5 Amino 2 Methylquinoline
quinoline thiophene imidazole thiazole

5-Amino-2-methylquinoline

Taiy Chemical

    Specifications

    HS Code

    888701

    Chemical Formula C10H10N2
    Molar Mass 158.20 g/mol
    Appearance Solid
    Color Typically white to off - white
    Melting Point Data needed
    Boiling Point Data needed
    Solubility In Water Low solubility
    Solubility In Organic Solvents Soluble in some organic solvents like ethanol, chloroform
    Density Data needed
    Odor Odorless or faint odor
    Pka Data needed
    Stability Stable under normal conditions

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    General Information
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    Frequently Asked Questions

    As a leading 5-Amino-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 are the main uses of 5-amino-2-methylquinoline?
    5-Hydroxy-2-methylbenzoic acid light is an important substance in the field of organic compounds. It has a wide range of uses and is of critical significance in many aspects.
    First, in the field of medicine, this substance is often used as a key intermediate for the synthesis of drugs. In the synthesis path of many drugs with special curative effects, 5-hydroxy-2-methylbenzoic acid light can be skillfully converted into pharmacologically active structural units through specific chemical reactions. For example, in the development and production of some drugs used to treat cardiovascular diseases, this compound can precisely construct a specific molecular structure, thereby endowing the drug with excellent efficacy and low side effects, bringing good news to the health of patients.
    Second, in the field of materials science, it plays a role that cannot be ignored. It can be used as a starting material for the synthesis of high-performance polymer materials. By polymerizing with other monomers, polymer materials with unique properties can be prepared, such as excellent heat resistance, chemical corrosion resistance, etc. Such materials are widely used in high-end fields such as aerospace, electronics and electrical appliances to meet the strict needs of different industries for special materials.
    Third, in the fine chemical industry, 5-hydroxy-2-methylbenzoic acid light is often used in the synthesis of various fine chemicals, such as fragrances, pigments, etc. In the synthesis of fragrances, it can impart a unique aroma to fragrances, improve the quality and uniqueness of fragrances; in the synthesis of pigments, it helps to prepare pigments with bright colors and good stability, which are widely used in paints, inks and other industries to add color to products.
    Fourth, in the agricultural field, this compound also shows certain potential. Can be used as raw materials for synthetic pesticides or plant growth regulators. Synthetic pesticides may have high efficiency and low toxicity, which can effectively control crop diseases and pests and ensure agricultural production; while plant growth regulators can precisely regulate the growth and development process of plants and improve crop yield and quality.
    In summary, 5-hydroxy-2-methylbenzoic acid light, with its unique chemical structure and reactivity, plays an important role in many fields such as medicine, materials, fine chemicals, and agriculture, and is invaluable in promoting the development of various industries.
    What are the physical properties of 5-amino-2-methylquinoline?
    5-Amino-2-methylbenzoic acid is an organic compound and is widely used in many fields. Its physical properties are described as follows:
    - ** Appearance **: Usually white to light yellow crystalline powder. This color and morphology are conducive to observation and identification in different environments and reaction systems. For example, in the laboratory synthesis process, by observing the appearance of the product, it can be preliminarily judged whether the reaction is successful.
    - ** Melting point **: Melting point is about 179-182 ° C. Melting point is an important physical property of organic compounds, which is of great significance for identification and purification. By accurately measuring the melting point, the purity of the compound can be judged. If the measured melting point is consistent with the standard value, it indicates that the purity is high; if there is a deviation, it may contain impurities. < Br > - ** Solubility **: Slightly soluble in water, soluble in ethanol, ether, hot benzene and other organic solvents. This solubility property determines its application in different solvent systems. In organic synthesis reactions, appropriate solvents can be selected accordingly to fully contact the reactants and improve the reaction efficiency. For example, in the reaction with ethanol as a solvent, 5-amino-2-methylbenzoic acid can dissolve well and promote the reaction.
    - ** Odor **: The compound has a weak and special odor. Although the odor is not strong, it is still necessary to pay attention to ventilation during operation and use to avoid long-term inhalation.
    - ** Stability **: Relatively stable under conventional conditions. However, when exposed to strong oxidizing agents, strong acids, and strong bases, chemical reactions may occur. For example, during storage and transportation, it is necessary to avoid contact with such substances to ensure their quality and safety.
    What are the chemical properties of 5-amino-2-methylquinoline?
    5-Amino-2-methylbenzoic acid is a kind of organic compound. It has the following chemical properties:
    - ** acidic **: This molecule contains a carboxyl group (-COOH), which can partially ionize hydrogen ions (H 🥰) in water, showing acidity. It can neutralize with bases to form corresponding carboxylic salts and water. For example, when reacting with sodium hydroxide (NaOH), the hydrogen ion in the carboxyl group combines with hydroxyl ion (OH) to form water, and the product is 5-amino-2-methylbenzoate sodium. This reaction reflects its acidic properties. In organic synthesis, this property is often used to separate and purify compounds.
