2 Hydroxy 3 Nitro 4 Methylpyridine
pyridine pyrrole pyrazine piperidine piperazine

2-Hydroxy-3-nitro-4-methylpyridine

    Specifications

    HS Code

    568988

    Name 2-Hydroxy-3-nitro-4-methylpyridine
    Molecular Formula C6H6N2O3
    Molar Mass 154.12 g/mol
    Appearance Solid (usually powder)
    Physical State At Room Temp Solid
    Melting Point Data needed
    Boiling Point Data needed
    Solubility In Water Data needed
    Solubility In Organic Solvents Data needed
    Density Data needed
    Pka Data needed
    Flash Point Data needed
    Hazard Class Data needed

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    Frequently Asked Questions

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    What is the chemistry of 2-Hydroxy-3-nitro-4-methylpyridine?
    2-Hydroxy-3-nitro-4-methylpyridine, this is an organic compound. Its chemical properties are unique, let me tell you in detail.
    Looking at its structure, the hydroxyl group, nitro group and methyl group are all connected to the pyridine ring. Hydroxy (-OH) is hydrophilic, which can make the compound exhibit some properties of alcohols to a certain extent. It can participate in the formation of hydrogen bonds, which in turn affects the physical and chemical properties of the compound, such as boiling point and solubility. For example, due to hydrogen bonding, its boiling point may be higher than that of similar pyridine compounds without hydroxyl groups.
    Nitro (-NO _ 2) is a strong electron-absorbing group. This property decreases the electron cloud density of the pyridine ring and increases the difficulty of electrophilic substitution reactions on the ring. However, at the same time, it enhances the acidity of the hydrogen atoms in the ortho and para-sites. Under appropriate conditions, these hydrogen atoms may be substituted and the corresponding substitution reaction occurs.
    Furthermore, methyl (-CH
    ) is an electron donor group, which also affects the electron cloud distribution of the pyridine ring. Although its electron supply capacity is not as significant as that of the hydroxyl group, it also has an effect on the reactivity of the pyridine ring. It may increase the electron cloud density of the methyl ortho and para-sites, which affects the selectivity of the reaction check point in specific reactions.
    This compound may participate in many chemical reactions. Under suitable reduction conditions, nitro groups can be reduced to amino groups to form corresponding amino-containing pyridine derivatives. Alternatively, hydroxyl groups can be esterified with acids to form ester compounds.
    In terms of solubility, due to the hydrophilicity of hydroxyl groups and the certain polarity of nitro and pyridine rings, it may have a certain solubility in some polar solvents such as alcohols and water.
    In short, the chemical properties of 2-hydroxy-3-nitro-4-methylpyridine are determined by the interaction of its functional groups with pyridine rings, and may have certain application potential in organic synthesis and other fields.
    What are 2-Hydroxy-3-nitro-4-methylpyridine synthesis methods?
    The synthesis method of 2-hydroxy-3-nitro-4-methylpyridine is rarely reported in ancient books, but today's chemical experts, after much research and practice, also have many ways.
    First, 4-methylpyridine can be started. First, under suitable temperature and reaction conditions, nitrify 4-methylpyridine with appropriate nitrifying reagents, such as concentrated nitric acid and concentrated sulfuric acid mixed acid, and introduce nitro groups into the 3-position of the pyridine ring. This step requires attention to the control of the reaction temperature. If it is too high, it is easy to cause side reactions such as polynitrification. After the successful introduction of nitro groups to obtain 3-nitro-4-methylpyridine, the 2-position of the pyridine ring is hydroxylated with a specific oxidizing agent, such as a suitable oxidizing agent in a suitable solvent system. This process requires careful selection of oxidizing agents and reaction conditions to achieve the purpose of high selectivity.
    Second, it can also start from pyridine derivatives containing specific substituents. If a pyridine compound with substituents that can be converted to hydroxyl groups, nitro groups and methyl groups is found, it is achieved by gradual functional group conversion. For example, a specific reaction first converts a substituent into methyl groups through a series of reactions, followed by the introduction of nitro groups, and finally converts another substituent into hydroxyl groups. This approach requires fine planning of the sequence of reactions in each step to ensure that each step proceeds smoothly with the least side reactions.
    Third, the reaction can still be catalyzed by transition metals. The substrate containing the pyridine structure is coupled with the reagent containing nitro, hydroxyl, and methyl in the presence of a transition metal catalyst. This method requires high requirements for the selection of catalysts, the design of reaction ligands, and the control of the reaction environment. However, if the conditions are suitable, the target product 2-hydroxy-3-nitro-4-methylpyridine can be synthesized efficiently and selectively.
    What are the main uses of 2-Hydroxy-3-nitro-4-methylpyridine?
    2-Hydroxy-3-nitro-4-methylpyridine is one of the organic compounds. It has a wide range of uses and is useful in various fields.
    First, in the field of pharmaceutical chemistry, this compound may be used as a key intermediate. Because of its unique structure, it can be chemically modified to construct structures similar to human physiologically active molecules, and then develop new drugs. Because drug development often relies on organic intermediates to build an active skeleton, the specific functional group combination of 2-hydroxy-3-nitro-4-methylpyridine may lead to unique biological activities, providing an opportunity for the creation of drugs against specific diseases.
