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

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

    Specifications

    HS Code

    473968

    Chemical Formula C8H6Cl2N2
    Molecular Weight 199.05
    Appearance Solid (predicted)
    Boiling Point Predicted to be around 325.9°C at 760 mmHg
    Density Predicted to be around 1.45 g/cm³
    Solubility In Water Low solubility (organic compound, non - polar nature)
    Logp Estimated to be around 2.3 (lipophilicity measure)
    Vapor Pressure Very low at room temperature
    Pka No common data found (but imidazo[1,2 - a]pyridine ring may have basic properties)

    As an accredited 6-Chloro-2-(chloromethyl)imidazo[1,2-a]pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing
    Storage
    Shipping
    Free Quote

    Competitive 6-Chloro-2-(chloromethyl)imidazo[1,2-a]pyridine prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615365036030 or mail to info@alchemist-chem.com.

    We will respond to you as soon as possible.

    Tel: +8615365036030

    Email: info@alchemist-chem.com

    General Information
    Where to Buy 6-Chloro-2-(chloromethyl)imidazo[1,2-a]pyridine in China?
    As a trusted 6-Chloro-2-(chloromethyl)imidazo[1,2-a]pyridine manufacturer, we deliver: Factory-Direct Value: Competitive pricing with no middleman markups, tailored for bulk orders and project-scale requirements. Technical Excellence: Precision-engineered solutions backed by R&D expertise, from formulation to end-to-end delivery. Whether you need industrial-grade quantities or specialized customizations, our team ensures reliability at every stage—from initial specification to post-delivery support.
    Frequently Asked Questions

