3 Methylthiophene 2 Carboxamide
quinoline thiophene imidazole thiazole

3-Methylthiophene-2-carboxamide

Taiy Chemical

    Specifications

    HS Code

    409652

    Name 3-Methylthiophene-2-carboxamide
    Chemical Formula C6H7NOS
    Molar Mass 141.19 g/mol
    Appearance Solid
    Color Off - white to light yellow
    Melting Point 128 - 130 °C
    Solubility In Water Low solubility
    Solubility In Organic Solvents Soluble in some organic solvents like ethanol, dichloromethane
    Odor May have a faint characteristic odor
    Purity Typically sold with high purity (e.g., 95%+)

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    General Information
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    Frequently Asked Questions

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    What is the chemistry of 3-Methylthiophene-2-carboxamide?
    3 - Methylthiophene - 2 - carboxamide is an organic compound. It is a solid and is mostly used in organic synthesis and medicinal chemistry. It has many unique chemical properties.
    From the structural point of view, its core is a thiophene ring with a formamide group at the 2nd position and a methyl group at the 3rd position. This specific structure gives it the properties that distinguish it from others. Formamide groups are polar and can cause hydrogen bonds between molecules, which affects physical properties such as melting point and boiling point. Methyl groups change the distribution of molecular electron clouds and affect the reactivity.
    On chemical activity, thiophene rings are electron-rich aromatic rings, which are prone to electrophilic substitution reactions. The presence of formamide groups and methyl groups affects the selectivity of the reaction check point. Due to the fact that formamide groups are electron-withdrawing groups, the electron cloud density of the thiophene ring decreases, but the 2,5 positions are relatively electron-rich, and electrophilic reagents are prone to attack these two positions. Methyl groups are electron-withdrawing groups, which increase the electron cloud density of adjacent and para-positions, and also affect the reaction selectivity.
    It can react with acids and bases. In an acidic environment, formamide groups can be protonated, enhancing their electron-withdrawing properties, or changing the reaction activity of thiophene rings. Under alkaline conditions, formamide groups or hydrolysis to form corresponding carboxylic acids and ammonia derivatives. The chemical properties of 3-Methylthiophene-2-carboxamide are determined by its structure. These properties can be used as intermediates in organic synthesis to build complex molecular structures through various reactions, laying the foundation for medical research and development and other fields, and helping to create compounds with specific biological activities.
    What are the physical properties of 3-Methylthiophene-2-carboxamide?
    3-Methylthiophene-2-formamide is an organic compound. Its physical properties are related to the external performance of substances, and have a great impact on the fields of chemical industry and materials.
    - ** Appearance properties **: At room temperature, it is mostly white to light yellow crystalline powder. This form is easy to store, transport and access. Its color is pure, reflecting the high purity of the substance and few impurities.
    - ** Melting boiling point **: Melting point is between 162-166 ° C, with a high boiling point. The melting point determines that it changes from solid to liquid at a specific temperature, which is of great significance to the processing process. A higher boiling point means that it needs high temperature to be vaporized, and it can maintain a stable solid or liquid state in a relatively wide temperature range. < Br > - ** Solubility **: It is soluble in common organic solvents such as methanol, ethanol, and dichloromethane, but has poor solubility in water. This property is conducive to selecting suitable solvents for reaction and separation during organic synthesis. According to the principle of similar phase dissolution, the intermolecular force between organic solvent molecules and the compound is appropriate to promote dissolution.
    - ** Density **: The density is 1.319g/cm ³, which is related to its quality and volume. During preparation and use, the dosage can be accurately calculated by density, which is of great significance to the accuracy of experiments and production.
    - ** Stability **: It is quite stable at room temperature and pressure, but when it encounters strong oxidants, strong acids, and strong bases, it is easy to cause chemical reactions to cause structural changes. When storing and using such substances, it is necessary to avoid them to ensure their stability and safe use.
    What are the common synthetic methods of 3-Methylthiophene-2-carboxamide?
    The common synthesis methods of 3-methylthiophene-2-formamide have been around for a long time. In the past, it followed the path of classical organic synthesis. First, starting from 3-methylthiophene, the carboxyl group can be introduced through the reaction of carboxylation. The Gainthiophene ring has a certain activity, and the methyl ortho-position on the thiophene ring can be carboxylated under specific conditions with suitable reagents, such as carbon dioxide. The conditions are quite critical, and the temperature, pressure and catalyst need to be carefully regulated. Often metal catalysts, such as magnesium, lithium and other organometallic reagents, help the reaction to proceed smoothly and generate 3-methylthiophene-2-carboxylic acid.
