6 Hydroxy 2 Oxo 1 2 3 4 Tetrahydro Quinoline
quinoline thiophene imidazole thiazole

6-hydroxy-2-oxo-1,2,3,4-tetrahydro quinoline

Taiy Chemical

    Specifications

    HS Code

    567400

    Name 6-hydroxy-2-oxo-1,2,3,4-tetrahydroquinoline
    Molecular Formula C9H9NO2
    Molecular Weight 163.173 g/mol
    Appearance Solid (predicted)
    Boiling Point 420.7°C at 760 mmHg (predicted)
    Melting Point 238 - 240°C
    Density 1.305 g/cm³ (predicted)
    Flash Point 208.2°C (predicted)
    Solubility Soluble in DMSO, methanol
    Pka 9.93 (predicted)
    Logp 0.96 (predicted)

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    General Information
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    Frequently Asked Questions

    As a leading 6-hydroxy-2-oxo-1,2,3,4-tetrahydro quinoline 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 6-hydroxy-2-oxo-1,2,3,4-tetrahydroquinoline?
    1,2,3,4-tetrahydrofuran-2-oxide, also known as furan oxide ethylene oxide, is quite rich in chemical properties.
    This compound has certain reactivity due to the existence of ethylene oxide structure. The ethylene oxide ring system has high ring tension, so it is chemically active and easy to open the ring for reaction. When encountering nucleophiles, nucleophilic substitution reactions are prone to occur. The nucleophilic reagents will attack the carbon atoms on the ethylene oxide ring, causing the ring to open and form new compounds. For example, when encountering water, water acts as a nucleophilic reagent to attack the epoxy ring to form products containing hydroxyl groups. When encountering alcohol compounds, the oxygen atom of the alcohol acts as a nucleophilic check point and reacts with the ethylene oxide ring to obtain ether products.
    1,2,3,4-tetrahydrofuran-2-oxide also has certain oxidative properties. Due to the presence of oxygen atoms in the molecule, it can participate in partial oxidation reactions. However, its oxidative properties are relatively weak compared to typical oxidants, such as potassium permanganate, etc., and usually require specific reaction conditions and substrates to exhibit oxidative properties.
    In addition, the compound may undergo rearrangement reactions under conditions such as heat or light. Under energy excitation of the ethylene oxide ring, the chemical bonds in the molecule are rearranged to form isomers with different structures. This rearrangement reaction provides a way to synthesize organic compounds with special structures.
    In the field of organic synthesis, 1,2,3,4-tetrahydrofuran-2-oxide is an important synthesis intermediate. With its diverse chemical properties, it can be used to construct various complex organic molecular structures, providing a powerful tool for the development of organic synthetic chemistry.
    What are the common synthesis methods of 6-hydroxy-2-oxo-1,2,3,4-tetrahydroquinoline?
    There are three methods for the synthesis of carbon tetrabromide. First, methane and bromine are substituted under light. Methane is the simplest hydrocarbon combined with carbon and hydrogen. Under light conditions, bromine replaces the hydrogen atom of methane step by step, and goes through one-bromomethane, dibromomethane, and tribromomethane to obtain carbon tetrabromide. However, there are many by-products of this reaction, which are difficult to separate and purify, and the yield is not high.
    Second, carbon tetrachloride and aluminum bromide are used as raw materials. Carbon tetrachloride is a common halogenated hydrocarbon. Under the action of appropriate temperature and catalyst aluminum bromide, chlorine atoms in carbon tetrachloride can be replaced by bromine atoms to form carbon tetrabromide. This method is relatively simple, and the catalyst aluminum bromide can promote the reaction and speed up the reaction rate. However, the preparation and use of aluminum bromide require certain conditions, and it is corrosive to the reaction equipment.
    Third, acetylene and bromine are used as raw materials. Acetylene, a hydrocarbon with unsaturated carbon-carbon bonds. Bromine can be added to it to obtain 1,2-dibromoethylene first, and then further added to bromine to form carbon tetrabromide for life. This reaction path is clear, the product is relatively single, and the yield is high. However, acetylene is a flammable and explosive gas, and special attention should be paid to safety during operation, and the control of reaction conditions is also stricter. < Br >
    These three are all common methods for synthesizing carbon tetrabromide, each with its own advantages and disadvantages. When applying, they should be selected according to actual needs and conditions.
    In what fields is 6-hydroxy-2-oxo-1,2,3,4-tetrahydroquinoline used?
    Silicon-based-2-oxide-1,2,3,4-tetrahydrofuran light is useful in many fields.
    In the field of materials, this light can help to form special silicon-based oxide materials. Due to its unique reaction properties, the microstructure and properties of materials can be precisely regulated. For example, in the preparation of high-performance optical films, the reaction of tetrahydrofuran light can make the film have better light transmission and stability, which is suitable for high-end optical instruments, such as telescopes, microscopes, and lens coatings, which can improve the clarity and accuracy of imaging.
    In the field of organic synthesis, its role cannot be ignored. It can be used as a special reaction condition to promote the synthesis of complex organic compounds. With tetrahydrofuran light irradiation, some chemical reactions that are difficult to achieve by conventional methods can be realized, and a unique molecular skeleton can be constructed. In pharmaceutical research and development, it helps to create new drug molecules, providing the possibility to overcome difficult diseases.
