2 Hydroxy 5 Fluoro 3 Nitropyridine
pyridine pyrrole pyrazine piperidine piperazine

2-hydroxy-5-fluoro-3-nitropyridine

    Specifications

    HS Code

    535413

    Chemical Formula C5H3FN2O3
    Appearance Solid (usually)
    Melting Point Data may vary, typically in a certain temperature range
    Solubility In Water Low solubility
    Solubility In Organic Solvents Soluble in some organic solvents like DMSO, DMF
    Pka Value relevant for its acidic or basic nature in solution
    Stability Can be sensitive to heat, light, and moisture

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    General Information
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    Frequently Asked Questions

    As a leading 2-hydroxy-5-fluoro-3-nitropyridine 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 main uses of 2-hydroxy-5-fluoro-3-nitropyridine?
    2-Hydroxy-5-fluoro-3-nitropyridine is an important member of organic compounds. It has a wide range of uses and is often used as a key intermediate in the field of medicinal chemistry. Due to the special chemical structure of this compound, it can be skillfully combined with other molecules through various chemical reactions in the process of drug synthesis, and then construct drug molecules with complex structures and specific biological activities.
    The development of modern medicine and the birth of many innovative drugs rely on such intermediates as the cornerstone. For example, in the creation of antibacterial drugs, 2-hydroxy-5-fluoro-3-nitropyridine can be integrated into the drug molecular framework through fine synthesis steps, giving the drug unique antibacterial properties, or interfering with the key metabolic pathways of bacteria, or destroying the integrity of their cell walls and cell membranes, in order to inhibit the growth and reproduction of bacteria.
    In the field of pesticide chemistry, it is also highly valued. It can be used as a raw material for the synthesis of new pesticides. Such pesticides may have high insecticidal and bactericidal effects, and are environmentally friendly and have low residues. Due to their special structure, they can precisely act on specific targets of pests or pathogens to achieve targeted control, ensuring a good harvest of crops while reducing the adverse impact on the ecological environment.
    Furthermore, in the field of materials science, 2-hydroxy-5-fluoro-3-nitropyridine may participate in the synthesis of some functional materials. After specific chemical reactions, it becomes a part of the material structure, endowing the material with special properties such as optics and electricity, providing a new way for the development of new functional materials.
    In short, 2-hydroxy-5-fluoro-3-nitropyridine, with its unique chemical structure, plays an indispensable role in many fields such as medicine, pesticides and materials science, providing important material basis and technical support for the development of related fields.
    What are 2-hydroxy-5-fluoro-3-nitropyridine synthesis methods?
    The synthesis method of 2-hydroxy-5-fluoro-3-nitropyridine is a common research in the field of organic synthesis. There are various synthetic routes, and the common ones are described here.
    First, it can be started from suitable pyridine derivatives. First, pyridine with corresponding substituents is used as raw materials, and nitro groups are introduced through nitrification reaction. Under suitable reaction conditions, such as using a mixed acid of nitric acid and sulfuric acid as nitrifying reagents, the reaction temperature, time and reagent ratio are controlled to selectively introduce nitro groups into specific positions of pyridine rings to obtain nitro-containing pyridine derivatives.
    Next, fluorine atoms are introduced through a halogenation reaction. A suitable fluorination reagent, such as Selectfluor, can be selected. In the presence of a suitable base and solvent, the reaction is carried out to introduce fluorine atoms into the pyridine ring to achieve the desired substitution position.
    Finally, through the hydroxylation reaction, with a suitable nucleophilic reagent, such as alkali metal hydroxide, under appropriate reaction conditions, the halogen atom is replaced by a hydroxyl group to obtain 2-hydroxy-5-fluoro-3-nitropyridine.
    Second, the strategy of constructing the pyridine ring can also be started. Using fluorine, nitro and small molecules that can potentially be converted into hydroxyl groups as raw materials, the pyridine ring structure is constructed through a multi-step reaction. If 1, 3-dicarbonyl compounds, fluoronitriles and nitro-substituted amines are used as starting materials, under suitable catalyst and reaction conditions, through condensation, cyclization and other reactions, a pyridine ring is formed. Subsequently, the obtained pyridine derivatives are converted into appropriate functional groups, so that each group meets the requirements of the target product, and finally 2-hydroxy-5-fluoro-3-nitropyridine is obtained.
    When synthesizing this compound, attention should be paid to the control of reaction conditions at each step, such as temperature, pH, reaction time, etc., to ensure the selectivity and yield of the reaction. After each step of the reaction, appropriate separation and purification should be carried out to remove impurities, maintain the purity of the product, and make the synthesis path more perfect.
    What are the physical properties of 2-hydroxy-5-fluoro-3-nitropyridine?
    2-Hydroxy-5-fluoro-3-nitropyridine, this is an organic compound. Its physical properties are quite important and are involved in various fields of chemistry.
    First of all, its appearance, under room temperature and pressure, is mostly white to light yellow crystalline powder. The characterization of this color state is often the basis for the identification of the substance at the beginning, and it is of great significance in experimental observation and substance identification.
