3 Chloro Pyrazine 2 Carbaldehyde
pyridine pyrrole pyrazine piperidine piperazine

3-CHLORO-PYRAZINE-2-CARBALDEHYDE

    Specifications

    HS Code

    373967

    Chemical Formula C5H3ClN2O
    Molar Mass 142.54 g/mol
    Appearance Solid (likely, based on similar compounds)
    Solubility In Water Limited solubility (due to non - polar nature of pyrazine ring and hydrophobic chloro group)
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, ethyl acetate
    Odor No common data, but may have a pungent or characteristic odor

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    Frequently Asked Questions

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    What is the chemistry of 3-CHLORO-PYRAZINE-2-CARBALDEHYDE?
    3-Chloro-pyrazine-2-formaldehyde, this is an organic compound. It has many unique chemical properties.
    Looking at its structure, it contains chlorine atoms and aldehyde groups, which give the compound a different reactivity. The aldehyde group has high reactivity and can participate in many organic reactions. Such as oxidation reactions, under the action of suitable oxidizing agents, the aldehyde group can be converted into carboxyl groups to obtain 3-chloro-pyrazine-2-carboxylic acids. It can also carry out reduction reactions. With the help of reducing agents, the aldehyde group can be changed into an alcohol hydroxyl group to obtain 3-chloro-pyrazine-2-methanol.
    Furthermore, aldehyde groups can react with compounds containing active hydrogen, such as alcohols, to form acetal structures. This structure is often used in organic synthesis as a means of protecting aldehyde groups to avoid the random participation of aldehyde groups in subsequent reactions. After the desired reaction is completed, the acetal is hydrolyzed under specific conditions to re-release the aldehyde group.
    And chlorine atoms also play an important role in compounds. Due to its high electronegativity, its ortho and para-electron cloud densities are reduced, and nucleophilic substitution reactions are more likely to occur. When nucleophilic reagents attack, chlorine atoms can be replaced, introducing different functional groups to expand the structure and properties of the compound. For example, when reacting with sodium alcohol, chlorine atoms can be replaced by alkoxy groups to form corresponding ether compounds.
    In addition, the pyrazine ring of the compound also affects its chemical properties. The pyrazine ring has a certain aromaticity, which makes its chemical properties relatively stable. However, due to the presence of nitrogen atoms on the ring, it imparts a certain alkalinity to the ring, which can react with acids to form salts, thereby changing the physical properties such as the solubility of the compound. This may have applications in operations such as separation and purification.
    3-chloro-pyrazine-2-formaldehyde has rich chemical properties. With the characteristics of aldehyde groups, chlorine atoms and pyrazine rings, it can participate in a variety of organic reactions and has high application value in the field of organic synthesis.
    What are the main uses of 3-CHLORO-PYRAZINE-2-CARBALDEHYDE?
    3-Chloropyrazine-2-formaldehyde, an organic compound, is widely used in chemical and scientific research fields.
    First, it is a key intermediate in drug synthesis. The structure of Geinpyrazine is common in many drug molecules and has unique biological activities and pharmacological properties. 3-Chloropyrazine-2-formaldehyde can be reacted in multiple steps to access specific functional groups to build a complex drug molecular skeleton. For example, when developing antibacterial and antiviral drugs, it can be used as a starting material, and the reaction route can be cleverly designed to synthesize new drugs with targeted effects, providing the possibility for pharmaceutical innovation.
    Second, in the field of materials science, it also has applications. It can participate in the preparation of functional materials, such as photoelectric materials. With its special structure, it can be polymerized or modified with other compounds to endow the material with unique optical and electrical properties. Or it can be used to synthesize photochromic materials that respond to specific wavelengths of light, showing potential in sensors, display technologies, etc.
    Third, it is an important building block in the field of organic synthesis chemistry. Chemists use the reactivity of aldehyde groups and chlorine atoms to carry out various classical organic reactions, such as condensation reactions of aldehyde groups and substitution reactions of chlorine atoms. With this, a diverse library of organic compounds is constructed, providing a basis for exploring new reaction mechanisms, expanding organic synthesis methods, and promoting the development of organic chemistry.
    What is 3-CHLORO-PYRAZINE-2-CARBALDEHYDE synthesis method?
    The synthesis of 3-chloro-pyrazine-2-formaldehyde is an important topic in the field of organic synthesis. This compound is valuable in the preparation of many drugs and functional materials. To synthesize this compound, there are several common methods.
    First, pyrazine-2-formaldehyde is used as the starting material. First, pyrazine-2-formaldehyde is dissolved in a suitable organic solvent, such as dichloromethane or tetrahydrofuran. Then, under low temperature environment, such as ice bath conditions, chlorine-containing reagents are slowly added. The commonly used chlorine-containing reagents are N-chlorosuccinimide (NCS) or thionyl chloride (SOCl ²). During the reaction, the reaction temperature and reaction process should be closely monitored. In the case of NCS, the reaction system will gradually change. The progress of the reaction is monitored by thin-layer chromatography (TLC). When the raw material point disappears, it indicates that the reaction is almost complete. Then, the reaction mixture is subjected to conventional post-treatment, such as extraction, washing, drying, and column chromatographic separation, to obtain pure 3-chloro-pyrazine-2-formaldehyde.
