(4S)-4-benzyl-1,3-oxazolidine-2,5-dione: A Key Chiral Intermediate for Pharmaceutical and Polymer Synthesis

(4S)-4-benzyl-1,3-oxazolidine-2,5-dione (CAS: 14825-82-2) stands as a cornerstone chiral building block, indispensable for crafting high-value pharmaceutical intermediates and advanced polymeric materials. Its unique stereochemical properties enable precise control in complex organic synthesis, making it a sought-after compound for manufacturers and researchers worldwide.

Get a Quote & Sample

Advantages of Sourcing Our Chiral Intermediates

Unmatched Stereochemical Control

Leverage the inherent chirality of (4S)-4-benzyl-1,3-oxazolidine-2,5-dione to achieve superior diastereoselectivity in your synthetic routes, minimizing unwanted byproducts and simplifying purification for your pharmaceutical intermediates.

Broad Synthetic Applicability

From aldol condensations and alkylations to polymerization, this compound is a versatile tool for organic chemists, empowering innovation in drug discovery and material science. Explore purchase options for your next project.

Consistent Quality & Availability

As a leading supplier, we guarantee consistent product quality and stable availability of (4S)-4-benzyl-1,3-oxazolidine-2,5-dione, ensuring uninterrupted production for your manufacturing needs.

Key Applications Driving Innovation

Pharmaceutical Synthesis

Essential for the stereoselective synthesis of complex APIs and drug candidates, including antibiotics and antiviral agents. Inquire about bulk purchase options and competitive pricing for your R&D pipeline.

Polymer Chemistry

Serves as a vital monomer in ring-opening polymerization, enabling the creation of advanced polypeptides and copolymers for drug delivery systems and biomaterials. Contact us for supplier information.

Chiral Auxiliary in Organic Synthesis

Facilitates highly enantioselective C-C bond formations, natural product synthesis, and the construction of complex chiral molecules. Request a free sample to test its efficacy.

Biochemical Research Tools

Used as a model compound for hydrogen bonding studies and as a substrate in enzyme activity research, furthering our understanding of biological processes.