Quinoline 8 Carboxaldehyde
quinoline thiophene imidazole thiazole

Quinoline-8-carboxaldehyde

Taiy Chemical

    Specifications

    HS Code

    332931

    Chemical Formula C10H7NO
    Molar Mass 157.17 g/mol
    Appearance Yellow to orange solid
    Melting Point 59 - 61 °C
    Boiling Point 145 - 147 °C at 10 mmHg
    Solubility Soluble in organic solvents like ethanol, dichloromethane
    Flash Point 129.7 °C
    Refractive Index N/A (solid, refractive index usually for liquids)
    Pka N/A (no acidic or basic hydrogens for simple pKa determination in common sense)
    Odor Characteristic organic odor

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    General Information
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    Frequently Asked Questions

    As a leading Quinoline-8-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 is the chemistry of Quinoline-8-carboxaldehyde?
    Quinoline-8-formaldehyde is a class of organic compounds. It is active and has a wide range of uses in the field of organic synthesis.
    This compound has the structure of an aldehyde group and a quinoline ring. The aldehyde group has the properties of a typical aldehyde group. It can react with nucleophiles, and if it is catalyzed by acids with alcohols, it will form acetals. This reaction is often used when protecting aldehyde groups or building complex organic molecules. And aldehyde groups can be oxidized, weak oxidants such as Toran reagent can oxidize them to carboxylic acids, and strong oxidants are even more serious.
    Quinoline ring also has properties. Its aromaticity gives the compound a certain stability. However, due to the characteristics of electron cloud distribution on the ring, electrophilic substitution reactions can occur at specific positions of the quinoline ring. Under appropriate conditions, halogenation, nitrification, sulfonation and other reactions can be carried out, providing a way for the introduction of different functional groups, and then derived a variety of derivatives.
    And because of its unique structure, quinoline-8-formaldehyde can participate in a variety of cyclization reactions to construct more complex multi-ring systems. This is of great significance in the fields of pharmaceutical chemistry and materials science. Because it can be used as a key intermediate to synthesize drug molecules with specific biological activities or to prepare materials with special properties. In short, quinoline-8-formaldehyde occupies an indispensable position in the fields of organic chemistry due to its special chemical properties.
    What are the main uses of Quinoline-8-carboxaldehyde?
    Quinoline-8-formaldehyde, this substance has a wide range of uses. In the field of medicine, it is a key raw material for the synthesis of many special drugs. Due to its unique chemical structure, it can precisely fit with biomolecules in the body. After ingenious modification and synthesis steps, it can produce various drugs such as antibacterial, anti-inflammatory and anti-tumor, which play an important role in healing diseases.
    In the field of materials science, it also has great value. It can participate in the synthesis of organic Light Emitting Diode (OLED) materials, endowing the materials with excellent optical properties, improving their luminous efficiency and stability, and helping display technology move towards a new level. At the same time, in the preparation of special functional polymer materials, quinoline-8-formaldehyde can be used as a key monomer to build a new polymer structure through polymerization reaction, endowing the material with specific properties such as fluorescence and adsorption, and showing its talents in sensors, separation membranes and other fields.
    In the field of organic synthesis chemistry, quinoline-8-formaldehyde often acts as an important intermediate. With its aldehyde group and quinoline ring activity, it can use a variety of organic reactions, such as condensation, addition, etc., to derive organic compounds with complex structures and specific functions, which greatly enriches the variety of organic compounds and contributes to the development of organic synthesis chemistry.
    What are Quinoline-8-carboxaldehyde synthesis methods?
    There are many different methods for synthesizing quinoline-8-formaldehyde. One method can also start from 8-hydroxyquinoline. First, 8-hydroxyquinoline reacts with halogenated alkanes in an alkaline environment to generate the corresponding 8-alkoxy quinoline. This reaction requires the selection of an appropriate base, such as potassium carbonate, in a suitable solvent, such as acetonitrile, etc., heating and refluxing for several hours, to obtain 8-alkoxy quinoline with a higher yield.
