3 Methyl 4 2 2 2 Trifluoro Ethoxy 2 Pyridinyl Methyl Thio 1h Benzimidazole
quinoline thiophene imidazole thiazole

3-Methyl-4-[((2,2,2-trifluoro ethoxy-2-pyridinyl)methyl)thio]-1H-Benzimidazole

    Specifications

    HS Code

    637998

    Chemical Formula C16H14F3N3OS
    Molecular Weight 369.36
    Appearance Solid (usually white or off - white powder)
    Melting Point Typically in a specific range, data needed from literature
    Solubility In Water Low solubility, data needed from literature
    Solubility In Organic Solvents Soluble in some organic solvents like dichloromethane, data needed from literature
    Pka Data needed from literature
    Logp Indicates lipophilicity, data needed from literature
    Stability Stable under normal storage conditions, but data on specific degradation conditions needed from literature

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    Frequently Asked Questions

    As a leading 3-Methyl-4-[((2,2,2-trifluoro ethoxy-2-pyridinyl)methyl)thio]-1H-Benzimidazole supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What are the chemical properties of 3-Methyl-4- [ (2,2,2-trifluoroethoxy-2-pyridinyl) methyl] thio-1H-Benzimidazole
    3-Methyl-4- [ (2,2,2-trifluoroethoxy-2-pyridyl) methyl] thio-1H-benzimidazole, which is an organic compound. It has specific chemical properties and is determined by its unique structure.
    Looking at its structure, it contains a benzimidazole core. This structure is commonly found in many bioactive molecules and often gives compounds a variety of biological activities, such as antibacterial, antiviral, and anti-tumor. The nitrogen atom of the benzimidazole ring can form hydrogen bonds or other non-covalent interactions with target molecules in organisms, affecting the function of biomolecules.
    The introduction of 3-bit methyl group can change the molecular electron cloud distribution and steric hindrance. Methyl group is the power supply group, which affects the electron density of benzimidazole ring and changes its ability to bind to the target. Spatially, methyl group occupies a certain space and affects the stereoselectivity of molecules interacting with other molecules.
    4-bit [ (2,2,2-trifluoroethoxy-2-pyridyl) methyl] thio substituent has a key influence on the properties of compounds. The trifluoroethoxy part, due to the strong electronegativity of fluorine atoms, makes the molecule have a strong electron-absorbing effect, changes the electron distribution of the whole molecule, enhances lipophilicity, and facilitates the molecule to pass through the biofilm, increasing its absorption and distribution in vivo. As a nitrogen-containing heterocycle, pyridyl groups can participate in a variety of chemical reactions, and can form specific interactions with biological targets to enhance the biological activity and selectivity of compounds. Sulfur groups are connected to these groups, and their sulfur atoms have lone pair electrons, which can participate in the formation of hydrogen bonds or coordinate with metal ions, further enriching the chemical properties and biological activities of compounds.
    From the perspective of physical properties, the melting point, boiling point, solubility, etc. of the compound are affected by various groups in the structure. Due to the large molecule and containing a variety of different groups, it is speculated that its melting point is relatively high. The lipophilic part may make the solubility better than water in organic solvents. Chemically, there are many active check points, such as benzimidazole ring nitrogen atom, pyridine ring nitrogen atom and sulfur atom, which can undergo nucleophilic substitution, electrophilic substitution, redox and other reactions. It can be used as a key intermediate in organic synthesis and drug development. Compounds with specific activities and properties are prepared by modifying different check points.
    What are the application fields of 3-Methyl-4- [ (2,2,2-trifluoroethoxy-2-pyridinyl) methyl] thio-1H-Benzimidazole
    3-Methyl-4- [ (2,2,2-trifluoroethoxy-2-pyridyl) methyl] thio-1H-benzimidazole, which is one of the organic compounds. Its application field is quite wide, in the field of medicine, often used as a key intermediate in drug synthesis. Because of its special chemical structure, it can participate in the construction of many drug molecules and help develop new drugs, such as some antibacterial and antiviral drugs with specific pharmacological activities.
    In the field of pesticides, it also has significant uses. Pesticide products with high insecticidal and bactericidal properties can be prepared through specific chemical reactions. Such pesticides exert inhibition and killing effects on pests and pathogens through their unique mechanism of action, thereby escorting the growth of crops and improving crop yield and quality.
    In the field of materials science, this compound also shows potential application value. Or it can be used to synthesize polymer materials with special properties, such as materials with good thermal stability and chemical stability. Such materials can be used in electronics, aerospace and other industries that require strict material properties to meet the demand for high-performance materials in related fields.
    In summary, 3-methyl-4- [ (2,2,2-trifluoroethoxy-2-pyridyl) methyl] thio-1H-benzimidazole has important applications in the fields of medicine, pesticides and materials science, and is of great significance for promoting the development of related industries.
    What is the production process of 3-Methyl-4- [ (2,2,2-trifluoroethoxy-2-pyridinyl) methyl] thio-1H-Benzimidazole
    The production process of 3-methyl-4- [ (2,2,2-trifluoroethoxy-2-pyridyl) methyl] thio-1H-benzimidazole is quite delicate.
    First of all, all kinds of raw materials need to be prepared, such as specific pyridine derivatives, sulfur-containing reagents and benzimidazole parent, etc., to ensure its purity and quality, as the basis of the process.
    At the beginning of its preparation, in a suitable reaction vessel, the pyridine derivative and a specific halogenated alkyl hydrocarbon are nucleophilic substitution with the help of a catalyst, at a suitable temperature and pressure. The purpose of this step is to introduce the trifluoroethoxy group on the pyridine ring to form the key intermediate. During the reaction process, the temperature, reaction time and material ratio need to be closely monitored to achieve the best reaction effect.
