6 Chloro 2 Methylthio 1h Benzo D Imidazole
quinoline thiophene imidazole thiazole

6-chloro-2-(methylthio)-1H-benzo[d]imidazole

    Specifications

    HS Code

    620876

    Chemical Formula C8H7ClN2S
    Molecular Weight 198.67
    Appearance Solid (usually)
    Solubility In Water Low (organic compound)
    Solubility In Organic Solvents Soluble in some organic solvents
    Stability Stable under normal conditions
    Hazard Class May have certain hazards, data required for exact classification

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    General Information
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    Frequently Asked Questions

    As a leading 6-chloro-2-(methylthio)-1H-benzo[d]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 are the chemical properties of 6-chloro-2- (methylthio) -1H-benzo [d] imidazole
    6-Chloro-2- (methylthio) -1H-benzo [d] imidazole, this is an organic compound with unique chemical properties. Its appearance is often white to light yellow crystalline powder, and the color is gradually changed under specific light and air environments, or due to oxidation and other reactions.
    When it comes to solubility, this compound is slightly soluble in water, because of its molecular structure, polar groups account for a limited proportion, and the force between water molecules is weak. However, it is soluble in some organic solvents, such as ethanol, dichloromethane, etc., because these organic solvents can form interactions with the compound molecules such as van der Waals force, which is conducive to its dispersion and dissolution.
    In terms of thermal stability, when heated moderately, the structure of the compound is still stable; but when the temperature is too high, the chemical bonds in the molecule may break due to energization, triggering decomposition reactions, resulting in sulfur-containing, chlorine-containing small molecules and other decomposition products.
    In terms of chemical activity, the chlorine atom in 6-chloro-2- (methylthio) -1H-benzo [d] imidazole has high activity, which can be replaced by various nucleophiles in nucleophilic substitution reactions to form new carbon-heteroatomic bonds, thereby deriving many compounds with different structures and functions. Methylthio groups also have certain activities, which can participate in oxidation reactions, change the valence state of sulfur atoms, and then affect the chemical properties and reactivity of the whole molecule. The benzimidazole ring system of this compound endows it with certain aromaticity and conjugate stability, which has a great influence on its physicochemical properties and chemical reaction pathways. It is often used as a reactive center or structural support part to participate in many organic synthesis reactions.
    What are the preparation methods of 6-chloro-2- (methylthio) -1H-benzo [d] imidazole
    The preparation method of 6-chloro-2- (methylthio) -1H-benzo [d] imidazole has been known for a long time. There are many methods, and they are described in this article.
    One is to start with o-phenylenediamine and chloroacetic acid, and under specific conditions, the two are blended and reacted. First, the o-phenylenediamine is dissolved in a suitable solvent, such as alcohol, and heated to a suitable temperature, usually tens of degrees Celsius, and then slowly dropped into the solution of chloroacetic acid. After adding it dropwise, stirring continuously, and reacting for several hours, until the reaction is complete, cooling, crystallizing, and filtering, the crude product can be obtained, and then purified by recrystallization. This is the classic way. < Br >
    Second, using o-nitroaniline as the starting material, the reduction reaction is first carried out to obtain o-phenylenediamine. Commonly used reducing agents, such as the combination of iron filings and hydrochloric acid, gradually reduce o-nitroaniline to o-phenylenediamine at moderate temperature and pressure. Then, according to the above method of reacting o-phenylenediamine with chloroacetic acid, 6-chloro-2- (methylthio) -1H-benzo [d] imidazole can be prepared.
    Third, sulfur-containing reagents can also be used to react with corresponding halogenated benzimidazole derivatives. If 2-chloro-6-nitrobenzimidazole is reacted with sodium methyl mercaptan, in an organic solvent, at a certain temperature range, the two interact, the nitro group is gradually converted, and the chlorine atom is replaced by the methylthio group to form the target product. This process needs to pay attention to the control of the reaction conditions, such as the temperature should not be too high to avoid side reactions.
    All kinds of preparation methods have their own advantages and disadvantages. In practical application, when considering the availability of raw materials, cost considerations, product purity requirements and many other factors, choose carefully.
    What is the main use of 6-chloro-2- (methylthio) -1H-benzo [d] imidazole?
