2 Phenylthiazole 4 Carboxylicacid Ethyl Ester
quinoline thiophene imidazole thiazole

2-Phenylthiazole-4-carboxylicacid ethyl ester

    Specifications

    HS Code

    329460

    Chemical Formula C12H11NO2S
    Molecular Weight 233.29
    Appearance Solid (likely, typical for such compounds)
    Solubility In Water Low (due to non - polar phenyl and thiazole groups)
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, dichloromethane

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    General Information
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    Frequently Asked Questions

    As a leading 2-Phenylthiazole-4-carboxylicacid 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 are the physical properties of 2-Phenylthiazole-4-carboxylic acid ethyl ester
    2-Phenylthiazole-4-carboxylic acid ethyl ester, this is an organic compound. Its physical properties are particularly important and are related to many practical applications.
    First of all, the appearance is white to light yellow crystalline powder at room temperature and pressure. This color and morphology are the key points for visual identification in many chemical production and drug preparation processes. Because of its powder shape, it can be better dispersed in subsequent mixing and reaction operations, which is conducive to the full progress of the reaction.
    And the melting point is about [X] ° C. The characteristic of melting point is of great significance in the purification and identification of compounds. By measuring the melting point, the purity of the substance can be judged. If the purity is high, the melting point range is narrow and close to the theoretical value; if it contains impurities, the melting point will be reduced and the melting range will be widened.
    In terms of boiling point, it is about [X] ° C. Boiling point data is indispensable for chemical operations such as distillation and separation. Knowing the boiling point can accurately control the distillation temperature, achieve effective separation of the compound from other substances, and obtain high-purity products.
    Solubility is also a key property. It is slightly soluble in water, but soluble in organic solvents such as ethanol, ether, and chloroform. This solubility characteristic affects the design of drug dosage forms and absorption in the body in drug development. In organic synthesis, it can help select suitable reaction solvents and create an environment conducive to reaction occurrence. < Br >
    The density is about [X] g/cm ³. Density data plays a significant role in the measurement of chemical production. Accurately knowing the density can accurately calculate the amount of substances, ensure that the reaction is carried out according to the expected stoichiometric ratio, and improve product quality and production efficiency.
    To sum up, the physical properties of 2-phenylthiazole-4-ethyl carboxylate play a key role in many fields such as chemical industry and medicine. In-depth understanding and accurate grasp of it are an important basis for research and production in related fields.
    What are the chemical properties of 2-Phenylthiazole-4-carboxylic acid ethyl ester
    Ethyl 2-phenylthiazole-4-carboxylate is an organic compound. It has unique chemical properties and has attracted much attention in the field of organic synthesis.
    Let's talk about its physical properties first. At room temperature, it is mostly a crystalline solid with a specific melting point and boiling point. Due to the presence of benzene and thiazole rings in the molecular structure, its relative density is slightly higher than that of water. Its solubility also has characteristics. It can be soluble in common organic solvents such as ethanol, ethyl ether, dichloromethane, etc., but it is difficult to dissolve in water. This solubility is due to the large proportion of hydrophobic groups in the molecule, which makes it weak in interacting with water molecules.
    Looking at the chemical properties, its molecule contains ester groups, so it has the typical properties of esters. In case of acid or base, hydrolysis reaction can occur. Under acidic conditions, hydrolysis generates 2-phenylthiazole-4-carboxylic acid and ethanol; under basic conditions, hydrolysis is more thorough, generating carboxylic salts and ethanol. This reaction is an important method for preparing corresponding carboxylic acids in organic synthesis.
    In addition, the thiazole ring and the benzene ring endow the molecule with certain aromatics and stability. The benzene ring can undergo electrophilic substitution reactions, such as halogenation, nitrification, sulfonation, etc. Although the activity of the thiazole ring is slightly lower than that of the benzene ring, it can also participate in some electrophilic or nucleophilic reactions under suitable conditions, adding complexity and diversity to the chemical properties of the compound. Due to the fact that the molecular structure contains multiple conjugated systems, it may have certain optical properties, such as fluorescence emission, under specific wavelengths of light, which may have potential applications in the field of optical materials.
    What is the synthesis method of 2-Phenylthiazole-4-carboxylic acid ethyl ester
    To prepare 2-phenylthiazole-4-carboxylic acid ethyl ester, the following method can be followed.
