4 Methyl 2 Thiophenecarboxylic Acid
quinoline thiophene imidazole thiazole

4-Methyl-2-thiophenecarboxylic acid

Taiy Chemical

    Specifications

    HS Code

    379045

    Name 4-Methyl-2-thiophenecarboxylic acid
    Molecular Formula C6H6O2S
    Molecular Weight 142.18 g/mol
    Appearance Solid
    Melting Point 138 - 142 °C
    Solubility In Water Insoluble
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, methanol, etc.
    Purity Typically available in high purity (e.g., 95%+)

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    General Information
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    Frequently Asked Questions

    As a leading 4-Methyl-2-thiophenecarboxylic acid 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 chemical structure of 4-Methyl-2-thiophenecarboxylic acid?
    4-Methyl-2-thiophenecarboxylic acid is 4-methyl-2-thiophenecarboxylic acid. Its chemical structure is as follows: the thiophene ring is a five-membered heterocyclic ring containing a sulfur atom. A carboxyl group (-COOH) is connected at position 2 of the thiophene ring, and a methyl group (-CH 🥰) is connected at position 4 of the thiophene ring. In this structure, the thiophene ring gives the compound unique properties such as aromaticity, while the carboxyl group makes it acidic. It can participate in various acid-base reactions and chemical reactions related to carboxyl groups. The presence of methyl groups affects the electron cloud distribution and spatial structure of the molecule, which in turn affects its physical and chemical properties. For example, in the electrophilic substitution reaction, the positioning effect of methyl and carboxyl groups will jointly determine the location and difficulty of the reaction. In this way, the unique chemical structure of 4-methyl-2-thiophenecarboxylic acid is formed.
    What are the main uses of 4-Methyl-2-thiophenecarboxylic acid?
    4-Methyl-2-thiophenecarboxylic acid, which has a wide range of uses. In the field of medicine, it is an important organic synthesis intermediate and is often the raw material for the synthesis of many special drugs. Due to the unique structure of thiophene rings, it has the potential to bind to specific targets in organisms, so it can help the development of antibacterial, anti-inflammatory, anti-tumor and other drugs, making great contributions to human health and well-being.
    In the field of materials science, it also has important value. It can be introduced into the structure of polymer materials through specific chemical reactions to improve the properties of materials, such as enhancing the stability and solubility of materials, and even endowing materials with some special optical and electrical properties, so as to meet the needs of different fields for special performance materials. It is widely used in electronic devices, optical materials and other industries.
    In organic synthesis chemistry, 4-methyl-2-thiophenecarboxylic acid is a key starting material or intermediate, participating in the construction of many complex organic compounds. With its active carboxyl groups and substituents on the thiophene ring, it can carry out a variety of chemical reactions such as esterification, amidation, halogenation, etc., providing organic synthesis chemists with a wealth of strategies and paths to create organic molecules with diverse structures and functions, and promoting the continuous development and innovation of organic synthesis chemistry.
    What are the synthesis methods of 4-Methyl-2-thiophenecarboxylic acid?
    The synthesis of 4-methyl-2-thiophenecarboxylic acid has various paths to follow.
    First, 4-methylthiophene can be used. First, 4-methylthiophene is halogenated with a suitable halogenating agent, such as bromine or chlorine, under suitable reaction conditions, 4-methylthiophene is halogenated, and a halogen atom is introduced at the 2-position of the thiophene ring to obtain 4-methyl-2-halothiophene. This halogenation reaction requires precise temperature control to ensure the selectivity of the reaction. Then the resulting 4-methyl-2-halothiophene is reacted with metal magnesium to form a Grignard reagent. Grignard's reagent is quite active, and then interacts with carbon dioxide gas or solid carbon dioxide such as dry ice, and then through the hydrolysis step, 4-methyl-2-thiophenecarboxylic acid can be obtained. This path step is slightly complicated, but the raw materials are relatively easy to obtain, and the reaction conditions for each step are relatively mature.
    Second, thiophene derivatives containing suitable substituents can also be started. If there are compounds containing methyl groups in the 4-position of the thiophene ring and the 2-position has a group that can be converted into carboxyl groups, such as 4-methyl-2-thiophene formaldehyde. The aldehyde group can be converted to carboxyl group by oxidation reaction. Commonly used oxidants include strong oxidants such as potassium permanganate, or mild oxidation systems, such as oxygen or air in the presence of specific catalysts. This method is relatively simple, but the requirements for starting materials are relatively high, and it may be difficult to obtain raw materials.
