4 Chloro 5 Fluoro 2 Methylquinoline
quinoline thiophene imidazole thiazole

4-chloro-5-fluoro-2-methylquinoline

Taiy Chemical

    Specifications

    HS Code

    147216

    Chemical Formula C10H7ClFN
    Appearance Solid (usually)
    Melting Point Specific value would need further research
    Boiling Point Specific value would need further research
    Solubility In Water Low solubility (organic compound)
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, acetone
    Density Specific value would need further research
    Odor May have a characteristic organic odor
    Pka Specific value would need further research
    Stability Stable under normal conditions, but may react with strong oxidizing agents

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    General Information
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    Frequently Asked Questions

    As a leading 4-chloro-5-fluoro-2-methylquinoline supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What is the chemistry of 4-chloro-5-fluoro-2-methylquinoline?
    4-Chloro-5-fluoro-2-methylquinoline, this is an organic compound with unique chemical properties. In its structure, the quinoline ring is the core, and chlorine, fluorine and methyl are the substituents. These substituents significantly affect its properties.
    In terms of physical properties, this compound is mostly solid under normal conditions, and the melting point and boiling point depend on the intermolecular force. Due to the high electronegativity of chlorine and fluorine atoms, the molecular polarity increases, the intermolecular force increases, and the melting point and boiling point are relatively high.
    In terms of chemical properties, it is aromatic, originates from the conjugated system of quinoline rings, and has high stability. It can undergo electrophilic substitution reactions. Due to the electron-absorbing effect of chlorine and fluorine, the electron cloud density of the quinoline ring decreases, and the electrophilic substitution reactivity may be lower than that of the quinoline itself. The check point of the substitution reaction may be affected by the localization effect of the substituent group. Methyl is the power supply radical, which also plays a role in the reactivity and check point.
    In addition, it can also participate in the nucleophilic substitution reaction. The chlorine atom can be used as a leaving group to react with the nucleophilic reagent to form new compounds. At the same time, the nitrogen-containing quinoline ring has a certain alkaline nature and can react with acids to form salts.
    4-chloro-5-fluoro-2-methylquinoline is widely used in In medicinal chemistry, it can be used as a lead compound to develop new drugs through structural modification; in materials science, it can be used to synthesize organic materials with specific properties.
    What are the physical properties of 4-chloro-5-fluoro-2-methylquinoline?
    4-Chloro-5-fluoro-2-methylquinoline is one of the organic compounds. Its physical properties are quite important and are related to many application fields.
    When it comes to appearance, this substance is often in a solid state, and the color may be white to light yellow. The characteristics of this color state are quite critical when identifying and preliminarily recognizing the compound. Looking at its texture, it is delicate and uniform, and it feels slightly rough to the touch, but it also varies according to the preparation process and purity.
    The melting point is an important physical property. After many experiments, its melting point is within a specific range, and this value provides an important basis for identifying and purifying the substance. The determination of the melting point is like a key to open the door to the characteristics of the compound. Accurate melting point data can judge the purity of the compound. If the melting point matches the standard value, the purity is higher; if there is a deviation, further purification is required.
    The boiling point is also not negligible. Its boiling point is in a certain range, and this value has important guiding significance in distillation separation and other processes. Knowing the boiling point can control the temperature in the relevant operation, so that the compound can be effectively separated from other substances for the purpose of purification or preparation.
    In terms of solubility, 4-chloro-5-fluoro-2-methylquinoline has a certain solubility in organic solvents, such as common ethanol, acetone, etc. In ethanol, with the increase of temperature, the solubility gradually increases, and a uniform and stable solution can be formed; in acetone, the dissolution rate is faster, and a clear solution can be obtained in a short time. However, in water, its solubility is poor, and only a very small amount can be dissolved. This property is closely related to the role of hydrophobic groups in the molecular structure.
    In addition, density is also one of its physical properties. Its density has a specific value, which has a great influence on chemical production, storage and other links. In the liquid state, density is related to the relationship between the volume and quality of a substance, and has important considerations in measurement, transportation and other aspects. The physical properties of 4-chloro-5-fluoro-2-methylquinoline are complex and interrelated, such as melting point, boiling point, solubility, density, etc., which play an important role in scientific research, chemical industry and many other fields, laying a solid foundation for the research and application of this compound.
    What are the main uses of 4-chloro-5-fluoro-2-methylquinoline?
    4-Chloro-5-fluoro-2-methylquinoline is a class of organic compounds. Its main use is quite important in the field of medicinal chemistry.
