3 Cyano 7 Ethoxy 4 Hydroxy 6 Acetylamino Quinoline
quinoline thiophene imidazole thiazole

3-Cyano-7-ethoxy-4-hydroxy-6-(acetylamino)quinoline

Taiy Chemical

    Specifications

    HS Code

    557790

    Chemical Formula C14H13N3O4
    Molecular Weight 287.27 g/mol

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    General Information
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    Frequently Asked Questions

    As a leading 3-Cyano-7-ethoxy-4-hydroxy-6-(acetylamino)quinoline 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 3-Cyano-7-ethoxy-4-hydroxy-6- (acetylamino) quinoline?
    3-Cyano-7-ethoxy-4-hydroxy-6- (acetamido) quinoline is used in the fields of medicine and chemical industry.
    In the field of medicine, it can be used as a key intermediate in drug synthesis. Drug developers often use it as a base and create new drugs with specific pharmacological activities through subtle chemical modification and transformation. Due to its unique chemical structure, it can be combined with specific targets in organisms to play a role in regulating physiological functions and treating diseases. For example, in the development of anti-tumor drugs, the compound can be modified to act precisely on specific proteins of tumor cells and inhibit the proliferation and metastasis of tumor cells. < Br >
    In the field of chemical industry, it also has outstanding performance in the synthesis of dyes and pigments. Because of its structure, it can give the product unique color and stability. Dyeers can use its characteristics to develop new dyes with bright colors, light resistance and washing resistance, which can be used in textile, printing and dyeing industries to make fabrics show brilliant and lasting colors. Furthermore, in the preparation of some high-performance materials, 3-cyano-7-ethoxy-4-hydroxy-6 - (acetamido) quinoline can be used as a functional additive to enhance the physical and chemical properties of the material, such as enhancing the material's oxidation resistance and thermal stability, thereby expanding the application range of the material.
    What are the physical properties of 3-Cyano-7-ethoxy-4-hydroxy-6- (acetylamino) quinoline
    3-Cyano-7-ethoxy-4-hydroxy-6- (acetamido) quinoline, this is an organic compound with unique physical properties. Its color state is mostly crystalline powder, which is solid at room temperature and pressure, stable and quiet.
    Looking at its solubility, it can be moderately dissolved in common organic solvents such as ethanol and dichloromethane. Just like fish entering water, although not completely fused, it can also be somewhat compatible. In water, its solubility is very small, just like the barrier between oil and water, it is difficult to be intimate.
    Melting point is a key indicator to measure its thermal change. The melting point of this compound is quite clear. At a specific temperature, it will gradually change from solid state to liquid state, just like ice melting under warm sun. This melting point characteristic is of great significance for its synthesis, purification and other operations, just like a beacon for navigation, guiding the choice of operating temperature.
    Its stability cannot be ignored. Under normal environmental conditions, it is quite stable and can resist the interference of many ordinary factors. However, in case of extreme conditions such as strong acid, strong alkali or high temperature, it will be like a gentle beast suddenly disturbed, and its chemical structure may change, triggering a chemical reaction.
    In addition, the spectral properties of this compound are also unique. Its infrared spectrum can accurately represent the vibration absorption peaks of specific chemical bonds in molecules like fingerprints, helping researchers to understand the mysteries of molecular structure. In the ultraviolet-visible spectrum, the absorption peaks at specific wavelengths can also reflect the electronic transition characteristics of molecules, just like the wonderful light and shadow changes in the microscopic world inside molecules. These spectral properties provide powerful tools for their analysis and identification, like a compass in the hands of an explorer, guiding the direction in the complex chemical world.
    What is the chemical synthesis method of 3-Cyano-7-ethoxy-4-hydroxy-6- (acetylamino) quinoline
    The chemical synthesis of 3-cyano-7-ethoxy-4-hydroxy-6- (acetamido) quinoline requires multiple steps of delicate reactions. First, suitable quinoline derivatives are often used as starting materials. Or take quinoline with appropriate substituents, such as those with modifiable groups at specific positions.
    The introduction of ethoxy groups can be used to obtain 7-ethoxy quinoline derivatives by nucleophilic substitution reaction of quinoline substrates with ethoxylating reagents, such as sodium ethanol and corresponding halogenated hydrocarbons, in suitable solvents. This reaction requires attention to the control of reaction temperature and time. If the temperature is too high or side reactions occur, if the time is too short, the reaction will not be fully functional.
    times and 4-hydroxyl groups are added. Or by hydrolysis, oxidation and other reactions, a specific group is converted into a hydroxyl group. For example, if the starting material has a hydrolyzable ester group or an oxidizable group, it is treated under the corresponding conditions to form a hydroxyl group at the 4 position. During hydrolysis, suitable acid and base conditions need to be selected. If the acid and base are too strong or damage other parts of the molecule.
