4 Chloro 2 Hydroxy 5 Nitropyridine
pyridine pyrrole pyrazine piperidine piperazine

4-Chloro-2-hydroxy-5-nitropyridine

    Specifications

    HS Code

    495554

    Name 4-Chloro-2-hydroxy-5-nitropyridine
    Molecular Formula C5H3ClN2O3
    Molecular Weight 174.54 g/mol
    Appearance Yellow solid
    Melting Point 185 - 188 °C
    Solubility In Water Slightly soluble
    Solubility In Organic Solvents Soluble in common organic solvents like DMSO, DMF
    Hazardous Nature May cause skin and eye irritation

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    General Information
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    Frequently Asked Questions

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    What is the chemistry of 4-Chloro-2-hydroxy-5-nitropyridine?
    4-Chloro-2-hydroxy-5-nitropyridine is also an organic compound. It is active and has a variety of chemical characteristics.
    In terms of its reactivity, the chlorine atom is above the pyridine ring, because the electron cloud of the pyridine ring is different, and the chlorogenic activity is different. It can participate in nucleophilic substitution reactions. If it encounters nucleophilic reagents, halogen atoms are easily replaced. This is because the electron-absorbing property of the pyridine ring makes the carbon sites attached to the chlorine atom partially positive, and nucleophilic reagents are easy to attack.
    Hydroxyl groups in this compound also show important chemical properties. Hydroxyl groups can be used as proton donors and participate in acid-base reactions. In the alkaline environment, hydroxyl groups easily lose protons and form corresponding negative ions. This negative ion has certain nucleophilic properties and can react with many electrophilic reagents.
    Furthermore, 5-nitro is a strong electron-absorbing group, which has a great influence on the electron cloud density of the pyridine ring. It not only enhances the electrophilic substitution activity of the ring, but also decreases the electron cloud density of the ortho and para-sites. This structure affects the stability and reaction path of the compound. The chemical properties of 4-chloro-2-hydroxy-5-nitropyridine are formed by the interaction of chlorine atoms, hydroxyl groups and nitro groups, and the conjugate system of pyridine rings. It has potential application value in the field of organic synthesis and can be used as intermediates to prepare various functional compounds.
    What are the main uses of 4-Chloro-2-hydroxy-5-nitropyridine?
    4-Chloro-2-hydroxy-5-nitropyridine, this compound has a wide range of uses and has its presence in many fields.
    In the field of medicinal chemistry, it is often a key intermediate for the synthesis of drugs. Due to its unique chemical structure, it can introduce other functional groups through a series of chemical reactions to construct compounds with specific pharmacological activities. For example, it may participate in the creation of antibacterial drugs, and interact with the target in the body of the bacteria through its structure, interfering with the normal physiological process of the bacteria, achieving antibacterial effect.
    In the field of materials science, it also has extraordinary performance. It can be chemically modified to integrate into polymer materials, giving the material special optical, electrical or thermal properties. For example, it can improve the conductivity of materials and find a place in the field of electronic device manufacturing; or enhance the ability of materials to absorb or emit light at specific wavelengths, for the research and development of optoelectronic devices, such as Light Emitting Diode.
    In the field of pesticide chemistry, 4-chloro-2-hydroxy-5-nitropyridine is also useful. It can be used as a raw material to synthesize new pesticides. With its chemical properties, it can inhibit or kill specific pests or weeds, assist agricultural production, and ensure crop yield and quality.
    In addition, in the field of organic synthetic chemistry, it is an important building block for organic synthesis reactions. Chemists can use it to perform nucleophilic substitution, electrophilic substitution and other reactions to build complex organic molecular structures, providing a powerful tool for the creation of new compounds and the study of organic synthesis methodologies.
    In short, 4-chloro-2-hydroxy-5-nitropyridine is of great significance in many fields such as medicine, materials, pesticides and organic synthesis, and has made great contributions to the development and innovation of various fields.
    What are 4-Chloro-2-hydroxy-5-nitropyridine synthesis methods?
    The synthesis method of 4-chloro-2-hydroxy-5-nitropyridine is quite complicated. However, although the ancient book "Tiangong Kaiwu" does not detail the synthesis method of this specific compound, the process idea contained in it may be useful for reference.
