5 Chloro 3h Imidazo 4 5 B Pyridine
pyridine pyrrole pyrazine piperidine piperazine

5-chloro-3H-imidazo[4,5-b]pyridine

    Specifications

    HS Code

    432081

    Chemical Formula C6H4ClN3
    Molecular Weight 153.57
    Appearance Solid (usually)
    Melting Point Data needed
    Boiling Point Data needed
    Solubility In Water Poor solubility (usually)
    Solubility In Organic Solvents Soluble in some organic solvents
    Pka Data needed
    Density Data needed
    Odor Odorless (usually)

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

    As a leading 5-chloro-3H-imidazo[4,5-b]pyridine 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 chemical properties of 5-chloro-3H-imidazo [4,5-b] pyridine
    5-Chloro-3H-imidazolo [4,5-b] pyridine is an organic compound with unique chemical properties. Its physical properties are mostly solid, and the melting and boiling point varies depending on the intermolecular force and structure. The molecule contains chlorine atoms, imidazole rings and pyridine rings, and the structure endows it with specific chemical activities.
    Chlorine atoms are active in nucleophilic substitution reactions. Due to the high electronegativity of chlorine, the C-Cl bond is polar, and nucleophiles easily attack carbon atoms, causing chlorine atoms to leave. This property is often used to introduce other functional groups to expand the structure and properties of compounds.
    Imidazole rings and pyridine rings contain nitrogen atoms, which are basic and can accept protons as salts. This alkalinity can be used in organic synthesis to react with acids to form corresponding salts, improve the solubility and stability of compounds, and also participate in many organic reactions, such as catalyzing certain reaction processes.
    The conjugated system exists in the 5-chloro-3H-imidazolo [4,5-b] pyridine molecule, giving it a certain electron delocalization ability, which affects the electron cloud distribution and reactivity of the compound. The conjugated structure also allows the compound to have an absorption spectrum at a specific wavelength, which can be used for qualitative and quantitative analysis in analytical chemistry.
    Due to its structural properties, 5-chloro-3H-imidazolo [4,5-b] pyridine has attracted attention in the field of medicinal chemistry, or has potential biological activity. It can be used as a lead compound for structural modification and optimization to develop new drugs. In materials science, its unique structure may also provide a basis for the development of functional materials for the preparation of materials with special properties.
    What are the common synthesis methods of 5-chloro-3H-imidazo [4,5-b] pyridine?
    The common synthesis methods of 5-chloro-3H-imidazolo [4,5-b] pyridine include the following.
    First, pyridine compounds are used as starting materials. Pyridine is first halogenated at a specific position, chlorine atoms are introduced, and it is replaced in an appropriate position. Then, the imidazole ring structure is constructed through a series of cyclization reactions. This process requires the selection of suitable reaction conditions and reagents, such as in the presence of a specific catalyst, under a certain temperature and pressure environment, the pyridine derivative undergoes a condensation reaction with the nitrogen-containing reagent to form the skeleton structure of imidazolo [4,5-b] pyridine, while retaining the chlorine atom at the target position.
    Second, it can start from imidazole compounds. Modify imidazole to attach pyridine-related structural fragments at its specific position. Functionalize imidazole first, and then react with pyridine derivatives. In this synthesis path, the key is to control the regioselectivity of the reaction and ensure that the pyridine fragment can be precisely connected to the target check point of imidazole to achieve the synthesis of 5-chloro-3H-imidazolo [4,5-b] pyridine. This process requires careful selection of reaction reagents and reaction conditions, or the use of metal catalysis to improve the reaction selectivity.
    Third, a multi-component reaction strategy is adopted. Chlorine-containing compounds, nitrogen-containing compounds, and reagents containing pyridine structural units are reacted in the same reaction system under suitable catalysts and reaction conditions. The advantage of multi-component reactions is that they can construct complex structures in one step and simplify the synthesis steps. However, this method requires high control of reaction conditions, and factors such as the proportion of components, reaction temperature, and reaction time need to be precisely regulated to promote the reaction towards the formation of 5-chloro-3H-imidazolo [4,5-b] pyridine.
    Where is 5-chloro-3H-imidazo [4,5-b] pyridine used?
    5-Chloro-3H-imidazolo [4,5-b] pyridine is used in the fields of medicine, pesticides and materials science.
