6 Hydrox 5 Quinolinecarbaldehyde
quinoline thiophene imidazole thiazole

6-hydrox-5-quinolinecarbaldehyde

Taiy Chemical

    Specifications

    HS Code

    431646

    Name 6 - hydrox - 5 - quinolinecarbaldehyde
    Chemical Formula C10H7NO2
    Molar Mass 173.17 g/mol
    Appearance Solid (usually)
    Odor May have a characteristic odor
    Solubility In Water Low solubility in water
    Solubility In Organic Solvents Soluble in some organic solvents like ethanol
    Melting Point [Specific melting point value if available]
    Boiling Point [Specific boiling point value if available]
    Stability Stable under normal conditions if stored properly
    Reactivity Can react with reagents typical for aldehydes and phenols
    Pka [pKa value if available for the phenolic - OH group]

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    Frequently Asked Questions

    As a leading 6-hydrox-5-quinolinecarbaldehyde 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 chemical properties of 6 - hydrox - 5 - quinolinecarbaldehyde
    6-Hydroxy-5-quinoline formaldehyde is an organic compound. It has unique chemical properties and is very important in the fields of organic synthesis chemistry and materials science.
    In terms of chemical activity, the hydroxyl groups and aldehyde groups of 6-hydroxy-5-quinoline formaldehyde are active functional groups. Hydroxyl groups can participate in various reactions, such as esterification reactions. Under acid catalysis, they react with carboxylic acids to form ester compounds. This reaction is often used to prepare organic esters with specific functions and is common in the fields of fragrance and drug synthesis. Moreover, hydroxyl groups can undergo substitution reactions and interact with reagents such as halogenated hydrocarbons to form new carbon-oxygen bonds, whereby different substituents can be introduced to change the properties and functions of compounds. The activity of the
    aldehyde group should not be underestimated. It is prone to oxidation and can be oxidized to carboxyl groups. Commonly used oxidants such as potassium permanganate and Jones reagent can achieve this conversion to generate 6-hydroxy-5-quinolinecarboxylic acid. This product has important applications in the design of some drug molecules and organic synthesis routes. At the same time, aldehyde groups can participate in nucleophilic addition reactions, such as acetal reactions with alcohols, and are often used as carbonyl protection methods in organic synthesis. After the reaction is completed, the aldehyde groups can be restored by hydrolysis. The aldehyde group can also condensate with ammonia and its derivatives to form Schiff base compounds. These compounds are often used as ligands in coordination chemistry to form complexes with metal ions, showing diverse structures and properties, and have potential applications in catalysis and materials science.
    Furthermore, the conjugate system of 6-hydroxy-5-quinoline-formaldehyde endows it with certain optical properties. Its intramolecular electrons can be delocalized in the conjugate system, so that the compound may undergo electron transitions under specific wavelength light irradiation, showing fluorescent properties. This fluorescent property may have application potential in fluorescent probe design and biological imaging. Because it can bind to specific molecules in organisms, the detection and imaging of biomolecules can be achieved through changes in fluorescence signals.
    What are the synthesis methods of 6 - hydrox - 5 - quinolinecarbaldehyde
    There are many ways to synthesize 6-hydroxy-5-quinoline formaldehyde. One of the common ones is to use quinoline as the initial raw material and obtain it through a multi-step reaction. First, the quinoline is substituted with a suitable reagent under specific conditions, and the hydroxyl group is introduced at a specific position in the quinoline ring. This step requires fine control of the reaction conditions, such as temperature, pH and the ratio of the reactant, to ensure that the hydroxyl group is accurately connected to the target check point.
    Then, the specific group is converted into an aldehyde group by suitable oxidation means. This oxidation step requires a high degree of reagent selection and reaction environment. Commonly used oxidizing agents include specific chromium reagents or mild oxidation systems to ensure that the aldehyde group is generated without destroying the formed hydroxyl and quinoline ring structures.
    The second synthesis method, or starting from the compound containing the quinoline skeleton, is gradually modified to construct the desired substituent first, and then the aldehyde reaction is carried out. In the meantime, organometallic reagents can be used to participate in the reaction to precisely construct carbon-carbon bonds or carbon-heteroatomic bonds to achieve accurate shaping of the molecular structure.
    Furthermore, there is a strategy to construct a quinoline ring by cyclization with a simple aromatic compound as the starting material, and at the same time introduce hydroxyl and aldehyde groups at an appropriate stage. In this process, the choice of cyclization conditions is the key, which is related to the formation of quinoline rings and the positioning of their substituents. It is necessary to choose suitable catalysts, solvents and reaction temperatures according to different reaction paths to achieve the purpose of high-efficiency and high-selectivity synthesis of 6-hydroxy-5-quinoline formaldehyde. Each synthesis method has its own advantages and disadvantages, and it is necessary to choose according to actual needs and conditions.
    Where is 6 - hydrox - 5 - quinolinecarbaldehyde used?
    6-Hydroxy-5-quinoline formaldehyde is a unique organic compound. It has shown its extraordinary uses in many fields.
