4 Formyl 2 Methoxypyridine
pyridine pyrrole pyrazine piperidine piperazine

4-formyl-2-methoxypyridine

    Specifications

    HS Code

    750094

    Name 4-formyl-2-methoxypyridine
    Molecular Formula C7H7NO2
    Molecular Weight 137.14 g/mol
    Appearance Off - white to light yellow solid
    Melting Point 48 - 52 °C
    Boiling Point 254 - 256 °C
    Solubility In Water Slightly soluble
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, dichloromethane
    Density 1.17 g/cm³
    Flash Point 115.6 °C
    Pka ~12.7 (for the pyridine nitrogen)

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    General Information
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    Frequently Asked Questions

    As a leading 4-formyl-2-methoxypyridine 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 4 - formyl - 2 - methoxypyridine
    4-Formyl-2-methoxypyridine is an organic compound with unique chemical properties. It contains formyl (-CHO) and methoxy (-OCH) groups at specific positions in the pyridine ring, and its structure endows it with a variety of chemical activities.
    The formyl group has high activity and can participate in many reactions. It can undergo oxidation reactions. If it encounters strong oxidants, it can be oxidized to carboxyl groups (-COOH) to form 4-carboxyl-2-methoxypyridine. This reaction is commonly used in the preparation of carboxyl-containing pyridine derivatives in organic synthesis. The reduction reaction can also be carried out. If a suitable reducing agent is used, the formyl group can be reduced to hydroxymethyl (-CH 2O OH) to obtain 4-hydroxymethyl-2-methoxypyridine. This product is an important intermediate in the preparation of alcohol hydroxypyridine compounds.
    Formyyl groups are also prone to condensation reactions with active hydrogen-containing compounds. For example, by reacting with amines, Schiff bases can be formed, which is widely used in the synthesis of nitrogen-containing heterocyclic compounds, because Schiff bases often have biological activity and coordination ability.
    Methoxy groups have an effect on the electron cloud distribution of the pyridine ring, which changes the electron cloud density of the pyridine ring and affects its electrophilic substitution activity and selectivity. Generally speaking, methoxy groups are the power supply groups, which will increase the electron cloud density of the pyridine ring, making the electrophilic substitution reaction more likely to occur, and the substituents often enter the pyridine ring and are in a suitable position with the methoxy group, such as the ortho-methoxy group or the para-position (due to the electron-absorbing action of the formyl group, it will have a certain impact on the selection of the electrophilic substitution position, and the specific substitution position will be determined by combining the two effects).
    4-formyl-2-methoxy pyridine is widely used in many fields such as medicine, In the field of medicine, it can be used as a key intermediate for the synthesis of specific biologically active drug molecules; in the field of materials, organic materials with special properties can be prepared through related reactions.
    What are the common synthesis methods of 4 - formyl - 2 - methoxypyridine
    4-formyl-2-methoxypyridine is also a key intermediate in organic synthesis. There are three common synthesis methods, as described below.
    One is chemical oxidation. Using 2-methoxypyridine as the initial raw material, with the power of oxidants, such as mild manganese dioxide or strong chromic acid, under suitable reaction conditions, the 4-methyl group of the pyridine ring is gradually oxidized to an aldehyde group. In this process, the properties of the solvent, the control of temperature, and the time of reaction are all critical. If dichloromethane is used as the solvent, the temperature is controlled near room temperature, and the oxidant is slowly added dropwise, a high yield can be obtained. However, the oxidizing agent may be toxic and corrosive, and the post-processing is complicated, so it needs to be handled with caution.
    The second is metal catalysis. Transition metals are used as catalysts, such as palladium and rhodium, and ligands are complemented to make formyl-containing reagents couple with 2-methoxypyridine. In this case, the structure of the ligand has a great influence on the selectivity and activity of the reaction. For example, 4-formyl-2-methoxypyridine can be precisely obtained by reacting with formylating reagents at a suitable temperature in the presence of a base with the participation of bipyridine ligands. This method has mild conditions and good selectivity. However, metal catalysts are expensive and difficult to recycle and reuse.