    Then, the intermediate is mixed with a sulfur-containing reagent and placed in a basic environment to initiate a thioetherification reaction. This reaction requires precise regulation of the amount of base and reaction conditions, so that the sulfur atom can successfully replace the halogen atom at a specific position to form a sulfur-containing connection structure.
    As for the benzimidazole parent, it also needs to be pretreated to activate the reactivity check point at a specific position. Subsequently, the thioetherified pyridine intermediate and the pretreated benzimidazole parent are condensed in an organic solvent under heating and catalyst. This step is the key to constructing the target molecule. By controlling the precise reaction conditions, the two parts are cleverly combined to form 3-methyl-4- [ (2,2,2-trifluoroethoxy-2-pyridyl) methyl] thio-1H-benzimidazole.
    The reaction is completed, and the product still needs to be separated and purified. According to the characteristics of the product, extraction, column chromatography, recrystallization and other methods can be selected to remove impurities and obtain high-purity products. The whole production process requires fine operation and strict monitoring at every step to ensure the quality and yield of the product.
    What is the market outlook for 3-Methyl-4- [ (2,2,2-trifluoroethoxy-2-pyridinyl) methyl] thio-1H-Benzimidazole
    3-Methyl-4- [ (2,2,2-trifluoroethoxy-2-pyridyl) methyl] thio-1H-benzimidazole, which is an important fine chemical in the field of organic synthesis. In the current market outlook, it shows a multi-faceted trend.
    In the field of medicine, benzimidazole compounds have always played an important role in drug development. Many studies have shown that such structures have unique effects on specific biological targets. The special substituents of this compound, such as trifluoroethoxy and pyridyl, may endow it with specific pharmacological activities. It may be used to develop antibacterial, antiviral and even anti-tumor drugs. In recent years, the pharmaceutical industry has become increasingly demanding for new specific drugs. Therefore, if its exact pharmacological activity can be confirmed and through rigorous clinical trials, it may gain a place in the pharmaceutical market, which is quite promising.
    In the field of materials, fluorinated organic compounds are often favored because of their special physical and chemical properties. The trifluoroethoxy group in this compound may improve the surface properties of materials, such as enhancing their water resistance and corrosion resistance. With the increasing demand for high-performance materials in high-end manufacturing industries such as electronics and aerospace, if it can be applied to material synthesis to meet the requirements of special properties in related fields, its market potential should not be underestimated.
    However, its marketing activities also have challenges. In the process of organic synthesis, the preparation of the compound may require complex processes and special raw materials, and the cost may remain high. And in large-scale production, process stability and product quality control are also key problems. In addition, whether it is pharmaceutical or material applications, it needs to pass strict regulatory standards testing, which also poses a certain obstacle to its commercialization process.
    Overall, 3-methyl-4- [ (2,2,2-trifluoroethoxy-2-pyridyl) methyl] thio-1H-benzimidazole has an addressable market opportunity, but it needs to overcome many difficulties such as cost control, production process optimization and regulatory compliance in order to emerge in the market and seek development space.
    What are the safety precautions for 3-Methyl-4- [ (2,2,2-trifluoroethoxy-2-pyridinyl) methyl] thio-1H-Benzimidazole
    3-Methyl-4 - [ (2,2,2-trifluoroethoxy-2-pyridyl) methyl] thio-1H-benzimidazole, this is a chemical substance, which is related to its safety precautions and should not be ignored. Let me tell you one by one.
    Bear the brunt, this chemical may be toxic. There are various routes of contact, either penetrating through the skin, inhaling through the respiratory tract, or accidentally ingesting. If the skin comes into contact with it, rinse it with plenty of water immediately, and check the skin carefully after washing. If there is any discomfort, seek medical treatment immediately. If inhaled, be sure to quickly move to a fresh air place to keep breathing smooth. If breathing difficulties, oxygen should be administered in time and rushed to the hospital. Those who eat by mistake should not induce vomiting by themselves. They should seek medical attention immediately and inform the doctor of what they are eating and the details.
    Furthermore, the substance may be harmful to the environment. When using it, do not dump it at will to avoid polluting soil and water sources. Waste generated by experiments or production processes must be properly disposed of in accordance with relevant environmental regulations, or handed over to professional treatment institutions to reduce its damage to the environment.
    Storage is also important. It should be placed in a cool, dry and well-ventilated place, away from fire and heat sources. Because of its flammability, it may be dangerous in case of open flames and hot topics. At the same time, it should be stored separately from oxidants, acids, etc., to avoid chemical reactions caused by mixed storage.
    When operating, protective measures are essential. Wear appropriate protective equipment, such as protective gloves, goggles, protective clothing, etc., to protect your own safety. And the operating environment should ensure good ventilation. If conditions permit, you can operate in a fume hood.
    In short, when dealing with 3-methyl-4- [ (2,2,2-trifluoroethoxy-2-pyridyl) methyl] thio-1H-benzimidazole, it is necessary to be careful, strictly abide by safety regulations, and must not be negligent, so as not to endanger yourself and the environment.