S Tert Butyl 2 5 4 Iodophenyl 1h Imidazol 2 Yl Pyrrilidine 1 Carboxylate

You are inquiring about the chemical structure of " (s) -tert-butyl 2- (5 - (4 - iodophenyl) -1h - imidazol - 2 - yl) pyrrilidine - 1 - carboxylate", which is a question related to the structure of organic compounds. Its structure analysis depends on the naming rules and structural characterization knowledge of organic chemistry.
In this compound nomenclature, " (s) " means that the chiral central configuration is S-type. "Tert-butyl" is tert-butyl, which is a branched alkyl group containing four carbons, and its structure is -C (CH). " 2 - (5 - (4 - iodophenyl) -1h - imidazol - 2 - yl) "part," 1h - imidazol - 2 - yl "refers to imidazole - 2 - group, imidazole is a five-membered heterocyclic ring containing two nitrogen atoms." 5 - (4 - iodophenyl) "indicates that there is a 4 - iodophenyl group in the 5 position of the imidazole ring, and the 4 - iodophenyl group is replaced by an iodine atom at the 4 position of the phenyl ring." Pyrrilidine-1-carboxylate "refers to pyrrolidine-1-carboxylate. Pyrrolidine is a five-membered heterocyclic ring containing one nitrogen atom, and the one position is connected with a carboxylate structure.
The structure of this compound is composed of a pyrrolidine ring as the core, with a tert-butyl carboxylate ester group in one position and an imidazole group containing an iodine-substituted phenyl group in the second position. Its structure is complex, and each group is connected to each other to form a unique spatial structure. Nitrogen-containing heterocyclic rings, benzene rings and iodine atoms endow it with specific chemical and physical properties. Its structure is of great significance for its application in organic

(S) -tert-butyl2- (5- (4-iodophenyl) -1H-imidazole-2-yl) pyrrolidine-1-carboxylate, which has a wide range of uses. In the field of medicinal chemistry, it is often a key intermediate for the creation of new drugs. Due to its unique molecular structure, it can closely fit with specific biological targets, helping to develop specific drugs for specific diseases, such as anti-cancer, anti-virus and the like.
In the field of organic synthesis, it also plays an important role. It can be used as a key building block to build complex organic compounds with the help of various organic reactions, such as coupling reactions, cyclization reactions, etc., laying the foundation for the synthesis of materials with specific properties and functions. At the same time, in materials science, materials prepared from this raw material may have unique electrical, optical or mechanical properties, making them stand out in electronic devices, optical materials, etc., and are expected to promote technological innovation and development in related fields.

To prepare (S) -tert-butyl2- (5- (4-iodophenyl) -1H-imidazole-2-yl) pyrrolidine-1-carboxylate, the following method can be followed.
First take suitable starting materials, such as pyrrolidine derivatives with specific chirality. The chiral central configuration of this derivative should be (S) type to ensure the correct chirality of the product. At the same time, another compound containing 5- (4-iodophenyl) -1H-imidazole-2-yl structure is prepared.
Then the two are reacted. During the reaction process, attention should be paid to the control of the reaction conditions. The temperature should be maintained within a certain moderate range. If the temperature is too high, it may cause side reactions to multiply and the purity of the product will be damaged. If the temperature is too low, the reaction rate will be slow and the time will be too long. In this reaction, a specific catalyst may be added to promote the reaction and make the reaction more efficient. The amount of catalyst also needs to be precisely controlled, and too much or too little may affect the reaction effect.
The choice of reaction solvent is also key. The selected solvent should be able to dissolve the reactants well and have no adverse effects on the reaction. Common organic solvents, such as dichloromethane, N, N-dimethylformamide, etc., may be selected after testing.
After the reaction is completed, the product needs to be separated and purified. Column chromatography can be used to select the appropriate stationary phase and mobile phase, and the separation of products and impurities can be achieved by the difference in the partition coefficients between the stationary phase and the mobile phase of different substances. Or supplemented by recrystallization, the purity of the product can be further improved according to the characteristics of the solubility of the product and impurities in different solvents changing with temperature.
After such steps, careful operation and fine control of each link, it is expected to obtain high-purity (S) -tert-butyl2- (5- (4-iodophenyl) -1H-imidazole-2-yl) pyrrolidine-1-carboxylate.

(S) -tert-butyl2- (5- (4-iodophenyl) -1H-imidazole-2-yl) pyrrolidine-1-carboxylic acid ester, which is an organic compound. Its physical properties are unique, related to the existence of substances, melting point, solubility, etc., and are quite important in chemical research and application.
First, the appearance is often solid powder, white and pure, delicate and uniform, which is due to the interaction and orderly arrangement of molecules. Its melting point, after precise determination, is about a certain temperature range. At this temperature, the molecule can break through the lattice binding and turn from solid to liquid state. The melting point is the key basis for the identification and purification of this compound.
Besides, the solubility is quite good in common organic solvents such as dichloromethane and chloroform. Because its molecular structure contains specific functional groups, it can form suitable interactions with organic solvent molecules, such as van der Waals force, hydrogen bonds, etc., to promote dissolution. However, the solubility in water is poor, because the hydrophobic part of the molecule accounts for a large proportion, and the interaction with water molecules is weak, making it difficult to disperse in the aqueous phase.
In addition, the density of the compound is also an important physical property. Although the specific value needs to be determined by precise experiments, it is speculated that the density may be within a certain range according to the structure and similar compounds, which is related to the molecular weight and the degree of packing.
Its vapor pressure is extremely low, and it evaporates slowly at room temperature. Due to the strong intermolecular force, it requires high energy for molecules to break away from the condensed phase and enter the gas phase.
In summary, the physical properties of (s) -tert-butyl2- (5- (4-iodophenyl) -1H-imidazole-2-yl) pyrrolidine-1-carboxylic acid esters, such as appearance, melting point, solubility, density and vapor pressure, are of great significance for their applications in organic synthesis, drug development and other fields. Therefore, researchers can better control their reaction conditions and application scenarios.

Nowadays, (S) -tert-butyl2- (5- (4-iodophenyl) -1H-imidazole-2-yl) pyrrolidine-1-carboxylate is an organic compound. Looking at its market prospects, it can be said that opportunities and challenges coexist.
In terms of demand, the field of pharmaceutical research and development may have a need for it. In the creation of new drugs, such compounds with specific structures may serve as key intermediates. Through delicate chemical reactions, molecular structures with unique pharmacological activities can be constructed to deal with many difficult diseases, such as some intractable tumor diseases or neurodegenerative diseases. Therefore, their demand at the forefront of medical research may grow.
However, the road to marketing activities has also been bumpy. The synthesis process of this compound may be complicated and costly. During synthesis, harsh reaction conditions may be required, such as precise temperature control, specific catalysts, and rare raw materials, which all cause production costs to rise, causing many companies to hesitate before large-scale production.
Furthermore, similar competitors are also obstacles to their market expansion. The field of chemical synthesis is changing with each passing day, or compounds with similar structures and similar properties have come out. In the competition for market share, (S) -tert-butyl2- (5- (4-iodophenyl) -1H-imidazole-2-yl) pyrrolidine-1-carboxylate must demonstrate its unique advantages in order to gain a place.
But overall, if it can break through the bottleneck of the synthesis process, reduce costs, and prove its unique value in pharmaceutical research and development, its market prospect is also promising, or it can bloom in the stage of pharmaceutical chemical industry.