2 Methylpyridine 3 Carboxylate
pyridine pyrrole pyrazine piperidine piperazine

2-methylpyridine-3-carboxylate

    Specifications

    HS Code

    193954

    Name 2 - methylpyridine - 3 - carboxylate
    Chemical Formula C7H7NO2
    Molar Mass 137.14 g/mol
    Appearance Solid (usually white or off - white)
    Odor May have a faint, characteristic odor
    Melting Point Varies depending on the specific carboxylate derivative
    Boiling Point Varies depending on the specific carboxylate derivative
    Solubility In Water Generally sparingly soluble
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, acetone
    Pka Related to the acidity of the pyridine - carboxylate system
    Stability Stable under normal conditions but may react with strong acids, bases, or oxidizing agents

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    Frequently Asked Questions

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    What is the chemistry of 2-methylpyridine-3-carboxylate?
    2-Methylpyridine-3-carboxylic acid ester, this is one of the organic compounds. Its chemical properties are unique and interesting.
    Looking at its structure, the pyridine ring is aromatic, which gives the substance a certain stability. The methyl group is attached to the second position of the pyridine ring, and the carboxylic acid ester group is in the third position, which has a great influence on its properties.
    In terms of physical properties, such compounds are mostly solid or liquid, depending on the specific structure and substituent. The melting point and boiling point are also determined by the intermolecular force. The polar carboxylic acid ester group is contained, or the intermolecular force is enhanced, and the melting boiling point is increased.
    In terms of chemical properties, carboxylic acid ester groups are active. Hydrolysis reactions can occur. Under acidic or alkaline conditions, ester groups are disconnected to form corresponding carboxylic acids and alcohols. In alkaline solutions, hydrolysis is easier to proceed, because bases can neutralize the formed carboxylic acids and promote the positive progress of the reaction.
    At the same time, the pyridine ring can participate in the electrophilic substitution reaction. However, due to the electron-absorbing nature of the pyridine ring nitrogen atom, the electron cloud density distribution is uneven, resulting in the electrophilic substitution reaction mainly occurring at the 4th or 6th position, rather than the 2nd or 3rd position.
    In addition, the methyl group of 2-methylpyridine-3-carboxylic acid esters may participate in certain reactions, such as halogenation reactions, where methyl hydrogen atoms can be replaced by halogen atoms under specific conditions.
    This compound has rich and diverse chemical properties and is widely used in the field of organic synthesis. It can be used as an intermediate and converted into other organic compounds through many reactions. It is of great value in pharmaceutical chemistry, materials science and many other aspects.
    What are the common uses of 2-methylpyridine-3-carboxylate?
    2-Methylpyridine-3-carboxylic acid ester, which is a class of compounds in organic chemistry. Its common uses are generally as follows.
    First, it is often used as a key intermediate in the field of drug synthesis. The construction of many drug molecules relies on this compound as the starting material, and through various chemical reactions, structures with specific pharmacological activities are gradually derived. Due to the structure of pyridine and carboxylic acid esters, it has unique chemical properties and can react with many reagents, laying the foundation for the synthesis of complex drug molecules.
    Second, it also has its uses in materials science. Can participate in the preparation of functional polymer materials. Through a specific polymerization reaction, the structure of 2-methylpyridine-3-carboxylic acid ester is introduced into the main chain or side chain of the polymer, thereby endowing the material with special properties, such as improving the solubility and thermal stability of the material, or endowing it with specific optical and electrical properties.
    Furthermore, in the study of organic synthetic chemistry, it is often used as a model compound. Due to its structure having both the aromatic properties of pyridine and the reactivity of carboxylic acid esters, researchers can deeply understand the organic reaction mechanism and develop novel synthesis methods by exploring its reactivity. Many organic reactions, such as nucleophilic substitution, electrophilic substitution, and metal-catalyzed reactions, can be studied with 2-methylpyridine-3-carboxylic acid esters as substrates, providing theoretical basis and practical experience for the development of organic synthetic chemistry.
    What are 2-methylpyridine-3-carboxylate synthesis methods?
    To prepare 2-methylpyridine-3-carboxylic acid ester, there are various methods. First, it can be obtained by esterification of 2-methylpyridine-3-carboxylic acid and alcohol under the condition of acid catalysis. If sulfuric acid is used as the catalyst, at a suitable temperature, the 2-methylpyridine-3-carboxylic acid is co-heated with ethanol, and the carboxyl group of the carboxylic acid is dehydrated and condensed with the hydroxyl group of the alcohol to form the corresponding ester. During the reaction, pay attention to the control of temperature. If the temperature is too high or side reactions are caused, the purity and yield of the product will be affected.
