2-(3-cyano-4-isobutoxyphenyl)-4-methylthiazole-5-carboxylic acid ethyl ester

2-%283-%E6%B0%B0%E5%9F%BA-4-%E5%BC%82%E4%B8%81%E6%B0%A7%E5%9F%BA%E8%8B%AF%E5%9F%BA%29-4-%E7%94%B2%E5%9F%BA%E5%99%BB%E5%94%91-5-%E7%BE%A7%E9%85%B8%E4%B9%99%E9%85%AF%E7%9A%84%E4%B8%BB%E8%A6%81%E7%94%A8%E9%80%94%E6%98%AF%E4%BB%80%E4%B9%88%3F%2C this is a question about the related uses of chemical substances. 2 - (3 - benzyl - 4 - isobutoxyphenyl) - 4 - methylimidazole - 5 - ethyl pyridinecarboxylate, this compound has important uses in many fields.
In the field of pharmaceutical chemistry, it is often used as a key intermediate. Because of its unique chemical structure, it can be modified by specific chemical reactions to synthesize drug molecules with specific pharmacological activities. For example, for some disease targets, after chemical modification, new therapeutic drugs may be developed, which may have significant effects on specific diseases such as cardiovascular diseases and neurological diseases.
In the field of materials science, it may be used to prepare functional materials. The properties given by the molecular structure may affect the physical and chemical properties of the material. If this compound is added to polymer materials, it may change the thermal stability and mechanical properties of the material, making it suitable for aerospace, electronic devices and other fields that require strict material properties.
In addition, in the field of organic synthetic chemistry, it can act as a reaction substrate or catalyst. Using its special structure and reactivity, it participates in the synthesis of complex organic compounds, promotes the development of organic synthetic chemistry, and provides an important foundation for the creation of new organic compounds.

To prepare 2 - (3 - amino - 4 - isohydroxybenzyl) - 4 - methylimidazole - 5 - formamide, the method is as follows:
First take the appropriate raw materials, and use the chemical method to gradually construct the molecular structure. The amino group can be introduced in a specific reaction first, and at a suitable reaction check point, after fine regulation, the construction of the 3 - amino group can be achieved. This process requires attention to the reaction conditions, such as temperature, pH, etc., which will affect the direction of the reaction and the purity of the product.
Then construct the 4 - isohydroxybenzyl moiety. Or select an appropriate benzyl derivative and combine it with the amino-containing structure through a series of nucleophilic substitution, redox and other reactions, and precisely control the isomeric form of the hydroxyl group to obtain the correct connection of 4-isohydroxybenzyl.
As for the formation of 4-methylimidazole, methyl can be introduced at a specific position through the synthesis of imidazole compounds through cyclization reaction. This step also requires careful selection of reaction reagents and conditions to ensure the smooth cyclization and the accuracy of methyl introduction.
Finally, the 5-formamide moiety is constructed, and the corresponding acylation reaction is often used to interact with the compound with the above structure with a suitable acylation reagent, so that the formamide group is successfully introduced at the specified position.
After each step of the reaction, it needs to be separated and purified, such as column chromatography, recrystallization, etc., to remove impurities and improve the purity of the product. And the connection between each step of the reaction also needs to be carefully planned, considering the stability and reactivity of the intermediate, so that the whole synthesis path is efficient and feasible. Thus, the synthesis of 2 - (3 - amino - 4 - isohydroxybenzyl) - 4 - methylimidazole - 5 - formamide is expected to be achieved by careful operation in multiple steps.

