1 4 Dihydro 4 Oxo 3 Quinolinecarboxylicacid
quinoline thiophene imidazole thiazole

1,4-dihydro-4-oxo-3-Quinolinecarboxylicacid

Taiy Chemical

    Specifications

    HS Code

    754767

    Name 1,4 - dihydro - 4 - oxo - 3 - Quinolinecarboxylic acid
    Chemical Formula C10H7NO3
    Molar Mass 189.17 g/mol
    Appearance Solid (usually powder)
    Melting Point Decomposes (no distinct melting point in common sense)
    Solubility In Water Slightly soluble
    Pka Around 4.5 (approximate value for carboxyl group)
    Odor Odorless (usually)
    Color Pale yellow to off - white
    Crystal Structure Can form various crystal structures depending on synthesis conditions

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    General Information
    Where to Buy 1,4-dihydro-4-oxo-3-Quinolinecarboxylicacid in China?
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    Frequently Asked Questions

    As a leading 1,4-dihydro-4-oxo-3-Quinolinecarboxylicacid supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What is the main use of 1,4-dihydro-4-oxo-3-quinoline carboxylic acid?
    1% 2C4-dihydro-4-oxo-3-pyridinecarboxylic acid has a wide range of uses. In the field of medicine, it can be used as a key intermediate to help synthesize many drugs with specific physiological activities. For example, when developing some anti-cancer drugs, with their unique chemical structure, they can participate in the construction of drug molecules, giving drugs the effect of targeting specific cancer cells and inhibiting tumor growth; in the synthesis of antibacterial drugs, they can also play a key role in enhancing the inhibitory effect of drugs on bacterial cell walls or metabolic pathways and enhancing antibacterial activity.
    In the field of materials science, 1% 2C4-dihydro-4-oxo-3-pyridinecarboxylic acid can be used to prepare functional materials. Due to its specific electron cloud distribution and reactivity, it can chemically react with other organic or inorganic materials to build unique composites. For example, by compounding with polymer, the mechanical properties, thermal stability or optical properties of materials can be improved, which can be used in many fields such as electronic device packaging materials, optical lenses, etc.
    In addition, in the agricultural field, it can be used as a raw material for potential plant growth regulators. By regulating the balance of hormones in plants or participating in plant metabolic processes, it affects the growth and development of plants, such as promoting plant root growth, enhancing plant resistance to stress, and then improving crop yield and quality.
    In summary, 1% 2C4-dihydro-4-oxo-3-pyridinecarboxylic acid has important uses in many fields such as medicine, materials, and agriculture. With the development of science and technology, its application prospects are expected to be broader.
    What are the physical properties of 1,4-dihydro-4-oxo-3-quinoline carboxylic acids?
    1% 2C4-dihydro-4-oxo-3-pentenoate, this is an organic compound with specific physical properties. Its properties are usually colorless to light yellow liquid, which exists stably at room temperature and pressure.
    Looking at its physical state, it is liquid at room temperature, with good fluidity, just like the agility of a clear spring, and it flows when it is poured, without stagnation. Its color is pure, colorless to light yellow, like the early morning sun shining on the clear liquid, without the disturbance of variegated colors.
    Smell its smell, emitting a light fragrance, not pungent or strong, just like the fragrance of the stamens in the spring breeze, giving people a sense of comfort. < Br >
    In terms of its solubility, it can be dissolved in common organic solvents, such as ethanol and ether. In ethanol, it can quickly blend, regardless of each other, just like a fish entering water, swimming freely, forming a uniform solution. This property is derived from the harmonious interaction between its molecular structure and the molecules of the organic solvent, so it can dissolve.
    Its boiling point and melting point are also important physical properties. The value of the boiling point makes it possible to transform from a liquid state to a gaseous state at a specific temperature. This temperature is the key node for molecules to break free from the liquid phase and escape into the gaseous phase. The melting point determines the temperature at which they change from a solid state to a liquid state. When the temperature rises to the melting point, the structure of the solid state gradually disintegrates, and the molecules are energized and agile, resulting in a liquid state. < Br >
    Density is also one of the characteristics. Compared with water, it is lighter or heavier, reflecting its mass per unit volume. This characteristic is of great significance in many practical applications, related to the hierarchical distribution when mixed with other substances.
    The physical properties of this compound are like its unique "business card", opening the door to explore its chemical mysteries and practical applications for those who know and use it.
    Is the chemical property of 1,4-dihydro-4-oxo-3-quinoline carboxylic acid stable?
