2 Methoxy 4 Methylpyridine 3 Carboxylic Acid
pyridine pyrrole pyrazine piperidine piperazine

2-Methoxy-4-methylpyridine-3-carboxylic acid

    Specifications

    HS Code

    105231

    Chemical Formula C8H9NO3
    Molar Mass 167.16 g/mol
    Appearance Solid (usually white or off - white)
    Physical State At Room Temperature Solid
    Solubility In Water Slightly soluble
    Solubility In Organic Solvents Soluble in some polar organic solvents like ethanol
    Melting Point 140 - 144 °C (approximate)
    Pka Value Related to acidic group, around 3 - 4 (approximate for carboxylic acid group)

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    General Information
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    Frequently Asked Questions

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    What are the physical properties of 2-methoxy-4-methylpyridine-3-carboxylic acid?
    2-% methoxy-4-methylpyridine-3-carboxylic acid is an organic compound with unique physical properties. The detailed description is as follows:
    Under normal temperature and pressure, 2-% methoxy-4-methylpyridine-3-carboxylic acid is often white to off-white crystalline powder. This form is easy to store and use, and it is easy to measure and mix in many chemical operations.
    When it comes to the melting point, the melting point of this compound is roughly within a specific range. The melting point is an important physical property of the substance, which can help to identify and determine the purity. Accurate determination of the melting point is of great significance for controlling the quality of 2-% methoxy-4-methylpyridine-3-carboxylic acid.
    In terms of solubility, 2-% methoxy-4-methylpyridine-3-carboxylic acid exhibits different solubility in specific solvents. Generally speaking, it has a certain solubility in organic solvents such as ethanol and dichloromethane. This property makes it soluble in organic synthesis reactions with suitable solvents, and then participates in various chemical reactions. In water, its solubility is relatively limited. Such solubility properties are of key guiding value in the separation, purification and preparation of compounds.
    As for stability, 2-% methoxy-4-methylpyridine-3-carboxylic acid is quite stable under conventional environmental conditions. However, if exposed to extreme temperatures, humidity or specific chemical substances, or cause chemical reactions, its structure and properties will change. Therefore, when storing the compound, it is necessary to choose a dry, cool and well-ventilated place to avoid contact with incompatible substances.
    In addition, the physical properties of 2-% methoxy-4-methylpyridine-3-carboxylic acid may be affected by impurities. The presence of trace impurities may change the properties of melting point and solubility. Therefore, in chemical research and industrial production, strict control of purity is of great significance to ensure the consistency of its physical properties and the stability of product quality.
    What are the chemical properties of 2-methoxy-4-methylpyridine-3-carboxylic acids?
    2-% methoxy-4-methylpentyl-3-butyric acid is an organic compound. It has the following chemical properties:
    1. ** Acidic **: This compound contains carboxyl groups, so it is acidic. It can react with bases to form corresponding carboxylic salts and water. For example, with sodium hydroxide: 2-% methoxy-4-methylpentyl-3-butyric acid + sodium hydroxide → 2-% methoxy-4-methylpentyl-3-butyrate sodium + water. This reaction is a typical acid-base neutralization reaction, reflecting the acidic characteristics of the compound.
    2. ** Esterification reaction **: Because it contains carboxyl groups, it can be esterified with alcohols under concentrated sulfuric acid catalysis and heating conditions to form esters and water. For example, when reacted with ethanol, 2-% methoxy-4-methylpentyl-3-butyrate ethyl ester and water will be formed. This reaction is a common method for preparing ester compounds in organic synthesis. The resulting esters often have special flavors and are widely used in the fragrance industry.
    3. ** Substitution Reaction **: Hydrogen atoms on groups such as methyl groups in molecules can be replaced by other atoms or groups under specific conditions. For example, when light is illuminated or there is a catalyst, hydrogen atoms on methyl groups may be replaced by halogen atoms, and halogenation reactions occur. This provides the possibility for further derivatization of the compound and the preparation of more functional organic compounds.
    4. ** Oxidation Reaction **: In theory, certain groups in molecules can be oxidized. Although the carboxyl group is relatively stable, other parts of the molecule, such as alkyl groups, may oxidize under the action of strong oxidants to form compounds containing more oxygen functional groups, but such reaction conditions are usually more severe.
    What is the main use of 2-methoxy-4-methylpyridine-3-carboxylic acid?
    2-% methoxy-4-methylpentanoic acid-3-carboxylic acid has many main uses. This compound is of great value in the field of medicine. Because of its unique structure, it can be used as a key intermediate for drug synthesis. The drugs prepared by it may have specific physiological activities, such as regulating human metabolism and fighting diseases. Doctors can use it to synthesize specific drugs to treat various diseases, or diseases of the digestive system, or diseases of the immune system. It is expected to help.
    In the chemical industry, it is also indispensable. It is often used as an important raw material for organic synthesis, and can be produced through a series of chemical reactions to produce a variety of high value-added chemical products. Polymer materials with special properties, such as some special properties, can be skillfully synthesized to give the material unique physical and chemical properties, such as better heat resistance, corrosion resistance, etc., and are widely used in high-end fields such as aerospace and electronic devices.