    In the field of electronics, silicon-based-2-oxide-1,2,3,4-tetrahydrofuran light can be used for the modification of semiconductor materials. Through its irradiation treatment, it can optimize the electrical properties of semiconductors, improve the electron mobility, and then improve the running speed and efficiency of electronic devices, such as computer chips, mobile phone processors, etc., which is expected to achieve a leap in performance.
    In addition, in environmental science, the reaction involved in light may be used for the degradation of pollutants. Under the action of tetrahydrofuran light, some organic pollutants can be accelerated to decompose into harmless small molecules, providing new ways and means for environmental purification.
    What are the market prospects for 6-hydroxy-2-oxo-1,2,3,4-tetrahydroquinoline?
    At present, the market prospect of 1,2,3,4-tetrahydrofuran-2-oxy-silicon-based is quite promising.
    Because 1,2,3,4-tetrahydrofuran-2-oxy-silicon-based has important uses in many fields. In the chemical industry, it is often a key intermediate in the synthesis of special materials. Through delicate chemical processes, it can react ingeniously with various compounds to derive new materials with outstanding properties, such as polymers with unique thermal stability and chemical stability. This is in high-end manufacturing, such as aerospace, electronic information and other fields. Aerospace equipment requires materials that can withstand extreme environments, and electronic information products also require materials with excellent electrical properties and stable chemical properties. Materials made of 1,2,3,4-tetrahydrofuran-2-oxy-silicon can just meet such stringent needs.
    Furthermore, in the field of pharmaceutical research and development, 1,2,3,4-tetrahydrofuran-2-oxy-silicon has also emerged. Its structural characteristics make it an important component of drug carriers. With precise design, it can achieve targeted delivery of drugs, improve drug efficacy, and reduce damage to normal tissues of the body. With the advance of medical science and technology, the concept of precision medicine has taken root in the hearts of the people, and the demand for efficient and safe drug carriers has surged. Under this trend, 1,2,3,4-tetrahydrofuran-2-oxy-silicon-based has broad development space.
    Looking at market dynamics, with the development of science and technology and industrial upgrading, the demand for 1,2,3,4-tetrahydrofuran-2-oxy-silicon-based is on the rise. Although there may be some challenges at present, such as the optimization of synthetic processes, cost control, etc., it is expected to be resolved one by one with the progress of scientific research and the accumulation of industrial experience. Therefore, the future market prospect of 1,2,3,4-tetrahydrofuran-2-oxy-silicon-based is promising, which may lead to new changes and breakthroughs in many fields.
    What are the precautions in the preparation of 6-hydroxy-2-oxo-1,2,3,4-tetrahydroquinoline?
    In the process of preparing tetrahydrofuran-2-oxide-1,2,3,4-tetraol, there are many precautions.
    First, the selection of raw materials must be cautious. The purity and quality of the starting materials used have a profound impact on the quality and yield of the final product. If there are too many impurities in the raw material, it will not only interfere with the reaction process, making it difficult to proceed smoothly, but also may generate many by-products, which greatly increases the difficulty of product separation and purification.
    Second, precise control of the reaction conditions is indispensable. In terms of temperature, the reaction is extremely sensitive to temperature. If the temperature is too high, the reaction rate will be accelerated, but it may cause side reactions, resulting in reduced product selectivity; if the temperature is too low, the reaction rate will be delayed, time-consuming will increase, and the production efficiency will drop significantly. Pressure is also a key factor. Appropriate pressure helps the reaction to advance in the direction of generating the target product. Improper pressure may make the reaction unable to proceed as expected. At the same time, the reaction time also needs to be strictly controlled. If the time is too short, the reaction is incomplete, and the product yield is low. If the time is too long, it will not only waste resources and time, but also cause product decomposition or other adverse changes due to the long-term reaction.
    Third, the cleanliness of the reaction environment cannot be ignored. The reaction system must be kept clean Even a very small amount of impurities may act as a catalyst or participate in the reaction, thereby changing the reaction path and seriously affecting the purity and quality of the product.
    Fourth, the operation process needs to be strictly regulated. When adding reactants, the order and speed are crucial. If the order is wrong or the speed is too fast, it may cause a violent reaction, posing a safety hazard, and it will also affect the normal progress of the reaction and the quality of the product. During the stirring process, it is necessary to ensure that the mixing is uniform and the reactants are fully contacted to ensure that the reaction can be carried out uniformly and efficiently.
    Fifth, the separation and purification of the product is crucial. After the reaction, appropriate separation and purification methods, such as distillation, extraction, recrystallization, etc. should be used to obtain high-purity target products. During operation, appropriate methods should be carefully selected according to the physical and chemical properties of the products and impurities. The operation process should be fine to avoid product loss or the introduction of new impurities.