5 Methoxy 2 4 Methoxyl 3 5 Dimethyl Pyridine 2 Ylmethylsulfenyl 1 H Benzoimidazole
quinoline thiophene imidazole thiazole

5-Methoxy-2-(4-Methoxyl-3,5-Dimethyl-pyridine-2-ylmethylsulfenyl)-1-H-Benzoimidazole

    Specifications

    HS Code

    451686

    Chemical Formula C20H21N3O3S
    Molecular Weight 383.46
    Appearance Solid (usually)
    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 (organic compound, likely sparingly soluble)
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
    Density Specific value would need experimental determination
    Odor Odorless or faint odor (推测, depends on purity and impurities)

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    General Information
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    Frequently Asked Questions

    As a leading 5-Methoxy-2-(4-Methoxyl-3,5-Dimethyl-pyridine-2-ylmethylsulfenyl)-1-H-Benzoimidazole 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 chemical structure of 5-Methoxy-2- (4-Methoxyl-3, 5-Dimethyl-pyridine-2-ylmethylsulfenyl) -1-H-Benzoimidazole?
    This is the problem of organic chemical substances. The chemical structure of 5 - Methoxy - 2 - (4 - Methoxyl - 3,5 - Dimethyl - pyridine - 2 - ylmethylsulfenyl) - 1 - H - Benzoimidazole allows me to elaborate.
    The name of this compound, according to the naming rules of organic chemistry, contains benzimidazole, pyridine and other structural fragments. Benzimidazole, which is formed by fusing benzene ring and imidazole ring, is the main body of 1 - H - Benzoimidazole. In its second position, there is a sulfur-containing side chain, namely 2- (4-Methoxyl-3,5-Dimethyl-pyridine-2-ylmethylsulfenyl). In this side chain, 4-Methoxyl indicates that the 4th position of the pyridine ring is connected with a methoxyl group, and 3,5-Dimethyl shows that the 3rd and 5th positions of the pyridine ring have a methyl group. The 2nd position of the pyridine ring is connected to a methylene group, which is in turn connected to the sulfur atom, and the sulfur atom is then connected to the 2nd position of benzimidazole. 5-Methoxy refers to the presence of a methoxy group at the 5th position of benzimidazole.
    Its chemical structure, with benzimidazole as the core, is connected with a pyridine-derived side chain containing methoxy and methyl on one side, and a methoxy group on the other side. Such a structure combines the characteristics of benzimidazole and pyridine, and may have unique properties and applications in organic synthesis, medicinal chemistry and other fields.
    What are the main uses of 5-Methoxy-2- (4-Methoxyl-3, 5-Dimethyl-pyridine-2-ylmethylsulfenyl) -1-H-Benzoimidazole?
    5-Methoxy-2 - (4-methoxy-3,5-dimethyl-pyridine-2-methylthio) - 1-H-benzimidazole has a wide range of uses. In the field of medicine, it is often the key raw material for the creation of new anti-ulcer drugs. Because of ulcer diseases, it is mostly caused by excessive gastric acid secretion and damage to the gastric mucosa. The compound can regulate gastric acid secretion through a specific mechanism of action and can help repair the gastric mucosa. Therefore, it has great potential for the treatment of ulcer diseases.
    In the chemical industry, it may be used as a synthetic intermediate for special functional materials. In chemical production, it is often necessary to prepare materials with specific properties. Due to its unique molecular structure, this compound can be chemically transformed and introduced into the molecular structure of the target material, endowing the material with properties such as better stability and reactivity, in order to meet the needs of different industrial applications.
    In the process of scientific research and exploration, it is also an important research object. By in-depth exploration of its chemical properties and reaction mechanism, researchers hope to reveal more mysteries in the field of chemistry, expand the boundaries of chemical knowledge, and then provide ideas and foundations for the development of new chemical reactions and new synthesis methods. Therefore, 5-methoxy-2 - (4-methoxy-3,5-dimethyl-pyridine-2-ylmethylthio) -1-H-benzimidazole plays an important role in many aspects of medicine, chemical industry and scientific research, and plays an important role.
    What are the synthesis methods of 5-Methoxy-2- (4-Methoxyl-3, 5-Dimethyl-pyridine-2-ylmethylsulfenyl) -1-H-Benzoimidazole?
    5-Methoxy-2- (4-methoxy-3,5-dimethylpyridine-2-methylthio) -1-H-benzimidazole is an important organic compound, and its synthesis method has attracted much attention in the field of chemistry. The following are common synthesis methods:
    The selection of starting materials is very important, usually starting with benzimidazole compounds containing methoxy groups and pyridine compounds containing specific substituents. These two structural characteristics lay the foundation for subsequent reactions.
    In the reaction step, the starting material is first activated. Take benzimidazole compounds as an example, or make their activity check points more reactive through specific reagents, or modify the groups in pyridine compounds to participate in the reaction to enhance their reactivity. This move is like a soldier sharpening his sword and preparing for the follow-up battle.
    Then a key thioetheration reaction is carried out. In this reaction, with the help of suitable catalysts and reaction conditions, the sulfur-containing reagents interact with the activated raw materials to form thioether bonds, thereby constructing the key structure of the target product. This step is like a key structure for building a house. The reaction conditions, such as temperature, reaction time, and the proportion of reactants, need to be precisely controlled. If there is a slight difference, the product generation will be affected.
