1 2 7 Chlorobenzo B Thien 3 Yl Methoxy 2 2 4 Dichlorophenyl Ethyl 1h Imidazole Mononitrate
quinoline thiophene imidazole thiazole

1-(2-((7-Chlorobenzo(b)thien-3-yl)methoxy)-2-(2,4-dichlorophenyl)ethyl)-1H-imidazole mononitrate

    Specifications

    HS Code

    551281

    Chemical Name 1-(2-((7-Chlorobenzo(b)thien-3-yl)methoxy)-2-(2,4-dichlorophenyl)ethyl)-1H-imidazole mononitrate
    Molecular Formula C22H17Cl3N4O4S
    Molecular Weight 541.82 g/mol
    Appearance Typically a solid, color may vary depending on purity
    Melting Point Specific melting point data would require experimental determination
    Solubility Solubility characteristics would depend on the solvent; likely sparingly soluble in water
    Pka No common pKa data available without specific experimental work
    Logp A value reflecting lipophilicity would need to be experimentally determined
    Stability Stability may be influenced by light, heat, and humidity
    Pharmacological Class Potential antifungal or other bio - active class (if applicable, based on imidazole structure)

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    Frequently Asked Questions

    As a leading 1-(2-((7-Chlorobenzo(b)thien-3-yl)methoxy)-2-(2,4-dichlorophenyl)ethyl)-1H-imidazole mononitrate 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- ((7-Chlorobenzo (b) thien-3-yl) methoxy) -2- (2,4-dichlorophenyl) ethyl) -1H-imidazole mononitrate?
    This is the chemical structure of 1- (2- ((7-chlorobenzo (b) thiophene-3-yl) methoxy) -2 - (2,4-dichlorophenyl) ethyl) -1H-imidazole mononitrate. I will explain it in the style of the ancient saying.
    The structure of this compound, 1H-imidazole is its core structure. In the case of imidazole, the five-membered nitrogen-containing heterocycle is also connected to the 2- ((7-chlorobenzo (b) thiophene-3-yl) methoxy) -2 - (2,4-dichlorophenyl) ethyl group at the first position on the ring.
    View 2- ((7-chlorobenzo (b) thiophene-3-yl) methoxy) -2 - (2,4-dichlorophenyl) ethyl moiety, in which the 2-position carbon atom is connected with (7-chlorobenzo (b) thiophene-3-yl) methoxy on one side. The benzo (b) thiophene is a structure formed by fusing the benzene ring with the thiophene ring. There is a chlorine atom substituted at the 7th position, and it is connected to the oxygen atom through methylene, and then to the carbon at the 2nd position of the main body. The other side is connected with 2,4-dichlorophenyl, that is, there is a chlorine atom substituted at the 2nd and 4th positions of the benzene ring.
    Furthermore, this compound is a mononitrate, which means that it is bound to one molecule of nitrate. The nitrate is formed by connecting the nitrogen atom to the three oxygen atoms in a specific chemical bond. This bonding method gives the compound unique chemical and physical properties.
    In summary, the chemical structure of 1- (2- ((7-chlorobenzo (b) thiophene-3-yl) methoxy) -2 - (2,4-dichlorophenyl) ethyl) -1H-imidazole mononitrate is composed of the above parts according to a specific connection method, and the parts interact with each other to co-construct this complex and unique chemical entity.
    What are the physical properties of 1- (2- ((7-Chlorobenzo (b) thien-3-yl) methoxy) -2- (2,4-dichlorophenyl) ethyl) -1H-imidazole mononitrate?
    1 - (2 - ((7 - chlorobenzo (b) thiophene - 3 - yl) methoxy) - 2 - (2,4 - dichlorophenyl) ethyl) - 1H - imidazole mononitrate, this is an organic compound. Its physical properties are unique, let me tell them one by one.
    Looking at its morphology, it is mostly solid at room temperature and pressure. White to off-white crystalline powders are common in appearance and delicate in texture, like finely crushed Qiongyu.
    When it comes to melting point, the melting point of this compound is in a specific range, but the exact value fluctuates slightly due to different measurement conditions, and is roughly within a certain temperature range. This temperature is the critical point for its transition from solid to liquid.
    Solubility is also an important physical property. In organic solvents, such as common ethanol and dichloromethane, it shows a certain solubility. Ethanol, as a common organic solvent, can dissolve some of the compounds, just like fish entering water, gradually dispersing and blending. In water, its solubility is relatively poor, and it mostly exists in the water body in a suspended state, like sand and stones entering water, which is difficult to melt and difficult to dissolve.
    Its density also has characteristics. Although it is not easily felt, this parameter is crucial in fine chemical operations and research. Density determines its distribution and behavior in a specific system, just as everything has its place in heaven and earth, and affects the state of many chemical reaction processes and matter mixing.
    In addition, the stability of this compound to light and heat is also a key physical property. Under light, it may cause structural changes, just like a delicate flower sees light, and its color and morphology gradually change; in a heated environment, if the temperature rises to a certain extent, it may also cause decomposition or other chemical changes, like a burning object, which is beyond recognition. Therefore, when storing and using, it is necessary to properly consider such properties to ensure its quality and efficiency.
    What is the use of 1- (2- ((7-Chlorobenzo (b) thien-3-yl) methoxy) -2- (2,4-dichlorophenyl) ethyl) -1H-imidazole mononitrate?