    Second, in the field of materials science, it also has its application. The structure and properties of organic compounds are closely related, and the structure composed of nitro, hydroxyl and methyl groups of this compound may endow the material with specific electrical and optical properties. For example, in the preparation of organic optoelectronic materials, by introducing them into the material system, the energy level structure and charge transport properties of the material can be adjusted to prepare devices such as Light Emitting Diode and solar cells with excellent performance.
    Furthermore, in the field of organic synthetic chemistry, 2-hydroxy-3-nitro-4-methylpyridine can be used as a multifunctional synthesizer due to its multifunctional group characteristics. Chemists can take advantage of the differences in the reactivity of each functional group to carry out a series of chemical reactions in an orderly manner to build complex organic molecules. By ingeniously designing reaction routes and using them as starting materials, many organic compounds with different functions and structures can be derived, which greatly enriches the variety and quantity of organic compounds and contributes to the development of organic synthetic chemistry.
    What are the precautions in storage and transportation of 2-Hydroxy-3-nitro-4-methylpyridine?
    2-Hydroxy-3-nitro-4-methylpyridine is also an organic compound. During storage and transportation, many matters must be paid attention to.
    First words storage, because of its specific chemical properties, should be stored in a cool, dry and well-ventilated place. If placed in a high temperature and humid place, it may cause deterioration of substances. For example, high temperature can enhance the activity of molecules and cause chemical reactions; humid environment may cause it to absorb moisture and affect purity. And should be kept away from fire and heat sources. This compound may be flammable or susceptible to thermal decomposition. In case of open flame, hot topic, or danger. In addition, it needs to be stored separately from oxidizing agents, acids, alkalis, etc. Because of its active chemical properties, contact with such substances can easily cause chemical reactions and even cause serious consequences such as explosions.
    As for transportation, be sure to ensure that the packaging is complete and sealed. To prevent leakage during transportation, it poses a threat to the environment and personal safety. The transportation process should follow relevant regulations and standards, and choose suitable transportation tools. And transportation personnel need to be professionally trained, familiar with the characteristics of the substance and emergency treatment methods. If a leak occurs during transportation, effective measures should be taken promptly, such as evacuating people, isolating contaminated areas, and cleaning up the leak in a professional way to prevent the harm from expanding.
    Therefore, when storing and transporting 2-hydroxy-3-nitro-4-methylpyridine, all precautions must be strictly adhered to to to ensure safety.
    What is the market price of 2-Hydroxy-3-nitro-4-methylpyridine?
    In today's world, business conditions are unpredictable, and it is difficult to determine the market price of 2-hydroxy-3-nitro-4-methylpyridine. The level of its price is often determined by many factors.
    The first to bear the brunt is the state of market supply and demand. If the demand for this product is strong and the demand exceeds the supply, the price will rise. For example, in the fields of medicine and chemical industry, if the amount of it is greatly increased, but the output is limited, the merchants will compete for it, and the price will be high. On the contrary, if the supply exceeds the demand and the market is saturated, the merchants will reduce their prices to promote their goods.
    Furthermore, the cost of raw materials is also the key. If the raw materials required for the preparation of 2-hydroxy-3-nitro-4-methylpyridine are reduced or difficult to purchase due to natural disasters, geopolitics or other reasons, the cost will increase, and the price of the product will also rise. On the contrary, if the supply of raw materials is sufficient and the cost is reduced, the price of the product is also expected to decline.
    The process technology should not be underestimated. Advanced production technology can improve production efficiency and reduce production costs. If a merchant has a unique and ingenious method, it can produce efficiently and of good quality, or it can have an advantage in market pricing. Those with lagging technology have high costs and low output, and the price may be constrained.
    In addition, the market competition situation also affects its price. If the competition in the same industry is fierce, various merchants compete for shares or fight price wars, resulting in lower prices. However, if the market is monopolized or oligopolistic, a few merchants can control the price, and the price may remain high.
    There are also the effects of policies and regulations. Stringent environmental protection policies may limit production, increase costs, and affect prices. Changes in tax policies may also increase or decrease enterprise costs, thus affecting product pricing.
    To sum up, in order to know the market price of 2-hydroxy-3-nitro-4-methylpyridine, it is necessary to carefully investigate many factors such as market supply and demand, raw material costs, process technology, competition situation and policies and regulations, in order to have a more accurate grasp of its price changes.