5 Methoxy 2 4 Methoxyl 3 5 Dimethyl Pyridine 2 Ylmethylsulfenyl 1 H Benzoimidazole
pyridine pyrrole pyrazine piperidine piperazine

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

    Specifications

    HS Code

    811977

    Chemical Formula C20H21N3O3S
    Molecular Weight 383.469 g/mol
    Appearance Typically a solid (physical state may vary based on purity and conditions)
    Melting Point Data may vary; needs specific experimental determination
    Solubility Solubility characteristics depend on solvent; likely has low solubility in water, better in organic solvents like DMSO, chloroform
    Pka Relevant acidic or basic groups' pKa values would need specific experimental determination
    Stability Stability can be affected by light, heat, and air; may be sensitive to oxidation
    Odor Likely odorless or with a faint, characteristic organic odor

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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?
    5 - Methoxy - 2 - (4 - Methoxyl - 3,5 - Dimethyl - pyridine - 2 - ylmethylsulfenyl) - 1 - H - Benzoimidazole, which is the English name of an organic compound. According to its naming rules, its chemical structure can be summarized as follows:
    The core structure of this compound is benzoimidazole (1 - H - Benzoimidazole). Benzoimidazole is formed by fusing the benzene ring with the imidazole ring. At position 2 of benzimidazole, there is a substituent, which is a sulfur-containing group, namely 2 - (4 - Methoxyl - 3,5 - Dimethyl - pyridine - 2 - ylmethylsulfenyl). Among them, the 4-Methoxyl-3,5-Dimethyl-pyridine-2-ylmethyl part is based on the pyridine ring. The 3 and 5 positions of the pyridine ring are each substituted with a methyl group (-CH < unk >), the 4 position is substituted with a methoxy group (-OCH < unk >), and the 2 position of the pyridine ring is connected to a methylene group (-CH < unk > -), which is then connected to the sulfur atom, and then connected to the 2 position of benzimidazole. At the 5 position of benzimidazole, there is a methoxy group (5-Methoxy). < Br >
    In summary, the chemical structure of this compound is determined by the connection of each group in a specific position. After this analysis, its structure is clear.
    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-dimethylpyridine-2-methylthio) -1-H-benzimidazole is an organic compound. It has the following physical properties:
    Under normal conditions, it is mostly white to off-white crystalline powder, which is conducive to distinguishing and distinguishing from other substances. In many chemical reactions and preparations, the powder form is conducive to full contact and reaction between substances.
    In terms of solubility, this compound is slightly soluble in water. Water is a common solvent, and its slightly soluble nature in water determines its form and reactivity in aqueous systems. However, it is soluble in some organic solvents, such as dichloromethane, N, N-dimethylformamide (DMF), etc. In dichloromethane, with its good solubility, it can be used for extraction, separation and specific organic synthesis reactions; in DMF, it can provide a suitable medium for some reactions that require a polar aprotic solvent environment.
    Melting point is also an important physical property. After determination, the melting point of the compound is in a specific temperature range (the specific value varies slightly due to test conditions). The determination of melting point can not only be used to determine purity, but also to provide clues for the study of the crystalline structure and intermolecular forces of compounds due to the presence of impurities.
    In addition, the compound has certain stability. Under normal temperature and humidity conditions, it can maintain the chemical structure unchanged for a certain period of time. However, in case of extreme conditions such as high temperature, strong oxidants or strong acids and bases, its structure may change, triggering chemical reactions and forming new substances.
    The above physical properties are of great significance for the application of this compound in organic synthesis, drug development and other fields. Knowing its solubility, the reaction solvent and subsequent separation and purification method can be reasonably selected; knowing the melting point and stability can control the reaction conditions and storage environment to ensure the quality and performance of the compound.
    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-dimethylpyridine-2-methylthio) - 1-H-benzimidazole The main use of this compound is particularly important. In the field of medicine, it is a key intermediate and is often indispensable in the synthesis of many drugs. Due to its unique structure, various active groups can be ingeniously introduced by organic synthesis, and then new drugs with excellent efficacy can be created.
    A drug for the treatment of gastric diseases, this compound may be modified to obtain a good drug that can effectively inhibit gastric acid secretion. With its structural characteristics, it can precisely act on specific targets of gastric cells, regulate the mechanism of gastric acid secretion, and relieve the pain of gastric patients.
