2 Chloro 5 7 Dimethyl 3 Quinolinecarbaldehyde
quinoline thiophene imidazole thiazole

2-CHLORO-5,7-DIMETHYL-3-QUINOLINECARBALDEHYDE

Taiy Chemical

    Specifications

    HS Code

    540746

    Chemical Formula C12H10ClNO
    Molecular Weight 219.67
    Physical State At Room Temp Solid
    Solubility In Water Low (due to non - polar nature of the aromatic ring)
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, dichloromethane (based on structure)

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    2-CHLORO-5, what is the chemical structure of 7-DIMETHYL-3-QUINOLINECARBALDEHYDE?
    2-Chloro-5,7-dimethyl-3-quinoline formaldehyde, according to its name, it can be known that it is a member of the family of organic compounds. The structure of this compound can be named according to the picture.
    "Quinoline" is a nitrogen-containing heterocyclic aromatic hydrocarbon with a skeleton fused with a benzene ring and a pyridine ring, just like the frame of a building, laying the basic structure. "3-quinoline formaldehyde" indicates that there is an aldehyde group (-CHO) connected to the third position of the quinoline ring, and the aldehyde group is like a unique logo protruding from the outside of the building, giving the compound specific chemical activity and reaction characteristics.
    "5,7-dimethyl" is shown at the 5th and 7th positions of the quinoline ring, each connected with a methyl group (-CH 🥰). The methyl group is like a small accessory of a building. Although it is small, it has subtle effects on the physical and chemical properties of the compound, such as changing the polarity of the molecule and the steric resistance.
    And "2-chlorine" means that at the 2nd position of the quinoline ring, a chlorine atom (-Cl) is connected. The chlorine atom is quite electronegative, and its existence is like adding a special component to the structure, which further affects the electron cloud distribution and reactivity of the molecule. In this way, the chemical structure of 2-chloro-5,7-dimethyl-3-quinoline formaldehyde is formed by the quinoline ring, and the aldehyde group, methyl group and chlorine atoms are respectively connected to specific positions. The interaction of each part together determines the unique chemical behavior and properties of the compound.
    2-CHLORO-5, what are the physical properties of 7-DIMETHYL-3-QUINOLINECARBALDEHYDE
    2-Chloro-5,7-dimethyl-3-quinoline formaldehyde, this is an organic compound with unique physical properties.
    Looking at its properties, it is often in a solid state. Due to the intermolecular force, it maintains a solid structure at room temperature and pressure. Its color may be white to light yellow. The formation of this color is due to the absorption and reflection characteristics of the molecular structure to light.
    Talking about the melting point, this compound has a specific melting point range. Due to the interaction and arrangement of molecules, when heated to a certain temperature range, the molecules are energized enough to overcome the lattice energy, and the lattice structure disintegrates and melts into a liquid state. However, the specific value of this melting point will vary slightly depending on the purity of the compound and the measurement method.
    As for solubility, its molecular structure contains polar aldehyde groups and relatively non-polar quinoline rings and methyl and chlorine atoms, which behave differently in different solvents. In polar organic solvents such as ethanol and acetone, the hydrogen bond between aldehyde groups and solvent molecules and partial polar interactions can show a certain solubility; in non-polar solvents such as n-hexane, the solubility is poor due to the limited polarity of the molecule as a whole.
    Furthermore, the density of the compound is also one of its physical properties. Density reflects the mass of the substance per unit volume, and is affected by the compactness of the molecular structure and the relative molecular mass. Its density values are helpful for the measurement and manipulation of substances in practical applications.
    In addition, the compound exhibits unique optical properties, such as absorption spectral characteristics, under specific wavelengths of light. This is due to the electron transition within the molecule, and the energy difference between different electron energy levels corresponds to the light absorption of specific wavelengths, which can provide a basis for the qualitative and quantitative analysis of the compound.
    The physical properties of 2-chloro-5,7-dimethyl-3-quinolinaldehyde are rich and diverse, and these properties are crucial for its application in organic synthesis, drug development and other fields.
    2-CHLORO-5, what is the main use of 7-DIMETHYL-3-QUINOLINECARBALDEHYDE
    2-Chloro-5,7-dimethyl-3-quinoline formaldehyde, this substance is widely used. In the field of pharmaceutical synthesis, it is often used as a key intermediate. In the preparation process of many drugs with specific curative effects, this substance is used as the starting material, through a series of delicate chemical reactions, to construct complex drug molecular structures, or used for antibacterial and anti-inflammatory, or for the treatment of specific diseases.
    In the field of materials science, 2-chloro-5,7-dimethyl-3-quinoline formaldehyde is also of great value. The research and development of some functional materials, with their unique chemical structures, endow materials with special properties such as fluorescence properties, and then apply to optical materials, sensors and many other aspects.
