5 Methoxy 2 4 Methoxy 3 5 Dimethyl 2 Pyridinyl Methylmercapto Benzimidazole
quinoline thiophene imidazole thiazole

5-Methoxy-2-(4-methoxy-3,5-dimethyl-2-pyridinyl) methylmercapto benzimidazole

    Specifications

    HS Code

    249110

    Chemical Formula C19H21N3O2S
    Molecular Weight 353.454 g/mol
    Appearance Typically a solid
    Melting Point Specific value depends on purity, usually in a certain temperature range
    Solubility Solubility characteristics vary in different solvents; often has limited solubility in water
    Odor May have a faint, characteristic odor
    Color May be white to off - white
    Purity Can be produced at different purity levels depending on manufacturing process
    Stability Stable under normal storage conditions away from strong oxidizing agents

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    General Information
    Where to Buy 5-Methoxy-2-(4-methoxy-3,5-dimethyl-2-pyridinyl) methylmercapto benzimidazole in China?
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    Frequently Asked Questions

    As a leading 5-Methoxy-2-(4-methoxy-3,5-dimethyl-2-pyridinyl) methylmercapto 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 is the chemical structure of 5-Methoxy-2- (4-methoxy-3, 5-dimethyl-2-pyridinyl) methylmercapto benzimidazole
    This is related to the chemical structure of 5-methoxy-2 - (4-methoxy-3,5-dimethyl-2-pyridyl) methylthiobenzimidazole. This compound belongs to benzimidazole derivatives. The nucleus of benzimidazole is the core of its structure, which is formed by fusing a benzene ring with an imidazole ring.
    Looking at its 5 position, there is a methoxy group. The existence of this methoxy group can affect the electron cloud distribution and polarity of molecules, and plays an important role in chemical reactions and biological activities.
    Look at the second position and connect (4-methoxy-3,5-dimethyl-2-pyridyl) methylthio. Pyridyl is also a nitrogen-containing heterocycle, with methoxy at the 4th position and methyl at the 3rd and 5th positions. Methoxy can increase the hydrophilicity of molecules, while methyl affects the steric hindrance and electronic effects. Methylthio is connected between the pyridyl group and the benzimidazole nucleus. The lone pair electron of the sulfur atom can participate in chemical reactions and affect the overall properties of the molecule.
    Such a structure makes the compound potentially active in the fields of medicine, pesticides, etc. The complexity and uniqueness of its structure provide a broad space for the study of its properties and applications.
    What are the main uses of 5-Methoxy-2- (4-methoxy-3, 5-dimethyl-2-pyridinyl) methylmercapto benzimidazole
    5-Methoxy-2 - (4-methoxy-3,5-dimethyl-2-pyridyl) methylthiobenzimidazole, which is widely used. In the field of medicine, it is often a key component of proton pump inhibitors. These drugs are effective in inhibiting gastric acid secretion and are mostly used in the treatment of digestive system diseases such as gastric ulcers, duodenal ulcers, and reflux esophagitis. It can effectively block the key link of gastric acid production, thereby creating an environment conducive to ulcer healing and alleviating the discomfort caused by excessive gastric acid in patients.
    In the chemical industry, it also has important uses. It can be used as an intermediate in organic synthesis to prepare a variety of organic compounds with special properties. With its unique chemical structure, it can participate in multiple chemical reactions, provide key starting materials for the synthesis of complex organic molecules, and help the research and development of new materials, fine chemicals, etc., which is of great significance to the innovation and development of the chemical industry.
    In addition, at the level of scientific research and exploration, due to its unique structure, it provides a good model for chemical and pharmaceutical research. By studying its reaction characteristics, pharmacological mechanisms, etc., researchers deepen their understanding of related chemical processes and biological activities, lay a theoretical foundation for the creation of new drugs and functional materials, and promote the continuous expansion of scientific research fields.
    What is the synthesis method of 5-Methoxy-2- (4-methoxy-3, 5-dimethyl-2-pyridinyl) methylmercapto benzimidazole
    The synthesis method of 5-methoxy-2 - (4-methoxy-3,5-dimethyl-2-pyridyl) methylthiobenzimidazole is as follows:
    First take an appropriate amount of starting materials, in which a specific substituent-containing pyridine derivative and benzimidazole-related substrates need to be prepared. In a clean and dry reaction vessel, put both in a certain molar ratio.
    Subsequently, add a suitable organic solvent, such as dichloromethane, N, N-dimethylformamide, etc., to create a homogeneous reaction environment to facilitate sufficient contact and reaction of the reactants. < Br >
