3 5 Dimethyl 1h Pyrrole 2 Carboxaldehyde
pyridine pyrrole pyrazine piperidine piperazine

3,5-dimethyl-1H-pyrrole-2-carboxaldehyde

    Specifications

    HS Code

    634784

    Chemical Formula C7H9NO
    Molar Mass 123.152 g/mol
    Appearance Typically a solid or liquid (appearance can vary)
    Solubility Soluble in organic solvents like ethanol, dichloromethane, due to its organic nature
    Density Estimated to be around 1.0 - 1.1 g/cm³ based on similar compounds
    Odor May have a characteristic organic odor, likely somewhat pungent
    Stability Stable under normal conditions, but may react with strong oxidizing or reducing agents
    Reactivity Can participate in reactions typical of aldehydes and pyrroles, such as nucleophilic addition at the aldehyde group

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    General Information
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    Frequently Asked Questions

    As a leading 3,5-dimethyl-1H-pyrrole-2-carboxaldehyde 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 physical properties of 3,5-dimethyl-1H-pyrrole-2-formaldehyde?
    3% 2C5 + - + dimethyl-1H-pyrrole-2-acetonitrile is one of the organic compounds. Its physical properties are quite important and are related to many applications of this compound.
    First of all, its appearance is often colorless to light yellow liquid. This color and shape are of great significance for intuitive identification. The view is warm and fluid, like a faint light liquid, standing in a container.
    Furthermore, on its melting point and boiling point. The melting point is the critical temperature at which a substance changes from solid to liquid. 3% 2C5-dimethyl-1H-pyrrole-2-acetonitrile has a low melting point and is in a liquid state under a relatively low temperature environment. The boiling point is the temperature limit for a substance to change from a liquid state to a gas state. Its boiling point is moderate. Within a certain temperature range, the stability of the liquid state can be maintained and it will not be easily volatilized. The characteristics of this melting point and boiling point are key factors to consider when separating, purifying and storing the compound.
    Solubility is also an important physical property. In common organic solvents, such as ethanol, ether, etc., 3% 2C5-dimethyl-1H-pyrrole-2-acetonitrile exhibits good solubility and can be fused with it. However, in water, its solubility is poor, which determines its application range in different solvent systems. In organic synthesis reactions, organic solvents that are soluble with it are often selected to promote the reaction.
    In terms of density, its density is slightly smaller than that of water. In stratification experiments, it can be seen that it floats on the water surface. This property has practical application value in operations such as mixture separation.
    In addition, 3% 2C5-dimethyl-1H-pyrrole-2-acetonitrile is volatile, and its amount will decrease over time in an exposed environment. However, its volatility is not extremely strong, and it can be effectively stored under appropriate sealing conditions. This volatility also affects its stability and existence in the environment.
    In summary, the physical properties of 3% 2C5-dimethyl-1H-pyrrole-2-acetonitrile, such as appearance, melting point, boiling point, solubility, density, and volatility, are interrelated to determine its application direction and operation mode in the field of organic chemistry, providing an important basis for related research and production practice.
    What are the chemical synthesis methods of 3,5-dimethyl-1H-pyrrole-2-formaldehyde
    To prepare 3% 2C5-dimethyl-1H-pyrrole-2-acetonitrile, there are many methods.
    First, it can be obtained by reacting a compound containing pyrrole structure with halogenated acetonitrile under suitable conditions. First take the pyrrole derivative, place it in a reactor, add an appropriate amount of organic solvent, such as tetrahydrofuran or dichloromethane, and stir well. Then slowly drop into the halogenated acetonitrile, and add an appropriate amount of base, such as potassium carbonate or triethylamine, to promote the reaction. Control the reaction temperature and time. This process needs to be closely monitored. It can be observed by thin-layer chromatography. After the reaction is completed, the target product is obtained through separation and purification steps, such as column chromatography or recrystallization.
    Second, it can also be synthesized from the corresponding aldose, amine and acetonitrile through multi-step reaction. First, the aldehyde and amine undergo a condensation reaction to form an imine intermediate. This reaction needs to be carried out under acidic or basic catalysis, depending on the nature of the aldehyde and amine used. The resulting imine is then reacted with acetonitrile under specific conditions, or with the help of suitable catalysts, such as metal catalysts, to promote its cyclization to form pyrrole rings, and then obtain the target 3% 2C5-dimethyl-1H-pyrrole-2-acetonitrile. After the reaction, it also needs to be separated and purified to remove impurities and obtain a purified product.
    Third, it can also be prepared from simple starting materials by constructing pyrrole rings and introducing acetonitrile groups. For example, using 1,4-dicarbonyl compounds and acetonitrile derivatives as raw materials, under suitable reaction conditions, pyrrole rings are formed by cyclization reaction, and acetonitrile groups are introduced at the same time. During the reaction, specific reagents may be added to regulate the selectivity and rate of the reaction. The final product can be obtained with high purity of 3% 2C5-dimethyl-1H-pyrrole-2-acetonitrile after regular separation and purification.
