2 Chloro N 2 Chloro 4 Methyl 3 Pyridyl 3 Pyridine Carboxamide
pyridine pyrrole pyrazine piperidine piperazine

2-chloro-N-(2-chloro-4-methyl-3-pyridyl)-3-pyridine carboxamide

    Specifications

    HS Code

    368662

    Chemical Formula C12H9Cl2N3O
    Molecular Weight 282.125 g/mol
    Appearance Solid (usually white to off - white powder)
    Solubility In Water Low solubility
    Solubility In Organic Solvents Soluble in some organic solvents like dichloromethane, acetone
    Melting Point 178 - 182 °C
    Boiling Point Decomposes before boiling
    Vapor Pressure Very low
    Logp 3.1 - 3.5 (estimation of lipophilicity)

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    General Information
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    Frequently Asked Questions

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    What is the chemical structure of 2-chloro-N- (2-chloro-4-methyl-3-pyridyl) -3-pyridine carboxamide
    This is an investigation into the chemical structure of 2-chloro-N- (2-chloro-4-methyl-3-pyridyl) - 3-pyridyl formamide. To clarify the details, it is necessary to analyze it from the principles of organic chemistry.
    Pyridine is a hexagonal nitrogen-containing heterocyclic compound with aromatic properties. In this compound, there are dipyridyl groups, one of which is the pyridine ring of 3-pyridineformamide, and the formamide group is attached to the carbon of the third position of the pyridine ring; the other is the 2-chloro-4-methyl-3-pyridyl group. The second position of the pyridine ring has a chlorine atom substitution, and the fourth position has a methyl substitution, and the nitrogen atom is connected to the pyridine ring of 3-pyridineformamide. Furthermore, the second position of the pyridine ring of 3-pyridineformamide also has a chlorine atom substitution. In this way, the chemical structure of this compound is based on a pyridine ring, modified by chlorine atoms, methyl groups, and formamide groups, and each atom is connected by a specific chemical bond, forming the unique structure of this organic compound.
    What are the main uses of 2-chloro-N- (2-chloro-4-methyl-3-pyridyl) -3-pyridine carboxamide
    2-Chloro-N- (2-chloro-4-methyl-3-pyridyl) -3-pyridyl formamide, which is widely used.
    In the field of agriculture, it is often used as an insecticide. With its unique chemical structure, it can precisely act on the nervous system of pests, interfere with nerve conduction, cause paralysis and death of pests, and effectively prevent and control many pests, such as aphids and planthoppers, etc., which greatly contribute to the harvest of crops and maintain the prosperity of agriculture.
    In the field of pharmaceutical research, it is also of great significance. Due to its special chemical activity, it can become a key intermediate for the development of new drugs. By modifying and modifying its structure, researchers can explore compounds with specific pharmacological activities, find new opportunities for disease treatment, or play an important role in the development of anti-cancer, anti-infection and other drugs, which is expected to bring good news to patients.
    In the field of materials science, this compound can participate in the synthesis of functional materials. Its chemical properties may endow materials with special properties, such as improving material stability and optical properties, and then expand the application range of materials. It has emerged in the fields of electronic devices, optical materials, etc., promoting the progress of materials science. Therefore, 2-chloro-N - (2-chloro-4-methyl-3-pyridyl) - 3 -pyridyl formamide has important uses in many fields and has a profound impact on the development of various industries.
    What are the physical properties of 2-chloro-N- (2-chloro-4-methyl-3-pyridyl) -3-pyridine carboxamide
    2-Chloro-N- (2-chloro-4-methyl-3-pyridyl) - 3-pyridyl formamide, this is an organic compound. Its physical properties are quite important, and it is related to its application in various fields.
    First appearance, under normal temperature and pressure, it is often in the shape of white to off-white crystalline powder, with fine texture and pure appearance. This appearance characteristic makes it easy to distinguish and deal with in preparation and other aspects.
    The melting point is about [X] ° C, and the melting point is relatively high, indicating that the intermolecular force is strong and the structure is relatively stable. During the heating process, a specific temperature is required to melt, which is crucial in the separation, purification and stability studies of substances.
    Another is solubility, which shows good solubility in organic solvents such as dichloromethane, N, N-dimethylformamide (DMF) and can be uniformly dispersed. However, the solubility in water is poor, because the molecular structure of the compound contains many hydrophobic groups, it interacts weakly with water molecules. Such solubility characteristics determine its reactivity and application scenarios in different solvent systems. In organic synthesis, suitable solvents can be selected to promote the reaction. < Br >
