Ethyl 6 7 Diisobutoxy 4 Hydroxyquinoline 3 Carboxylate
quinoline thiophene imidazole thiazole

Ethyl 6,7-diisobutoxy-4-hydroxyquinoline-3-carboxylate

Taiy Chemical

    Specifications

    HS Code

    473575

    Chemical Formula C24H35NO6
    Molecular Weight 433.54
    Appearance Solid (usually)
    Physical State At Room Temp Solid
    Solubility In Water Low solubility
    Solubility In Organic Solvents Soluble in some organic solvents like ethanol, acetone
    Melting Point Specific value would require experimental determination
    Boiling Point Estimated to be high, specific value needs experiment
    Odor Typically odorless or very faint odor
    Stability Stable under normal conditions, but may decompose under extreme heat or in presence of strong oxidizing agents

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    General Information
    Where to Buy Ethyl 6,7-diisobutoxy-4-hydroxyquinoline-3-carboxylate in China?
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    Frequently Asked Questions

    As a leading Ethyl 6,7-diisobutoxy-4-hydroxyquinoline-3-carboxylate 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 Ethyl 6, 7-diisobutoxy-4-hydroxyquinoline-3-carboxylate?
    Ethyl 6,7-diisobutoxy-4-hydroxyquinoline-3-carboxylate is an organic compound with unique chemical properties. Its molecule contains a quinoline ring, which endows it with certain stability and conjugation properties. Isobutoxy at 6 and 7 positions, isobutyl has certain spatial resistance and electronic effects, which affect the physical and chemical properties of the molecule as a whole. Spatial resistance can change the interaction between molecules, affecting its solubility, melting point and other physical properties; in terms of electronic effects, alkoxy is the power supply, which can increase the electron cloud density of the quinoline ring, enhance its nucleophilicity, and easily participate in electrophilic substitution reactions. The hydroxyl group at the
    4 position has active hydrogen and is acidic, which can participate in acid-base reactions and react with bases to form corresponding salts. At the same time, the hydroxyl group can form intramolecular or intermolecular hydrogen bonds, which has a great influence on the stability, melting point, boiling point and solubility of the compound in solvents. The carboxyl ethyl ester structure in the molecule, the carbonyl group in -COOEt has electron-absorbing properties, which makes the ester carbons partially positively charged and vulnerable to attack by nucleophiles. Hydrolysis, alcoholysis, aminolysis and other reactions occur. Under acidic or basic conditions, ester groups can be hydrolyzed into corresponding carboxylic acids and ethanol.
    In summary, the chemical properties of Ethyl 6,7 - diisobutoxy - 4 - hydroxyquinoline - 3 - carboxylate are determined by the interaction of functional groups, which makes it potentially useful in organic synthesis, medicinal chemistry and other fields.
    What are the main uses of Ethyl 6, 7-diisobutoxy-4-hydroxyquinoline-3-carboxylate
    Ethyl 6,7-diisobutoxy-4-hydroxyquinoline-3-carboxylate (6,7-diisobutoxy-4-hydroxyquinoline-3-carboxylate) is a widely used compound. In the field of medicinal chemistry, it may be a key intermediate for the synthesis of specific drugs. Due to its unique chemical structure, it contains quinoline parent nuclei and specific substituents. These structures are often biologically active and can be chemically modified to meet the needs of specific drug targets, and then drugs for the treatment of various diseases, such as anti-malaria, anti-tumor drugs, etc.
    also has potential applications in materials science. Its structure endows it with certain optical and electrical properties, or it can be used to prepare organic optoelectronic materials. For example, in the study of organic Light Emitting Diode (OLED) or organic solar cells, rational design and modification may optimize the charge transport performance, luminous efficiency and other key parameters of the material, which can promote the development of such new energy and display materials.
    Furthermore, in the field of organic synthetic chemistry, it can be used as a multifunctional synthetic building block. With its multiple reactive activity check points, it can construct more complex organic molecular structures through various organic reactions, such as nucleophilic substitution, oxidation reduction, etc., providing an important cornerstone for organic synthetic chemists to explore the synthesis path of novel compounds. In conclusion, Ethyl 6,7 - diisobutoxy - 4 - hydroxyquinoline - 3 - carboxylate has shown important value and application prospects in many scientific fields.
    What is the synthesis method of Ethyl 6, 7-diisobutoxy-4-hydroxyquinoline-3-carboxylate
    The method of preparing Ethyl 6, 7 - diisobutoxy - 4 - hydroxyquinoline - 3 - carboxylate (6, 7 - diisobutoxy - 4 - hydroxyquinoline - 3 - carboxylate ethyl ester), ancient wisdom or according to the principle of chemistry, follow the path of organic synthesis.
    Initially, choose a suitable starting material, or choose a quinoline skeleton, or from the basic compound that can be derived from this structure. For example, starting with an active aromatic compound, after multiple steps of ingenious transformation, the quinoline parent nucleus is constructed.