    The third is biosynthesis. Using the catalytic properties of biological enzymes, enzymes have high selectivity and mild reaction conditions. For example, some aldehyde transferases can catalyze substrates to generate target products in specific environments in vivo or in mild environments simulated in vitro. Although biosynthesis is green and environmentally friendly, the extraction and purification of enzymes is not easy, and the reaction system is complex. Industrialization will take time.
    Where is 4 - formyl - 2 - methoxypyridine used?
    4-formyl-2-methoxypyridine is useful in various fields. In the field of medicinal chemistry, it is a key building block for organic synthesis. It can be combined with other compounds through ingenious chemical reactions to create drug molecules with unique structures and specific functions. The chemical activity check point of this compound can be precisely combined with specific targets in organisms, so in the process of drug development, it provides broad possibilities for finding new drugs with high efficiency and low toxicity.
    In the field of materials science, 4-formyl-2-methoxypyridine also has extraordinary performance. It can participate in the synthesis of polymers and endow materials with novel physical and chemical properties. For example, by polymerizing with specific monomers, the resulting polymers may have excellent optical and electrical properties, which are suitable for frontier fields such as optoelectronic devices and sensors. Its special molecular structure can introduce a unique electron cloud distribution to the material, affecting key parameters such as conductivity and fluorescence of the material.
    Furthermore, in the field of organic synthesis chemistry, 4-formyl-2-methoxy pyridine is used as a reaction substrate to participate in a variety of classic organic reactions. Such as condensation reactions, addition reactions, etc., with its formyl and methoxy activities, it can build a complex and diverse organic molecular skeleton. Chemists can use this to expand the structural diversity of organic compounds, contribute to the development of organic synthetic chemistry, and promote the exploration and innovation of new reactions and methods.
    What is the market price of 4 - formyl - 2 - methoxypyridine
    I don't know the market value of 4-formyl-2-methoxypyridine. This compound may be due to demand, quantity, availability, and cost of raw materials. If you want to find it, you can explore it.
    First, the trading of chemical raw materials is flat. This market is a collection of multiple suppliers and suppliers, and the price or quantity, quality, and supplier can be tested.
    Second, chemical suppliers. Multi-chemical raw material suppliers are available for sale, and can sell their specific quantities, 4-formyl-2-methoxypyridine, and can be purchased in batches due to long-term cooperation.
    Third, the research and development of the city will be announced. The chemical industry has worked hard to research the market, and the supply and demand of specific compounds will not change, which can help determine the direction of their performance.
    In addition, if you want to know the market value of 4-formyl-2-methoxypyridine, it is appropriate to combine multiple paths and consider various factors in order to obtain a comprehensive solution.
    What are the storage conditions for 4 - formyl - 2 - methoxypyridine
    4-Formyl-2-methoxypyridine is an organic compound. The storage conditions are crucial and related to the stability and quality of this substance.
    Cover 4-formyl-2-methoxypyridine is active and easy to react with surrounding substances, so it is necessary to choose a suitable storage. First, when placed in a cool place, away from direct sunlight. Hot sunlight can promote photochemical reactions, causing structural changes and damaging its inherent properties. And if the temperature is too high, the molecular movement will intensify, and it is easy to cause decomposition or deterioration. Therefore, storing in a cool place can reduce this risk. < Br >
    Second, it should be placed in a dry place. Water vapor in the air is easy to interact with 4-formyl-2-methoxypyridine. Or hydrolysis, or participation in other reactions, can damage its purity and efficiency. Therefore, if it is stored in a dry environment, it can be protected from water vapor.
    Furthermore, this substance should be sealed and stored. It is volatile and easy to react with oxygen and other components in the air. The sealed device can isolate the outside air to prevent the disaster of volatilization and oxidation.
    If stored in a cool, dry, and sealed manner, 4-formyl-2-methoxypyridine can retain its properties for a long time, ready for scientific research and production, without losing its original characteristics and effectiveness. It can also be used in organic synthesis and other fields.