1 2 4 Chlorophenyl Methoxy 2 2 4 Dichlorophenyl Ethyl 1h Imidazole Mononitrate
quinoline thiophene imidazole thiazole

1-[2-[(4-chlorophenyl)methoxy]-2-(2,4-dichlorophenyl)-ethyl]-1h-imidazole mononitrate

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    HS Code

    160942

    Chemical Name 1-[2-[(4-chlorophenyl)methoxy]-2-(2,4-dichlorophenyl)ethyl]-1H-imidazole mononitrate

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    General Information
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    Frequently Asked Questions

    As a leading 1-[2-[(4-chlorophenyl)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- [ (4-chlorophenyl) methoxy] -2- (2,4-dichlorophenyl) -ethyl] -1h-imidazole mononitrate?
    This is the problem of the chemical substance 1- [2- [ (4-chlorophenyl) methoxy] -2 - (2,4-dichlorophenyl) -ethyl] -1H-imidazole mononitrate. To clarify its chemical structure, it is necessary to analyze its naming.
    The main body is "1H-imidazole", which is a five-membered nitrogen-containing heterocycle with two nitrogen atoms. There is a long chain substituent at the first position, namely "[2 - [ (4-chlorophenyl) methoxy] -2 - (2,4-dichlorophenyl) -ethyl]". In this long chain, there are two phenyl groups attached to the 2-position carbon, one is " (4-chlorophenyl) ", which has a chlorine atom substituted at the 4-position of the benzene ring; the other is " (2,4-dichlorophenyl) ", which has chlorine atoms at the 2 and 4 positions of the benzene ring. And the 2-position carbon is also connected with " (4-chlorophenyl) methoxy]", which means that 4-chlorophenyl is connected to the main chain 2-position carbon through methylene and oxygen. And because it is a mononitrate, it indicates that this organic molecule forms a salt with one molecule of nitric acid.
    So, the structure of this chemical substance is based on 1H-imidazole as the core, with a specific long chain substituent in 1 position, and forms a salt with nitric acid. After this analysis, the appearance of its chemical structure is gradually clear.
    What are the main uses of 1- [2- [ (4-chlorophenyl) methoxy] -2- (2,4-dichlorophenyl) -ethyl] -1h-imidazole mononitrate?
    1 - [2 - [ (4 - chlorophenyl) methoxy] - 2 - (2,4 - dichlorophenyl) -ethyl] - 1H - imidazole mononitrate, this is an organic compound. Its main uses are quite extensive, in the field of medicine, or as a key component of antibacterial drugs. Because its structure contains specific phenyl and imidazole groups, or it has inhibitory and killing effects on specific pathogens, it can help humans resist infectious diseases and seek well-being for patients.
    In the field of chemical synthesis, it may be used as an important intermediate. With its unique chemical structure and specific reactions with other compounds, new materials with special properties can be prepared, such as new polymer materials, which play a role in promoting the development of materials science.
    At the level of scientific research and exploration, this compound may be a research hotspot. By studying its chemical properties and reaction mechanism, researchers can expand the boundaries of organic chemistry knowledge and contribute to the theoretical development of related fields. And its properties change under different conditions, or lay the foundation for the development of innovative applications.
    Its uses span many fields such as medicine, chemical industry and scientific research, and are of great significance to human life and scientific progress.
    What is the safety of 1- [2- [ (4-chlorophenyl) methoxy] -2- (2,4-dichlorophenyl) -ethyl] -1h-imidazole mononitrate?
    1-% 5B2-% 5B% 284 -chlorophenyl% 29 methoxy% 5D - 2 - (2,4 -dichlorophenyl) -ethyl% 5D - 1H -imidazole mononitrate This product is related to its safety and needs to be investigated in detail.
    Ancient times discuss the safety of things, and its properties, sources, and uses are often observed. From this perspective, in terms of its chemical structure, the presence of chlorine atoms containing chlorophenyl and imidazole groups may affect its chemical activity and stability. In chemical reactions, chlorine atoms may easily cause reactions such as substitution and addition. This process may produce new chemical substances. If not handled properly, it may be potentially harmful.
    Looking at its use, if it is used in the field of medicine, its safety review must be strict. Drugs need to undergo many clinical trials to consider their efficacy and side effects on the human body. The structure of this compound is complex, or unknown metabolites are produced during metabolism in the body, which affects the normal physiological function of the human body. If it involves industrial use, the use of raw materials in the production process and the control of reaction conditions are all related to safety. If the reaction temperature and pressure are not properly controlled, or the reaction is out of control, causing a safety accident. And if this substance is released into the environment, due to its chemical properties, or difficult to degrade, it accumulates in the environment, affects the ecological balance, and endangers the survival of organisms.
