2 Quinolinecarbaldehyde
quinoline thiophene imidazole thiazole

2-Quinolinecarbaldehyde

Taiy Chemical

    Specifications

    HS Code

    735246

    Chemical Formula C10H7NO
    Molar Mass 157.17 g/mol
    Appearance Yellow solid
    Melting Point 64 - 66 °C
    Boiling Point 305 - 307 °C
    Solubility In Water Insoluble
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, chloroform
    Odor Characteristic odor
    Flash Point 134.2 °C
    Stability Stable under normal conditions, but sensitive to strong oxidizing agents

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    General Information
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    Frequently Asked Questions

    As a leading 2-Quinolinecarbaldehyde 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 2-Quinolinecarbaldehyde?
    2-Quinoline formaldehyde is one of the organic compounds with unique chemical properties. Its appearance is light yellow to yellow crystalline powder, and it is widely used in scientific research and organic synthesis.
    This compound contains a quinoline ring and an aldehyde group, which gives it a variety of chemical activities. The aldehyde group has high reactivity and can participate in many important organic reactions. For example, it can condensate with amine compounds to form imine products, which is commonly used in the construction of nitrogen-containing heterocyclic compounds and the synthesis of biologically active molecules. At the same time, the aldehyde group can undergo oxidation reaction and be converted into corresponding carboxylic acids; it can also be reduced to hydroxyl alcohol groups under the action of reducing agents.
    Furthermore, the quinoline ring structure of 2-quinoline formaldehyde makes it have certain aromaticity and stability. The compound can be used as a ligand to form complexes with metal ions, showing important application potential in the field of catalytic reactions and materials science. Due to its structural properties, 2-quinoline formaldehyde also has research value in fluorescent materials. Some derivatives have fluorescent properties and can be used in the design of fluorescent probes to detect specific ions or biomolecules.
    In addition, 2-quinoline formaldehyde is often used as a key intermediate in the design of organic synthesis routes. A series of derivatives with various structures can be synthesized by chemically modifying different positions on the aldehyde group and quinoline ring, providing the possibility for the creation of new functional molecules in the fields of medicinal chemistry and materials science. Its unique chemical properties and structural characteristics make it an object of much attention in the research and application fields of organic chemistry.
    What are the common synthetic methods of 2-Quinolinecarbaldehyde?
    2-Quinoline formaldehyde is a key intermediate in organic synthesis. It has a wide range of uses and is important in the fields of medicine, pesticides and materials. The common synthesis methods are about the following.
    One is the oxidation method of quinoline derivatives. Using a specific derivative of quinoline as the starting material, with the action of a suitable oxidant, it can reach 2-quinoline formaldehyde. Commonly used oxidants such as chromate, permanganate, etc. In this way, appropriate reaction conditions need to be selected to control the degree of oxidation and avoid impurities or low yields of products caused by excessive oxidation. For example, a quinoline derivative, in a specific solvent, with an appropriate amount of chromate as the oxidant, temperature control and reaction time, the target product can be obtained. < Br >
    The second is the metal catalytic coupling method. With the help of transition metal catalysts, the substrate containing the quinoline structure is coupled with the reagent containing the aldehyde group. Metal catalysts such as palladium and copper are often used. This method has the advantages of high selectivity and mild reaction conditions. For example, with palladium catalyst, in the presence of ligands, quinoline halide and a certain aldehyde-based reagent can be obtained under the action of suitable solvents and bases through a specific reaction process.
    The third is the quinoline ring construction method. Starting from basic raw materials, quinoline rings are constructed through a series of reactions, and aldehyde groups are introduced at the same time. This process often involves multi-step reactions, and the reaction sequence and conditions need to be carefully planned. For example, an aromatic amine is condensed with a carbonyl compound first, and then cyclized and functional group converted to obtain 2-quinoline formaldehyde. Each step of the reaction needs to be carefully regulated to ensure the high efficiency and high selectivity of the overall synthesis.
    In what areas is 2-Quinolinecarbaldehyde applied?
    2-Quinoline formaldehyde is useful in many fields.
