3h Imidazo 4 5 C Quinoline
quinoline thiophene imidazole thiazole

3H-imidazo[4,5-c]quinoline

Taiy Chemical

    Specifications

    HS Code

    713773

    Molecular Formula C10H7N3
    Molecular Weight 169.183 g/mol
    Melting Point Data may vary, typically organic heterocyclic compound melting point range
    Boiling Point Data may vary based on purity and conditions
    Appearance Solid (usually)
    Solubility In Water Low solubility, organic heterocyclic compounds often have poor water solubility
    Solubility In Organic Solvents May dissolve in some common organic solvents like DMSO, chloroform
    Uv Vis Absorption Absorbs in UV - Vis region characteristic of aromatic heterocyclic systems
    Pka Data may vary depending on substitution and environment
    Stability Stable under normal conditions but may react with strong oxidizing or reducing agents

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    General Information
    Where to Buy 3H-imidazo[4,5-c]quinoline in China?
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    Frequently Asked Questions

    As a leading 3H-imidazo[4,5-c]quinoline supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What are the main application fields of 3H-imidazo [4,5-c] quinoline
    3H-imidazolo [4,5-c] quinoline is a class of organic compounds with unique chemical structures. It has important applications in many fields.
    In the field of medicinal chemistry, this compound is often used as a potential drug precursor. Due to its structural properties, it can interact with specific targets in organisms, or exhibit pharmacological activities such as antibacterial, antiviral, and antitumor. For example, some drugs developed on this basis can precisely act on the specific signaling pathways of tumor cells, inhibit the proliferation and metastasis of tumor cells, and open up new avenues for tumor treatment.
    In the field of materials science, 3H-imidazolo [4,5-c] quinoline also has extraordinary performance. Due to its specific optical and electrical properties, it can be applied to the preparation of optoelectronic devices such as organic Light Emitting Diodes (OLEDs) and solar cells. It can improve the luminous efficiency, stability and charge transport performance of the device, and enhance the overall efficiency of optoelectronic devices.
    Furthermore, in the field of analytical chemistry, its special structure and properties can be used to develop highly sensitive analytical detection methods. For example, as a fluorescent probe, it can selectively identify and detect specific ions or biomolecules, assisting in environmental monitoring, biomedical diagnosis, etc., to achieve accurate determination of trace substances.
    In conclusion, 3H-imidazolo [4,5-c] quinoline, with its unique structure, has demonstrated important value in many fields such as medicine, materials, and analysis, providing strong support and innovation opportunities for the development of various fields.
    What are the synthesis methods of 3H-imidazo [4,5-c] quinoline
    The synthesis method of 3H-imidazolo [4,5-c] quinoline has been known for a long time. In the past, Fang family often used subtle methods to make this compound.
    One method is to use quinoline as the base, supplemented by the genus imidazole, to promote the synthesis of the two by suitable reaction conditions. First, put the quinoline in a special vessel, add an appropriate amount of solvent to make a uniform solution. Next, slowly add imidazole reagents. This process requires fine temperature control and cannot be ignored. When the temperature reaches a specific value and remains at a certain level, the two begin to combine, and after complex reactions, gradually produce 3H-imidazolo [4,5-c] quinoline. < Br >
    Another method is to use the heterocyclic nitrogen-containing ring as the starting material. First, the heterocyclic ring is modified to have a specific active group. Then, another reactant suitable for it is introduced, and the two can also obtain this compound through ingenious reaction. In the meantime, the choice of catalyst is crucial. Choosing a good catalyst can promote the reaction speed and increase the purity of the product.
    In addition, there is also a concept of molecular design to carefully plan the reaction path. According to the structural characteristics of 3H-imidazolo [4,5-c] quinoline, the required raw materials and reaction steps are inferred. After repeated experiments, the reaction parameters, such as temperature, pressure, and the ratio of reactants, were adjusted, and the reaction was carried out according to the envisaged route, and the final product was pure.
    All these synthesis methods have their own strengths and weaknesses, and they all rely on the ingenuity and experience of the Fang family to enable the smooth synthesis of 3H-imidazo [4,5-c] quinoline.
    What are the physicochemical properties of 3H-imidazo [4,5-c] quinoline?
    3H-imidazolo [4,5-c] quinoline is a class of organic compounds with a special structure. Its physical and chemical properties are quite important in the academic community.
