Ethyl 4 Nitro 1h Imidazole 2 Carboxylate
quinoline thiophene imidazole thiazole

Ethyl 4-Nitro-1H-Imidazole-2-Carboxylate

    Specifications

    HS Code

    446350

    Chemical Formula C6H5N3O4
    Molar Mass 183.12 g/mol
    Appearance Typically a solid (color may vary based on purity)
    Solubility In Water Limited solubility (organic compounds with this structure generally have low water solubility)
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
    Pka No specific pKa data provided (acid - base properties related to imidazole ring)
    Stability Stable under normal conditions, but sensitive to strong acids, bases and reducing agents

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    General Information
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    Frequently Asked Questions

    As a leading Ethyl 4-Nitro-1H-Imidazole-2-Carboxylate 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 main uses of Ethyl 4-Nitro-1H-Imidazole-2-Carboxylate?
    Ethyl 4 - Nitro - 1H - Imidazole - 2 - Carboxylate, Chinese name ethyl 4 - nitro - 1H - imidazole - 2 - carboxylate, this substance has a wide range of uses. In the field of medicinal chemistry, it is often a key intermediate for the synthesis of many drugs. The unique structure of the genimidazole ring can be precisely combined with targets in vivo in the design of drugs, adding drug activity and specificity. Taking some antibacterial and antiviral drugs as an example, this compound can introduce suitable functional groups through specific reaction steps, which can construct drug molecules with excellent biological activity, or can effectively inhibit the growth and reproduction of pathogens. < Br >
    In the field of materials science, it also has important uses. It can be introduced into polymer materials by specific reactions to give new properties to the materials. For example, after adding some functional polymer materials, it can improve the thermal stability and mechanical properties of the materials, or even endow the materials with special optical and electrical properties, making the materials more widely used in electronic devices, optical materials and other fields.
    Furthermore, in the field of organic synthetic chemistry, it is an important synthetic building block. With its functional groups such as ester groups and nitro groups, it can participate in many classical organic reactions, such as nucleophilic substitution and reduction reactions. Chemists can follow different reaction paths and conditions, ingeniously design synthetic routes, and prepare organic compounds with diverse structures and functions, providing a rich material foundation and diverse synthesis strategies for the development of organic synthetic chemistry.
    What are the physical properties of Ethyl 4-Nitro-1H-Imidazole-2-Carboxylate?
    Ethyl 4-nitro-1H-imidazole-2-carboxylic acid ester is one of the organic compounds. Its physical properties are quite important and are related to many chemical applications.
    First of all, its appearance, at room temperature, is mostly solid, and the color is either white or slightly yellowish, depending on the purity and preparation method. Its texture is fine, and the powder is common, which is easy to use and experimental operation.
    The melting point is the key physical property. After many experiments, its melting point is about a specific temperature range, but the exact value varies slightly due to differences in experimental conditions. The characteristics of the melting point are significant in identifying and purifying this substance. The purity can be determined by means of melting point measurement. If the purity is high, the melting point will be sharp and approach the theoretical value; if it contains impurities, the melting point will decrease and the melting range will be widened.
    Furthermore, the solubility of this substance is also the focus. In organic solvents, such as common ethanol and dichloromethane, etc., it shows a certain solubility. Ethanol has a moderate polarity and can form a moderate interaction with ethyl 4-nitro-1H-imidazole-2-carboxylate molecules to partially dissolve it. Dichloromethane can also dissolve a certain amount of this substance due to its unique molecular structure and weak polarity. However, in water, due to the large proportion of hydrophobic groups in its structure, the solubility is very small.
    In addition, the density of this substance is also one of the physical properties. Although the relevant data may vary depending on the measurement method and the environment, the density is roughly in a certain range, which is indispensable for experiments and industrial applications involving mass and volume conversion.
    The physical properties of ethyl 4-nitro-1H-imidazole-2-carboxylic acid esters, such as appearance, melting point, solubility and density, are of great significance in chemical research, identification of substances in industrial production, purification, and setting of reaction conditions. They are key basic information in related fields.
    What is the chemical synthesis method of Ethyl 4-Nitro-1H-Imidazole-2-Carboxylate?