    1 - {2 - [ (7 -chlorobenzo (b) thiophene-3-yl) methoxy] -2 - (2,4 -dichlorophenyl) ethyl} -1H -imidazolium mononitrate, this is a complex organic compound. It has a wide range of uses and is often used as an important active ingredient in the field of medicine. Many studies have shown that it has potential antibacterial, anti-inflammatory and other pharmacological activities, or can be used to develop new antibacterial drugs against bacteria that are resistant to traditional drugs.
    Looking back at the past, this compound may be a key link in the process of drug development. Although there was no such advanced technology as modern times in ancient times, the ancestors also tried to find ways to cure diseases and save people from natural substances through unremitting exploration. Today, chemical synthesis technology has advanced, and our research on such compounds is also more in-depth.
    In agriculture, it may be used as a raw material for pesticides. With its special chemical structure, it may be used to prepare pesticides or fungicides to protect crops from pests and diseases, ensure a bumper grain harvest, and help the development of agriculture.
    In the process of scientific research and exploration, it provides scientists with samples for research. Scholars can use the study of its structure and properties to gain a deeper understanding of the reaction mechanism of organic compounds, contributing to the progress of organic synthesis chemistry. Perhaps more novel compounds could be derived from this, providing new opportunities for fields such as materials science.
    What are the synthesis methods of 1- (2- ((7-Chlorobenzo (b) thien-3-yl) methoxy) -2- (2,4-dichlorophenyl) ethyl) -1H-imidazole mononitrate?
    1 - (2 - ((7 - chlorobenzo (b) thiophene - 3 - yl) methoxy) - 2 - (2,4 - dichlorophenyl) ethyl) - 1H - imidazole mononitrate synthesis method, there are various ways.
    First, the selection of raw materials is the key. When 7 - chlorobenzo (b) thiophene - 3 - formaldehyde, 2,4 - dichloroacetophenone, etc. are used as the starting materials. These two need to be selected with the best quality, and the reaction will be smooth if there are few impurities.
    times, the reaction steps should be carefully arranged. First, 7-chlorobenzo (b) thiophene-3-formaldehyde is reacted with suitable reagents to obtain (7-chlorobenzo (b) thiophene-3-yl) methanol. This step requires temperature control and control. If the temperature is too high or too low, the product can be impure. 2,4-dichloroacetophenone is converted into the corresponding intermediate through a specific reaction. Then, (7-chlorobenzo (b) thiophene-3-yl) methanol is reacted with intermediates derived from 2,4-dichloroacetophenone to form key intermediates. The reaction conditions at this step are rather particular. The choice of solvent and the amount of catalyst affect the reaction process and product yield.
    Then, react with imidazole with key intermediates to generate 1- (2- ((7-chlorobenzo (b) thiophene-3-yl) methoxy) -2- (2,4-dichlorophenyl) ethyl) -1H-imidazole. When reacting, pay attention to the pH of the reaction environment and adjust it in time to make the reaction perfect. At the end of
    , the imidazole product is reacted with nitric acid to obtain 1- (2- ((7-chlorobenzo (b) thiophene-3-yl) methoxy) -2- (2,4-dichlorophenyl) ethyl) -1H -imidazole mononitrate. This step should pay attention to the concentration of nitric acid and the reaction temperature to prevent overreaction.
    The whole process of synthesis, separation and purification cannot be ignored. Each step of the product is purified by recrystallization, column chromatography, etc., to remove impurities, and to obtain high purity of 1- (2- ((7-chlorobenzo (b) thiophene-3-yl) methoxy) -2- (2,4-dichlorophenyl) ethyl) -1H-imidazole mononitrate.
    What is the safety of 1- (2- ((7-Chlorobenzo (b) thien-3-yl) methoxy) -2- (2,4-dichlorophenyl) ethyl) -1H-imidazole mononitrate?
    1-%282-%28%287-Chlorobenzo%28b%29thien-3-yl%29methoxy%29-2-%282%2C4-dichlorophenyl%29ethyl%29-1H-imidazole mononitrate, this is a complex chemical substance. Looking at its safety, when examining various data in detail, there is no conclusive conclusion today.
    In the past, Shennong tasted all kinds of herbs to observe the physical properties. In order to know the safety of this substance, it needs to be explored many times. In laboratory research, it should be observed that it affects cells and animals. If it is applied to cells, it should be observed whether there are toxic reactions, such as apoptosis and abnormal proliferation. In animal experiments, it should be observed that it affects physiological functions, such as organ function and behavioral changes.
    At the environmental level, it is necessary to explore its degradation in nature after discharge, and its impact on the ecosystem. If it is difficult to degrade or enriched in organisms, it may pose a threat to the ecological balance.
    In human application, more caution is required. Although its specific use is not known, if it involves medical drugs, it must undergo rigorous clinical trials to check its efficacy and safety. If a drug is a clinical trial, it needs to be carried out in stages, from a small number of healthy subjects to a large number of patients, and adverse reactions should be carefully observed.
    The safety of this substance needs comprehensive multi-faceted research, and rigorous scientific verification can only be understood, and no conclusions can be made.