2 N Propyl 4 Methyl 6 1 Methylbenzimidazole 2 Yl 1h Benzimidazole
quinoline thiophene imidazole thiazole

2-N-Propyl-4-methyl-6-(1-methylbenzimidazole-2-yl)-1H-benzimidazole

    Specifications

    HS Code

    644568

    Chemical Formula C20H21N3
    Molecular Weight 303.401 g/mol
    Appearance Solid (usually white to off - white powder)
    Melting Point Typically in a specific range (data may vary, e.g., around 170 - 180°C)
    Solubility In Water Low solubility in water
    Solubility In Organic Solvents Soluble in some organic solvents like DMSO, chloroform
    Odor Odorless or very faint odor
    Stability Stable under normal storage conditions away from strong oxidizing agents
    Pka Value Relevant acid - base dissociation constant value (specific value depending on the environment)

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    General Information
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    Frequently Asked Questions

    As a leading 2-N-Propyl-4-methyl-6-(1-methylbenzimidazole-2-yl)-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 is the chemical structure of 2-N-Propyl-4-methyl-6- (1-methylbenzimidazole-2-yl) -1H-benzimidazole
    This is the chemical structure analysis of 2-n-propyl-4-methyl-6- (1-methylbenzimidazole-2-yl) -1H-benzimidazole. Its structure contains the core structure of benzimidazole, which is the key component.
    One, the 2-position is connected with n-propyl, which is an alkyl group connected by three carbon atoms in a straight chain. It gives the molecule specific spatial and chemical properties, and affects the physical and chemical properties of the molecule, such as solubility and lipophilicity.
    The second, the 4-position has a methyl group, which contains only one carbon atom and three hydrogen atoms. Although the structure is simple, it has an effect on the distribution and overall properties of molecular electron clouds, or changes the polarity of molecules, affecting their interactions with other molecules.
    The third, 6 positions are connected with 1-methylbenzimidazole-2-group, which is another benzimidazole structure connected to the main benzimidazole, and 1 position has methyl. This fused ring structure endows the molecule with a unique electron conjugation system, which affects its optical, electrical and biological activities and other properties. The connection of two benzimidazole structures enhances the overall rigidity of the molecule, and the spatial structure is complex. In the fields of drug design or materials science, this special structure may exhibit unique properties and application potential.
    The synergistic action of various parts of this chemical structure determines the physical, chemical and biological properties of the compound, which is of great significance in the research fields of chemistry, pharmacy and materials science.
    What are the main uses of 2-N-Propyl-4-methyl-6- (1-methylbenzimidazole-2-yl) -1H-benzimidazole
    2-N-propyl-4-methyl-6- (1-methylbenzimidazole-2-yl) -1H-benzimidazole, this substance has its uses in various fields. Viewing its use in medicine, or its ability to resist diseases, it can be the basis for the development of new agents. Geiinbenzimidazole compounds have many pharmacological activities, or can act on specific targets to regulate the physiology of the body and inhibit the reproduction of pathogens.
    In the field of materials, it also has its function. Its structure is unique, or it can be used to prepare materials with special properties, such as those with good stability or special optical and electrical properties. Using it as a raw material, through exquisite methods, new materials suitable for electronic devices and optical instruments can be prepared.
    Furthermore, it is an important chemical reagent in the path of scientific research and exploration. Scientists can use it to explore the mechanism of chemical reactions and investigate their interactions with other substances, so as to expand the boundaries of chemical understanding and pave the way for the creation of new reactions and new synthesis methods. This compound has its unique uses in medicine, materials and scientific research, and has promising prospects.
    What is the production method of 2-N-Propyl-4-methyl-6- (1-methylbenzimidazole-2-yl) -1H-benzimidazole?
    To prepare 2-N-propyl-4-methyl-6- (1-methylbenzimidazole-2-yl) -1H-benzimidazole, the following method can be followed.
    Take suitable raw materials first, among which benzimidazole-related compounds are the key starting materials. In the reaction vessel, add an appropriate amount of reaction solvent, such as organic solvent xylene, which can provide a suitable environment for the reaction, so that the reactants are uniformly dispersed and conducive to contact reaction.
    Then, add a specific catalyst. The choice of this catalyst is related to the reaction rate and yield. Metal salt catalysts with specific activities can often be selected, such as salts of some transition metals, which can effectively reduce the activation energy of the reaction and promote the reaction to occur more easily.
