1h Benzimidazole 2 3 4 Dichlorophenyl Methyl
quinoline thiophene imidazole thiazole

1H-Benzimidazole, 2-[(3,4-dichlorophenyl)methyl]-

    Specifications

    HS Code

    665025

    Chemical Formula C14H10Cl2N2
    Molecular Weight 277.15
    Appearance Solid
    Solubility In Water Low
    Solubility In Organic Solvents Moderate in some organic solvents
    Stability Stable under normal conditions
    Main Uses Potential pharmaceutical or chemical intermediate

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    General Information
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    Frequently Asked Questions

    As a leading 1H-Benzimidazole, 2-[(3,4-dichlorophenyl)methyl]- 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 property of 1H-Benzimidazole, 2- [ (3,4-dichlorophenyl) methyl] -
    2 - [ (3,4 -dichlorophenyl) methyl] -1H -benzimidazole, this is an organic compound. Its physical properties are often solid at room temperature, with a high melting point, and it needs a specific temperature to melt into a liquid state. Because its molecular structure contains benzimidazole ring and dichlorophenyl methyl, it is endowed with certain stability and is not easy to volatilize.
    In terms of chemical properties, benzimidazole ring is rich in nitrogen atoms and has a certain alkalinity, which can react with acids to form corresponding salts. The chlorine atom connected to the benzene ring in this compound is less active than the general aliphatic chlorine atom due to the influence of the benzene ring conjugation system, but under specific conditions, such as under the action of strong nucleophiles and suitable catalysts, substitution reactions can still occur, and the chlorine atom is replaced by other groups. The benzimidazole ring and dichlorophenyl group in the
    molecule give this compound a certain conjugate system, so that it has characteristic absorption in the ultraviolet region, which can be analyzed and identified by ultraviolet spectroscopy. In the field of organic synthesis, it is often used as a key intermediate. With the reactivity of benzimidazole ring and dichlorophenyl methyl, it participates in the construction of more complex organic molecular structures, and has potential application value in many fields such as medicinal chemistry and materials science.
    What are the uses of 1H-Benzimidazole, 2- [ (3,4-dichlorophenyl) methyl] -
    2 - [ (3,4 -dichlorophenyl) methyl] -1H -benzimidazole, this is an organic compound. It has a wide range of uses and can play an important role in many fields.
    In the field of medicine, it may become a key intermediate in drug synthesis. Inbenzimidazole compounds often have a variety of biological activities, such as antibacterial, antiviral, anti-tumor, etc. Based on this compound, through a series of chemical reactions, specific drugs for specific diseases may be prepared. For example, by modifying and modifying its structure, it may be able to show inhibitory activity on some stubborn tumor cells, providing new drug options for tumor treatment.
    In the field of pesticides, it also has potential uses. Due to its special chemical structure, it may have certain insecticidal and bactericidal properties. It can be used to develop new pesticides to help crops resist pest attacks and improve crop yield and quality. For example, through reasonable design and experimentation, it may be possible to develop high-efficiency insecticides for specific pests, which are relatively friendly to the environment and have low residues, which meets the needs of modern green agriculture development.
    In the field of materials science, it may be used as a component of functional materials. With its unique chemical properties, it can be combined with other materials, or it can give new properties to materials. For example, adding this compound to polymer materials can improve the thermal stability and mechanical properties of materials, and broaden the application range of materials, such as in aerospace, electronic devices and other fields that require strict material properties.
    In short, the chemical structure of 2- [ (3,4-dichlorophenyl) methyl] -1H-benzimidazoline itself shows potential application value in many fields such as medicine, pesticides, and materials science. With in-depth research, it is expected to bring new opportunities for the development of various fields.
    What is the synthesis method of 1H-Benzimidazole, 2- [ (3,4-dichlorophenyl) methyl] -
    There are currently methods for the synthesis of 2- [ (3,4-dichlorophenyl) methyl] -1H-benzimidazole, which are described in detail below.
    First take 3,4-dichlorobenzaldehyde and o-phenylenediamine and dissolve them in an appropriate organic solvent, such as ethanol. Mix the two in an appropriate ratio, which is related to the effectiveness of the reaction and should be carefully considered. After mixing, an appropriate amount of acid can be added as a catalyst, such as acetic acid, which can promote the reaction. < Br >
