3 Methyl 1 Benzothiophene 2 Carboxylate
quinoline thiophene imidazole thiazole

3-methyl-1-benzothiophene-2-carboxylate

Taiy Chemical

    Specifications

    HS Code

    561947

    Chemical Formula C10H8O2S
    Molecular Weight 192.24 g/mol
    Appearance Solid (usually)
    Odor Typical of benzothiophene derivatives (odor description can vary)
    Melting Point Data may vary, specific value needs further research
    Boiling Point Data may vary, specific value needs further research
    Solubility In Water Low solubility in water
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, acetone
    Density Data may vary, specific value needs further research
    Stability Stable under normal conditions, may react with strong oxidizing agents

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    General Information
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    Frequently Asked Questions

    As a leading 3-methyl-1-benzothiophene-2-carboxylate 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 3-methyl-1-benzothiophene-2-carboxylate?
    3-Methyl-1-benzothiophene-2-carboxylic acid ester, this is one of the organic compounds. It has unique chemical properties.
    View its structure, containing benzothiophene ring and carboxyl-derived ester group. The benzothiophene ring is fused from the benzene ring and the thiophene ring, which endows the compound with certain aromatic and stability. Due to the existence of the conjugate system, the electron cloud distribution has a specific law, which has a great influence on its physical and chemical properties.
    The existence of ester groups makes this compound hydrolyzed under specific conditions. When exposed to acids or bases, ester bonds are easily broken, and acid-catalyzed hydrolysis generates corresponding carboxylic acids and alcohols; alkali-catalyzed hydrolysis generates carboxylic salts and alcohols. This hydrolysis reaction is widely used in organic synthesis and analysis.
    3-methyl-1-benzothiophene-2-carboxylic acid esters may also participate in nucleophilic substitution reactions. Carbonyl carbons of ester groups have certain electrophilicity and are vulnerable to attack by nucleophiles. Nucleophiles can replace the original groups in ester groups to realize the modification and transformation of compound structures, which is an important way to synthesize more complex organic compounds.
    In addition, due to the special structure of the benzothiophene ring, the compound may have certain optical and electrical properties, which may have potential applications in the field of materials science, such as in organic optoelectronic materials, or it may exhibit unique optoelectronic properties, providing a direction for the research and development of new functional materials.
    What are the main uses of 3-methyl-1-benzothiophene-2-carboxylate?
    3-Methyl-1-benzothiophene-2-carboxylic acid ester, an important compound in organic chemistry, has a wide range of uses in various fields.
    In the field of medicinal chemistry, it is often used as a key intermediate. Due to its special chemical structure, it can participate in the synthesis of a variety of drug molecules. Many drugs with specific biological activities, in the development and preparation of many drugs, 3-methyl-1-benzothiophene-2-carboxylic acid esters can be used as starting materials or key reaction fragments. After clever chemical modification and reaction, it can be constructed into a complex drug structure with specific pharmacological activities to deal with diseases such as inflammation and tumors. < Br >
    has also made its mark in the field of materials science. Due to its structural properties, materials are endowed with specific optical, electrical or thermal properties. For example, it can be introduced into polymer materials to improve material stability, conductivity or fluorescence properties by changing the molecular structure and interaction of the material. In the research of organic Light Emitting Diode (OLED) materials, containing such structural compounds may optimize the luminous efficiency and stability, contributing to the development of display technology.
    In the field of pesticide chemistry, it also plays an important role. It can be used as a key component in the synthesis of new pesticides, providing a new way for crop pest control. Through rational design and modification, compounds based on 3-methyl-1-benzothiophene-2-carboxylic acid esters can effectively inhibit and kill specific pests or bacteria, and have little impact on the environment and non-target organisms, which meets the needs of modern green pesticide development.
    In short, 3-methyl-1-benzothiophene-2-carboxylic acid esters play an important role in the fields of medicine, materials, pesticides, etc., providing an important material basis for technological innovation and Product Research & Development in related fields.
    What are 3-methyl-1-benzothiophene-2-carboxylate synthesis methods?
    The synthesis method of 3-methyl-1-benzothiophene-2-carboxylic acid ester has been used by many parties throughout the ages. Common ones are to use specific starting materials and carefully designed reaction steps to gradually build the target molecular structure with the help of chemical reagents. The starting material or the benzothiophene derivative with suitable substituents, supplemented by the corresponding carboxylating reagents, under suitable reaction conditions, such as under specific temperature, pressure and catalyst action, make it chemically react to form this ester compound.
