1-Azabicyclo[2.2.2]octan-8-yl (1S)-1-phenyl-3,4-dihydro-1H-isoquinoline-2-carboxylate butanedioic acid

This is a complex organic compound, and its chemical structure is composed of many parts. The 1-azabicyclo [2.2.2] octyl-8-base part is like the cornerstone of building a pavilion and supports a corner of the overall structure. (1S) -1-phenyl-3,4-dihydro-1H-isoquinoline-2-carboxylate part, like the delicate decoration of a pavilion, carries a unique phenyl and isoquinoline structure, giving the compound different characteristics. The succinic acid part, like a bridge, connects the front and rear structures, making it a tight whole.
Looking at its structure, the 1-azabicyclic [2.2.2] octyl-8-matrix has a rigid bilicyclic structure, which brings specific spatial orientation and stability to the molecule, just like a stable beam supporting a pavilion. In (1S) -1-phenyl-3,4-dihydro-1H-isoquinoline-2-carboxylic acid esters, the chiral center (1S) determines its optical activity, and the phenyl and isoquinoline rings endow it with aromatics and electronic effects, which affect the reactivity and biological activity of the compounds, just like the decoration of a pavilion adds a unique charm. As a dicarboxylic acid, succinic acid can participate in a variety of reactions and is connected to the front and rear structures, which has a great impact on the overall solubility and the distribution of reaction check points. It acts as a bridge to connect all parties, so that molecular functions can be integrated and displayed. The complex and delicate structure of this compound contains rich chemical mysteries and potential application value.

1-Azabicyclo [2.2.2] octyl-8-yl (1S) -1-phenyl-3,4-dihydro-1H-isoquinoline-2-carboxylate succinic acid, which is widely used. In medicine, it is often the key raw material for the creation of new drugs. Because of its special chemical structure, it can act on specific physiological targets in the human body, or can regulate the biochemical reactions of the body, and has potential effects on the treatment of specific diseases. For example, in the drug development of nervous system diseases or cardiovascular diseases, it can be delicately designed and modified to become an active ingredient with unique efficacy.
In the field of scientific research, it is an important intermediate in organic synthetic chemistry. Chemists can explore novel chemical reaction paths by ingeniously modifying its structure, synthesizing organic compounds with more complex structures and more specific functions, which will help to expand the theory of organic chemistry and improve the actual synthesis technology. Furthermore, in the field of materials science, if it is properly introduced into the material system, it may endow the material with unique physical and chemical properties, such as improving the stability and solubility of the material, or even endowing it with special optical and electrical properties, providing an opportunity for the creation of new functional materials.

The synthesis of 1-azabicyclic [2.2.2] octyl-8-yl (1S) -1-phenyl-3,4-dihydro-1H-isoquinoline-2-carboxylic succinic acid has various paths to follow.
First, the key structure can be built from the starting material through multi-step reaction. First, a specific 1-phenyl-3,4-dihydro-1H-isoquinoline-2-carboxylic acid derivative is used as a base. With suitable reagents, under appropriate reaction conditions, such as mild temperature and suitable solvent, it can be esterified with azabicyclo [2.2.2] octyl-8-ol. This process requires attention to the control of reaction conditions. If the temperature is too high, side reactions will occur, and if it is too low, the reaction will be delayed. The properties of the solvent are also related to the effect of the reaction. Non-polar or weakly polar solvents may be more suitable.
Furthermore, the raw materials can be modified first. The 1-phenyl-3,4-dihydro-1H-isoquinoline-2-carboxylic acid is introduced into the activating group at a specific check point, which greatly increases its activity, and then reacts with the pretreated azabicyclic [2.2.2] octyl-8-based reagent. When pretreating the azabicyclic [2.2.2] octyl-8-based reagent, it may need to be activated with a base agent to increase its nucleophilicity and make the reaction smooth.
can also be constructed by the method of intermediates. First synthesize the intermediate containing part of the target structure, and then skillfully transform it to gradually approach the target product. If the intermediate containing phenyl-dihydroisoquinoline-carboxylic acid and a specific linker is prepared first, the linker needs to have a transformable activity check point, and then the linker is reacted with azabicyclo [2.2.2] octyl-8-group, and then the subsequent modification is carried out to obtain the target product and succinic acid. Each step requires detailed observation of the reaction process to ensure the purity and yield of the product.

1-Azabicyclo [2.2.2] octyl-8-yl (1S) -1-phenyl-3,4-dihydro-1H-isoquinoline-2-carboxylate succinic acid, which is a chemical substance. However, its safety is not detailed in ancient books, and it is difficult to judge based on the old theory today.
In today's discussion of the safety of chemical substances, it is often involved in toxicity, stability, reactivity and many other aspects. Toxicity is related to the harm to life, or damage to the organs, disordered metabolism, and hindered development. Stability is related to whether one can survive for a long time, and whether it can change in case of heat, light, and moisture. The reactive person is related to what kind of reaction it is prone to when encountering other things, such as explosion, combustion, or toxicity.
However, there is a lack of research on this thing. Without a large number of animal experiments, how can we know the geometry of its acute and slow toxicity. Without long-term environmental monitoring, Aneng knows the state of decomposition and transformation in nature, and what impact it has on the ecology. Without precise physical and chemical analysis, how can we know the details of its stability and reactivity.
To know the safety of this thing, we should do detailed experiments, collect data, and discuss it many times in accordance with today's scientific law, in order to obtain a definite theory, so as to preserve the safety of life and the environment.

I don't know if 1 - Azabicyclo [2.2.2] octan - 8 - yl (1S) -1 - phenyl - 3,4 - dihydro - 1H - isoquinoline - 2 - carboxylate butanedioic acid is in the market price range. The name of this compound is extremely diverse, and it belongs to a specific substance in the field of professional chemistry. Its price is often determined by many factors, such as purity geometry, ease of preparation, market demand, and different suppliers.
If the purity is very high, the preparation process is complicated, and the market demand is strong, the price will be high; conversely, if the purity is ordinary, the preparation is relatively simple, and the demand is small, the price will be low. However, we have not investigated the specific situation of this compound under various factors, so it is difficult to determine its price range. Or you need to ask the merchants specializing in chemical reagents, or inquire about the relevant professional chemical product trading platforms to get a more accurate price range.