    Then, the carboxylic acid reacts with ammonia or amine compounds to form an amide. This step of the reaction is mostly assisted by a condensing agent. If a condensing agent such as dicyclohexyl carbodiimide (DCC) is used, it can promote the dehydration and condensation between the carboxylic acid and ammonia or amine. This condensing agent can activate the carboxyl group, making it easier to react with ammonia or amine to form an amide bond, and finally obtain 3-methylthiophene-2-formamide.
    There are other methods. It can be started by thiophene derivatives containing corresponding substituents, and the desired structure can be gradually constructed through multi-step reactions. The thiophene ring is modified first, and a suitable substituent is introduced, and then it is converted into a carboxylamide group through functional group transformation. Although this approach is a little complicated, it can be flexibly adjusted according to different raw materials and conditions to achieve the purpose of synthesis. And each step of the reaction needs to be carefully operated, pay attention to the selectivity and yield of the reaction, and carefully control each step to obtain a pure 3-methylthiophene-2-formamide product.
    3-Methylthiophene-2-carboxamide in what areas?
    3-Methylthiophene-2-formamide is useful in various fields. In the field of medicine, it can be a key raw material for the creation of new drugs. Due to its unique chemical structure, it can interact with specific targets in the body, thereby regulating physiological functions, or has antibacterial, anti-inflammatory, anti-tumor and other effects. It is a way of medical research and development. Many medical scientists use it as a basis to explore new therapeutic drugs.
    In the field of materials science, 3-methylthiophene-2-formamide is also highly valued. It can be integrated into polymer materials through specific chemical reactions to improve the properties of materials. For example, making it have better electrical conductivity, stability or optical properties is of great benefit in the manufacture of electronic devices and optical materials, or can lead to the birth of new display screens, sensors and other devices.
    Furthermore, in the agricultural field, it may be used to prepare new pesticides. With its chemical properties, it may have the effect of inhibiting or killing diseases and insects in crops, and compared with traditional pesticides, it may have lower toxicity and better environmental compatibility. When ensuring crop yield and quality, it can also reduce the harm to the environment.
    In addition, in the world of organic synthetic chemistry, 3-methylthiophene-2-formamide is often used as an important intermediate. Chemists can modify and derive their structures through various organic reactions, thus constructing more complex and functional organic compounds, which contribute to the development of organic synthetic chemistry and promote the continuous development of this field.
    What is the market outlook for 3-Methylthiophene-2-carboxamide?
    3-Methylthiophene-2-formamide is one of the organic compounds. Looking at its market prospects, it can be discussed from various perspectives.
    First talk about the field of chemical synthesis, which is a key intermediate and can be used to prepare other fine chemicals. Nowadays, the chemical industry is advancing, and there is a growing demand for high-purity and characteristic structure intermediates. 3-Methylthiophene-2-formamide has emerged in new materials, pharmaceutical synthesis and other branches due to its unique structure. For example, in pharmaceutical research and development, it is often necessary to build a special molecular structure. This compound may be an ideal starting material to help chemists build the required active molecules. Therefore, in the chemical synthesis chain, its prospects are bright, and the demand is expected to increase with the expansion of research and development.
    Second talk about the field of materials science. With the development of science and technology, new functional materials have attracted much attention. 3-methylthiophene-2-formamide or modified, polymerized and other means are integrated into the polymer material system to endow the material with specific properties such as conductivity and optics. For example, in the field of organic semiconductor materials, there is an urgent need for compounds with specific electronic structures. This compound may be able to find a place in this field by virtue of its own structural advantages and promote the upgrading of materials. Therefore, in the direction of materials science, it also has broad development space.
    However, its market prospects are not without challenges. The complexity of the synthesis process or the high production cost limit large-scale application. And the market competition is fierce, and similar substitutes may continue to emerge. To open up the market, researchers need to improve the synthesis process to reduce costs, and enterprises must also strengthen innovation and highlight the unique advantages of products in order to gain an advantage in the changing market and enjoy the rich potential of 3-methylthiophene-2-formamide.