3 Aminopyrazine 2 Carbohydrazide
pyridine pyrrole pyrazine piperidine piperazine

3-aminopyrazine-2-carbohydrazide

    Specifications

    HS Code

    243542

    Chemical Formula C5H7N5O
    Molar Mass 153.14 g/mol
    Appearance Solid (usually white or off - white powder)
    Melting Point Approximately 240 - 245 °C (decomposition may occur)
    Solubility In Water Slightly soluble
    Solubility In Organic Solvents Soluble in some polar organic solvents like dimethylformamide (DMF)
    Pka Value Relevant to its acidic - basic properties in solution, but specific value may vary with conditions
    Crystal Structure Can crystallize under appropriate conditions, specific structure details depend on crystallization method
    Odor Odorless or very faint odor

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    Frequently Asked Questions

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    What are the chemical properties of 3-aminopyrazine-2-formylhydrazide?
    3-Hydroxybutyric acid-2-methylchloroester is an organic compound with unique chemical properties. It is mostly white crystalline powder at room temperature, smelling slightly fishy, tasting slightly bitter, and soluble in common solvents such as water and ethanol.
    From the perspective of chemical activity, 3-hydroxybutyric acid-2-methylchloroester can participate in multiple chemical reactions because it contains hydroxyl groups and ester groups. Hydroxyl groups are nucleophilic, and are prone to acylation reactions when exposed to acyl halides, acid anhydrides, etc., to form corresponding ester compounds. This reaction is often a key step in the construction of complex ester structures in organic synthesis. At the same time, the hydroxyl group can also react with active metals such as sodium metal to release hydrogen gas to form sodium alcohol compounds, which can introduce specific functional groups to achieve molecular structure modification.
    The ester group is also active, and can undergo hydrolysis under acidic or basic conditions. In acidic hydrolysis, 3-hydroxybutyric acid and methanol are formed; in alkaline hydrolysis, 3-hydroxybutyrate and methanol are formed. This hydrolysis property is of great significance in the fields of drug metabolism and organic synthesis raw material recovery.
    Furthermore, the molecular structure of 3-hydroxybutyric acid-2-methylchloride gives it a certain lipid solubility, which affects its absorption, distribution and metabolism in living organisms. Because the cell membrane is composed of a lipid bilayer, fat-soluble substances are easier to penetrate, so the compound can enter the inside of the cell relatively easily, play a physiological role or participate in intracellular chemical reactions. However, its fat solubility also affects its excretion rate in the body. Compared with water-soluble substances, more complex metabolic processes may be required to excrete it from the body.
    What are the physical properties of 3-aminopyrazine-2-formylhydrazide?
    3-Aminopyridine-2-formamide is one of the organic compounds. Its physical properties are as follows:
    Looking at its appearance, under room temperature and pressure, it often shows a white to light yellow crystalline powder. This form is easy to observe and use. In many chemical experiments and industrial production processes, this form is conducive to accurate measurement and subsequent processing.
    When it comes to melting point, it is between 155-159 ° C. Melting point is one of the inherent characteristics of the substance. This value can help identify the compound and is of great significance in the synthesis and purification process. By precisely controlling the temperature, according to the melting point characteristics, the purpose of separation and purification can be effectively achieved.
    As for solubility, it is slightly soluble in water. Water is a common solvent, and this property indicates that the compound has limited dispersion in aqueous systems. However, it is soluble in common organic solvents, such as ethanol, dichloromethane, etc. This solubility characteristic provides a variety of choices in the field of organic synthesis. Due to the different solubility properties and reaction environments of different organic solvents, the rational selection of solvents can regulate the reaction process and improve the purity of the product.
    Furthermore, the compound has certain stability. Under conventional environmental conditions, it can maintain its own chemical structure and properties unchanged. However, it should be noted that although it is stable, when it encounters special chemicals such as strong oxidants, strong acids, and strong bases, it may still cause chemical reactions and cause changes in its structure and properties. Therefore, during storage and use, contact with the above substances should be avoided. This stability feature makes the compound relatively controllable in environmental conditions during storage and transportation, laying the foundation for its wide application.
    What are the main applications of 3-aminopyrazine-2-formylhydrazide?
    3-Aminopyridine-2-formamide is mainly used in multiple domains. "Tiangong" does not directly mention this substance, but it can be roughly used in the present based on ancient principles.
    The first is the chemical domain. This compound can be used as an important synthetic compound for the core skeleton of polymers. Ancient home-made, often seeking the delicate ratio of various plants, trees, and gold stones in order to eliminate diseases. Today's chemical synthesis also follows this path. Due to its special chemical properties, 3-aminopyridine-2-formamide can be synthesized with specific biological activities by multi-step reaction, introducing different functionalities, such as compounds for treating certain diseases such as inflammation and tumors.
