7 Chloroimidazo 1 2 Pyridine
pyridine pyrrole pyrazine piperidine piperazine

7-chloroimidazo[1,2-伪]pyridine

    Specifications

    HS Code

    515615

    Chemical Formula C6H4ClN3
    Molar Mass 153.57 g/mol
    Appearance Solid (usually white or off - white)
    Melting Point Data may vary depending on purity, typically in a certain range
    Solubility In Water Poorly soluble in water
    Solubility In Organic Solvents Soluble in some organic solvents like dichloromethane, chloroform
    Density Data may be available based on experimental determination
    Pka Value Relevant for its acidic - basic properties in solution
    Stability Stable under normal conditions, but may react with strong oxidizing or reducing agents

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    Frequently Asked Questions

    As a leading 7-chloroimidazo[1,2-伪]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 7-chloroimidazo [1,2-a] pyridine?
    7-Chlorimidazolo [1,2-a] pyridine, this is an organic compound. It has a wide range of uses and is often used as a key intermediate in the field of medicinal chemistry. It can be converted into biologically active drug molecules through specific chemical reactions, which is of great significance for the development of therapeutic drugs for a variety of diseases. Due to its unique structure, it can interact with specific targets in organisms, or have antibacterial, antiviral, antitumor and other effects, contributing to the creation of new drugs.
    It also has its uses in the field of materials science. Because of its chemical stability and special structure, it can be used to synthesize materials with special properties, such as optoelectronic materials. It can endow materials with unique optical or electrical properties, and play a role in the manufacture of optoelectronic devices, such as Light Emitting Diodes, solar cells, etc., to improve device performance.
    Furthermore, in the field of organic synthetic chemistry, 7-chlorimidazolo [1,2-a] pyridine is an important synthetic building block. With its structural chlorine atoms and imidazolo-pyridine skeleton, it can construct more complex organic molecular structures through various organic reactions, such as nucleophilic substitution, coupling reactions, etc., to promote the development of organic synthetic chemistry and expand the synthesis path of new organic compounds.
    What are the synthesis methods of 7-chloroimidazo [1,2-a] pyridine
    The synthesis of 7-chlorimidazolo [1,2-a] pyridine has been around for a long time, and with the evolution of the times, the methods have become increasingly diverse and exquisite.
    In the past, the original synthesis method was often based on basic organic reactions. Pyridine derivatives are used as starting materials, and chlorine atoms are introduced at specific locations through halogenation reactions. This process requires careful control of reaction conditions, such as temperature, reactant ratio, and catalyst use. Too high or too low temperature may cause the reaction to favor side reactions or slow down the reaction rate. The choice of catalyst is also crucial, and different catalysts have a significant impact on the selectivity and rate of the reaction.
    Subsequently, with the development of chemical theory, new synthesis strategies have gradually emerged. The method of constructing the imidazole ring as the key step has attracted much attention. The imidazole precursor containing a specific functional group is first prepared, and then it is cyclized with pyridine derivatives to form the target product. The mechanism of this cyclization reaction is quite complex, involving many processes such as nucleophilic substitution and electron rearrangement in molecules. The reaction conditions need to be precisely regulated to improve the yield and purity of the product.
    In recent years, the concept of green chemistry has prevailed, and the green synthesis method for the synthesis of 7-chlorimidazolo [1,2-a] pyridine has also come into being. For example, the use of environmentally friendly solvents to replace traditional toxic and harmful solvents, or the use of catalysts with high catalytic efficiency and recyclability, to reduce the impact on the environment and reduce production costs. In addition, microwave-assisted synthesis technology has also emerged. Through microwave radiation, the reaction process can be accelerated, the reaction time can be shortened, and the selectivity of the reaction can be improved, opening up a new path for the synthesis of the compound.
    Synthesis of 7-chlorimidazolo [1,2-a] pyridine, from simple to complex, from traditional to green innovation, chemists continue to explore, laying a solid foundation for the wide application of this compound.
    What are the physical properties of 7-chloroimidazo [1,2-a] pyridine
    7-Chlorimidazolo [1,2-a] pyridine, this is an organic compound. Its physical properties are particularly important and are related to many practical applications.
    First of all, its appearance, under room temperature and pressure, is mostly white to light yellow crystalline powder. This color and shape are easy to identify and preliminary judgment, and are the initial characterization in experiments and production.
    Besides the melting point, the melting point of this compound is quite high, about 160-165 ℃. The melting point is determined by the intermolecular force. The high melting point means that the molecules are closely bound and the structure is stable. This property is very critical in purification, separation and other operations, and can be purified by the difference in melting point. The boiling point of
