7 Fluoro 1 4 Dihydro 6 Methoxy 4 Oxo 3 Quinolinecarbonitrile
quinoline thiophene imidazole thiazole

7-fluoro-1,4-dihydro-6-methoxy-4-oxo-3-Quinolinecarbonitrile

Taiy Chemical

    Specifications

    HS Code

    813024

    Chemical Formula C12H7FN2O2
    Molecular Weight 230.195
    Appearance Solid
    Color Unknown
    Odor Unknown
    Melting Point Unknown
    Boiling Point Unknown
    Solubility In Water Unknown
    Solubility In Organic Solvents Unknown
    Density Unknown
    Pka Unknown
    Logp Unknown
    Stability Unknown
    Hazardous Nature Unknown

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    General Information
    Where to Buy 7-fluoro-1,4-dihydro-6-methoxy-4-oxo-3-Quinolinecarbonitrile in China?
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    As a leading 7-fluoro-1,4-dihydro-6-methoxy-4-oxo-3-Quinolinecarbonitrile 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 physical properties of 7-fluoro-1, 4-dihydro-6-methoxy-4-oxo-3-Quinolinecarbonitrile?
    7 - fluoro - 1,4 - dihydro - 6 - methoxy - 4 - oxo - 3 - Quinolinecarbonitrile is an organic compound. Its physical properties are quite important, and it is related to the performance and application of this substance in various scenarios.
    When it comes to appearance, it is usually solid, mostly powdery, and the color is often white or almost white. This is a common state of many organic compounds. It has a fine texture, is easy to handle and weigh, and provides convenience for experiments and production operations.
    Melting point is also a key physical property. It has been experimentally determined that its melting point is within a specific range, and this value is of great significance for the identification and purification of this compound. If the melting point is accurate and sharp, it indicates that the purity of the substance is quite high; if the melting point range is wide, it indicates that there may be impurities. Knowing the melting point, during the synthesis and preparation process, the temperature can be precisely controlled to ensure the quality of the product.
    In terms of solubility, it has a certain solubility in common organic solvents such as ethanol and dichloromethane. In ethanol, moderate heating can enhance dissolution, which is convenient for integrating it into solution systems for chemical reactions or formulations. However, the solubility in water is very small, which is related to the hydrophobic groups contained in its molecular structure. This property determines its limited application in aqueous systems.
    In addition, the compound has certain stability. Under normal storage conditions, in a dry and cool place, the chemical structure and properties can remain unchanged for a long time. However, under extreme conditions such as strong acid, strong alkali or high temperature, the structure may change, triggering decomposition or other chemical reactions.
    The above physical properties lay the foundation for the research and application of 7-fluoro-1,4-dihydro-6-methoxy-4-oxo-3-Quinolinecarbonitrile, and help researchers and producers to rationally plan experiments and production processes according to their characteristics to realize the value of the compound.
    What are the chemical synthesis methods of 7-fluoro-1, 4-dihydro-6-methoxy-4-oxo-3-Quinolinecarbonitrile
    To prepare 7-fluoro-1,4-dihydro-6-methoxy-4-oxo-3-quinoline-formonitrile, there are many methods. In the past, Fang family mostly followed the classic method, first taking suitable aromatic compounds, such as benzene derivatives with specific substituents, and gradually constructing the quinoline mother nucleus through ingenious reactions, such as nucleophilic substitution, cyclization condensation and other steps.
    At the beginning, the benzene ring containing methoxy and fluorine atoms is often used as the starting material, and the active material containing nitrile groups is first introduced into the benzene ring in the appropriate alkali and solvent environment. This step requires attention to the precise control of the reaction conditions. The strength of the base and the polarity of the solvent are all related to the success or failure of the reaction and the yield. Afterwards, with a suitable cyclization reagent, at a suitable temperature and time, the benzene ring and the introduced group are cyclized to form a quinoline ring. However, in this process, the introduction of 4-position carbonyl is very critical, either through oxidation reaction or the selection of reactants with carbonyl groups to participate in the cyclization, so as to achieve the purpose of 4-oxygen substitution. < Br >
    There are also improved methods. Reactions catalyzed by transition metals, such as palladium-catalyzed coupling reactions, can introduce each substituent more accurately, and can effectively improve the selectivity and efficiency of the reaction. With palladium complexes as catalysts, the selection of ligands is also extremely important, which can affect the activity and selectivity of the catalyst. In this method, the design of the starting materials needs to meet the requirements of palladium-catalyzed reactions, and the positioning and activity of each substituent need to be carefully considered.
    Another synthetic approach guided by the concept of green chemistry attempts to use more environmentally friendly solvents, such as aqueous reaction systems, or the use of biocatalysis, with the help of enzyme efficiency and specificity, to catalyze the reaction of specific steps. Although the implementation is slightly more difficult, it has broad prospects and is expected to reduce the impact of the reaction on the environment and improve the sustainability of the synthesis.
    What is the main use of 7-fluoro-1, 4-dihydro-6-methoxy-4-oxo-3-Quinolinecarbonitrile?
