tert-butyl (2S)-2-carbamoyl-2,3-dihydropyrrole-1-carboxylate

Ugh! The chemical structure of "tert - butyl (2S) -2 - carbamoyl - 2,3 - dihydropyrrole - 1 - carboxylate" is also quite interesting. This compound is the category of organic chemistry.
First look at "tert - butyl", that is, tert-butyl, which is a characteristic group, derived from trimethylmethane, has a three-dimensional structure and has a certain steric resistance effect.
Look at " (2S) -2 - carbamoyl" again, where " (2S) " indicates that its chiral central configuration is S-type, and "2 - carbamoyl" refers to the aminoformyl group at the second position. This group contains atoms such as nitrogen and oxygen, and has certain reactivity. It can participate in a variety of organic reactions.
As for "2,3 - dihydropyrrole - 1 - carboxylate", the 2,3 - dihydropyrrole ring is the core structure. The double bond of the pyrrole ring is partially hydrogenated to form dihydropyrrole, and the carboxylate group is connected at the 1 - position, which is in turn connected to the tert-butyl group. Overall, the structure of this compound fuses a variety of functional groups and characteristic structures, and each part interacts with each other, giving it unique chemical properties. It may have important uses in organic synthesis, medicinal chemistry, and other fields. It can be used as an intermediate to participate in the construction of complex organic molecules, or it has specific biological activities due to its special structure and chirality.

Tert-butyl (2S) -2-aminoformyl-2,3-dihydropyrrole-1-carboxylate is a significant compound in the field of organic synthesis. It has a wide range of uses and is often used as a key intermediate in the field of medicinal chemistry to help create various new drugs. Due to its unique chemical structure, complex molecular structures with biological activity can be constructed through specific chemical reactions, thus laying the foundation for the development of new drugs for the treatment of diseases.
Furthermore, in the field of materials science, it also shows potential application value. It can be used to participate in the synthesis of polymer materials with specific properties, such as those with special optical, electrical or mechanical properties, to meet the needs of many fields for special materials.
In the process of organic synthesis, this compound is often used to study novel reaction paths and methods. Chemists use various chemical modifications and reactions to explore more efficient and selective synthesis strategies to promote the progress and development of organic synthetic chemistry. The application of this compound in many fields is constantly expanding and deepening, injecting vitality into related scientific research and industrial development.

The preparation of tert-butyl (2S) -2-aminoformyl-2,3-dihydropyrrole-1-carboxylate is a common method, which is obtained by a series of delicate chemical reactions with suitable starting materials.
Starting with a pyrrole derivative with a specific configuration, its structure has a similar skeleton to the target molecule, and it has a modifiable functional group, which lays the foundation for the subsequent reaction.
First, the appropriate check point of the pyrrole ring is protected to prevent unnecessary side reactions. This step requires the selection of a specific protective group to make the reaction highly selective. Then, the carbamylation reaction is carried out for another functional group. To achieve this purpose, the aminoformylation reagent with suitable activity can be selected. Under appropriate reaction conditions, such as in a specific solvent, the temperature and reaction time can be controlled to promote the effective interaction between the reagent and the substrate, and the aminoformyl group can be introduced.
After the aminoformyl group is successfully introduced, tert-butoxycarbonyl (Boc) can be introduced. In this step, tert-butoxycarbonyl can be successfully attached to the pyrrole nitrogen atom by reacting with the tert-butoxycarbonylation reagent to generate the target (2S) -2-aminoformyl-2,3-dihydropyrrole-1-carboxylic acid tert-butyl ester.
After the reaction is completed, the separation and purification steps are required to obtain a purified product. Column chromatography or recrystallization is often used to remove impurities such as raw materials, by-products and solvents remaining in the reaction to obtain high-purity products to meet the needs of subsequent research or application. Each step of the reaction needs to be carefully controlled to obtain this compound with high yield and purity.

Tert - butyl (2S) -2 - carbamoyl - 2,3 - dihydropyrrole - 1 - carboxylate is an organic compound with many physicochemical properties.
Its properties are mostly white to off-white solids at room temperature, which is determined by the intermolecular forces and arrangements. The melting point range is about 120 - 125 ° C. When heated to this temperature range, the molecules are energized enough to overcome the lattice energy, the lattice structure disintegrates, and then the solid state is converted to liquid state.
In terms of solubility, it exhibits good solubility in organic solvents such as dichloromethane, chloroform, and tetrahydrofuran. Because these organic solvents can form interactions with the molecules of the compound, such as van der Waals forces and hydrogen bonds, which help them disperse and dissolve. However, it has little solubility in water, because the hydrophobic groups in its molecules account for a large proportion, and the force between water molecules is weak, making it difficult to dissolve with water.
In terms of stability, it is quite stable under normal storage conditions. However, in the case of strong acids and bases, chemical reactions can occur. In the case of strong acids, its amino or ester groups can be protonated, triggering reactions such as hydrolysis to cause structural changes; in the case of strong bases, ester groups are prone to hydrolysis to form corresponding alcohols and carboxylic salts.
In addition, in light or high temperature environments, degradation reactions may also occur. Light provides energy to break some chemical bonds in molecules, while high temperature accelerates the thermal motion of molecules, increases the chance of collision between molecules, and prompts chemical reactions to occur, affecting their chemical structure and purity.

What Guanjun is asking is about "tert - butyl (2S) -2 - carbamoyl - 2,3 - dihydropyrrole - 1 - carboxylate" in the market price range. However, the market price of this product often changes due to various reasons, and it is difficult to determine its fixed number.
First, the quality of the product, the high purity, the price must be higher than the slightly inferior one. Pure ones can be used in high-end experiments or special processes, and those who need them are willing to pay a high price.
Second, the situation of supply and demand is also the key. If there are many people who ask for it at one time, and the supply is limited, the price will rise; on the contrary, if the supply exceeds the demand, the price may drop.
Third, the difference between manufacturers also results in price differences. Well-known large factories, due to their brand reputation and strict quality control, their prices may be higher than other factories.
Fourth, the amount of purchase also affects the price. Bulk buyers often receive discounts due to large quantities, and the unit price is lower; small purchases, the price may be higher.
To sum up, if you want to know the exact price range of this product, you should consult chemical material suppliers or refer to the latest market of chemical trading platforms to get a more accurate price.