1h Imidazole 2 Carboxamide
quinoline thiophene imidazole thiazole

1H-Imidazole-2-carboxamide

    Specifications

    HS Code

    472810

    Chemical Formula C4H5N3O
    Molar Mass 111.10 g/mol
    Appearance White to off - white solid
    Odor Odorless
    Melting Point 199 - 201 °C
    Solubility In Water Soluble
    Pka Value 3.9 (approximate value for imidazole ring)
    Density 1.40 g/cm³ (estimated)
    Stability Stable under normal conditions

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    General Information
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    Frequently Asked Questions

    As a leading 1H-Imidazole-2-carboxamide 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 chemistry of 1H-Imidazole-2-carboxamide?
    1H-imidazole-2-formamide, this is an organic compound. Its physical properties are mostly white to light yellow crystalline powder at room temperature, which can remain relatively stable in air. Its melting point is in a specific range, about [specific melting point value], which is convenient for experimental and industrial production to determine the purity by melting point.
    Regarding chemical properties, 1H-imidazole-2-formamide contains imidazole ring and formamide group, which give it unique chemical activity. The imidazole ring is aromatic and the electron cloud is specially distributed, which makes the compound easy to participate in electrophilic substitution reactions. For example, under certain conditions, it can react with halogenated hydrocarbons, and the halogen atom replaces the hydrogen atom at a specific position on the imidazole ring to form the corresponding substituted product. This reaction is of great significance for the preparation of various derivatives in organic synthesis. The
    formamide group allows 1H-imidazole-2-formamide to participate in a variety of condensation reactions. For example, under the action of appropriate catalysts, condensation can occur with aldehyde compounds to form new compounds containing carbon-nitrogen double bonds, expanding its application in the field of organic synthesis. At the same time, the formamide group can also be hydrolyzed. Under acidic or basic conditions, the amide bond breaks to form the corresponding carboxylic acid or carboxylate and ammonia or amine substances. This hydrolysis reaction is crucial for studying its metabolic pathway and stability in different environments.
    In addition, 1H-imidazole-2-formamide can be used as a ligand to form complexes with metal ions due to the lone pair electrons on the nitrogen atom in the structure. In the field of coordination chemistry, it combines with transition metal ions to form complexes with diverse structures and unique properties. These complexes have shown potential application value in catalysis, materials science and other fields.
    What are the common uses of 1H-Imidazole-2-carboxamide?
    1H-imidazole-2-formamide has a wide range of uses. In the field of medicine, it is often used as a key intermediate in drug synthesis. In the process of creating many new anti-cancer drugs and antiviral agents, 1H-imidazole-2-formamide plays a cornerstone role. Due to its unique chemical structure, it can precisely bind to specific biological targets and help drugs achieve therapeutic purposes.
    In the field of materials science, it also shows extraordinary value. It can act as an excellent modifier in the preparation of certain high-performance polymer materials. By adding 1H-imidazole-2-formamide, the mechanical properties and thermal stability of the material can be significantly improved. For example, special polymer materials used in the aerospace field can be modified to meet the strict environmental requirements.
    In the field of chemical production, 1H-imidazole-2-formamide can participate in the synthesis of a variety of fine chemicals. In the preparation of some functional dyes and catalysts, it is used as an important raw material to endow products with unique properties. For example, after the synthesis of catalysts with specific structures is participated in, the catalytic activity is greatly enhanced and the reaction efficiency is significantly improved, thereby optimizing the chemical production process and reducing production costs.
    Furthermore, in biochemical research, it is used as a biochemical reagent to explore the chemical reaction mechanism in living organisms. With its interaction characteristics with biomolecules, researchers can gain in-depth insight into biological processes and contribute to the development of life sciences. In short, 1H-imidazole-2-formamide plays an important role in many fields due to its diverse uses.
    What is the preparation method of 1H-Imidazole-2-carboxamide?
    The preparation method of 1H-imidazole-2-formamide has been widely investigated in the field of chemistry throughout the ages. In the past, the preparation of this compound often followed various paths.
    First, it can be started from raw materials containing imidazole structure. For example, a carboxyl group is introduced through a carboxylation reaction with a specific substituted imidazole as a group, and then the carboxyl group is converted into a formamide group. First, a suitable imidazole derivative is reacted with a carboxylating agent, such as carbon dioxide or its equivalent, in a specific solvent, such as an organic solvent, under the catalysis of a base, to form an imidazole-2-carboxylic acid derivative. Bases, such as potassium carbonate and sodium carbonate, can promote the reaction to proceed. Subsequently, a suitable amidation reagent, such as dichlorosulfoxide, works synergistically with ammonia or amine substances to convert the carboxyl group into a formamide group. In this process, dichlorosulfoxide first reacts with carboxylic acid to form a more active acid chloride intermediate, and then ammonia or amine attacks the acid chloride to achieve amidation, resulting in 1H-imidazole-2-formamide.
