Diethyl Quinoline 2 3 Dicarboxylate
quinoline thiophene imidazole thiazole

diethyl quinoline-2,3-dicarboxylate

Taiy Chemical

    Specifications

    HS Code

    314243

    Chemical Formula C15H17NO4
    Molecular Weight 275.30
    Appearance Solid (Typical)
    Solubility In Water Insoluble
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, chloroform

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    Frequently Asked Questions

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    What is the main use of diethylquinoline-2,3-dicarboxylate?
    What is the main use of diethyl ether-2,3-type acid anhydride?
    Diethyl ether is an organic compound. It is a colorless, odorless liquid at room temperature, highly volatile and flammable. It has a wide range of uses. In the field of organic synthesis, it is often used as a solvent. Many organic reactions need to be carried out smoothly in an inert solvent environment. Diethyl ether has become a common choice because of its good solubility and relatively stable chemical properties. It can dissolve various organic substances such as fats, resins, alkaloids, etc. In the field of medicine, it used to be used as a general anesthetic, but due to its flammability and some adverse effects on the human body, it is now less used.
    As for the second type of acid anhydride, it is an important class of organic compounds. The main use is in organic synthesis. First, it can be used as an acylating agent to react with alcohols, amines and other compounds to form important organic compounds such as esters and amides, which is of great significance in drug synthesis and polymer material preparation. Second, in the polymerization reaction, the second type of acid anhydride can be used as a monomer to participate in the reaction to prepare polyesters, polyimides and other polymers. These polymers are widely used in aerospace, electronics and other fields due to their excellent properties, such as high strength and high temperature resistance. Third, in the design of organic synthesis routes, the second type of acid anhydride is often used as a key intermediate, which is converted into other more complex organic compounds through a series of chemical reactions, greatly enriching the strategies and approaches of organic synthesis.
    What are the synthesis methods of diethylquinoline-2,3-dicarboxylate?
    To prepare diethyl benzyl ether, there are two methods. The first is to co-heat diethoxy borane with benzyl halogen under the catalysis of alkali. The capping base can activate the ethoxy group of borane, and the halogen atom of benzyl halogen is easily replaced. The two are combined to obtain diethyl benzyl ether. This reaction condition is milder and the yield is also good.
    The second is to react with benzyl alcohol and haloethane under the action of alkali. The base promotes the deprotonation of the hydroxyl group of benzyl alcohol, and the generated oxygen anion has strong nucleophilicity, which can attack the carbon atom of haloethane, and the halogen atom leaves, so as to obtain the target product. In this process, the activity of haloethane and the type and dosage of bases have a great influence on If the activity of haloethane is insufficient, the reaction is difficult to proceed; the amount of alkali is inappropriate, or the side reaction may increase.
    However, no matter what method, it is necessary to pay attention to the precise control of the reaction conditions, such as temperature, time, and the proportion of reactants. If the temperature is too high, or the side reaction is triggered, the product is impure; if the time is too short, the reaction is not completed, and the yield is reduced. And the proportion of reactants is out of balance, which will also affect the reaction process and product yield. Therefore, in order to obtain pure and high-yield two-ethyl benzyl ether, the experimenter should consider it carefully and operate cautiously.
    What are the physical properties of diethylquinoline-2,3-dicarboxylate
    The physical properties of diethyl ether-2,3-type acid anhydrides cover these two types of acid anhydrides, and have special properties. Its melting and boiling point is particularly important. The melting and boiling point of the second type of acid anhydride varies depending on the structure, usually with a relatively low melting point and a higher boiling point. This is due to the intermolecular force, and there are van der Waals forces and hydrogen bonds between molecules, which affect the melting and boiling point.
    In addition, the solubility of the second type of acid anhydride is also a key physical property. In organic solvents, such as ether and chloroform, the second type of acid anhydride has good solubility. This is because the second type of acid anhydride and the organic solvent molecules can have a similar miscibility effect, so that the two can be miscible. However, in water, the solubility of the second type of acid anhydride may not be good, because of the force between the water molecules or the strong force of the hydrogen bond between the water molecules.
