O-Benzyl-L-serine (CAS 4726-96-9) is more than just a chemical compound; it's a valuable tool that empowers scientific discovery across various disciplines. For research and development scientists, understanding the capabilities and applications of such specialized amino acid derivatives can unlock new possibilities in their work. This article explores the scientific significance of O-Benzyl-L-serine, highlighting its roles in biochemical studies and organic synthesis, and guiding researchers on where to effectively buy this essential compound.

At its core, O-Benzyl-L-serine is an L-serine derivative where the hydroxyl group is protected by a benzyl ether. This structural modification is critical for its use in complex chemical reactions. In biochemical studies, researchers leverage this protection to selectively manipulate other functional groups or to control the reactivity of the serine residue during protein or peptide synthesis. The benzyl group is relatively stable under many reaction conditions but can be cleaved selectively later in the synthesis process, typically via hydrogenolysis, making it a versatile protecting group.

The applications in R&D are diverse. Scientists utilize O-Benzyl-L-serine in the synthesis of specific peptide sequences that are designed to mimic natural proteins or to act as therapeutic agents. For instance, in the development of enzyme inhibitors or receptor agonists, precise control over the amino acid sequence and side-chain modifications is crucial. The ability to reliably purchase O-Benzyl-L-serine from a trusted supplier ensures that these complex synthetic strategies can be executed with confidence. Its use is also prevalent in academic research focused on understanding protein-ligand interactions and enzyme mechanisms.

Beyond biochemical applications, O-Benzyl-L-serine serves as a chiral building block in advanced organic synthesis. Its defined stereochemistry (L-configuration) makes it valuable for creating enantiomerically pure target molecules. For organic chemists, having access to high-quality derivatives like this from a dependable manufacturer is essential for ensuring the stereochemical integrity of their final products. The molecular formula C10H13NO3 and molecular weight of 195.22 are fundamental properties, but its chemical reactivity and protective group strategy are what truly define its scientific utility.

For researchers requiring O-Benzyl-L-serine for their R&D projects, sourcing from a reputable chemical company is vital. Whether you are in a university lab or a pharmaceutical R&D department, ensuring the consistent quality and availability of CAS 4726-96-9 will directly impact the success of your experiments. We invite you to explore our offerings and learn more about obtaining this critical reagent. Understanding the price and availability from reliable sources can help optimize research budgets and accelerate discovery timelines.

In essence, O-Benzyl-L-serine is a testament to the power of chemical modification in facilitating scientific advancement. Its specific properties make it an invaluable component for scientists pushing the boundaries in peptide chemistry, drug discovery, and organic synthesis. By choosing the right supplier, researchers can confidently integrate this versatile derivative into their groundbreaking work.