2 3 Methyl 4 2 2 2 Trifluoroethoxy Methylthio 1h Benzimidazole
quinoline thiophene imidazole thiazole

2-[3-Methyl-4-(2,2,2-Trifluoroethoxy)Methylthio-1H-Benzimidazole

    Specifications

    HS Code

    476650

    Chemical Formula C12H12F3N2OS2
    Molecular Weight 322.36
    Appearance Solid (usually white or off - white powder)
    Physical State At Room Temperature Solid
    Melting Point Specific value would need experimental determination
    Boiling Point Specific value would need experimental determination
    Solubility In Water Low solubility in water, likely hydrophobic
    Solubility In Organic Solvents May be soluble in common organic solvents like dichloromethane, chloroform
    Density Value would need experimental determination
    Stability Stable under normal conditions, may decompose under extreme heat or strong oxidizing agents
    Pka Value would need experimental determination for acidic/basic groups in the molecule
    Odor Odorless or very faint odor

    As an accredited 2-[3-Methyl-4-(2,2,2-Trifluoroethoxy)Methylthio-1H-Benzimidazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    General Information
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    Frequently Asked Questions

    As a leading 2-[3-Methyl-4-(2,2,2-Trifluoroethoxy)Methylthio-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 main application fields of 2- [3-Methyl-4- (2,2,2-Trifluoroethoxy) Methylthio-1H-Benzimidazole
    2-% 5B3-methyl-4- (2,2,2-trifluoroethoxy) methionyl-1H-benzimidazole has a very important application in the field of medicine. This compound is outstanding in the field of deworming drugs, often used as a key active ingredient. With its unique chemical structure and characteristics, it shows high-efficiency inhibition and killing ability against a variety of parasites. Taking livestock and poultry breeding as an example, animals are susceptible to parasite infestation, which affects growth and health. Drugs containing this compound can precisely act on specific physiological links of parasites, destroy their survival and reproduction conditions, ensure the healthy growth of livestock and poultry, and improve breeding benefits.
    In the field of pesticides, it also plays an important role. It can effectively resist crop parasites and pests, reduce the use of chemical pesticides, and conform to the development trend of green and environmentally friendly agriculture. By interfering with the physiological metabolism of pests, efficient control is achieved, negative impact on the environment is reduced, and ecological balance is safeguarded.
    In the field of drug research and development, due to its unique structure, it provides a key idea and material basis for the creation of new drugs. Scientists use it as a starting material or lead compound, and through structural modification and optimization, explore innovative drugs with higher activity, lower toxicity, and better pharmacokinetic properties, bringing new hope for the development of drugs to overcome difficult diseases.
    What is the production process of 2- [3-Methyl-4- (2,2,2-Trifluoroethoxy) Methylthio-1H-Benzimidazole
    To prepare 2 - [3-methyl-4 - (2,2,2-trifluoroethoxy) methylthio-1H-benzimidazole], the process steps are as follows:
    First, prepare the corresponding starting materials. Based on a suitable benzimidazole derivative, this derivative needs to have an activity check point for subsequent reactions, usually reserved at specific positions for the introduction of methyl, trifluoroethoxy and methylthio groups.
    The first step is to carry out a methylation reaction. Take an appropriate amount of the above-mentioned benzimidazole derivative, place it in a reactor, and add a suitable methylation agent, such as iodomethane or dimethyl sulfate. At the same time, an appropriate amount of base is added as a catalyst, such as potassium carbonate or sodium carbonate, etc. At a certain temperature, for example 50 - 80 ° C, the reaction is continuously stirred for a certain time, about 3 - 6 hours, so that the specific position of benzimidazole is successfully introduced into the methyl group.
    The second step, the introduction of trifluoroethoxy. In the product that has completed the methylation, the reagent containing trifluoroethoxy is added, such as the active intermediate formed by the reaction of trifluoroethanol with p-toluenesulfonyl chloride, or the direct use of trifluoroethyl halide. Under basic conditions, such as the presence of sodium hydride or potassium tert-butoxide, react at a suitable temperature, such as 60-90 ° C, for 4-8 hours to induce the trifluoroethoxy group to connect to the designated position on the benzimidazole molecule.
    Third step, add methyl thioyl group. To the product that has introduced methyl and trifluoroethoxy groups, add a methyl mercaptan salt reagent, such as sodium methyl thioalcohol or potassium methyl mercaptan, etc. In a suitable organic solvent, such as N, N-dimethylformamide or dimethylsulfoxide, the reaction is carried out at 40-70 ° C for 3-5 hours, so that the methylthio group is successfully attached to the benzimidazole molecule, and the final product is obtained 2 - [3-methyl-4 - (2,2,2-trifluoroethoxy) methylthio-1H-benzimidazole]. After the reaction is completed, the high-purity product can be obtained by separation, purification and other operations, such as column chromatography or recrystallization.
    What is the market outlook for 2- [3-Methyl-4- (2,2,2-Trifluoroethoxy) Methylthio-1H-Benzimidazole?
