4 Fluoro 2 Pyridinecarbonitrile
pyridine pyrrole pyrazine piperidine piperazine

4-Fluoro-2-pyridinecarbonitrile

    Specifications

    HS Code

    261194

    Chemical Formula C6H3FN2
    Molar Mass 122.099 g/mol
    Appearance Typically a solid
    Physical State At Room Temp Solid
    Solubility In Water Low solubility
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane
    Stability Stable under normal conditions, avoid strong oxidizing agents

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    General Information
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    Frequently Asked Questions

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    What is the chemistry of 4-Fluoro-2-pyridinecarbonitrile?
    4-Fluoro-2-pyridinecarbonitrile, or 4-fluoro-2-pyridylmethonitrile, is one of the organic compounds. Its chemical properties are unique and have attracted much attention in the field of organic synthesis.
    In this compound, fluorine atoms and cyanyl groups are attached to the pyridine ring. The pyridine ring is aromatic, which endows the compound with certain stability. Fluorine atoms have high electronegativity, which can affect the electron cloud distribution of molecules by inducing effects, causing the density of adjacent and para-electron clouds to change, which in turn affects the reactivity.
    4-fluoro-2-pyridylmethonitrile can participate in a variety of chemical reactions. One is the nucleophilic substitution reaction. Due to the high activity of fluorine atoms, it is easy to be replaced when encountering nucleophilic reagents. For example, when reacting with sodium alcohol, fluorine atoms can be replaced by alkoxy groups to generate corresponding ether derivatives. This reaction condition usually needs to be carried out under the catalysis of appropriate organic solvents and bases.
    Second, cyanyl groups are active and can undergo many reactions. If hydrolyzed under acidic or alkaline conditions, cyanyl groups can be converted into carboxyl groups to generate 4-fluoro-2-pyridinecarboxylic acid; they can also be reduced to amino groups under the action of reducing agents to obtain 4-fluoro-2-aminopyridine. These reactions are of great significance in the field of drug synthesis and other fields.
    In addition, the hydrogen atoms on the pyridine ring can undergo electrophilic substitution reactions such as halogenation and nitrification under specific conditions. Due to the influence of fluorine atoms and cyanyl groups, the reaction check points are mainly concentrated at specific locations of the pyridine ring.
    4-fluoro-2-pyridylmethonitrile plays a key role in organic synthesis, drug development and other fields due to its unique chemical properties, providing an important basis for the creation of new organic compounds and drugs.
    What are 4-Fluoro-2-pyridinecarbonitrile synthesis methods?
    The synthesis method of 4-fluoro-2-pyridyl methanonitrile has been used by many parties throughout the ages. First, the compound containing the pyridine ring is used as the starting material, and fluorine atoms are introduced after a halogenation reaction. This process requires fine control of the reaction conditions, such as temperature, reagent ratio, etc. When halogenating, a suitable halogenating reagent, such as a fluorine-containing halogen, can precisely replace the hydrogen atom at a specific position to obtain a fluorine-containing pyridyl intermediate. Subsequently, the cyanide group is introduced through a cyanidation reaction. This step requires the help of a specific catalyst to improve the reaction efficiency and selectivity, and finally achieve 4-fluoro-2-pyridyl methanonitrile.
    Second, fluorine-containing and pyridine structural fragments are used as starting materials, and they are cleverly spliced through coupling reaction. In this path, the coupling reaction conditions are very critical, including the type and amount of reaction solvent, base, etc. Carefully select suitable coupling reagents and catalysts to efficiently connect fluorine-containing fragments with pyridine-containing fragments, and then synthesize the target product.
    In addition, pyridine derivatives are used as starting materials, and cyanylation is first carried out, and then fluoridation is carried out. When cyanylation, appropriate cyanide reagents and reaction conditions are selected to ensure the smooth introduction of cyanide groups. The fluorination step also needs to be careful, and the appropriate fluorination reagent and reaction environment should be selected to replace the fluorine atoms according to the expected position to achieve the synthesis of 4-fluoro-2-pyridyl formonitrile.
    Synthesis methods have their own advantages and disadvantages, and need to be selected according to the actual situation, such as raw material availability, cost, reaction difficulty and other factors, in order to obtain this compound efficiently.
    4-Fluoro-2-pyridinecarbonitrile in what areas
    4-Fluoro-2-pyridinecarbonitrile, which translates to 4-fluoro-2-pyrimethanonitrile, has wonderful uses in various fields.
    In the field of medicinal chemistry, it is the key raw material for the synthesis of many special drugs. Due to its unique chemical structure, it can introduce drug molecules and endow drugs with specific biological activities and pharmacological properties. For example, when developing targeted drugs for specific diseases, 4-fluoro-2-pyrimethanonitrile can precisely bind to the target of diseased cells, enhance the efficacy of drugs, and reduce the damage to normal cells, just like good medicine, precise treatment, medicine to cure the disease.
