1 2 Dihydro 4 Oxo Quinoline 3 Carboxylic Acid
quinoline thiophene imidazole thiazole

1,2-Dihydro-4-oxo-quinoline-3-carboxylic acid

Taiy Chemical

    Specifications

    HS Code

    726741

    Chemical Formula C10H7NO3
    Molar Mass 189.17 g/mol
    Appearance Solid (presumably, common for such organic compounds)
    Physical State At Room Temperature Solid
    Solubility In Water Low solubility (as many quinoline - carboxylic acids have poor water solubility)
    Solubility In Organic Solvents Soluble in some polar organic solvents like DMSO, DMF
    Melting Point Specific value would require experimental determination but likely in a range typical for such aromatic carboxylic acids
    Acidity Carboxylic acid group makes it acidic
    Pka Value Value around 4 - 5 typical for simple aromatic carboxylic acids
    Color Colorless to light - colored solid (usually)
    Odor Odorless or very faint odor

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    General Information
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    Frequently Asked Questions

    As a leading 1,2-Dihydro-4-oxo-quinoline-3-carboxylic acid 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 1,2-dihydro-4-oxyquinoline-3-carboxylic acid?
    1% 2C2-dioxo-4-oxo-3-quinolinocarboxylic acid, which is acidic and can partially ionize hydrogen ions in water due to its carboxyl group. It has certain stability, but can react under specific conditions. In case of strong oxidants, unsaturated bonds and related groups in its structure may be affected, which may cause oxidation reactions to cause structural changes.
    From the perspective of nucleophilic substitution, due to the presence of suitable leaving groups and reaction check points in the molecule, under suitable nucleophilic reagents and conditions, nucleophilic substitution can occur. Nucleophilic reagents such as hydroxyl and amino groups can replace specific atoms or groups in molecules. < Br >
    In terms of solubility, it has a certain solubility in polar solvents such as water due to its polar carboxyl group, but because the molecule also contains a large non-polar part, the solubility may be limited, and the solubility may be relatively higher in organic solvents such as ethanol and acetone.
    In the field of organic synthesis, it can be used as a key intermediate. With its own structural characteristics, it can construct more complex organic compounds through a series of reactions, which can be used to prepare drugs, materials and other organic products with specific structures and functions, and plays an important role in organic chemistry research and industrial production.
    What are the main uses of 1,2-dihydro-4-oxyquinoline-3-carboxylic acid?
    1% 2C2-dicyano-4-oxyvaleric acid-3-enoic acid, this compound has important uses in many fields.
    In the field of medicine, it can be used as a key intermediate in drug synthesis. With the delicate modification and modification of its structure, drugs with unique effects can be developed. For example, in the synthesis process of some anti-cancer drugs, this compound can be used as a starting material to build a molecular structure with specific anti-cancer activity through a series of precise chemical reactions, helping medicine to overcome cancer problems.
    In the field of materials science, it can participate in the creation of high-performance materials. Due to its special chemical structure, it can give materials unique properties. For example, when preparing some functional materials with special requirements for stability, conductivity, etc., the introduction of this compound can optimize the molecular arrangement and interaction of the material, thereby improving the comprehensive properties of the material and meeting the stringent requirements of high-end fields such as aerospace and electronic equipment.
    In the agricultural field, it may be used to develop new pesticides. With its chemical properties, it is possible to develop green pesticides that are highly effective in killing specific pests and are environmentally friendly to non-target organisms. While ensuring crop yield, it is possible to reduce the negative impact on the ecological environment and promote the sustainable development of agriculture.
    This compound has shown great application potential in many fields such as medicine, materials science, agriculture, etc. With the in-depth advancement of scientific research, it is expected to bring more significant breakthroughs and development to various fields.
    What are the synthesis methods of 1,2-dihydro-4-oxyquinoline-3-carboxylic acid?
    To prepare 1,2-dichloro-4-oxo-cyclopentane-3-enocarboxylic acid, there are three methods.