    Furthermore, the field of material science is also indispensable. It can be used for the synthesis of polymer materials and improve the properties of materials. Ancient techniques such as fabrics and fabrics have been used to improve the properties of materials. Polymer materials synthesized from 3-aminopyridine-2-formamide raw materials may have better mechanical properties and qualitative properties. For example, in the production of high-performance engineering plastics, the addition of this compound can interact with the arrangement of whole molecules, making the plastic more durable, and can be used in aerospace, automotive manufacturing, and other materials with high performance requirements.
    In addition, it is also useful in the field of cultivation. It can be used to create new types of plastics and increase the disease resistance of crops. Ancient farming, using natural materials to prevent seedlings. Today, with chemical means, 3-aminopyridine-2-formamide can be used to synthesize high-efficiency and low-toxicity plastics, protecting crops from disease invasion, improving food intake, and protecting people's livelihood.
    Therefore, 3-aminopyridine-2-formamide plays an important role in the development of various fields, such as modern technology, materials, and engineering.
    What is the synthesis method of 3-aminopyrazine-2-formylhydrazide?
    The synthesis of 3-aminopyridine-2-formamide is an important topic in the field of organic synthesis. There are many methods, and the commonly used methods are described in detail below.
    One of the methods is to use 3-aminopyridine as the starting material. First, 3-aminopyridine is reacted with an appropriate acylating agent. The acylating agent is often an acyl halide or an acid anhydride. If an acyl halide, such as acetyl chloride, is used in a suitable solvent, such as dichloromethane, the reaction is carried out under the catalysis of a base. The base can be selected from triethylamine or pyridine, and its function is to neutralize the hydrogen halide generated by the reaction and promote the forward reaction. During the reaction, the temperature is controlled at a low temperature, such as between 0 ° C and room temperature, to ensure the selectivity of the reaction. After the reaction is completed, 3-aminopyridine-2-formamide can be obtained by separation and purification methods such as extraction and column chromatography.
    Second, it can be synthesized from pyridine derivatives through multi-step reactions. For example, pyridine is first substituted at a specific position, a suitable functional group is introduced, and then the functional group is converted to gradually construct the target molecular structure. For example, a halogen atom is first introduced at the 2-position of the pyridine ring, and then an amino group is introduced through a nucleophilic substitution reaction, and then an amidation reaction is carried out. During amidation, it can react with the corresponding carboxylic acid or its activated derivatives, such as carboxylic acid and carbodiated diamine reagents to form active intermediates, and then react with amino groups to form amide bonds, and finally obtain 3-aminopyridine-2-formamide.
    Third, there is also a synthesis path catalyzed by metals. Transition metal catalysts, such as palladium, copper, etc., are used to catalyze the coupling reaction between substrate molecules. For example, in the presence of metal catalysts and ligands, a coupling reaction occurs under appropriate reaction conditions, such as specific temperatures, bases, and solvent systems, to form the structure of the target product. The advantage of this method is that it can achieve the formation of selective carbon-carbon or carbon-heteroatomic bonds, improving the synthesis efficiency and product purity.
    All these synthesis methods have their own advantages and disadvantages. According to the actual situation, such as the availability of raw materials, the controllability of reaction conditions, and the purity requirements of the product, etc., choose the appropriate method to synthesize 3-aminopyridine-2-formamide.
    What are the precautions for the storage and transportation of 3-aminopyrazine-2-formylhydrazide?
    3-Aminopyridine and 2-methylpyridine should be paid attention to during storage and transportation.
    Fu 3-aminopyridine, which is alkaline and has certain chemical activity. When storing, be sure to choose a dry, cool and well-ventilated place. Because it is easy to react with acidic substances and water vapor in the air, the packaging must be tight to prevent moisture intrusion and deterioration. For example, if the seal is not tight, water vapor seeps in, or causes it to hydrolyze, it will affect its chemical properties and quality. When transporting, also pay attention to avoid moisture and high temperature. High temperature environment may cause chemical reactions, and even cause danger. And because of its certain toxicity, it is necessary to operate in accordance with the relevant toxic chemicals during transportation to ensure the safety of transporters and the safety of the environment.
    As for 2-methylpyridine, it also has specific chemical properties. Storage should be kept away from fire sources and oxidants. 2-methylpyridine is a flammable organic compound. If it is close to the fire source, it may cause a fire if it is not careful. Contact with oxidants can easily trigger violent oxidation reactions and cause accidents. During transportation, ensure that the container is stable and will not be damaged and leaked due to bumps and collisions. If it leaks, it will not only cause pollution to the environment, such as soil and water pollution, but also the volatile gas will pose a threat to the health of surrounding people.
    Both are required to strictly follow the relevant regulations on chemical management during storage and transportation, and make labels to identify and distinguish them, so that operators can clarify their characteristics and potential hazards, and then take appropriate protection and response measures. This will ensure the safety of storage and transportation.