2 Amino Thiophene 3 Carboxylic Acid Ethyl Ester
quinoline thiophene imidazole thiazole

2-Amino-thiophene-3-carboxylic acid ethyl ester

Taiy Chemical

    Specifications

    HS Code

    452302

    Chemical Formula C7H9NO2S
    Molar Mass 171.217 g/mol
    Appearance Typically a solid (description may vary based on purity and conditions)
    Melting Point Data may vary, specific value depends on purity
    Solubility In Water Low solubility in water (organic nature of thiophene ring)
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, dichloromethane
    Density Data may vary, experimental determination needed for accurate value
    Pka No widely - known standard value, related to acidic or basic groups in the molecule

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    General Information
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    Frequently Asked Questions

    As a leading 2-Amino-thiophene-3-carboxylic acid ethyl 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 2-Amino-thiophene-3-carboxylic acid ethyl ester?
    2-Amino-thiophene-3-carboxylic acid ethyl ester, this substance has a wide range of uses. In the field of medicinal chemistry, it is a key class of organic synthesis intermediates. It can be used to construct many drug molecules containing thiophene structures, such as some drugs with antibacterial and anti-inflammatory effects. The thiophene core structure often depends on this ethyl ester for initial synthesis. Due to the unique electronic properties of thiophene rings, it can endow drugs with specific biological activities and better pharmacological properties.
    It has also made a name for itself in materials science. Polymer systems can be introduced through specific reactions to improve the electrical and optical properties of materials. For example, conjugated polymers with specific photoelectric response can be synthesized for use in organic Light Emitting Diodes (OLEDs), solar cells and other optoelectronic devices to improve their performance.
    In the field of pesticides, it also has potential application value. It may be able to derive pesticide active ingredients containing thiophene structures, which show unique inhibitory and killing effects on pests and pathogens. Due to the special structure of thiophene rings, it may have the advantages of environmental friendliness, low toxicity and high efficiency, providing a possible path for the creation of new pesticides. In short, 2-amino-thiophene-3-carboxylate ethyl ester has important uses in many fields, laying the foundation for many research and applications.
    What are the synthesis methods of 2-Amino-thiophene-3-carboxylic acid ethyl ester
    The synthesis method of 2-amino-thiophene-3-carboxylic acid ethyl ester has been known for a long time. Now I will describe it as follows.
    First, using thiophene as the starting material, the thiophene is first substituted under specific conditions to introduce carboxyl groups. In this step, attention should be paid to the temperature of the reaction and the proportion of reagents. If the cap temperature is too high or too low, and the proportion of reagents is unbalanced, the yield and purity of the reaction can be affected. Then the carboxyl group is esterified, and ethanol and an appropriate catalyst are used to promote the conversion of carboxyl groups into ethyl ester groups. In this esterification process, the choice and amount of catalyst are very critical, which is related to the rate of reaction and the quality of the final product. Finally, the amino group is introduced at a specific position in the thiophene ring through a clever method. This step requires fine control of the reaction conditions to obtain a higher yield of the target product 2-amino-thiophene-3-carboxylic acid ethyl ester.
    Second, there are also thiophene derivatives containing specific substituents as starters. First, the specific group is properly transformed to construct a structure similar to the target product. Then through a series of reactions, carboxyl, ethyl ester and amino groups are gradually introduced. This approach requires careful planning of the sequence of each step of the reaction, which affects the purity and yield of the product due to different reaction sequences or the number of side reactions. Each step of the reaction requires careful consideration of the reaction conditions, such as the choice of solvent and the control of the reaction time.
    Third, there are those who use other heterocyclic compounds as starting materials and convert them into 2-amino-thiophene-3-carboxylic acid ethyl ester through multi-step reactions. This method requires a deep understanding of the reactivity of heterocyclic compounds and the use of their special reactivity to gradually construct the structure of the target product. This process often involves complex reaction mechanisms and optimization of conditions. It requires the experimenter to have a deep chemical foundation and rich practical experience in order to effectively improve the yield and purity of the product and achieve the purpose of synthesis.
    What are the physical and chemical properties of 2-Amino-thiophene-3-carboxylic acid ethyl ester
