Ethyl 2-amino-4-phenylthiazole-5-carboxylate

Ethyl ethyl ethyl-2-amino-4-phenylthiazole-5-carboxylate, an organic compound, has important uses in many fields.
First, in the field of medicinal chemistry, it can be used as a key intermediate. Due to the unique biological activity of the thiazole ring structure, it can interact with specific targets in organisms. For example, by modifying and modifying the structure of the compound, antibacterial drugs can be developed. Some thiazole antibacterial drugs can effectively inhibit bacterial cell wall synthesis or interfere with bacterial metabolic processes, thereby achieving antibacterial effect. In the development of anti-tumor drugs, it may also have potential value. Studies have shown that some thiazole-containing compounds can affect the proliferation and apoptosis-related signaling pathways of tumor cells, providing a direction for the development of new anti-tumor drugs.
Second, in the field of materials science, it can be used to prepare functional materials. Because the molecular structure contains specific functional groups, it can endow the material with special properties. For example, in optical materials, the compound may exhibit unique photophysical properties due to structural conjugation properties, such as fluorescence emission, and then be used to prepare luminescent materials. It is applied to devices such as organic Light Emitting Diode (OLED) to improve its luminous efficiency and stability.
Third, in the field of organic synthetic chemistry, as an important synthetic building block. With its active functional groups, more complex organic molecular structures can be constructed through various organic reactions, such as nucleophilic substitution, cyclization, etc. Chemists can use this to expand the structural diversity of compounds, synthesize organic compounds with novel structures and properties, and promote the development of organic synthesis chemistry.
In summary, ethyl ethyl ethyl ethyl ethyl ethyl carboxylate with 2-amino-4-phenylthiazole-5-carboxylate has important uses in many fields such as drug development, material preparation, and organic synthesis, providing a key material basis for related scientific research and industrial production.

The synthesis method of Ethyl 2-amino-4-phenylthiazole-5-carboxylate (2-amino-4-phenylthiazole-5-carboxylate), although the ancient books do not directly describe the method of this specific substance, it can be deduced from the ancient methods of related chemical synthesis.
In the past, various heterocyclic compounds were synthesized, often using raw materials containing sulfur, nitrogen and other elements, through condensation and cyclization. When synthesizing the 2-amino-4-phenylthiazole-5-carboxylic acid ethyl ester, the halogenate containing benzene ring and the nucleophilic reagent containing sulfur can be taken first, and the sulfur atom can be connected to the benzene ring by the method of nucleophilic substitution to obtain the thiobenzene derivative.
Then, the nitrogen-containing amine compound and the obtained thiobenzene derivative are condensed under a suitable acid-base environment and temperature, so that the nitrogen atom is also incorporated into its structure, and the prototype of the thiazole ring is preliminarily constructed.
Then, with the above preliminary products, ethyl carboxylate groups are introduced through esterification and other reactions to obtain Ethyl 2-amino-4-phenylthiazole-5-carboxylate.
Or there are other methods, such as substitution reactions with parent compounds containing thiazole rings, and the gradual introduction of amino groups, phenyl groups and ethyl carboxylate groups. However, no matter what method, it is necessary to carefully observe the reaction conditions, such as temperature, pressure, and catalyst selection, in order to promote the smooth reaction and increase the purity and yield of the product.

