3 Fluoro 5 Methoxypyridine 4 Carbaldehyde
pyridine pyrrole pyrazine piperidine piperazine

3-Fluoro-5-Methoxypyridine-4-carbaldehyde

    Specifications

    HS Code

    822265

    Name 3-Fluoro-5-methoxypyridine-4-carbaldehyde
    Molecular Formula C7H6FNO2
    Molecular Weight 155.13

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    General Information
    Where to Buy 3-Fluoro-5-Methoxypyridine-4-carbaldehyde in China?
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    Frequently Asked Questions

    As a leading 3-Fluoro-5-Methoxypyridine-4-carbaldehyde 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 3-Fluoro-5-Methoxypyridine-4-carbaldehyde?
    3-Fluoro-5-methoxypyridine-4-formaldehyde, which has a wide range of uses, is an important intermediate in organic synthesis in the field of medicinal chemistry.
    In the creation of new drugs, its key role is obvious. In the process of many drug research and development, this is the starting material, and with the help of delicate organic synthesis reactions, a molecular structure with specific biological activities can be built. Due to the unique chemical properties of pyridine and aldehyde groups, complex drug molecules can be constructed through various functional group conversion reactions, such as oxidation, reduction, condensation, etc. For example, when developing antibacterial drugs, using their structural characteristics, specific groups are introduced to synthesize new compounds that have inhibitory effects on pathogenic bacteria, injecting vitality into pharmaceutical innovation. < Br >
    In the field of materials science, it also has outstanding performance. It can be used as a basic unit for the construction of functional materials. With the synergy effect of fluorine atoms, methoxy groups and aldehyde groups, it can give novel properties to materials by compounding or reacting with other organic or inorganic materials. For example, when preparing photoelectric functional materials, they are integrated into the material system through specific reactions to improve the electronic transport properties of the materials, thereby enhancing the application efficiency of the materials in optoelectronic devices, such as organic Light Emitting Diodes (OLEDs), solar cells and other fields.
    In the field of fine chemicals, it is also indispensable. It can be used to synthesize high-value-added fine chemicals, such as special fragrances, dyes and auxiliaries. With its unique structure, it endows fine chemicals with unique properties and functions. Such as synthesizing fragrances with special flavors, or preparing dyes with excellent dyeing properties for specific fibers, helping fine chemical products to develop into high-end and differentiated products.
    What are 3-Fluoro-5-Methoxypyridine-4-carbaldehyde synthesis methods?
    There are various ways to synthesize 3-fluoro-5-methoxypyridine-4-formaldehyde. First, the compound containing the pyridine structure can be used as the starting material and converted in multiple steps. If the pyridine derivative is properly substituted, the fluorine atom is introduced at a specific position in the pyridine ring first, which can be done by means of nucleophilic substitution reaction or halogenation reaction. Under suitable conditions, the fluorine-containing reagent is reacted with the pyridine substrate to control the reaction temperature, time and reagent dosage, so that the fluorine atom is precisely connected to the required check point.
    Then, the methoxy group is introduced. Methoxylating reagents, such as sodium methoxide, dimethyl carbonate, etc., are often used to react with pyridine derivatives in an alkaline environment or under the action of a phase transfer catalyst, so that the methoxy group replaces the group at a specific position, and then the fluorine-containing and methoxy-containing pyridine intermediates are obtained.
    As for the introduction of aldehyde groups, a mild oxidation method can be used. If the pyridine intermediate has oxidizable groups, such as alcohol hydroxyl groups, etc., the alcohol hydroxyl group is oxidized to the aldehyde group by a suitable oxidizing agent, such as Dass-Martin oxidizing agent (DMP), in an organic solvent, at low temperature, and this oxidizing agent has good selectivity and does not affect the fluorine and methoxy groups on the pyridine ring.
    Or, in another strategy, the pyridine ring is first constructed, and then fluorine, methoxy and aldehyde groups are introduced in sequence. Pyridine rings can be formed by cyclization of small molecules containing nitrogen and carbon, and then each substituent is introduced step by step according to the above similar method. Such various synthesis methods need to be weighed according to various factors such as the availability of raw materials, the difficulty of reaction conditions, the purity and yield of the product, so as to achieve the purpose of efficient synthesis of 3-fluoro-5-methoxy pyridine-4-formaldehyde.
    What are the physical properties of 3-Fluoro-5-Methoxypyridine-4-carbaldehyde?
    3-Fluoro-5-methoxypyridine-4-formaldehyde is an organic compound. Its physical properties are crucial and indispensable in chemical research and practical applications.
    Looking at its appearance, under room temperature and pressure, it is mostly colorless to light yellow liquid, or white to light yellow crystalline powder. This appearance feature can provide an intuitive basis for identifying the substance.
    Melting point is about a specific temperature range, but the exact value may vary slightly due to different experimental conditions. The determination of melting point is often done by means of thermal analysis, such as differential scanning calorimetry. This parameter is of great significance for determining the purity and stability of the substance. For those with high purity, the melting point range is narrow and close to the theoretical value; if there are many impurities, the melting point is reduced and the melting range is widened.