    - ** Amino reaction **: The amino group in the molecule (-NH2O) is basic and can react with acids to form salts. Like interacting with hydrochloric acid (HCl), the lone pair electrons on the amino nitrogen atom will combine with hydrogen ions to form ammonium salts. In addition, amino groups are nucleophilic and easily participate in nucleophilic substitution reactions. Under appropriate conditions, they can react with electrophilic reagents such as halogenated hydrocarbons. Nitrogen atoms attack the carbon atoms attached to halogens in halogenated hydrocarbons. Halogen atoms leave to form new nitrogen-containing compounds, which are crucial in building complex organic molecular structures. < Br > - ** Benzene ring reaction **: The benzene ring in 5-amino-2-methylbenzoic acid has aromatic properties and can undergo a variety of electrophilic substitution reactions. For example, halogenation reactions, under the action of catalysts, hydrogen atoms on the benzene ring can be replaced by halogen atoms; nitration reactions, the benzene ring will introduce nitro groups (-NO ²); sulfonation reactions, sulfonic acid groups (-SO 🥰 H) can be introduced. These reaction products are widely used in the field of organic synthesis and can be used as important intermediates for the synthesis of drugs, dyes, pesticides, etc.
    - ** Redox reactions **: In this compound, the amino group is connected to the benzene ring, and under certain conditions, the amino group may be oxidized. At the same time, if there is a suitable reducing agent, the benzene ring may also undergo hydrogenation reduction reaction, but the benzene ring is relatively stable, and hydrogenation reduction usually requires more severe conditions.
    What are the synthesis methods of 5-amino-2-methylquinoline?
    5-Amino-2-methylbenzoic acid is an important intermediate in organic synthesis and is widely used in medicine, dyes and other fields. There are many synthesis methods. Although the synthesis method is not described in detail in "Tiangong Kaizi", the following common synthesis paths can be summarized with reference to many ancient and modern chemical books and research results.
    First, o-toluic acid is used as the starting material. First, nitro is introduced at a specific position in the benzene ring of o-toluic acid through a nitration reaction. This reaction usually uses a mixed acid of concentrated nitric acid and concentrated sulfuric acid as the nitrifying agent. At a suitable temperature, a nitro-containing o-toluic acid derivative can be obtained. Then, the nitro group is converted into an amino group by a reduction reaction. The commonly used reducing agents are iron filings and hydrochloric acid, hydrogen and catalysts (such as palladium carbon). After this two-step reaction, 5-amino-2-methylbenzoic acid can be prepared.
    Second, use 2-methyl-5-nitrobenzoate methyl ester as raw material. First, use appropriate reducing agents, such as sodium borohydride, lithium aluminum hydride, etc., to reduce the methyl ester group to an alcohol hydroxyl group to obtain 2-methyl-5-nitrobenzyl alcohol. Then through oxidation, the alcohol hydroxyl group is oxidized to a carboxyl group, and oxidizing agents such as potassium permanganate and potassium dichromate can be selected. Finally, the target product can also be synthesized by reducing the nitro group to an amino group as described above.
    Third, o-xylene is used as the starting material. First, a sulfonation reaction is carried out to introduce a sulfonate group into the benzene ring of o-xylene to determine the position of the subsequent reaction. Then, a nitro group is introduced through a nitration reaction. Then, the sulfonate group is removed through a hydrolysis reaction, and the methyl group is oxidized to a carboxyl group to generate 2-methyl-5-nitrobenzoic acid. Finally, the nitro group is reduced to an amino group to achieve the synthesis of 5-amino-2-methylbenzoic acid.
    The above synthesis methods have their own advantages and disadvantages. In practical application, it is necessary to comprehensively consider many factors such as raw material availability, reaction conditions, yield and cost, and select the appropriate synthesis path.
    What are the precautions for using 5-amino-2-methylquinoline?
    5-Hydroxy-2-methylbenzoic acid is an important organic compound and is widely used in many fields. However, many matters need to be paid attention to during use. The details are as follows:
    First, it is related to storage conditions. This compound has certain chemical activity and is highly susceptible to environmental factors. It should be stored in a cool, dry and well-ventilated place, avoiding direct sunlight and high temperature environments. Due to high temperature, its chemical reactivity will be enhanced, or it will cause decomposition and deterioration. Direct sunlight may also induce luminescent chemical reactions, change its chemical structure, reduce quality and purity, and affect the use effect.
    Second, pay attention to operating specifications. When handling 5-hydroxy-2-methylbenzoic acid, be sure to wear appropriate protective equipment, such as gloves, goggles and lab clothes. Because of its irritating effect on the skin, eyes and respiratory tract, direct contact or inhalation of its dust may cause discomfort or even damage. The operation process needs to be rigorous to avoid its leakage. If it is accidentally spilled, it should be cleaned up immediately according to the corresponding emergency treatment procedures to prevent harm to the environment and personnel.
    Third, pay attention to chemical reaction characteristics. 5-hydroxy-2-methylbenzoic acid contains active functional groups such as hydroxyl and carboxyl groups, and is chemically active and easy to react with a variety of substances. When using, it is necessary to fully understand the reaction characteristics of it with other reagents, and strictly control the reaction conditions, such as temperature, pH and reaction time. Otherwise, the reaction may be out of control, the expected product cannot be obtained, and even dangerous conditions may be caused.
    Fourth, pay attention to waste disposal. After use, the remaining 5-hydroxy-2-methylbenzoic acid and related waste cannot be discarded at will. It needs to be properly disposed of in accordance with local environmental protection regulations and laboratory regulations. Usually it needs to be collected by classification and delivered to a professional organization for harmless treatment to prevent pollution to the environment. The use of 5-hydroxy-2-methylbenzoic acid requires attention from various aspects such as storage, operation, reaction characteristics, and waste disposal to ensure safe and effective use, while reducing the harm to the environment and people.