Imidazo 1 2 A Pyridine 2 Carboxylic Acid 7 Methyl
pyridine pyrrole pyrazine piperidine piperazine

imidazo[1,2-a]pyridine-2-carboxylic acid, 7-methyl-

    Specifications

    HS Code

    836133

    Name imidazo[1,2-a]pyridine-2-carboxylic acid, 7-methyl-
    Chemical Formula C9H8N2O2
    Molar Mass 176.17 g/mol
    Appearance Solid (usually)
    Physical State At Room Temp Solid
    Melting Point N/A (specific value may vary by source)
    Boiling Point N/A (specific value may vary by source)
    Solubility In Water Low (expected, based on structure)
    Solubility In Organic Solvents Soluble in some organic solvents like DMSO, methanol (general prediction)
    Pka N/A (specific value may vary by source)
    Logp N/A (specific value may vary by source)
    Density N/A (specific value may vary by source)

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    General Information
    Where to Buy imidazo[1,2-a]pyridine-2-carboxylic acid, 7-methyl- in China?
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    Frequently Asked Questions

    As a leading imidazo[1,2-a]pyridine-2-carboxylic acid, 7-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 is the chemical property of the product imidazo [1,2-a] pyridine-2-carboxylic acid, 7-methyl-
    This is a compound of 7-methyl-imidazolo [1,2-a] pyridine-2-carboxylic acid. Its physical properties are either solid at room temperature or white to pale yellow crystalline powder, which is caused by the arrangement and interaction of atoms in the molecular structure. Its solubility may have a certain solubility in organic solvents such as dichloromethane and ethanol. Due to the principle of similar miscibility, the partial structure of the compound is similar to that of organic solvents. However, its solubility in water may be limited, because its molecules are not highly hydrophilic.
    Regarding chemical properties, this compound contains carboxyl groups and is acidic. It can neutralize with bases to form corresponding carboxylate and water. The carboxyl group can also participate in the esterification reaction, and form ester compounds with alcohols under acid catalysis. The structural part of imidazolopyridine, due to its nitrogen heterocycle, has certain basic and nucleophilic properties, which can participate in nucleophilic substitution reactions, and the lone pair of nitrogen atoms can attack electrophilic reagents. It may also participate in cyclization reactions to further construct complex cyclic compounds, which are widely used in the field of organic synthesis. In short, 7-methyl-imidazolo [1,2-a] pyridine-2-carboxylic acids have diverse chemical properties due to their unique structures, and are important raw materials in the fields of organic synthesis and drug development.
    What are the main uses of imidazo [1,2-a] pyridine-2-carboxylic acid, 7-methyl-
    Imidazolo [1,2-a] pyridine-2-carboxylic acid, 7-methyl-this substance has a wide range of uses and has its impact in many fields.
    In the process of pharmaceutical research and development, it is often a key intermediate. Gain has a unique chemical structure, which can be combined with specific targets in organisms, or can help create new drugs to treat various diseases. For example, in the exploration of anti-cancer drugs, researchers hope to develop drugs that can precisely act on cancer cells, inhibit their proliferation or induce apoptosis by chemically modifying them.
    In the field of materials science, it also shows extraordinary potential. It can participate in the synthesis of materials with specific functions, such as materials with unique optical and electrical properties. After ingenious design and reaction, the material has specific response characteristics, which are applied to sensors, optoelectronic devices, etc., providing new paths for material performance improvement and functional expansion.
    In the field of organic synthetic chemistry, it is an important building block. Chemists can use various reactions to build complex organic molecular structures on the basis of them, expand the variety of organic compounds, and inject vitality into the research and development of new organic materials and the progress of organic synthesis methodologies.
    Because of its special structure, it has also emerged in the field of catalysis. It can also act as a ligand to coordinate with metal ions to form a highly efficient catalyst, promoting the smooth progress of specific chemical reactions, improving reaction efficiency and selectivity, and providing a more green and efficient way for chemical production.
    What is the preparation method of imidazo [1,2-a] pyridine-2-carboxylic acid, 7-methyl-
    To prepare 7-methyl-imidazolo [1,2-a] pyridine-2-carboxylic acid, the following method can be followed.
    First take the appropriate pyridine derivative, which is the starting material of the reaction. In a suitable reaction vessel, add the pyridine derivative and an appropriate amount of reaction solvent, such as an organic solvent, to disperse it uniformly.