    In terms of boiling point, it also has specific values. The determination of boiling point requires precise control of pressure conditions and is mostly carried out under standard atmospheric pressure. The boiling point data is of great significance for the separation and purification of substances. Separation techniques such as distillation are realized according to the difference in boiling points of different substances.
    In terms of solubility, 3-fluoro-5-methoxypyridine-4-formaldehyde behaves differently in organic solvents. Common organic solvents such as ethanol, ether, dichloromethane, etc., have good solubility to them. Due to intermolecular forces, the substance can interact with these organic solvent molecules to form hydrogen bonds or van der Waals forces. In water, its solubility is relatively limited, because the molecular structure of hydrophilic groups accounts for a small proportion, and the hydrophobic part affects its interaction with water molecules.
    density is also an important physical property, reflecting the mass of the substance per unit volume. Density determination mostly uses the pictogram method, etc. Accurate density data is of great significance for quantitative analysis of substances and chemical production material ratio.
    In addition, the substance is volatile to a certain extent and will evaporate slowly at room temperature. This characteristic needs to be taken into account when storing and using, and should be properly sealed to prevent volatilization loss and impact on the environment and people.
    In summary, the physical properties of 3-fluoro-5-methoxypyridine-4-formaldehyde, such as appearance, melting point, boiling point, solubility, density and volatility, are all key parameters in chemical research, chemical production and related fields. In-depth understanding will help to better control and use this substance.
    What are the chemical properties of 3-Fluoro-5-Methoxypyridine-4-carbaldehyde?
    3-Fluoro-5-methoxypyridine-4-formaldehyde is one of the organic compounds. Its chemical properties are unique and contain many characteristics.
    This compound has an aldehyde group with high aldehyde activity and can participate in many reactions. For example, in a typical oxidation reaction, under the action of an appropriate oxidant, the aldehyde group can be oxidized to a carboxyl group, which can then be converted into 3-fluoro-5-methoxypyridine-4-carboxylic acid. This reaction process is like a metamorphosis of a substance, and the aldehyde group is "baptized" by oxidation and converted into a carboxyl group, and the chemical structure and properties are also changed accordingly.
    At the same time, the aldehyde group can also undergo a reduction reaction. With the help of the reducing agent, it can be reduced to the alcohol hydroxyl group, which is changed to 3-fluoro-5-methoxypyridine-4-methanol. This is the conversion from aldehyde to alcohol, which is like a "transformation", and the chemical activity and physical properties are different.
    Furthermore, the fluorine atom and methoxy group in this compound also have special chemical properties. The strong electronegativity of fluorine atoms will affect the distribution of molecular electron clouds, causing the polarity of molecules to change, which in turn affects their physical properties and reactivity. The methoxy group, as the power supply group, can increase the electron cloud density of the pyridine ring, and in the electrophilic substitution reaction, it will affect the reaction check point and reactivity. For example, in the electrophilic substitution reaction, the power supply action of the methoxy group will guide the electrophilic reagent to attack the specific position of the pyridine ring, showing a unique reaction selectivity.
    The pyridine ring in this compound, as a nitrogen-containing heterocycle, has a certain alkaline nature and can react with acids to form salts. Because there are lone pairs of electrons on the nitrogen atom, it can accept protons, which is the source of its alkalinity. Pyridine rings can also participate in various reactions on the ring, such as nucleophilic substitution, electrophilic substitution, etc. These reactions lay the foundation for the derivation Many chemical properties are intertwined to form a unique chemical "picture" of 3-fluoro-5-methoxypyridine-4-formaldehyde, which has important application value and research significance in organic synthesis and other fields.
    What is the price range of 3-Fluoro-5-Methoxypyridine-4-carbaldehyde in the market?
    I have not heard the exact price of 3-fluoro-5-methoxypyridine-4-formaldehyde in the market. However, if you want to measure the range of its price, you can consider various things.
    First, the source of the material and the difficulty of obtaining it. If the raw materials are easy to buy, it is not difficult to make, and the quantity is sufficient, the price may not be high. On the contrary, if the raw materials are rare, difficult to make, or special methods and utensils are required, the price will be high.
    Second, the amount you want. If there is a lot of demand for this product in the chemical, pharmaceutical and other industries, the supply is not enough, and the price will also rise. If there is a shortage of those who need it, the supply will exceed the demand, and the price will drop. < Br >
    Third, the method of system. The method of high efficiency and low cost can reduce the cost, and the price is also low. The method of extravagance and expense makes the cost increase and the price increase.
    Fourth, the competition in the city. If there are many of these, the competition is intense, and it is for customers, or the price is reduced. There are few camp owners, and there is a appearance of a ridge, the price is controllable and high.
    Overall, the price of 3-fluoro-5-methoxypyridine-4-formaldehyde varies from tens to hundreds of yuan per gram, but this is only an idea. The actual price needs to be carefully examined by market conditions and consulted by businesspeople.