6 Chloro 5 Iodo 2 Methylsulfonyl 1h Benzimidazole
quinoline thiophene imidazole thiazole

6-chloro-5-iodo-2-(Methylsulfonyl)-1H-benziMidazole

    Specifications

    HS Code

    237128

    Chemical Formula C9H8ClIN2O2S
    Molar Mass 386.596 g/mol

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    General Information
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    Frequently Asked Questions

    As a leading 6-chloro-5-iodo-2-(Methylsulfonyl)-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 6-chloro-5-iodo-2- (Methylsulfonyl) -1H-benziMidazole?
    6-Chloro-5-iodine-2- (methylsulfonyl) -1H-benzimidazole, this is an organic compound. Looking at its structure, the benzimidazole ring system is the core, and there are substituents such as chlorine, iodine and methyl sulfonyl groups connected to it.
    First talk about its physical properties, usually solid, due to intermolecular forces, the melting point may be quite high. Its solubility is due to organic solvents, such as dichloromethane, N, N-dimethylformamide, etc., or has a certain solubility. Due to the principle of similar compatibility, its organic structure has a certain affinity with organic solvents; in water, due to its limited polarity, its solubility may be low.
    In addition to chemical properties, the benzimidazole ring has certain aromatic properties and is quite stable. However, the substituents on the ring give it a variety of reactivity. Chlorine and iodine atoms can participate in nucleophilic substitution reactions. When there are suitable nucleophilic reagents, chlorine and iodine can be replaced to form new derivatives. In the methylsulfonyl group, the sulfur atom has a higher oxidation state, which makes the group electron-absorbing, which affects the electron cloud distribution of the benzimidazole ring, causing the electron cloud density on the ring to decrease, and the electrophilic substitution reaction activity may be reduced. And methylsulfonyl groups can participate in some reactions involving sulfonyl transformation, such as reacting with nucleophilic reagents to achieve sulfonyl modification. < Br >
    In chemical reactions, this compound can be used as a raw material to participate in a variety of organic synthesis and construct more complex compounds. However, because its structure contains halogen atoms and sulfonyl groups, the reaction needs to select suitable conditions, control the reaction process and selectivity, in order to achieve the expected synthesis target.
    What are the preparation methods of 6-chloro-5-iodo-2- (Methylsulfonyl) -1H-benziMidazole?
    The methods for preparing 6-chloro-5-iodine-2- (methylsulfonyl) -1H-benzimidazole are as follows:
    First, a suitable substituted benzene is used as the starting material. The chlorine atom is first introduced into the benzene ring at a specific position, which can be achieved by electrophilic substitution with chlorine-containing reagents such as thionyl chloride and phosphorus oxychloride under suitable reaction conditions. Subsequently, in another suitable step, an iodine atom is introduced into the chlorinated benzene ring, for example by means of an iodide reagent, and the reaction is carried out in the presence of a catalyst. Finally, the methylsulfonyl group is introduced into a specific position of the benzene ring. Methylsulfonyl chloride and other reagents can be used to react with the previously halogenated benzene ring derivative in the presence of a base. After a series of reaction steps, the target product 6-chloro-5-iodine-2 - (methylsulfonyl) -1H-benzimidazole can be obtained.
    Second, benzimidazole derivatives are used as starting materials. First, a halogenation reaction is carried out at a specific position on the benzimidazole ring to introduce chlorine atoms and iodine atoms. This halogenation reaction requires the selection of appropriate halogenation reagents and reaction conditions according to the activity of the benzimidazole ring. After that, through an appropriate nucleophilic substitution reaction, the methyl sulfonyl group is introduced into the benzimidazole ring to obtain the target product. This process requires precise control of the reaction conditions, such as temperature, reaction time, and ratio of reactants, to ensure the selectivity and yield of the reaction.
    Third, a multi-step tandem reaction strategy can be considered. In the same reaction system, a compound with a certain functional group can be used as the starting material. In the same reaction system, through ingenious design of the reaction sequence and conditions, chlorine atoms, iodine atoms and methyl sulfonyl groups are introduced in sequence, and 6-chloro-5-iodine-2 - (methylsulfonyl) -1H-benzimidazole is directly generated by a one-pot tandem reaction. Although this method is challenging, the successful implementation can greatly simplify the operation process and improve the production efficiency, but the reaction mechanism and conditions need to be deeply studied and optimized.
    What is the main use of 6-chloro-5-iodo-2- (Methylsulfonyl) -1H-benziMidazole?
    6-Chloro-5-iodine-2- (methylsulfonyl) -1H-benzimidazole, this substance has a wide range of uses. In the field of medicinal chemistry, it is often used as a precursor of active ingredients. Its unique structure endows compounds with specific biological activities, or can be combined with specific targets in organisms. By precisely regulating biological processes, it has become the cornerstone of potential drug development. Physicians hope to develop new drugs to treat various diseases, such as tumors, inflammation and neurological diseases.
