Ethyl 2-(3-bromo-4-isobutoxyphenyl)-4-methyl-5-thiazolecarboxylate

Alas! This "Ethyl 2- (3 - bromo - 4 - isobutoxyphenyl) -4 - methyl - 5 - thiazolecarboxylate" has the name of the compound. To know its chemical properties, it remains to be analyzed.
In its name, "Ethyl" means ethyl, which is often referred to as "ethyl", and its - C ² H, which is at the end of this compound. "2- (3 - bromo - 4 - isobutoxyphenyl) " part, "phenyl" is phenyl, which is an aromatic group composed of six carbon atoms, and its - C H. " For "3-bromo-4-isobutoxy", it is said that the third position of the phenyl group has a bromine atom (Br) substitution, and the fourth position has a butoxy (-O-CH-CH (CH) ³) substitution. In the butoxy group, the oxygen atom is a phenyl phase, and its part is butyl.
"4-methyl-5-thiazolecarboxylate" is one, "thiazole" is a thiazole, a sulfur-containing, nitrogen-containing quintile, its basic value. " 4-Methyl "indicates that the fourth position of thiazolyl has a methyl (CH 🥰) substitution," 5-carboxylate "refers to the fifth position of thiazolyl has a carboxylic acid ester group, and the" Ethyl "of the carboxylic acid ester group has a carboxylic acid ester group, which forms a carboxylic acid ethyl ester, that is, -COO-C-H.
As described above, the chemical compound of this compound has a methyl group containing a specific substituent, a methyl group at the fourth position of thiazolyl, an ethyl carboxylic acid ester at the fifth position, and a 3-bromo-4-butoxy-substituted phenyl group at the second position of thiazolyl. This collection is based on a wide range of fundamental principles, showcasing the sophistication of chemical compounds.

Ethyl 2- (3 - bromo - 4 - isobutoxyphenyl) -4 - methyl - 5 - thiazolecarboxylate is an organic compound. Its main use is more common in the fields of medicinal chemistry and organic synthesis.
In medicinal chemistry, such compounds containing thiazole rings often have potential biological activities. Many studies have shown that thiazole structures can interact with specific targets in organisms. It can either participate in the inhibition process of enzymes to regulate biochemical reactions in vivo; or bind to receptors to affect cell signaling pathways. Therefore, ethyl 2- (3-bromo-4-isobutoxyphenyl) -4-methyl-5-thiazolecarboxylate is very likely to be used as a lead compound for medical researchers to explore in depth, and then develop new therapeutic drugs for treating diseases such as inflammation and tumors.
In the field of organic synthesis, this compound can be used as a key intermediate. Because its molecular structure contains bromine atoms, isobutoxy groups and thiazolecarboxylate and other active groups. Bromine atoms can participate in halogenation reactions, coupling reactions, etc., and can introduce other specific functional groups or build carbon-carbon bonds, thereby expanding the complexity of molecules; isobutoxy groups can endow molecules with specific spatial structures and physical properties; thiazole carboxylate ethyl ester can also be modified by various reactions, such as hydrolysis, esterification, amidation, etc., to synthesize organic compounds with more diverse structures to meet the needs of different fields for special structural organic molecules.

