Imidazo 1 2 A Pyridine 6 Carboxylic Acid
pyridine pyrrole pyrazine piperidine piperazine

IMIDAZO[1,2-A]PYRIDINE-6-CARBOXYLIC ACID

    Specifications

    HS Code

    570271

    Chemical Formula C9H8N2O2
    Molar Mass 176.172 g/mol
    Appearance Solid (usually white or off - white)
    Melting Point Data may vary depending on purity
    Solubility In Water Low solubility
    Solubility In Organic Solvents Soluble in some polar organic solvents like DMSO
    Pka Value Related to its acidic nature, specific values depend on experimental conditions
    Boiling Point Data may vary depending on purity and pressure
    Density Value depends on physical state and conditions
    Stability Stable under normal conditions, but may react with strong oxidizing agents

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    General Information
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    Frequently Asked Questions

    As a leading IMIDAZO[1,2-A]PYRIDINE-6-CARBOXYLIC ACID 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 structure of IMIDAZO [1,2-A] PYRIDINE-6-CARBOXYLIC ACID?
    Imidazolo [1,2-A] pyridine-6-carboxylic acid (IMIDAZO [1,2-A] PYRIDINE-6-CARBOXYLIC ACID), an organic compound, belongs to nitrogen-containing heterocyclic carboxylic acids. Its structure is quite characteristic. It is formed by fusing the imidazole ring with the pyridine ring, and the carboxyl group is connected at the 6 position.
    The preview imidazole ring is composed of two nitrogen atoms and three carbon atoms to form a five-membered heterocyclic ring, which is aromatic. The solitary pair electrons of the nitrogen atom participate in the conjugation system to stabilize the ring. The pyridine ring is a six-membered heterocyclic ring containing one nitrogen atom, which is also aromatic. The two fused together to form a unique double-ring structure, which endows the compound with special physical and chemical properties.
    The 6-carboxyl group (-COOH) contains carbonyl (C = O) and hydroxyl (-OH). The electron cloud density distribution of carbon-oxygen double bonds in carbonyl groups is uneven, polar, and prone to nucleophilic addition and other reactions; hydroxyl hydrogen is acidic and can undergo acid-base reactions. Under specific conditions, it can esterify with alcohols to form ester compounds.
    The structure of imidazolo [1,2-A] pyridine-6-carboxylic acid has attracted much attention in the fields of medicine, pesticides, and materials science. In the field of medicine, due to its unique structure, it can interact with specific targets in organisms, or has potential biological activity, and can be used as a lead compound for drug development; in the field of pesticides, it can inhibit or kill specific pests and bacteria; in materials science, its structural properties may be used to design and synthesize materials with special properties, such as photoelectric materials.
    What are the main physical properties of IMIDAZO [1,2-A] PYRIDINE-6-CARBOXYLIC ACID
    Imidazolo [1,2-A] pyridine-6-carboxylic acid, this is an organic compound. It has many important physical properties.
    Looking at its appearance, under room temperature and pressure, it is mostly white to light yellow crystalline powder, like fine sand, fine and uniform. This state is easy to store and use, and in many chemical reactions, it can provide a large reaction contact area, which is conducive to the efficient progress of the reaction.
    When it comes to the melting point, it is about 180-185 ° C. The melting point is an inherent property of the substance, and this specific melting point range can be used to identify the purity of the compound. If the purity is high, the melting point is close to this range; if impurities are contained, the melting point tends to decrease and the melting range becomes wider. < Br >
    Its solubility is also a key property. In common organic solvents, such as dimethyl sulfoxide (DMSO), N, N-dimethylformamide (DMF), it has good solubility and can be quickly dispersed and dissolved to form a uniform solution. However, in water, the solubility is relatively small. This difference in solubility is of great significance in the separation, purification and preparation of compounds. According to the target requirements, a suitable solvent can be selected to achieve the best treatment effect.
    In addition, the compound has good stability. Under normal storage conditions, in a dry and cool environment, it can be stored for a long time without significant chemical changes. However, under extreme conditions such as strong acid, strong alkali or high temperature, strong oxidant, the structure may change and chemical reactions occur. This stability feature provides certain convenience and limitations for its storage and use in various application scenarios. It is necessary to reasonably control external conditions to ensure that its performance is not affected.
    IMIDAZO [1,2-A] In which areas PYRIDINE-6-CARBOXYLIC ACID is used
    Imidazolo [1,2-A] pyridine-6-carboxylic acid is useful in many fields. In the field of medicine, this compound has great potential. After long-term research, doctors and pharmacists have found that its structure is unique and can be combined with specific targets in the body by subtle methods. Or like ancient doctors who used herbal medicine to treat diseases, this compound can precisely regulate the physiological mechanism of the human body, and is like a key in the development of drugs to treat various diseases. Or used to develop drugs for neurological diseases to relieve pain, just like the ancients used good remedies to solve patients' diseases.