    In the way of reaction, the step of etherification is indispensable. Using isobutanol or its corresponding halide as a reagent, etherification occurs with phenolic hydroxyl groups, and the reaction conditions, such as temperature, solvent, and catalyst type and dosage, are carefully regulated. If the temperature is too high, side reactions may occur; if the temperature is too low, the reaction will be slow. The solvent used must have good solubility to the reactants and be in harmony with the reaction system, such as aprotic polar solvents, which can promote the smooth progress of the reaction. The choice of catalyst, or acidic or basic substances, depends on the reaction mechanism, to accelerate the formation of ether bonds, so that isobutoxy groups are introduced at positions 6 and 7.
    When both the quinoline parent nucleus and the ether bond are formed, the reaction of carboxyl ethylation is carried out. A suitable carboxylic acid derivative, such as acyl chloride or acid anhydride, is reacted with ethanol under appropriate conditions to convert the carboxyl group to ethyl ester group. This step also requires attention to the precise control of the reaction conditions to avoid damage to the formed structure.
    As for the introduction of hydroxyl groups, or reserve transformable groups in the early reaction, and then introduce 4-hydroxyl groups precisely through hydrolysis, oxidation and other reactions. After each step of the reaction, it is necessary to separate and purify the impurities to obtain a pure product, which can provide high-quality raw materials for the next reaction. In this way, after many delicate operations, Ethyl 6,7 - diisobutoxy - 4 - hydroxyquinoline - 3 - carboxylate can be obtained.
    Ethyl 6, 7-diisobutoxy-4-hydroxyquinoline-3-carboxylate What are the precautions during storage and transportation?
    Ethyl 6,7 - diisobutoxy - 4 - hydroxyquinoline - 3 - carboxylate is a fine chemical substance. During storage and transportation, many matters must be paid attention to to to ensure its quality and safety.
    First storage environment. This compound should be stored in a cool, dry and well-ventilated place. If it is in a high temperature environment, its chemical properties may change due to excessive temperature, and even cause adverse reactions such as decomposition. Humid gas is also a big taboo, because it may cause the compound to be damp, resulting in impaired purity and affecting subsequent use. If stored in an open and humid place, moisture can easily interact with it and destroy its structure.
    Furthermore, the packaging must be tight. It must be packed with suitable packaging materials to ensure that there is no risk of leakage. Usually a sealed container is used to prevent contact with external factors such as air and moisture. If the packaging is not strict, the oxygen in the air may react with the compound and change its chemical composition.
    When transporting, also be cautious. Avoid violent vibration and collision. The compound may be damaged by shock and reduce its stability. And the environment in the transportation vehicle needs to be controlled to maintain a suitable temperature and humidity. If the temperature and humidity fluctuate too much during transportation, the quality of the compound will be affected.
    In addition, its storage and transportation need to be strictly operated in accordance with relevant regulations and standards. Operators should also be familiar with its characteristics and safety precautions to ensure that Ethyl 6,7-diisobutoxy-4-hydroxyquinoline-3-carboxylate remains stable during storage and transportation without quality problems and safety hazards.
    What is the market outlook for Ethyl 6, 7-diisobutoxy-4-hydroxyquinoline-3-carboxylate?
    Guanfu "Ethyl 6,7 - diisobutoxy - 4 - hydroxyquinoline - 3 - carboxylate" is a genus of organic compounds. To analyze its market prospects, it is necessary to look at it from multiple perspectives.
    From the perspective of the pharmaceutical field, many pharmaceutical companies are currently focusing on new drugs. This compound contains a specific chemical structure, or has biological activity, can interact with human biological targets, and can be used as potential drug intermediates. Nowadays, there is a growing demand for innovative drugs. If it exhibits unique effects in pharmacological research, it will surely gain the attention of the pharmaceutical industry, and market demand may surge.
    As for the field of materials, organic compounds are often the basis for the development of new materials. This substance may have unique optical, electrical or thermal properties due to structural properties. With the development of science and technology, the demand for high-performance materials is increasing. If in-depth research and development is carried out, it may have broad applications in electronic devices, optical materials, etc., and the market prospect is promising.
    However, its marketing activities also have challenges. The synthesis process may be complex, the cost is difficult to control, the price is high, and the market competitiveness is affected. And new compounds enter the market, subject to strict regulatory approval and security evaluation, which is time-consuming and laborious.
    To sum up, "Ethyl 6,7 - diisobutoxy - 4 - hydroxyquinoline - 3 - carboxylate" has potential, but to fully explore the market prospects, it is still necessary for researchers and enterprises to work together to overcome technical and regulatory problems in order to emerge in the market and open up a wide world.