    Therefore, to clarify the safety of 1-% 5B2-% 5B% 284 -chlorophenyl% 29 methoxy% 5D-2 - (2,4 -dichlorophenyl) -ethyl% 5D-1H -imidazole mononitrate, it is necessary to comprehensively investigate its chemical properties, uses and potential effects on human body and the environment.
    What is the market outlook for 1- [2- [ (4-chlorophenyl) methoxy] -2- (2,4-dichlorophenyl) -ethyl] -1h-imidazole mononitrate?
    1-%5B2-%5B%284-chlorophenyl%29methoxy%5D-2-%282%2C4-dichlorophenyl%29-ethyl%5D-1h-imidazole mononitrate, this is a specific chemical, often referred to as itraconazole mononitrate. Itraconazole is a commonly used antifungal drug in the field of medicine and can effectively treat infections caused by a variety of fungi.
    Looking at its market prospects, with the increasing incidence of fungal infections, its demand is also on the rise. Today, changes in living environments, the aging of the population, and the increase in the number of immunosuppressed people have made fungal infections more common. Such as deep fungal infections, which pose a great threat to the health and life of patients, itraconazole plays an important role in the treatment of such diseases due to its good efficacy and safety.
    Furthermore, in the pharmaceutical industry, the research and development and production of high-efficiency and safe antifungal drugs are highly valued. 1-%5B2-%5B%284-chlorophenyl%29methoxy%5D-2-%282%2C4-dichlorophenyl%29-ethyl%5D-1h-imidazole mononitrate as a mature antifungal ingredient, the relevant pharmaceutical technology has become mature, and the large-scale capacity is also guaranteed, which can better meet the market demand.
    However, market competition should not be underestimated. Many pharmaceutical companies have ventured into the field of antifungal drugs and developed and launched similar products. To stand out in the market, companies need to make efforts in product quality, price and R & D innovation. On the one hand, strictly control the production process to ensure the stable and reliable quality of drugs; on the other hand, optimize costs and attract customers at competitive prices. At the same time, continue to invest in research and development, improve product dosage forms, improve curative effect or expand the scope of application, in order to occupy a stable place in the fierce market competition. Although the market prospect is broad, challenges also exist.
    What is the production process of 1- [2- [ (4-chlorophenyl) methoxy] -2- (2,4-dichlorophenyl) -ethyl] -1h-imidazole mononitrate?
    1 - [2 - [ (4 - chlorophenyl) methoxy] - 2 - (2,4 - dichlorophenyl) -ethyl] - 1H - imidazole mononitrate, which is an important product in the synthesis of medicine. Its production process is exquisite and requires careful preparation through multi-step reactions.
    The first step is to take a specific halogenated aromatic hydrocarbon, such as 4 - chlorobenzyl chloride, and an appropriate alcohol. Under the catalysis of a base, through a nucleophilic substitution reaction, an intermediate containing (4 - chlorophenyl) methoxy is obtained. In this step, the amount of alkali, reaction temperature and time are all key, and precise control can obtain a high yield intermediate.
    In the next step, the obtained intermediate is mixed with 2,4-dichloroacetophenone in a specific solvent. Under the action of strong base, a condensation reaction occurs to generate 2- [ (4-chlorophenyl) methoxy] -2- (2,4-dichlorophenyl) -acetone. In this process, the polarity of the solvent, the type and amount of strong base have a great impact on the reaction process and the purity of the product.
    Subsequently, the above-mentioned acetone intermediates are reduced with suitable reducing agents, such as sodium borohydride, etc., and the carbonyl group is reduced to a hydroxyl group to obtain the corresponding alcohol intermediate. Whether the reduction reaction conditions are mild or not, the accuracy of the amount of reducing agent depends on the configuration and purity of the product.
    Then, the alcohol intermediate and imidazole are condensed with the help of a condensing agent to form 1 - [2 - [ (4-chlorophenyl) methoxy] - 2 - (2,4-dichlorophenyl) - ethyl] - 1H - imidazole. The activity of the condensation agent and the pH of the reaction system are all factors that affect the success or failure of the reaction.
    Finally, the above imidazole products are salted with nitric acid, and the concentration and dosage of nitric acid are strictly controlled, and the reaction temperature and time are strictly controlled to obtain 1 - [2 - [ (4 - chlorophenyl) methoxy] - 2 - (2,4 - dichlorophenyl) -ethyl] - 1H - imidazole mononitrate. After each step of the reaction, it needs to go through separation and purification processes, such as extraction, crystallization, column chromatography, etc., to ensure the high purity of the product and meet the strict requirements of pharmaceutical production.