2 Methyl 3 Thiophenecarboxylic Acid
quinoline thiophene imidazole thiazole

2-Methyl-3-thiophenecarboxylic acid

Taiy Chemical

    Specifications

    HS Code

    831662

    Chemical Formula C6H6O2S
    Molar Mass 142.18 g/mol
    Appearance Solid
    Color White to off - white
    Odor Characteristic
    Solubility In Water Slightly soluble
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, acetone
    Melting Point 145 - 149 °C
    Boiling Point Decomposes before boiling
    Pka Value Around 3.9 (approximate value for carboxylic acid group)

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    General Information
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    Frequently Asked Questions

    As a leading 2-Methyl-3-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 are the chemical properties of 2-Methyl-3-thiophenecarboxylic acid?
    2-Methyl-3-thiophenecarboxylic acid is one of the organic compounds. It has unique chemical properties and is of great significance to organic synthesis chemistry.
    This compound is in solid form and has relatively stable properties at room temperature and pressure. When it encounters hot topics, it may decompose and release harmful gases such as sulfur. It has certain solubility in common organic solvents such as ethanol and ether, which is convenient for participating in many reactions as reactants or intermediates in organic reaction systems.
    In terms of its chemical activity, the carboxyl group and the methyl group on the thiophene ring give it special reaction properties. Carboxyl groups can undergo many typical reactions, such as esterification with alcohols under acid catalysis, to form corresponding ester compounds. This reaction condition usually requires mild heating, and strong acids such as concentrated sulfuric acid are used as catalysts, which can effectively promote the forward reaction. At the same time, the carboxyl group can also neutralize with the base to form the corresponding carboxylate, which is rapid and thorough, providing a convenient way for its separation and purification. The presence of methyl groups on the
    thiophene ring also affects the distribution of molecular electron clouds, making the thiophene ring more reactive at specific positions. For example, in the electrophilic substitution reaction, the electron cloud density of the methyl group increases relatively, and it is more vulnerable to the attack of electrophilic reagents, and electrophilic substitution reactions such as halogenation and nitrification occur. These reaction conditions vary depending on the electrophilic reagents. Iron halide is commonly used as a catalyst for halogenation reactions, while nitrification reactions generally require a mixed acid system of concentrated sulfuric acid and concentrated nitric acid.
    2-methyl-3-thiophenecarboxylic acid is widely used in organic synthesis in the fields of medicine, pesticides and materials due to these chemical properties, laying the foundation for the creation of new compounds and the development of functional materials.
    What are the main uses of 2-Methyl-3-thiophenecarboxylic acid?
    2-Methyl-3-thiophenecarboxylic acid has a wide range of uses. In the field of medicine, it is an important intermediate in organic synthesis, which can be combined with other compounds through specific reaction steps to create a variety of drugs. For example, in the development of some antibacterial drugs, 2-methyl-3-thiophenecarboxylic acid is a key starting material, participating in the construction of the core structure of the drug, and through its unique chemical structure, giving the drug specific antibacterial activity.
    In the field of materials science, it also has important functions. In the preparation of certain high-performance polymer materials, 2-methyl-3-thiophenecarboxylic acid can be introduced into the polymer backbone as a functional monomer. In this way, the prepared polymer material has special optoelectronic properties, such as good fluorescence properties, which can be applied to optoelectronic devices such as organic Light Emitting Diode (OLED) to improve the luminous efficiency and stability of the device.
    In addition, in the field of fine chemicals, 2-methyl-3-thiophenecarboxylic acid is often used to synthesize various fine chemicals. For example, it can be used to prepare special fragrances to add unique aroma characteristics to fragrances; it can also be used to prepare high-performance coating additives to enhance coating adhesion, corrosion resistance and other properties. In short, 2-methyl-3-thiophenecarboxylic acid plays a key role in many fields due to its unique chemical properties, providing an important material basis for the development of various fields.
    What are the synthetic methods of 2-Methyl-3-thiophenecarboxylic acid?
    To prepare 2-methyl-3-thiophenecarboxylic acid, there are many methods, and each has its advantages and disadvantages. The choice of method depends on the actual situation. The following are common synthesis methods:
    First, 2-methyl-3-thiophenylformaldehyde is used as the starting material. The target product can be obtained by oxidation reaction. In this way, various oxidants can be selected, such as potassium permanganate, which has strong oxidation and is easy to occur. However, the reaction conditions are relatively harsh, and the reaction temperature and pH must be strictly controlled, otherwise it is easy to cause excessive oxidation and reduce the yield. Manganese dioxide can also be used as an oxidant, which is relatively mild, the reaction conditions are easy to control, and the product purity is high. However, the reaction rate is slightly slower and the reaction time is longer. < Br >
