Ethyl 5 Bromo 2 Phenyl 1 3 Thiazole 4 Carboxylate
quinoline thiophene imidazole thiazole

ethyl 5-bromo-2-phenyl-1,3-thiazole-4-carboxylate

    Specifications

    HS Code

    324397

    Chemical Formula C12H10BrNO2S
    Molar Mass 312.18 g/mol
    Appearance Solid (usually)
    Color Off - white to light yellow (typical)
    Melting Point Varies (but generally in a certain range, data needed for exact value)
    Solubility In Water Low (practically insoluble)
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
    Density Data needed for exact value
    Stability Stable under normal conditions but may react with strong oxidizing agents

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    General Information
    Where to Buy ethyl 5-bromo-2-phenyl-1,3-thiazole-4-carboxylate in China?
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    Frequently Asked Questions

    As a leading ethyl 5-bromo-2-phenyl-1,3-thiazole-4-carboxylate supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    Ethyl 5-bromo-2-phenyl-1, what is the chemical structure of 3-thiazole-4-carboxylate
    Ethyl-5-bromo-2-phenyl-1,3-thiazole-4-carboxylic acid ester, its chemical structure is as follows:
    The core of this compound is a thiazole ring, which is a five-membered heterocyclic ring composed of a sulfur atom and a nitrogen atom at positions 1,3. A phenyl group is connected at position 2 of the thiazole ring, a bromine atom is connected at position 5, and a carboxylic acid ester is connected at position 4 through a carboxyl group and an ethyl ester group to form a carboxylic acid ester structure, namely -COOCH -2 CH. The phenyl group is composed of a benzene ring composed of six carbon atoms, which adds aromaticity to the compound. Bromine atoms have strong electronegativity, which can affect the electron cloud distribution and reactivity of the compound. As an electron-withdrawing group, ethyl ester groups also play an role in the chemical properties of the thiazole ring. These different groups are connected to the thiazole ring, endowing the compound with unique physical and chemical properties, which may have potential application value in the fields of organic synthesis and medicinal chemistry.
    Ethyl 5-bromo-2-phenyl-1, what are the main uses of 3-thiazole-4-carboxylate
    Ethyl 5-bromo-2-phenyl-1,3-thiazole-4-carboxylate, the Chinese name can be called ethyl 5-bromo-2-phenyl-1,3-thiazole-4-carboxylate. This compound has a wide range of uses and is often a key intermediate in the synthesis of medicine.
    Gainthiazole compounds have a variety of biological activities, such as antibacterial, anti-inflammatory, anti-tumor, etc. This compound can introduce specific functional groups through clever chemical transformation to construct molecules with unique pharmacological activities. For example, bromine atoms can be replaced by specific groups through substitution reactions, thereby modifying the molecular structure, improving the affinity and activity for specific targets, or optimizing the pharmacokinetic properties, laying the foundation for the creation of new and efficient drugs.
    In the field of pesticides, it also has its uses. Thiazole derivatives are mostly insecticidal, bactericidal, weeding and other effects. This compound can be used as a starting material for the construction of new pesticide active ingredients. By means of organic synthesis, high-efficiency and low-toxicity pesticide products for specific crop diseases and insect pests can be developed to protect farmers and mulberry and ensure the abundance of crops.
    Furthermore, in the field of materials science, it has also emerged. Some compounds containing thiazole structures show unique properties in optical and electrical materials. Ethyl 5 - bromo - 2 - phenyl - 1, 3 - thiazole - 4 - carboxylate or can be polymerized to construct polymer materials with special photoelectric properties, which are used in the research and development of Light Emitting Diodes, solar cells and other devices, and open up new fields of material application.
    Ethyl 5-bromo-2-phenyl-1, what is the synthesis method of 3-thiazole-4-carboxylate
    There are currently methods for synthesizing ethyl 5-bromo-2-phenyl-1,3-thiazole-4-carboxylate, which are described in detail below.
    First, suitable starting materials, such as sulfur-containing compounds, nitrogen-containing compounds and benzene derivatives with corresponding substituents, are used as bases. After condensation reaction, the structures of each part are initially connected. During this process, the reaction conditions, such as temperature, pressure, reaction duration and molar ratio of the reactants, need to be precisely regulated to ensure that the reaction proceeds in the desired direction. Too high or too low temperature may cause an increase in side reactions, affecting the yield and purity of the target product. < Br >
