1 2 2 4 Dichlorophenyl 2 4 Phenylthio Phenyl Methoxy Ethyl 1h Imidazole
quinoline thiophene imidazole thiazole

1-[2-(2,4-Dichlorophenyl)-2-[[4-(Phenylthio)Phenyl]Methoxy]Ethyl]-1H-Imidazole

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    HS Code

    721972

    Chemical Name 1-[2-(2,4-Dichlorophenyl)-2-[[4-(Phenylthio)Phenyl]Methoxy]Ethyl]-1H-Imidazole

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    Frequently Asked Questions

    As a leading 1-[2-(2,4-Dichlorophenyl)-2-[[4-(Phenylthio)Phenyl]Methoxy]Ethyl]-1H-Imidazole 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 main use of 1- [2- (2,4-dichlorophenyl) -2- [[4- (phenylthio) phenyl] methoxy] ethyl] -1H-imidazole
    1 - [2 - (2,4 -dihydroxyphenyl) - 2 - [[4 - (phenyl) phenyl] ethoxy] ethyl] -1H -indole, although this substance is not directly recorded in Tiangong Kaiwu, it can be used from similar materials.
    This compound contains a specific group structure, or has unique chemical and physical properties. In ancient China, although there is no modern precise chemical understanding, it has long been used for materials with similar properties.
    Like ancient dyeing and weaving, materials with color change and color fixing are often sought. If this material has similar properties, it can be used for dyeing improvement. Ancient craftsmen took colors from herbs and minerals. If this compound can stabilize the color under specific conditions, it can increase the color gamut and fastness of dyes.
    Ancient medicine, focusing on herbal pharmacology. Although the exact molecular structure of this compound is unknown, if it has some activity, it may be used for medicinal exploration. The ancients tested medicine with experience. If this compound has potential effects such as anti-inflammatory and antibacterial, it may be included in the category of medicinal use after trying.
    Like ancient incense making, the pursuit of a unique and lasting aroma. If this compound can emit a pleasant aroma or has a fragrance-enhancing effect, or is used by incense makers, it will enhance the charm of fragrance products. Although there is no exact ancient book on its use, it is analogous to ancient technological applications according to its characteristics, or has potential applications in the fields of dyeing, weaving, medicine, and incense making.
    What are the chemical properties of 1- [2- (2,4-dichlorophenyl) -2- [[4- (phenylthio) phenyl] methoxy] ethyl] -1H-imidazole
    1-% [2- (2,4-dihydroxyphenyl) -2- [4- (phenyl) phenyl] ethoxy] ethyl-1H-imidazole is a complex organic compound. Its chemical properties are as follows:
    This compound is basic because it contains an imidazole ring, and can react with acids to form corresponding salts. Under suitable conditions, the imidazole ring can participate in nucleophilic substitution reactions. The nitrogen atom acts as a nucleophilic check point and combines with electrophilic reagents such as halogenated hydrocarbons to realize functionalization, thereby introducing various substituents to expand its chemical properties and application scope. The phenyl ring in the
    molecule endows the compound with certain stability and conjugation system. Due to the conjugation effect, the benzene ring can absorb light of specific wavelengths, so that the compound may have certain optical properties, such as a characteristic absorption peak in the ultraviolet-visible region, which can be used for qualitative and quantitative analysis. At the same time, the benzene ring is prone to electrophilic substitution reactions, such as halogenation, nitrification, sulfonation, etc., which can modify the molecular structure to meet different needs.
    And the hydroxyl group in it has active hydrogen, which can participate in the formation of hydrogen bonds and affect the physical properties of the compound, such as melting point, boiling point, and solubility. The hydroxyl group can also undergo esterification reaction, and the acid can form ester compounds under the action of the catalyst; or under the action of appropriate oxidizing agents, it can be converted into other functional groups such as aldehyde groups and carboxyl groups. The
    ether bond is relatively stable under general conditions, but under special conditions such as strong acids, it may break and produce corresponding alcohols and halogenated hydrocarbons. The compound is rich in chemical properties, and it can be modified and transformed through rational design of reaction conditions, which shows potential application value in many fields such as materials science and medicinal chemistry.
    What is the production process of 1- [2- (2,4-dichlorophenyl) -2- [[4- (phenylthio) phenyl] methoxy] ethyl] -1H-imidazole
    The production process of 1-% [2- (2,4-dioxybenzyl) -2- [[4- (silicon carboxyl) benzyl] ethoxy] ethyl] -1H-imidazole is a delicate and complicated process, so let me go through it in detail.
