Imidazo 1 2 A Pyridine 2 Chloromethyl 6 Methyl
pyridine pyrrole pyrazine piperidine piperazine

imidazo[1,2-a]pyridine, 2-(chloromethyl)-6-methyl-

    Specifications

    HS Code

    558683

    Chemical Formula C10H11ClN2
    Molecular Weight 194.66
    Appearance Solid (usually)
    Physical State At Room Temp Solid
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform, etc.

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    General Information
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    Frequently Asked Questions

    As a leading imidazo[1,2-a]pyridine, 2-(chloromethyl)-6-methyl- 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 physical properties of imidazo [1,2-a] pyridine, 2- (chloromethyl) -6-methyl-
    Imidazo [1,2 - a] pyridine, 2- (chloromethyl) -6-methyl - This compound is an organic compound, and its physical properties are quite critical. Looking at its properties, it is mostly solid or crystalline under normal conditions, and the quality is relatively stable.
    When it comes to the melting point, after many experiments, it is found that within a certain temperature range, this temperature is of great significance to its physical state transformation, which is related to its existence in different environments. In terms of boiling point, it is also in a specific range. When this temperature is reached, the compound will change from liquid to gaseous state, which is very important in chemical operations such as separation and purification.
    In terms of solubility, in organic solvents, such as common ethanol, ether, etc., there is a certain solubility, but the degree of solubility in water is relatively limited. This property is derived from its molecular structural characteristics, which cause weak interaction with water molecules and more affinity with organic solvent molecules.
    In terms of density, after accurate measurement, there is a specific value. This value reflects its mass per unit volume and has a profound impact on its distribution in various mixed systems and related applications.
    In addition, its appearance may have a specific color, mostly colorless to yellowish. This appearance characteristic can be used as an important basis for actual identification and quality control.
    It can be seen from the above that the many physical properties of imidazo [1,2 - a] pyridine, 2- (chloromethyl) -6-methyl- play a key role in guiding its application in many fields such as chemical industry and scientific research.
    What are the chemical properties of imidazo [1,2-a] pyridine, 2- (chloromethyl) -6-methyl-
    Alas! There are chemical things today, called imidazo [1,2 - a] pyridine, 2- (chloromethyl) -6-methyl-, which is a genus of organic compounds. Their properties are unique and have a variety of chemical characteristics.
    First of all, its physical properties, under room temperature, or in a solid state, or in a crystalline state, its color or white or nearly colorless, texture or powder. Its melting point is determined by the intermolecular force and structure. Intermolecular hydrogen bonds, van der Waals forces, etc., cause its melting point to be quite high. To make it melt, it needs to be at a suitable temperature.
    As for chemical activity, chloromethyl is very active in this compound. The chlorine atom is highly electronegative, and chloromethyl is electrophilic, which is easy to react with electron-rich groups or molecules. In case of nucleophilic reagents, the chlorine atom of chloromethyl is easily replaced by nucleophilic reagents, forming new chemical bonds and causing changes in molecular structure.
    Furthermore, the conjugate system of the pyridine ring and the imidazole ring gives the molecule a certain stability, but also gives it a special electron cloud distribution. Although the methyl group on the ring is small, it affects the electron cloud density and spatial resistance of the molecule. The property of the methyl supply makes the electron cloud density on the ring increase, which may affect the reaction check point and activity during the electrophilic substitution reaction. < Br >
    In addition, due to its nitrogen-containing heterocycle, it can complex with protons or metal ions. In acidic environments, nitrogen atoms can be protonated, changing the charge distribution and solubility of molecules. When metal ions exist, they may coordinate with metal ions with lone pairs of electrons of nitrogen atoms to form stable complexes, which have potential applications in catalysis, materials science and other fields.
    In summary, this imidazo [1,2-a] pyridine, 2- (chloromethyl) -6-methyl-compound, with its unique structure, exhibits diverse chemical properties, and is of great significance for chemical research and industrial applications.
    What is the main use of imidazo [1,2-a] pyridine, 2- (chloromethyl) -6-methyl-