    In the process of Guanfu's pharmaceutical creation, this compound is often used as a key intermediate. Due to its unique chemical structure, it can be used to synthesize various biologically active molecules through various chemical reactions. In the development of antibacterial drugs, it can provide a framework for the construction of new antibacterial agents, or it can enhance the inhibitory activity against specific bacteria by modifying its structure, helping to create better antibacterial drugs with less side effects.
    In the field of materials science, 4-chloro-5-fluoro-2-methylquinoline may also have wonderful uses. Because it contains special functional groups, it may participate in polymerization reactions to obtain polymer materials with unique photoelectric properties. These materials may be emerging in organic Light Emitting Diodes (OLEDs), solar cells and other devices, which are expected to improve the performance of devices, such as improving photoelectric conversion efficiency and prolonging service life.
    Furthermore, in the field of agricultural chemistry, it may contribute to the creation of new pesticides. Relying on the study of the mechanism of action of insects, plant pathogens and other organisms, using it as a starting material, chemically modified, or highly efficient, low-toxicity and environmentally friendly pesticide products can be developed, which helps to ensure the growth of crops, increase yield, and reduce the adverse impact on the ecological environment.
    In summary, 4-chloro-5-fluoro-2-methylquinoline has potential application value in many fields such as medicine, materials and agricultural chemistry, providing many possibilities for the development of related fields. Its research and development is of great significance.
    What are 4-chloro-5-fluoro-2-methylquinoline synthesis methods?
    The synthesis method of 4-chloro-5-fluoro-2-methylquinoline has been recorded in many books in the past, and the ways are different. One common one is to use an appropriate aromatic compound as the starting material, and introduce chlorine and fluorine atoms precisely through halogenation reaction. If a specific substituted quinoline substrate is selected, under suitable reaction conditions, it is skillfully treated with a halogenating agent, so that the chlorine and fluorine atoms are connected to the molecular structure according to the designed check point. In this process, the selection of halogenating reagents, reaction temperature, reaction time, and the nature of the solvent all have a great impact on the reaction effect.
    Furthermore, for the introduction of methyl groups, methylating reagents are often used. For example, the use of halogenated methane, under the catalytic action of alkali, undergoes nucleophilic substitution reaction with the halogenated quinoline intermediate to achieve a 2-position-based bonding. The type and amount of base, the pH of the reaction system, and the anhydrous degree of the reaction environment are all key factors to consider.
    A multi-step tandem reaction method is also used. The quinoline parent nucleus is first constructed by a specific cyclization reaction, and then halogenation and methylation are carried out in an orderly manner. This strategy requires fine regulation of the reaction conditions at each step to ensure that the reaction proceeds in the expected direction, avoid the growth of side reactions, and improve the yield and purity of the target product. After each step of the reaction, it is often necessary to use separation and purification methods, such as column chromatography, recrystallization, etc., to obtain pure intermediates and final products to ensure the efficiency and accuracy of the synthesis path.
    4-chloro-5-fluoro-2-methylquinoline What are the precautions during storage and transportation?
    4-Chloro-5-fluoro-2-methylquinoline is also an organic compound. During storage and transportation, many matters must be paid attention to.
    First words storage, this compound should be placed in a cool, dry and well-ventilated place. Due to its nature or sensitivity to temperature and humidity, high temperature and humidity may cause its qualitative change. Therefore, the warehouse temperature should be controlled within a suitable range, not too high, and the humidity must be maintained within a reasonable range to prevent moisture decomposition or other chemical reactions.
    Furthermore, this compound should be stored separately from oxidants, acids, bases and other substances. Due to its chemical properties, if it is mixed with the above substances, it is easy to cause chemical reactions, or cause combustion, explosion and other dangerous situations. Therefore, when storing, it is necessary to carefully check the surrounding stored materials and strictly classify them to prevent the disadvantages of mixed storage.
    As for transportation, there are also many details. The transportation vehicle must ensure that the vehicle is in good condition and has corresponding protective measures. It is necessary to properly fix the transportation container to prevent bumps and collisions on the way, causing damage to the container and leakage of the compound.
    Transportation personnel should also be familiar with the characteristics of this compound and emergency treatment methods. In the event of an accident such as leakage, it can be quickly disposed of according to the established methods to reduce the harm. And during transportation, it is advisable to avoid high temperature periods and densely populated areas and choose a safe route to ensure safety.
    In short, 4-chloro-5-fluoro-2-methylquinoline has strict requirements on the environment, storage methods, transportation conditions and personnel quality during storage and transportation. Only by being cautious can we ensure its safety and avoid disasters.