The preparation of ethyl 2 - (3 - bromo - 4 - isobutoxy phenyl) -4 - methyl - 5 - thiazole carboxylic acid ester often involves several steps. The first step may be to prepare an aromatic compound containing isobutoxy. Take appropriate phenols, such as 4 - hydroxybenzene derivatives, and isobutyl halides, in the presence of bases such as potassium carbonate, in suitable solvents such as acetone, heat and stir, through nucleophilic substitution reaction, 4 - isobutoxy benzene derivatives can be obtained. < Br >
Next, the resulting 4-isobutoxybenzene derivative is combined with a bromine-containing reagent, such as N-bromosuccinimide (NBS), in the presence of an initiator such as benzoyl peroxide, in a suitable solvent such as carbon tetrachloride, heated and refluxed, and a bromination reaction is carried out to introduce bromine atoms at specific positions in the benzene ring to obtain 3-bromo-4-isobutoxybenzene derivatives.
Furthermore, a thiazole ring is prepared. Using ethyl acetoacetate as a starting material, it is heated and refluxed with thiourea in ethanol to form an intermediate of ethyl 4-methyl-5-thiazole carboxylate. Subsequently, the 3-bromo-4-isobutoxybenzene derivative and ethyl 4-methyl-5-thiazole carboxylate intermediates are reacted at low temperature in an anhydrous tetrahydrofuran solvent under the action of a strong base such as potassium tert-butyl alcohol. After nucleophilic substitution, the aryl group is connected to the thiazole ring to obtain ethyl 2- (3-bromo-4-isobutoxyphenyl) -4-methyl-5-thiazole carboxylate. After each step of the reaction, the product needs to be purified by extraction, column chromatography or recrystallization to achieve high purity.

Ethyl 2- (3 - bromo - 4 - isobutoxyphenyl) -4 - methyl - 5 - thiazolecarboxylate is an organic compound. Its physical properties are as follows:
This substance is usually solid and relatively stable at room temperature and pressure. Looking at its properties, it may be a white to light yellow crystalline powder, because this kind of compound containing heterocyclic and aromatic ring structures mostly shows this appearance.
Its melting point is quite critical, but the specific value varies due to factors such as preparation purity, and is roughly in a specific temperature range. This melting point characteristic can be used as an important basis for the identification and purification of this compound.
In terms of solubility, it may have a certain solubility in organic solvents such as dichloromethane, chloroform, acetone, etc. Due to the polarity and molecular structure of these organic solvents, it can form intermolecular forces with the compound to promote dissolution. However, the solubility in water is low, because the molecular structure of hydrophobic aromatic rings, heterocycles and alkyl groups accounts for a large proportion, and the interaction with water is weak.
In addition, the density of the compound is also one of its physical properties. Although the exact value needs to be accurately determined, its density is related to the degree of molecular accumulation and relative molecular mass. When it comes to the separation and extraction of the compound, the density factor also needs to be considered.
The physical properties of this substance are of great significance in the fields of organic synthesis and drug development. Knowing its melting point, solubility and other properties is convenient for separation, purification and identification in experimental operations, which lays a foundation for further research on its chemical properties and biological activities.

Ethyl 2- (3 - bromo - 4 - isobutoxyphenyl) -4 - methyl - 5 - thiazolecarboxylate is an organic compound. Its market prospects are influenced by many factors.
From the perspective of the pharmaceutical field, this compound may have potential medicinal value. Today, there is a strong demand for new, efficient and low-toxic compounds in pharmaceutical research and development. If this compound is proven to have specific biological activities, such as anti-tumor, anti-bacterial or anti-inflammatory effects, it will find a broad space in the drug development market. For example, many new drugs are derived from in-depth research and optimization of organic compounds with unique structures.
In the field of materials science, organic compounds are often used to prepare functional materials. If Ethyl 2- (3 - bromo - 4 - isobutoxyphenyl) -4 - methyl - 5 - thiazolecarboxylate has special optical, electrical or thermal properties, it can be applied to fields such as optoelectronic materials and sensor materials. With the rapid development of science and technology, the demand for new functional materials is also increasing, which provides opportunities for this compound.
However, its market prospects also face challenges. First, the process of synthesizing the compound may be complex and expensive. If the synthesis route cannot be optimized to reduce costs, it will be difficult to gain an advantage in the market competition. Secondly, research on its performance and application is still lacking, requiring a lot of time and resources to explore in depth, which is also a hindrance to marketing activities.
Overall, Ethyl 2- (3 - bromo - 4 - isobutoxyphenyl) -4 - methyl - 5 - thiazolecarboxylate has addressable market opportunities, especially in the fields of medicine and materials science, but needs to overcome the problems of synthesis cost and insufficient research in order to emerge in the market.