4 Methyl 3 Phenylpyridine
pyridine pyrrole pyrazine piperidine piperazine

4-Methyl-3-phenylpyridine

    Specifications

    HS Code

    529114

    Chemical Formula C12H11N
    Molecular Weight 167.22 g/mol
    Appearance Solid (usually white to off - white)
    Solubility In Water Poorly soluble
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, dichloromethane
    Odor Typical of aromatic organic compounds, likely faint and pungent
    Stability Stable under normal conditions, but may react with strong oxidizing agents

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    Frequently Asked Questions

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    What are the chemical properties of 4-Methyl-3-phenylpyridine?
    4-Methyl-3-phenylpyridine, which is a kind of organic compound. Its chemical properties are unique, containing the structure of the pyridine ring, and there are methyl and phenyl groups connected at specific positions.
    In terms of physical properties, it is usually in a solid or liquid state, depending on environmental conditions. Its melting point and boiling point are affected by intermolecular forces. The presence of the pyridine ring makes the molecule have a certain polarity. However, the substitution of phenyl and methyl makes the intermolecular forces more complex.
    In terms of chemical properties, the nitrogen atom of the pyridine ring is rich in electrons, so 4-methyl-3-phenylpyridine exhibits alkalinity and can react with acids to form salts. This property is very important in organic synthesis, which can be separated, purified or participated in specific reactions by acid-base reactions.
    Furthermore, the benzene ring part also endows the compound with unique properties. Benzene rings are aromatic, stable and can participate in electrophilic substitution reactions. For example, under suitable conditions, halogenation, nitration, sulfonation and other electrophilic substitution reactions can occur on benzene rings to generate corresponding derivatives.
    The α and β positions of the pyridine ring also have different reactivity due to the electronic effect of nitrogen atoms. In nucleophilic substitution or electrophilic addition reactions, the reaction check point and reaction activity of the pyridine ring are affected by the electronic and spatial effects of methyl and phenyl groups.
    In addition, the carbon-carbon and carbon-nitrogen bonds in 4-methyl-3-phenylpyridine molecules are relatively stable. However, under extreme conditions, such as high temperature, strong oxidants or strong reducing agents, cracking and transformation may also occur, and various new compounds may be derived.
    In summary, 4-methyl-3-phenylpyridine has rich and diverse chemical properties and has wide application and research value in organic synthesis, pharmaceutical chemistry and other fields.
    What are the physical properties of 4-Methyl-3-phenylpyridine?
    4-Methyl-3-phenylpyridine is one of the organic compounds. Its physical properties are worthy of detailed investigation.
    When it comes to appearance, at room temperature, it is mostly crystalline solid, like fine grains, uniform texture and certain luster. This appearance characteristic is quite critical when identifying and preliminarily recognizing this substance.
    When looking at its melting point, it is about [X] ° C. The melting point is the critical temperature at which a substance changes from solid to liquid. This specific melting point is not only an important basis for identifying the compound, but also has great significance in practical applications, such as separation and purification. When the temperature gradually rises to the melting point, 4-methyl-3-phenylpyridine slowly melts from the solid state to the liquid state. During this process, the physical state of the substance changes significantly.
    As for the boiling point, it is probably at [X] ° C. The boiling point is the temperature limit at which a substance changes from a liquid state to a gaseous state under a specific pressure. The value of the boiling point is related to the stability and volatility of the compound in a high temperature environment. At this temperature, 4-methyl-3-phenylpyridine will vaporize in large quantities and escape into space.
    Solubility is also one of the important physical properties. 4-Methyl-3-phenylpyridine is soluble in common organic solvents such as ethanol, ether, etc. In ethanol, it can be uniformly dispersed in a certain proportion to form a clear solution. This solubility property provides convenience for its application in organic synthesis and chemical analysis. However, its solubility in water is poor and only slightly soluble. The solubility of this difference is due to the difference in the molecular structure of the compound and the interaction between water molecules and organic solvent molecules.
    In terms of density, its value is about [X] g/cm ³. The density reflects the mass per unit volume of a substance and is of reference value in the measurement, mixing and process design of substances. The density of 4-methyl-3-phenylpyridine makes it exhibit a specific distribution state according to its own mass and volume relationship when mixed with other substances.
    In summary, the physical properties of 4-methyl-3-phenylpyridine, including appearance, melting point, boiling point, solubility and density, each have their own unique characteristics and are related to each other. They all play an important role in organic chemistry research and practical applications.
    What are the main applications of 4-Methyl-3-phenylpyridine?
    4-Methyl-3-phenylpyridine has a wide range of uses and has applications in many fields.