    Second, it is also prepared by the strategy of constructing an imidazole ring. Small molecule raw materials containing nitrogen and carbon were selected, and imidazole rings were constructed through multi-step reactions and formamide groups were introduced at the same time. For example, glyoxal, ammonia and cyanamide are used as starting materials. In aqueous solution, at a suitable temperature and in the presence of a catalyst, a condensation reaction occurs first to form the prototype of the imidazole ring, and then a formamide group is introduced at the second position of the ring through subsequent modification reactions. In this process, the choice of temperature and catalyst is very critical. The temperature may be controlled in an appropriate range, such as between 50 and 80 degrees Celsius. The catalyst or a specific acid or base guides the reaction in the desired direction, and the target product 1H-imidazole-2-formamide is gradually synthesized.
    Third, there are still methods for catalyzing by transition metals. Using suitable metal catalysts, such as palladium, copper, etc., catalyze the reaction between specific substrates. Select imidazole derivatives containing halogen atoms and nucleophiles containing formamide groups. Under the combined action of metal catalysts, ligands and bases, a coupling reaction occurs to construct the structure of 1H-imidazole-2-formamide. The ligand can enhance the activity and selectivity of the metal catalyst, and the base helps to regulate the chemical environment of the reaction and promote the efficient occurrence of the reaction, so as to achieve the preparation of 1H-imidazole-2-formamide.
    What are the differences in the application of 1H-Imidazole-2-carboxamide in different fields?
    1H-imidazole-2-formamide has a wide range of uses and can be used in different fields.
    In the field of medicine, it is a key raw material for the synthesis of many drugs. Because the imidazole structure can interact with a variety of targets in vivo, it can be modified with 1H-imidazole-2-formamide to produce antibacterial, antiviral, antitumor and other drugs. For example, some new anti-tumor drugs, with their structural advantages, precisely act on specific targets of tumor cells and inhibit tumor growth, contributing to the solution of cancer problems.
    In the field of materials science, 1H-imidazole-2-formamide also has outstanding performance. It can participate in the preparation of high-performance polymer materials. Due to its nitrogen-containing heterocyclic structure, it can enhance the force between polymer molecules, improve the mechanical properties and thermal stability of materials. Composite materials made with it as an additive are used in industries with strict material performance requirements such as aerospace and automobile manufacturing to manufacture key components and help devices withstand extreme conditions.
    In agricultural chemistry, it is an important intermediate for the synthesis of pesticides. Through rational design and synthesis, pesticides with high insecticidal, bactericidal and herbicidal activities can be prepared. Such pesticides are highly selective to target organisms, which can not only effectively control pests and diseases, weeds, ensure crop yield and quality, but also reduce environmental and non-target biological hazards, which meets the needs of modern green agriculture development.
    In the field of organic synthetic chemistry, 1H-imidazole-2-formamide is a unique organic reagent and participates in the synthesis of many complex organic compounds. Due to its active structure, it can occur a variety of chemical reactions, such as nucleophilic substitution, cyclization, etc., providing a powerful tool for organic synthetic chemists to construct novel organic structures, help explore new compounds, and expand the boundaries of organic chemistry research.
    What is the market outlook for 1H-Imidazole-2-carboxamide?
    1H-imidazole-2-formamide, this product has both challenges and opportunities in the current market prospect.
    Looking at its application field, it has attracted much attention in the field of pharmaceutical and chemical industry. Because of its unique structure, it may act as a key intermediate in the process of drug research and development, helping to create new special drugs to fight various diseases, so the demand for it in the pharmaceutical industry may grow. In this field, the market prospect is quite bright, and many pharmaceutical companies are bound to invest more attention and resources in order to seek innovation and breakthroughs.
    However, at the level of market competition, there are also many challenges. With the in-depth research on it, many manufacturers have flooded in, and the market competition has become increasingly fierce. To emerge in the market, manufacturers need to have superb production processes to ensure high product quality and cost control. Otherwise, it is very easy to be eliminated in the fierce competition.
    Furthermore, the impact of regulations and policies should not be underestimated. In the field of chemical production, regulations and policies are becoming increasingly stringent. The production and sales of 1H-imidazole-2-formamide need to follow relevant regulations. If regulations change, manufacturers may need to invest additional costs to adapt to the new regulations, which is also one of the major factors affecting the market outlook.
    Overall, although 1H-imidazole-2-formamide has broad application space in the fields of medicine and chemical industry, it also needs to face challenges such as market competition and regulations and policies. If manufacturers can make good use of opportunities and actively respond to challenges, they may be able to obtain good development prospects in this market.