    Guanfu 3-methyl-4- (2,2,2-trifluoroethoxy) methionyl-1H-benzimidazole is a promising product in the current market. This compound has potential uses in the fields of medicine and pesticides.
    In the field of medicine, its structure is unique, or it can be modified to fit specific targets, and it is expected to be developed into new therapeutic drugs. In view of the current situation of pharmaceutical research and development, there is a growing demand for compounds with novel structures and diverse biological activities. If this benzimidazole derivative can be further explored in its pharmacological mechanism, it may emerge in the treatment of diseases such as anti-inflammation and anti-tumor.
    In the field of pesticides, with the popularization of green environmental protection concepts, the demand for high-efficiency, low-toxicity and environmentally friendly pesticides has increased greatly. The introduction of groups such as trifluoroethoxy in this compound may endow it with unique insecticidal and bactericidal activities, and may have better environmental stability and bioavailability due to the characteristics of fluorine atoms.
    However, in order to make it shine in the market, it also faces many challenges. Control of R & D costs is one of them. From the optimization of the synthesis process to reduce costs, to the investment in pre-clinical and clinical trials, all need to be carefully planned. Furthermore, compliance with regulations is also crucial, and it is necessary to meet the strict approval standards of various countries for pharmaceuticals and pesticides.
    Overall, 3-methyl-4- (2,2,2-trifluoroethoxy) methionyl-1H-benzimidazole has promising prospects, but practitioners need to work hard in R & D, regulations and other aspects to achieve good results.
    2- [3-Methyl-4- (2,2,2-Trifluoroethoxy) Methylthio-1H-Benzimidazole Quality Standards
    The Quality Standard of 2-% 5B3-methyl-4- (2,2,2-trifluoroethoxy) methylthio-1H-benzimidazole is not exactly recorded in Tiangong Kaiwu, but according to modern chemical analysis, the Quality Standard of such compounds has many exquisite aspects.
    First of all, its purity is crucial. The purity of this compound needs to reach a very high level, generally speaking, it should not be less than 98%, in order to ensure its stability and reliability in various chemical reactions and applications. The presence of impurities, or the increase of reaction by-products, affects the quality of the product.
    Secondly, the inspection of related substances cannot be ignored. It is necessary to strictly control the content of related impurities. For example, the content of specific organic impurities should be controlled in a very low range, usually not more than 0.1%, to prevent impurities from interfering with its chemical properties and functions.
    Furthermore, the melting point range is also a key indicator. The melting point of the compound usually needs to be maintained in a specific range, such as [specific melting point range]. The deviation of the melting point may suggest that its purity changes or crystal form differences affect its physical and chemical properties.
    In addition, the drying weight loss index also needs to be paid attention to. The drying weight loss should be controlled within a certain limit, such as no more than 0.5%, to ensure that the moisture content of the compound is appropriate and to avoid adverse effects of moisture on its properties, such as affecting its storage stability and reactivity.
    Finally, there are strict requirements for heavy metal content. The content of heavy metals such as lead and mercury must be extremely low, generally measured in ppm level, to ensure the safety of their application in medicine, electronics and other fields and prevent the harm of heavy metal pollution.
    What are the storage conditions for 2- [3-Methyl-4- (2,2,2-Trifluoroethoxy) Methylthio-1H-Benzimidazole
    3-Methyl-4- (2,2,2-trifluoroethoxy) methylthio-1H-benzimidazole is an organic compound, and its storage conditions are crucial to the stability and quality of this compound.
    According to the "Tiangongkai" and common sense inference, such organic compounds should generally be stored in a cool, dry and well-ventilated place. A cool environment can prevent the molecular movement of the compound from intensifying due to excessive temperature, triggering decomposition or deterioration. If it is at high temperature, the chemical bond can obtain more energy, which is easy to break and cause structural changes. A dry environment is also indispensable, because most organic compounds are afraid of water, moisture or hydrolysis reactions, which destroy the molecular structure. If this substance contains groups that are easy to react with water, such as ester groups, acyl chloride groups, etc., it is easy to hydrolyze in contact with water and lose its original characteristics.
    Furthermore, good ventilation can disperse harmful gases that may be volatilized in time to avoid potential safety hazards caused by accumulation, and can maintain fresh air in the storage space and reduce adverse reactions such as oxidation. In addition, it should be kept away from fire sources, heat sources and strong oxidants, because many of them are flammable or reducing. When storing,
    should be contained in a suitable container to ensure a good seal to prevent the intrusion of impurities such as air and moisture. Strict control of the storage conditions of the compound can effectively ensure its quality and performance for subsequent use.