    is also an important property. However, due to the complex structure, the exact boiling point is difficult to determine accurately. It is roughly speculated that under a specific pressure, the boiling point is in a higher temperature range. The significance of boiling point is that in separation methods such as distillation, it can be separated from the mixture according to the difference in boiling point.
    In terms of solubility, 7-chlorimidazolo [1,2-a] pyridine is slightly soluble in water. This is because water is a polar solvent, and the polar groups in the structure of this compound are limited, and the interaction with water molecules is weak. However, in some organic solvents, such as dichloromethane, chloroform, N, N-dimethylformamide (DMF), it has good solubility. This solubility characteristic provides a basis for the selection of solvents in organic synthesis reactions. Suitable solvents can promote the reaction and improve the yield.
    In terms of density, although the exact value is difficult to obtain, its density should be slightly higher than that of water based on the speculation of similar structural compounds. The size of the density has important reference value when it involves operations such as phase separation.
    In addition, the compound has certain stability and can maintain structural integrity under conventional environmental conditions. In case of extreme conditions such as strong oxidants, strong acids and alkalis, the structure may change. This stability knowledge needs to be taken into account when storing and transporting, and it is necessary to ensure that the environment is suitable to prevent deterioration.
    In conclusion, the physical properties of 7-chlorimidazolo [1,2-a] pyridine are of great significance in the fields of organic synthesis, drug development, and materials science. Only by deeply understanding these properties can we better apply this compound.
    What are the chemical properties of 7-chloroimidazo [1,2-a] pyridine
    7-Chlorimidazolo [1,2-a] pyridine, this is an organic compound with interesting chemical properties and important uses in many fields.
    First, in terms of its physical properties, this compound is usually solid, although its specific appearance may vary depending on purity and crystallization conditions. In terms of solubility, it has a certain solubility in some organic solvents such as dichloromethane, N, N-dimethylformamide, but it has a low solubility in water. This solubility characteristic is related to the chlorine atom contained in the molecule and the heterocyclic structure of imidazolopyridine. The presence of chlorine atoms enhances the polarity of the molecule, but the overall heterocyclic structure limits its dissolution in strongly polar solvents such as water.
    Furthermore, in terms of its chemical properties, the chlorine atom in 7-chlorimidazolo [1,2-a] pyridine is extremely active. This chlorine atom can participate in a variety of nucleophilic substitution reactions. For example, when co-heated with alcohols under basic conditions, the chlorine atom can be replaced by alkoxy groups to form corresponding ether derivatives. And if it reacts with amine compounds, it can form nitrogen-containing substitution products. The activity of this nucleophilic substitution reaction stems from the fact that the carbon atom connected to the chlorine atom is affected by the electronic effect of the imidazolo-pyridine ring, making it positive and vulnerable to attack by nucleophiles.
    In addition, the imidazolo-pyridine ring itself has a certain alkalinity. This is because the nitrogen atom in the ring has a lone pair of electrons and can accept protons. This basicity allows the compound to react with acids to form salts, which is particularly important in the field of medicinal chemistry, because the formation of salts can improve the solubility and stability of compounds, which is conducive to the preparation and application of drugs. Moreover, imidazolopyridine rings can also participate in various cyclization reactions and addition reactions, further expanding the possibility of its derivatization, providing a basis for the synthesis of compounds with more complex structures.
    In conclusion, 7-chlorimidazolo [1,2-a] pyridine has shown broad application prospects in organic synthesis, drug development and other fields due to its unique chemical properties. Chemists can use this to develop many compounds with specific functions.
    What is the price range of 7-chloroimidazo [1,2-a] pyridine in the market?
    The price of 7-chlorimidazolo [1,2-a] pyridine in the market is difficult to determine. The price of this substance often changes for various reasons.
    First, the price of the raw material of this substance fluctuates, often causing the price of 7-chlorimidazolo [1,2-a] pyridine to fluctuate. If the raw material is rare or difficult to prepare, the price will be high; conversely, if the raw material is easy to obtain, the price may be slightly cheaper.
    Second, the method of preparing this compound is also relevant. < Br >
    Third, the supply and demand in the market is the key reason.
    If there are many people who want it, but there are few suppliers, the price will rise; if the supply exceeds the demand, the price will fall.
    Fourth, the factory that makes this product is located in different regions, and its taxes, labor costs, etc. are different, which can also make the price different.
    Looking at the past, in the field of fine chemicals, the price of such compounds ranges from tens to hundreds of yuan per gram. However, today, due to the above-mentioned factors, the determination of the price of 7-chlorimidazolo [1,2-a] pyridine requires detailed consideration of the current raw material conditions, preparation process, market supply and demand, and factory conditions. It is difficult to determine the range of its price.