5 Methoxy 2 4 Methoxyl 3 5 Dimethyl Pyridine 2 Ylmethylsulfenyl 1h Benzimida
pyridine pyrrole pyrazine piperidine piperazine

5-Methoxy-2-(4-Methoxyl-3,5-Dimethyl-Pyridine-2-Ylmethylsulfenyl)- 1H- Benzimida

    Specifications

    HS Code

    510016

    Chemical Formula C20H21N3O2S
    Molecular Weight 367.469 g/mol
    Appearance Solid (likely, based on similar benzimidazole derivatives)
    Solubility In Water Low (due to non - polar aromatic and heterocyclic structure)
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform (typical for such compounds)
    Logp Positive value (hydrophobic due to aromatic rings, would need calculation or experimental determination)
    Stability Stable under normal conditions, but may react with strong oxidizing or reducing agents

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    Frequently Asked Questions

    As a leading 5-Methoxy-2-(4-Methoxyl-3,5-Dimethyl-Pyridine-2-Ylmethylsulfenyl)- 1H- Benzimida 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) -1H-Benzimida
    This is to investigate the chemical structure of 5-methoxy-2- (4-methoxy-3,5-dimethylpyridine-2-ylmethylthio) -1H-benzimidazole. This compound is derived from the parent nucleus of benzimidazole. The benzimidazole part is a fused heterocyclic structure containing two nitrogen atoms, which is aromatic and is common in many drugs and bioactive molecules.
    At the 2-position of benzimidazole, there is a complex side chain connected. The side chain starts as a sulfur atom, which is connected to 4-methoxy-3,5-dimethylpyridine-2-ylmethyl. The pyridine ring is a six-membered nitrogen-containing heterocycle and is also aromatic. There is a methyl substitution at the 3,5-position of the pyridine ring, and a methoxy substitution at the 4-position. These substituents affect the electron cloud density and spatial structure of the pyridine ring, which in turn affects the physicochemical properties and biological activities of the whole molecule.
    The 5-position of benzimidazole contains a methoxy group. Methoxy is a power supply group, which can change the electron cloud distribution of the benzimidazole ring and affect its reactivity and intermolecular interactions. The overall structure of this compound, due to the interaction of various parts, endows it with unique physical, chemical and biological properties, which may have potential applications in medicinal chemistry, materials science and other fields.
    What are the main uses of 5-Methoxy-2- (4-Methoxyl-3,5-Dimethyl-Pyridine-2-Ylmethylsulfenyl) -1H-Benzimida
    5-Methoxy-2- (4-methoxy-3,5-dimethylpyridine-2-methylthio) -1H-benzimidazole is a crucial compound in the field of organic synthesis. It has a wide range of uses and can be used as a key intermediate in the field of medicinal chemistry to create drugs with specific biological activities. The structure of benzimidazole and pyridine gives the compound unique pharmacological properties, which may exhibit antibacterial, antiviral, anti-tumor and other effects, paving the way for the development of new drugs.
    In the field of materials science, this compound also has great potential. Due to its unique molecular structure, it may participate in the construction of functional materials with excellent performance. For example, with its electronic properties and structural stability, it may be applied to the preparation of organic optoelectronic materials, which is expected to improve the photoelectric conversion efficiency of materials and shine in the fields of Light Emitting Diode and solar cells.
    Furthermore, in pesticide chemistry, 5-methoxy-2- (4-methoxy-3,5-dimethylpyridine-2-methylthio) -1H-benzimidazole may be used as the basis for the development of new pesticides. Its specific mechanism of action against certain pests or pathogens may provide an opportunity for the creation of high-efficiency, low-toxicity and environmentally friendly pesticides, contributing to the sustainable development of agriculture. In short, this substance has significant potential application value in many fields, opening a new chapter in related scientific research and industrial development.
    What is the market outlook for 5-Methoxy-2- (4-Methoxyl-3,5-Dimethyl-Pyridine-2-Ylmethylsulfenyl) - 1H-Benzimida?
    5-Methoxy-2- (4-methoxy-3,5-dimethylpyridine-2-methylthio) -1H-benzimidazole, although this product has not been widely spread in this world, it has gradually shown its extraordinary appearance in the fields of various specialties.
    Look at the research and development of its products, and in the realm of scientific research, it is gradually getting better. Many scientific researchers have devoted their efforts to studying its properties and applications, and have come to the fore in a corner of medical chemistry. Its unique structure is like a secret weapon made by ancient craftsmen, hiding endless wonders. Scientists use it as the key to open the door to new ways of medicine and explore new paths of disease healing.
