5 G Quinoline 7 Carboxylicacid 5 Ethyl 5 8 Dihydro 8 Oxo 3 Dioxolo 4
quinoline thiophene imidazole thiazole

5-g)quinoline-7-carboxylicacid,5-ethyl-5,8-dihydro-8-oxo-3-dioxolo(4

    Specifications

    HS Code

    452388

    Chemical Formula C14H11NO6
    Molecular Weight 289.24
    Appearance Solid (presumed, based on common quinoline - carboxylic acid derivatives)
    Physical State At Room Temperature Solid
    Solubility In Water Low (quinoline - carboxylic acid derivatives often have low water solubility)
    Solubility In Organic Solvents Soluble in some organic solvents like ethanol, DMSO (common for such compounds)
    Stability Stable under normal conditions, but may decompose under extreme heat or in the presence of strong oxidizing agents

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    General Information
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    Frequently Asked Questions

    As a leading 5-g)quinoline-7-carboxylicacid,5-ethyl-5,8-dihydro-8-oxo-3-dioxolo(4 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 chemical structure of 5-ethyl-5,8-dihydro-8-oxo-3-dioxacyclopenteno (4) [5-g] quinoline-7-carboxylic acid?
    The chemical structure of boric acid is quite unique. In terms of boron atoms, they are connected to surrounding atoms by covalent bonds.
    Boron atoms are usually in a trivalent state and combine with three hydroxyl groups (-OH), thus forming the basic structure of boric acid. The three hydroxyl groups are distributed at a specific angle in space, giving boric acid a unique three-dimensional configuration.
    And between boric acid molecules, hydrogen bonds can be used to interact. Hydrogen atoms in hydroxyl groups can form hydrogen bonds with oxygen atoms in adjacent boric acid molecules. The force of this hydrogen bond has a great influence on the physical and chemical properties of boric acid. For example, its melting point and boiling point have a certain performance, which also affects its solubility in water.
    Furthermore, the structure of boric acid makes it acidic to a certain extent. However, the reason for its acidity is that the hydroxyl group directly dissociates the hydrogen ion, because the p-orbit of the boron atom can accept the lone pair of electrons provided by the oxygen atom in the water molecule, which prompts the water molecule to dissociate the hydrogen ion, and then it becomes acidic.
    To sum up, the chemical structure of boric acid, with boron atoms as the core, forms a molecule with hydroxyl groups, and because of the hydrogen bond interaction, and has a special acidic mechanism, which is the beauty of its structure.
    What are the physical properties of 5-ethyl-5,8-dihydro-8-oxo-3-dioxacyclopenteno (4) [5-g] quinoline-7-carboxylic acid?
    "Tian Gong Kai Wu" has a saying: "Alkali is strong in nature. There are many kinds of alkali, common ones such as alkali taken from plant ash, and artificial alkali. Its color is white or gray, and it is mostly powdery. Alkali is hygroscopic, and when placed in air, it will deliquescent for a long time. And alkali is soluble in water, and its aqueous solution is alkaline, which can turn purple litmus test solution blue. The density of alkali is greater than that of water. When put into water, it sinks to the bottom. When heated in fire, alkali is stable and not easy to decompose. In addition, alkali can neutralize and react with acids to form salts and water. It can also decompose with some salts to form new salts and new bases. Alkali has a wide range of uses and is indispensable in soap making, papermaking, textiles and other industries."
    What are the preparation methods of 5-ethyl-5,8-dihydro-8-oxo-3-dioxacyclopenteno (4) [5-g] quinoline-7-carboxylic acid?
    There are several methods for making acid. In the past, many people have studied it.
    First, the amyl group is combined with dioxy. First take amyl five, dioxy eight, and mix it in the device. Then heat is applied to make it react. During this time, the oxygen generation occurs, and the amyl group changes and has different properties. If the amount of amyl group is five grams, after the change, the relevant quality can be obtained, which is the base for making acid.
    Second, burn the dioxane heterocycle. This thing is easy to change after fire. When burned, the atoms clutch and combine to produce new compounds. After this change, it can be used to make acid.
    The third is to use amyl and dioxy substances, supplemented by light. Light can promote its transformation. Pentyl and dioxy meet light, and molecules move and merge. The five of amyl and the eight of dioxy interact under light to form the quality required for the production of acid.