    In the field of organic synthetic chemistry, due to its special functional group combination, it can participate in various classical organic reactions, such as nucleophilic addition, redox, etc., to help synthesize a series of organic compounds with novel structures, opening up new paths for the development of organic chemistry, and playing an important role in exploring new reaction mechanisms and synthesis strategies.
    In short, 2-chloro-5,7-dimethyl-3-quinoline formaldehyde is indispensable in many fields. With its unique chemical properties, it provides key support and infinite possibilities for the development of various fields.
    2-CHLORO-5, what are the synthesis methods of 7-DIMETHYL-3-QUINOLINECARBALDEHYDE
    The synthesis method of 2-chloro-5,7-dimethyl-3-quinoline formaldehyde has been described in many books in the past, but now it is Jun Chen or one.
    One method is to use 2-chloro-5,7-dimethyl-quinoline as the starting material. After halogenation, a specific halogen atom is introduced into a suitable check point. This halogen atom is active and lays the foundation for the subsequent reaction. Then a suitable nucleophilic reagent, such as a reagent with an aldehyde precursor, undergoes a nucleophilic substitution reaction with it. The nucleophilic reagent attacks the carbon position attached to the halogen atom, and the halogen atom leaves to form a new carbon-nucleophilic bond. This step requires careful control of the reaction conditions, such as temperature, solvent and catalyst. If the temperature is too high, or side reactions occur frequently, the product is impure; if the temperature is too low, the reaction rate will be slow and take a long time. The selection of an appropriate solvent can help the reactants dissolve, promote the reaction, and also affect the reaction selectivity. The addition of a suitable catalyst can reduce the activation energy of the reaction and speed up the reaction process. Finally, the aldehyde precursor is converted into the target aldehyde group by hydrolysis or other appropriate post-processing steps, so as to obtain 2-chloro-5,7-dimethyl-3-quinoline formaldehyde.
    The second method is to use aromatic hydrocarbons containing corresponding substituents as starting materials to construct quinoline rings through cyclization reaction. First, the activity check point of aromatic hydrocarbons is used to condensate with specific reagents to gradually construct the ring system. During the cyclization process, the reaction conditions are cleverly controlled, and the substitutions are introduced based on the expected position to form 2-chloro-5,7-dimethylquinoline structures. Then the specific position of the quinoline ring is functionalized, and the specific group is converted into an aldehyde group through oxidation or other suitable conversion steps to obtain the target product. In this process, the control of the cyclization reaction conditions is extremely critical, which is related to the selectivity and yield of cyclization. The oxidation step also needs to consider factors such as the type, dosage and reaction time of the oxidizing agent to ensure the efficient generation of aldehyde groups and avoid side reactions such as excessive oxidation.
    Synthesis methods have advantages and disadvantages. They need to be used according to the actual situation, such as the availability of raw materials, cost considerations, and product purity requirements.
    2-CHLORO-5, What is the market outlook for 7-DIMETHYL-3-QUINOLINECARBALDEHYDE?
    Today, there are 2-chloro-5,7-dimethyl-3-quinoline formaldehyde. I would like to know what its market prospects are. This is an organic compound with potential uses in many fields such as medicine and materials.
    Looking at the field of medicine, quinoline compounds are often biologically active or can be used to create new drugs. The unique structure of 2-chloro-5,7-dimethyl-3-quinoline formaldehyde may provide an opportunity for the development of anti-cancer, antibacterial and antiviral drugs. At present, the pharmaceutical industry has a strong demand for new active ingredients. If the medicinal potential of this compound can be confirmed, it will definitely open up a broad market.
    As for the field of materials, it may be used as an intermediate for the synthesis of special functional materials. With the advance of science and technology, the demand for high-performance materials is increasing day by day, such as photoelectric materials, sensor materials, etc. If this compound can participate in the synthesis of materials with unique optical and electrical properties, it will also usher in considerable market opportunities.
    However, its market prospects are also facing challenges. The first to bear the brunt is the synthesis process. Efficient, economical and environmentally friendly synthesis routes need to be developed. If the synthesis cost is too high, its large-scale application will be limited. Furthermore, safety and Environmental Impact Assessment are indispensable. Only through detailed testing can it be confirmed that it is harmless to the human body and the environment before it can be recognized by the market.
    Overall, 2-chloro-5,7-dimethyl-3-quinoline formaldehyde has potential opportunities in the field of medicine and materials due to its special structure. However, in order to realize its market value, it is still necessary to overcome the problems of synthesis process and security evaluation. If it can be properly solved, it will emerge in the market and have a promising future.