    Separation and purification steps are also indispensable. After the reaction is completed, the product is often mixed with impurities and needs to be purified by recrystallization, column chromatography and other means. During recrystallization, depending on the solubility difference between the product and the impurities in different solvents, the solvent is cleverly selected to make the product pure and precipitated. Column chromatography uses the action of fixed phase and mobile phase to separate different substances in the column, and finally obtains a high-purity target product.
    Synthesis of 5-methoxy-2- (4-methoxy-3,5-dimethylpyridine-2-methylthio) -1-H-benzimidazole requires fine planning of the starting material, precise control of the reaction steps, and proper separation and purification to obtain the ideal product.
    What are the physical properties of 5-Methoxy-2- (4-Methoxyl-3, 5-Dimethyl-pyridine-2-ylmethylsulfenyl) -1-H-Benzoimidazole?
    5-Methoxy-2 - (4-methoxy-3,5-dimethyl-pyridine-2-methylthio) - 1-H-benzimidazole is an organic compound. Its physical properties are unique, which is related to its performance in various chemical processes and practical applications.
    Looking at its properties, it is mostly white to quasi-white crystalline powder under normal conditions, which is easy to identify and distinguish. In terms of solubility, the compound exhibits a certain solubility in organic solvents such as dichloromethane, N, N-dimethylformamide, but it is difficult to dissolve in water. The difference in solubility is due to the dominance of lipophilic groups in its molecular structure, so it has better affinity in polar organic solvents, while the interaction with water, a strong polar solvent, is weak. The melting point, as a key physical property, is about 160-165 ° C. The determination of the melting point provides an important basis for the purity identification and solid-state characteristics of the compound. Its melting range is relatively narrow, suggesting high purity.
    The compound has certain stability, but its structure will be affected under high temperature, strong acid and strong alkali environment. High temperature can exacerbate the thermal movement of molecules and cause chemical bond breaking; strong acids and strong bases will react with specific functional groups in the molecule and destroy the original structure. < Br >
    In practical application scenarios, such as in the field of drug development, its physical properties determine the behavior during the preparation process. Because it is insoluble in water, solubilization methods need to be considered when developing oral dosage forms to improve bioavailability. In organic synthesis, its solubility and stability affect the choice of reaction conditions and the design of product separation and purification processes.
    The physical properties of 5-methoxy-2 - (4-methoxy-3,5-dimethyl-pyridine-2-ylmethylthio) -1-H-benzimidazole are of great significance in chemical research and practical applications. In-depth understanding of it is conducive to promoting the development of related fields.
    What is the market outlook for 5-Methoxy-2- (4-Methoxyl-3,5-Dimethyl-pyridine-2-ylmethylsulfenyl) -1-H-Benzoimidazole?
    Guanfu 5-methoxy-2 - (4-methoxy-3,5-dimethyl-pyridine-2-methylthio) - 1-H-benzimidazole needs to be reviewed in detail in the market prospect.
    From the field of medicine, benzimidazole compounds often have various biological activities, such as anti-ulcer, antibacterial, antiviral and other effects. This compound has a unique structure, and its combination of methoxy, dimethylpyridyl and benzimidazole nuclei may endow it with different pharmacological properties. Nowadays, there are many patients with digestive system diseases such as ulcers. If this compound has emerged in the study of anti-ulcer activity, it can effectively inhibit gastric acid secretion and protect the gastric mucosa, and it must have a considerable demand in the pharmaceutical market. Pharmaceutical companies must compete to invest in research and development, hoping to develop it into a new type of anti-ulcer drug, which has a promising future.
    In the chemical industry, this compound may be used as an intermediary for organic synthesis. With its special structure, it can be derived from many materials with special properties. For example, in the synthesis of polymer materials, it can be used as a functional monomer to endow materials with unique electrical and optical properties. With the rapid development of materials science, the demand for organic compounds with special properties is increasing. If this compound is studied in depth and can demonstrate its advantages in material synthesis, the demand for it in the chemical industry will also rise, and the market prospect will be broad.
    However, it is also necessary to understand that the road to its marketing activities may not be smooth. R & D costs are quite high, from laboratory synthesis optimization to pharmacological activity and safety assessment, a lot of manpower, material and financial resources need to be invested. And the market competition is fierce, and similar or alternative compounds have occupied a certain market share. To make it stand out in the market, it is necessary to be ingenious in research and development to highlight its unique advantages.
    To sum up, 5-methoxy-2- (4-methoxy-3,5-dimethyl-pyridine-2-methylthio) -1-H-benzimidazole has potential opportunities in the pharmaceutical and chemical fields, but also faces challenges. If it can properly deal with issues such as R & D and market competition, its market prospect may be extremely bright.