    In the field of materials science, it has also emerged. New polymer materials can be constructed through specific chemical reactions. These materials may have excellent electrical and optical properties and are suitable for the preparation of advanced electronic devices, such as high-efficiency Light Emitting Diodes, sensitive sensors, etc. Just like the selection of materials by craftsmen, they are based on them to create exquisite instruments and shine at the forefront of science and technology.
    In the field of pesticide research and development, 4-fluoro-2-pyridinetrile also plays an important role. It can be used as an important intermediate for the synthesis of high-efficiency and low-toxicity pesticides. The prepared pesticides can effectively kill pests, while reducing environmental pollution and impact on non-target organisms. Just like a farmer treating insects, it not only ensures a good harvest of crops, but also protects ecological harmony.
    In addition, in the field of organic synthetic chemistry, it is often used as a key building block to participate in the construction of complex organic molecules. Chemists use its unique reactivity to synthesize organic compounds with various novel structures and functions through ingenious design and regulation of reaction conditions, which continuously injects new vitality into the development of organic synthetic chemistry. Just like the literati, they use it as ink to paint a brilliant picture of organic chemistry.
    What is the market price of 4-Fluoro-2-pyridinecarbonitrile?
    4-Fluoro-2-pyridineformonitrile, this product is in the market, and its price often changes for many reasons.
    First, it is related to output. If the production is abundant and the market supply is abundant, the price may become more affordable; if the production is scarce, the demand exceeds the supply, and the price will rise. Second, the price of raw materials is also a major factor. The production requires specific raw materials. If the price of raw materials increases, the cost of this product will increase, and the market price will rise accordingly. On the contrary, the price of raw materials may decrease, and the price may also decrease. Furthermore, the progress of technology also affects its price. If the new production method can reduce consumption and improve production, reduce its cost, and the price may change accordingly.
    Looking at past transactions, the state of price fluctuations varies with the changes of the above factors. At certain times, due to the increase in production or the decrease in raw material prices, the price can be as low as [X] yuan per unit; however, at other times, due to the scarcity of raw materials, technical bottlenecks, etc., the price may be as high as [Y] yuan per unit.
    Merchants in the market often set different prices according to changes in the market and their own cost considerations. Therefore, if you want to know the exact price, you can consult various suppliers or observe the details of recent market transactions to get a price close to the actual situation.
    What are 4-Fluoro-2-pyridinecarbonitrile storage conditions?
    4-Fluoro-2-pyrimethonitrile is also an organic compound. Its storage conditions are crucial, related to the stability and quality of this substance.
    Cover this substance should be stored in a cool, dry and well ventilated place. In a cool place, the temperature should not be too high. If it is too high, it is easy to cause the compound to undergo thermal decomposition or accelerate its chemical reaction, which will damage its original chemical structure and properties. Therefore, it is usually appropriate to not exceed 30 ° C. It can be placed in a warehouse with temperature control, or in an ordinary warehouse with air conditioning to adjust the temperature.
    Drying is also the key. If this substance encounters water vapor, or reacts such as hydrolysis, the quality will deteriorate. It is necessary to avoid moisture in the storage place, and a desiccant can be placed next to it, such as calcium chloride, silica gel, etc., to absorb water vapor in the air and keep the environment dry.
    Good ventilation is indispensable. If the storage space is closed, the accumulation of volatile gas from the compound will increase the risk of fire and explosion, and the second is the accumulation of gas or interaction with the compound, which will affect its stability. Therefore, the warehouse should be equipped with ventilation equipment to ensure air circulation.
    And when stored, it should be separated from oxidants, acids, alkalis, etc. These substances may react chemically with 4-fluoro-2-pyridinonitrile, causing danger. In a special container, it is tightly sealed to prevent leakage and contact with air and water vapor. The material of the container must also be carefully selected and should not react with the compound, such as glass or specific plastic materials, depending on the specific properties of the compound. In short, the stability and safety of 4-fluoro-2-pyridinonitrile can be maintained by storing under these conditions.