    Furthermore, through the construction strategy of thiophene rings. Using small molecules containing sulfur and methyl as starting materials, under suitable catalyst and reaction conditions, thiophene rings are first constructed, and methyl groups are introduced at the 4-position at the same time, and a check point that can be converted into carboxyl groups is reserved at the 2-position. The target product 4-methyl-2-thiophenecarboxylic acid can be obtained by converting the reserved check point into a carboxyl group through appropriate conversion reaction. This strategy requires in-depth understanding and control of the thiophene ring construction reaction, and requires strict reaction conditions. However, if it can be successfully implemented, it may have unique advantages.
    What are the precautions for 4-Methyl-2-thiophenecarboxylic acid in storage and transportation?
    4-Methyl-2-thiophenecarboxylic acid is an organic compound. During storage and transportation, many matters need to be paid attention to.
    When storing, the first environment. It must be placed in a cool, dry and well-ventilated place. This is due to its fear of heat, moisture, high temperature and humidity, or cause it to deteriorate. If heated, the molecular structure may change, which affects the quality; if exposed to moisture, it may cause a chemical reaction and damage its purity.
    Furthermore, the packaging must be tight. When it is placed in a sealed container, it should be prevented from excessive contact with air. Oxygen, water vapor and other components in the air may react with the substance, causing it to oxidize or hydrolyze, reducing the quality.
    In addition, the storage place should be kept away from fire and heat sources, because it is flammable to a certain extent, in case of open flames, hot topics or dangerous. And it should be stored separately from oxidants, acids, alkalis, etc., because of its active chemical properties, mixed with these substances, or triggered a violent reaction.
    When transporting, there are also important points. It is necessary to ensure that the packaging is stable, and the road is bumpy so that the container will not be damaged and leaked. Transportation vehicles should be equipped with corresponding fire protection equipment to deal with sudden fires. During transportation, avoid high temperature periods and high temperature areas to prevent excessive temperature from affecting the stability of substances.
    And transportation personnel should be familiar with its nature and emergency treatment methods. In case of leakage and other situations, it can be handled quickly and properly to minimize harm. In conclusion, the storage and transportation of 4-methyl-2-thiophenecarboxylic acid should be handled with caution and in accordance with regulations to ensure safety and quality.
    What is the market price range for 4-Methyl-2-thiophenecarboxylic acid?
    4-Methyl-2-thiophenecarboxylic acid, the price of this product in the market is difficult to determine. The range of its price often varies due to various factors.
    First, the amount of output affects its price. If the origin is abundant, the output is abundant, and the supply in the market is abundant, the price may be flat; conversely, if the origin is thin and the supply is insufficient, the price will rise.
    Second, the demand trend is also the key. In the chemical and pharmaceutical industries, if the demand for this product is strong, the demand exceeds the supply, and the price will rise; if the industry demand is low and the supply exceeds the demand, the price will decline.
    Furthermore, the difficulty and cost of preparation also affect its price. If the preparation method is complicated, the materials used are expensive, the process is difficult, and the cost must be high, the price is not cheap; if the preparation is simple, the cost is low, and the price is close to the people.
    In addition, the competition situation of the market, trade policy, transportation costs, etc., can all affect its price. In a fiercely competitive city, merchants may reduce their price in order to occupy a share; changes in trade policies, increases or decreases in tariff rates, also make prices fluctuate; long transportation distances, increased costs, will also cause prices to rise or fall. < Br >
    Overall, the market price of 4-methyl-2-thiophenecarboxylic acid, or due to the above factors, fluctuates over a wide range, ranging from tens of yuan per kilogram to hundreds of yuan. It is difficult to determine an exact value.