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What is the chemical structure of quinoline-3-carboxylate Ethyl-6, 7-Difluoro-1-methyl-4-oxo-4H- (1,3) thiazole (3,2-a)
Eh, this is the name of an organic compound. To know its chemical structure, you need to analyze its naming rules in detail. The name is "Ethyl-6,7-Difluoro-1-methyl-4-oxo-4H - (1,3) thiazole (3,2 - a) quinoline-3 - carboxylate". From the perspective, "Ethyl" epethyl group is a simple alkyl group, which seems to be a small branch connected to the main structure. "6,7-Difluoro" clearly states that there are difluorine atoms at the 6th and 7th positions of the main structure. Fluorine atoms affect many properties of molecules due to their reactivity. " 1 - methyl "indicates that there is a methyl group in the first position, which is also an alkyl group, adding a branch to the structure." 4 - oxo "has a carbonyl group in the fourth position, and the carbonyl group is a carbon-oxygen double bond, which has a unique chemical activity." 4H - (1,3) thiazole (3,2 - a) quinoline "This part constructs the fused ring structure of the main body. The thiazole ring and the quinoline ring are fused in a specific way. This fused ring structure gives the molecule a specific rigid and conjugated system. And" 3 - carboxylate "indicates that there is a carboxylic acid ester group attached to the third position, which gives the molecule a different reactivity. Overall, the chemical structure of this compound is complex and delicate, and the interaction of various groups jointly determines its unique chemical and physical properties.
What are the main uses of Ethyl-6, 7-Difluoro-1-methyl-4-oxo-4H- (1,3) thiazole (3,2-a) quinoline-3-carboxylate
Ethyl - 6,7 - Difluoro - 1 - methyl - 4 - oxo - 4H - (1,3) thiazole (3,2 - a) quinoline - 3 - carboxylate is also an organic compound. Its main uses are quite extensive, and it has important applications in the field of medicinal chemistry.
First, this compound may have potential antibacterial activity in the development of antibacterial drugs. Due to the fact that substances of this type of structure can often affect the physiological process of bacteria, such as interfering with the synthesis of bacterial cell walls, inhibiting the generation of bacterial proteins, etc., so as to achieve antibacterial effect, it is expected to provide key lead compounds for the creation of new antibacterial drugs to deal with the increasingly serious problem of bacterial drug resistance.
Second, in the study of the structure-activity relationship of pharmaceutical chemistry, its unique structure, containing fluorine atoms, heterocycles and other special groups, provides a good example for exploring the relationship between structure and biological activity. Scientists can modify and modify its structure to study the effect of different substituents on activity, so as to design drug molecules with better activity and greater selectivity.
Third, in the field of organic synthetic chemistry, as an intermediate with a special structure, it can be used to construct more complex organic molecules. Its unique structural characteristics can participate in a variety of organic reactions, such as nucleophilic substitution, cyclization, etc., providing an effective way for the synthesis of organic materials with specific functions and the total synthesis of natural products, etc., and promoting the development and innovation of organic synthetic chemistry.
What is the synthesis method of Ethyl-6, 7-Difluoro-1-methyl-4-oxo-4H- (1,3) thiazole (3,2-a) quinoline-3-carboxylate
The synthesis of Ethyl - 6,7 - Difluoro - 1 - methyl - 4 - oxo - 4H - (1,3) thiazole (3,2 - a) quinoline - 3 - carboxylate requires many steps, and according to chemical principles, step by step.
The first step often involves the selection and preparation of starting materials. This compound has a complex structure, and the precise selection of starting materials is crucial. It may need to be based on specific compounds containing nitrogen, sulfur and fluorine, and carefully treated to make it reactive.
Second, the reaction process of chemical synthesis. In the common reaction path, there may be a cyclization reaction. Under suitable reaction conditions, such as specific temperature, pressure and catalyst, the raw material molecules are cyclized and gradually form the basic structure of this compound. Among them, the formation and remodeling of chemical bonds such as carbon-nitrogen, carbon-sulfur and carbon-fluorine are involved.