    In the reaction system, a specific catalyst needs to be added. The choice of this catalyst is very critical, and it can effectively promote the progress of the reaction, such as some metal salt catalysts or organic base catalysts, depending on the specific needs of the reaction.
    It is essential to properly regulate the reaction temperature and reaction time. Generally speaking, the reaction temperature is maintained at a certain range, such as between 40 ° C and 80 ° C, for several hours, such as 3 to 8 hours. During this period, the reaction process must be closely monitored. The consumption of the reaction substrate and the formation of the product can be observed in a timely manner by means of thin-layer chromatography.
    After the reaction is completed, cool the reaction system, and then use conventional separation and purification methods. Steps such as extraction and column chromatography to obtain high-purity 5-methoxy-2 - (4-methoxy-3,5-dimethyl-2-pyridyl) methylthiobenzimidazole products. During extraction, select a suitable extractant and extract multiple times to improve the product collection rate. During column chromatography, carefully select suitable stationary and mobile phases to ensure effective separation and purification of the product.
    What are the physical and chemical properties of 5-Methoxy-2- (4-methoxy-3, 5-dimethyl-2-pyridinyl) methylmercapto benzimidazole
    5-Methoxy-2 - (4-methoxy-3,5-dimethyl-2-pyridyl) methylthiobenzimidazole, an organic compound. Its physicochemical properties are crucial for its applications in various fields.
    Let's talk about its physical properties first. Under normal temperature and pressure, this substance is mostly in a solid state. Due to the strong intermolecular forces, the molecules are closely arranged. Its appearance is often white or off-white powder, which is determined by the reflection and scattering characteristics of the molecular structure to light. In terms of melting point, it is about a specific temperature range. This temperature is the critical value for the molecule to overcome the lattice energy and change from solid to liquid state, which is of great significance for its purification and identification.
    Re-discuss its chemical properties. This compound contains benzimidazole core structure, which has certain aromaticity and stability. The presence of methoxy and methylthio groups endows it with unique chemical activity. Methoxy is a power supply group, which can increase the electron cloud density of the benzene ring and make the benzene ring more prone to electrophilic substitution. The sulfur atom in the methylthio group has lone pair electrons, which not only has certain nucleophilic properties, but also participates in coordination. In acidic or basic environments, the stability of the compound may change, because acid and base can react with some of the groups, such as methoxy under strong acidic conditions or hydrolysis. In addition, it also has specific behaviors in redox reactions, and sulfur atoms can be oxidized to higher valence states, which affects the overall properties of the compound.
    In this way, the physicochemical properties of 5-methoxy-2- (4-methoxy-3,5-dimethyl-2-pyridyl) methylthiobenzimidazole lay the foundation for its application in chemical, pharmaceutical and other fields.
    What is the price of 5-Methoxy-2- (4-methoxy-3, 5-dimethyl-2-pyridinyl) methylmercapto benzimidazole in the market?
    5-Methoxy-2 - (4-methoxy-3,5-dimethyl-2-pyridyl) methylthiobenzimidazole, the price of which is difficult to determine in the market. The cover is due to its special use and demand, and is disturbed by factors such as changes in supply and demand over time, the quality of production methods, and high quality.
    In the pharmaceutical industry, it is a key raw material for the production of proton pump inhibitors, which are mostly used to treat gastric acid-related diseases, and the demand is quite large. If the pharmaceutical market is prosperous for acid suppressants, and this raw material is in short supply, its price will rise; if the supply is abundant and the competition is fierce, the price may decline.
    Furthermore, the preparation method is also related to its price. The subtle and efficient method can reduce costs and increase production, so that the market supply can increase, and the price may stabilize; if the preparation is difficult and the cost is high, the price will be high.
    Quality is also the main reason. Those with high purity and excellent quality are used in high-end applications such as pharmaceuticals, and the price must be higher than ordinary ones.
    It varies from time to time, and the price is also different. Where supply and demand are unbalanced, the price may rise and fall sharply; and where supply and demand are balanced, the price may be stable.
    The reason is to observe it. To determine the price between the markets, it is necessary to consider various factors in detail and pay attention to market changes from time to time.