Pyridine 4 Carboxylic Acid Phenylamide
pyridine pyrrole pyrazine piperidine piperazine

Pyridine-4-carboxylic acid phenylamide

    Specifications

    HS Code

    904214

    Chemical Formula C12H10N2O
    Molecular Weight 198.22 g/mol
    Appearance Solid (usually white or off - white powder)
    Odor May have a faint, characteristic odor
    Melting Point Typically in a certain temperature range (e.g., around 180 - 190°C, approximate)
    Boiling Point Decomposes before boiling in normal conditions
    Solubility In Water Poorly soluble in water
    Solubility In Organic Solvents Soluble in some organic solvents like ethanol, DMSO

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    Frequently Asked Questions

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    What is the chemical structure of Pyridine-4-carboxylic acid phenylamide?
    The chemical structure of pyridine-4-carboxylic acid phenamide should be described by chemical principles and molecular deconstruction. This compound is mainly composed of pyridine ring, carboxyl-derived amide group and phenyl group.
    From the perspective of its pyridine ring, it is a six-membered nitrogen-containing heterocyclic ring with aromatic properties. The nitrogen atom in the ring participates in the conjugate system with its one pair electron, so that the electron cloud distribution of the pyridine ring is different from that of the benzene ring, with specific electronic properties and chemical activities. At the 4th position of the pyridine ring, there is an amide structure derived from carboxyl groups. The amide group is formed by the condensation of the carboxyl group and the amino group. In this amide bond (-CONH -), the carbon, oxygen and nitrogen atoms are connected to the bond length at a specific bond angle. The lone pair electrons of the nitrogen atom in the amide group form p-π conjugate with the π bond of the carbonyl group, resulting in the partial double bond properties of the amide bond and relatively stable structure.
    And phenyl is a group derived from the benzene ring, which is also aromatic. The benzene ring is composed of six carbon atoms with a sp ² hybrid orbital to form a six-membered ring structure, and its large π bond endows the benzene ring with unique stability and chemical properties. The phenyl group is attached to the amide structure formed by the pyridine-4-carboxylic acid, so that the whole molecule has the characteristics of both the pyridine ring, the amide group and the benzene ring. The various parts interact with each other, such as electronic effects, spatial effects, etc., which in turn affect the physical and chemical properties of the compound, such as solubility, acidity and alkalinity, and reactivity. In this way, the chemical structure of the phenamide of the pyridine-4-carboxylic acid is an exquisite combination of the pyridine ring, the amide group and the phenyl group. The synergistic action of each part together determines its unique chemical behavior and properties.
    What are the physical properties of Pyridine-4-carboxylic acid phenylamide?
    Phenamide, pyridine-4-carboxylic acid, has various physical properties. In terms of its color state, it is often in the form of white to off-white crystalline powder. The texture is fine and the color is pure. This state is easy to identify and handle, and it is easy to distinguish and use in many experiments and production processes.
    Melting point is about a specific range, usually [specific melting point range]. Melting point is its important characteristic, which can be used to judge the purity of the substance. If the purity is high, the melting point range is narrow and close to the theoretical value; if it contains impurities, the melting point is often reduced and the range is wider.
    Solubility is also critical. In organic solvents, such as ethanol, dichloromethane, etc., it has a certain solubility. Ethanol is a common organic solvent in which pyridine-4-carboxylic acid benzamide can be moderately dissolved to form a uniform solution. This property makes it a reactant or intermediate in organic synthesis reactions, with the help of solvents such as ethanol well dispersed to promote the reaction. However, in water, its solubility is poor and only slightly soluble. This difference is due to its molecular structure, containing hydrophobic groups such as benzene ring and amide group, which makes it weak in hydrophilicity.
    Furthermore, its density is also fixed, about [specific density value]. Density in practical applications is related to material measurement, storage and transportation. For example, during production and preparation, the dosage can be accurately calculated according to the density to ensure that the reaction proceeds according to the expected proportion.
    In addition, the stability of pyridine-4-carboxylic acid benzamide is quite good. Under normal temperature and environmental conditions, it can maintain its own structure and properties for a long time. In case of extreme conditions such as strong acid, strong alkali or high temperature, the structure may change, and reactions such as hydrolysis and decomposition occur. Therefore, it is necessary to choose a dry, cool place and avoid acid and alkali when storing.
    What are the main uses of Pyridine-4-carboxylic acid phenylamide?
    Pyridine-4-carboxylic acid benzamide, this substance has a wide range of uses. In the field of medicine, it is often a key intermediate for the creation of new drugs. Due to its specific chemical structure and activity, it can participate in many drug synthesis reactions. By ingeniously combining with other compounds, drugs with unique pharmacological activities can be prepared, or used to treat specific diseases, or to improve drug efficacy and reduce adverse reactions, opening up new paths for pharmaceutical research and development.
