Discover the exceptional versatility of rac-tert-Butyl (3R,5R)-3-amino-5-fluoropiperidine-1-carboxylate, a premium-quality chemical compound with a CAS number of 1638772-27-6. This fluorinated piperidine derivative boasts a molecular weight of 218.27g/mol and a melting point of 67°C, making it a valuable asset for your advanced research and development projects.
Crafted with meticulous attention to detail, this compound offers a purity of at least 95%, ensuring consistent and reliable results in your experiments. Its unique chemical structure, featuring a fluorine atom and an amino group, unlocks a world of possibilities in the fields of pharmaceuticals, agrochemicals, and beyond. Harness the power of this exceptional building block to elevate your scientific endeavors to new heights.
Unlock the versatile potential of rac-tert-Butyl (3R,5R)-3-amino-5-fluoropiperidine-1-carboxylate, a highly specialized chemical compound that holds immense value for researchers and scientists across diverse fields. This Fluorinated Compound, identified by its CAS number 1638772-27-6, boasts a unique molecular structure that enables a wide range of applications, from pharmaceutical development to material science innovations.
rac-tert-Butyl (3R,5R)-3-amino-5-fluoropiperidine-1-carboxylate presents itself as a high-quality chemical, with a purity of at least 95%. Its molecular formula, C10H19FN2O2, and a molecular weight of 218.27 g/mol, provide a clear chemical identity. The compound's melting point of 67°C and its MDL number, MFCD28987727, further contribute to its precise characterization.
This Fluorinated Compound's exceptional purity and well-defined technical specifications make it a reliable and trustworthy choice for researchers seeking to push the boundaries of scientific discovery.
rac-tert-Butyl (3R,5R)-3-amino-5-fluoropiperidine-1-carboxylate is a versatile chemical that finds its applications in various scientific domains, each offering unique opportunities for innovation and advancement.
In the realm of pharmaceutical research, this compound serves as a valuable building block in the synthesis of novel drug candidates. Its fluorinated piperidine moiety and carboxylate functionality provide a versatile platform for the development of targeted therapies addressing a wide range of health conditions, from neurological disorders to metabolic diseases. Researchers can leverage the compound's distinct properties to unlock new possibilities in the quest for more effective and safer pharmaceutical solutions.
The agricultural industry also benefits from the unique properties of rac-tert-Butyl (3R,5R)-3-amino-5-fluoropiperidine-1-carboxylate. This compound serves as a crucial building block in the synthesis of advanced crop protection agents, such as pesticides and herbicides. Its fluorinated structure and specific functional groups contribute to the development of more potent and selective agrochemicals, helping to safeguard crops, enhance yields, and minimize environmental impact.
Beyond the pharmaceutical and agrochemical realms, rac-tert-Butyl (3R,5R)-3-amino-5-fluoropiperidine-1-carboxylate finds applications in the field of material science. Researchers in this domain utilize the compound's unique properties to engineer novel materials with enhanced performance characteristics, such as improved thermal stability, mechanical strength, or optical properties. These advancements can lead to the creation of cutting-edge products with diverse applications, from advanced coatings to high-performance composites.
To ensure the long-term stability and integrity of rac-tert-Butyl (3R,5R)-3-amino-5-fluoropiperidine-1-carboxylate, it is essential to follow proper handling and storage guidelines. The compound should be stored in a cool, well-ventilated area, protected from moisture and direct sunlight. Appropriate personal protective equipment, such as gloves and eye protection, should be used when handling the material to minimize the risk of exposure.
Embrace the versatility of rac-tert-Butyl (3R,5R)-3-amino-5-fluoropiperidine-1-carboxylate and unlock new possibilities in your research and development endeavors