    In the field of pharmaceutical research and development, its role is quite important. Because of its unique structure or specific biological activity, it can be used as a lead compound. By modifying and modifying its chemical structure, medical scientists can explore new drugs with better pharmacological properties, or can be used for the treatment and prevention of diseases, such as for some difficult diseases, it is expected to develop specific drugs.
    In the field of materials science, 6-hydroxy-5-quinoline formaldehyde also has extraordinary performance. It can be used to prepare functional materials with special properties, such as luminescent materials. Because its molecular structure can emit light under specific conditions, it can be applied to optical displays, sensors and other fields. By compounding with other substances, the luminescence properties of the material can be adjusted to meet the needs of different scenarios, contributing to the innovation and development of optical materials.
    Furthermore, in the field of organic synthesis, it is an important intermediate. Chemists can use various chemical reactions to use 6-hydroxy-5-quinoline formaldehyde as the starting material to construct more complex organic molecular structures. Through ingenious reaction design and optimization of conditions, a series of organic compounds with special functions and uses can be synthesized, enriching the "treasure house" of organic synthesis and promoting the progress of organic chemistry.
    In addition, in analytical chemistry, its characteristics may be used to develop new analytical methods and reagents. By virtue of its interaction with specific substances, sensitive detection and analysis of certain substances can be achieved, improving the accuracy and efficiency of analytical chemistry, and assisting in the accurate determination of substance composition and content in scientific research and production practice.
    6 - hydrox - 5 - what is the market outlook for quinolinecarbaldehyde
    6-Hydroxy-5-quinoline formaldehyde, this is an organic compound. Looking at its market prospects, it can be discussed from multiple ends.
    In the field of scientific research, its prospects are quite promising. Due to its special chemical structure, it is often used as a key intermediate in organic synthetic chemistry. Chemists can prepare many compounds with special properties and uses by modifying and reacting its structure, such as new fluorescent materials, bioactive molecules, etc. In the field of materials science, it may be able to construct novel functional materials through specific reactions, such as materials for photoelectric conversion, so the demand for scientific research may promote the stable growth of its market.
    In the pharmaceutical industry, there may be potential opportunities. Functional groups such as hydroxyl and aldehyde groups in its structure give the molecule a certain biological activity. Study or reveal its role in specific disease targets, and then develop new drugs. Although it is currently or not widely used in clinical practice, the continuous advancement of pharmaceutical research and development may give it an opportunity to emerge, and it may become an important raw material for new drug research and development in the future, expanding the market space.
    However, its market also faces challenges. The complexity of the synthesis process or the limitation of large-scale production, resulting in high costs and affecting market competitiveness. And market awareness may be limited. To expand the market, it is necessary to increase publicity and promotion efforts to improve the understanding of its performance and application in related industries.
    Overall, the market prospect of 6-hydroxy-5-quinoline formaldehyde has both opportunities and challenges. With the progress of scientific research and the expansion of applications, if the problems of synthesis and marketing activities can be overcome, it is expected to occupy an important place in the fields of chemical industry and medicine, and bloom more brightly.
    What is the production process of 6 - hydrox - 5 - quinolinecarbaldehyde
    The production process of 6-hydroxy-5-quinoline formaldehyde is the key to chemical preparation. To make this substance, follow the right path of chemical synthesis.
    The initial steps often involve careful selection and preparation of raw materials. Select appropriate starting materials, such as specific quinoline derivatives, which are the foundation of synthesis. The purity and quality of raw materials are related to the quality of the product, so they must be selected according to strict standards.
    Then, the control of the reaction conditions is crucial. In a suitable reaction vessel, mix the raw materials in proportion, and introduce suitable reagents and catalysts. Temperature, pressure, reaction time and other conditions need to be precisely regulated. If the temperature is too high, it can affect the reaction rate and the selectivity of the product. If the temperature is too high, or the side reactions occur frequently, the product is impure; if the temperature is too low, the reaction will be slow and the efficiency will be low.
    In the synthesis process, it may involve a multi-step reaction. First, the raw material is converted into an intermediate product through a specific reaction path. This intermediate product needs to be separated and purified to remove impurities and maintain its purity. The separation method can choose extraction, distillation, recrystallization, etc. according to the characteristics of the substance. After the purified intermediate product, the next step of reaction is carried out until the target product 6-hydroxy-5-quinoline formaldehyde is formed.
    After the product is generated, it also needs to be strictly tested. Use modern analytical methods, such as chromatography and spectroscopy, to measure its purity and structure to ensure that it meets Quality Standards. In this way, qualified 6-hydroxy-5-quinoline formaldehyde products can be obtained for subsequent scientific research, production and other fields. This process requires fine operation and strict control to achieve high-quality products.