    In the field of materials science, it also has its own shadow. Just as ancient craftsmen used different materials to build delicate things, today's scientists use imidazolo [1,2-A] pyridine-6-carboxylic acids as the basis to develop new materials. It may endow the material with unique properties, such as enhancing the stability of the material, making it strong and durable in different environments, just like the good materials used to build strong palaces in ancient times.
    Furthermore, in the field of agriculture, there is also the possibility of application. Ancient farmers worked with experience, and now this compound can be used to develop new pesticides or plant growth regulators. It may be able to effectively resist pests and diseases and ensure the strong growth of crops, just like the ancient method of protecting seedlings and protecting harvests, contributing to the harvest of agriculture. In this way, imidazolo [1,2-A] pyridine-6-carboxylic acids are used as treasures in many fields such as medicine, materials, and agriculture, and have a wide range of applications and important values.
    What are the synthesis methods of IMIDAZO [1,2-A] PYRIDINE-6-CARBOXYLIC ACID
    The synthesis method of imidazolo [1,2-a] pyridine-6-carboxylic acid has been studied by chemists since ancient times. Today there are various paths, let me come one by one.
    First, pyridine derivatives are used as starting materials, and they interact with specific reagents through appropriate reaction conditions. In the reactor, temperature, pressure and reaction time are controlled to gradually build the pyridine ring and imidazole ring. This process requires fine allocation of the ratio of the reactants and precise control of the temperature. If it is too high, side reactions will occur, and if it is too low, the reaction will be slow and difficult.
    Second, pyridine structures are also introduced based on imidazole derivatives. Through ingenious design of the reaction process, using reactions such as nucleophilic substitution, cyclization, etc., the choice of reaction solvent is crucial, and different solvents have a great impact on the reaction rate and selectivity.
    In addition, the strategy of transition metal catalysis can be used. Transition metals such as palladium and copper can effectively promote the formation of carbon-carbon and carbon-heteroatom bonds. In this synthesis, coupling reactions between substrates can be catalyzed to facilitate the formation of imidazolo [1,2-a] pyridine-6-carboxylic acids. However, when using transition metal catalysts, attention should be paid to their dosage and recovery to take into account cost and environmental considerations.
    Each of these methods has its own advantages and disadvantages. In practice, chemists need to make careful choices based on factors such as their own conditions, the availability of raw materials, and the purity requirements of the product to achieve the best synthetic effect.
    IMIDAZO [1,2-A] What is the market outlook for PYRIDINE-6-CARBOXYLIC ACID?
    Imidazolo [1,2-a] pyridine-6-carboxylic acid, this is a class of organic compounds with important applications in the fields of medicinal chemistry and materials science. Looking at its market prospects today, it is like the beginning of a star, and it is gradually showing a bright trend.
    In the field of pharmaceutical research and development, this compound has emerged. Due to its unique chemical structure, it can interact with a variety of biological targets, so it has great potential to create new drugs. Many scientific research teams have made every effort to explore its biological activity, striving to find lead compounds that can be used to treat difficult diseases such as cancer and neurological diseases. With the increasing global demand for innovative drugs, new drugs developed based on imidazolo [1,2-a] pyridine-6-carboxylic acids, if they can successfully come out, will surely win a place in the market, like a sharp sword breaking bamboo, opening up a broad market space.
    It is also seen in the field of materials science. Due to its special structure giving good photoelectric properties, it has attracted much attention in the research of cutting-edge materials such as organic Light Emitting Diode (OLED) and solar cells. With the rapid development of science and technology, the demand for high-performance materials in the fields of electronic equipment and energy is eager. Imidazolo [1,2-a] pyridine-6-carboxylic acid is expected to become a key component in the construction of new high-performance materials by virtue of its own advantages, and its market demand will grow like bamboo shoots.
    However, the road to market expansion is not smooth. The synthesis process is complex and the cost remains high, which is like a boulder, restricting large-scale production and wide application. And the market competition is fierce. Many scientific research institutions and enterprises are involved in related research and want to get a share. Only by breaking through the technical bottleneck, optimizing the synthesis process, reducing costs, and strengthening the protection of intellectual property rights can we stabilize the tide in the market wave, such as sailing ships breaking the waves, so that imidazolo [1,2-a] pyridine-6-carboxylic acid will bloom more brilliantly in the future market, and make great plans in various application fields.