Ethyl-2-amino-4-phenylthiazole-5-carboxylic acid ester is an organic compound. Its physical properties are quite important, and it is related to its performance in various chemical processes and practical applications.
First of all, its appearance is usually white to light yellow crystalline powder, which is convenient for preliminary identification and distinction. Looking at it, its texture is fine, and there is no obvious color deviation. This appearance characteristic also reflects one of its purity spots.
As for the melting point, it has been determined by many experiments to be around [specific value] ℃. The stability and exact value of the melting point are crucial for identifying the compound and controlling its quality. If the melting point deviates from the normal range, it may suggest that its purity is poor, or impurities are mixed, which affects its chemical activity and reaction effect.
In terms of solubility, it has a certain solubility in common organic solvents such as ethanol and acetone. Ethanol can form a uniform solution with it, which facilitates its application as a reactant or intermediate in organic synthesis. However, in water, its solubility is very small. Due to the large proportion of hydrophobic groups in the molecular structure and the weak force between water molecules.
Density is also one of the important physical properties, about [specific value] g/cm ³. The determination of density is of great significance for the separation, purification, distribution and behavior of substances in specific systems. In chemical production and laboratory operations, appropriate separation methods and reaction vessels can be selected according to their density characteristics.
In addition, the compound is quite stable, and can be stored for a long time without significant chemical changes at room temperature and pressure. This stability is derived from the molecular structure, the strength of chemical bonds and the rationality of spatial arrangement, making it less susceptible to external factors such as light and air oxidation.
The physical properties of ethyl-2-amino-4-phenylthiazole-5-carboxylic acid esters lay the foundation for their application in organic synthesis, medicinal chemistry and other fields. Researchers can design reasonable reaction paths and application plans according to their characteristics.

Ethyl 2 - amino - 4 - phenylthiazole - 5 - carboxylate is an organic compound with unique chemical properties. It contains amino, phenyl, thiazole ring and carboxylate ethyl group, and the interaction of each group endows it with various characteristics.
The amino group of this compound is basic and can react with acids to form salts. Because its nitrogen atom has lone pairs of electrons, it can provide electron pairs to bind to protons. For example, when it encounters hydrochloric acid, the amino nitrogen atom will bind to hydrogen ions to form corresponding salts. This property can be used in organic synthesis to introduce specific functional groups or change the solubility of compounds.
The presence of phenyl groups, because the phenyl ring has a conjugated system, adds stability to the compound and gives it a certain hydrophobicity. The benzene ring can undergo electrophilic substitution reactions, such as halogenation, nitrification, sulfonation, etc. If suitable reagents and conditions are available, bromine can replace the hydrogen atoms on the benzene ring to form bromine-containing substituents, which can expand the reactivity and application scope of the compound.
Thiazole ring, as the core structure of the compound, has aromatic properties, which affect the overall electron cloud distribution and stability of the molecule. The nitrogen and sulfur atoms on the thiazole ring have lone pair electrons, which can participate in coordination and form complexes with metal ions, which may have potential applications in the fields of materials science and catalysis.
Carboxylic acid ethyl ester group is hydrolytic, and can undergo hydrolysis reaction under acid or base catalysis. In acidic conditions, hydrolysis generates carboxylic acids and ethanol; in alkaline environments, carboxylate and ethanol are formed. This hydrolytic property can be used in organic synthesis to prepare corresponding carboxylic acids or perform functional group transformation.
Ethyl 2-amino-4-phenylthiazole-5-carboxylate's various chemical properties make it show potential application value in many fields such as medicinal chemistry, materials science, organic synthesis, etc. It can be used as a key intermediate for the synthesis of more complex and functional organic compounds.

I don't know the price of "Ethyl 2 - amino - 4 - phenylthiazole - 5 - carboxylate" in the market. The price of this unusually easy-to-obtain thing may change due to many reasons. If it is difficult to prepare, the price of the raw materials used, and the number of applicants can affect its price.
If its preparation requires rare raw materials and the process is complicated, the price will be high. And if there are many applicants in the market, and there are few producers, the price will also be high. On the contrary, if the raw materials are easy to produce, it is not difficult to prepare, and there are few applicants, the price may be cheap.
If you want to know its exact price, you should consult chemical material suppliers and chemical reagent suppliers. You can visit the city, check the Internet, or consult people in the industry, who may be able to tell the current price. Unfortunately, I have not personally involved the market, nor have I investigated its situation in detail, so it is difficult to determine the price.