2-(6-hydroxy-1,3-benzothiazol-2-yl)-4,5-dihydro-1,3-thiazole-4-carboxylic acid

This is the chemical structure analysis of 2- (6-hydroxy-1,3-benzothiazole-2-yl) -4,5-dihydro-1,3-thiazole-4-carboxylic acid.
Looking at its structure, this compound is formed by fusing two parts. One is the benzothiazole ring, which contains the fusion structure of the benzene ring and the thiazole ring. At the 6-position of the benzothiazole ring, there is a hydroxyl group connected. This hydroxyl group has active hydrogen and can participate in various chemical reactions, such as the formation of hydrogen bonds, which in turn affects the physical and chemical properties of the compound. The second is a 4,5-dihydro-1,3-thiazole ring, which is connected with a carboxyl group at the 4-position. The carboxyl group is a strongly polar group, which is acidic and can undergo acid-base neutralization, esterification and other reactions. The two rings are connected at the 2-position to form a unique fused ring structure. This structure endows the compound with a specific spatial configuration and electron cloud distribution, making it potentially useful in pharmaceutical chemistry, materials science and other fields. For example, in drug development, such structures may interact with specific biological targets to exhibit biological activity; in the field of materials, their special structures may affect the optical and electrical properties of the material. In short, the chemical structure of this compound determines its unique physical and chemical properties and potential application value.

2-% (6-hydroxy-1,3-benzothiazole-2-yl) -4,5-dihydro-1,3-thiazole-4-carboxylic acid, this is an organic compound. It has several unique physical properties.
Looking at its appearance, it is often in a solid state or a crystalline powder. Due to intermolecular forces, it aggregates into a solid structure at room temperature and pressure. The powder shape is conducive to its uniform dispersion in the reaction system, which is quite beneficial for chemical synthesis and other operations.
When it comes to melting point, this compound has a specific melting point value. Determination of melting point can help identify and identify purity. When heated to this specific temperature, the molecule obtains enough energy to overcome the lattice energy, the lattice structure disintegrates, and then it converts from solid to liquid. The determination of precise melting point can be one of the key indicators to determine the purity of the compound, and the melting point range of high-purity compounds is narrow.
In terms of solubility, it varies in different solvents. In polar organic solvents, such as ethanol and dimethyl sulfoxide (DMSO), it may have a certain solubility. This is because polar solvents and polar groups in compounds, such as hydroxyl groups, carboxyl groups, etc., can form hydrogen bonds or other intermolecular forces to promote dissolution. In non-polar solvents, such as n-hexane and toluene, the solubility is very low. Due to the large polar difference between non-polar solvents and the compound, the intermolecular forces are weak.
In addition, the compound may have a certain stability. Under normal temperature and conventional environmental conditions, the chemical properties are relatively stable, and it is not easy to spontaneously undergo chemical reactions. However, under specific conditions, such as high temperature, strong acid, strong base or the presence of specific catalysts, active check points in its molecular structure, such as carboxyl groups, thiazole rings, etc., may participate in chemical reactions and exhibit different chemical activities. This balance of stability and reactivity is of great significance for its applications in chemical synthesis, drug development and other fields.

2-% (6-hydroxy-1,3-benzothiazole-2-yl) -4,5-dihydro-1,3-thiazole-4-carboxylic acid. The common synthesis methods of this compound are as follows:
The starting material can be selected from benzothiazole compounds and thiazoline precursors containing appropriate substituents. First, the 6-position of benzothiazole is hydroxylated on the basis of benzothiazole. Under appropriate reaction conditions, a suitable hydroxylating agent, such as a mixed acid system of sulfuric acid and nitric acid, or a specific metal salt catalysis, is used to introduce the hydroxyl group at the 6-position of benzothiazole.
Then, the 4,5-dihydro-1,3-thiazole-4-carboxylic acid moiety is prepared. The thiazole ring structure is usually constructed by cyclization of sulfur-containing organic compounds with aldides and ketones under the action of basic catalysts. For example, in the presence of weak bases such as sodium carbonate or potassium carbonate, mercaptoacetic acid derivatives and suitable aldides are heated and refluxed in a suitable organic solvent such as ethanol or dichloromethane to promote cyclization, resulting in the formation of precursors of 4,5-dihydro-1,3-thiazole-4-carboxylic acids.
Finally, the modified benzothiazole moiety was condensed with a 4,5-dihydro-1,3-thiazole-4-carboxylic acid precursor. In the presence of condensing agents such as dicyclohexyl carbodiimide (DCC) or 1-ethyl-3- (3-dimethylaminopropyl) carbodiimide hydrochloride (EDC · HCl), in a suitable reaction solvent such as N, N-dimethylformamide (DMF), react under mild temperature conditions, so that the two are joined to form the target compound 2-% (6-hydroxy-1,3-benzothiazole-2-yl) -4,5-dihydro-1,3-thiazole-4-carboxylic acid. After the reaction is completed, a pure target product is obtained by conventional separation and purification methods such as column chromatography, recrystallization, etc.

