5 6 Dimethoxy 1h Benzimidazole
quinoline thiophene imidazole thiazole

5,6-dimethoxy-1H-benzimidazole

    Specifications

    HS Code

    970678

    Chemical Formula C9H10N2O2
    Molar Mass 178.19 g/mol
    Appearance Solid
    Melting Point 187 - 190 °C
    Solubility In Water Insoluble
    Solubility In Organic Solvents Soluble in some organic solvents like ethanol
    Logp Estimated to have certain lipophilicity
    Crystal Structure Specific crystal structure details require X - ray diffraction analysis
    Odor Odorless or very faint odor

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    General Information
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    Frequently Asked Questions

    As a leading 5,6-dimethoxy-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 5,6-dimethoxy-1H-benzimidazole?
    5,6-Dimethoxy-1H-indolopyrazole is very useful in the field of pharmaceutical and chemical industry.
    First, it can be used as a key intermediate for drug research and development. When creating new anti-cancer drugs, their structures have been cleverly modified and modified, which can precisely combine with specific targets of cancer cells, effectively inhibit the proliferation and metastasis of cancer cells, and contribute to overcoming cancer problems. Just like the early research stage of many cutting-edge anti-cancer drugs, 5,6-dimethoxy-1H-indolopyrazole is often the raw material that researchers focus on. After many experiments and optimizations, it is hoped to breed new anti-cancer drugs with high efficiency and low toxicity.
    Second, it also has potential in the development of drugs for the treatment of neurological diseases. Because it has a unique mechanism of action on specific receptors or enzymes of the nervous system, after in-depth research and development, it may become an effective drug for the treatment of neurodegenerative diseases such as Parkinson's disease and Alzheimer's disease. For example, by adjusting its chemical structure, it can enhance the protection and repair ability of diseased nerve cells, bringing new hope to patients with neurological diseases.
    Third, it has emerged in the field of materials science. Due to its special chemical structure and photoelectric properties, it can be applied to organic Light Emitting Diode (OLED) materials. The OLED materials developed on this basis may have higher luminous efficiency, stability, and color purity, which will help to upgrade the display technology and promote the development of the display screen towards a clearer, more energy-efficient, and thinner direction.
    What are the physical properties of 5,6-dimethoxy-1H-benzimidazole?
    5% 2C6-dimethoxy-1H-indolopyrrole is one of the organic compounds. Its physical properties are quite important, so let me tell them one by one.
    Looking at its properties, under room temperature and pressure, it is mostly in a solid state. The color of this substance, or white to light yellow powder, is pure in color and fine in texture.
    As for the melting point, this is one of the key physical properties. After many studies, its melting point is within a certain range. This value is slightly different or slightly different due to experimental conditions, but it is roughly stable in the interval, which can be an important basis for identifying this compound.
    In terms of solubility, 5% 2C6-dimethoxy-1H-indole-pyrrole exhibits unique solubility properties in common organic solvents. In some organic solvents, such as ethanol, dichloromethane, etc., it has certain solubility. In ethanol, with the increase of temperature, the solubility increases, showing a good dissolution trend. This property makes it possible to use solvents such as ethanol for dissolution, separation, and purification in chemical synthesis and related fields.
    Its density is also an important component of physical properties. After accurate measurement, the density value is relatively stable. This value is of great significance for the calculation of substance dosage and the ratio of reaction systems in practical application scenarios such as chemical production.
    In addition, the stability of the compound also needs to be considered. Under normal environmental conditions, if properly stored to avoid extreme conditions such as light, high temperature, and humidity, 5% 2C6-dimethoxy-1H-indole-pyrrole can maintain a relatively stable chemical structure, and its physical properties have not changed significantly. However, if exposed to adverse environments or in contact with specific chemicals, it may cause structural changes, which in turn may cause physical properties to change.
    Is the chemical property of 5,6-dimethoxy-1H-benzimidazole stable?
    5,6-Dimethoxy-1H-indolocarbazole has stable properties. Due to its special chemical structure, it forms a stable conjugated system within the molecule, resulting in its chemical properties stabilizing. Intermolecular interactions, such as hydrogen bonds, van der Waals forces, etc., also contribute to its stability.
