(S)-(-)-4-Isobutyl-5,5-diphenyl-2-oxazolidinone

Introducing (S)-(-)-4-Isobutyl-5,5-diphenyl-2-oxazolidinone, a versatile and highly pure chemical compound that holds immense potential for researchers and scientists across various fields. With its unique structural features and exceptional quality, this Oxazolidinone derivative is poised to unlock new possibilities in pharmaceutical development, organic synthesis, and beyond.

At the heart of this compound lies a captivating molecular structure, characterized by the presence of an isobutyl group, two phenyl rings, and an oxazolidinone core. This intricate arrangement of atoms not only bestows it with distinct physical and chemical properties but also endows it with a remarkable level of versatility. The (S)-configuration of the chiral center further enhances the compound's utility, allowing for the selective synthesis of targeted molecules with enhanced biological activity or desired properties.

Pharmaceutical Applications

In the realm of pharmaceutical research, (S)-(-)-4-Isobutyl-5,5-diphenyl-2-oxazolidinone shines as a valuable building block. Its unique structural features make it an essential component in the development of innovative drug candidates, particularly those targeting neurological disorders, metabolic conditions, and a wide range of other therapeutic areas. Researchers can leverage the compound's inherent reactivity and stereochemistry to design and synthesize novel pharmaceutical compounds with improved pharmacological profiles, enhanced potency, and increased selectivity.

The compound's versatility extends beyond its use as a starting material, as it can also serve as a chiral auxiliary or a key intermediate in the synthesis of more complex pharmaceutical molecules. This versatility allows researchers to explore diverse synthetic pathways, ultimately leading to the creation of novel therapeutic solutions that can positively impact patient lives.

Organic Synthesis and Chemical Applications

Beyond the pharmaceutical realm, (S)-(-)-4-Isobutyl-5,5-diphenyl-2-oxazolidinone finds its place as a valuable tool in the world of organic synthesis and chemical research. Its unique structural features, including the presence of the isobutyl group and the two phenyl rings, make it a highly reactive and selective reagent in a wide range of chemical transformations.

Chemists and organic synthesis experts can leverage the compound's reactivity to construct more complex molecules with tailored properties, such as improved stability, enhanced reactivity, or increased selectivity. This versatility opens up new avenues for the development of advanced materials, functional molecules, and other innovative chemical products that can address the evolving needs of various industries.

Quality and Purity

At the core of (S)-(-)-4-Isobutyl-5,5-diphenyl-2-oxazolidinone's value lies its exceptional quality and purity. Meticulously synthesized and rigorously tested, this compound boasts a purity level of 97%, ensuring reliable and consistent results in research and development applications. Its CAS number, 191090-34-3, and MDL number, MFCD03093532, provide unique identifiers that allow researchers to easily track and reference this valuable chemical asset.

To maintain the compound's integrity and stability, it is recommended to store (S)-(-)-4-Isobutyl-5,5-diphenyl-2-oxazolidinone in a cool, dry, and well-ventilated environment, away from direct light exposure. Proper handling and storage protocols are crucial to preserve the compound's exceptional quality and ensure its long-term viability in your research endeavors.

Unlock the Potential

As you embark on your research journey, let (S)-(-)-4-Isobutyl-5,5-diphenyl-2-oxazolidinone be your trusted companion. This versatile compound, with its unique structural features and exceptional purity, holds the key to unlocking new possibilities in the realms of pharmaceutical development, organic synthesis, and beyond. Explore its diverse applications, leverage its inherent reactivity, and let it inspire your next groundbreaking discovery. The