Ethyl 6 7 8 Trifluoro 4 Oxo 1 4 Dihydroquinoline 3 Carboxylate
quinoline thiophene imidazole thiazole

ethyl 6,7,8-trifluoro-4-oxo-1,4-dihydroquinoline-3-carboxylate

Taiy Chemical

    Specifications

    HS Code

    766841

    Chemical Formula C12H8F3NO3
    Molar Mass 273.19 g/mol
    Appearance Solid (usually white or off - white)
    Physical State At Room Temperature Solid
    Solubility In Water Low solubility
    Solubility In Organic Solvents Soluble in some organic solvents like DMSO, acetone
    Melting Point Specific value would need experimental determination
    Pka Related to the acidic or basic functional groups in the molecule, value would need experimental determination
    Uv Vis Absorption Absorbs in specific UV - Vis regions characteristic of the quinoline moiety

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    Frequently Asked Questions

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    What is the chemical structure of ethyl 6, 7, 8 - trifluoro - 4 - oxo - 1, 4 - dihydroquinoline - 3 - carboxylate
    This is the chemical structure analysis of 6,7,8-trifluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid ethyl ester. Looking at this name, "ethyl ester" refers to the structural characteristics of carboxylic acid and ethanol esters, indicating that it contains ester-COOCH -2 CH. "6,7,8-trifluoro" expressly states that there is a fluorine atom substitution at the 6th, 7th, and 8th positions of the quinoline ring. The fluorine atom has strong electronegativity, which has a great influence on molecular properties. "4-oxo" has a carbonyl group at the 4th position, which plays a key role in chemical reactions and molecular activities. " 1,4-Dihydroquinoline "outlines the structure of the parent nucleus as a partially hydrogenated quinoline ring. The hydrogen atoms at positions 1 and 4 make the electron cloud distribution of the ring different from that of quinoline, resulting in its unique chemical activity." 3-carboxylic acid "refers to the carboxyl-COOH connected to the 3 position of the quinoline ring, which is acidic and can participate in many reactions. Overall, the structure of this compound is complex, and each substituent affects each other. Its unique chemical structure endows it with diverse chemical properties and potential application value.
    What are the main uses of ethyl 6, 7, 8 - trifluoro - 4 - oxo - 1, 4 - dihydroquinoline - 3 - carboxylate
    Ethyl 6,7,8-trifluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid ester, which is widely used and has important applications in the fields of medicine, pesticides and materials.
    In the field of medicine, it is often a key intermediate for the creation of many new antibacterial drugs. Due to its unique chemical structure, it can be derived and modified rationally to obtain compounds that exhibit high inhibitory activity against specific bacteria. By interfering with specific physiological processes of bacteria, such as nucleic acid synthesis or protein synthesis, it achieves antibacterial effect and provides a powerful weapon for humans to fight against bacterial infections and diseases.
    In the field of pesticides, it also plays an important role. Can be used to develop new pesticides, fungicides and other pesticide products. For common crop pests and diseases, scientifically designed and synthesized pesticides based on them can accurately act on pests or pathogens, effectively inhibit their growth and reproduction, thereby protecting the healthy growth of crops, improving crop yield and quality, and ensuring agricultural harvest.
    In the field of materials, ethyl 6,7,8-trifluoro-4-oxo-1,4-dihydroquinoline-3-carboxylate can be used to prepare materials with special properties. For example, by introducing it into a polymer material through a special process, it can change the optical, electrical or thermal properties of the material, imparting unique properties such as fluorescence properties, improved electrical conductivity or enhanced thermal stability to the material, thus meeting the needs of different fields for special materials and promoting the continuous development and progress of materials science.
    What is the synthesis method of ethyl 6, 7, 8 - trifluoro - 4 - oxo - 1, 4 - dihydroquinoline - 3 - carboxylate
    The author of "Tiangong Kaiwu" is an ancient book of science and technology, but it does not contain the synthesis method of "ethyl 6,7,8-trifluoro-4-oxo-1,4-dihydroquinoline-3-carboxylate". This compound is a product of modern organic chemistry.
    To synthesize this compound, it is commonly used in today's organic synthesis methods. First, a quinoline skeleton can be constructed by a multi-step reaction from a suitable starting material. For example, a fluorine-containing aromatic compound and a carbonyl-containing compound are condensed to form a preliminary structure.
    Times, the resulting intermediate is oxidized, reduced or substituted to introduce specific functional groups. For example, a specific group is converted into a carbonyl group by oxidation reaction, and then its oxidation state is adjusted by reduction reaction.
    In addition, the control of reaction conditions is crucial. Temperature, pressure, catalyst selection and dosage all affect the rate and yield of the reaction. For example, some reactions need to be carried out at low temperature to avoid side reactions; for others, high temperature and high pressure are required to promote the occurrence of the reaction.