    In the field of agriculture, it can also play a role. Or it can be developed as a new type of pesticide or plant growth regulator. As a pesticide, it has inhibitory or killing effects on specific pests or pathogens, and compared with traditional pesticides, it may have higher selectivity and lower toxicity, which can reduce the harm to the environment and the impact on non-target organisms; if it is a plant growth regulator, it can precisely regulate the growth and development process of crops, improve crop yield and quality, such as promoting fruit expansion, enhancing fruit color and sweetness, etc. In summary, 2-% methoxy-4-methylvaleric acid-3-carboxylic acid has shown important uses in many fields such as medicine, chemical industry, and agriculture, providing strong support for the development of various industries.
    What are the synthesis methods of 2-methoxy-4-methylpyridine-3-carboxylic acid?
    To prepare 2-methoxy-4-methylpyridine-3-carboxylic acid, the following method can be used.
    First, a suitable pyridine derivative is used as the starting material. First, a methoxy group is introduced at a specific position on the pyridine ring, which can be achieved by nucleophilic substitution reaction. Select a suitable halogenated pyridine derivative with activity, and co-react with alkoxylation reagents such as sodium methoxide to control the reaction temperature, time and material ratio, so that the halogen atom is smoothly replaced by methoxy group. Subsequently, the methyl group is introduced at another designated position of the pyridine ring, which can be condensed with a methylating agent such as chloromethane and a suitable catalyst, such as anhydrous aluminum trichloride, in a suitable solvent by Fu-gram alkylation reaction. Finally, the methyl group is oxidized to a carboxyl group, and a strong oxidizing agent such as potassium permanganate is used to realize the conversion under suitable reaction conditions to obtain the target product.
    Second, start with the construction of the pyridine ring. Take a suitable raw material containing methoxy group and methyl group and form a ring through multi-step reaction. For example, first, β-ketoate with corresponding substituents is condensed with ammonia or amine compounds to form the prototype of the pyridine ring. Next, the substituents on the ring are adjusted and modified to make the methoxy group and methyl group in the target position. In the process, protection and de-protection steps may be required to prevent undesired reactions from occurring. When the structure of the pyridine ring and the substituent are properly arranged, the specific group is converted into a carboxyl group through an appropriate oxidation reaction, and the final product is 2-methoxy-4-methylpyridine-3-carboxylic acid.
    Third, the coupling reaction catalyzed by transition metals can also be used. Select pyridine derivatives containing methoxy and methyl groups, and reagents containing carboxyl precursors, under the action of transition metal catalysts such as palladium catalysts, to construct the target molecule through coupling reaction. In the reaction, suitable ligands should be selected, the reaction conditions should be optimized, and the selectivity and yield of the reaction should be improved to obtain pure 2-methoxy-4-methylpyridine-3-carboxylic acid.
    What are the precautions for 2-methoxy-4-methylpyridine-3-carboxylic acid in storage and transportation?
    2-Methoxy-4-methylphenyl-3-pyridylic acid in storage and transportation, need to pay attention to many key matters.
    One, related to the storage environment. This substance should be stored in a cool, dry and well-ventilated place. Because of the cool environment, it can avoid the chemical properties of its chemical properties and even decomposition due to excessive temperature; drying can prevent moisture from causing deliquescence, affecting its purity and quality; good ventilation can disperse harmful gases that may be generated in time to maintain environmental safety. It is necessary to keep away from fires and heat sources, because the substance may be flammable, and there is a risk of burning and explosion in case of open flames, hot topics or combustion. At the same time, it should be stored separately from oxidants, acids, alkalis, etc., to avoid chemical reactions caused by mixed storage, resulting in dangerous accidents.
    Second, the transportation aspect should not be underestimated. Before transportation, make sure that the packaging is complete and sealed tightly to prevent material leakage during transportation. Select suitable transportation tools, and ensure that the container does not leak, collapse, fall, or damage during transportation. When transporting, follow the specified route, and do not stop in densely populated areas and residential areas, just in case of leakage and harm to many people. Transportation vehicles should be equipped with corresponding varieties and quantities of fire fighting equipment and leakage emergency treatment equipment. In the event of an accident, response measures can be quickly launched to reduce losses and hazards.
    In addition, whether it is storage or transportation, the relevant operators must undergo special training and strictly abide by the operating procedures. Warehouse management personnel should regularly check the stored 2-methoxy-4-methylphenyl-3-pyridine acid to see if the packaging is intact and whether the environmental conditions meet the requirements. Transportation personnel should pay close attention to the transportation situation during transportation. If any abnormalities are found, timely and effective measures should be taken to ensure the safety of 2-methoxy-4-methylphenyl-3-pyridine acid during storage and transportation.