    In the field of organic synthesis, it is a key intermediate. Organic synthesizers can modify and carve its structure through various chemical reactions, and introduce various functional groups to build complex and functional organic molecules. With the activity of chlorine, iodine and methyl sulfonyl groups in its structure, it can trigger nucleophilic substitution, coupling and other reactions, paving the way for the synthesis of new materials and total synthesis of natural products.
    In the field of materials science, or can participate in the creation of special materials. Because of its chemical stability and specific electronic properties, it can prepare materials with unique electrical and optical properties, such as optoelectronic materials, semiconductor materials, etc., injecting new opportunities for the development of electronic devices, optical equipment and other industries. In summary, 6-chloro-5-iodine-2 - (methylsulfonyl) -1H-benzimidazole has important value and broad application prospects in many fields.
    What is the market outlook for 6-chloro-5-iodo-2- (Methylsulfonyl) -1H-benziMidazole?
    6-Chloro-5-iodine-2- (methylsulfonyl) -1H-benzimidazole, the market prospect of this product is related to many aspects, and now it is the king.
    In the field of medicine, this compound may have unique pharmacological activities. In today's medical research and development, there is a hunger for new kinds of special drugs. Many researchers are tirelessly exploring, hoping to find a cure for difficult diseases. If 6-chloro-5-iodine-2- (methylsulfonyl) -1H-benzimidazole can exhibit outstanding pharmacological properties, such as high affinity and selectivity for specific disease targets, it may become a key intermediate for innovative drug development. Based on this, the development of new drugs with significant efficacy and small side effects will surely be able to gain a place in the highly competitive pharmaceutical market, and its market prospects are naturally vast.
    As for the field of materials science, the development of emerging materials has been rapid in recent years. The demand for functional materials is on the rise. Due to the unique molecular structure of this compound, it may endow materials with different properties. For example, in optoelectronic materials, it may affect the conductivity and luminescence characteristics of the material; in polymer materials, it may improve its mechanical properties and stability. If there is a breakthrough in this regard, it will be applied to new electronic devices, high-performance polymers and other industries, which will open up a new market space, attract the attention and investment of many material companies, and the market potential is immeasurable.
    However, it is also necessary to understand that there may be obstacles to its marketing activities. If the process of synthesizing this compound is complicated and cumbersome, and the cost remains high, it will limit its large-scale production and application. Furthermore, the entry of new compounds into the market requires strict regulatory approval, especially in the field of medicine, and the verification of safety and effectiveness is time-consuming and laborious. Only by overcoming these problems can 6-chloro-5-iodine-2- (methylsulfonyl) -1H-benzimidazole be unimpeded in the market, fully unleashing its potential value, and the future will be bright from obscurity.
    What are the precautions for 6-chloro-5-iodo-2- (Methylsulfonyl) -1H-benziMidazole during storage and transportation?
    6-Chloro-5-iodine-2- (methylsulfonyl) -1H-benzimidazole This product has several precautions during storage and transportation, and it needs to be taken with care.
    One is related to the storage environment. This compound should be placed in a cool, dry and well-ventilated place. The cover may be sensitive to temperature and humidity due to its nature. If it is placed in a high temperature and humid place, it may cause deterioration. Under high temperature, its structure may change, affecting its chemical properties; humid environment, it is easy to make it absorb moisture, or cause chemical reactions to occur without reason. Therefore, choosing a suitable storage environment is the first thing.
    Second, when transporting, the packaging must be solid and stable. It is necessary to ensure that it will not be damaged and leaked during the bumpy transfer. Appropriate packaging materials should be selected, which can not only effectively protect, but also meet the relevant transportation specifications. And during transportation, it is necessary to avoid mixing with other substances that may react with it. Because the chemical structure of the compound, chlorine, iodine and methyl sulfonyl groups, etc., may have certain reactivity, if it comes into contact with improper substances, it may cause violent reactions and endanger transportation safety.
    Third, whether it is stored or transported, it must be strictly marked. Clearly indicate its name, nature and precautions and other key information. In this way, the relevant personnel can see at a glance, know how to properly dispose of it, and in case of emergencies, they can quickly take the correct response according to the identification information to prevent the harm from expanding.
    Furthermore, operators need to be professionally trained. When exposed to the compound, be familiar with its characteristics and latent risks, and follow standard operating procedures. Regular inspections during storage to see if there are any abnormalities; pay close attention to transportation conditions during transportation to ensure that the whole process is safe, so as to ensure the safety and stability of this compound during storage and transportation.