    These methods have all been tried by predecessors. Each has its own reason and has its own use. Although the methods are different, they all seek to make acid. Or because of the difference in materials, or because of the convenience of the device, and choose different methods. If you want to be good at something, you should carefully observe its reason and act according to the review, and you can get the best effect.
    In which fields is 5-ethyl-5,8-dihydro-8-oxo-3-dioxacyclopenteno (4) [5-g] quinoline-7-carboxylic acid used?
    "Tiangong Kaiwu" says: "The sprouts and malts are used for saccharification in ancient times. The method is to use rice and wheat to germinate and dry, and the length of the sprouts is small, and it is used for brewing and boiling." This is the application of sprouts and malts in brewing and making wine.
    And the application of carboxyl groups is also quite extensive. In the field of medicine, many drug molecules contain carboxyl structures, which can help drugs bind specifically to targets and enhance their efficacy. For example, aspirin, whose core structure contains carboxyl groups, has antipyretic, analgesic and anti-inflammatory effects, and is a commonly used drug.
    In materials science, carboxyl groups can participate in the synthesis of polymer materials. Through the reaction of carboxyl groups with other functional groups, polymers with different properties can be prepared. For example, polyester materials, prepared by the condensation reaction of carboxyl groups and hydroxyl groups, are widely used in fiber, plastic and other industries, such as common polyester fibers, with crisp anti-wrinkle, easy to wash and dry characteristics.
    In the food industry, organic acids containing carboxyl groups are commonly found in food additives. Citric acid contains carboxyl groups, which have a sour taste and good chelating ability. It is often used as a sour agent and antioxidant synergist in beverages, candies and other foods, which can adjust food flavor and improve stability.
    In biochemistry, carboxyl groups play a key role in the structure and function of biological macromolecules such as proteins and nucleic acids. Amino acids contain carboxyl groups, which are interconnected to form protein polypeptide chains. Carboxyl groups participate in the formation of peptide bonds, and also have important effects on the regulation of protein spatial structure and function.
    What is the market prospect of 5-ethyl-5,8-dihydro-8-oxo-3-dioxacyclopenteno (4) [5-g] quinoline-7-carboxylic acid?
    The market prospect of heptanoic acid today is like a changing celestial phenomenon, which is difficult to predict. However, if you study it carefully, you can also get clues.
    heptanoic acid, in today's world, is in a quite unique situation. Everything from hardware, such as magnesium base in the ratio of 5 and 8, to chemical products, such as carbon dioxide in 8, epoxy in 3, and photolysis in 5 grams, is related to it, and everything is linked to each other, affecting its market trend.
    As far as the scene is concerned, heptanoic acid is useful in many fields. In the field of industry, it is indispensable because it is related to magnesium-based, carbon dioxide, and epoxy compounds, or can be used as a catalytic agent, or as a synthetic material to help industrial processes. Therefore, in the industrial market, its demand may have a certain foundation, and with the development of industry, the progress of science and technology, new uses may increase. If the industry expands and new technologies are introduced, the demand for seven acids may grow accordingly.
    However, the change of the market is not limited to one end of demand. Its supply is also the key. The production capacity and the quality of technology in the factories that produce seven acids all determine the market. If there is excess capacity and oversupply, the price will fall; if the technology is stagnant and the quality is not high, it will be difficult to take advantage of the market.
    Looking at the competition in the market, it is also fierce. Similar products may have substitutes, or better performance, or cheaper prices. If Seven Acids wants to win a place in it, we must think of ways to improve.
    Then discuss the external factors of the market, the orientation of policies, and the requirements of environmental protection, all of which affect the market of Seven Acids. If policies encourage its use and environmental protection standards are conducive to production, the market prospect is promising; on the contrary, if policies restrict and environmental protection is strict, the road ahead may be difficult.
    The market prospect of Seven Acids, opportunities and challenges coexist. It is necessary to understand the changes in the market, improve technology, and adapt to policies in order to seek opportunities for development and gain market benefits in the turbulent market.