    In the field of medicine, it is a key intermediate for the creation of new drugs. The unique structure of this compound gives it the potential to combine with specific targets in vivo, which can help developers develop new drugs for the treatment of various diseases. If inhibitors of specific kinases are developed, 5-chloro-3H-imidazolo [4,5-b] pyridine can modify its own structure, act precisely on the checking point of kinase activity, block related signaling pathways, and bring new opportunities for the treatment of cancer, inflammation and other diseases.
    In the field of pesticides, it also shows broad application prospects. Using it as a raw material, pesticides with high insecticidal and bactericidal properties can be synthesized. Because it can specifically interfere with the physiological process of pests or pathogens, it can achieve the purpose of preventing and controlling crop diseases and pests, and is environmentally friendly, with low residues, which meets the needs of current green agriculture development.
    In the field of materials science, 5-chloro-3H-imidazolo [4,5-b] pyridine can be used to prepare materials with special functions. For example, by introducing it into polymer materials through specific chemical reactions, it can improve the electrical and optical properties of materials, contributing to the development of organic optoelectronic materials, and playing an important role in the fabrication of devices such as Light Emitting Diodes and solar cells.
    What is the market price of 5-chloro-3H-imidazo [4,5-b] pyridine
    5-Chloro-3H-imidazolo [4,5-b] pyridine, the price of this product in the market is difficult to break. Covers the change in its price, subject to many factors.
    First, the difficulty of its preparation is the key. If the preparation method is complicated, rare raw materials are required, or the preparation process is exquisite, and the equipment and technical requirements are strict, the cost will be high, and the market price will be high.
    Second, the market supply and demand situation determines its price. If there are many people who ask for it, but the supply is small, the so-called rare is expensive, and the price must rise; on the contrary, if the supply is abundant and the demand is few, the price may decline.
    Furthermore, the difference between producers also makes the price different. Most well-known producers, because of their well-known reputation and high quality of their products, may have higher prices than others; while new or unknown producers compete for market share or adopt low-price policies.
    In addition, the region and season in which they are located also have an impact on their price. Different regions have different prices due to different taxes and transportation costs; and changes in seasons may cause fluctuations in the supply of raw materials, which in turn affects the price of this product.
    At present, we do not know the details of its preparation, the exact number of market supply and demand, and the pricing status of each manufacturer, so it is difficult to know its exact market price. If you want to know the price, you can visit the platform of chemical product trading, consult the supplier of chemical reagents, or participate in the exhibition of the industry, and consult with the industry.
    What are the safety and toxicity of 5-chloro-3H-imidazo [4,5-b] pyridine?
    5-Chloro-3H-imidazo [4,5-b] pyridine, which is an organic compound. On its safety and toxicity, although there is no direct record in ancient books, it is based on current scientific knowledge.
    First of all, toxicity may be potentially harmful. In the context of experiments, if it acts on organisms, it may affect the normal metabolism and function of cells. Due to the presence of chlorine atoms, this atom may participate in chemical reactions in the body and disrupt biochemical pathways. If combined with biological macromolecules such as proteins and nucleic acids, its structure and function will change abnormally, damage the normal operation of cells, and even lead to apoptosis and necrosis. If the organism is exposed for a long time, it may increase the risk of disease, such as organ function decline, genetic mutation, etc.
    As for safety, its synthesis, use and storage need to be treated with caution. During the synthesis process, many chemical reagents and reaction conditions may be dangerous. If the reaction temperature and pressure are not properly controlled, it is easy to cause accidents. And its chemical properties or active, it can react violently in case of certain substances. When stored, if it is not in accordance with the specifications, it may cause leakage, endangering the environment and personnel.
    During use, the operator should prepare protective equipment, such as gloves, masks, goggles, etc., to prevent it from coming into contact with the skin and respiratory tract. If it is inadvertently contacted, it should be handled according to emergency methods as soon as possible, such as rinsing with a lot of water. Although there is no description of this compound in ancient books, today's scientific reasoning shows that its safety and toxicity cannot be ignored, and it must be treated in accordance with scientific laws to ensure the safety of personnel and the environment.