    As for the construction of 6 - (acetamide), the amino group is often introduced first with an amination reagent and then reacted with an acetylation reagent. For example, ammonia gas or ammonia derivatives react with substrates to form aminoquinoline, and then react with acetyl chloride or acetic anhydride under the catalysis of an appropriate base to form a 6- (acetamido) structure. In this process, the amount and activity of the base are also key, which are related to the selectivity and yield of the reaction.
    The formation of 3-cyano groups can be reacted with cyanide reagents by halogenated compounds. The 3-halogenated quinoline derivatives react with cyanidating agents such as potassium cyanide or sodium cyanide in an organic solvent in the presence of a phase transfer catalyst to obtain a 3-cyano product. The choice and amount of phase transfer catalyst have a great impact on the reaction rate and efficiency.
    After each step of the reaction, separation and purification techniques, such as column chromatography, recrystallization, etc. are required to remove impurities and obtain pure 3-cyano-7-ethoxy-4-hydroxy-6 - (acetamido) quinoline. Each step of the reaction needs to be carefully regulated to make the synthesis process smooth and obtain the desired product.
    3-Cyano-7-ethoxy-4-hydroxy-6- (acetylamino) quinoline is used in which areas
    3-Cyano-7-ethoxy-4-hydroxy-6- (acetamido) quinoline, which has a wide range of uses and is involved in many fields such as medicinal chemistry and materials science.
    In the field of medicinal chemistry, such compounds containing quinoline structure often have unique biological activities. The quinoline skeleton is an important structural unit of many drugs. Due to its special chemical structure, it can interact with specific targets in organisms. Functional groups such as cyano, ethoxy, hydroxyl and acetamido in this compound can affect its pharmacological properties. For example, hydroxyl groups can enhance the hydrophilicity of compounds, which is conducive to transport and metabolism in living organisms; cyanyl groups can change the distribution of molecular electron clouds and affect the ability to bind to targets, so they may exhibit biological activities such as antibacterial, anti-inflammatory, and anti-tumor, or lay the foundation for the development of new drugs.
    In the field of materials science, due to its orderly and stable molecular structure, or with unique optical and electrical properties. In the field of organic optoelectronic materials, compounds with quinoline structures are often used as luminescent materials or charge transport materials. The compounds have different functional groups or endow them with specific light absorption and emission characteristics, which can be used to prepare materials such as Light Organic Emitting Diode (OLED) and fluorescence sensors. In addition, its stability may make it stand out in some material applications that require stable structure, such as additives for some special coating materials or polymer composites to enhance material properties.
    In summary, 3-cyano-7-ethoxy-4-hydroxy-6 - (acetamido) quinoline has potential application value in the field of medicine and materials. With the deepening of research, it is expected to bring new opportunities for the development of related fields.
    What is the market outlook for 3-Cyano-7-ethoxy-4-hydroxy-6- (acetylamino) quinoline?
    3-Cyano-7-ethoxy-4-hydroxy-6- (acetamido) quinoline, the market prospect of this substance today, just like the ancient books say "the rise and fall of things, the time is also, the trend is also". Its market situation is related to many parties, like a complex chess game.
    From the perspective of the medical field, quinoline compounds often have unique biological activities, or can be used to develop new drugs. The cyano, hydroxy, acetamido and other groups of this compound may endow it with antibacterial, anti-inflammatory, anti-tumor and other potential effects. If we can deeply explore its pharmacological mechanism and develop corresponding drug products, we may be able to occupy a place in the pharmaceutical market, just like Gu Yun "good medicine and good medicine, the power of helping the world".
    Looking at the chemical industry, it may be used as a key intermediate in organic synthesis. With its special chemical structure, a variety of high-value-added fine chemicals can be derived through various reactions. However, the chemical market is changing and the competition is fierce. If you want to emerge in this field, you need advanced synthesis technology to ensure the quality and output of products, so as to "win people with technology and win with quality".
    Furthermore, market demand is the key factor. At present, with the deepening of scientific research and the development of the industry, the demand for organic compounds with special structures is gradually increasing. If this compound can meet the specific needs of the market, and the supply is stable and the price is reasonable, its future may be bright. However, the market is also influenced by policies and regulations, and environmental protection requirements are becoming stricter, or its production and application are limited. Enterprises need to comply with regulations, "change with time, and follow the trend" in order to move forward steadily in the market wave.
    To sum up, the market prospects, opportunities and challenges of 3-cyano-7-ethoxy-4-hydroxy-6- (acetamido) quinoline coexist. It is necessary to gain insight into the market, improve technology, and adapt to the times in order to seize the opportunity and achieve a career.