What is the chemical structure of 1-azabicyclo [2.2.2] octyl-3-yl (1S) -1-phenyl-3,4-dihydroisoquinoline-2 (1H) -carboxylate

Looking at this "1-%E6%B0%AE%E6%9D%82%E5%8F%8C%E7%8E%AF [2.2.2] %E8%BE%9B-3-%E5%9F%BA+ (1S) -1-%E8%8B%AF%E5%9F%BA-3, 4-%E4%BA%8C%E6%B0%A2%E5%BC%82%E5%96%B9%E5%95%89-2 (1H) -%E7%BE%A7%E9%85%B8%E9%85%AF%E7%9A%84%E5%8C%96%E5%AD%A6%E7%BB%93%E6%9E%84", it is actually a complex organic matter represented by a specific chemical naming convention.

Among them, "%E6%B0%AE%E6%9D%82%E5%8F%8C%E7%8E%AF [2.2.2]% E8% BE% 9B" seems to refer to a group with a dicyclic [2.2.2] octane structure and a heteroatom substitution on it. The positions marked by "1 -" and "3 -" may be the check point where the key substituent is located. "% E5% 9F% BA" is unclear, so it must be an important structural fragment. " ( 1S) -1 -% E8% 8B% AF% E5% 9F% BA ", (1S) indicates that the three-dimensional configuration of benzol based on position 1 is S-type.

" 3,4 - %E4%BA%8C%E6%B0%A2%E5%BC%82%E5%96%B9%E5%95%89 ", showing that there are dihydroisocoumarins at positions 3 and 4." 2 (1H) -%E7%BE%A7%E9%85%B8%E9%85%AF ", this part may be a quinolinic acid ester-related structure containing a specific hydrogen atom, and is connected to the whole.

In summary, the organic compound has a complex structure, fusing multiple types of cyclic structures and specific three-dimensional configuration substituents, and each part is interconnected to form a unique chemical structure. However, more spectroscopic data are needed to confirm its precise structure.

What are the main uses of 1-azabicyclo [2.2.2] octyl-3-yl (1S) -1-phenyl-3,4-dihydroisoquinoline-2 (1H) -carboxylate

1-% octyl-3-yl + (1S) -1-naphthyl-3,4-diquinoline-2 (1H) -carboxylic acid ester, this compound has a wide range of uses. It can be used in the field of chemical engineering. Because of its specialization, or it can be modified by a specific method, it can improve the biological activity and performance of the product. For example, it can be used to treat certain diseases or enzymes, and it is expected to develop new therapeutic compounds.

In the materials department, compounds or special functional materials can be used. Because of its specific molecular and empty type, or can develop the characteristics of optical materials, such as used in optical diodes (OLEDs), improve the qualitative properties of the material's optical efficiency; it may also be in liquid crystal materials, affecting the molecular arrangement and phase alignment, and a new type of liquid crystal material with excellent performance.

In the field of chemical synthesis, it is often used as a synthesizer. The Naphthalene, Naphthalene, and Quinoline carboxylate parts in it can introduce different functionalities, expand the versatility of compounds, and provide important groups for the synthesis of molecules with specific functions. In addition, 1-% [2.2.2] octyl-3-yl + (1S) -1-naphthyl-3,4-diquinoline-2 (1H) -carboxylic acid esters have great performance in the polymorphism phase.

What is the synthesis method of 1-azabicyclo [2.2.2] octyl-3-yl (1S) -1-phenyl-3,4-dihydroisoquinoline-2 (1H) -carboxylate

To prepare 1-% [2.2.2] octyl-3-yl + (1S) -1-phenyl-3,4-diquinoline-2 (1H) -ketoanhydride, the following ancient method can be carried out.

The first amount of 1-% [2.2.2] octyl-3-ol is prepared with (1S) -1-phenyl-3,4-diquinoline-2 (1H) -one and placed in the reactor. The reactor is first removed with nitrogen to maintain its oxygen environment. Adding appropriate catalysts, such as a specific gold complex, can promote the reaction activity of the two.