    Then, introduce a specific reagent, which needs to be able to react with the pyridine derivative to construct the imidazolo structure. During the reaction process, the reaction temperature, time and other conditions need to be carefully adjusted. Too high or too low temperature may affect the process of the reaction and the purity of the product. It can be slowly warmed to a specific temperature range and maintained for a period of time to allow the reaction to proceed fully.
    After the imidazole structure is constructed, the methylation step is carried out. Select the appropriate methylation reagent and add it carefully to the reaction system. This step also needs to pay attention to the control of reaction conditions, such as pH. A suitable pH environment helps to introduce methyl into the target position precisely to obtain the product of 7-methyl.
    After the methylation reaction is completed, the product needs to be separated and purified. Classical methods such as column chromatography and recrystallization can be used. Column chromatography can achieve the separation of the product and the impurity according to the difference in the distribution coefficient between the stationary phase and the mobile phase. Recrystallization is achieved by controlling the temperature and solvent to precipitate the product in a pure crystal state, thereby improving the purity of the product, and finally obtaining 7-methyl-imidazolo [1,2-a] pyridine-2-carboxylic acid.
    What is the market price range for imidazo [1,2-a] pyridine-2-carboxylic acid, 7-methyl-
    It is difficult to determine the market price of fuimidazolo [1,2-a] pyridine-2-carboxylic acid, 7-methyl. The price of the market is often changed due to various factors and cannot be generalized.
    If you study its price, the first thing to look at is its quality. The quality is high, the price is high; the quality is low, the price must be low. And the method of its production and the place of its source are also related to the price. The variety of the system, the scarcity of the source, the price is high; otherwise, the price is flat.
    In addition, the supply and demand of the market are also the main reasons for the price. If more is needed and less is supplied, the price will rise; if the supply exceeds the demand, the price will fall.
    Looking at "Tiangong Kaiwu", although the price of this product is not bluntly stated, it is reasonable. The book says that all kinds of works are made, the quality of the materials is good, and the difficulty of making is easy, all of which involve price. This imidazolo [1,2-a] pyridine-2-carboxylic acid, 7-methyl is also the same.
    Roughly speaking, its price is uncertain, or varies according to time, place, quality, supply and demand. Or a few tens of dollars for one tael, or a few gold taels, are unknown. The market person should carefully observe the current situation to get the actual price.
    What are the safety precautions for imidazo [1,2-a] pyridine-2-carboxylic acid, 7-methyl-
    "Tiangong Kaiwu" is written in ancient classical Chinese, which may be difficult to accurately fit the content of modern chemistry. Today, it answers in a style similar to ancient Chinese, and tries its best to meet the needs.
    "imidazo [1,2-a] pyridine-2-carboxylic acid, 7-methyl -" that is, 7-methyl-imidazo [1,2-a] pyridine-2-carboxylic acid. This substance is related to safety and needs to be paid attention to many matters.
    First, this substance is chemically active. When storing, it should be placed in a cool, dry and well-ventilated place. Do not co-store with strong oxidants, strong acids, strong alkalis, etc., to prevent violent chemical reactions from occurring, resulting in the risk of fire and explosion. If the ancients stored medicine, they must be divided into their own characteristics to avoid their offenses.
    Second, when operating, be properly protected. Wear protective clothing, protective gloves and goggles. If you accidentally touch their skin, you should immediately rinse with a lot of water, just like the ancients when they were injured by poisons, and quickly ask for water to wash them. If it enters the eyes, it is even more urgent to rinse with flowing water or normal saline, and seek medical attention quickly without a slight delay.
    Third, the use of this object should be carried out in a fume hood to prevent harmful gases from escaping and endangering the human body. If indoors, it is necessary to ensure smooth air circulation, and the homes of the Jews should also be heavily ventilated.
    Fourth, the disposal of waste must be in compliance. Do not dump at will to prevent pollution to the environment. It needs to be properly disposed of in accordance with relevant laws and regulations. Just as the ancients knew that waste should not be discarded indiscriminately to ensure the purity of the water and soil in the mountains.
    In short, the operation, storage, and disposal of 7-methyl-imidazolo [1,2-a] pyridine-2-carboxylic acids should be done with caution and strict procedures should be followed to ensure personal and environmental safety.