    The mixture is heated and refluxed at a certain temperature. This temperature is also a key factor. It is usually controlled in a moderate range, such as between 80 ° C and 100 ° C. After several hours of reaction, the process of the reaction is closely observed, which can be monitored by thin layer chromatography.
    After the reaction is completed, the mixture is cooled, and solid precipitation can be seen. The solid is collected by filtration, and then washed with a suitable solvent to remove impurities. The crude product needs to be further purified, often by recrystallization. Select a suitable solvent, such as ethanol-water mixed solvent, heat to dissolve the crude product, then slowly cool to precipitate the crystals, filter again, dry, and obtain a pure 2- [ (3,4-dichlorophenyl) methyl] -1H -benzimidazole product. This synthesis method requires fine operation in each step to obtain satisfactory results.
    What is the market outlook for 1H-Benzimidazole, 2- [ (3,4-dichlorophenyl) methyl] -?
    Today there are 1H-benzimidazole, 2- [ (3,4-dichlorophenyl) methyl], what is the market prospect? Let me know in detail.
    This compound may have considerable potential in the field of medicine. Due to its unique molecular structure, chemists speculate that it may have an affinity for specific biological targets or can be developed into new drugs. Looking at today's pharmaceutical market, there is a hunger for innovative drugs, and many pharmaceutical companies have invested heavily in research and development. If this compound is studied in depth and confirmed to have pharmacological activity and meet safety standards, it will surely gain a place in the market.
    In the field of pesticides, it should not be underestimated. Today's agriculture pursues efficient and environmentally friendly pesticides, and this compound may be developed into a new type of pesticide due to its special mechanism of action on pests. Nowadays, environmental regulations are becoming increasingly strict, and traditional pesticides are mostly limited due to toxicity and other issues. If this compound can fit the concept of green environmental protection, it may shine in the pesticide market.
    However, it also faces many challenges if it wants to succeed in the market. The research and development process requires a huge amount of money and a long time. From laboratory research to clinical trials or field trials, rigorous demonstration is required. And the market competition is fierce, and there are many potential compounds of the same kind. To stand out, you need to have advantages in terms of activity, safety, and cost-effectiveness.
    In conclusion, although 1H-benzimidazole, 2- [ (3,4-dichlorophenyl) methyl] has promising prospects, it also needs to overcome many difficulties in order to bloom in the market.
    1H-Benzimidazole, 2- [ (3,4-dichlorophenyl) methyl] - What are the related derivatives?
    There are many derivatives related to 2 - [ (3,4 -dichlorophenyl) methyl] -1H -benzimidazole, each with wonderful properties and uses.
    In the past, there have been Fang Fang's research on this compound, and many variants have been derived. First, in some derivatives, different substituents are introduced at specific positions of benzimidazole, which is like adding unique accessories to it, which greatly improves its chemical properties. For example, connecting a specific alkyl group to the side chain is like giving it a different "dress", which changes the intermolecular forces and affects its solubility and stability. This is like ancient craftsmen carefully carving and decorating the utensils to make their performance better.
    Furthermore, changing the number or position of chlorine atoms on 3,4-dichlorophenyl groups is like adjusting the delicate mechanism layout, which greatly affects the ability of the derivative to bind to biological targets. If it is cleverly changed, it may improve its biological activity and find a new way in the field of medicine, or explore a new path to the treasure house of health.
    There are other heterocycles replacing the benzimidazole part, which seems to reshape the foundation and derive compounds with different structures. The distribution of its electron cloud and the spatial configuration are changed, showing a new physical and chemical properties, which seems to open a new door to the unknown field.
    Derivatives, either in pharmaceutical research and development, help treat diseases; or in materials science, become the cornerstone of building novel materials, just like stars dotted in the vast sky of science, each shining brightly, waiting for the world to explore in depth and tap its endless potential.