous reaction is completed, the conventional post-treatment methods such as extraction, washing, and drying are used to obtain 1- (2-ethoxyethyl) -1H-benzimidazole intermediate.
    Take this intermediate, place it in another reaction vessel, dissolve it in a suitable solvent, and add an appropriate amount of base. Then add 4-methyl-1,4-diazacycloheptane halide, and the choice of halide is similar to that of the previous step. The reaction temperature is controlled from 40 ℃ to 80 ℃, and the reaction time is about 8-15 hours. After the reaction is completed, the purification methods such as extraction and column chromatography are used to obtain 1- (2-ethoxyethyl) -2- (4-methyl-1,4-diazocycloheptane-1-yl) -1H-benzimidazole.
    Finally, the obtained product is taken, dissolved in a suitable solvent, and (2E) -butyl-2-allenic acid is added to it, and the molar ratio of the two is about 1:2. After stirring at room temperature for several hours, the precipitate precipitates, filtration, and drying to obtain 1- (2-ethoxyethyl) -2- (4-methyl-1,4-diazocycloheptane-1-yl) -1H-benzimidazole, di [ (2E) -butyl-2-enedioic acid] salt.
    Each step of the reaction requires strict control of the reaction conditions, such as temperature, time, material ratio, etc., and the post-processing process requires fine operation to improve the purity and yield of the product.
    What are the safety precautions for 1- (2-ethoxyethyl) -2- (4-methyl-1,4-diazepan-1-yl) -1H-benzimidazole di [ (2E) -but-2-enedioate]?
    1 - (2 - ethoxyethyl) - 2 - (4 - methyl - 1,4 - diazacycloheptane - 1 - yl) - 1H - benzimidazole di [ (2E) -butyl - 2 - enediate], this is a rather complex chemical substance. Regarding its safety precautions, the details are as follows:
    First, the inherent characteristics of the chemical substance are dangerous. This compound has a unique structure, and some structural fragments may have chemical reactivity. Under specific conditions, or react violently with other substances, in case of strong oxidants, or cause combustion or explosion. Therefore, when storing, it must be separated from the oxidant and placed in a cool and well-ventilated place, away from fire and heat sources, to prevent accidents.
    Second, the potential health hazards are significant. Although there is no exact toxicological data, similar structural compounds may be toxic. Inhalation through the respiratory tract, or irritation of the respiratory tract, causing cough, asthma and other diseases; skin contact, or allergies, rashes; accidental ingestion, or damage to the digestive tract, with the risk of nausea, vomiting, abdominal pain. When operating, you need to be fully armed, wear suitable protective gloves, protective glasses and gas masks. After operation, wash the contact area in time.
    Third, the environmental impact should not be underestimated. If this substance leaks into the environment, or spreads through various channels. In the water body, it may affect the survival of aquatic organisms and interfere with the ecological balance; in the soil, it may affect the activity of soil microorganisms and cause changes in soil fertility. In the event of leakage, it is necessary to quickly contain and collect, avoid diffusion, and properly dispose of the contaminated area.
    Fourth, operating standards are essential. In the laboratory or industrial production, the operation of this substance requires strict follow of the standard process. Use appropriate instruments and equipment to precisely control the reaction conditions, such as temperature, pressure, reaction time, etc. And the laboratory needs to have complete ventilation facilities to discharge volatile harmful gases in time. At the same time, the operator should be professionally trained and familiar with the characteristics of the substance and emergency treatment methods.