    The next time, 8-alkoxy quinoline is treated with a suitable oxidizing agent. Common, such as selenium dioxide, in an inert solvent, such as dichloromethane, heating reaction. In this process, selenium dioxide oxidizes the methyl group of the alkoxy ortho-position to an aldehyde group to obtain quinoline-8-formaldehyde. After the reaction is completed, the purified product can be obtained by column chromatography.
    Another method uses quinoline as the starting material. First, quinoline is lithiated, often with a reagent such as n-butyl lithium, at a low temperature, such as minus 70 to 80 degrees Celsius, in an anhydrous and oxygen-free environment, the 8-position of quinoline is introduced into the lithium atom. Then, with dimethylformamide, this step can connect the lithiated quinoline 8-position to a formyl group, thereby generating quinoline-8-formaldehyde. After the reaction is completed, the target product can be obtained through various post-treatment steps such as acidification, extraction, drying, and distillation.
    Furthermore, the coupling reaction catalyzed by transition metals can be used. For example, 8-halogenated quinoline and formaldehyde derivatives, such as methyl formate, are heated in an organic solvent in the presence of a palladium catalyst, such as tetra (triphenylphosphine) palladium, and suitable ligands and bases. This reaction can selectively introduce an aldehyde group at the 8-position of quinoline, and after subsequent separation and purification operations, quinoline-8-formaldehyde can also be obtained.
    Quinoline-8-carboxaldehyde What are the precautions in storage and transportation?
    Quinoline-8-formaldehyde is an important compound in organic chemistry. When storing and transporting, many matters must be paid attention to.
    Bear the brunt, the storage place should be dry and cool. This is because quinoline-8-formaldehyde is active, and it is easy to deteriorate if it is in a humid and warm place. For example, humid gas can cause it to hydrolyze, warm environment, or promote chemical reactions, which will damage its purity and quality. Therefore, choose a dry and cool place, such as a cool warehouse, and hold it in a glass or ceramic container, tightly sealed to prevent moisture from invading.
    Furthermore, during transportation, shock resistance and collision prevention are essential. This compound, the texture or brittle, if during transportation, the turbulence is severe, the container is damaged, and it leaks out, or it is dangerous. Therefore, the packaging must be sturdy and lined with soft materials such as foam and cotton to ensure stable transportation.
    In addition, quinoline-8-formaldehyde may have certain toxicity and irritation. People who store and transport it should be equipped with protective equipment, such as gloves, masks, goggles, etc. If they accidentally touch it, they should be rinsed with plenty of water as soon as possible, and in severe cases, they should seek medical treatment.
    In addition, storage and transportation should be kept away from fire sources and oxidants. Quinoline-8-formaldehyde is flammable and will burn in case of fire, and in case of oxidants, it is easy to react violently and cause danger. Therefore, in the place of storage and transportation, fireworks are prohibited, and co-storage and co-transportation with oxidants are not allowed.
    In short, when storing and transporting quinoline-8-formaldehyde, care must be taken, and attention must be paid to dry and cool, shockproof and anti-collision, comprehensive protection, and keeping away from fire and oxidants to ensure safety and quality.
    What is the market price range for Quinoline-8-carboxaldehyde?
    In the case of quinoline-8-formaldehyde, its market price has been directly affected. The market is determined, and there are general factors. First and foremost, its efficiency is easy to achieve. If the method of propagation is low, high-quality raw materials or multiple precision steps are required, and the cost will rise, and the price will be high. Furthermore, the supply and demand of the market are low. If the demand is low and the supply is low, it must be low; on the contrary, if the supply is low and the demand is low, it will decline. In addition, the difference between the land also has implications. In different places, due to the cost of sources and labor, there may be waves. And the quality of the poor is also the quality of the price, and the high quality is often higher than the ordinary one.
    Past market conditions, the price per gram may be between 10 and 100 yuan. However, this is not fixed, and the world is changing, the market is changing, and the price is also changing. If you want to obtain a refined product, a supplier of a customized product, or a transaction in the recent market, you can get it.