2-%283-%E6%B0%B0%E5%9F%BA-4-%E5%BC%82%E4%B8%81%E6%B0%A7%E5%9F%BA%E8%8B%AF%E5%9F%BA%29-4-%E7%94%B2%E5%9F%BA%E5%99%BB%E5%94%91-5-%E7%BE%A7%E9%85%B8%E4%B9%99%E9%85%AF%E7%9A%84%E5%85%B7%E4%BD%93%E5%8C%96%E5%AD%A6%E5%BC%8F%E4%B8%BA $C_ {13} H_ {18} O_4 $, this compound has the following physical and chemical properties:
In terms of appearance properties, it is usually a colorless to light yellow liquid, has a special odor, and exists stably at room temperature and pressure. Its boiling point is about a certain temperature range, which varies slightly due to specific environmental factors, which makes it undergo a phase transition from liquid to gaseous under specific temperature conditions. The boiling point characteristic is closely related to the intermolecular force.
In terms of solubility, it is slightly soluble in water, but miscible in any ratio with most organic solvents such as ethanol and ether. This is because its molecular structure has both relatively polar and non-polar parts. According to the principle of similarity and miscibility, it is difficult to dissolve with water with strong polarity in large quantities, but it can mix well with organic solvents.
In terms of chemical stability, it is generally stable, but when certain conditions such as high temperature, strong acid, strong base or strong oxidant exist, chemical reactions will occur. For example, under acidic conditions, its ester groups may undergo hydrolysis reactions to generate corresponding acids and alcohols; under the action of strong oxidants, some groups in the molecule may be oxidized, resulting in changes in its chemical structure and properties.
In terms of optical properties, the compound may have a certain refractive index. As one of the characteristic constants of the substance, refractive index is of great significance for the identification and analysis of the compound. By measuring its refractive index, it can assist in judging its purity and concentration.
In addition, its density is also a specific value. This physical property plays an important role in practical application scenarios such as separation and mixing of the substance. Substances of different densities will exhibit different distribution states due to density differences in the mixed system. This can be used for related processing and analysis.

I look at your words and ask about the price range of 2 - (3 - amino - 4 - isohydroxybenzyl) - 4 - methylimidazole - 5 - ethyl carboxylate in the market. However, this compound is quite professional, and its price varies depending on factors such as quality, purity, and market supply and demand.
In the ordinary chemical reagent market, if it is laboratory grade, the purity is about 95%, and the price per gram may be around tens of yuan to hundreds of yuan. This is because the preparation process may require specific processes and raw materials, so the cost varies.
If it is industrial grade, and the purity requirements are slightly lower, due to mass production, the cost of scale effect is reduced, and the price per ton may be in the tens of thousands. However, if the purity requirements are extremely high, reaching more than 99%, and used in high-end pharmaceutical research and development and other fields, the price will increase, or more than 100 yuan per gram, or even higher.
Furthermore, the pricing of different suppliers is also different. Well-known large manufacturers may have high prices due to quality control and brand effect; while emerging manufacturers may have discounts for expanding the market. And the market fluctuates frequently, and changes in raw material prices and policies and regulations can affect their prices. Therefore, it is difficult to accurately describe its price range, but only according to common circumstances.

2-%283-%E6%B0%B0%E5%9F%BA-4-%E5%BC%82%E4%B8%81%E6%B0%A7%E5%9F%BA%E8%8B%AF%E5%9F%BA%29-4-%E7%94%B2%E5%9F%BA%E5%99%BB%E5%94%91-5-%E7%BE%A7%E9%85%B8%E4%B9%99%E9%85%AF%E7%9A%84%E5%BA%94%E7%94%A8%E9%A2%86%E5%9F%9F%E6%9C%89%E5%A4%9A%E7%A7%8D%EF%BC%8C%E5%88%97%E4%B8%8B%E4%B8%8B%E6%96%87%E6%89%80%E8%BF%B0%EF%BC%9A
First, in the field of medicinal chemistry, this compound is often a key intermediate in drug synthesis. Because of its active groups such as amine and hydroxyl, it can be precisely combined with other molecules through various chemical reactions to construct complex structures with specific pharmacological activities. For example, it is used to prepare drugs for the treatment of cardiovascular diseases. Its unique chemical structure can precisely interact with specific receptors in the cardiovascular system, regulate physiological functions, and achieve therapeutic effects.
Second, in the field of materials science, 2- (3-amino-4-isobutoxyphenyl) -4-methylquinazoline-5-carboxylate ethyl ester can exhibit special properties. Due to its molecular structure properties, it can be used to prepare functional polymer materials. By chemical modification, it is introduced into the polymer skeleton to give the material special electrical, optical or mechanical properties, such as the preparation of materials with special electrical conductivity, which is used in the field of electronic devices.
Third, in the field of organic synthetic chemistry, it is an extremely important synthetic building block. Its rich reaction check point can be used to construct various organic compounds through halogenation, alkylation, acylation and other reactions. Chemists can use this to build a library of organic molecules with diverse structures, providing rich raw materials for the discovery and synthesis of new compounds, and promoting the development of organic synthetic chemistry.
Fourth, in agricultural chemistry, it can be developed as a new type of pesticide or plant growth regulator. With its chemical structure and biological activity, it can affect plant physiological processes, such as regulating plant growth, enhancing plant resistance, or inhibiting and killing specific pests and pathogens, thus contributing to the green and sustainable development of agriculture.