    In the field of chemical materials, it also has potential. Or it can be used as a special additive to add specific materials to give materials different properties. Such as enhancing the stability and corrosion resistance of materials, or improving their optical and electrical properties, so that materials can be used more widely in different fields.
    Furthermore, in the path of scientific research and exploration, it is an important research object. Scientists can use their in-depth research to gain insight into the relationship between the reaction mechanism, structure and properties of organic compounds, contributing to the development of organic chemistry, inspiring the birth of more novel synthesis paths and methods, and opening up a broader field for the creation of subsequent compounds.
    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-dimethyl-pyridine-2-methylthio) - 1-H-benzimidazole is an important organic compound, and its synthesis methods are diverse and each has its own advantages.
    One is a benzimidazole derivative containing methoxy group and a pyridine mercaptan derivative containing a specific substituent as raw materials. Under moderate temperature, in an organic solvent, under the catalysis of a base, the two undergo nucleophilic substitution reactions. The base can help the pyridine mercaptan derivatives to form sulfur anions, which can then attack the activity check point in the benzimidazole derivatives and realize the construction of carbon-sulfur bonds, so as to obtain the target product. The raw materials of this method are relatively easy to obtain, and the reaction conditions are relatively mild, but the reaction selectivity needs to be carefully controlled to prevent side reactions.
    The second method can be used to construct step by step. Pyridine-containing structural units are synthesized first, and then sulfur atoms are introduced through thioetherization reaction, and then spliced with benzimidazole structure. In this process, the reaction conditions need to be precisely controlled at each step to ensure the correct transformation of each functional group. For example, in the thioetheration step, an appropriate sulfur source and reaction reagent need to be selected to accurately connect the sulfur atoms to the pyridine methyl position. Although this method is slightly complicated, it is easier to control the intermediates in each step of the reaction, which is conducive to improving the purity of the product.
    Third, the coupling reaction can be catalyzed by transition metals. Appropriate transition metal catalysts, such as palladium and copper, are selected to catalyze the coupling of halogenated benzimidazole derivatives with pyridine-containing thioreagents. Transition metal catalysts can effectively activate the reaction substrate, reduce the activation energy of the reaction, and make the reaction proceed efficiently. However, this method requires higher reaction equipment and operation, and the catalyst cost may also be higher. It is necessary to comprehensively consider the economic cost and reaction effect.
    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 - Methoxyl - 3,5 - Dimethyl - pyridine - 2 - ylmethylsulfenyl) - 1 - H - Benzimidazole This product, in today's market prospects, is like a cloud in the sky, changing and unpredictable, but it also holds infinite opportunities.
    This compound is emerging in the field of pharmaceutical and chemical industry. Its unique molecular structure seems to contain a wonderful method, which can attract the attention of researchers. In the process of pharmaceutical research and development, it may become the basis of targeted drugs and hold promise for the cure of specific diseases. Due to the synergy of various groups in the causative molecule, such as tenon-mortise fit, it can precisely act on the lesion and achieve high-efficiency treatment.
    In the chemical industry, it may be a key component of new materials. With its special chemical properties, it can improve material properties, such as enhancing stability and enhancing reactivity. Although it is not widely used at present, it is like the beginning of a spark, and it is gradually becoming a prairie fire.
    However, the road to market prospects is not smooth. The high cost of research and development is like a boulder. From micro-trials in the laboratory to large-scale production, a huge amount of resources are required. And the constraints of regulations should not be underestimated. In the field of medicine and chemical industry, strict regulations, product approval takes a long time, and various safety and Quality Standards need to be met.
    In addition, the market competition is fierce, such as a hundred competing. Similar compounds or potential substitutes continue to emerge. To stand out in this field requires technical refinement and outstanding quality. If we can break through many difficulties and make good use of our own advantages, with time, 5 - Methoxy - 2 - (4 - Methoxyl - 3,5 - Dimethyl - pyridine - 2 - ylmethylsulfenyl) - 1 - H - Benzimidazole will be able to occupy a place in the market, shine brightly, contribute to the development of the industry, and become a strong driving force for the progress of the industry.