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What is the main use of 6-Chloroimidazo [1,2-a] pyridine-3-carbaldehyde?
6-Chlorimidazolo [1,2-a] pyridine-3-formaldehyde is a crucial compound in the field of organic synthesis. Its main uses are quite extensive, especially in the field of medicinal chemistry.
The unique structure of this compound gives it the ability to interact with specific targets in organisms. In the process of many drug development, 6-chlorimidazolo [1,2-a] pyridine-3-formaldehyde is often used as the key intermediate. Through a series of chemical reactions, different functional groups are added, and then drug molecules with specific pharmacological activities are constructed. For example, in the creation of anti-inflammatory, anti-tumor and other drugs, this compound often plays an important role. Scientists hope to find new drugs with better efficacy and less side effects by modifying and optimizing its structure.
In the field of materials science, 6-chlorimidazolo [1,2-a] pyridine-3-formaldehyde also has outstanding performance. It can participate in the preparation of materials with special photoelectric properties, such as organic Light Emitting Diode (OLED) materials. Because its structure can affect the electronic transport and luminescence properties of materials, rational design and synthesis can improve the luminescence efficiency and stability of OLED materials, contributing to the development of display technology.
In addition, it is also indispensable in the synthesis of fine chemical products. In the preparation of fine chemicals such as some high-end dyes and fragrances, 6-chlorimidazolo [1,2-a] pyridine-3-formaldehyde can be used as an important starting material or reaction intermediate to help synthesize fine chemical products with complex structures and excellent performance, meeting the needs of different industries for high-quality chemicals.
What are the synthesis methods of 6-Chloroimidazo [1,2-a] pyridine-3-carbaldehyde
The synthesis method of 6-chlorimidazolo [1,2-a] pyridine-3-formaldehyde can be described below.
The first one can follow the conventional path of organic synthesis. Using suitable pyridine derivatives as starting materials, chlorine atoms are introduced at specific positions through halogenation reaction. This halogenation reaction requires careful selection of halogenating reagents and reaction conditions, such as a specific chlorination agent, carried out under appropriate solvents and temperatures, so that chlorine atoms fall precisely at the target check point of the pyridine ring.
Then, through cyclization, the cyclic structure of imidazolo [1,2-a] pyridine is constructed. This step requires a suitable catalyst and reaction environment to promote the formation of intramolecular rings to achieve the construction of an imidazole-pyridine skeleton.
Furthermore, for the introduction of aldehyde groups, specific organic reactions can be used. For example, with suitable reagents, through a series of operations such as oxidation and substitution, the aldehyde groups are successfully introduced at the 3 positions of the pyridine ring. In this process, the selectivity and yield of the reaction need to be carefully controlled. Due to the high activity of aldehyde groups and the slightly poor reaction conditions, side reactions can easily occur.
Or, you can refer to the existing synthesis strategies of similar compounds in the relevant literature and adjust and optimize them according to their principles and steps. Due to the method of organic synthesis, it is often possible to learn from the experience of similar structure synthesis, take the essence and remove the dross, so that the synthesis route is simpler and more efficient, and can effectively improve the purity and yield of the product.
When synthesizing this compound, each step of the reaction requires precise control of raw materials, reagents, temperature, time and other factors in order to make the synthesis path smooth and achieve the expected synthesis goal.
What are the physical properties of 6-Chloroimidazo [1,2-a] pyridine-3-carbaldehyde
6-Chlorimidazolo [1,2-a] pyridine-3-formaldehyde is an organic compound. Its physical properties are crucial for many uses and reaction characteristics of this compound.
This compound is mostly solid or crystalline at room temperature. The texture may be fine, and the appearance may be white to pale yellow powder or crystal. This color and morphology are derived from the molecular structure and internal arrangement.
In terms of melting point, the melting point is determined by precise experiments to be in a specific temperature range, which is of great significance for the identification and purity evaluation of compounds. When heated to this temperature range, the molecule is energized, the lattice structure disintegrates, and the solid state gradually melts into a liquid state.
In terms of solubility, some organic solvents have good solubility in common organic solvents. For example, in polar organic solvents such as dimethyl sulfoxide (DMSO) and N, N-dimethylformamide (DMF), it can exhibit good solubility, which is attributed to the interaction between molecules and solvents, such as hydrogen bonds, van der Waals forces, etc. However, the solubility in water is poor, and the interaction with water molecules is weak due to the polar distribution of molecular structure.