Furthermore, substitution reactions are often key. On the established basic structure, groups such as 1-methyl and 3-carboxylate ethyl are introduced through clever substitution reactions. In this regard, precise control of the reaction check point is extremely important. Suitable reaction reagents and conditions are required to ensure that the substitution is in the correct position without generating by-products. < Br >
Control of the reaction conditions is also essential for synthesis. The temperature may affect the reaction rate and product selectivity. The regulation of pressure, in some reactions, is related to the direction and process of the reaction. The choice of catalyst can greatly change the difficulty and yield of the reaction. For example, some metal catalysts can effectively promote the formation of specific chemical bonds and improve the reaction efficiency. The steps after
are the separation and purification of the product. The mixture obtained by synthesis often contains unreacted raw materials, by-products, etc. The target product Ethyl - 6,7 - Difluoro - 1 - methyl - 4 - oxo - 4H - (1,3) thiazole (3,2 - a) quinoline - 3 - carboxylate needs to be finely separated by means such as column chromatography and recrystallization to obtain a pure product with the desired quality and purity.
What are the physical properties of quinoline-3-carboxylate Ethyl-6, 7-Difluoro-1-methyl-4-oxo-4H- (1,3) thiazole (3,2-a)
Ethyl-6,7-difluoro-1-methyl-4-oxo-4H- (1,3) thiazolo (3,2-a) quinoline-3-carboxylic acid ester, this is an organic compound. It has some physical properties, let me tell you one by one.
This substance may be a solid under normal conditions, but due to the presence of complex conjugated systems and polar groups in its molecular structure, the intermolecular force is quite strong. Looking at its melting point, or due to the close arrangement of molecules, the melting point is relatively high. Due to the interaction between the conjugated structure and the polar groups, the molecules need higher energy to overcome the mutual binding and melt.
As for solubility, because the compound contains polar carboxyl ester groups and non-polar aromatic rings and thiazole rings, its solubility in organic solvents may be unique. In polar organic solvents such as ethanol and acetone, polar groups can form hydrogen bonds or dipole-dipole interactions with solvent molecules, or have a certain solubility. However, in non-polar organic solvents such as n-hexane, because the non-polar part is not enough to be well miscible with the solvent, the solubility may be very small.
Its density is inferred from its molecular composition and structure, and the relative density may be greater than that of water. Because the molecule contains elements with relatively large atomic mass such as fluorine atoms, and the structure is compact, the mass per unit volume is large. < Br >
Its appearance may be a white to pale yellow powdery solid, which is determined by the light absorption and reflection properties of the conjugated system. The conjugated structure allows the molecule to absorb visible light of a specific wavelength and reflect light of the corresponding color, thus presenting such appearance characteristics.
What is the market outlook for Ethyl-6, 7-Difluoro-1-methyl-4-oxo-4H- (1,3) thiazole (3,2-a) quinoline-3-carboxylate
Ethyl - 6,7 - Difluoro - 1 - methyl - 4 - oxo - 4H - (1,3) thiazole (3,2 - a) quinoline - 3 - carboxylate is one of the organic compounds. Looking at its market prospects, there are really considerable things.
At present, the field of pharmaceutical research and development is booming, and this compound may have unique uses in it. Because of its unique structure, or can be used as a key intermediate in the drug synthesis path. The pharmaceutical industry's thirst for innovative drugs has never ceased. New compounds such as Ethyl - 6,7 - Difluoro - 1 - methyl - 4 - oxo - 4H - (1,3) thiazole (3,2 - a) quinoline - 3 - carboxylate may open up new avenues for the creation of specific new drugs.
Furthermore, the field of pesticides is also its potential stage. Today's agricultural production has a growing demand for high-efficiency, low-toxicity and targeted pesticides. If this compound can be studied to show inhibitory or killing activity against specific pests or bacteria, it will definitely gain a place in the pesticide market. Its unique chemical structure, or endow it with unique biological activities, lays the foundation for the development of new pesticides.
However, looking at its market prospects, there are also challenges. The process of synthesizing this compound may require fine control, and the cost may be the key to affecting its large-scale application. If there can be breakthroughs in synthesis technology and reduce production costs, it will definitely expand its market space. And before it is put into the market, it needs to undergo strict safety assessments and environmental impact considerations to ensure that it is harmless to the ecological environment and users.
Overall, Ethyl - 6,7 - Difluoro - 1 - methyl - 4 - oxo - 4H - (1,3) thiazole (3,2 - a) quinoline - 3 - carboxylate market prospects are bright and challenges coexist. If we can do good research and rational development, we will be able to bloom in the fields of medicine and pesticides.