    Second, starting from 2-methylthiophene. Carboxyl groups are first introduced through carboxylation reaction. This process can be used Grignard reagent method, 2-methylthiophene is made into Grignard reagent, and then reacted with carbon dioxide, and then acidified to obtain 2-methyl-3-thiophenecarboxylic acid. This method has good selectivity and can accurately introduce carboxyl groups at specific positions. However, Grignard reagent requires strict preparation requirements, anhydrous and anaerobic environment, complicated operation, and high skill requirements for experimenters.
    Third, thiophene is used as raw material. Methylation reaction is carried out first, methyl groups are introduced on the thiophene ring, and then carboxylation reaction is carried out. This route has many steps, the reaction process is complicated, and the separation and purification of intermediate products is difficult. However, the raw material thiophene has a wide range of sources and low cost. If the reaction conditions and separation technology can be optimized, it also has certain application value.
    In summary, the methods for synthesizing 2-methyl-3-thiophenecarboxylic acid have their own advantages. In actual synthesis, when factors such as raw material cost, reaction conditions, yield, purity and difficulty of operation are comprehensively considered, the most suitable synthesis method is selected.
    What are the precautions for 2-Methyl-3-thiophenecarboxylic acid during storage and transportation?
    2-Methyl-3-thiophenecarboxylic acid is an organic compound, and many matters need to be paid attention to when storing and transporting.
    First, when storing, it should be placed in a cool, dry and well-ventilated place. This is because if it is in a high temperature and humid place, it is easy to react with water vapor and other components in the air, causing it to deteriorate. For example, if the storage environment is humid, it may cause deliquescence and change its physical and chemical properties.
    Second, it is necessary to keep away from fires and heat sources. Because of its flammability, there is a risk of burning in case of open flames and hot topics, and in severe cases, it may cause fire, endangering the safety of people and property.
    Third, it should be stored separately from oxidants, acids, alkalis, etc., and should not be mixed with storage. Because of its active chemical properties, contact with oxidants or cause violent oxidation reactions; contact with acid and alkali, or damage its structure due to acid-base reactions, affecting quality.
    Fourth, during transportation, make sure that the container does not leak, collapse, fall, or damage. The packaging should be firm to prevent the package from being damaged due to bumps and collisions during transportation, causing material leakage.
    Fifth, during transportation, it should be driven according to the specified route, and do not stop in residential areas and densely populated areas. Just in case of leakage and other accidents, which will affect many people and cause serious consequences. In conclusion, 2-methyl-3-thiophenecarboxylic acid must be stored and transported in strict accordance with relevant regulations to ensure safety and material quality.
    What is the market price of 2-Methyl-3-thiophenecarboxylic acid?
    I look at your question and ask about the market price of 2-methyl-3-thiophenecarboxylic acid. However, this price is not static, and it often fluctuates due to many factors.
    In terms of raw materials, if the raw materials for the production of 2-methyl-3-thiophenecarboxylic acid are abundant and affordable, the cost of this product can be reduced, and the market price may also be reduced; on the contrary, if the raw materials are scarce and expensive, the cost will rise, and the price will be higher.
    The production process is also the key. If there is an advanced and efficient process, it can reduce energy consumption, increase productivity, and reduce costs, which will have a downward pull on prices. If the process is outdated, the cost is high, and the price is difficult to drop.
    The market supply and demand situation is the main reason for the price. If the market has strong demand for this product, but the supply is limited, it is like a rare product is expensive, and the price is bound to rise. If the supply exceeds the demand, the merchant may sell the goods at a reduced price.
    The price varies from region to region. In places where the chemical industry is concentrated and logistics is convenient, the price may be slightly lower due to lower transportation costs; in remote and logistics inconvenient places, the cost increases and the price may be higher.
    Brand and quality also affect the price. Well-known brands and high-quality ones often have higher prices than others due to quality assurance and reputation.
    In summary, in order to determine the exact market price of 2-methyl-3-thiophenecarboxylic acid, it is necessary to carefully investigate factors such as raw materials, processes, supply and demand, regions and brand quality, and it is advisable to pay attention to market trends in real time, or inquire from chemical product trading platforms, industry merchants and other parties to obtain more accurate prices.