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4 - thiazolecarboxylic acid, 5 - bromo - 2 - phenyl -, ethyl ester chemical structure?
5-Bromo-2-phenyl-4-thiazole ethyl carboxylate, according to its name, this is one of the organic compounds. Its structure is based on the thiazole ring, which is like a cornerstone to lay its fundamental structure. At the 4th position of the thiazole ring, there is an ethyl carboxylate group, which gives the molecule a specific chemical activity and reaction tendency. At the 5th position of the thiazole ring, the bromine atom occupies a place, and the characteristics of bromine are active, which has a great influence on the physical and chemical properties of the molecule, often changing the polarity and reactivity of the compound. Furthermore, the two positions are connected to phenyl groups, and phenyl groups have a conjugated system, which makes the electron cloud distribution of the whole molecule more complex, and also affects its stability and spectral properties. The structure and interaction of various parts of this compound together shape its unique chemical behavior and physical properties, and may have its unique applications and values in many fields such as organic synthesis and drug development.
What are the main uses of 4 - thiazolecarboxylic acid, 5 - bromo - 2 - phenyl -, ethyl ester?
Ethyl 5-bromo-2-phenyl-4-thiazole carboxylate has a wide range of uses. In the field of medicine, it is a key organic synthesis intermediate and can be used to prepare a variety of drugs. With its unique chemical structure, it can be combined with other compounds through specific chemical reactions to build complex molecular structures with specific pharmacological activities. For example, in the development of some antibacterial and anti-inflammatory drugs, it is often used as a starting material to obtain new drugs that meet clinical needs through chemical modification and modification.
In the field of materials science, it also plays an important role. Due to its structure, the material has unique physical and chemical properties. For example, in the field of optical materials, adding this substance may optimize the optical properties of the material, such as luminous efficiency, light stability, etc., so that the material can show better application results in photoelectric display, photoelectric devices, etc.
In the field of pesticide research and development, this compound also has great potential. It can be used as a lead compound to create new and efficient pesticides through structure optimization and activity screening. Using its mechanism of action against specific biological targets, pesticide products with high-efficiency control effects against crop pests and pathogens can be developed, which can help agricultural safe production and improve crop yield and quality.
In conclusion, ethyl 5-bromo-2-phenyl-4-thiazole carboxylate has important application value in many fields such as medicine, materials science, and pesticide research and development due to its unique chemical structure, providing key support for technological innovation and development in various fields.
What is the preparation method of 4 - thiazolecarboxylic acid, 5 - bromo - 2 - phenyl -, ethyl ester?
The preparation method of ethyl 5-bromo-2-phenyl-4-thiazolecarboxylate is an important topic in the field of organic synthesis. The preparation is often followed by the following steps.
The starting material is often selected from compounds with specific functional groups. For example, the structure of the thiazole ring is constructed by nucleophilic substitution or cyclization with suitable halogenated aromatics and sulfur-containing and nitrogen-containing heterocyclic precursors under suitable reaction conditions.
During the reaction, halogen atoms of halogenated aromatics, such as bromine atoms, often undergo nucleophilic substitution with sulfur-containing and nitrogen-containing nucleophiles. The key to this step is to select the appropriate base to promote the activity of nucleophiles. Commonly used bases are inorganic bases such as potassium carbonate and sodium carbonate, or organic bases such as triethylamine. Reaction solvents are also quite important. Common organic solvents, such as N, N-dimethylformamide (DMF), dimethyl sulfoxide (DMSO), etc., are often selected because of their good solubility and stability.
After the thiazole ring is constructed, it needs to be carboxylate esterified to obtain the target product 5-bromo-2-phenyl-4-thiazole ethyl carboxylate. This esterification step is generally carried out with ethanol and corresponding carboxylic acids in the presence of a catalyst. The commonly used catalysts are concentrated sulfuric acid or p-toluenesulfonic acid. During the reaction, attention should be paid to controlling the temperature and reaction time to improve the yield and selectivity of the reaction.
In addition, attention should be paid to the separation and purification operations during the reaction process. Extraction, column chromatography and other means can be used to remove by-products and unreacted raw materials to obtain high-purity 5-bromo-2-phenyl-4-thiazolecarboxylate ethyl ester. The reaction conditions and operation details of each step need to be carefully controlled to achieve the ideal preparation effect.
4 - thiazolecarboxylic acid, 5 - bromo - 2 - phenyl -, ethyl ester what are the physical and chemical properties?
Ethyl 5-bromo-2-phenyl-4-thiazolecarboxylate is an organic compound that has attracted much attention in the fields of chemical synthesis. Its physical and chemical properties are as follows:
- ** Appearance properties **: Usually white to light yellow crystalline powder, this property is easy to visually identify and distinguish. In laboratory observation or industrial production quality inspection, the substance can be preliminarily judged based on this.
- ** Melting point **: About [specific melting point value], the melting point is of great significance in the identification and purity judgment of the substance. By measuring the melting point, it can be compared with the theoretical value to evaluate its purity. If the melting point is consistent with the theoretical value and the melting range is narrow, it indicates high purity; conversely, the wide melting range is poor purity.
- ** Boiling point **: About [specific boiling point value], the boiling point information is of great significance for the separation and purification of substances. In separation operations such as distillation, the effective separation of the substance from other components can be achieved according to the difference in boiling point.
- ** Solubility **: Soluble in organic solvents such as dichloromethane, chloroform, N, N-dimethylformamide, etc. This property is conducive to the selection of suitable solvents in organic synthesis reactions to create a good environment for the reaction. For example, in some synthesis that requires a homogeneous reaction system, suitable solvents can promote full contact of the reactants and improve the reaction efficiency.
- ** Stability **: It is relatively stable under conventional conditions, but when it encounters strong oxidants, strong acids or strong bases, it is prone to chemical reactions. This requires that during storage and use, it is necessary to avoid contact with these substances. For example, when storing, you should choose a dry, cool environment away from strong acids and bases and oxidants to prevent deterioration.
- ** Spectral Properties **: Its infrared spectrum will have characteristic absorption peaks at specific wavenumbers, such as C = O stretching vibration peaks located at about [specific wavenumber], which helps to confirm the structure. In the identification of unknown objects, the infrared spectrum is like a "fingerprint" of the substance. By comparing it with the standard spectrum, the structure of the substance can be quickly and accurately determined.
4 - thiazolecarboxylic acid, 5 - bromo - 2 - phenyl -, ethyl ester What are the common purity grades on the market?
Ethyl 5-bromo-2-phenyl-4-thiazole carboxylate sold in the market has the following common purity grades.
One is industrial grade, and the purity of this grade is about 80% to 90%. The lid is mostly used in industrial production processes that do not require strict purity, such as some large-scale but not very high-purity chemical synthesis processes.
The second is chemical purity, with a purity of about 95%. Such purity products, the impurity content has been greatly reduced, suitable for most general chemical experiments and research, can meet the needs of common chemical reactions, and are commonly used in laboratories.
The third is analytical purity, and the purity can reach more than 98%. This grade of products is extremely pure, with very few impurities, and is often used in analytical testing work that requires strict purity, such as high-precision quantitative analysis experiments, preparation of reference materials, etc., to ensure the accuracy and reliability of experimental results.
The fourth is excellent purity, with a purity of nearly 99% or even higher. Premium pure 5-bromo-2-phenyl-4-thiazole carboxylate ethyl ester, with minimal impurity content, is mainly used in high-end scientific research projects, drug research and development and other fields with extreme requirements for purity, which can ensure the accuracy of experimental data and the stability of product quality.