    As for the market, although it is still in its infancy, it has attracted attention from all parties. Just like the germinating of spring, although it is not flourishing, its vitality is hidden. Among pharmaceutical R & D institutions, it is a potential choice and is expected to become the cornerstone of new drug creation. Pharmaceutical companies regard it as jade, hoping to shine after carving. Although it is difficult to find it in the current market, it has been found in professional trading houses, and it is cherished by those who know the goods.
    In the future, if the research and development goes well and breaks through many barriers, or like a dragon getting water, it will rise in the pharmaceutical market. It can be used as a sharp blade to fight diseases and heal sentient beings; it can also be used as a ladder for scientific research to help the study of medicine climb to a new high. At that time, the market scene will be like the first blooming flowers, which are very gorgeous.
    What are the preparation methods of 5-Methoxy-2- (4-Methoxyl-3,5-Dimethyl-Pyridine-2-Ylmethylsulfenyl) -1H-Benzimida
    The preparation method of 5-methoxy-2- (4-methoxy-3,5-dimethylpyridine-2-methylthio) -1H-benzimidazole is not directly mentioned in the book "Tiangong Kaiji", but the preparation method can be deduced according to the principle of similar substances.
    Looking at this compound, its preparation may require multiple steps. The first step is to focus on the construction of the structure of pyridine and benzimidazole. For the pyridine part, or take the related precursor of 3,5-dimethyl-4-methoxy pyridine, and use an appropriate halogenated reagent, such as hydrogen halide or halogenated alkane, under suitable solvent and base catalysis conditions, introduce halogen atoms at the 2-position of pyridine to obtain halogenated pyridine derivatives. This step is similar to the metallurgical setting in "Tiangong Kaiji". The amount of solvent, base and reaction temperature must be precisely controlled, otherwise it is easy to cause side reactions, such as halogenated position deviation.
    The second step is for the structure of benzimidazole, or by the condensation and cyclization of o-phenylenediamine and an appropriate carbonyl compound under acid catalysis. In this reaction, it is necessary to pay attention to the proportion of the reactants. If the proportion is out of balance, it is difficult to obtain the ideal benzimidazole product.
    Furthermore, the halogenated pyridine derivative obtained above is reacted with a sulfur-containing reagent, such as mercaptan or thioether salt, in an alkaline environment, so that the sulfur atom is connected to the pyridine 2-position methyl group to form the desired sulfur-based structure. This process is like the shaping of ceramics in "Tiangong Kaiwu". The strength of the base and the reaction time all affect the purity and yield of the product.
    Finally, the sulfur-containing pyridine derivative is connected to the benzimidazole intermediate through a suitable coupling reaction. Or use transition metal catalysis, such as palladium-catalyzed coupling reaction, under the protection of inert gas, strictly control the reaction temperature and time, so that the two can be precisely combined to obtain the target product 5-methoxy-2 - (4-methoxy-3,5-dimethylpyridine-2-methylthio) -1H-benzimidazole. After each step of the reaction, the product needs to be purified by extraction, crystallization, column chromatography, etc., to ensure the smooth follow-up reaction, such as the fine processing of various products in "Tiangongkai", in order to obtain pure target compounds.
    What are the safety and toxicity of 5-Methoxy-2- (4-Methoxyl-3, 5-Dimethyl-Pyridine-2-Ylmethylsulfenyl) -1H-Benzimida?
    I don't know what "5-Methoxy-2- (4-Methoxyl-3, 5-Dimethyl-Pyridine-2-Ylmethylsulfenyl) -1H-Benzimida" is. This name may be a highly specialized chemical term. It has not been found in ancient books, nor has it been studied in the past. Its safety and toxicity.
    However, in terms of the safety and toxicity of the investigated substance, it is common sense to follow the scientific method. To clarify its details, it may be necessary to conduct multiple experiments to observe its interaction with biological systems. If you take animals as a test to observe its impact on animal physiology, behavior, and organs, this is the first way to understand toxicity. It is also necessary to consider its chemical properties. If the structure is similar to that of known toxic substances, you need to be extra vigilant.
    Furthermore, in the environment, this substance may react with surrounding substances, which affects its safety and toxicity. If it decomposes or transforms in water, air, and soil, the product also needs to be studied in detail.
    In addition, the route of human contact is also the key, and the effects caused by oral, percutaneous, and inhalation may be different. However, because we do not know the specific reasons for this chemical, it is difficult to accurately determine its safety and toxicity. It needs to be based on scientific experiments and research to be sure.