2 5 Dimethyl 1h Benzimidazole
quinoline thiophene imidazole thiazole

2,5-DIMETHYL-1H-BENZIMIDAZOLE

    Specifications

    HS Code

    486079

    Chemical Formula C9H10N2
    Molar Mass 146.19 g/mol
    Appearance Solid
    Physical State At Room Temp Solid
    Solubility In Water Insoluble
    Solubility In Organic Solvents Soluble in some organic solvents

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    General Information
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    Frequently Asked Questions

    As a leading 2,5-DIMETHYL-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 main use of 2,5-dimethyl-1H-benzimidazole?
    2% 2C5-dimethyl-1H-indolocarbazole, this substance has important uses in many fields. In the field of pharmaceutical research, it shows potential medicinal value. Due to its unique structure, chemists speculate that it may have an affinity for specific biological targets, and it is expected to be developed into new drugs. For some difficult diseases, it can precisely act on diseased cells, bringing new opportunities for conquering diseases.
    In the field of materials science, 2% 2C5-dimethyl-1H-indolocarbazole also has outstanding performance. Because of its special optoelectronic properties, it can emerge in optoelectronic devices. For example, when applied to organic Light Emitting Diode (OLED), it can optimize the luminous efficiency and stability, improve the display effect, and make the screen picture clearer and more vivid; in the field of solar cells, it may help improve the photoelectric conversion efficiency and promote the development of clean energy.
    In the field of chemical synthesis, it acts as a key intermediate, providing the possibility for the synthesis of more complex and special functional compounds. Chemists can use it as a foundation to build molecular structures with diverse structures and functions through ingenious chemical reactions, further expanding the boundaries of chemical species and properties, and laying the foundation for the innovative development of materials, medicine and other related industries.
    What are the physical properties of 2,5-dimethyl-1H-benzimidazole?
    2% 2C5-dimethyl-1H-benzimidazole is one of the organic compounds. Its physical properties are complex, let me tell them one by one.
    Looking at its properties, under room temperature and pressure, this substance is mostly white to light yellow crystalline powder, with a delicate texture, as if it has been carefully ground by artisans.
    When it comes to the melting point, it is between 290 ° C and 295 ° C. This temperature range is like the node of its transformation. At this temperature, the solid body begins to melt into a liquid state, just like ice disappearing under the warm sun and quietly changing its form.
    As for solubility, this compound is slightly soluble in water, just like a passer-by in water, and it is difficult to blend with water. However, in organic solvents, such as ethanol, chloroform, dichloromethane, etc., it can show good solubility, just like a wanderer returning home, and can blend with these solvents and coexist harmoniously.
    Furthermore, its density is also an important physical property. Although the specific value varies slightly according to the experimental conditions, it is roughly within a certain range. This density characteristic affects its settlement and floating states in different media, as well as its distribution and behavior in various chemical reaction systems.
    Its sublimation characteristics are also worth mentioning. Under specific temperature and pressure conditions, it can be directly transformed from solid to gaseous without going through the liquid state. This process is like the emergence of immortals, which is quiet and mysterious. This property provides a unique way and method for its separation, purification and other operations.
    In summary, the physical properties of 2% 2C5-dimethyl-1H-benzimidazole are diverse, and each property is interrelated, which jointly determines its application and behavior in the chemical field and related industries. It is a delicate product of natural creation.
    Is the chemical property of 2,5-dimethyl-1H-benzimidazole stable?
    The chemical properties of 2% 2C5-dimethyl-1H-indolo-pyrrole are quite stable. This compound has a unique structure and its stability is due to multiple factors.
    From the perspective of its molecular structure, 2,5-dimethyl-1H-indolo-pyrrole contains a fused ring system, which endows the molecule with high rigidity and stability. The atoms in the ring are closely connected by covalent bonds to form a stable structure, which resists molecular deformation or bond breakage caused by external factors. The introduction of
    methyl also makes an important contribution to the stability. Methyl is an electron-supplying group, which increases the density of cyclic electrons through induction and superconjugation effects, resulting in a decrease in the energy and enhanced stability of the system. This electronic effect changes the reactivity of the molecule to the electrophilic reagent, and it is not easy to react against the attack of external electrophilic substances, thereby maintaining molecular stability.
    Furthermore, there is a conjugate system in the molecule, and the electrons are delocalized from the entire conjugate structure, reducing the molecular energy and enhancing the stability. The conjugate effect makes the electron distribution more uniform, avoids the local charge caused by the concentration of electrons in specific atoms, reduces the reactivity check point, and keeps the molecule stable under normal conditions.
    However, although its stability is quite high, in the case of extreme chemical environments such as strong oxidants, strong acids, and strong bases, or special physical conditions such as high temperature and high radiation, the chemical structure of 2,5-dimethyl-1H-indole-pyrrole may be affected, triggering chemical reactions and changing its chemical properties. However, in conventional experiments and application environments, without specific excitation conditions, this compound can maintain good stability and provide a reliable basis for applications in related fields.
    What are the synthesis methods of 2,5-dimethyl-1H-benzimidazole?
    The synthesis method of 2% 2C5-dimethyl-1H-benzimidazole covers several pathways. One is to use o-phenylenediamine and acetic acid as raw materials. Under appropriate reaction conditions, such as in the presence of a specific temperature and catalyst, the two interact and undergo a condensation reaction to form the target product. In this process, the control of temperature is extremely critical, and either too high or too low may affect the rate and yield of the reaction.
    There are also those who use o-nitroaniline as the starting material. First, o-nitroaniline is converted into o-phenylenediamine through a reduction reaction. This reduction step may require a specific reducing agent and a suitable reaction environment. Then, with the corresponding acids, such as acetic acid, according to the above-mentioned similar condensation reaction steps, the purpose of synthesizing 2% 2C5-dimethyl-1H-benzimidazole can be achieved.
    In addition, other compounds containing benzene rings and amino groups are used as starting materials, and the structure of the target molecule is gradually constructed through a series of carefully designed reaction steps. These reactions may involve many common reaction types in organic chemistry such as substitution, addition, cyclization, etc. Careful planning of reaction sequence and conditions between each step is required to effectively and efficiently obtain 2% 2C5-dimethyl-1H-benzimidazole. Each synthetic method has its own advantages and disadvantages. In practical applications, the appropriate synthetic route should be carefully selected according to specific requirements, such as cost, yield, purity, and other factors.
    In which fields is 2,5-dimethyl-1H-benzimidazole used?
    2% 2C5-dimethyl-1H-indolocarbazole is used in many fields such as medicine and materials.
    In the field of medicine, it has potential anti-cancer activity. After many studies, it can effectively inhibit the proliferation and metastasis of cancer cells. Gain can precisely act on specific signaling pathways in cancer cells, such as regulating the expression of key proteins, thereby blocking the growth and division process of cancer cells, just like strangling the raging throat of cancer cells, opening up a new path for the development of anti-cancer drugs.
    In the field of materials, it exhibits unique optoelectronic properties. Its molecular structure imparts good fluorescence properties and can be used to prepare organic Light Emitting Diode (OLED) materials. OLED devices made of such materials have high luminous efficiency and good color performance, and have broad prospects in the field of display technology, or can make the screen image quality more gorgeous and realistic. And because of its specific electrical properties, it can also be used in organic semiconductor materials, or help improve the performance of electronic devices, such as speeding up the electron transfer rate, so that electronic devices operate more efficiently and quickly.
    In summary, 2% 2C5-dimethyl-1H-indolocarbazole plays a significant role in the field of medicine and materials, like a hidden treasure, which needs to be further explored and utilized to contribute to human health and scientific and technological progress.