    In which fields is 3,5-dimethyl-1H-pyrrole-2-formaldehyde used?
    "Tiangong Kaiwu" says: "Dimethyl is a rare thing. It is widely used and has implications in various fields." Dimethyl is used in the chemical industry, mostly as a raw material. For example, the synthesis of various fine chemicals, with its unique structure, can produce a variety of compounds, adding to the chemical industry. In the field of materials, it also has wonderful uses. It can optimize material properties, such as enhancing the stability and flexibility of materials, making materials more suitable for various scenarios, or for construction, or as an auxiliary material for electronic devices. In the field of medicine, it can also be seen. Or participate in the drug synthesis process to help form a specific molecular structure to achieve the desired pharmacological effect, bringing convenience to pharmacies. In agriculture, dimethyl can also play a role. It can be used as a special additive, or it can help crops grow, or it can enhance their resistance to stress, resist the invasion of pests and diseases, and ensure crop yield and quality. All of this shows that Erjia has functions that cannot be ignored in many fields, and it is an important thing in the world.
    What is the market price of 3,5-dimethyl-1H-pyrrole-2-formaldehyde?
    At present, the price of dimethyl-1H-pyrrole-2-acetonitrile in the market is related to many factors.
    Looking at its raw materials, the price of dimethyl, 1H-pyrrole, acetonitrile and other raw materials has a huge impact on its cost. If the raw materials are abundant and the supply is plentiful, the price may be stable and low; if the raw materials are reduced in disaster or the supply is blocked, the price will rise.
    Furthermore, the simplicity of the process is also tied to the price. To prepare this product, if exquisite methods and strict conditions are required, the process cost will be high, and the price will also rise; if the process is refined, labor and materials will be saved, and the cost will be reduced or the price will be lower.
    Market supply and demand is the top priority. If the demand for this product in the pharmaceutical, chemical and other industries is strong, but the output is not enough, the demand exceeds the supply, and the price rises; on the contrary, if the market is weak, the demand is weak, the output is surplus, and the supply exceeds the demand, the price will fall.
    Technological innovation also has an impact. New technologies may improve production and quality, reduce costs, and lead to lower prices; while technical blockade may cause production difficulties and high costs, and prices will rise.
    The price varies from region to region. In areas where the origin of raw materials is close and the transportation is convenient, the logistics cost is low, and the price may be excellent; in remote areas, the logistics is disrupted, and the cost increases and the price is high.
    In summary, the market price of dimethyl-1H-pyrrole-2-acetonitrile varies with factors such as raw materials, processes, supply and demand, technology, and geography. It is difficult to determine the number. It is necessary to observe it in real time and analyze the market situation in detail to know the price.
    What are the storage conditions for 3,5-dimethyl-1H-pyrrole-2-formaldehyde?
    3% 2C5-dimethyl-1H-pyrrole-2-acetonitrile is an extremely rare chemical substance. Its storage conditions are harsh and crucial. A slight poor pool may cause it to deteriorate or deactivate, which may affect subsequent experiments and applications.
    This substance is suitable for storage in a low temperature environment, with the optimal temperature range being -20 ° C to -80 ° C. Low temperature can effectively slow down molecular movement, inhibit chemical reactions, and prolong its shelf life. Due to the increase in temperature, molecular activity will be accelerated, causing it to react with oxygen, moisture and other substances in the air, causing its chemical structure to change, reducing purity and activity.
    At the same time, it is necessary to ensure that the storage environment is dry. Because it has a certain hydrophilicity, it is easy to absorb moisture in the air. The presence of moisture will trigger reactions such as hydrolysis and destroy its chemical structure. Therefore, when storing, it should be placed in a dryer, or a desiccant should be added to maintain a dry environment.
    Furthermore, avoid light. Light may provide energy and induce chemical reactions that lead to material decomposition or structural changes. Therefore, it should be stored in a brown bottle or a container wrapped in aluminum foil and stored in a dark place.
    Caution is also required during access. It should be operated in a protective atmosphere of inert gases such as nitrogen or argon to prevent it from contacting with oxygen and moisture in the air. The equipment must be dry and clean to avoid the introduction of impurities. After each access, quickly seal the container and put it back into the original storage environment. In this way, the stability and purity of 3% 2C5-dimethyl-1H-pyrrole-2-acetonitrile can be guaranteed to meet various scientific research and production needs.