The product, Factory Supply (S)-(-)-1-tert-Butoxycarbonyl-3-aminopyrrolidine with CAS 147081-44-5, is a high - quality chemical compound. The CAS number, 147081 - 44 - 5, serves as a unique identifier in the chemical world, allowing for easy reference and tracking in scientific research, industry applications, and regulatory compliance. Its chiral purity, being the (S)-(-) isomer, is a crucial characteristic, as chirality can significantly affect the compound's biological activity and chemical reactivity.
When it comes to price, it offers a competitive edge in the market, making it an attractive option for various users, from academic research institutions to large - scale pharmaceutical manufacturers. The factory - supply nature of this product ensures a stable and reliable source, which is essential for continuous production processes.
This compound has a wide range of applications in the pharmaceutical and chemical industries. In pharmaceutical research, it can serve as a building block for the synthesis of new drugs. The amino - pyrrolidine structure provides a versatile platform for further chemical modifications, enabling the creation of compounds with specific biological activities, such as antibacterial, antiviral, or anticancer properties. For example, it can be used in the development of novel central nervous system (CNS) agents, as the pyrrolidine ring is often found in many CNS - active drugs.
In the chemical industry, it can be used in the synthesis of specialty chemicals. It can participate in various chemical reactions, such as nucleophilic substitution and amide bond formation, to produce high - value - added products. Additionally, it can be used as a chiral ligand in asymmetric catalysis, facilitating the production of enantiomerically pure compounds, which are in high demand in the fine - chemical and pharmaceutical sectors.
When using (S)-(-)-1-tert-Butoxycarbonyl-3-aminopyrrolidine, proper handling procedures must be followed. First, it should be stored in a cool, dry place away from direct sunlight and sources of heat. The storage container should be tightly sealed to prevent moisture and air from entering, as this can potentially degrade the compound.
During the synthesis process, appropriate protective equipment, such as gloves, goggles, and a lab coat, should be worn. The compound should be added to the reaction mixture slowly and under controlled conditions, taking into account the reaction's exothermic or endothermic nature. It is also important to monitor the reaction progress using analytical techniques, such as thin - layer chromatography (TLC) or nuclear magnetic resonance (NMR) spectroscopy, to ensure the desired product is being formed.
Case 1: A pharmaceutical research company was working on the development of a new antidepressant drug. They used (S)-(-)-1-tert-Butoxycarbonyl-3-aminopyrrolidine as a key building block. By modifying the pyrrolidine ring, they were able to introduce specific functional groups that interacted with neurotransmitter receptors in the brain. After several rounds of synthesis and biological testing, they successfully obtained a compound with promising antidepressant activity. In pre - clinical trials, the compound showed significant improvement in animal models of depression, demonstrating the potential of this compound in drug discovery.
Case 2: A chemical manufacturing company was interested in producing a chiral intermediate for a high - value fine chemical. They employed (S)-(-)-1-tert-Butoxycarbonyl-3-aminopyrrolidine as a chiral ligand in an asymmetric catalytic reaction. By optimizing the reaction conditions, they were able to achieve a high enantiomeric excess (ee) of the product, which was crucial for the subsequent steps in the synthesis. This not only increased the overall yield of the final product but also reduced the production cost, as less purification was required.
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