ethyl 2-[3-formyl-4-(2-methylpropoxy)phenyl]-4-methyl-1,3-thiazole-5-carboxylate

Alas! For ethyl + 2 - [3 - formyl - 4 - (2 - methylpropoxy) phenyl] - 4 - methyl - 1,3 - thiazole - 5 - carboxylate, analyze the group contained in its name.
"ethyl", is ethyl, containing an alkyl group of two carbons, which is -CH ² CH 😉.
"2 - [3 - formyl - 4 - (2 - methylpropoxy) phenyl]", where "phenyl" is phenyl, and the hexavalent aromatic group C H; "3 - formyl" means that the third position of benzene has formyl-CHO; "4 - (2 - methylpropoxy) " The fourth position of epiphenyl has 2 - methylpropoxy, and the fourth position of 2 - methylpropoxy has 2 - methylpropoxy (CH 🥰) -2 CH2-, the oxygen atomic phase is formed into -O- (CH 🥰) ▽ CH2-, which is connected to benzene.
In "4-methyl-1,3-thiazole-5-carboxylate", "1,3-thiazole" is thiazole, which contains the five elements of nitrogen and sulfur; "4-methyl" refers to thiazole with methyl-CH at the 4th position; "5-carboxylate" indicates that thiazole has a carboxylate group at the 5th position, and this ethyl phase forms -COOCH ² CH. On
, the chemical composition of this compound consists of ethyl group in the carboxylic acid ester group at the 5 position of thiazole, methyl group at the 4 position of thiazole, and phenyl group containing formyl group and 2-methylpropoxy group at the 2 position of thiazole. In this way, its shape is clear.

ethyl+2-%5B3-formyl-4-%282-methylpropoxy%29phenyl%5D-4-methyl-1%2C3-thiazole-5-carboxylate is an organic compound with the Chinese name 2- [3-formyl-4- (2-methylpropoxy) phenyl] -4-methyl-1,3-thiazole-5-carboxylic acid ethyl ester. This compound has important uses in many fields.
In the field of medicinal chemistry, it may be used as a lead compound. Its structure contains specific functional groups such as thiazole ring, phenyl ring and ester group, which endow it with potential biological activity. Researchers can explore new drugs with better pharmacological activity and pharmacokinetic properties by modifying and optimizing its structure. For example, it may be able to show inhibitory or regulatory effects on specific disease-related targets, such as anti-tumor, antibacterial, anti-inflammatory, etc., providing a key starting point for the development of new drugs.
In the field of materials science, the compound also has potential applications. Due to its unique molecular structure, it may be used to prepare functional materials. For example, by combining with other materials or self-assembling, materials with special optical, electrical or thermal properties can be prepared. For example, in organic optoelectronic materials, it may be able to adjust the charge transport and luminescence properties of materials, laying the foundation for the development of new optoelectronic materials.
In the field of organic synthetic chemistry, it can be used as an important intermediate. With its structural functional group reactivity, it can construct more complex organic molecular structures through various organic reactions, such as nucleophilic substitution, addition, redox, etc. Synthetic chemists can use it to synthesize a series of organic compounds with special structures and functions to expand the research scope and compound library of organic synthetic chemistry.

To prepare ethyl 2- [3-formyl-4- (2-methylpropoxy) phenyl] -4-methyl-1, 3-thiazole-5-carboxylate, you can follow the following ancient method.
First take the appropriate 4- (2-methylpropoxy) -3 -nitrotoluene as the starting material. A suitable reducing agent, such as the combination of iron powder and hydrochloric acid, undergoes a reduction reaction to convert the nitro group into an amino group to obtain 4- (2-methylpoproxy) -3 -aminotoluene.
Then, 4- (2 - methylpropoxy) - 3 - aminotoluene is combined with potassium thiocyanate and benzyl bromide to form 2 - (4 - (2 - methylpropoxy) phenyl) -4 - methyl - 1,3 - thiazole - 5 - carboxylic acid ethyl ester through condensation reaction. This reaction requires appropriate organic solvents such as ethanol, controlled temperature and reaction time to obtain higher yields.
Then 2 - (4 - (2 - methylpropoxy) phenyl) -4 - methyl - 1,3 - thiazole - 5 - carboxylic acid ethyl ester is formylated. Vilsmeier - Haack reagent can be used, that is, a mixture of N, N - dimethylformamide and phosphorus oxychloride. In this reaction, the substrate is dissolved in an appropriate amount of N, N - dimethylformamide, slowly added at low temperature phosphorus oxychloride, then heated to an appropriate temperature and stirred for a certain time, so that the reaction is complete, can be in the 3 - position of the benzene ring is introduced into the formyl group, the final ethyl 2- [3 - formyl - 4 - (2 - methylpropoxy) phenyl] -4 - methyl - 1,3 - thiazole - 5 - carboxylate. < Br >
The reaction process requires attention to the reaction conditions of each step, such as temperature, reactant ratio, and reaction time, and the products of each step need to be purified, such as recrystallization, column chromatography, etc., to ensure the purity of the product.