    Furthermore, or use a different approach to start from different raw materials and use different reaction mechanisms to achieve synthesis. Or build a benzothiophene skeleton first, and then introduce methyl and carboxylic acid ester groups. This process requires a good grasp of various chemical reactions, and precise control of reaction conditions, such as the choice of solvent and the control of reaction time, are all critical to success or failure.
    During synthesis, temperature control is crucial. If the temperature is too high, or side reactions may occur, and the product is impure; if the temperature is too low, the reaction rate will be slow and take a long time. The use of catalysts is also indispensable, which can accelerate the reaction process and increase the yield. Different catalysts have different effects on the selectivity and activity of the reaction, so careful selection is required.
    In addition, the nature of the reaction solvent also affects the synthesis effect. The choice of polar solvent or non-polar solvent depends on the reaction mechanism and the characteristics of the raw materials. A suitable solvent can promote the dissolution of the reactants, facilitate the collision between molecules, and then promote the smooth progress of the reaction. In short, the synthesis of 3-methyl-1-benzothiophene-2-carboxylate requires comprehensive consideration of various factors and careful design of the experimental process to obtain the ideal product.
    What is the price of 3-methyl-1-benzothiophene-2-carboxylate in the market?
    The price of 3-methyl-1-benzothiophene-2-carboxylic acid ester in the market is difficult to determine. This compound is not a common general product, and its price is determined by many factors.
    The first to bear the brunt is the difficulty of preparation. If its preparation requires complicated steps, rare raw materials, or high and difficult technologies, the price will be high. During its synthesis, the procurement of raw materials, the control of reactions, and the purification of products require a lot of manpower, material and financial resources.
    Furthermore, market demand is also the key. If there is a strong demand for this product in a specific field, such as pharmaceutical research and development, materials science, etc., but the supply is limited, the price will rise according to the reason of supply and demand. On the contrary, if there is little demand, the price may be relatively easy.
    In addition, the difference in suppliers also affects the price. Different merchants, due to their own cost structure and business strategies, set different prices. Some merchants will sell at a lower price in order to expand the market and increase their share; those who focus on quality and service may have a slightly higher price.
    However, after checking the market records of the past, there is no detailed record of the exact price of 3-methyl-1-benzothiophene-2-carboxylate. To know the exact price, the best way is to consult chemical product suppliers, browse professional chemical trading platforms, or attend industry exhibitions and consult with industry insiders, so as to obtain the current market price.
    What are 3-methyl-1-benzothiophene-2-carboxylate storage conditions?
    3-Methyl-1-benzothiophene-2-carboxylic acid ester is one of the organic chemicals. The key to its storage is related to the properties and long-term survival of this substance.
    This substance should be placed in a cool, dry and well-ventilated place. A cool environment can slow its change due to heat, and avoid its decomposition or chemical change caused by high temperature. Dry place, to prevent moisture damage. Moisture often causes decay and hydrolysis of primers, especially in organic compounds, so it is necessary to prevent moisture intrusion. In a well-ventilated place, the accumulated volatile gas can be removed to avoid gas accumulation and life risk, and the storage environment can be kept fresh.
    Furthermore, keep away from fire and heat sources. Many of these chemicals are flammable, and in case of fire and heat sources, it is easy to cause combustion or even explosion. It should also be stored in isolation from oxidizing agents. The oxidizing agent has strong oxidizing properties and meets with 3-methyl-1-benzothiophene-2-carboxylic acid ester, or causes violent chemical reactions, resulting in accidents.
    The packaging should not be neglected. It is necessary to ensure that the packaging is complete and sealed. The complete packaging can be isolated from external adverse factors; the sealed state prevents volatilization and leakage, and keeps the material pure to avoid pollution to the environment.
    When handling, it should be handled with care to avoid package damage. Damage will cause the material to leak, which is useless and pollutes the environment, and the leaked material may be at risk around. According to the above, store it carefully to ensure the safety and quality of 3-methyl-1-benzothiophene-2-carboxylate.