Imidazo 1 2 A Pyridine 2 Carboxylic Acid Ethyl Ester
pyridine pyrrole pyrazine piperidine piperazine

Imidazo[1,2-a]pyridine-2-carboxylic acid ethyl ester

    Specifications

    HS Code

    949907

    Chemical Formula C10H10N2O2
    Molecular Weight 190.2 g/mol
    Appearance Solid (usually white or off - white powder)
    Melting Point Specific value depends on purity, typically in a certain range
    Boiling Point Specific value under certain pressure conditions
    Solubility In Water Low solubility
    Solubility In Organic Solvents Soluble in some organic solvents like ethanol, dichloromethane
    Pka Value Relevant to its acidic - basic properties in solution
    Density A specific density value (g/cm³)
    Flash Point A certain flash point value (°C)

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    General Information
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    Frequently Asked Questions

    As a leading Imidazo[1,2-a]pyridine-2-carboxylic acid ethyl ester 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 chemical properties of imidazolo [1,2-a] pyridine-2-carboxylate ethyl ester
    What are the chemical properties of saltpeter [1,2-a] pyridine to its -2-ethyl carboxylate? This question is related to the transformation characteristics of chemical substances and is of great value for investigation. In ancient Chinese, try to solve it for you.
    For saltpeter and [1,2-a] pyridine, it wants to be converted to -2-ethyl carboxylate, which involves many chemical changes. This process often depends on the mechanism of chemical reaction and requires suitable conditions to be achieved.
    First of all, the activity of the reaction is discussed. Saltpeter and [1,2-a] pyridine have a specific structure and electron cloud distribution, resulting in its unique activity in the reaction. In case of specific reagents, such as with reactants containing ethyl ester groups, under appropriate catalyst, temperature, pressure and other conditions, bond cracking and recombination can be initiated.
    Furthermore, the selectivity of the reaction is also key. Chemical changes are complex, and if you want to obtain ethyl 2-carboxylate accurately, you need to choose a specific reaction path and conditions to ensure that the reaction proceeds in the desired direction and avoid excessive by-products.
    In addition, the rate of reaction cannot be ignored. Factors such as temperature, type and dosage of catalysts all have a significant impact on it. When the temperature increases, the molecular thermal motion intensifies, and the reaction rate may be accelerated; and a suitable catalyst can reduce the activation energy of the reaction, making the reaction more prone to occur, and can also regulate the rate.
    In summary, the chemical properties of the conversion of saltpeter to [1,2-a] pyridine to -2-carboxylate ethyl ester are reflected in many aspects such as activity, selectivity and reaction rate, and various factors need to be considered in detail to achieve the ideal conversion effect.
    What are the common synthesis methods of imidazolo [1,2-a] pyridine-2-carboxylate ethyl ester
    There are several common methods for the synthesis of polynitro [1,2-a] to ethyl carboxylate as follows.
    One is nitrification. First, the corresponding aromatic hydrocarbon is nitrified and nitro groups are introduced. This process requires precise regulation of reaction conditions, such as temperature and the ratio of nitric acid to sulfuric acid, to prevent excessive nitrification. Subsequently, under suitable reduction conditions, such as metal and acid or catalytic hydrogenation, the nitro group is converted to amino group. Next, through the diazotization reaction, the amino group is converted into diazonium salt, and then the carboxyl group is introduced through the treatment of specific reagents. Finally, the esterification reaction with ethanol is carried out to obtain ethyl nitrosulfono [1,2-a] -2-carboxylate. Although this approach is complex, the raw materials are easy to obtain, and it has certain applications in industrial production.
    The second is halogenated carboxylation. Using aromatic derivatives containing halogen atoms as starting materials, under the action of metal catalysts, react with carbon monoxide and ethanol to directly realize the carboxylation and esterification of halogen atoms, and generate the target product in one step. This method has high atomic economy and relatively simple reaction steps, but it requires strict catalyst requirements and harsh reaction conditions, which need to be carried out under high temperature and high pressure.
    The third is the cyclization method. Select suitable sulfur-containing, nitrogen-containing and carboxyl-containing linear compounds, and under the action of acidic or basic catalysts, an intramolecular cyclization reaction occurs to construct the parent nuclear structure of nitrosulfono [1,2-a], and then appropriately modified to achieve esterification to obtain this product. The key to this method is the design and synthesis of linear raw materials, which can effectively avoid cumbersome operations and side reactions caused by multi-step reactions.
    All kinds of synthesis methods have their own advantages and disadvantages. It is necessary to consider many factors such as raw material cost, reaction conditions, yield and purity according to actual needs, and choose the appropriate one.
    In which fields is imidazolo [1,2-a] pyridine-2-carboxylate ethyl ester used?
    Sunburn [1,2-a] has a wonderful effect in many fields, and it is a magical thing.
    In many fields, this product can be used as an active ingredient, and it is the best of many materials. Because of its special properties, it has certain biological activity, or it can help people with certain physiological systems and help heal diseases. For example, in the treatment of some chronic diseases, it can solve diseases and improve the effect of the disease, just like a good product in the hands of the patient, and the patient removes the pain.
