5 Fluoro 2 Methoxy Pyridine 3 Carbaldehyde
pyridine pyrrole pyrazine piperidine piperazine

5-fluoro-2-methoxy-pyridine-3-carbaldehyde

    Specifications

    HS Code

    217681

    Chemical Formula C7H6FNO2
    Molar Mass 155.13 g/mol
    Appearance Solid (Typical for this type of compound)
    Boiling Point Data may vary depending on purity and conditions
    Melting Point Data may vary depending on purity and conditions
    Solubility In Water Low (due to non - polar parts in the molecule)
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
    Density Data may vary depending on conditions
    Flash Point Data may vary depending on purity and conditions
    Pka Data related to the acidic - basic properties may vary

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    General Information
    Where to Buy 5-fluoro-2-methoxy-pyridine-3-carbaldehyde in China?
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    Frequently Asked Questions

    As a leading 5-fluoro-2-methoxy-pyridine-3-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 chemical properties of 5-fluoro-2-methoxy-pyridine-3-carbaldehyde?
    5-Fluoro-2-methoxy-pyridine-3-formaldehyde is a member of the family of organic compounds. Looking at its structure, the fluorine atom, methoxy group and aldehyde group are each based on the specific position of the pyridine ring, and this unique structure endows it with various chemical properties.
    Let's talk about the fluorine atom first, because of its high electronegativity, it can enhance the polarity of the molecule and affect the intermolecular force. Its introduction often improves the stability of the compound, and in the nucleophilic substitution reaction, the fluorine atom in the ortho or para position can change the electron cloud density of the pyridine ring, making the reaction activity and selectivity extraordinary.
    Looking at the methoxy group again, as the power supply group, it will increase the electron cloud density of the pyridine ring, especially in the ortho and para-sites. This not only affects the electrophilic substitution activity of the compound, but also makes the reaction check point tend to be methoxy ortho and para-sites. The existence of the
    aldehyde group endows this compound with typical aldehyde chemical properties. It is very active, easy to participate in oxidation reactions, and can be oxidized to carboxyl groups; and it can react with alcohols under suitable conditions to form acetals, which are often used to protect aldehyde groups. At the same time, aldehyde groups can undergo nucleophilic addition reactions with ammonia and its derivatives to generate products such as oxime and hydrazone.
    In the field of organic synthesis, 5-fluoro-2-methoxy-pyridine-3-formaldehyde is often used as a key intermediate to construct more complex organic molecules due to its rich reaction check point and unique properties. It has important application potential in many fields such as medicinal chemistry and materials science.
    What are the common synthetic methods of 5-fluoro-2-methoxy-pyridine-3-carbaldehyde?
    The synthesis of 5-fluoro-2-methoxy-pyridine-3-formaldehyde is common. First, fluoropyridine is used as the starting material, and the order is methoxylated and formylated. First, take the appropriate fluoropyridine, under specific reaction conditions, cowarm with a methoxylating agent, such as potassium carbonate as a base, in a polar solvent such as N, N-dimethylformamide, react with a methylating agent, so that the fluorine atom is replaced by a methoxy group to obtain 2-methoxy-fluoropyridine. After the introduction of formyl group by the Wilsmeier-Hack reaction, the intermediate is mixed with dimethylformamide and phosphorus oxychloride, heated, and hydrolyzed to obtain the target 5-fluoro-2-methoxy-pyridine-3-formaldehyde.
    Second, starting from the pyridine derivative, the methoxy group and the pyridine ring are first constructed, and then the fluorine atom and the formyl group are introduced. With suitable pyridine derivatives, methoxylated to obtain 2-methoxy pyridine derivatives, and then halogenated to introduce fluorine atoms by nucleophilic substitution or electrophilic substitution, and then formylated. Under the catalyst of copper salt, 5-fluoro-2-methoxy-pyridine-3-formaldehyde can be obtained by the reaction of carbon monoxide and suitable reagents.
    Another heterocyclic construction method is used to construct pyridine rings from simple raw materials and introduce methoxy groups, fluorine atoms and formyl groups at the same time. For example, small molecules containing fluorine and methoxy groups are used to form pyridine rings through multi-step cyclization reactions under the action of condensing agents and catalysts to obtain 5-fluoro-2-methoxy-pyridine-3-formaldehyde. These methods have their own advantages and disadvantages, and they need to be carefully selected according to the availability of raw materials, reaction conditions, yield and purity requirements.