    In the reaction system, a suitable catalyst can be selected to speed up the reaction rate and reduce the activation energy of the reaction. At the same time, the selection of a suitable solvent can not only dissolve the reactants and help them fully contact, but also affect the selectivity of the reaction.
    After the condensation reaction is completed, the product may need to go through the steps of separation and purification. Commonly used methods include distillation, recrystallization, column chromatography, etc. Distillation can be separated according to the difference in boiling points of different substances; recrystallization can precipitate the target product in crystal form due to the difference in solubility; column chromatography can achieve effective separation according to the interaction between the substance and the stationary phase and the mobile phase.
    After many operations and strict control of each link, ethyl 5-bromo-2-phenyl-1,3-thiazole-4-carboxylate of higher purity can be obtained. The way of synthesis requires caution and insight into various details to achieve the desired effect.
    Ethyl 5-bromo-2-phenyl-1, what are the physical properties of 3-thiazole-4-carboxylate
    "Tiangong Kaiwu" is an ancient scientific and technological masterpiece in our country, but it does not contain "ethyl 5-bromo-2-phenyl-1,3-thiazole-4-carboxylate". However, according to today's chemical knowledge, the physical properties of this compound can be described as follows:
    This compound is called 5-bromo-2-phenyl-1,3-thiazole-4-carboxylic acid ethyl ester. Looking at its structure, it contains bromine atom, phenyl group, thiazole ring and carboxylic acid ethyl ester group.
    It may be a solid at room temperature, and due to the structure of benzene ring and heterocycle, the intermolecular force is relatively large. The melting point may be higher due to its tight structure, but the exact value needs to be determined experimentally.
    This substance is insoluble in water because of its large proportion of hydrocarbons in the molecule, which is highly hydrophobic, while water is a polar solvent. However, it can be soluble in common organic solvents, such as dichloromethane, chloroform, tetrahydrofuran, etc., because these organic solvents are similar in structure to this compound, and follow the principle of "similar miscibility".
    Its density may be slightly higher than that of water. Due to the presence of bromine atoms in the molecule, the relative weight of bromine atoms is larger, resulting in an increase in molecular weight and an increase in unit volume mass.
    Appearance may be white to light yellow powder or crystalline, which is a common appearance form of benzene-containing ring and heterocyc And because it contains a conjugated system or has certain ultraviolet absorption characteristics, characteristic absorption peaks can be found in ultraviolet spectral analysis, providing a basis for its identification and analysis.
    Ethyl 5-bromo-2-phenyl-1, 3-thiazole-4-carboxylate market prospects
    Nowadays, there are compounds ethyl + 5 - bromo - 2 - phenyl - 1,3 - thiazole - 4 - carboxylate, and their market prospects are related to many aspects. This substance may have potential utility in the field of medicine. The research and development of medicine in Guanggu often makes breakthroughs due to the discovery of new compounds. If this compound can exhibit unique pharmacological activity, it can become a key ingredient of new drugs, and benefit patients, the market prospect will be broad.
    In the chemical industry, or as an important intermediate. In ancient chemical production, intermediates are the cornerstone of building complex compounds. If it can participate in various chemical reactions and synthesize high-value products, the demand for it by chemical companies will increase, and the market will also expand.
    However, its market prospects also pose challenges. If the synthesis process is complex and costly, it is difficult to produce on a large scale like the ancient method of refining, and its marketing activities must be limited. And the competition of similar compounds is fierce, and it is necessary to highlight unique advantages in order to win the favor of the market. If it can stand out in terms of performance and cost, just like the heroes of the ancient times who can win, it can take the lead in the market and have a bright future; otherwise, it may be trapped in the market and the prospect is worrying.