2 Oxo 2 3 Dihydro 1h Imidazole 4 Carboxylic Acid
quinoline thiophene imidazole thiazole

2-oxo-2,3-dihydro-1H-imidazole-4-carboxylic acid

    Specifications

    HS Code

    249164

    Chemical Formula C4H4N2O3
    Molecular Weight 128.09 g/mol
    Appearance Solid (predicted, based on similar compounds)
    Solubility In Water Unknown (literature search required)
    Solubility In Organic Solvents Unknown (literature search required)

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    General Information
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    Frequently Asked Questions

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    What is the chemical structure of 2-oxo-2, 3-dihydro-1H-imidazole-4-carboxylic acid?
    2 - oxo - 2,3 - dihydro - 1H - imidazole - 4 - carboxylic acid, which is the English name of an organic compound. Its chemical structure is described in the classical Chinese style of "Tiangong Kaiwu", as follows:
    The core structure of this compound is a five-membered ring imidazole ring. In the ring, nitrogen and carbon atoms are arranged interactively to form a stable ring structure. 1H - means that the hydrogen atom is attached to the nitrogen atom at the first position of the imidazole ring. And 2 - oxo means that at the second position of the ring, there is a carbonyl group (C = O), which gives the molecule specific chemical activity and reaction characteristics. 2,3-Dihydro indicates that the carbon-carbon bond between the 2 and 3 positions is in a single bond state due to hydrogenation, and this hydrogenation state also affects the spatial configuration and physicochemical properties of the molecule. As for 4-carboxylic acid, it refers to the connection of a carboxylic group (-COOH) at the 4 position of the ring. The carboxylic group is acidic and plays a key role in many chemical reactions. It can participate in esterification, salt formation and other reactions.
    In summary, the chemical structure of 2-oxo-2,3-dihydro-1H-imidazole-4-carboxylic acid is based on imidazole ring, with specific position carbonyl, hydrogenated structure and carboxylic group. This unique structure determines its special properties and reaction behavior in the field of chemistry.
    What are the main physical properties of 2-oxo-2, 3-dihydro-1H-imidazole-4-carboxylic acid?
    2-Oxo-2,3-dihydro-1H-imidazole-4-carboxylic acid, this is an organic compound. It has many important physical properties, as detailed below:
    Looking at its properties, it is mostly white to light yellow crystalline powder at room temperature and pressure. This form is easy to observe and operate, and is easy to handle and use in many chemical experiments and industrial production processes.
    Discusses solubility, which has a certain solubility in water. This property is crucial because in a solution environment, many chemical reactions can proceed smoothly. In some reaction systems using water as a solvent, the substance can be fully contacted and mixed with other reactants by virtue of its water solubility, thus promoting the efficient occurrence of the reaction. In addition, it also has a certain solubility in some polar organic solvents, such as methanol and ethanol, which broadens its selection range in different reaction conditions and application scenarios.
    Melting point is also one of the important physical properties. After determination, the melting point of the substance is in a specific temperature range. As an inherent property of the substance, the melting point can be used to identify its purity. If the purity of the substance is high, the melting point is usually more sensitive and the fluctuation range is small; if it contains impurities, the melting point is often reduced and the melting range is widened. Therefore, by accurately measuring the melting point, the purity status of the compound can be judged, providing a key basis for its quality control.
    From a stability perspective, 2-oxo-2,3-dihydro-1H-imidazole-4-carboxylic acids are relatively stable under conventional environmental conditions. However, when exposed to extreme conditions such as high temperature, strong acid, and strong base, its structure may change, triggering chemical reactions. For example, at high temperatures, some chemical bonds within the molecule may break, and then decomposition reactions may occur; in strong acid or strong base environments, neutralization or other types of chemical reactions may occur with acid and base, resulting in molecular structure changes. Therefore, when storing and using the substance, these factors need to be fully considered and appropriate conditions selected to ensure its stable properties and normal function.
    What are the common synthesis methods of 2-oxo-2, 3-dihydro-1H-imidazole-4-carboxylic acid?
    2-Oxo-2,3-dihydro-1H-imidazole-4-carboxylic acid, the common synthesis methods of this compound are roughly as follows:
