2 Aminothiophene 3 Carboxylic Acid Methyl Ester
quinoline thiophene imidazole thiazole

2-Aminothiophene-3-carboxylic acid methyl ester

Taiy Chemical

    Specifications

    HS Code

    629208

    Chemical Formula C6H7NO2S
    Molar Mass 157.19 g/mol
    Appearance Solid
    Color Typically white to off - white
    Odor May have a characteristic organic odor
    Solubility In Water Poorly soluble
    Solubility In Organic Solvents Soluble in some common organic solvents like dichloromethane, chloroform
    Melting Point Varies, but around [specific value if known] °C
    Boiling Point Varies depending on conditions, around [estimated value if known] °C
    Pka Related to its acidic and basic nature, value around [if known]
    Density [Value if known] g/cm³

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    General Information
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    Frequently Asked Questions

    As a leading 2-Aminothiophene-3-carboxylic acid methyl ester 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 main use of methyl 2-aminothiophene-3-carboxylate?
    Ethyl 2-% hydroxysuccinic acid-3-malonate, this is an organic compound, its main uses are as follows:
    One is the raw material for organic synthesis. In the field of organic synthesis, it can be used as a key intermediate. Taking the preparation of carboxylic acid compounds with specific structures as an example, by performing specific chemical reactions on 2-hydroxysuccinic acid-3-malonate ethyl ester, such as hydrolysis, esterification, condensation, etc., complex carboxylic acid structures with specific functional groups can be constructed. For example, when constructing a polycyclic compound, the active functional group of the compound can initiate a cyclization reaction, and then generate a ring-like product with rich structure, providing a variety of options for organic synthesis chemistry.
    The second is related to pharmaceutical research and development. In the field of medicinal chemistry, it can be used as a structural fragment of a lead compound. Because it has a specific chemical structure and activity, it can interact with specific targets in organisms. Some studies have tried to integrate it into the molecular structure of drugs, modify and optimize it to improve the activity, selectivity and bioavailability of drugs. For example, in the development of some anti-cancer drugs, this structural fragment is introduced, hoping to improve the targeting of drugs to cancer cells, enhance the anti-cancer efficacy, and reduce the toxic and side effects on normal cells.
    The third is the application of materials science. In the field of materials science, it can be used to prepare polymer materials with special properties. Introducing it into the polymer polymerization system as a monomer or modifier can endow the polymer material with unique properties due to its special functional groups. For example, improving the solubility, thermal stability or mechanical properties of the material. When preparing functional film materials, adding this compound may make the film have better flexibility and stability, and expand the application of the material in packaging, electronic devices and other fields.
    What are the synthesis methods of methyl 2-aminothiophene-3-carboxylate?
    The synthesis method of 2-% hydroxybutyric acid-3-hexenoic acid ethyl ester has various paths, which are described as follows:
    First, the esterification reaction of hydroxybutyric acid and hexenol is made by using hydroxybutyric acid and hexenol as raw materials. This reaction often requires acid as a catalyst, such as sulfuric acid, p-toluenesulfonic acid and the like. Place the two in a reaction vessel in an appropriate ratio, add an appropriate amount of catalyst, heat and stir, so that the reaction can proceed. During the reaction, the catalysis of the acid can promote the dehydration and condensation of the hydroxyl group and the carboxyl group to form an ester structure. However, in this process, it is necessary to pay attention to the control of the reaction temperature and time. If the temperature is too high, or the side reaction will lead to At the same time, timely removal of the water generated by the reaction can shift the equilibrium to the right and improve the yield of the ester.
    Second, by the acid chloride method. First, 2-hydroxybutyric acid is converted into acid chloride, which is often obtained by reagents such as thionyl chloride and phosphorus trichloride interacting with acids. The activity of acid chloride is higher than that of acid, and it is easier to react with hexenol. The resulting acid chloride reacts with hexenol in an appropriate solvent, such as dichloromethane, ethyl ether, etc., in the presence of a base, which can bind the acid and promote a smooth reaction. This way has a faster reaction rate and a higher yield. However, the acid chloride is corrosive, and the operation needs to be cautious, and the cost of reagents may be high. < Br >
    Third, use the transesterification reaction. If there are suitable esters, such as methyl or ethyl esters of 2-hydroxybutyric acid, and hexenol under the action of catalysts, transesterification can occur. Commonly used catalysts include metal alkoxides, Lewis acids, etc. The conditions of this method are relatively mild, and the raw materials may be more accessible. However, the reaction also needs to be carefully controlled, such as the amount of catalyst, the proportion of reactants and the reaction time, etc., in order to achieve good yield and purity.
    Synthesis of 2-hydroxybutyric acid-3-hexenoic acid ethyl ester, according to the actual situation, such as the availability of raw materials, cost, equipment conditions, etc., the appropriate synthesis method can be selected.
    What are the physical properties of methyl 2-aminothiophene-3-carboxylate?
    2-Aminopyridine and 3-carboxypyridine methyl esters are both organic compounds with unique physical properties.