    Put in the starting material, and mix the reagents containing propyl, methyl and other functional groups with benzimidazole derivatives appropriately in a precise ratio. Heat up to a suitable temperature, usually within a certain range, such as between 150 ° C and 200 ° C. At this temperature, the thermal motion of the molecules intensifies, and the reactant molecules are more likely to overcome the reaction energy barrier and chemically react to form the required carbon-carbon bonds, carbon-nitrogen bonds and other key chemical bonds.
    During the reaction process, close monitoring is required. Chromatography and other analytical methods can be used to observe the degree of reaction. When the reaction reaches the expected level, the reaction can be stopped in time. After
    terminates, the reaction mixture is treated. First, the system temperature is cooled to reduce, and then the organic phase containing the target product is separated by extraction and other methods. Then, the solvent and unreacted raw materials are removed by distillation and other operations to obtain a crude product.
    The crude product still needs to be purified, and the method of recrystallization can be adopted. A suitable recrystallization solvent is selected, and the target product is dissolved in it. After slow cooling and other operations, the crystallization is precipitated, and finally the high-purity 2-N-propyl-4-methyl-6- (1-methylbenzimidazole-2-yl) -1H-benzimidazole product is obtained.
    2-N-Propyl-4-methyl-6- (1-methylbenzimidazole-2-yl) How safe is -1H-benzimidazole?
    2 - N - propyl - 4 - methyl - 6 - (1 - methylbenzimidazole - 2 - yl) - 1H - benzimidazole, the safety of this substance is related to many aspects.
    Looking at its chemical structure, this compound contains the structural unit of benzimidazole. Benzimidazole substances, many of which have biological activities, but some or latent risk. In terms of its stability, under normal environmental conditions, the structure of the compound is relatively stable and not easy to decompose spontaneously. In case of extreme conditions such as high temperature and strong acid and base, it may cause structural changes or release harmful components.
    When it comes to toxicity, because the relevant books do not contain detailed toxicity data of this specific substance, it can only be speculated from similar structural compounds. Many benzimidazole derivatives have been shown by animal experiments, or have certain acute toxicity, and can involve organs such as liver and kidney. And some may have mutagenicity and carcinogenicity, but this is only an inference based on structural similarity, and more experimental verification is needed.
    In terms of environmental impact, if the substance enters the environment, its degradability is quite critical. Depending on the complexity of its structure, it may not be easy to degrade in the natural environment, or accumulate in soil and water bodies, causing long-term impact on the ecosystem. And its toxic effects on aquatic and terrestrial organisms also need to be considered, or affect the growth, reproduction and survival of organisms.
    In terms of safety of use, if used in industrial production, workers who come into contact with the substance can pose a threat to health if they are not properly protected, inhaled through the respiratory tract, exposed to the skin or accidentally ingested. When storing, it is also necessary to pay attention to environmental conditions to prevent its leakage from causing safety accidents.
    In summary, although the current safety knowledge of 2-N-propyl-4-methyl-6- (1-methylbenzimidazole-2-yl) -1H-benzimidazole is limited, it should be treated with caution based on its structure and characteristics of similar substances. More experimental studies are urgently needed to clarify its safety profile.
    What are the relevant market application cases of 2-N-Propyl-4-methyl-6- (1-methylbenzimidazole-2-yl) -1H-benzimidazole?
    2-N-propyl-4-methyl-6- (1-methylbenzimidazole-2-yl) -1H-benzimidazole, this is an organic compound, which has many relevant applications in the fields of medicine and chemical industry.
    In the field of medicine, it may be a key intermediate for the development of new anti-parasite drugs. In the past, in the study of combating intestinal parasite infestation, we have observed that compounds containing benzimidazole structure have the ability to inhibit specific parasite enzymes, which can cause parasite metabolic disorders and death. This compound has been cleverly modified, which may enhance the targeting and inhibitory effect on specific parasites. In the past, physicians explored insect repellent formulas and used precise medicinal flavors to achieve the purpose of removing evil and improving health. Today, this compound is used in the research and development of anti-parasitic drugs, and it also follows this concept of precise action, hoping to become a good medicine with high efficiency and low toxicity.
    In the chemical industry, it may be used as a synthetic monomer of special polymer materials. In ancient times, for example, firing exquisite porcelain in ancient times required exquisite proportions of raw materials and superb skills. Today, the synthesis of special polymer materials, due to its unique structure, may endow the material with special properties, such as excellent heat resistance and chemical stability. After polymerization, it can be used to prepare high-performance materials for high-precision fields such as aerospace and electronic devices, helping related industries to flourish.