2 3 Formyl 4 Hydroxy Phenyl 4 Methyl Thiazole 5 Carboxylic Acid Ethyl Ester
quinoline thiophene imidazole thiazole

(2-(3-Formyl-4-hydroxy-phenyl)-4-methyl-thiazole-5-carboxylic acid ethyl ester

    Specifications

    HS Code

    789233

    Chemical Formula C14H15NO4S
    Molecular Weight 293.34
    Appearance Solid (usually)
    Physical State At Room Temp Solid
    Solubility In Water Low
    Solubility In Organic Solvents Moderate in some organic solvents
    Melting Point Specific value would need experimental determination
    Boiling Point Specific value would need experimental determination
    Pka Related to the carboxylic acid group, value needs determination
    Uv Vis Absorption Absorption peaks would be characteristic of aromatic and thiazole moieties

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    General Information
    Where to Buy (2-(3-Formyl-4-hydroxy-phenyl)-4-methyl-thiazole-5-carboxylic acid ethyl ester in China?
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    As a leading (2-(3-Formyl-4-hydroxy-phenyl)-4-methyl-thiazole-5-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 chemical structure of (2- (3-Formyl-4-hydroxy-phenyl) 4-methyl-thiazole-5-carboxylic acid ethyl ester)?
    This is the name of an organic compound, based on modern chemical analysis, " (2- (3-formyl-4-hydroxy-phenyl) -4-methyl-thiazole-5-carboxylate ethyl ester) ", its chemical structure can be deduced as follows.
    In this compound, the thiazole ring is the core structure. The thiazole ring is a five-membered heterocycle containing sulfur and nitrogen, numbered from the carbon atom adjacent to the sulfur atom, sequentially 1, 2, 3, 4, and 5. At the 4 position, there is a methyl group, that is, a group composed of one carbon atom and three hydrogen atoms. < Br >
    The 5th position is connected to a carboxylic acid ethyl ester group, which is obtained by the esterification reaction of carboxyl group (-COOH) with ethanol (C ³ H OH), that is, -COOC ³ H.
    The 2nd position is connected to a phenyl group, which is the group after removing a hydrogen atom from the benzene ring. The phenyl group has formyl (-CHO) at the 3rd position and hydroxyl (-OH) at the 4th position.
    In summary, the chemical structure of this compound is formed by connecting a specific substituent at a specific position with a thiazole ring as the center. Compounds with such structures may exhibit specific chemical properties and reactivity due to the characteristics and interactions of each group, and may have potential uses in organic synthesis, medicinal chemistry, and other fields.
    What are the main uses of (2- (3-Formyl-4-hydroxy-phenyl) 4-methyl-thiazole-5-carboxylic acid ethyl ester)?
    (2- (3-formyl-4-hydroxy-phenyl) -4-methyl-thiazole-5-carboxylic acid ethyl ester) This substance has its uses in many fields.
    In the development of medicine, it can be used as a key intermediate. The unique structure of the genome may interact with specific targets in organisms, helping to develop novel drugs, such as therapeutic drugs for specific diseases. Doctors use it as a basis, carefully formulated, or can create a cure and save people.
    In the field of organic synthesis, its importance should not be underestimated. With its own structural characteristics, it can participate in a variety of chemical reactions, paving the way for the synthesis of more complex organic compounds with special functions. Those who use this substance skillfully may be able to create new materials with excellent properties.
    In the field of materials science, this material can be used as a starting material, and after specific reactions and treatments, materials with special optical, electrical or mechanical properties can be prepared. These materials can play a great role in electronic devices, optical instruments and other fields, contributing to scientific and technological progress.
    In short, (2 - (3 - formyl - 4 - hydroxy - phenyl) - 4 - methyl - thiazole - 5 - carboxylic acid ethyl ester) in medicine, organic synthesis, materials science and many other important fields, all have functions that cannot be ignored, and are actually important substances to promote the development of related fields.
    What is the synthesis method of (2- (3-Formyl-4-hydroxy-phenyl) 4-methyl-thiazole-5-carboxylic acid ethyl ester)?
    The synthesis of (2 - (3-formyl-4-hydroxy-phenyl) -4-methyl-thiazole-5-carboxylic acid ethyl ester) is a key exploration in organic synthetic chemistry. Its synthesis path needs to follow the principle of organic reaction and the method of chemical transformation.
    Initially, the raw materials containing specific substituents can be selected, such as compounds containing 3-formyl-4-hydroxy-phenyl structure, and those containing 4-methyl-thiazole-5-carboxylic acid ethyl ester related fragments. For the two to react effectively, appropriate reaction conditions need to be carefully selected.
    In the creation of the reaction environment, the choice of solvent is crucial. Appropriate solvents can help the reactants to mix fully and promote the reaction. Or polar organic solvents can be selected, because they can effectively dissolve the reactants and have a positive impact on the reactivity and selectivity.
    The intervention of catalysts is also indispensable. Appropriate catalysts can reduce the reaction activation energy, accelerate the reaction rate, and promote the reaction to form the target product. Or specific acid-base catalysts can be selected, depending on the characteristics of the reactants and the type of reaction.
