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What is the chemical structure of 7-Chloro-3- (1- (2,4-dichlorophenyl) -2- (1H-imidazol-1-yl) ethoxy-methyl) benzo (b) thiophene
This is the chemical name of an organic compound. In order to clarify its chemical structure, it is necessary to analyze the meaning of each part of the name. This name follows the naming rules of organic chemistry, and its structure can be inferred according to this rule.
"7 - Chloro - 3 - (1 - (2,4 - dichlorophenyl) - 2 - (1H - imidazol - 1 - yl) ethoxymethyl) benzo (b) thiophene" In "benzo (b) thiophene", the epitome is a benzo [b] thiophene structure, which is a fused ring system composed of a benzene ring and a thiophene ring.
"7-Chloro" is shown to have a monochlorine atom substituted at position 7 of the parent nucleus of benzo [b] thiophene.
"3 - (1- (2,4 - dichlorophenyl) -2- (1H - imidazol - 1 - yl) ethoxymethyl) " part, indicating that there is a complex substituent at position 3 of the parent nucleus. Among this substituent, "ethoxymethyl" is an ethoxy methyl group, that is, the structure of -CH -2 OCH -2 CH. And "1 - (2,4 - dichlorophenyl) - 2 - (1H - imidazol - 1 - yl) " indicates that the 1 position of ethoxy methyl is connected with 2,4 - dichlorophenyl, and the 2 position is connected with 1H - imidazole - 1 - group. 2,4 - dichlorophenyl is the structure where the 2 and 4 positions of the benzene ring are replaced by chlorine atoms; 1H - imidazole - 1 - group is the part left after the hydrogen atom at the 1 position is removed from the imidazole ring.
In summary, the chemical structure of this compound is benzo [b] thiophene as the parent nucleus, with a chlorine atom at position 7 and a substituent containing 2,4-dichlorophenyl, 1H-imidazole-1-group and ethoxy methyl at position 3. Its structure is complex, and all parts of the groups are connected to each other to form the unique chemical structure of this organic compound.
What are the physical properties of 7-Chloro-3- (1- (2,4-dichlorophenyl) -2- (1H-imidazol-1-yl) ethoxy-methyl) benzo (b) thiophene
7-Chloro-3- (1- (2,4-dichlorophenyl) -2- (1H-imidazole-1-yl) ethoxy-methyl) benzo (b) thiophene This substance has considerable physical properties.
Looking at its shape, under normal circumstances, it may be a solid powder with a white or similar color. This is the common appearance of many such organic compounds. It is delicate and homogeneous. It is twisted in the hand and feels smooth to the touch. Although its smell is not strong and pungent, it also has a unique smell under the fine smell. It has a light fragrance unique to organic chemicals, which is not comparable to the ordinary fragrance in the world.
When it comes to the melting point, its melting point is quite high, and it needs to reach a specific temperature to disintegrate the ordered structure of its lattice and turn it into a liquid state. The number of melting points, determined by rigorous experiments, is accurate, due to the delicate combination of intermolecular forces and crystal structures. The boiling point is higher, and to make it boil and vaporize, more energy needs to be applied, which also highlights the strong intermolecular interactions.
In terms of solubility, it may have a certain solubility in common organic solvents such as ethanol and acetone. The polarity of ethanol, which is in agreement with some groups of the compound, can be dispersed and dissolved by the force of intermolecules, resulting in a uniform solution. However, in water, its molecular structure has many hydrophobic groups, so its solubility is very small. In water, it is like oil floating on water, and it is distinct and difficult to blend.
The determination of density is also one of the keys to its physical properties. After fine measurement, its density value can be obtained. This value reflects the mass of its unit volume. It is related to its mixing and stratification with other substances in practical applications. It is of important significance in chemical, pharmaceutical and other fields.
Such various physical properties are intertwined to form the unique physical properties of this compound, which lays a solid foundation for its application in scientific research and industrial practice.
What is the main use of 7-Chloro-3- (1- (2,4-dichlorophenyl) -2- (1H-imidazol-1-yl) ethoxy-methyl) benzo (b) thiophene
7-Chloro-3- (1- (2,4-dichlorophenyl) -2- (1H-imidazole-1-yl) ethoxy-methyl) benzo (b) thiophene, an organic compound. Its main uses are quite extensive, and it is often used as a key intermediate in drug synthesis in the field of medicine.
In the development of Guanfu Pharmaceutical, many antifungal drugs rely on this compound as the cornerstone. Due to its unique chemical structure, it can combine with specific targets in fungal cells to interfere with the metabolic process of fungi or the formation of cell membranes, thereby achieving the effect of inhibiting and even killing fungi. In the context of scientific research, this compound is also an indispensable tool to help researchers gain insight into the physiological mechanisms of fungi and the principles of drug action.