    In the field of chemical synthesis, sunburn [1,2-a] also plays an important role in the treatment of 2-carboxyl ethyl esters. It can be used as a medium for the synthesis of more complex chemical compounds. Chemists use its unique chemical properties to combine with other compounds in an ingenious way to create new materials with special properties, such as materials with special optical and chemical properties, such as skilled craftsmen using fine parts to create magical objects.
    Furthermore, in the field of biological research, this compound can be used as a tool to explore some biochemical reactions of biological agents. Scientists use it to investigate its reaction process in biological agents, the interaction of biological macromolecules, etc., to uncover the mystery of life, just like explorers exploring the unknown world, using it to play a big role in the truth.
    In addition, the reaction of [1,2-a] to its-2-carboxyl ethyl ester is like a shining star in many fields such as chemistry, chemical synthesis, and biological research.
    What is the market prospect of imidazolo [1,2-a] pyridine-2-carboxylate ethyl ester?
    #What is the market prospect of nitrate [1,2-a] pyridine to its-2-carboxyethyl ester?
    In today's world, there is a lot of business. In order to explore the market prospect of nitrate [1,2-a] pyridine to its-2-carboxyethyl ester, it is necessary to increase the degree of general sentiment.
    Since the cost of self-production is high, this kind of product has an important value in many rows. In the field of production, it may be in the process of production. Today's demand is increasing, and new research and development are not released. The demand for this refined product is also high. If we can efficiently synthesize its 2-carboxylethyl ester with nitro [1,2-a] pyridyl group, it will be able to meet the needs of the industry and occupy a place in this booming market.
    Furthermore, the field of transformation cannot be ignored. The main purpose of this system is to determine the demand. Some new types of research and development, or the development of this transformation. The development of high-quality, high-efficiency, and the derivation of nitro [1,2-a] pyridyl to its 2-carboxylethyl ester, if it can conform to the concept of protection and high-efficiency, it will definitely be able to achieve the world in the market.
    However, there are many challenges in the market. First, it is important that the synthesis process is easy to achieve. If the synthesis process is not easy and the cost is high, it must be controlled and promoted in the market. It is necessary to maintain research and development, reduce chemical production, and reduce costs and increase efficiency. Second, the cost of the same product is also a difficult matter. There may already be substitutes for similar functions in the market. How to develop them in terms of product quality, cost, service quality, etc., needs to be carefully considered.
    In this regard, the market prospect of nitro [1,2-a] pyridine to its 2-carboxylethyl ester is like a jade to be cut, which cannot be selected and stored in case of problems. Good insight into the market, fine research in the industry, and those who are good, can grasp the first, in this market. Prosperity.
    What are the precautions in the preparation of imidazolo [1,2-a] pyridine-2-carboxylate ethyl ester
    In the preparation process of making Li wine and\ [1,2-a\] to its-2-ethyl acetate, you need to pay attention to all things and listen to me carefully.
    At the beginning, the ratio of materials must be accurate. When brewing Li wine, the ratio of rice, water and koji has a great impact. If there is more rice, the wine will be strong, but it is easy to cause poor fermentation; if there is more water, the wine will be weak and the flavor will be poor; if the amount of koji is improper, the fermentation will be slow and abnormal. When preparing ethyl acetate, the ratio of ethanol to acetic acid is also critical. The ratio is unbalanced, the yield of the product will decrease, and impurities will increase.
    Temperature control is the most important thing. Liquor fermentation, temperature is too high, microbial metabolism is too fast, easy to produce bacteria, bad wine quality; temperature is too low, fermentation is slow, time-consuming. For the preparation of ethyl acetate, the reaction temperature needs to conform to the active temperature range of the catalyst, otherwise the reaction rate and balance will be disturbed, affecting the yield.
    The reaction time cannot be ignored. Liquor fermentation has not reached enough time, the taste of the wine is weak, and the aroma is insufficient; if the fermentation is too long, the wine quality will deteriorate. Ethyl acetate preparation, the reaction time is short, the raw materials are not fully reacted, and the yield is low; if the time is long, the side reactions will increase, and the purity of the product will decrease.
    Furthermore, cleaning utensils is about success or failure. The utensils used to make Li wine and ethyl acetate are unclean, bacteria are mixed in, Li wine deteriorates, and the reaction of ethyl acetate is disturbed, resulting in impure products.
    The operation process needs to be rigorous. When making Li wine, the stirring frequency and intensity affect the uniformity of fermentation; when preparing ethyl acetate, improper feeding sequence and mixing method can cause abnormal reactions.
    These precautions are related to the quality of Li wine and ethyl acetate. They must not be taken lightly. They must be carefully operated to achieve a good product.