    The way of chemical synthesis, or the number-following method can be used to prepare 4-chloro-2-hydroxy-5-nitropyridine. First, pyridine is used as the initial raw material, and chlorine atoms are introduced at specific positions in the pyridine ring by halogenation. To obtain precise positioning, the reaction conditions, such as temperature and catalyst genus, must be carefully considered. Then, through nitration, nitro is re-added to the pyridine ring. This step also needs to be carefully regulated to achieve the ideal substitution check point. Finally, by hydroxylation, a hydroxyl group is formed at a specific position, and the target product is obtained.
    Second, pyridine can be hydroxylated and nitrified first, and then halogenated. The key to this path is also the delicate control of the reaction conditions at each step. Each step is related to the purity and yield of the final product.
    Or another method can be found, using another compound as the starting material, and then converted into 4-chloro-2-hydroxy-5-nitropyridine through a series of reactions. However, no matter what method is used, it is necessary to be familiar with various reaction mechanisms and conditions, and to weigh the advantages and disadvantages in order to achieve efficient and accurate synthesis. Although there is no "Tiangong Kaiwu" method to follow, the spirit of research and innovation advocated by it is actually the standard required for the synthesis of this compound and even the field of chemical synthesis.
    4-Chloro-2-hydroxy-5-nitropyridine What are the precautions during storage and transportation?
    4-Chloro-2-hydroxy-5-nitropyridine is also a chemical substance. During storage and transportation, many matters must not be ignored.
    Let's talk about storage first. This substance needs to be placed in a cool, dry and well-ventilated place. If it is placed in a high temperature or humid place, its chemical properties may change. High temperature can promote its reaction to speed up, and humid gas can easily make the substance damp, or cause reactions such as hydrolysis, which will damage its purity and quality. It should be kept away from fire and heat sources to prevent the risk of fire and explosion. Because it may be flammable, or after contact with fire sources, it will react violently. And it should be stored separately from oxidants, acids, bases, etc., and should not be mixed. There may be a chemical reaction between different chemical substances, resulting in danger.
    Let's talk about transportation. During transportation, the packaging must be stable and tight. The selected packaging material must be able to resist general vibration, collision and friction, so as not to leak the material. During transportation, the speed of the vehicle should not be too fast to prevent package damage caused by sudden braking. Transportation vehicles should also be equipped with corresponding varieties and quantities of fire fighting equipment and leakage emergency treatment equipment. If there is an accident such as leakage on the way, it can be dealt with in time. And the transportation personnel should be professionally trained and familiar with the nature of this substance and emergency treatment methods, so as to ensure the safety of storage and transportation.
    What is the market outlook for 4-Chloro-2-hydroxy-5-nitropyridine?
    4-Chloro-2-hydroxy-5-nitropyridine, this substance is quite promising in the field of chemical medicine.
    Looking back at the past, with the improvement of chemical technology, the method of organic synthesis is improving. This pyridine derivative, due to its unique chemical conformation, has gradually entered the field of vision of Fang. It is at the end of drug creation and can be used as a key intermediate. When physicians search for new drugs, the combination of chlorine, hydroxyl and nitro in its structure can respond to various reactions and derive other active molecules, which is expected to treat various diseases.
    Among the markets, the demand is also gradually emerging. Pharmaceutical companies expand production capacity and develop new products, and the demand for this substance continues unabated. Research institutes explore new reaction paths, optimize synthesis processes, and increase their usage. Furthermore, in the field of fine chemicals, paints, pigments, electronic chemicals, and other branches, there are also needs for them, either for structural modification or as reaction starting materials.
    However, its market is not without danger. Although the synthesis method has made progress, the cost remains high, and some processes are complicated, making its price difficult to reach the people and restricting market expansion. And environmental regulations are becoming stricter, and the three wastes treatment in the production process must be in compliance, which increases the cost of enterprises. But in the long run, with the innovation and scale effect of the green synthesis method appearing, the cost may drop, and the market prospect is still considerable. When the technology breaks through the bottleneck, its application in various fields will be more extensive, and the market situation will also be more prosperous.