    Second, pyrazine derivatives can also be used. For example, selecting a specific pyrazine derivative, which has a suitable substituent in its structure, can gradually introduce chlorine atoms and aldehyde groups through a multi-step reaction. First, the pyrazine derivative undergoes a substitution reaction at a specific position, and a functional group that can be converted into an aldehyde group, such as a nitrile group (-CN), can be converted into an aldehyde group through a hydrolysis reaction. At the same time, in a suitable reaction step, chlorine atoms are introduced at the target position through nucleophilic substitution or electrophilic substitution. Although this path is a little complicated, it requires high precision control of the reaction conditions and purification of the intermediate product. However, its advantage is that the substituents on the pyrazine ring can be designed and regulated more flexibly to meet different synthesis needs.
    Third, the reaction can also be catalyzed by transition metals. Taking palladium catalysis as an example, select suitable palladium catalysts, such as tetra (triphenylphosphine) palladium (0) [Pd (PPh) ] or palladium acetate [Pd (OAc) 2O], etc. The substrate containing pyrazine structure and the reagents containing chlorine and aldehyde groups are reacted in the presence of specific ligands, bases and solvents. This reaction condition is relatively mild and the selectivity is good, but the activity and stability of the catalyst are very high, and the cost of the catalyst is high. Its economy and practicality need to be comprehensively considered.
    There are many methods for the synthesis of 3-chloro-pyrazine-2-formaldehyde. The specific method to be selected needs to be carefully selected according to the availability of starting materials, reaction cost, purity requirements of target products, and experimental conditions, etc., in order to achieve efficient, economical and high-quality synthesis.
    What are the precautions in storage and transportation of 3-CHLORO-PYRAZINE-2-CARBALDEHYDE?
    3-Chloro-pyrazine-2-formaldehyde is also a chemical substance. When storing and transporting, many matters need to be paid attention to.
    First words storage. This substance should be stored in a cool, dry and well-ventilated place. The cover may be sensitive to heat and moisture, and if placed in a warm and humid place, it may cause chemical changes or cause deterioration. Furthermore, it should be kept away from fires and heat sources, because it is flammable or prone to dangerous reactions in contact with fire and heat. And it must be stored separately from oxidizing agents, acids, alkalis, etc., to prevent interaction, chemical reactions, and dangerous accidents. The storage place should have suitable containment materials for emergency use.
    Times and transportation. The packaging must be in good condition during transportation to ensure that there is no risk of leakage. During transportation, the vehicle should be equipped with the corresponding variety and quantity of fire protection equipment and leakage emergency treatment equipment. During driving, it should be protected from exposure to the sun, rain and high temperature. Do not mix with oxidants, acids, alkalis, etc. Drivers and escorts must be familiar with its chemical properties and emergency disposal methods. Pay close attention during transportation. If there is any abnormality, deal with it immediately.
    All of these are for the storage and transportation of 3-chloro-pyrazine-2-formaldehyde, so as to ensure the safety of personnel and the stability of the material.
    What is the market price of 3-CHLORO-PYRAZINE-2-CARBALDEHYDE?
    The market price of 3-chloro-pyrazine-2-formaldehyde is difficult to determine. This is due to the changing situation of the chemical market, and the price varies with many factors.
    The price of raw materials is also the first to bear the brunt. If the raw materials for synthesizing this compound, such as chlorine compounds, pyrazine derivatives, etc., fluctuate in price, the price of 3-chloro-pyrazine-2-formaldehyde will be implicated. The raw materials are abundant and cheap, and the price of finished products may decline; if the price of raw materials is scarce and the price rises, the price of finished products will also rise.
    Furthermore, the preparation process is related to the cost. Advanced and efficient processes can reduce energy consumption and yield, resulting in lower costs and lower market prices; if the process is complicated, the yield is low, the cost rises, and the price is also high.
    Market supply and demand conditions also affect its price. If many industries, such as medicine, pesticide synthesis, etc., have strong demand for 3-chloro-pyrazine-2-formaldehyde, but limited supply, prices will rise; conversely, if there is little demand and more supply, prices will fall.
    Regional differences cannot be ignored. Different places have different prices due to differences in transportation costs, tax policies, and industrial agglomeration. In places where the chemical industry gathers, due to the scale effect and convenient logistics, the price may be relatively low; in remote places, the transportation cost is high, and the price may be high.
    And the market competition situation is different. When there are many manufacturers and the competition is fierce, the market may be dominated or the price may be reduced; if the market monopoly is strong, the price may be controlled by a few manufacturers and is at a high level.
    Therefore, in order to know the current market price of 3-chloro-pyrazine-2-formaldehyde, it is necessary to gain real-time insight into the chemical raw material market, process progress, supply and demand pattern and regional economy.