Methyl 2-(3-cyano-4-isobutoxyphenyl)-4-methyl-5-thiazolecarboxylate

"Methyl 2- (3 - cyano - 4 - isobutoxyphenyl) -4 - methyl - 5 - thiazolecarboxylate" is the English name of an organic compound. Its chemical structure is described in the ancient style of "Tiangong Kaiwu", as follows:
The main frame of this compound is the thiazole ring. At the 4th position of the thiazole ring, there is a methyl group; at the 5th position, there is a carboxylic acid methyl ester group. At the 2nd position of the thiazole ring, there is a phenyl group, and at the 3rd position of this phenyl group, there is a cyano group, and at the 4th position there is an isobutoxy group.
The isobutoxy group is one of the branches of the butyl group, which is isomeric. The cyano group is a functional group containing carbon and nitrogen three bonds. Carboxylic acid methyl ester group, formed by esterification of carboxyl and methyl groups. The thiazole ring is a five-membered aromatic ring with sulfur and nitrogen heteroatoms. The phenyl group is a six-membered aromatic hydrocarbon group.
This compound has a unique chemical structure due to the combination and connection of various groups. It is used in organic synthesis and related fields, or has specific chemical properties and uses.

Methyl-2- (3-cyano-4-isobutoxyphenyl) -4-methyl-5-thiazole carboxylic acid ester, this is an organic compound. Its use is quite extensive, in the field of medicine, often used as an intermediate for drug synthesis. Due to specific structures and properties, complex compounds with specific pharmacological activities can be constructed through a series of reactions to assist the development of new drugs.
In the field of pesticides, it also has important functions. It can be used as a key raw material for the creation of new pesticides. Through chemical modification and transformation, pesticide products with efficient pest control effect and environmental friendliness can be prepared to escort agricultural harvests.
In the field of materials science, this compound may be used to synthesize materials with special properties. With its unique chemical structure, it endows materials with good stability, optical properties, etc., expanding the application range of materials, such as in electronic devices, optical materials, etc.
In addition, in the study of organic synthetic chemistry, it is often used as a key block for chemists to explore new reaction paths and synthesis strategies, to promote the continuous development of organic synthetic chemistry, and to help discover more novel and valuable organic compounds.

To prepare methyl 2 - (3 - cyano - 4 - isobutoxy phenyl) - 4 - methyl - 5 - thiazole carboxylic acid ester, the method is as follows:
First, all raw materials must be prepared, such as aromatic compounds containing cyanyl groups, reagents with isobutoxy groups, thiazole derivatives containing methyl groups, etc., all of which must be of good texture and appropriate purity.
In a clean reactor, according to the appropriate ratio, add raw materials. First, mix the aromatic compound containing cyanyl groups with the reagent containing isobutoxy groups, and add an appropriate amount of catalyst. This catalyst should effectively promote the reaction of the two, so that the isobutoxy groups are successfully connected to the aromatic ring. The reaction temperature needs to be carefully controlled, often maintained in a moderate temperature range, or the temperature needs to be controlled by a condensing device to prevent side reactions from occurring due to excessive temperature.
After this step of reaction is completed, an intermediate product is obtained. Then, the intermediate product and the methyl-containing thiazole derivative are co-placed in the reaction system, and then accompanied by suitable reaction conditions, or the temperature is changed or other additives are added, so that the two are condensed to form methyl 2 - (3-cyano-4-isobutoxy phenyl) - 4-methyl-5-thiazole carboxylic acid ester.
The reaction is completed, and the product still contains impurities, which needs to be purified by extraction, distillation, recrystallization and other methods. During extraction, a suitable extractant is selected to separate the product from impurities; distillation can remove volatile or difficult-to-volatile impurities according to the difference in boiling point; recrystallization can obtain pure crystal products. After these steps, high-purity methyl 2 - (3-cyano-4-isobutoxy phenyl) - 4-methyl-5-thiazole carboxylate can be obtained.

Methyl 2 - (3 -cyano-4 -isobutoxy phenyl) - 4 -methyl-5 -thiazole carboxylic acid ester is a kind of organic compound. Its physicochemical properties are particularly important, related to its performance in various chemical reactions and practical applications.
Looking at its physical properties, this substance is either a solid or a viscous liquid under normal conditions, depending on the strength of the intermolecular forces. Its melting point and boiling point are fixed due to the specific arrangement of the molecular structure. Intermolecular cyano, isobutoxy, methyl and thiazole ring groups interact, resulting in complex intermolecular forces. If the molecules are arranged in a regular manner and the interaction force is strong, the melting point and boiling point will be higher; otherwise, it will be lower.
In terms of its chemical properties, cyanyl groups have high reactivity and can participate in many nucleophilic addition reactions. When encountering nucleophilic reagents, the three bonds in the cyanyl group can be opened and new functional groups can be introduced. The oxygen atom in the isobutoxyl group has a solitary pair of electrons, which can be used as a nucleophilic check point or participate in coordination in some reactions. The thiazole ring also has unique chemical activity, because it is a heterocyclic ring containing nitrogen and sulfur, and the distribution of electron clouds is specific, which can participate in aromatic electrophilic substitution reactions. Although the 4-methyl group is relatively stable, under certain conditions, the substitution of methyl groups may also occur. The carboxylic acid ester groups of this compound can be hydrolyzed to form corresponding carboxylic acids and alcohols. Under acidic or alkaline environments, the hydrolysis rate varies. Under alkaline conditions, hydrolysis is usually more rapid, because bases can catalyze the cleavage of ester bonds.
In summary, the physicochemical properties of methyl 2 - (3-cyano-4-isobutoxy phenyl) - 4-methyl-5-thiazole carboxylic acid esters depend on the synergistic action of various groups in their molecules, indicating that these properties are of great significance in organic synthesis, drug development and other fields.

The market price of methyl 2 - (3-cyano-4-isobutoxyphenyl) - 4-methyl-5-thiazole carboxylic acid ester is difficult to determine. This compound may be involved in the field of fine chemical and pharmaceutical synthesis, and its price often varies depending on the purity of the quality, the amount of supply, and the urgency of demand.
Looking at the past, the price of such fine chemicals often depends on various factors. If the quality is pure and the supply is sufficient and the demand is small, the price may decrease; conversely, if the quality is high and the supply is small and the demand is strong, the price must rise.
Those who are looking for this product in the city are mostly the genus of chemical factories and pharmaceutical companies. However, the market situation changes, and one end cannot be stuck.
Or there are sellers of this product, because of its quantity and quality, the price is different. Less is expensive, more or negotiable. And the buyer's ability to negotiate the price also affects the price.
Although there is no exact number to report, if you want to know the price, you can consult the brokers in the chemical raw material market, or on the online commerce platform, check the same product, compare its price, measure its extent, and get its approximate price range.