    The regulation of reaction temperature and time is also a key factor. If the temperature is too high, it may cause side reactions to breed, and the purity of the product will be damaged; if the temperature is too low, the reaction rate will be slow and it will take a long time. Therefore, experimental exploration is required to find the best reaction temperature range. Time control should also be accurate to ensure that the reaction is fully completed without overreaction.
    During the reaction process, appropriate analytical methods, such as thin layer chromatography (TLC), need to be used to monitor the reaction progress in real time. When the reaction reaches the expected level, the product should be separated and purified. Column chromatography, recrystallization and other means can be used to remove impurities, improve the purity of the product, and finally obtain pure (2 - (3 - formyl - 4 - hydroxy - phenyl) - 4 - methyl - thiazole - 5 - carboxylic acid ethyl ester). This synthesis process requires rigorous operation by the experimenter, according to chemical principles and practical experience, in order to achieve efficient and high-quality synthesis.
    What are the physical properties of (2- (3-Formyl-4-hydroxy-phenyl) 4-methyl-thiazole-5-carboxylic acid ethyl ester)?
    (2 - (3 - formyl - 4 - hydroxy - phenyl) - 4 - methyl - thiazole - 5 - carboxylic acid ethyl ester) The physical properties of this product are quite important and are related to many practical applications.
    Looking at its shape, it is mostly solid at room temperature and pressure. The appearance of crystallization is often delicate and consistent, and the crystal form may vary depending on the preparation method. Its color is usually white to off-white. When it is pure, the color is uniform, like the first snow in winter, clean and flawless.
    As for the melting point, it is one of the key physical properties. It has been determined by many experiments that it is about a certain temperature range. This temperature range may fluctuate slightly due to subtle differences in experimental conditions. At this temperature, the substance gradually melts from the solid state to the liquid state, just like ice and snow in spring, quietly changing its form.
    The solubility cannot be ignored. In organic solvents, such as common ethanol and acetone, it exhibits a certain solubility. In ethanol, with moderate stirring, it can be partially dissolved to form a uniform solution, just like salt melts in water, and it melts seamlessly. In water, the solubility is very small. Due to its molecular structure characteristics, it interacts weakly with water molecules, so it is difficult to dissolve. It is like oil floating in water, and it is distinct.
    In addition, density is also one of its physical properties. Although the specific value needs to be determined by precise instruments, it can be seen that its density may be different from that of common organic solvents. This difference also affects its distribution in the mixed system, just like the weight of other objects, in their respective positions in the medium.
    Its refractive index reflects the degree of deflection of light when passing through, and is closely related to the internal structure of the material. The specific refractive index is like the unique fingerprint of the material, providing an important basis for the identification of this substance.
    These physical properties are of critical significance in many fields such as chemical synthesis and drug research and development, just like the foundation of a building, laying the foundation for its application.
    What is the market outlook for (2- (3-Formyl-4-hydroxy-phenyl) 4-methyl-thiazole-5-carboxylic acid ethyl ester)?
    (2 - (3 - formyl - 4 - hydroxy - phenyl) - 4 - methyl - thiazole - 5 - carboxylic acid ethyl ester) This product has considerable market prospects today.
    In the field of medicine, its unique chemical structure may be a key building block for the creation of new drugs. Today's pharmaceutical research and development is increasingly targeting precisely. The structural characteristics of this compound may enable it to act precisely on specific biological targets. For example, in cancer treatment research, many new targeted drugs are derived from small molecule compounds with specific structures, (2- (3-formyl-4-hydroxy-phenyl) -4-methyl-thiazole-5-carboxylic acid ethyl ester) or because the structure is compatible with specific receptors of cancer cells, it is expected to be developed into new anti-cancer drugs. Therefore, the anti-cancer drug research and development market has great potential.
    In the field of materials science, it also has potential to be tapped. There is a growing demand for functional compounds in the field of materials. The formyl group, hydroxy group and other functional groups of this compound may endow the material with unique properties. For example, in optical materials, its structural characteristics can be used to improve the fluorescence performance or light stability of the material, and it can be applied to new display materials, optical sensors, etc., to open up new fields in the material market.
    However, its market development is not smooth sailing. The complexity of the synthesis process may be a major obstacle. Complex synthesis routes not only increase production costs, but also affect production efficiency and product purity. To open up the market, it is necessary to optimize the synthesis process, reduce costs and improve efficiency. And the market competition is fierce, with many similar or similar functional compounds. To stand out, it is necessary to highlight its own advantages, such as unique performance and higher safety.
    Overall, the (2 - (3 - formyl - 4 - hydroxy - phenyl) - 4 - methyl - thiazole - 5 - ethyl carboxylate) market has a bright future, but it also faces challenges. If we can overcome the difficulties, we will be able to occupy a place in the market.