    Density is also one of the physical properties of the second type of acid anhydride. Its density varies depending on the specific structure and composition, and is generally within a certain range compared with the density of common organic compounds. The different densities have important effects in practical applications, such as separation and mixing.
    The refractive index of the second type of acid anhydride is also an observable physical property. The refractive index reflects the refractive property of light propagating in the second type of acid anhydride, which is related to the molecular structure of the second type of acid anhydride and the distribution of electron clouds. The accurate determination of refractive index can help identify the second type of acid anhydride, and provide a key basis for studying its purity and concentration.
    View the color state of the second type of acid anhydride, under normal conditions, it is mostly liquid or solid, and the color may be colorless and transparent, or microstrip color, due to the influence of impurities or special structures. These physical properties are of great significance in many fields such as chemicals and pharmaceuticals, and are related to the storage, transportation, and use of the second type of acid anhydride.
    What are the chemical properties of diethylquinoline-2,3-dicarboxylate
    The chemical properties of diethyl ether-2,3-dicarboxylic anhydride have various characteristics. This compound has the generality of acid anhydride, and it is easy to hydrolyze in contact with water, resulting in the corresponding two-carboxylic acid. In the structure of capped anhydride, the acid anhydride bond breaks when attacked by water molecules to form a carboxyl group. The hydrolysis reaction is quite rapid, and can be carried out spontaneously in the water environment at room temperature.
    And because it contains diethoxy groups, it has certain lipophilic properties. It has good solubility in the organic phase and can be miscible with many organic solvents such as benzene and chloroform. This property makes the compound often used as a solvent or intermediate in organic synthesis.
    Furthermore, diethyl ether-2,3-dicarboxylic acid anhydride can participate in the esterification reaction. By interacting with alcohols, ester products can be formed under appropriate catalyst and reaction conditions. In this reaction, the acyl group of the acid anhydride is combined with the hydroxyl group of the alcohol to remove a molecule of carboxylic acid to achieve the purpose of esterification.
    When heated, diethyl ether-2,3-dicarboxylic acid anhydride can also undergo reactions such as rearrangement. Due to the influence of the electron cloud distribution of each atom in the structure and the steric resistance, heating can promote the rearrangement of atoms in the molecule to form products with different structures, which is one end of its thermochemical properties.
    All these chemical properties make diethyl ether-2,3-dicarboxylic anhydride have important applications and values in the synthesis and reaction research of organic chemistry.
    What is the price range of diethylquinoline-2,3-dicarboxylate in the market?
    Today, there are diisoyl square light-2,3-dicarboxylic acid anhydride, and it is difficult to determine the price range in the market. However, the theory of "Tiangong Kaiwu" may be referred to.
    "Tiangong Kaiwu" is a great achievement of all kinds of skills and products. Sadly, it is not detailed in which diisoyl square light-2,3-dicarboxylic acid anhydride is mentioned. At that time, it was not covered or there was no such thing, or it was a very common genus, so it was not included in the book.
    However, looking at the method of "Tiangong Kaiwu" on things, it is probably based on its production, use, and convenience. From this, if the preparation of diiso-2,3-dicarboxylic anhydride is difficult and the use is rare, the price will be high; if the preparation is easy and the use is wide, the price will be easy.
    In this world, the price of things on the market is also related to supply and demand, labor costs, decrees, etc. If there are many people seeking this thing, there are few suppliers, and the cost of labor is not cheap, and the decree is regulated, the price will be high. On the contrary, if the supply exceeds the demand, the cost of labor is very cheap, and the decree is loose, the price may be low.
    Although we have not been able to obtain the exact price of diisoyl square light-2,3-dicarboxylic acid anhydride according to "Tiangong Kaiwu", we can know the approximate trend of its price by referring to the current market conditions. Or consult the city Jia, industry, you can also get the truth.