    And the solvent used also needs to be selected according to the characteristics of the reaction. Polar or non-polar solvents have an impact on the stability of the intermediate and the reaction path of the reaction.
    Although there is no such synthesis method in "Tiangong Kaiwu", the scientific ideas contained in it are also in common with today's synthesis concepts. They all focus on the selection of raw materials, the precision of the process, and the control of conditions in order to achieve the quality of the product.
    What are the physical properties of ethyl 6, 7, 8 - trifluoro - 4 - oxo - 1, 4 - dihydroquinoline - 3 - carboxylate
    Ethyl 6,7,8 - trifluoro - 4 - oxo - 1,4 - dihydroquinoline - 3 - carboxylate, this is an organic compound, often found in the field of medicinal chemistry and organic synthesis. The following is an explanation of its physical properties:
    Looking at its properties, this substance is usually in the state of a crystalline solid, which is caused by intermolecular interactions, such as van der Waals forces, hydrogen bonds, etc., resulting in the orderly arrangement of molecules, and then the formation of a crystalline structure.
    As for the melting point, because the exact value is affected by impurities and measurement conditions, it is roughly in a specific temperature range. At this temperature, the molecule is energized enough to overcome the lattice energy, and the lattice structure disintegrates, so it changes from a solid state to a liquid state. < Br >
    In terms of solubility, in organic solvents, such as common ethanol, dichloromethane, acetone, etc., there is a certain solubility. This is because the compound molecules and organic solvent molecules can form interactions such as van der Waals forces, hydrogen bonds, etc., which help them disperse in solvents. In water, the solubility is relatively low, and due to the lack of sufficient hydrophilic groups in its molecular structure, it is difficult to form effective interactions with water molecules.
    Its density is slightly larger than that of water. This is determined by its molecular weight and molecular accumulation mode. Higher molecular mass and tight molecular accumulation increase the mass of the substance per unit volume, so the density is relatively large.
    In terms of stability, it is relatively stable under conventional environmental conditions. However, under extreme conditions such as high temperature, strong acid, strong base or strong oxidant, the molecular structure may change. Because there are active checking points such as carbonyl and double bonds in the molecular structure, it can participate in chemical reactions, such as hydrolysis of ester groups under the catalysis of strong acid or strong base.
    The above physical properties are crucial in the process of organic synthesis and drug development. Such as solubility, which affects its dispersion and mass transfer in the reaction system, is related to the reaction rate and yield; stability determines its storage conditions and use range. Therefore, familiarity with the physical properties of this substance can be better used in chemical practice.
    Ethyl 6, 7, 8 - trifluoro - 4 - oxo - 1, 4 - dihydroquinoline - 3 - carboxylate
    Ethyl-6,7,8-trifluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid esters are a class of compounds that have attracted much attention in the field of organic synthesis. As far as its market prospects are concerned, it presents a complex and diverse situation.
    In the field of pharmaceutical research and development, with the in-depth exploration of new antibacterial and anti-inflammatory drugs, such compounds exhibit significant biological activity due to their unique molecular structures or can be used as lead compounds after modification and optimization. This has opened up a broad market space for them. Many pharmaceutical companies and scientific research institutions are interested in their potential medicinal value and actively participate in related research. Therefore, under the background of driving pharmaceutical innovation, there may be a certain market demand growth in the future.
    In the field of materials science, due to its special electronic properties and chemical stability, it may be applied to the preparation of optoelectronic materials and high-performance polymers. With the continuous advancement of science and technology, the demand for new functional materials is increasing day by day. If technological breakthroughs and application expansion can be achieved in this field, its market potential is also considerable.
    However, the market development of this compound also faces several challenges. Its synthesis process may involve complex reaction steps and expensive raw materials, resulting in high production costs, which may hinder its large-scale production and marketing activities. Furthermore, the market competition is also quite fierce, and compounds with similar structures or functions are also competing for market share.
    Overall, ethyl-6,7,8-trifluoro-4-oxo-1,4-dihydroquinoline-3-carboxylate has potential market opportunities, but it also needs to overcome cost control, technological innovation and other problems in order to gain a place in the market. The prospect still requires practitioners to take stock of the situation, seize opportunities and actively respond to challenges.