    As a leading 6-Chloro-2-(chloromethyl)imidazo[1,2-a]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 6-Chloro-2- (chloromethyl) imidazo [1,2-a] pyridine?
    6-Chloro-2- (chloromethyl) imidazolo [1,2-a] pyridine is widely used in the field of organic synthesis.
    First, it is often a key intermediate for the creation of new drugs. In the way of pharmaceutical research and development, it is often relied on such compounds to construct novel molecular structures to find potential drugs with unique biological activities. Given its structural characteristics, it can be modified by chemical reactions to bind to specific biological targets, thereby regulating physiological processes in organisms. For example, it participates in the inhibition of protein kinases related to specific diseases, paving a new way for the conquest of cancer, inflammation and other diseases.
    Second, it also has important functions in the field of pesticide creation. Using it as a starting material, it can be chemically converted to produce high-efficiency, low-toxicity and environmentally friendly pesticides. Its structure can give pesticides high selectivity to specific pests or pathogens, enhance the control effect, and reduce the adverse effects on non-target organisms, which is in line with the current needs of green agriculture development.
    Furthermore, it has made a name for itself in the field of materials science. It can be introduced into polymer materials through specific reactions to endow the materials with special properties. For example, organic materials with specific optical and electrical properties can be prepared and applied to electronic devices such as organic Light Emitting Diodes (OLEDs) and sensors to expand the functions and application scope of materials.
    This compound, with its unique structure, provides an important foundation for scientific research and industrial production in various fields such as medicine, pesticides, and materials, and contributes to technological innovation and development in various fields.
    What are the synthesis methods of 6-Chloro-2- (chloromethyl) imidazo [1,2-a] pyridine
    The synthesis method of 6-chloro-2 - (chloromethyl) imidazolo [1,2-a] pyridine is of great interest in the field of chemical synthesis. There are many synthetic paths, and the following are the main ones.
    First, the pyridine derivative can be used as the starting material. First, a suitable substituent is introduced into the specific position of the pyridine, and the imidazole ring is constructed through a series of reactions. For example, selecting a suitable pyridine derivative, reacting with a chloromethyl-containing reagent under suitable conditions, introducing the chloromethyl group into the designated position, and then forming an imidazolo [1,2-a] pyridine structure through cyclization. During this process, the reaction conditions, such as temperature, reaction time, and the proportion of reactants, need to be precisely controlled to ensure that the reaction proceeds in the desired direction and improve the yield of the target product.
    Second, using imidazole derivatives as the starting material is also a method. Imidazole derivatives are modified to gradually introduce the pyridine ring structure and the desired chlorine atom. Each part can be connected in sequence through specific organic reactions, such as nucleophilic substitution, condensation, etc., to synthesize the target compound. In the reaction process, each step of the reaction product needs to be carefully separated and purified to prevent the accumulation of impurities from affecting the quality of the final product.
    Third, with the help of the reaction strategy of transition metal catalysis. Transition metal catalysts often play a unique role in organic synthesis, which can promote the formation of carbon-carbon and carbon-heteroatomic bonds. Using suitable transition metal catalysts to catalyze the reaction between reactants, the reaction is guided to precisely generate 6-chloro-2 - (chloromethyl) imidazolo [1,2-a] pyridine. However, this method requires high requirements for the selection of catalysts and the optimization of the reaction system, and various parameters need to be carefully adjusted to achieve the best reaction effect.
    All these synthetic methods have their own advantages and disadvantages. In practice, it is necessary to comprehensively consider many factors such as the availability of raw materials, cost, difficulty in controlling reaction conditions, and the purity requirements of the target product, and then choose the most suitable synthetic path.
    What are the physicochemical properties of 6-Chloro-2- (chloromethyl) imidazo [1,2-a] pyridine
    6-Chloro-2- (chloromethyl) imidazolo [1,2-a] pyridine, this is an organic compound. Its physicochemical properties are quite critical and are widely used in chemical research and related fields.
    In terms of physical properties, the compound is often in a solid state at room temperature and pressure, but the specific appearance may vary depending on purity and crystallization conditions, or it is a white to light yellow crystalline powder. Determination of melting point is of great significance for identification and purity evaluation. After verifying the relevant data, its melting point is about [specific value] ° C. This characteristic can help to determine the purity of the substance by melting point measurement in experiments. If the melting point of the sample matches the standard value and the melting range is narrow, the purity is higher; on the contrary, if the melting range is wide, it may contain impurities.
    Furthermore, its solubility is also an important physical property. In common organic solvents, such as ethanol, dichloromethane, etc., it has a certain solubility. In ethanol, under certain temperature conditions, it can dissolve a certain proportion, which is convenient for use as a reaction solvent in organic synthesis or for separation and purification steps. In water, the solubility is relatively poor, which is related to the large proportion of hydrophobic groups in the molecular structure.
    In terms of chemical properties, the presence of chlorine atoms in the molecule of the compound endows it with active chemical activity. Chlorine atoms can participate in nucleophilic substitution reactions, for example, react with nucleophilic reagents such as sodium alcohols and amines, etc., which can modify the molecular structure and generate new derivatives. Among them, the chloromethyl moiety at the 2-position is particularly active and vulnerable to nucleophilic reagents, and substitution reactions occur to form carbon-heteroatom bonds. This reaction property is widely used in the construction of complex organic molecular structures. At the same time, the imidazolo [1,2-a] pyridine parent nucleus also has unique chemical properties, which can participate in some aromatic electrophilic substitution reactions. Under suitable conditions, other functional groups are introduced into the parent nucleus, thereby expanding the compound's application in medicinal chemistry, materials science and other fields.
    6-Chloro-2- (chloromethyl) imidazo [1,2-a] pyridine What are the precautions in storage and transportation
    6-Chloro-2- (chloromethyl) imidazolo [1,2-a] pyridine is an organic chemical. During storage and transportation, careful attention should be paid to many matters to ensure safety.
    First words storage, this chemical should be placed in a cool and dry place. Cover it or be sensitive to temperature and humidity. If it is in a high temperature and humid place, it may cause chemical reactions and cause changes in properties. For example, if the ambient humidity is high, water vapor or interaction with the substance will promote reactions such as hydrolysis, which will damage its quality. And it must be stored in a well-ventilated place to prevent the accumulation of volatile gases, causing excessive concentration and potential danger.
    Furthermore, the storage place should be kept away from fire and heat sources. This chemical may be flammable. In case of open flames and hot topics, it is easy to catch fire and burn, and even cause explosions, endangering the safety of the surrounding area. At the same time, it should also be stored separately from oxidants, acids, alkalis and other substances. Due to its active chemical properties, it can mix with the above substances, or trigger violent chemical reactions, generating harmful gases and causing safety accidents.
    As for transportation, it is necessary to ensure that the packaging is intact. If the packaging is damaged, the substance may leak, polluting the environment and posing a threat to the transportation personnel. During transportation, the speed of the vehicle should be stable, and sudden braking and bumps should be avoided to prevent damage to the packaging due to vibration. Transportation vehicles should also be equipped with corresponding fire protection equipment and leakage emergency treatment equipment. In case of emergencies, they can respond in time. And transportation personnel should be professionally trained, familiar with the characteristics of the chemical and emergency treatment methods, pay close attention to the status of the goods during transportation, and take immediate measures if there is any abnormality.
    What is the market situation for 6-Chloro-2- (chloromethyl) imidazo [1,2-a] pyridine?
    6-Chloro-2- (chloromethyl) imidazolo [1,2-a] pyridine, this product has a considerable trend in today's chemical market.
    From the demand side, it is widely used in the field of medicinal chemistry. It is often used as a key intermediate in the development of many new drugs. Taking a class of anti-infective drugs as an example, the structural properties of this compound can endow drug molecules with unique biological activities and help drugs act more precisely on pathogen targets, so the demand for it in the pharmaceutical industry continues to rise. Furthermore, in the field of pesticide chemistry, it has also emerged. Due to its certain insecticidal and bactericidal properties, it can be made into highly efficient and low-toxic pesticide products after rational design and transformation, which meets the current needs of green agriculture development, and the agricultural market also has considerable demand potential for it.
    When it comes to the supply level, with the growth of market demand, many chemical companies have paid attention to this. Many companies with advanced synthesis processes constantly optimize their production processes and strive to increase production capacity. However, the process of synthesizing this compound often involves complex reaction steps and harsh reaction conditions, which requires high production technology and equipment. Although some companies have the will to produce, it is difficult to achieve large-scale stable supply due to technical bottlenecks. Therefore, although the current market supply is growing, it has not yet fully met the demand.
    In terms of market competition, companies that have been involved in this field have gained a place in the high-end product market by virtue of their first-mover advantages and technological accumulation. New entrants need to work hard on technological innovation and cost control if they want to get a piece of the pie. Only by continuously developing more efficient and environmentally friendly synthetic routes and reducing production costs can they seek development in the highly competitive market.
    In summary, the 6-chloro-2- (chloromethyl) imidazolo [1,2-a] pyridine market has broad prospects, but they also face various challenges such as technology and competition. All parties still need to make unremitting efforts to promote the steady development of this market segment.