    In the field of medicine, this compound is often a key raw material for the creation of new drugs. Due to its special chemical structure, it can interact with specific biological targets to regulate human physiology. For example, the development of certain drugs with antibacterial, anti-inflammatory and even anti-cancer activities, 4-methyl-3-phenylpyridine may play an important role in helping researchers explore more effective treatments for diseases.
    In the field of materials science, it also has significant value. Or can participate in the synthesis of special functional materials, such as organic Light Emitting Diode (OLED) materials. During the synthesis of such materials, the structural properties of 4-methyl-3-phenylpyridine may optimize the photoelectric properties of the materials, improve the luminous efficiency and stability, and thus promote the progress of display technology.
    Furthermore, in the field of organic synthetic chemistry, 4-methyl-3-phenylpyridine is often used as a key intermediate. Chemists can build more complex and diverse organic molecules through various chemical reactions based on their structures, expand the types and properties of organic compounds, inject new vitality into the development of organic synthetic chemistry, and help explore novel synthesis paths and methods.
    To sum up, 4-methyl-3-phenylpyridine plays an indispensable role in the fields of medicine, materials science, and organic synthetic chemistry, and is of great significance for progress and innovation in various fields.
    What are 4-Methyl-3-phenylpyridine synthesis methods?
    4-Methyl-3-phenylpyridine is also an organic compound. Its synthesis method is so ingenious, let me come one by one.
    One method can be started by a suitable pyridine derivative. Take the pyridine first, and introduce the methyl group at a specific position. This can be done by reacting halogenated methane with the corresponding pyridine salt. Halogenated methanes such as iodomethane can undergo nucleophilic substitution with the pyridine salt in the presence of a base, and methyl groups can be successfully introduced into the pyridine ring. To introduce phenyl groups at the third position, a coupling reaction catalyzed by palladium can be used. Using 3-halo-4-methylpyridine and phenylboronic acid as raw materials, in palladium catalyst, base and suitable solvent system, the two are coupled to obtain 4-methyl-3-phenylpyridine.
    In addition, benzaldehyde and specific nitrogen-containing compounds can also be used as starting materials. Benzaldehyde and nitrogen-containing compounds with active hydrogen, catalyzed by acid or base, are condensed to form a pyridine ring structure. In this process, the reaction conditions, such as temperature, pH, and the ratio of reactants, are controlled to form methyl and phenyl groups at specific positions in the pyridine ring. After subsequent purification and separation steps, pure 4-methyl-3-phenylpyridine can be obtained.
    Another synthesis route can be started from simple aromatic hydrocarbons and nitrogen-containing heterocyclic precursors. The electrophilic substitution activity of aromatic hydrocarbons is used to react with nitrogen-containing heterocyclic precursors under appropriate conditions to gradually construct the structure of the target molecule. During the reaction, the reaction check point is precisely controlled to achieve the purpose of introducing methyl and phenyl at specific positions on the pyridine ring.
    The synthesis process requires attention to the control of reaction conditions, such as temperature, reaction time, catalyst dosage, etc., which have a great impact on the formation and purity of the product. The purification and separation steps are also crucial. Distillation, recrystallization, column chromatography, etc. can be used to obtain high-purity 4-methyl-3-phenylpyridine to meet the needs of different fields.
    4-Methyl-3-phenylpyridine what are the precautions during use?
    For 4-methyl-3-phenylpyridine, all matters must be paid attention to. The first to bear the brunt is the toxicity of this substance. Its toxicity or cause various physical discomfort, such as dizziness, nausea, vomiting, and even damage to the liver and kidneys. Therefore, when taking it, it is necessary to wear protective gear, such as masks, gloves, and anti-goggles, to prevent it from touching the skin, eyes, and breathing into the body.
    In addition, the chemical activity of 4-methyl-3-phenylpyridine is active. In case of open flames and hot topics, it is very easy to explode. Where it is stored and used, it must be kept away from fire and heat sources, and it must be well ventilated. When storing, it should also be separated from oxidants, acids, and bases, and must not be mixed, so as not to cause chemical reactions and cause danger.
    During use, accurate measurement is also crucial. Because in different reactions, the required amount is different, the dosage is improper, or the reaction is not as expected, or other side reactions are generated. Therefore, it is necessary to measure with an accurate measuring tool according to the requirements of the reaction.
    In addition, after use, the residue should not be discarded at will. It must be properly disposed of in accordance with relevant regulations to prevent environmental pollution. The utensils used should also be cleaned in time to remove the residue for next use.
    The operation of this compound requires a professional site and is carried out by a person who is familiar with the operation specifications. In the operation room, if there is any abnormality, such as abnormal smell, color change, etc., the operation should be stopped immediately to check the cause to ensure safety. In this way, 4-methyl-3-phenylpyridine can be used smoothly without accident.