    At the beginning, various raw materials, such as organic compounds containing specific groups, need to be prepared, which is the cornerstone of the reaction. First take the reactant containing 2,4-dioxybenzyl structure, put it in a suitable reaction vessel, and add an appropriate amount of catalyst and solvent. This solvent needs to be able to dissolve the reactants without interfering with the reaction process. Like common organic solvents, its polarity and boiling point have been carefully considered.
    Then, the temperature is raised to a specific range, which is obtained by repeated experiments and affects the reaction rate and product purity. At this temperature, a benzyl reactant containing silicon carboxyl groups is introduced, and the two interact to form an intermediate through a series of complex chemical reactions. The structure and properties of this intermediate have a profound impact on subsequent reactions.
    Subsequently, the ethoxy reactant is added, and the reaction conditions are adjusted again, or the temperature is changed, or the ratio of the reactants is adjusted, so that the reaction proceeds in the direction of generating the target product 1-% [2- (2,4-dioxybenzyl) -2- [4- (silicon carboxyl) benzyl] ethoxy] ethyl] -1H-imidazole. After the
    reaction is completed, the product is still mixed in the reaction system, and needs to be separated and purified. Commonly used methods include distillation, extraction, recrystallization, etc. Distillation can separate the target product according to the difference in the boiling point of each substance; extraction uses different solvents to have different solubility of the product and impurities to achieve preliminary separation; recrystallization can further improve the purity of the product and remove trace impurities.
    Through this multi-step process, a pure 1-% [2- (2,4-dioxybenzyl) -2- [[4- (silicon carboxyl) benzyl] ethoxy] ethyl] -1H-imidazole product can be obtained to meet the needs of industry or scientific research.
    What is the market price of 1- [2- (2,4-dichlorophenyl) -2- [[4- (phenylthio) phenyl] methoxy] ethyl] -1H-imidazole?
    The question asked by the watcher is about the price of 1 - [2 - (2,4 - dihydroxyphenyl) - 2 - [[4 - (phenyl) phenyl] ethoxy] ethyl] -1H - indole in the market. However, this chemical substance is extremely complicated and unusual.
    Although "Tiangong Kaiwu" is a strange book, it involves most of the skills of agriculture and industry, the source and production of products, and the price of such fine chemicals is really difficult to cover. If the art of chemistry at that time has not been realized, how can there be such a thing in the market?
    If you want to know the price of this substance today, you can only get it if you consult the industry and vendors in the market of chemical materials and specialized chemical trading platforms in this world. Because the price of chemical substances often varies with the abundance of raw materials, the difficulty of production methods, and the amount of demand, it cannot be said in a word. Or in the field of fine chemicals, there are specialized companies that sell this rare substance, and its price may vary due to purity and quantity. To obtain the exact number, you must search for information widely and ask all parties in the industry to know its actual price in the market.
    What are the relevant safety precautions for 1- [2- (2,4-dichlorophenyl) -2- [[4- (phenylthio) phenyl] methoxy] ethyl] -1H-imidazole?
    1 - [2 - (2,4 - diethylamino) - 2 - [[4 - (silicon carboxyl) silicon] ethoxy] ethyl] - 1H - imidazole related safety precautions are as follows:
    This substance contains special chemical groups, and its chemical activity should be paid attention to during operation. 2,4 - diethylamino groups are alkaline and come into contact with the skin or eyes, which may cause irritation and burns. Be sure to wear complete protective equipment, such as protective gloves, goggles and lab clothes, to avoid direct contact. < Br >
    [4- (silicon carboxyl) silyl] ethoxyethyl moiety, its chemical properties or react with surrounding substances. When using, keep away from strong oxidizing agents, strong acids and strong bases to prevent violent chemical reactions, and even cause explosions or release toxic gases.
    1H-imidazole has a lively structure and can participate in a variety of chemical reactions under specific conditions. When storing, it should be placed in a cool, dry and well-ventilated place, away from fire and heat sources to prevent its properties from changing due to changes in temperature and humidity.
    When using products containing this ingredient or conducting related experiments, the experimental site should be equipped with good ventilation facilities to disperse possible harmful gases. If you accidentally come into contact with this substance, skin contact should be rinsed with a large amount of water as soon as possible, and then seek medical attention according to the specific situation; eye contact should be immediately rinsed with flowing water and seek medical attention quickly. After the operation is completed, properly dispose of the remaining substances and waste, follow relevant environmental protection and safety regulations, and must not be discarded at will to avoid polluting the environment or causing safety accidents.