    In terms of density, it is about [X] g/cm ³. This value reflects the mass per unit volume. When mixed with other substances, it affects the density of the system, which in turn affects the physical state and separation operation of the mixed system.
    In addition, the compound has certain stability and can maintain its chemical structure and properties for a long time under conventional storage conditions. However, when exposed to specific chemicals such as strong oxidizing agents, strong acids or strong bases, chemical reactions may occur, causing changes in its structure and properties.
    In summary, the physical properties of 2-chloro-N- (2-chloro-4-methyl-3-pyridyl) -3-pyridyl formamide, from appearance, melting point, solubility, density to stability, etc., have their own characteristics and are related to each other, which has a profound impact on its application and research in many fields such as chemical industry and medicine.
    What is the synthesis method of 2-chloro-N- (2-chloro-4-methyl-3-pyridyl) -3-pyridine carboxamide
    To prepare 2-chloro-N- (2-chloro-4-methyl-3-pyridyl) - 3-pyridyl formamide, the method is as follows:
    First, appropriate starting materials are taken, and pyridine compounds are used as groups. Pyridine derivatives containing suitable substituents can be selected, such as 2-chloro-4-methyl-3-aminopyridine and 2-chloro-3-pyridyl chloride. Of these two, 2-chloro-4-methyl-3-aminopyridine needs to be finely prepared, or obtained from the corresponding pyridine compound through a series of reactions such as halogenation and methylation. 2-chloro-3-pyridyl chloride can be prepared by the reaction of 2-chloro-3-pyridyl carboxylic acid with chlorinated reagents such as dichlorosulfoxide under suitable conditions.
    Then, 2-chloro-4-methyl-3-aminopyridine is amidated with 2-chloro-3-pyridyl chloride. This reaction should be carried out in an inert organic solvent, such as dichloromethane, N, N-dimethylformamide, etc. And an appropriate amount of alkali, such as triethylamine, pyridine, etc., is added to neutralize the hydrogen chloride generated by the reaction and promote the reaction to proceed in a positive direction. The reaction temperature can be controlled in the range of low temperature to room temperature, depending on the specific situation. The reaction time needs to be monitored and determined. The reaction process is often tracked by thin-layer chromatography.
    After the reaction is completed, the mixture is post-treated. First, the organic phase is extracted with an appropriate solvent, and then the organic phase is separated, and then washed and dried. A desiccant such as anhydrous sodium sulfate can be used for drying. Subsequently, the solvent is The crude product is further purified by column chromatography or recrystallization to obtain high purity 2-chloro-N - (2-chloro-4-methyl-3-pyridyl) - 3-pyridyl formamide. This is the approximate synthetic route, and the actual operation needs to be carefully adjusted according to the specific experimental conditions and requirements to achieve satisfactory results.
    What are the precautions for using 2-chloro-N- (2-chloro-4-methyl-3-pyridyl) -3-pyridine carboxamide?
    2-Chloro-N - (2-chloro-4-methyl-3-pyridyl) - 3-pyridyl formamide. When using this product, many things need to be paid attention to.
    Bear the brunt of safety, and do not ignore it. This compound may be toxic, contact with the human body, or cause damage. When operating, be sure to wear appropriate protective equipment, such as gloves, goggles, protective clothing, etc., to ensure your own safety. And it is necessary to work in a well-ventilated place to prevent the accumulation of harmful gases and endanger health.
    Furthermore, accurate weighing and use are related to experimental accuracy. Due to the special properties of the substance, the dosage is slightly poor, or the experimental results are deviated. When taking it, when using a precise measuring tool, take it accurately according to the experimental requirements, and do not be careless.
    Storage is also exquisite. It should be placed in a dry, cool and ventilated place, away from fire and heat sources. Because of its active chemical properties, improper storage or deterioration will affect the use effect.
    During use, the chemical reaction conditions need to be strictly controlled. Temperature, reaction time, proportion of reactants, etc., all have a significant impact on the reaction process and product generation. If there is a slight carelessness, the reaction may fail, or other by-products may be generated.
    It should be noted that after the experiment is completed, the remaining materials cannot be discarded at will. It should be properly handled in accordance with relevant regulations to avoid polluting the environment.
    In short, the use of 2-chloro-N - (2-chloro-4-methyl-3-pyridyl) -3-pyridyl formamide requires caution and careful attention in all aspects to ensure the smooth operation of the experiment and the safety of personnel and the environment.