    2-Aminopyridine, in the form of white to pale yellow crystalline powder, soluble in water, ethanol and ether and other common solvents. Its melting point is about 58-62 ° C, and its boiling point is 272-273 ° C. This substance is basic due to the presence of amino groups and can react with acids to form salts. It is often used as an intermediate in the field of organic synthesis and participates in the preparation of many nitrogen-containing compounds.
    3-Carboxypyridine methyl ester also has a white to off-white solid appearance. It is slightly soluble in water, but easily soluble in organic solvents such as ethanol and chloroform. The melting point is in the range of 38-42 ° C, and the boiling point is about 270 ° C. The carboxyl group and the methyl ester group endow the compound with special chemical activity. The carboxyl group can undergo esterification, salt formation and other reactions, and the methyl ester group can undergo hydrolysis and other transformations. It is an important raw material in pharmaceutical chemistry and organic synthesis, and is of great significance for the construction of complex organic molecular structures.
    The two have different solubility in physical properties. 2-aminopyridine has relatively good water solubility due to the formation of hydrogen bonds between amino groups and water. The melting point and boiling point are also different due to different molecular structures and forces. These differences in physical properties make them unique in the selection of separation, purification, and application scenarios. In many fields such as organic synthesis and drug development, they can achieve precise chemical conversion and product preparation based on their physical properties.
    What is the market price of methyl 2-aminothiophene-3-carboxylate?
    At present, the prices of 2-hydroxypyridine and 3-carboxybenzaldehyde in the market vary with changes in market conditions.
    As far as 2-hydroxypyridine is concerned, it has a wide range of uses in the field of chemical and pharmaceutical synthesis. The method of its preparation may be obtained from a specific reaction path. In the market, its quality is different, and it has few impurities. It is required in high-end pharmaceutical and fine chemical synthesis, and the price is also high. Second, it may contain some impurities and is used in general industrial synthesis, and the price is slightly lower. And the output of the place of origin and the trend of supply and demand all affect its price. If the place of origin is abundant in raw materials, the process is advanced, the output is greatly increased, and the demand is limited, the price will decline; conversely, the raw materials are scarce, and the number of seekers will increase, and the price will increase. Common, its price per kilogram or in the range of gold to gold.
    As for 3-carboxybenzaldehyde, it is also indispensable in many fields such as organic synthesis and materials science. Its preparation or through complex chemical steps. Its market price is also made by many factors. Its purity is essential, high purity, used in cutting-edge scientific research and high-end material preparation, valuable; lower purity, used in general production, the price is relatively low. Market supply and demand conditions also affect its price. If there is a surge in demand from emerging industries and the production capacity is temporarily difficult to cope, the price will rise; if the supply exceeds the demand, the price will fall. Roughly speaking, the price per kilogram may range from hundreds to thousands of gold.
    In short, the market price of the two is influenced by various factors such as quality, supply and demand, raw materials, and craftsmanship. To know the exact price, you should carefully observe the current market situation and transaction details.
    What are the precautions for methyl 2-aminothiophene-3-carboxylate in storage and transportation?
    2-% aminopyridine and 3-carboxybenzaldehyde have a lot to pay attention to during storage and transportation.
    The first word is storage, both of which need to be stored in a cool, dry and well-ventilated place. 2-aminopyridine is alkaline and easy to react with acidic substances, so it must be stored separately from acids to prevent chemical reactions. And its hygroscopicity is strong. If the storage environment humidity is high, it is easy to be damp and deteriorated, so the humidity at the storage place should be controlled within a reasonable range. 3-carboxybenzaldehyde needs to avoid contact with oxidants, strong bases, etc. due to the active chemical properties of its aldehyde group to prevent oxidation or other chemical reactions. It is also sensitive to light. Long-term light exposure may cause it to undergo photochemical reactions and deteriorate, so it should be stored in a container protected from light.
    Second talk about transportation, when transporting 2-aminopyridine, it is necessary to ensure that the packaging is complete and well sealed to prevent leakage. Because it is a chemical dangerous substance, the transportation vehicle must meet relevant safety standards and be equipped with necessary emergency treatment equipment and protective equipment. During transportation, it should be protected from sun exposure, rain and high temperature. 3-Carboxybenzaldehyde transportation also needs to be properly packaged to prevent package damage caused by collision and friction. Because of its lively nature, it should also be kept away from fire and heat sources during transportation to avoid mixing with incompatible substances. Transportation personnel should also be familiar with the characteristics and emergency treatment methods of these two substances. In the event of leakage and other accidents, they can be disposed of quickly and properly to avoid the expansion of harm. In short, 2-aminopyridine and 3-carboxybenzaldehyde should not be taken lightly during storage and transportation. They must adhere to their chemical properties and adhere to relevant regulations to ensure safety.