    Ethyl 2-amino-thiophene-3-carboxylate is a class of organic compounds. It has specific physical and chemical properties and is used in many fields.
    When it comes to physical properties, this compound is mostly in solid form at room temperature, but the exact melting point, boiling point and other properties often vary due to the preparation process and purity. Generally speaking, the melting point is about a certain range, because the exact value needs to be determined by experiments. Its appearance is usually white to light yellow powder or crystalline, and the texture is fine. The substance is insoluble in water due to the fact that it contains hydrophobic groups in its molecular structure, but it can be soluble in organic solvents such as ethanol and dichloromethane. It exhibits a certain solubility in organic solvents. This property provides convenience for its use in organic synthesis operations.
    As for chemical properties, in 2-amino-thiophene-3-carboxylic acid ethyl ester, the amino group is alkaline and can react with acids to form corresponding salts; while the ester group has ester properties, and hydrolysis can occur when exposed to acids or bases. Under basic conditions, 2-amino-thiophene-3-carboxylate and ethanol can be obtained by hydrolysis; under acidic conditions, 2-amino-thiophene-3-carboxylic acid and ethanol can be obtained. In addition, thiophene rings can participate in electrophilic substitution reactions due to their aromaticity. Under specific conditions, other functional groups can be introduced on thiophene rings, which provides the possibility for their use in organic synthesis to construct complex structural compounds. And amino groups and ester groups may also affect each other, thereby affecting the overall molecular reactivity and selectivity.
    What is the price range of 2-Amino-thiophene-3-carboxylic acid ethyl ester in the market?
    I look at your question, but I am inquiring about the price range of ethyl 2-amino-thiophene-3-carboxylate in the market. However, the price of this chemical often varies due to various factors, which is difficult to determine.
    First, quality is the key. If it has high purity and few impurities, it is suitable for high-end scientific research or pharmaceutical and other fine fields, and the price is not cheap; if the purity is slightly lower, it is only used for general industrial purposes, and the price may be relatively easy.
    Second, the supply channel also has an impact. Through regular large factories, the quality is guaranteed, but the price may be high due to brand, cost and other factors; if it is obtained from some small suppliers, the price may be favorable, but the quality may remain variable.
    Third, the market supply and demand situation determines the price. If the demand is strong for a while and the supply is limited, if a pharmaceutical project urgently needs a large amount of this product, the price will rise; on the contrary, if the market is saturated and the supply exceeds the demand, the price may be lowered.
    Fourth, the amount of purchase is also related to the price. Bulk purchase, suppliers or for promotional quantities, give discounts; small purchases, unit price or higher.
    As far as I know, in the past market, the price of this product was between a few yuan and tens of yuan per gram. However, this is only a rough number. Today, it is necessary to consult major chemical raw material suppliers and chemical trading platforms in detail to obtain an accurate price range.
    What are the storage conditions for 2-Amino-thiophene-3-carboxylic acid ethyl ester?
    2-Amino-thiophene-3-carboxylic acid ethyl ester is also an organic compound. Its storage conditions are crucial to the stability and quality of this compound.
    This compound should be stored in a cool place. High temperature can easily cause its chemical reaction, damaging its structure and properties. A cool place can slow down its molecular movement and reduce its interaction with external factors to maintain its chemical stability.
    And when placed in a dry place. Because moisture is easy to cause reactions such as hydrolysis, when there is water vapor, water molecules may attack its chemical bonds, causing it to decompose or deteriorate. Therefore, a dry environment can prevent the occurrence of this adverse reaction.
    In addition, it should be avoided from contact with oxidants. Ethyl 2-amino-thiophene-3-carboxylate has specific chemical activity, and its chemical composition and properties will be changed when it encounters oxidants or undergoes violent oxidation reactions, causing dangers such as combustion and explosion.
    When storing, it needs to be sealed. Sealing can prevent its volatilization and escape, and can also isolate external air, water vapor and impurities, making the storage environment stable, thereby ensuring that the compound maintains its inherent characteristics in long-term storage for subsequent experiments, production and other uses. In this way, 2-amino-thiophene-3-carboxylic acid ethyl ester must be properly stored to make it play its due role.