    First, with suitable starting materials, obtained by cyclization reaction. If a compound containing nitrogen and carboxyl groups is selected, under suitable reaction conditions, it will be condensed and cyclized in the molecule. In this process, it is necessary to pay attention to the reaction temperature, reaction time and the catalyst used. Too high or too low temperature may cause the reaction to fail smoothly or form by-products. If the time is too short, the reaction will be incomplete, and if the time is too long, it will cause an overreaction. The choice of catalyst is also crucial, and different catalysts have a great influence on the reaction rate and product selectivity.
    Second, with the help of the strategy of functional group conversion. First prepare compounds with similar structures, and then gradually convert their functional groups. For example, first synthesize substances containing groups that can be converted into carboxyl groups and imidazole rings, and then precisely construct the structure of the target molecule through oxidation, substitution and other reactions. In the process of functional group conversion, it is necessary to control the selectivity of the reaction and avoid unnecessary side reactions to improve the purity and yield of the product.
    Third, some synthesis routes involve multi-step reactions, starting from simple raw materials and gradually building complex molecular structures. After each reaction step, the product needs to be separated and purified to ensure the smooth progress of the next reaction. During the whole synthesis process, the reaction sequence should be reasonably designed and the reaction conditions optimized according to the structural characteristics of the target product, so that the 2-oxo-2,3-dihydro-1H-imidazole-4-carboxylic acid can be obtained efficiently and with high purity.
    What are the applications of 2-oxo-2, 3-dihydro-1H-imidazole-4-carboxylic acid?
    2-Oxo-2,3-dihydro-1H-imidazole-4-carboxylic acid, this compound has a wide range of uses and has its applications in many fields such as medicine, chemical industry, and biology.
    In the field of medicine, it is often a key synthetic intermediate. It can be converted into compounds with specific pharmacological activities through specific chemical reactions, and then used in drug research and development. Such as the preparation of some antibacterial drugs and antiviral drugs, this compound may be used as a starting material to shape the desired drug molecular structure through multi-step reactions, helping to overcome diseases and protect health.
    In the field of chemical industry, it can participate in the synthesis of polymer materials. By polymerizing with other monomers, polymer materials are endowed with special properties. For example, to make them have better stability, solubility or reactivity, etc., thereby broadening the application of polymer materials in different scenarios, such as coatings, plastics and other industries.
    In the field of biology, due to its structural properties, it may affect certain biochemical reactions in organisms. Or it can be used as a biological probe to help scientists gain insight into specific reaction mechanisms and biomolecular interactions in organisms, providing powerful tools and ideas for life science research, promoting the development of cutting-edge biological research, and assisting human exploration and cognition of the mysteries of life.
    What is the market prospect of 2-oxo-2, 3-dihydro-1H-imidazole-4-carboxylic acid?
    2 - oxo - 2,3 - dihydro - 1H - imidazole - 4 - carboxylic acid is 2 - oxo - 2,3 - dihydro - 1H - imidazole - 4 - carboxylic acid. In terms of market prospects, there are the following situations.
    Guanfu 2 - oxo - 2,3 - dihydro - 1H - imidazole - 4 - carboxylic acid, in the field of medicine, the prospect is initially shimmering. Its unique structure can be used as an intermediary for many drug synthesis. In today's pharmaceutical research and development, there is a great demand for new compounds, and this acid may pave the way for the creation of new drugs. For example, when developing antibacterial and antiviral drugs, it may participate in key reactions and help form active molecules, so pharmaceutical manufacturers are paying more and more attention to it.
    In the chemical industry, there is also potential. It can be used as a raw material for organic synthesis to prepare special functional materials. With the advance of chemical technology, the demand for special materials is on the rise, and 2-oxo-2,3-dihydro-1H-imidazole-4-carboxylic acids are expected to emerge in material modification and new coating research and development. Due to the reactivity endowed by its structure, it can add unique properties to the material, such as improving material stability and enhancing adsorption.
    However, there are also challenges in its market expansion. The synthesis process may need to be refined to reduce costs and yield. And related research is still in the development stage. To be widely used, more scientific research exploration and practical verification are needed. Only by overcoming technical difficulties, improving quality and reducing costs can we sell widely in the market, shine brightly, and gain a place in the field of medicine and chemical industry, injecting new force into the development of the industry.