In addition, the compound also has a certain volatility. Although the volatility is not strong, under certain conditions, such as heating or high vacuum environment, some molecules can escape the solid or liquid surface and enter the gas phase. This property needs to be taken into account in some separation and purification processes.
Its density is also an important physical property. Through accurate measurement, the mass of the compound per unit volume can be known, which is of great significance in the fields of preparation and reaction measurement.
The above physical properties provide a solid foundation for the research and application of 6-chlorimidazo [1,2-a] pyridine-3-formaldehyde, and help researchers to deeply understand its behavior and achieve better utilization.
What is the price range of 6-Chloroimidazo [1,2-a] pyridine-3-carbaldehyde in the market?
6-Chlorimidazolo [1,2-a] pyridine-3-formaldehyde, the price of this substance in the market varies for many reasons.
First, the preparation method is poor in simplicity. If exquisite craftsmanship and rare raw materials are required, the price will be high; if the simple method is common, the price will be slightly lower.
Second, the state of supply and demand also affects its price. If there are many people in the market, and the supply is limited, the price will rise; conversely, if the supply exceeds the demand, the price may drop.
Third, the quality, high purity, and few impurities, the price will be higher than that of ordinary ones.
However, after searching the past records, no exact price can be obtained. Based on common sense, it is important in the field of fine chemicals or the pharmaceutical industry. Due to the characteristics of the industry, its price may fluctuate from a few yuan to several hundred yuan per gram. This is only speculation, and the market situation is fickle. The actual price must be consulted in detail with chemical raw material suppliers or relevant market practitioners to obtain an accurate number.
6-Chloroimidazo [1,2-a] What are the relevant safety precautions pyridine-3-carbaldehyde
6-Chlorimidazolo [1,2-a] pyridine-3-formaldehyde is an organic compound that is occasionally involved in chemical experiments and industrial production. The safety precautions related to this compound are detailed as follows:
First, protective contact is extremely important. This compound may irritate the skin, eyes and respiratory props. Therefore, when operating, you must wear appropriate protective equipment, such as laboratory clothes, protective gloves and safety goggles. If the skin comes into contact accidentally, you should immediately rinse with plenty of water and then seek medical treatment; if it splashes into the eyes, you need to rinse with running water immediately for a few minutes and seek medical attention quickly.
Second, pay attention to inhalation prevention. When handling this compound, it is necessary to ensure that it is well ventilated, and it is best to operate in a fume hood. Due to its dust or volatile gaseous substances, if inhaled, it may cause respiratory discomfort. If inhaled, it should be quickly moved to a place with fresh air. If symptoms do not subside, seek medical attention.
Third, properly dispose of chemical waste. The remaining 6-chlorimidazolo [1,2-a] pyridine-3-formaldehyde, or solutions containing this compound, must not be dumped at will. According to the waste treatment procedures established by the laboratory or factory, it must be collected and properly disposed of to prevent pollution to the environment.
Fourth, carefully store. It should be stored in a cool, dry and ventilated place, away from fire and heat sources, and avoid mixing with oxidants, acids, alkalis and other substances to prevent dangerous chemical reactions.
Fifth, know the emergency treatment method. The operation site should be equipped with corresponding emergency treatment equipment and medicines. In the event of a leak, personnel from the leaked contaminated area should be quickly evacuated to a safe area and isolated, strictly restricting access. Emergency personnel must wear self-contained positive pressure breathing apparatus and anti-toxic clothing. Do not let leaks come into contact with combustible substances (such as wood, paper, oil, etc.), cut off the source of leakage as much as possible, and prevent it from flowing into restricted spaces such as sewers and flood drains. Small leakage: mix with sand, dry lime or soda ash. It can also be rinsed with a large amount of water, diluted with washing water and placed in the wastewater system. Large leaks: build a dike or dig a pit for containment. Cover with foam to reduce vapor hazards. Transfer to a tanker or special collector by pump, recycle or transport to a waste treatment site for disposal.
All operations involving 6-chlorimidazolo [1,2-a] pyridine-3-formaldehyde should be handled with caution and strict compliance with safety procedures to ensure the safety of personnel and the environment is not damaged.