    6-Chloro-2- (methylthio) -1H-benzo [d] imidazole has a wide range of uses. In the field of medicine, it is often the key raw material for the creation of new antibacterial and antiviral drugs. Due to its unique structure, it can precisely combine with specific biological targets, block the metabolic pathway of bacteria, achieve antibacterial and antiviral effects, and help humans resist various diseases.
    In the field of materials science, it also shows extraordinary potential. It can be modified by specific processes to introduce polymer materials, endowing materials with special properties, such as improving stability and enhancing anti-aging ability, so that materials can maintain good performance in different environments. It is used in aerospace, automobile manufacturing and other fields to promote industry progress.
    In agriculture, it also has important contributions. It can be used as a new type of pesticide active ingredient to inhibit and kill crop pests and pathogens. Compared with traditional pesticides, it has the characteristics of high efficiency, low toxicity and environmental friendliness, which can not only ensure the harvest of crops, but also reduce the damage to the ecological environment, which is in line with the needs of sustainable development of modern agriculture.
    In addition, in the field of scientific research, as an organic synthesis intermediate, researchers can use it to construct complex organic molecular structures, explore new chemical reaction paths and material properties, inject new vitality into the development of chemistry, and open up more unknown fields.
    What is the market outlook for 6-chloro-2- (methylthio) -1H-benzo [d] imidazole?
    6-Chloro-2- (methylthio) -1H-benzo [d] imidazole, this is an organic compound. Looking at its market prospects, it can be described as complex, with both opportunities and challenges.
    In the field of medicine, such compounds are often key intermediates in drug development. Due to their unique chemical structure, they can be modified to obtain a variety of biological activities, such as antibacterial and antiviral. In recent years, the pharmaceutical industry has continued to thrive, and the demand for new drugs has increased unabated. This compound may emerge in the development of innovative drugs, and market demand may rise with the progress of new drug development.
    In the field of materials science, some benzimidazole-containing structural compounds exhibit unique electrical and optical properties, which can be used to prepare organic Light Emitting Diodes, sensors and other materials. With the rapid progress of science and technology, the demand for advanced materials is on the rise. If 6-chloro-2- (methylthio) -1H-benzo [d] imidazole can mine unique properties and applications in this field, it is also expected to open up a vast market.
    However, its marketing activities also face many obstacles. The synthesis process may be complex and the cost remains high, which affects large-scale production and application. And the market competition is fierce, with many similar or alternative products. In order to stand out, it is necessary to make great efforts in technological innovation and cost control.
    Even though there are challenges, with the continuous advancement of science and technology, the fields of medicine and materials continue to expand. 6-chloro-2- (methylthio) -1H-benzo [d] imidazole, with its own structural characteristics, is likely to find a place in the future market and bloom with unique brilliance if it is deeply researched and developed.
    What are the precautions for 6-chloro-2- (methylthio) -1H-benzo [d] imidazole in storage and transportation?
    6-Chloro-2- (methylthio) -1H-benzo [d] imidazole should be stored with caution, and many matters should not be ignored.
    When hiding, the first environment. It must be placed in a cool, dry place, protected from direct sunlight, covering the heat and light of sunlight, or causing this material to denature and lose its inherent nature. And it must be kept away from fires and heat sources to prevent unexpected fires. If this substance is heated or biochemically changed, it may even cause danger.
    Also, it should be isolated from oxidants, acids, etc. When these substances meet with 6-chloro-2- (methylthio) -1H-benzo [d] imidazole, they are prone to chemical reactions, or raw gas, heat, or even explosion, endangering the surroundings.
    As for losing, there are also important rules. The packaging must be solid to prevent damage and leakage on the way. When handling, the operator should be careful, pack lightly and unload lightly, so as not to damage the container. If there is any leakage, dispose of it quickly according to the procedures, and do not be lazy.
    In addition, the transportation vehicle must also be clean, free of other pollutants, and equipped with fire and explosion-proof equipment. During driving, drive slowly to avoid bumps and sudden brakes to ensure the safety of transportation. In short, 6-chloro-2- (methylthio) -1H-benzo [d] imidazole storage and transportation are all related to safety, and everything needs to be done in accordance with regulations to be worry-free.