Methyl 2 Phenylpyridine 3 Carboxylate
pyridine pyrrole pyrazine piperidine piperazine

methyl 2-phenylpyridine-3-carboxylate

    Specifications

    HS Code

    377488

    Chemical Formula C13H11NO2
    Molar Mass 213.23 g/mol
    Appearance Solid (usually)
    Odor Typically odorless or faint
    Melting Point Specific value would need experimental determination
    Boiling Point Specific value would need experimental determination
    Solubility In Water Low solubility
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, chloroform
    Density Specific value would need experimental determination
    Stability Stable under normal conditions

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    Frequently Asked Questions

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    What are the chemical properties of methyl 2-phenylpyridine-3-carboxylate?
    Methyl-2-phenylpyridine-3-carboxylic acid ester, which is a kind of organic compound. Its physical properties are often solid or liquid, and the exact properties vary depending on the specific conditions.
    In terms of its chemical properties, the ester groups it contains can participate in the hydrolysis reaction. In an acid or base environment, the ester groups will hydrolyze. In an acidic environment, the hydrolysis process is relatively slow, and after a gradual reaction, the corresponding carboxylic acids and alcohols are finally formed; in an alkaline environment, the hydrolysis reaction is more rapid, resulting in carboxylic salts and alcohols.
    Furthermore, the pyridine ring in this compound also has unique chemical activity. The pyridine ring is rich in nitrogen atoms. Due to the high electronegativity of nitrogen atoms, the pyridine ring can exhibit certain alkalinity and can react with acids to form pyridine salts. At the same time, the pyridine ring can participate in the electrophilic substitution reaction, but its reactivity is slightly lower than that of the benzene ring. Due to the electron-absorbing effect of nitrogen atoms, the electrophilic substitution reaction mostly occurs at the β position of the pyridine ring.
    In addition, the benzene ring part also exhibits the typical chemical properties of benzene. For example, it can participate in electrophilic substitution reactions, such as halogenation, nitration, sulfonation and other reactions can occur. Because the benzene ring is an electron-rich system, it is vulnerable to the attack of electrophilic reagents. < Br >
    The methyl group in the compound is relatively stable, but under certain conditions, such as the action of strong oxidants, the methyl group can be oxidized to form other functional groups such as carboxyl groups.
    The chemical properties of methyl-2-phenylpyridine-3-carboxylic acid esters are rich and diverse. In the field of organic synthesis, with these properties, organic compounds with more complex structures and unique functions can be prepared through various reaction paths.
    What are the preparation methods of methyl 2-phenylpyridine-3-carboxylate
    There are several common methods for preparing methyl 2-phenylpyridine-3-carboxylic acid esters.
    First, the esterification reaction can occur through pyridine-3-carboxylic acid and methanol catalyzed by concentrated sulfuric acid. This process requires placing pyridine-3-carboxylic acid and excess methanol into a reaction vessel, slowly adding concentrated sulfuric acid as a catalyst, heating to an appropriate temperature and continuously stirring. Concentrated sulfuric acid can promote the equilibrium of the esterification reaction to move in the direction of ester formation, and improve the yield of the product. After the reaction, the reaction mixture needs to be treated, and the sulfuric acid is neutralized in sodium bicarbonate solution, and then the product is extracted with organic solvent, and the pure methyl 2-phenylpyridine-3-carboxylic acid ester is obtained by distillation and other operations.
    Second, prepare by reacting 2-phenylpyridine-3-formyl chloride with methanol. First dissolve 2-phenylpyridine-3-formyl chloride in a suitable organic solvent, such as dichloromethane, and slowly add methanol dropwise under low temperature and stirring conditions. This reaction is relatively fast, because the activity of formyl chloride is quite high. After the reaction is completed, the organic phase is washed with water, dried, and the solvent is evaporated to obtain the product. However, the toxicity and corrosiveness of ethyl chloride need to be taken into account during operation.
    Third, 2-phenylpyridine-3-carboxylic acid anhydride can be reacted with methanol. Mix carboxylic acid anhydride with methanol and add an appropriate amount of organic bases such as pyridine to catalyze. Pyridine can promote the reaction, so that carboxylic acid anhydride and methanol can react smoothly to form the target product. After the reaction, pure methyl 2-phenylpyridine-3-carboxylic acid ester is obtained by conventional separation methods such as filtration and distillation.
    The above methods have their own advantages and disadvantages. In actual operation, the most suitable method should be selected according to the comprehensive consideration of factors such as raw material availability, cost, and reaction conditions.
    Where is methyl 2-phenylpyridine-3-carboxylate used?
    Methyl-2-phenylpyridine-3-carboxylic acid ester, an organic compound. It has applications in many fields.
    In the field of medicinal chemistry, it is often a key intermediate for drug development. Due to its special chemical structure, molecules with specific biological activities can be constructed by chemical synthesis. For example, using it as a starting material and through a series of reactions, drugs targeting specific disease targets may be created, such as anti-tumor and antiviral drugs. By modifying and optimizing its structure, the activity, selectivity and pharmacokinetic properties of the drug can be adjusted.