    7 - fluoro - 1,4 - dihydro - 6 - methoxy - 4 - oxo - 3 - Quinolinecarbonitrile, this is an organic compound, Chinese or can be called 7 - fluoro - 1,4 - dihydro - 6 - methoxy - 4 - oxo - 3 - quinolinocarbonitrile. Its main use is more common in the field of pharmaceutical chemistry in organic synthesis.
    In the development of medicine, it is often used as a key intermediate. Due to the structure of quinoline, it has a variety of biological activities, such as antibacterial, anti-inflammatory, anti-tumor, etc. After specific chemical modifications and reactions, this compound can build more complex molecular structures with specific biological activities. Taking the development of anti-tumor drugs as an example, researchers try to develop new drugs that can precisely act on specific targets of tumor cells by modifying and modifying their structures, or enhance the affinity and lethality of drugs to tumor cells, while reducing the damage to normal cells.
    In the field of materials science, it may also have potential uses. The special structure and electronic properties of organic compounds may endow materials with unique optical and electrical properties. The fluorine atoms, methoxy groups and other functional groups contained in this compound may affect the electron cloud distribution of the material and the interaction between molecules, thereby changing the conductivity and fluorescence properties of the material. Or it can be used to prepare fluorescent materials with special optical properties, which can be used in photoelectric display, biological imaging, etc.
    In the field of pesticide chemistry, there are also applications. Quinoline compounds have inhibitory or killing effects on some pests and pathogens. With this compound as the starting material, after structural optimization and derivatization, new pesticides with high efficiency, low toxicity and environmental friendliness can be developed, which can be used for crop pest control and ensure the yield and quality of agricultural production.
    What is the market outlook for 7-fluoro-1, 4-dihydro-6-methoxy-4-oxo-3-Quinolinecarbonitrile?
    7-Fluoro-1,4-dihydro-6-methoxy-4-oxo-3-quinolinoformonitrile, which has considerable market prospects at present.
    In the field of Guanfu Chemical and Pharmaceutical, this compound is a key intermediate with a wide range of uses. In the process of drug synthesis, it can provide a cornerstone for the creation of new drugs. Due to the research and development of modern medicine, there is a growing demand for compounds with specific structures and activities. The unique structure of 7-fluoro-1,4-dihydro-6-methoxy-4-oxo-3-quinolinocarbonitrile makes it possible to derive drug molecules with excellent pharmacological activities, such as antibacterial, anti-inflammatory, anti-tumor and other fields.
    Furthermore, with the advancement of science and technology, the field of materials science has also emerged for its demand. It may find a place in organic optoelectronic materials. Due to its structural characteristics or unique optical and electrical properties, it can help develop new display materials, sensor materials, etc., and contribute to the progress of materials science.
    From the perspective of market supply and demand, with the vigorous development of the pharmaceutical and materials industries, the demand for 7-fluoro-1,4-dihydro-6-methoxy-4-oxo-3-quinoline formonitrile is expected to continue to rise. However, its production and preparation also face challenges, and it is necessary to optimize the process and increase the yield to meet the growing market demand. Overall, 7-fluoro-1,4-dihydro-6-methoxy-4-oxo-3-quinolinocarbonitrile is a promising market with both opportunities and challenges.
    7-Fluoro-1, 4-dihydro-6-methoxy-4-oxo-3-Quinolinecarbonitrile what are the precautions during storage and transportation
    7-Fluoro-1,4-dihydro-6-methoxy-4-oxo-3-quinolinoformonitrile is a fine chemical material. When storing and transporting, many matters must be paid attention to.
    First words storage. This compound should be placed in a cool, dry and well-ventilated place. Due to high temperature, or its chemical properties change, it may even cause reactions such as decomposition; excessive humidity makes it easy to absorb moisture, affecting purity and quality. The storage place should be kept away from fire, heat sources, and direct sunlight. This is because both light and high temperature may promote its chemical reaction and damage the stability of the material. Furthermore, it should be stored separately from oxidizing agents, acids, alkalis, etc., and must not be mixed. Due to the chemical structure of this compound, or violent reaction with the above substances, it is dangerous. At the same time, the storage area should be equipped with suitable materials to contain leaks, so as to prevent accidental leakage and deal with them in time to reduce hazards.
    Second talk about transportation. Be sure to ensure that the packaging is complete and sealed before transportation. Packaging materials must be able to resist vibration, collision and friction, and prevent material leakage caused by package damage. During transportation, vehicles should be equipped with corresponding varieties and quantities of fire-fighting equipment and leakage emergency treatment equipment. Driving routes should avoid passing through sensitive areas such as densely populated areas and water source protection areas. When transporting, follow the prescribed route and do not stop in residential areas and densely populated areas. And transport personnel need to be professionally trained to be familiar with the properties, hazards and emergency treatment methods of the compound. When loading and unloading, it should be handled lightly, and it is strictly forbidden to drop, touch, and collide, so as to avoid packaging damage and cause safety accidents.
    7-fluoro-1,4-dihydro-6-methoxy-4-oxo-3-quinoline formonitrile must be strictly followed throughout the storage and transportation process to ensure the safety of personnel, environmental safety and material quality.