1h Imidazo 4 5 B Pyridine
pyridine pyrrole pyrazine piperidine piperazine

1H-Imidazo[4,5-b]pyridine

    Specifications

    HS Code

    755083

    Chemical Formula C6H5N3
    Molar Mass 119.125 g/mol
    Appearance Solid
    Melting Point 182 - 186 °C
    Solubility In Water Slightly soluble
    Stability Stable under normal conditions

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    General Information
    Where to Buy 1H-Imidazo[4,5-b]pyridine in China?
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    Frequently Asked Questions

    As a leading 1H-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 is the main use of 1H-Imidazo [4,5-b] pyridine?
    1H-imidazolo [4,5-b] pyridine is an organic compound. It has a wide range of uses and is of great significance in many fields.
    In the field of medicine, it is often a key intermediate for drug development. The design and synthesis of many drug molecules rely on this as the basic framework. Due to its specific chemical structure, it can interact with specific targets in organisms. For example, in the development of anti-tumor drugs, with the help of modification and modification of the structure of 1H-imidazolo [4,5-b] pyridine, drugs that can precisely act on tumor cell-related proteins or enzymes can be developed to inhibit tumor cell growth, proliferation or induce apoptosis.
    In the field of materials science, it also shows unique value. It can be used to prepare functional materials with special properties. For example, polymer materials constructed from it may have excellent electrical, optical or thermal properties, and have potential applications in electronic devices, optical sensors, etc. The presence of nitrogen atoms in its structure can affect the electron cloud distribution and charge transport characteristics of materials.
    In the field of pesticides, 1H-imidazolo [4,5-b] pyridine also has a place. It can be reasonably designed to synthesize pesticide ingredients with high insecticidal, bactericidal or herbicidal activities. Its structure can fit with specific biomolecules in pests, pathogens or weeds, interfering with their normal physiological and biochemical processes, and achieving the purpose of control.
    1H-imidazolo [4,5-b] pyridine plays an important role in the fields of medicine, materials science, pesticides, etc. With the continuous progress of science and technology, its application prospects will be broader, and it is expected to bring new breakthroughs and opportunities for the development of various fields.
    What are the physical properties of 1H-Imidazo [4,5-b] pyridine
    1H-imidazolo [4,5-b] pyridine, an organic compound, has unique physical properties and is of great research value.
    Its appearance is often solid, but the specific color varies depending on the purity and preparation method, or it is white to light yellow powder, or it is crystalline.
    In terms of melting point, it is usually in a relatively high temperature range, and the specific value varies according to the exact structure and substituent. This property is crucial for the identification and purification of compounds, and its purity can be tested by melting point measurement.
    Solubility is also a key physical property. In organic solvents, such as dichloromethane, chloroform, N, N-dimethylformamide, etc., show some solubility, but the solubility in water is relatively limited. This difference in solubility provides a basis for selecting suitable solvents in chemical synthesis and separation and purification steps.
    In addition, the density of the compound also has a specific value. Although it is not a property that is frequently considered in daily life, it cannot be ignored in some scenarios involving accurate measurement and reaction system construction. Its density is closely related to the molecular structure, reflecting the accumulation mode and interaction between molecules. The physical properties of 1H-imidazolo [4,5-b] pyridine are of great significance in the fields of organic synthesis and medicinal chemistry, which lay the foundation for its further research and application.
    What are the chemical synthesis methods of 1H-Imidazo [4,5-b] pyridine
    The common methods for the chemical synthesis of 1H-imidazolo [4,5-b] pyridine are as follows.
    One is to obtain a suitable pyridine derivative and a nitrogen-containing heterocyclic precursor by cyclization under suitable reaction conditions. In this case, the reaction substrate needs to be carefully selected, and the reaction temperature, time and solvent should be precisely controlled. For example, the pyridine compound with a specific substituent and the imidazole precursor with an active functional group should be cyclized and condensed in an inert gas atmosphere under high temperature and the presence of a suitable catalyst. In this way, the pyridine ring can be cleverly connected to the imidazole ring to construct the target 1H-imidazolo [4,5-b] pyridine structure.
    The second can be constructed by a multi-step reaction. The pyridine ring is first modified to introduce a specific functional group, and then the functional group is converted to connect with the synthesis step of the imidazole ring. For example, a halogen atom is introduced into the pyridine ring first, and then the nucleophilic substitution reaction is used to access the intermediate required for the synthesis of the imidazole ring. After further cyclization reaction, the formation of the imidazolo [4,5-b] pyridine structure is promoted. Although this method is a little complicated, the control of the reaction conditions is more precise, which can effectively improve the purity and yield of the product.
    The third is the reaction strategy using transition metal catalysis. Transition metals are used as catalysts to activate substrate molecules and promote the bonding of pyridine rings and imidazole rings. Common transition metal catalysts such as palladium and copper can efficiently catalyze related reactions with the assistance of specific ligands. In suitable base and solvent systems, substrate molecules undergo coupling and cyclization reactions catalyzed by transition metals to generate 1H-imidazolo [4,5-b] pyridine. This method has the advantages of mild reaction conditions and high selectivity, and is widely used in modern organic synthesis.
    What is the price range of 1H-Imidazo [4,5-b] pyridine in the market?
    The price of 1H-imidazolo [4,5-b] pyridine in the market is difficult to determine. The price often varies due to various factors such as the quality, the state of supply and demand, the method of preparation, and the place of sale.
    If the quality is high and pure, and it is worth the time of high supply and thin supply, the price will be high; if the quality is slightly inferior, and the supply exceeds the demand, the price will decrease. Furthermore, the preparation method is different in complexity and simplicity, and the cost is also different, which also affects the price. In different places, the price is also different due to taxes, freight, etc.
    The price of such chemicals in the market varies from a few dollars to tens of dollars per gram, or even more than 100 yuan. However, this is only a rough estimate. The actual price should be obtained by consulting the merchants in the market or checking in detail on the chemical product trading platform.
    What are the relevant safety precautions for 1H-Imidazo [4,5-b] pyridine?
    1H-imidazolo [4,5-b] pyridine is an important organic compound. It is important to know the safety precautions for this substance.
    This substance may have specific chemical activities, and the experimental procedures must be strictly followed when operating. During use, appropriate protective equipment should be worn, such as gloves, goggles, lab clothes, etc., to prevent it from coming into contact with the skin and eyes. Because it may be irritating, if you accidentally touch it, you should immediately rinse it with plenty of water and seek medical treatment if necessary.
    When storing, pay attention to environmental conditions. It should be placed in a dry, cool and well-ventilated place, away from fire sources and oxidants, due to its chemical properties or risk of fire or chemical reactions. Properly sealed and stored to prevent it from interacting with air or moisture, causing quality changes or forming dangerous products.
    During use, its chemical reaction should be treated with caution. Clarify the characteristics and conditions of its participation in the reaction to avoid the reaction getting out of control. Operate in a fume hood to discharge the harmful gases that may be generated to ensure the safety of the experimental environment.
    When heating or other operations, strictly control the temperature and reaction time. Excessive heating or too long time may cause side reactions or cause serious consequences such as explosion.
    In addition, the waste after use should also be properly disposed of in accordance with regulations. Do not discard at will to prevent pollution of the environment. Appropriate treatment methods should be selected according to its chemical characteristics to ensure safety and environmental protection. In conclusion, the use of 1H-imidazolo [4,5-b] pyridine requires rigorous treatment of every step, and must not be negligent in order to ensure the safety of the experimenter and the smooth progress of the experiment.