    In the field of medicine, it can be used as a key raw material for the synthesis of traditional Chinese medicine. Because 2-quinoline formaldehyde has a specific chemical structure and activity, it can be converted into biologically active compounds through a series of chemical reactions. For example, it may be used in the development of antimicrobial drugs, which combine with some key targets in bacteria to inhibit bacterial growth and reproduction; or it may play a role in the development of anticancer drugs, inhibiting the proliferation of cancer cells by affecting the metabolic pathways or signal transduction pathways of cancer cells, providing new possibilities for solving cancer problems.
    In the field of materials science, 2-quinoline formaldehyde is also indispensable. It can participate in the preparation of functional materials, such as luminescent materials. Due to its structural characteristics, or endowing the material with unique optical properties, after rational design and synthesis, the obtained material may have high luminous efficiency and good stability, which can be applied to organic Light Emitting Diode (OLED) and other fields to improve the performance of display technology and make the display screen clearer and brighter.
    In the field of organic synthetic chemistry, 2-quinoline formaldehyde is an important synthetic block. Due to the existence of aldehyde groups and quinoline rings, a variety of classical organic reactions can occur, such as the condensation reaction of aldehyde groups, and the reaction with other compounds containing active hydrogen to construct complex organic molecular structures, providing a convenient way for the synthesis of new organic compounds. This helps organic synthetic chemistry to continuously expand the boundaries and create more organic compounds with novel structures and unique properties.
    What are the physical properties of 2-Quinolinecarbaldehyde?
    2-Quinoline formaldehyde is one of the organic compounds. Its physical properties are quite unique. Looking at its appearance, it is mostly light yellow to yellow crystalline powder under normal circumstances, just like fine sand accumulation, and like a delicate powder aggregate. Under light, it may also emit a faint and unique luster.
    When it comes to the melting point, it is about 56-59 ° C. This property is like a "key" to temperature. When the temperature rises to this range, it gradually moves from solid to liquid, just like ice and snow melting when warm, completing the transformation of the state of matter.
    In terms of boiling point, it is about 321.3 ° C. Under such high temperature, it will further transform from liquid to gaseous state, rising like a curl of blue smoke, showing the wonderful changes of matter under different temperature conditions.
    2-Quinoline formaldehyde is slightly soluble in water, like a shy dancer, only a little integrated in the water stage, and most of them still maintain their own independence. However, it is easily soluble in organic solvents such as ethanol and ether. In these solvents, it can disperse freely like a duck to water and blend intimately with the solvent, fully reflecting its solubility preference.
    In addition, it has a certain smell, which is difficult to describe exactly, but it has a unique smell of organic compounds, maybe with a light aroma, or maybe mixed with a slightly irritating taste, like a unique logo, showing its own existence. In short, the physical properties of 2-quinoline formaldehyde are like its unique "business card", which makes it show a different style in the field of organic chemistry.
    What are the storage requirements for 2-Quinolinecarbaldehyde?
    2-Quinoline formaldehyde is an organic compound with certain chemical activity. It needs to follow specific requirements when storing to ensure its quality and stability.
    First, the temperature of the storage environment is very important. It should be stored in a cool place. Generally speaking, the temperature should be maintained at 2-8 ° C. This is because the temperature is too high to cause the compound to undergo chemical reactions and accelerate the rate of deterioration; while the temperature is too low, although it can inhibit the reaction, it may cause the compound to crystallize or solidify, affecting subsequent use and use.
    Second, the humidity should not be ignored. It should be stored in a dry environment, and the humidity should be controlled at 40% - 60%. If the ambient humidity is too high, 2-quinoline formaldehyde is easy to absorb water and cause reactions such as hydrolysis, resulting in a decrease in its purity.
    Third, 2-quinoline formaldehyde is quite sensitive to light, so it needs to be stored away from light. It can be stored in brown bottles or opaque containers to prevent photochemical reactions caused by light exposure and damage to its molecular structure.
    Fourth, the storage place must be kept away from fire sources and oxidants. 2-quinoline formaldehyde is an organic substance, which is flammable and easy to cause fires when exposed to fire sources; and oxidants will have violent oxidation reactions with it, which not only affects its quality, but also may bring safety hazards.
    Fifth, the material of the storage container is also exquisite. Glass or specific plastic containers should be selected. Such materials are chemically stable and not easy to react with 2-quinoline formaldehyde, which can effectively ensure their quality. And the container must be well sealed to prevent air from entering and avoid contact between compounds and oxygen, moisture and other components in the air.