    First, cyclopentadiene is used as the starting point, and it can be obtained through diene addition, oxidation, halogenation, hydrolysis and other steps. First, cyclopentadiene is added to the diene body by diene addition reaction to obtain the corresponding adduct. This adduct can be oxidized at a specific location under suitable oxidation conditions, such as treatment with a specific oxidant. Then halogenated, chlorine atoms are introduced, and finally hydrolyzed to convert a specific group into a carboxyl group, thereby obtaining the target product.
    Second, a specific cyclopentene-containing compound can be started. The compound is first modified by functional groups, so that a suitable substituent is introduced at a certain position on cyclopentene, and then the specific atom is oxidized to the desired valence state through the oxidation process to form an oxygen-containing structure. Then halogenation, chlorine atoms are introduced at a specific position precisely, and finally the carboxyl group is adjusted through suitable reaction conditions to obtain 1,2-dichloro-4-oxycyclopentane-3-enocarboxylic acid.
    Third, other similar structures are used as raw materials. First, the ring is rearranged by ring opening or ring expansion to construct a suitable carbon frame. Then it is oxidized, halogenated and carboxylated in multiple steps. During oxidation, the conditions are strictly controlled to enable specific atoms to reach the desired oxidation state; during halogenation, the appropriate halogenating agent and conditions are selected to ensure the accurate introduction of chlorine atoms; the carboxylation step adjusts the reaction conditions so that the product finally forms the target carboxyl group structure, and then 1,2-dichloro-4-oxo-cyclopentane-3-enocarboxylic acid is obtained.
    What is the price range of 1,2-dihydro-4-oxyquinoline-3-carboxylic acid in the market?
    1% 2C2-dibromo-4-oxovaleric acid-3-enoic acid is in the market, and its price range is quite difficult to determine. The price often varies due to various reasons, such as the output of the place of origin, the supply and demand of the city, the production process, and the quality.
    If its origin is wide and the output is abundant, and it is supplied in the market, but there are few people in need, the price may decline. On the contrary, if the origin is narrow, the output is thin, and there are many people in demand, the supply will exceed the demand, and the price will rise.
    Furthermore, the complexity of the preparation process is also related to the price. If the process is complicated, expensive, time-consuming, and labor-intensive, the price will be higher; if it is simple, the price may be slightly lower.
    As for the quality, the better one is expensive, and the second one is less expensive.
    In summary, in order to determine the price range between markets, it is necessary to check the dynamics of the market in real time, consult suppliers and industry players, and obtain a more accurate number. However, according to common sense, the price of this compound may be between tens of yuan and hundreds of yuan per gram due to use, demand, etc., or there are more than one. It is difficult to generalize, and it all changes with the market.
    What are the storage conditions for 1,2-dihydro-4-oxyquinoline-3-carboxylic acid?
    1% 2C2-dicyanobicyclo [3.2.0] heptyl-3-enoic acid, this thing is highly toxic and dangerous, so its storage needs to be extremely cautious, according to ancient regulations, as follows.
    The hiding place must be selected in a remote, quiet and inaccessible place, and it must be dry and ventilated to prevent moisture and corrosion. There should be no fireworks around, nor near flammable and explosive things. Because of its strong nature, it may cause a dramatic explosion in case of fire or hot topic, and it will affect the four sides.
    The reservoir should be specially made of a sturdy container, and the material should be resistant to corrosion to prevent leakage. The words "highly toxic" should be written on the outside of the container, which is conspicuously displayed, so that everyone who sees it knows the danger.
    The storage place should be guarded by a special person, and those who trespass should be severely punished. Those on duty must be familiar with the nature of this thing and always have measures to deal with it. If there is an accidental leakage, cover it with lime and sand as soon as possible, and do not touch it rashly. Urgent report to the company and deal with it quickly.
    The temperature of storage should be constant and moderate, and it should not be suddenly cold and hot. In summer, it should be cooled by an ice cellar or water cooling method; in winter, it should be wrapped in felt cotton to prevent freezing.
    In short, the storage of 1% 2C2-dicyano-4-oxobicyclo [3.2.0] heptyl-3-enoic acid is related to human life and safety, and the well-being of mountains and rivers. It is necessary to follow the ancient law and strictly implement it.