    Let's talk about its physical properties first. This substance is often in a solid state, which is mostly caused by the interaction between molecules. The level of its melting point depends on the tightness of the molecular structure and the strength of the interaction force. If there are strong interactions such as hydrogen bonds and van der Waals forces between molecules, the melting point is often higher; if the molecular structure is loose and the interaction is weak, the melting point is relatively low. Its color is either colorless or light yellow, which is related to the intramolecular electron transition and conjugation system. When the conjugated system is large or contains specific chromogenic groups, it absorbs light differently and causes color changes.
    Re-discussion of chemical properties. It has a certain alkalinity, and the nitrogen atom of the imidazole ring and the quinoline ring can accept protons. In an acidic environment, it is easy to combine with protons to form salts, which makes it an important use in the field of organic synthesis and medicinal chemistry. Because it can react with acidic substances, it can be used to prepare salt compounds with specific structures and change the solubility and stability of the compounds. And because of its conjugate system, it has certain aromaticity and can undergo electrophilic substitution reactions. In case of electrophilic reagents, it can be substituted at specific positions on the ring, introducing various functional groups, laying the foundation for the synthesis of complex organic molecules. At the same time, the nitrogen atom of the compound can also act as a nucleophilic center, participate in nucleophilic reactions, and combine with electrophilic reagents to expand the diversity of molecular structures.
    In summary, the physical and chemical properties of 3H-imidazolo [4,5-c] quinoline are unique, and have potential application value in many fields such as organic synthesis and drug development, providing an important basis for chemists to explore new compounds and develop new drugs.
    What is the price range of 3H-imidazo [4,5-c] quinoline in the market?
    3H-imidazolo [4,5-c] quinoline is difficult to determine within the range of market prices. Its price is subject to many reasons.
    First, the difficulty of its preparation is of great importance. If the preparation method is cumbersome, rare or expensive raw materials are required, and the reaction conditions are severe, special equipment and exquisite skills are required, the cost will increase greatly, and the price will be high. On the contrary, if the preparation method is simple, the raw materials are common and cheap, the price may be lower.
    Second, the market supply and demand is also the key. If there is a large demand for this product in the fields of pharmaceutical research and development, materials science, etc., but the supply is limited, the price will rise according to the reason of supply and demand. On the contrary, if there is little demand and excess output, the price will fall.
    Furthermore, the differences in manufacturers also have an impact. Different manufacturers offer different prices due to different technical levels, management efficiency, and cost control. Large factories may reduce costs due to scale effects, and their prices may be competitive; while small factories may have higher prices due to higher costs.
    In summary, the market price of 3H-imidazolo [4,5-c] quinoline can range from tens of yuan per gram to hundreds of yuan per gram, or even higher. It is difficult to determine the exact range, depending on the actual market conditions and specific product specifications.
    What are the manufacturers of 3H-imidazo [4,5-c] quinoline?
    3H-imidazolo [4,5-c] quinoline is an organic compound, which is widely used in medicine, pesticides, material science and other fields. However, in today's world, there is no one who has recorded the manufacturer of this compound in ancient words. With the knowledge of today's people, I will briefly describe the relevant manufacturers for you.
    In the land of Huaxia, many chemical companies are involved in the production of this compound. For example, ** A chemical company in Jiangsu **, which has been focusing on the field of organic synthesis for a long time, with its profound technical background and advanced equipment, it can stably produce high-quality 3H-imidazolo [4,5-c] quinoline, supplying raw materials for many downstream industries. Furthermore, a fine chemical company in Zhejiang is also listed. The company focuses on R & D innovation and constantly optimizes the production process. Its products are not only sold well in China, but also exported overseas.
    There are also many such manufacturers overseas. ** A well-known chemical company in the United States **, its scientific research strength is strong, the production scale is huge, and the 3H-imidazolo [4,5 - c] quinoline produced is quite reputable in the international market. Another example is ** A well-known chemical company in Germany **, adhering to the concept of rigorous process and excellent quality, its products are very popular in the high-end application field.
    In short, there are many manufacturers of this compound, distributed all over the world, all of which use their own advantages to promote the development of this compound-related industry.