    The method for the synthesis of ethyl 4-nitro-1H-imidazole-2-carboxylic acid esters is often followed by a number of paths. First, imidazole can be used as the starting point. Under suitable reaction conditions, imidazole can be nitrified with appropriate nitrifying reagents, such as concentrated nitric acid and concentrated sulfuric acid mixed acid, to obtain 4-nitroimidazole. This step requires careful control of the reaction temperature and time to prevent excessive nitrification.
    After 4-nitroimidazole is obtained, it is then reacted with carboxylic acid esterification reagents, such as ethyl chloroformate, under base catalysis. The base can be selected from potassium carbonate, sodium carbonate, etc., in an organic solvent such as dichloromethane, N, N-dimethylformamide, maintain a certain temperature, and then stir the reaction to cause a substitution reaction between the two to generate ethyl 4-nitro-1H-imidazole-2-carboxylate. After the reaction is completed, the post-treatment steps such as extraction, washing, drying, column chromatography, etc. are used to obtain a pure product.
    Or another way is to use compounds containing specific substituents as raw materials and gradually construct imidazole rings through multi-step reactions. For example, with suitable nitro-substituted amine compounds and compounds containing carbonyl and carboxyl groups, under suitable condensation reagents and catalytic conditions, the imidazole structure is first formed into a ring, and then esterification is carried out to introduce ethyl ester groups. Although this path is a little complicated, it is also a feasible method if the raw materials are readily available and the reaction conditions are mild and controllable. In short, there are various methods for synthesizing this compound, and the best one should be used according to the actual raw materials, equipment and process requirements.
    What are the precautions for Ethyl 4-Nitro-1H-Imidazole-2-Carboxylate during storage?
    Ethyl + 4 - Nitro - 1H - Imidazole - 2 - Carboxylate is also an organic compound. During storage, many matters should be paid attention to.
    First, it is quite sensitive to environmental conditions. In terms of temperature, it should be stored in a cool place to avoid high temperature hot topics. Hot topics can easily cause the molecular movement of compounds to intensify, or cause the risk of decomposition and deterioration. If the temperature is too high, the energy between molecules increases, and chemical bonds may be damaged, thereby damaging their chemical structure and properties.
    Second, humidity cannot be ignored. When the storage environment is kept dry and the compound is damp, the water molecules may interact with the molecular structure, or initiate reactions such as hydrolysis, which will reduce the purity and affect subsequent use. If the water binds to some groups in the molecule, it will change its chemical activity.
    Furthermore, the light factor should not be underestimated. Direct exposure to strong light should be avoided, and the light energy or the photochemical reaction of the compound will cause the structure to change. Especially high-energy light such as ultraviolet light can break chemical bonds and generate new substances.
    In addition, it needs to be properly isolated from other chemicals during storage. Because of its specific chemical properties, if it comes into contact with improper substances or triggers violent reactions, such as oxidation and reduction, it will not only damage itself, but also lead to safety accidents.
    In conclusion, when storing Ethyl + 4 - Nitro - 1H - Imidazole - 2 - Carboxylate, it is necessary to pay attention to temperature, humidity, light and chemical isolation to ensure its quality and stability.
    What is the market price range for Ethyl 4-Nitro-1H-Imidazole-2-Carboxylate?
    Ethyl 4 - Nitro - 1H - Imidazole - 2 - Carboxylate is a specific compound in the chemical field. However, its market price range is difficult to determine with certainty. Because the market price often changes with many factors.
    First, the price fluctuation of raw materials has a great impact on it. If the price of various raw materials required for the synthesis of this compound fluctuates, the cost of Ethyl 4 - Nitro - 1H - Imidazole - 2 - Carboxylate also changes, which in turn affects its market price.
    Second, the difficulty and advanced degree of production process are also key factors. If the production process is complex, requires a lot of manpower, material resources and time, or requires special equipment and technology, the cost will be high, and the price will be high. And advanced technology, if it can improve production efficiency and reduce loss, may reduce the price.
    Third, the market supply and demand relationship, the price is very large. If the market demand for this compound is strong and the supply is limited, the price will often rise; conversely, if the supply exceeds the demand, the price will tend to decline.
    Fourth, different manufacturers will have different pricing due to their own operating costs and market strategies. In general, the market price of this compound may vary from a few to several tens of dollars per gram, but this is only a rough estimate. The actual price needs to be investigated in detail according to specific market conditions.