    Under normal chemical conditions, 5,6-dimethoxy-1H-indolocarbazole can resist the action of common chemical reagents and is not easy to react spontaneously at room temperature and pressure. In the case of oxidizing agents, due to the ingenious distribution of electron clouds in the structure, the oxidizing agent cannot capture its electrons, so it is not easy to oxidize; in the case of reducing agents, the same is true, the reducing agent is difficult to cause its electronic structure to change.
    Under the influence of temperature, it is difficult to change its chemical structure when it is moderately heated. When it reaches a specific high temperature, the molecular vibration intensifies, and the covalent bond may be challenged, but the high temperature far exceeds the usual conditions. On the pH again, in the range of common acids and bases, its molecular structure can remain intact, and acid and base are difficult to break its covalent bond and conjugate system. Only extreme acid and base conditions may affect it.
    From this perspective, the chemical properties of 5,6-dimethoxy-1H-indole-carbazole are quite stable, and they can maintain their inherent structure and properties under conventional chemical and physical environments.
    What are the synthesis methods of 5,6-dimethoxy-1H-benzimidazole?
    The synthesis method of 5,6-dimethoxy-1H-indolocarbazole involves many chemical channels, among which are delicate, and let me explain in detail.
    First, it can be obtained from a specific starting material through a multi-step reaction. The initial raw material is carried out in the first step under suitable reaction conditions, such as at a specific temperature, pressure and in the presence of a catalyst. This step may be a substitution reaction, in which some groups in the raw material are replaced by specific reagents to build the basic framework of the molecule.
    Then, it goes through a series of modification steps. Or through oxidation reactions, the oxidation state of specific atoms in the molecule is precisely adjusted to give the molecule the desired chemical properties. Or by means of a reduction reaction, the saturation of a specific chemical bond is changed, paving the way for subsequent reactions.
    Furthermore, the cyclization reaction is a key step. Under cleverly designed reaction conditions, specific atoms interact within the molecule to form the core ring structure of indole carbazole. This process requires fine control of reaction kinetics and thermodynamics to ensure that the cyclization reaction occurs with high selectivity and high yield.
    In addition, during the reaction process, the control of the reaction intermediate is crucial. The stability and activity of the intermediate affect the formation of the final product. Appropriate reaction solvents and additives need to be selected to optimize the reaction environment to promote the smooth conversion of the intermediate to the target product.
    Synthesis of this compound requires attention to the purity and yield of the reaction. Through fine reaction control and post-processing steps, such as column chromatography separation, recrystallization, etc., the purity of the product can be improved and high-quality 5,6-dimethoxy-1H-indolocarbazole can be obtained. This synthesis requires a good understanding of chemical principles and careful design of reaction paths.
    What is the price of 5,6-dimethoxy-1H-benzimidazole in the market?
    Wuwei Wen has the price of 5,6-dimethoxy-1H-indolo-pyridine in the market. This is a fine chemical, or it is used in specialized fields such as scientific research and pharmaceutical research and development. It is not a common product in circulation, and it is difficult to find it in the market, so the price is difficult to determine.
    If you want to know its price, you should consult a professional chemical supplier. This generation is often involved in various fine chemical transactions, or you can tell you the approximate price. However, its price is also subject to multiple factors, such as purity, demand, production difficulty, etc.
    Those with high purity must be expensive. For scientific research, high purity is often required, so the price is also high. Changes in demand can also affect its price. If there is a large increase in demand for pharmaceutical research and development at a certain time, the price may increase accordingly. Furthermore, the difficulty of production is related to the cost. If the synthesis steps are complicated and the raw materials are rare, the cost will be high and the price will be high.
    To know the exact price, you must consult the merchant in detail, and the conditions at the time of the specific transaction shall prevail. The market conditions are changeable, and the price is also unstable. The actual price can only be obtained by careful investigation.