    Second, 2-methylpyridine-3-carboxylic acid can be converted into its acyl chloride first, and the hydroxyl group of the carboxylic acid can be replaced by chlorine to obtain 2-methylpyridine-3-formyl chloride. Then, the acyl chloride reacts with the alcohol in the presence of a base, which can bind the acid, prompts the reaction to proceed to the right, and efficiently obtains the target ester product. This route has high reactivity, but the acyl chloride is highly corrosive and irritating. It must be handled with caution, in a well-ventilated environment, and properly handle the exhaust gas.
    or through the corresponding pyridine derivatives, through a series of substitution, oxidation, esterification and other steps to synthesize. First, a specific position on the pyridine ring is substituted, a group such as methyl is introduced, and then oxidized to construct a carboxyl group at a suitable position, and finally esterified to obtain 2-methyl pyridine-3-carboxylic acid ester. This route has many steps, and it is necessary to precisely control the reaction conditions of each step to ensure that the reaction proceeds in the expected direction and improve the overall yield and product purity. Each method has its own advantages and disadvantages. According to the actual situation, such as the availability of raw materials, cost, requirements for product purity, etc., choose the appropriate method.
    How 2-methylpyridine-3-carboxylate applied in different fields
    2-Methylpyridine-3-carboxylic acid esters are useful in various fields.
    In the field of medicine, it can be a key intermediate. The structure of Geinpyridine and carboxylic acid esters has unique chemical and biological activities. Chemists can make a variety of compounds with specific pharmacological activities by modifying their structures. If you want to develop drugs for specific diseases, or use 2-methylpyridine-3-carboxylic acid esters as starting materials, introduce different functional groups through multi-step reactions to obtain drugs with good curative effect and low side effects.
    It is also useful in the field of material chemistry. This compound can participate in the preparation of polymer materials with special properties. Due to the presence of pyridine rings, it can form strong interactions with other molecules, such as π-π stacking, hydrogen bonding, etc. On this basis, polymers with specific optical, electrical or mechanical properties can be synthesized. For example, in the preparation of optoelectronic materials, the introduction of 2-methylpyridine-3-carboxylate structure into the main chain or side chain of the polymer is expected to improve the charge transport performance and photostability of the material.
    In organic synthetic chemistry, it is an important building block. Chemists often use it as a substrate to carry out various reactions, such as nucleophilic substitution, redox, cyclization, etc. Through clever design of reaction paths, complex organic molecular structures can be constructed. Due to the existence of pyridine ring and carboxylic acid ester group, it can provide different reaction check points and facilitate the synthesis of various organic compounds.
    In agricultural chemistry, 2-methylpyridine-3-carboxylate may be used as pesticide raw materials. After appropriate modification, high-efficiency, low-toxicity and environmentally friendly pesticides may be prepared. Because of its special structure, or highly selective inhibition or killing of specific pests and pathogens, it provides a new way for pest control in agricultural production.
    What is the market outlook for 2-methylpyridine-3-carboxylate?
    2-Methylpyridine-3-carboxylic acid ester is one of the organic compounds. In today's chemical and pharmaceutical fields, it is gradually emerging.
    Looking at its chemical field, this compound is often the key raw material for the synthesis of many fine chemicals. Because of its unique molecular structure, it gives it specific reactivity and chemical properties, and can be converted into various compounds with different functions through various chemical reaction paths. In the synthesis of fragrances, it can be used as an intermediate to add a different flavor to the fragrance, making its aroma more fragrant and unique. In the preparation of coatings and plastic additives, it participates in the reaction and may improve the properties of the product, such as enhancing its stability and durability.
    As for the field of medicine, the potential of 2-methylpyridine-3-carboxylate cannot be underestimated. Research has gradually shown that it may have certain biological activities, which can provide new opportunities for drug research and development. It may be used as a lead compound, which can be modified and optimized to create new drugs with better efficacy and less side effects. In the research and development of therapeutic drugs for certain diseases, this is the basis for exploration, and it is expected to find innovative treatment methods.
    Looking at its market prospects, opportunities and challenges coexist. On the one hand, with the vigorous development of the chemical and pharmaceutical industries, the demand for fine chemicals and innovative drugs is increasing, creating a broad market space for 2-methylpyridine-3-carboxylic acid esters. On the other hand, its synthesis process may have complex and high-cost problems, and market competition is also fierce. To occupy a place in the market, it is necessary to continue to innovate in synthesis technology, reduce costs and increase efficiency, and strengthen product quality control to cope with the competitive situation.