Therefore, the control of the reaction rate should be carried out by the method of rising to a certain degree of temperature. The degree of temperature depends on the previous period of temperature, and it is generally here that the reaction rate can be improved. And in this process, it is necessary to mix quickly with a magnetic mixer to make the reaction material fully connected.

After the reaction rate is completed for a period of 15 days, the reaction process can be reversed by a thin color method or other suitable means. If it is found that the reaction rate has been completed, it can be cooled to the chamber.

However, the resulting mixture is added to the solution amount, and the solution needs to be able to dissolve the unreversed material and by-products, and the object can be precipitated as a solid substance.

The crude product still needs to be refined, so as to re-crystallize the product, and obtain a suitable solution, such as the mixed solution of a certain alcohol, add a solution to dissolve the crude product, and then cool the product to make the target product precipitate in the shape of a crystal. The best, the dry process, can obtain a high degree of 1-% [2.2.2] octyl-3-yl + (1S) -1-phenyl-3,4-diquinoline-2 (1H) -ketoanhydride. The whole process, the operation of Zunhua, and the control of each step of the product, can obtain the ideal result.

Physicochemical Properties of 1-azabicyclo [2.2.2] octyl-3-yl (1S) -1-phenyl-3,4-dihydroisoquinoline-2 (1H) -carboxylate

1-% [2.2.2] octyl-3-yl + (1S) -1-phenyl-3,4-dicoumarin-2 (1H) -one, which is a characteristic chemical compound, its physicalization is very important, and it has a very important impact on the synthesis and physicochemical fields.

As far as physical properties are concerned, its external properties are often solid, and there are multiple forces on the multi-factor molecules, such as van der force,, etc., to promote the orderly arrangement of molecules. In terms of melting, due to the properties of molecules, different substituents will affect them. In general, the amount of molecules increases, the molecular force increases, and the melting also increases. For example, if methyl and other daughter groups are introduced into benzene, the molecular force may be increased and the melting rate may be improved.

In terms of solubility, the compound has a certain solubility due to its hydrophobic and aromatic properties, but it is less soluble in water molecules. For example, in chloroform and dichloromethane, it often has a certain solubility. However, in water, the solubility of water molecules is very small, and the difference between the compounds is large, so as to form an effective interaction.






























< b The aryl moiety is easy to generate and reverse, because benzene has rich properties, such as bromination, nitrification and other reactions are possible. And the carbonyl in the dicoumarin ketone is the functional function of the activity, which can generate multiple nuclei, such as Grignard's addition, and derive more valuable compounds. This property is especially important in the synthesis process, which can be used to build more valuable compound molecules.

What is the market prospect of 1-azabicyclo [2.2.2] octyl-3-yl (1S) -1-phenyl-3,4-dihydroisoquinoline-2 (1H) -carboxylate?

There is now a market prospect of 1-octyl-3-yl + (1S) -1-phenyl-3,4-diphenyl-coumarin-2 (1H) -keto, which is a matter of concern.

This compound, 1-octyl-3-yl-2 (1H) -keto, (1S) -1-phenyl-3,4-diphenyl-coumarin-2 (1H) -keto also has properties. In this field, or due to the characteristics of the combination of the two, new research agreements can be obtained. For example, in the treatment of certain diseases, a specific compound is required to act on a specific receptor or enzyme of a living organism. This compound may have a good effect due to its special effects, so there may be a demand for it.

Furthermore, in terms of material science, it may be able to give new properties to the material by means of its own specialization. For example, increasing the quality of the material, changing the quality or light properties of the material, etc. With the development of science and technology, the demand for new materials is increasing. If this compound can play a role in material modification, it will be able to expand the market.

However, its market prospects are also constrained by many factors. The synthesis of this compound is difficult and expensive, which will affect its large-scale production and market promotion. Moreover, the acceptance of new compounds in the market also needs to be cultivated, and the cooperation of peers should not be ignored. If other similar compounds are already in the market, if this compound wants to be released, it needs to be special.

Therefore, the market prospect of 1-octyl [2.2.2] octyl-3-yl + (1S) -1 -phenyl-3,4-diphenyl-couscous-2 (1H) -ketone contains both problems and challenges. Only by grasping the problems and overcoming the problems can we win a place in the market.