    In the field of materials science, pyridine-4-carboxylic acid benzamide also has important functions. It can be used as a synthetic raw material for functional materials, and it can be treated by special processes to endow the materials with special properties such as good thermal stability, optical properties or electrical properties. For example, in the preparation of high-performance polymer materials, the addition of this material can optimize the material structure, enhance its mechanical properties and stability, and make the material suitable for aerospace, electronic equipment and other fields with strict performance requirements.
    In agriculture, it also shows potential value. It may become an important component in the development of new pesticides or plant growth regulators. With its chemical properties, it may inhibit crop diseases and pests, or regulate plant growth and development, improve crop yield and quality, and provide support for sustainable agricultural development.
    In addition, in the field of organic synthetic chemistry, pyridine-4-carboxylic acid benzamide is often used as an important reagent and catalyst to promote the efficient progress of various organic reactions, assist in the synthesis of many complex organic compounds with special functions, and contribute to the development of organic synthetic chemistry. In short, pyridine-4-carboxylic acid benzamide has key uses in many fields and is of great significance to scientific and technological progress and industrial development.
    What are the preparation methods of Pyridine-4-carboxylic acid phenylamide?
    The method of making pyridine-4-carboxylic acid benzamide has been explored by many scholars in the past. There are many methods, and each has its own advantages and disadvantages.
    One method is to use pyridine-4-carboxylic acid as the base to interact with benzoyl chloride in a suitable reaction environment. First prepare an appropriate amount of pyridine-4-carboxylic acid, place it in a clean reactor, add an appropriate amount of organic solvent, such as dichloromethane or tetrahydrofuran, and dissolve the carboxylic acid uniformly. After that, under low temperature and stirring, slowly drop benzoyl chloride. When dropping, the temperature of the reaction should be strictly monitored to prevent the temperature from rising sharply and causing side reactions. Pure pyridine-4-carboxylic acid phenamide is obtained by conventional separation and purification methods, such as extraction, column chromatography, etc.
    The second method can be obtained by reacting pyridine-4-formyl chloride with aniline. Pyridine-4-formyl chloride is first prepared, and pyridine-4-carboxylic acid is reacted with chlorination reagents, such as dichlorosulfoxide, under suitable conditions to obtain pyridine-4-formyl chloride. After that, pyridine-4-formyl chloride is dissolved in a suitable solvent, such as ether or toluene, and then stirred at low temperature, and aniline is gradually added. During the reaction process, pay close attention to the changes of the system. When the reaction is complete, the product is also purified by extraction and recrystallization.
    The third method uses pyridine-4-nitrile and benzoic acid derivatives as raw materials. Pyridine-4-nitrile is first converted into pyridine-4-carboxylic acid-related intermediates through hydrolysis and other steps, and then reacts with benzoic acid derivatives in appropriate solvents with the help of condensing agents, such as dicyclohexyl carbodiimide (DCC). After subsequent treatment, pyridine-4-carboxylic acid benzamide can also be prepared.
    Although this number method can prepare pyridine-4-carboxylic acid benzamide, each method has different requirements for reaction conditions, raw material cost, product purity and yield. It is necessary to choose carefully according to actual needs.
    What are the precautions for Pyridine-4-carboxylic acid phenylamide in storage and transportation?
    Pyridine-4-carboxylic acid benzamide is an important organic compound. During storage and transportation, many matters need to be paid careful attention.
    First talk about storage, this compound should be stored in a cool, dry and well-ventilated place. Because pyridine-4-carboxylic acid benzamide is exposed to high temperature environment, it may cause its chemical properties to change, and even cause adverse reactions such as decomposition. And humid environment may promote its moisture absorption, affecting purity and stability. Storage must be kept away from fire and heat sources. Because it may be flammable, it is easy to cause danger in case of open flames and hot topics. At the same time, it should be stored separately from oxidants, acids, bases, etc., to avoid mixed storage to prevent violent chemical reactions. There are also requirements for storage containers, which need to be well sealed to prevent leakage. The integrity of the container and the state of the compound should also be checked regularly. If any abnormalities are detected, such as container damage, compound properties change, etc., they need to be dealt with in time.
    As for transportation, ensure that the packaging is complete and sealed before transportation. Packaging materials must be able to effectively protect pyridine-4-carboxylate benzamide from vibration and collision to avoid leakage. During transportation, vehicles should be equipped with corresponding fire fighting equipment and leakage emergency treatment equipment. Drive carefully to prevent collisions, rollover and other accidents. Transportation personnel also need to know the basic properties of pyridine-4-carboxylate benzamide and emergency treatment methods. In the event of leakage and other accidents, they can respond quickly and correctly. Do not mix with other contraindicated items to prevent dangerous interactions during transportation. Transportation route planning should also be reasonable, avoiding densely populated areas and environmentally sensitive areas to reduce latent risks.