    Imidazolo [1,2-a] pyridine-2- (chloromethyl) -6-methyl is a widely used substance. In the field of medicinal chemistry, it is often a key intermediate for the synthesis of specific new drugs. Due to its unique chemical structure, it can be precisely combined with specific targets in organisms. Through modification and modification, it may be possible to develop innovative drugs for specific diseases, such as tumors and nervous system diseases.
    In the field of materials science, it also has outstanding performance. Or it can be specially treated to give novel optical and electrical properties to materials, which can be used to make high-performance optoelectronic materials, such as organic Light Emitting Diodes, sensors and other components, so that materials have better performance and application value.
    In the field of pesticide research and development, it also plays an important role. It can be used as an active ingredient. After rational design and preparation, a new type of pesticide with high efficiency, low toxicity and environmental friendliness can be developed. It has significant control effect on crop pests, helps agricultural yield increase, and ensures the quality and safety of agricultural products. In short, imidazolo [1,2-a] pyridine-2- (chloromethyl) -6-methyl has important applications in many fields, promoting technological innovation and development in various fields.
    What is the synthesis method of imidazo [1,2-a] pyridine, 2- (chloromethyl) -6-methyl-
    The method for synthesizing 2- (chloromethyl) -6-methylimidazolo [1,2-a] pyridine can follow the following steps.
    First take an appropriate amount of 6-methylpyridine-2-amine, place it in a clean reactor, dissolve it with an appropriate amount of organic solvent such as dichloromethane, stir well to form a homogeneous solution.
    Take chloroacetaldehyde for the second time, slowly add it dropwise to the above solution, while maintaining a low temperature environment, about 0 to 5 degrees Celsius. Add it dropwise, raise it to room temperature, and continue to stir for a few times when the reaction is completed. In this process, 6-methylpyridine-2-amine interacts with chloroacetaldehyde to gradually form the precursor of the target product.
    After the reaction is completed, the reaction solution is poured into the separation funnel, washed with an appropriate amount of saturated salt water, and the organic phase is separated. Then the organic phase is dried with anhydrous sodium sulfate, the desiccant is filtered off, and the desiccant is distilled under reduced pressure to remove the organic solvent to obtain the crude product.
    After the crude product is separated by column chromatography, and eluted with a suitable eluent, such as a mixture of petroleum ether and ethyl acetate in a certain proportion. The fractions containing the target product are collected and concentrated by rotary distillation to obtain pure 2- (chloromethyl) -6-methylimidazolo [1,2-a] pyridine. During the operation, attention should be paid to the control of temperature, dripping speed and reaction time to ensure the smooth progress of the synthesis reaction and obtain a product with high yield and purity.
    What are the precautions for imidazo [1,2-a] pyridine, 2- (chloromethyl) -6-methyl-in storage and transportation?
    2 - (chloromethyl) -6 -methylimidazolo [1,2 - a] pyridine in storage and transportation, need to pay attention to many key matters. This substance has a certain chemical activity, when exposed to water or moisture, or chemical reaction, forming corrosive or harmful products. Therefore, it should be placed in a dry, well-ventilated place, away from water sources and moisture, and the packaging used must be waterproof.
    It is flammable, and there is a risk of combustion and explosion in high temperature, open flame or strong oxidant environment. When storing, it should be isolated from oxidants, fire sources, etc. The warehouse needs to have fire and explosion-proof facilities, and fireworks are strictly prohibited. During transportation, high temperature environment and impact should also be avoided to ensure the fire safety of transportation vehicles.
    Due to its chemical structure characteristics, or harmful to human health. When operating and contacting, be sure to take protective measures, such as wearing protective gloves, goggles and gas masks, to prevent inhalation, contact with skin or ingestion. In the event of a leak, do not touch it directly. People should be evacuated quickly, the contaminated area should be isolated, and corresponding treatment measures should be taken according to the amount of leakage and the specific situation, such as absorption with inert materials such as sand and vermiculite, or neutralization with suitable chemical reagents.
    Furthermore, warehousing and transportation must follow relevant regulations and standards to ensure their safety. Management personnel and transportation personnel should be professionally trained and familiar with the characteristics of this substance and emergency treatment methods in order to effectively prevent accidents and ensure the safety of personnel and the environment.