    The melting point is related to the key node of its phase transition. After many experiments, the melting point of 2-hydroxy-5-fluoro-3-nitropyridine is roughly in a specific range. The value of the melting point is of great significance to its purification, separation and identification work. The purity geometry of the substance can be determined by the melting point measurement.
    Solubility is also an important physical property. In common organic solvents, its solubility varies. In some polar organic solvents, such as dimethyl sulfoxide (DMSO), it exhibits good solubility and can be uniformly dispersed to form a solution; however, in non-polar solvents, such as n-hexane, the solubility is poor, insoluble or slightly soluble. This difference in solubility provides a basis for the selection of suitable solvents in the process of chemical synthesis, separation and purification to achieve the desired reaction or separation effect.
    Furthermore, the stability of the compound cannot be ignored. Due to the fact that its structure contains fluorine atoms, nitro and hydroxyl groups and other groups, its chemical activity is unique. Nitro has strong electron absorption, and hydroxyl groups have a certain electron supply effect. The interaction between the two makes the substance possible to chemically react under specific conditions. Although it is relatively stable at room temperature and pressure, in case of extreme conditions such as high temperature, strong acid and strong base, the structure may change, triggering reactions such as decomposition and substitution. Knowing its stability characteristics is crucial to control the conditions of storage, transportation and use, so as to avoid deterioration of the substance due to improper conditions or cause safety problems.
    The physical properties of 2-hydroxy-5-fluoro-3-nitropyridine, such as appearance, melting point, solubility and stability, are indispensable basic information in chemical research, industrial production and related application fields.
    What are the precautions in storage and transportation of 2-hydroxy-5-fluoro-3-nitropyridine?
    2-Hydroxy-5-fluoro-3-nitropyridine is a chemical substance, and care must be taken when storing and transporting it to prevent accidents.
    First, the storage place must be dry and cool. This chemical is susceptible to moisture. If the environment is humid or causes it to deteriorate, it will affect the quality and performance. Furthermore, a cool environment can reduce the risk of reactions caused by excessive temperature.
    Second, the material must be kept away from fire and heat sources. Because of its certain chemical activity, in case of open flames, hot topics, or the risk of combustion or even explosion, it is strictly forbidden to store and transport fireworks, and to control the temperature, good insulation measures.
    Third, this chemical should be stored separately from oxidants, reducing agents, acids, alkalis, etc. Because of its special chemical properties, it is mixed with these substances, or violent chemical reactions occur, endangering safety. When transporting, it is also not allowed to mix such substances with vehicles.
    Fourth, storage and transportation containers must be well sealed. First, it can prevent it from evaporating and polluting the environment; second, it can avoid contact with external substances and cause unnecessary reactions. The material of the container used must be compatible with the chemical and not react with it.
    Fifth, the operation and transportation personnel must be professionally trained, familiar with its characteristics, safety precautions and emergency handling methods. When working, appropriate protective equipment should be worn, such as protective clothing, gloves, goggles, etc., to ensure their own safety.
    In short, the storage and transportation of 2-hydroxy-5-fluoro-3-nitropyridine, every step is related to safety. If there is a slight carelessness, it may lead to disaster, and the relevant regulations and operating procedures must be strictly followed.
    What is the market outlook for 2-hydroxy-5-fluoro-3-nitropyridine?
    2-Hydroxy-5-fluoro-3-nitropyridine is an important compound in organic synthetic chemistry. Looking at its market prospects, there is much to discuss.
    From the perspective of the chemical industry, this compound is often a key intermediate in the pharmaceutical synthesis path. Today's pharmaceutical research and development has made great progress in targeted drugs, antibacterial drugs and other categories. Due to its unique chemical structure, 2-hydroxy-5-fluoro-3-nitropyridine can participate in many reactions to build complex drug molecular structures. For example, in the creation of specific antimicrobial drugs, it can be used as a starting material to introduce necessary functional groups through multi-step reactions to obtain pharmaceutical entities with specific biological activities. With the increasing global demand for new and efficient drugs, the position of this compound in the pharmaceutical and chemical industry chain is also becoming increasingly important, and the market demand for it may increase.
    In the field of materials science, although the application is not as extensive as that in the field of medicine, it is also emerging. With the development of high-tech industries, there is an increasing demand for materials with special properties. 2-Hydroxy-5-fluoro-3-nitropyridine may be chemically modified to prepare materials with specific electrical and optical properties, such as organic semiconductor materials. Although the current relevant research may be in the preliminary stage, if the technology breaks through over time, the market potential cannot be underestimated.
    However, its marketing activities also face challenges. The complexity of the synthesis process has led to high production costs. To expand market share, it is necessary to optimize the synthesis route and reduce costs. And its related application research still needs to be in-depth to enable more potential application fields to be developed. Only by solving such problems can 2-hydroxy-5-fluoro-3-nitropyridine expand more space in the market and usher in a broader prospect.