Furthermore, in the field of materials science, this compound may emerge in the preparation of some functional materials due to its specific electronic structure and chemical properties. Or it can be used as an important raw material for the construction of materials with special structures and properties, opening up a way for the research and development of new materials.
In summary, 7-chloro-3- (1- (2,4-dichlorophenyl) -2- (1H-imidazole-1-yl) ethoxy-methyl) benzo (b) thiophene has important uses in the fields of medicine and materials. It is like the key to open many scientific research and application doors, leading our generation to explore the unknown and promote the progress and development of science and technology.
What are the synthesis methods of 7-Chloro-3- (1- (2,4-dichlorophenyl) -2- (1H-imidazol-1-yl) ethoxy-methyl) benzo (b) thiophene
7-Chloro-3- (1- (2,4-dichlorophenyl) -2- (1H-imidazole-1-yl) ethoxy-methyl) benzo (b) thiophene-an organic compound. The synthesis method of this compound is quite critical in the field of organic synthesis. There are several common methods for the synthesis of this compound.
First, a compound containing a thiophene structure is used as the starting material. The chlorine atom is introduced at a specific position in the thiophene ring first, which can be achieved by halogenation reaction. In the halogenation reaction, suitable halogenating reagents, such as chlorine, N-chlorosuccinimide, etc., are selected to control the reaction conditions, such as temperature, solvent, catalyst, etc., to ensure that chlorine atoms are introduced into the desired position precisely.
Then, the structure of benzothiophene is constructed. Nucleophilic substitution or cyclization can be used to connect and cyclize the thiophene ring with the reagent containing the benzene ring to form the benzothiophene parent nucleus.
Second, for the construction of the 1 - (2,4-dichlorophenyl) -2 - (1H-imidazole-1-yl) ethoxy moiety. First, 2,4-dichlorobenzene is connected to an ethoxy-containing reagent through a substitution reaction to form a 2,4-dichlorophenyl ethoxy compound. Next, the compound undergoes a nucleophilic substitution reaction with imidazole, and the nitrogen atom of imidazole attacks the appropriate check point of the ethoxy compound, and introduces a 1- (1H-imidazole-1-yl) group.
Finally, the constructed 1- (2,4-dichlorophenyl) -2- (1H-imidazole-1-yl) ethoxy moiety is connected to the formed chlorobenzothiophene-containing structure. In this step, the nucleophilic substitution reaction can be used to attack the appropriate substitution check point on the benzothiophene ring with the oxygen atom of ethoxy to form the target product 7-chloro-3- (1- (2,4-dichlorophenyl) -2- (1H-imidazole-1-yl) ethoxymethyl) benzo (b) thiophene.
The whole synthesis process needs to carefully control the reaction conditions of each step to ensure the selectivity and yield of the reaction, so as to achieve the purpose of efficient synthesis of the target compound.
How competitive is 7-Chloro-3- (1- (2,4-dichlorophenyl) -2- (1H-imidazol-1-yl) ethoxy-methyl) benzo (b) thiophene in the market?
7-Chloro-3- (1- (2,4-dichlorophenyl) -2- (1H-imidazole-1-yl) ethoxymethyl) benzo (b) thiophene, how competitive is this product in the city? I will use the ancient saying of "Tiangong Kaiwu".
Now look at this 7-chloro-3- (1- (2,4-dichlorophenyl) -2- (1H-imidazole-1-yl) ethoxymethyl) benzo (b) thiophene, its competitiveness in the city is related to multiple ends. First, it depends on its function. If it is a raw material for medicine, has a unique healing effect, can cure diseases, and among the same kind, has better curative effect and fewer side effects, it will be favored by doctors and patients, and the competitiveness of the city will be self-strengthening.
The second is about its manufacturing cost. If the manufacturing method is exquisite, the materials used are saved and the labor efficiency is high, the price can be close to the people, and it will be widely sold in the city. On the contrary, if the cost is high, the price is high and few people care about it, the competitiveness will be weak.
Furthermore, the situation of market supply and demand is also important. If the world is hungry for this thing, and there are few suppliers, its competitiveness is self-evident. However, if there is an oversupply, even if there are all kinds of wonders, it is also necessary to compete for a place.
There is also a way of marketing. If it can be widely publicized, so that everyone knows its goodness, it can also increase its competitiveness. On the contrary, although it has good ability, but the world does not know it, it is difficult to develop its growth.
In summary, the competitiveness of 7-chloro-3- (1- (2,4-dichlorophenyl) -2- (1H-imidazole-1-yl) ethoxymethyl) benzo (b) thiophene in the city depends on the function, cost, supply and demand and marketing. One cannot be ignored.