2-% (6-hydroxy-1,3-benzothiazole-2-yl) -4,5-dihydro-1,3-thiazole-4-carboxylic acid, this compound is used in many fields such as medicine, materials science, agriculture, etc.
In the field of medicine, due to its unique chemical structure, or diverse biological activities. If it may exhibit antibacterial activity, it has inhibitory effect on some bacteria, and can interfere with bacterial cell wall synthesis and metabolic processes, it is expected to develop new antibacterial drugs to deal with drug-resistant bacterial infections. In anti-cancer research, it may regulate cancer cell signaling pathways, induce cancer cell apoptosis, provide a new direction for the development of anti-cancer drugs, and help develop high-efficiency and low-toxicity anti-cancer drugs.
In the field of materials science, this compound can be used as a functional material. With its specific structure and properties, it may be used to prepare optoelectronic materials, and in optoelectronic devices such as Light Emitting Diode and solar cells, it can improve the photoelectric conversion efficiency and stability of the device, and promote the development of the optoelectronic industry. At the same time, because of its interaction with some materials, it can also be used to prepare special adsorption materials, selectively adsorb specific substances, and use them for the treatment of environmental pollutants or the separation and purification of substances.
In the agricultural field, it may have potential application value. It may have plant growth regulation activity, regulate plant hormone levels, promote plant growth and development, and improve crop yield and quality. It may also be used as a new type of pesticide lead compound to develop green and environmentally friendly pesticides, which have repellent, inhibitory or toxic effects on pests, and are environmentally friendly, reducing the damage to the ecological environment caused by the use of chemical pesticides.

2-%286-hydroxy-1%2C3-benzothiazol-2-yl%29-4%2C5-dihydro-1%2C3-thiazole-4-carboxylic acid, which is the English name of the chemical substance, in Chinese or 2- (6-hydroxy-1,3-benzothiazole-2-yl) -4,5-dihydro-1,3-thiazole-4-carboxylic acid. In terms of its market prospects, let me tell you in detail.
Looking at the current field of chemical research, new organic compounds are often the focus of scientific research. This compound may have emerged in the field of medicinal chemistry due to its unique molecular structure. In today's pharmaceutical research and development, new molecules with biological activity are often explored for the treatment of diseases. If this acid compound is shown to have biological activities such as antibacterial, anti-inflammatory or anti-tumor, it will attract the attention of pharmaceutical companies and scientific research institutions, and the market prospect is broad.
Let's talk about the field of materials science. The research and development of new materials often depends on the help of new compounds. If this acid compound has special physical and chemical properties, such as good thermal stability, optical properties, etc., it may be used to prepare new polymer materials and optical materials. If this compound can meet this demand, the market potential cannot be underestimated.
However, its marketing activities also have challenges. In terms of chemical synthesis, it is necessary to optimize the synthesis process, reduce costs, and improve yield in order to gain an advantage in the market competition. Furthermore, a large amount of experimental data is required to clarify its safety and stability, which is the key to whether it can enter the practical field.
Overall, although 2- (6-hydroxy-1,3-benzothiazole-2-yl) -4,5-dihydro-1,3-thiazole-4-carboxylic acid has addressable market opportunities, it also needs to overcome many difficulties. If it can be properly dealt with, it will be necessary for the chemical-related industries to bloom.