    First take an appropriate amount of 2-aminothiophenol and dissolve it in a suitable organic solvent, such as ethanol, dichloromethane, etc., to create a reaction environment. Then slowly add α-bromoacetoacetate ethyl ester. This process needs to be carefully controlled and maintained at a low temperature, such as 0-5 ° C, to prevent side reactions. Add an appropriate amount of acid binding agents, such as potassium carbonate, triethylamine, etc., to regulate the pH of the reaction system and promote the smooth progress of the reaction. Stir for a few hours at this low temperature, then gradually heat up to room temperature, and continue to stir the reaction, usually for several hours, until the reaction reaches a moderate process.
    After the reaction is completed, pour the reaction solution into an appropriate amount of water, and extract the product with an organic solvent such as ethyl acetate. The extract is dried with anhydrous sodium sulfate to remove the moisture. Subsequently, the organic solvent is removed by vacuum distillation to obtain a crude product.
    To obtain pure 2-phenylthiazole-4-carboxylate ethyl ester, the crude product needs to be further purified. In the method of regular mining column chromatography, silica gel is used as the fixed phase, and a suitable eluent, such as the mixture of petroleum ether and ethyl acetate, can be obtained by elution and collection according to a specific ratio. During the whole process, the control of the conditions of each step is the key, which is related to the yield and purity of the product.
    2-Phenylthiazole-4-carboxylic acid ethyl ester is used in which areas
    2-Phenylthiazole-4-ethyl carboxylate is useful in various fields. In the field of medicine, it can be used as a key raw material for the synthesis of drugs. The structure of Geiinthiazole and benzene ring gives it unique chemical properties and can interact with specific targets in organisms. Physicians can develop new drugs with antibacterial and anti-inflammatory effects by modifying the structure of the compound. For example, through delicate chemical modification, antibacterial drugs targeting specific bacteria may be obtained to treat related diseases.
    In the field of materials science, it is also quite useful. Because of its specific molecular structure and properties, it can be used to prepare special functional materials. If involved in the synthesis of polymer materials with unique optical and electrical properties, they can be applied to optoelectronic components, such as organic Light Emitting Diode (OLED), to help improve the luminous efficiency and stability of the components.
    In the agricultural field, pesticides with insecticidal and bactericidal activities can be prepared through derivatization reactions. With its chemical properties, it interferes with the physiological and metabolic processes of pests or pathogens, so as to achieve the purpose of controlling pests and diseases, ensuring the robust growth of crops and improving yields.
    Furthermore, in the field of organic synthetic chemistry, 2-phenylthiazole-4-carboxylate is often an important intermediate. Chemists can use a variety of organic reactions, such as nucleophilic substitution, addition reactions, etc., to build more complex and functional organic compounds, expand the boundaries of organic synthesis, and lay the foundation for the development of new materials and new drugs.
    2-Phenylthiazole-4-carboxylic acid ethyl ester market prospects
    2-Phenylthiazole-4-carboxylate ethyl ester, the current market prospect of this product is the main point of concern for everyone. Looking back at the past, the field of organic synthesis has developed rapidly, and many new compounds have emerged, bringing new opportunities to various industries. This compound has great potential in many fields such as medicine and materials due to its unique chemical structure.
    In the field of medicine, with the in-depth study of disease mechanisms, new drug R & D requests are on the rise. The special structure of 2-phenylthiazole-4-carboxylate ethyl ester may provide novel ideas for drug design. For example, some studies have revealed that compounds containing similar structures have certain affinity for specific disease targets, or can be developed as drugs for the treatment of related diseases, so they are expected to occupy a place in the pharmaceutical research and development market.
    As for the field of materials, with the advancement of science and technology, the demand for high-performance materials continues to grow. The compound may be useful in photoelectric materials, polymer material modification and other aspects due to its unique chemical and physical properties. For example, in some organic photoelectric material systems, the introduction of such structures may improve the photoelectric properties of materials and enhance their application value in devices such as Light Emitting Diodes and solar cells.
    However, its activity marketing also faces challenges. On the one hand, the optimization of the synthesis process and cost control are extremely critical. If efficient and low-cost synthesis cannot be achieved, large-scale production and market popularization will be hindered. On the other hand, the market competition is fierce, with many similar compounds competing for a limited market share. Only by relying on technological innovation to highlight its own unique advantages can it stand out in the market.
    Overall, although 2-phenylthiazole-4-carboxylate ethyl ester faces challenges, given its structural characteristics and potential application value, if it can overcome the problems of synthesis and market competition, the future market prospect may be quite broad.