Ethyl + 2 - [3 - formyl - 4 - (2 - methylpropoxy) phenyl] - 4 - methyl - 1,3 - thiazole - 5 - carboxylate, Chinese name or 2 - [3 - formyl - 4 - (2 - methylpropoxy) phenyl] - 4 - methyl - 1,3 - thiazole - 5 - carboxylate ethyl ester. The physical properties of this substance, let me tell them one by one.
Looking at its state, it may be solid under normal circumstances, mostly crystalline, crystalline or regular, with a certain luster. This is a common form of many such organic compounds, due to the orderly arrangement of molecular interactions.
As for the color, it is most likely to be nearly colorless or light, because there are not too many groups in the molecular structure that can cause strong color. Organic compounds without the huge chromophore of the conjugated system are mostly of this color.
When it comes to the melting point, the melting point should have a specific value. Due to the existence of various interaction forces in the molecule, such as van der Waals force, hydrogen bonds, etc., the molecules are closely arranged, and specific energy is required to melt them, so the melting point is relatively fixed. The boiling point is also related to it. Under a specific pressure and reaching a certain temperature, the molecule obtains enough energy to break free from the liquid phase and transform into the gas phase. < Br >
In terms of solubility, it shows different performances in organic solvents. Because the compound has both lipophilicity and a certain polarity. In polar organic solvents such as ethanol and acetone, it may have a certain solubility, because the polar part of the molecule can form interactions with polar solvent molecules, such as hydrogen bonds, dipole-dipole interactions. In non-polar organic solvents such as n-hexane, the solubility is low, because the non-polar part is not enough to be well miscible with non-polar solvents.
Density is also one of its physical properties, and the relative density may be similar to that of common organic solvents. The specific value depends on the molecular weight and the degree of molecular packing compactness. The molecular structure of this compound determines its density or is in a specific range, which provides a reference for practical applications such as separation and mixing.

The market prospect of ethyl + 2 - [3 - formyl - 4 - (2 - methylpropoxy) phenyl] - 4 - methyl - 1,3 - thiazole - 5 - carboxylate is related to many aspects.
From the perspective of the pharmaceutical field, such compounds may have unique biological activities. In their structures, specific functional groups, such as thiazole rings and substituents on benzene rings, may be able to bind to specific targets in organisms. For example, the presence of 3-formyl and 4- (2-methylpropoxy) may affect its interaction with protein receptors, and then show potential in the treatment of diseases. To introduce it into the pharmaceutical market, it must go through rigorous pharmacological research, clinical trials and other stages. This process is time-consuming and expensive, and many difficulties need to be overcome, such as drug safety and effectiveness verification.
In the field of materials science, the properties of this compound may make it a potential raw material for new materials. The particularity of its structure may endow the material with unique physical and chemical properties, such as optical and electrical properties. If it can be effectively utilized, it may give birth to new material application fields. However, in order to achieve this goal, it is necessary to deeply explore its compatibility with other materials, processing properties, etc., which is not an easy task.
Furthermore, from the perspective of market competition, although it has a unique structure and potential application value, the field of chemical synthesis is developing rapidly today, and compounds of the same kind or similar functions are emerging in an endless stream. In order to gain a place in this market, it is necessary to continuously improve research and development and production processes to reduce costs and improve quality in order to attract customers and expand market share.
In summary, ethyl + 2 - [3 - formyl - 4 - (2 - methylpropoxy) phenyl] - 4 - methyl - 1,3 - thiazole - 5 - carboxylate is promising, but it also faces many challenges. Only by prudent response and unremitting exploration can we have the opportunity to emerge in the market.