    In the field of materials science, methyl-2-phenylpyridine-3-carboxylate may be used to prepare functional materials. For example, copolymerization with specific polymers imparts unique optical, electrical or thermal properties to the material. It may be used as a component of luminescent materials for optoelectronic devices such as organic Light Emitting Diodes (OLEDs) to improve the luminous efficiency and color purity of the device.
    In the field of organic synthetic chemistry, it is an important synthetic building block. Chemists can use it to participate in various organic reactions, such as nucleophilic substitution, metal-catalyzed coupling reactions, etc., to synthesize complex organic molecules. Through these reactions, the structural diversity of compounds can be expanded, providing rich materials for the development of organic synthetic chemistry.
    In the fragrance and flavor industry, because it has certain odor characteristics, it can be used as a fragrance ingredient. After blending and optimizing, it adds a unique aroma to the product, and is used in perfumes, cosmetics, food additives and other industries to improve the sensory quality of the product.
    What is the market outlook for methyl 2-phenylpyridine-3-carboxylate?
    Methyl-2-phenylpyridine-3-carboxylic acid ester, which is a special compound in organic chemistry. Its market prospect is related to many levels.
    Looking at the field of chemical synthesis, organic synthesis technology has advanced rapidly in recent years, and the demand for fine chemicals is increasing day by day. Methyl-2-phenylpyridine-3-carboxylic acid ester can be used as a key intermediate in many organic synthesis reactions due to its unique chemical structure. With the improvement of synthesis technology, its preparation efficiency and cost are improved, so its supply in the chemical raw material market is expected to increase, and it can meet the needs of more downstream industries.
    At the level of pharmaceutical research and development, the research and development of many new drugs focuses on the screening and optimization of specific structural compounds. The structure of methyl-2-phenylpyridine-3-carboxylic acid esters may endow them with certain biological activities, providing pharmaceutical chemists with novel structural templates. If its potential medicinal value is discovered in pharmacological research, it will greatly expand its market space, causing many pharmaceutical companies to invest in R & D and production, and promoting its market scale to expand sharply.
    In the field of materials science, with the increasing demand for high-performance materials, organic compounds with special functions have attracted much attention. Methyl-2-phenylpyridine-3-carboxylic acid ester may be applied to optical materials, polymer materials and other fields by means of modification, injecting new vitality into the development of materials science. The application and expansion of this field will create new market opportunities for it, attract the attention and investment of materials companies, and promote its market share growth.
    However, it should also be noted that although the market prospect is broad, its development is still restricted by many factors. If environmental regulations are increasingly stringent, its production process must meet green chemistry requirements, otherwise it may face production restrictions. And the market competition is fierce, and new synthetic methods and alternative products emerge, all posing challenges to its market position. Only by continuously innovating, optimizing processes, and expanding applications can we gain a competitive advantage in the market and enjoy the opportunities offered by the vast market prospect.
    What are the physical properties of methyl 2-phenylpyridine-3-carboxylate?
    The methyl-2-phenylpyridine-3-carboxylic acid ester is one of the organic compounds. Its physical properties are particularly important and relevant to its application in various fields.
    First of all, its appearance is usually white to light yellow crystalline powder. This is the property that can be observed by the naked eye. In the laboratory or industrial production environment, this characteristic can be used to preliminarily identify this substance.
    As for the melting point, it is about a certain range, such as [specific melting point range]. The determination of the melting point is crucial in the identification and purification of the compound. If the melting point of the sample is similar to the theoretical value, it can be proved that the purity is high; if the deviation is large, it may contain impurities.
    The boiling point is also a key physical property. Under specific pressure conditions, such as standard atmospheric pressure, its boiling point is [specific boiling point value]. Knowing the boiling point helps to grasp the appropriate temperature in separation and purification operations such as distillation to achieve effective separation.
    In terms of solubility, this substance exhibits unique properties in organic solvents. In common organic solvents such as ethanol and ether, it has a certain solubility. This property can help in the selection of suitable solvents in organic synthesis reactions, so that the reaction can proceed smoothly. For example, if a reaction needs to occur in a homogeneous system, the appropriate solubility is the basis for the successful reaction.
    density is also one of the considerations. Its density is [specific density value]. This parameter is indispensable when it comes to mass and volume conversion, or when judging the distribution of substances in mixed systems.
    In addition, the stability of methyl-2-phenylpyridine-3-carboxylic acid esters is also related to their physical properties. It is relatively stable at room temperature and pressure, but may change under specific conditions such as high temperature and strong oxidizing agent. The understanding of this stability is of great significance for the storage and transportation of this substance. In short, knowing its physical properties makes it possible to properly apply methyl-2-phenylpyridine-3-carboxylic acid esters in many fields such as organic synthesis and materials science.