    In what areas is 5-fluoro-2-methoxy-pyridine-3-carbaldehyde applied?
    5-Fluoro-2-methoxy-3-pyridine-formaldehyde is an organic compound. It has extraordinary applications in the fields of medicinal chemistry, materials science, etc.
    is often used as a key intermediate in the field of medicinal chemistry. Taking the synthesis of specific targeted drugs as an example, its unique chemical structure can be cleverly designed to be spliced with other molecules. Due to the existence of pyridine rings and aldehyde groups, it can participate in various chemical reactions. For example, aldehyde groups can undergo condensation reactions with amine compounds to construct nitrogen-containing heterocyclic structures. This structure is common in many drug molecules and is of great significance for regulating drug activity and enhancing affinity with targets.
    Materials science category, or can be used to prepare special functional materials. With its structural properties, it can be used as a building unit to form materials with specific photoelectric properties through polymerization or cross-linking reactions. For example, the introduction of fluorine atoms and methoxy groups, or the change of intermolecular forces and electron cloud distribution of materials, endow materials with unique electrical and optical properties, and show potential in the preparation of organic Light Emitting Diode (OLED) or sensor materials.
    Furthermore, in the field of organic synthetic chemistry, it is an important starting material for the synthesis of complex organic molecules. Through a series of organic reactions, such as nucleophilic addition and nucleophilic substitution, rich carbon-carbon and carbon-heteroatom bonds can be constructed, and the molecular structure complexity can be expanded, which lays the foundation for the synthesis of organic compounds with specific functions and structures.
    What is the market price of 5-fluoro-2-methoxy-pyridine-3-carbaldehyde?
    I don't know what the market value of 5-fluoro-2-methoxy-pyridine-3-carbalaldehyde is. However, if you want to estimate it, you need to consider all factors.
    First, the degree of this product is of paramount importance. If the degree of production is high, it will be necessary for high-end applications such as refined synthesis or chemical research; if the degree of production is low, it can be used for general industrial purposes, and the cost will be low.
    Furthermore, the ease of production also affects the price. If the synthesis is slow and complex, special raw materials or reverse parts are required, the cost will be high, and the market will also rise; if the production is slow, the cost will be controllable, and the cost will be reduced.
    In addition, the situation of supply and demand in the market also affects the market. If the demand is strong and the supply is limited, the merchant will offer high profits; if the market is in harmony, the supply is in demand, and the price will drop.
    In addition, the price is also different from the family. Well-known big brands, due to factors such as brand reputation, quantity control, etc., the price of the product may be high; while small families and cities, the price or more people.
    However, I have not yet obtained the price, and what is the market. To know the quality, you can use chemical raw material suppliers, check the chemical trading platform, or test the recent market conditions to get the price.
    What are 5-fluoro-2-methoxy-pyridine-3-carbaldehyde storage conditions?
    5-Fluoro-2-methoxy-pyridine-3-formaldehyde is an organic compound whose storage conditions are critical. This compound should be stored in a cool, dry and well-ventilated place. Because it is sensitive to light and heat, it should be avoided in light and high temperature environments to prevent decomposition and deterioration.
    When storing, make sure that the container is tightly sealed to prevent contact with air, moisture and other substances. Because moisture may cause hydrolysis reactions, and oxygen in the air may also oxidize the compound, which in turn affects its quality and purity.
    Furthermore, in view of the toxicity and irritation of this compound, it is necessary to keep away from fire, heat and incompatible substances during storage to prevent dangerous reactions. When using this compound, it is also necessary to follow relevant safety operating procedures, such as wearing appropriate protective equipment.
    In addition, in order to ensure the stability of its quality, it is recommended to set a suitable storage period according to its characteristics and the manufacturer's suggestion, and regularly conduct quality inspections. In this way, it is possible to ensure that 5-fluoro-2-methoxy-pyridine-3-formaldehyde maintains good quality during storage for subsequent use.