    1% 2C4-dihydro-4-oxo-3-pyridinecarboxylic acid is a relatively stable chemical substance. Its stability is due to various structural properties. From the perspective of the structure of the pyridine ring, the pyridine ring has a certain aromaticity, and the aromatic system usually has high stability. The delocalized distribution of electron clouds reduces the molecular energy and enhances the overall stability.
    In this substance, the 1,4-dihydro and 4-oxo structural parts, although they have unsaturated bonds, form a conjugate system with the pyridine ring, which further disperses electrons and stabilizes the molecule. The carboxyl group of the 3-pyridinecarboxylic acid part has some activity, but under the influence of the whole molecular conjugation system and pyridine ring, the molecular stability is not significantly damaged.
    However, the stability of this substance is also affected by external conditions. In a strong acid or strong base environment, the carboxyl group may react, changing the molecular structure and affecting the stability. Under high temperature conditions, the thermal motion of the molecule intensifies, which may cause chemical bond cracking and damage the stability. In the presence of specific oxidizing agents or reducing agents, unsaturated bonds and related groups may also participate in the reaction, resulting in changes in stability. However, 1% 2C4-dihydro-4-oxo-3-pyridinecarboxylic acid can maintain good stability under normal conditions, such as normal temperature, normal pressure, neutral environment and no special chemical reagents.
    What are the preparation methods of 1,4-dihydro-4-oxo-3-quinoline carboxylic acid?
    1% 2C4-dihydro-4-oxo-3-quinolinecarboxylic acid. The preparation method of this substance is also covered in ancient books.
    One method may be initiated by a suitable aromatic compound. First, the benzene substance with a specific substituent should be condensed with the nitrogen-containing heterocyclic precursor under appropriate reaction conditions. During this condensation process, attention should be paid to the temperature, pressure and catalyst selection of the reaction. For example, a metal salt with a specific activity can be selected as a catalyst, and the combination of the two can be promoted under moderate heating and pressure to form a preliminary intermediate product. < Br >
    Furthermore, the step of oxidation is applied to the intermediate product. Suitable oxidants, such as a certain type of high-valent metal oxide, can be used to oxidize specific groups in it to achieve the structural requirements of 4-oxygen substitution. During oxidation, the pH and reaction time of the reaction system need to be carefully controlled to prevent excessive oxidation from impurities or low yields of the product.
    Another method can start from carboxylic acid derivatives containing specific carbon chain structures. First, the functional groups on the carboxylic acid derivatives are modified to have the activity of nucleophilic substitution or addition reactions with subsequent reactants. Afterwards, they are combined with nitrogen-containing heterocyclic fragments to form key intermediates. In this binding step, the choice of solvent is very important, and it is necessary to choose a solvent that can dissolve the reactants and has no adverse interference with the reaction. Then, the resulting intermediate is cyclized, and the reaction conditions are adjusted, such as heating, adding specific dehydrating agents or cyclization accelerators, to promote the formation of the basic skeleton of 3-quinolinecarboxylic acid. Finally, depending on specific needs, the resulting product may be subjected to post-treatment operations such as reduction to obtain 1% 2C4-dihydro-4-oxo-3-quinolinecarboxylic acid.
    The process of preparation, all details are related to success or failure, from the purity of the reactants, the precise control of the reaction conditions, to the fine operation of the post-processing, cannot be ignored. It is necessary to carefully consider and act cautiously according to the actual situation in order to obtain high-purity target products.
    What is the price range of 1,4-dihydro-4-oxo-3-quinoline carboxylic acid in the market?
    1% 2C4-dihydro-4-oxo-3-pyridinecarboxylic acid, the price of this product varies from market to market, and it often varies depending on the quality, supply and demand, where it is produced and where it is sold.
    High-quality products, pure in quality and less miscellaneous, and many in the market, the price may be slightly higher. If the origin is close to the user, the transportation cost will be reduced, and the price may also drop. There are also those who sell in bulk, and the purchase quantity is large, and the price will be profitable.
    However, the current price is difficult to determine. With changes in market conditions, it is different in an instant. Or a few gold per gram, or dozens of gold per gram. If you want to know the exact price, you should consult the company of chemical raw materials, the dealer of reagents, or visit the platform of chemical trading to get the real-time price.