Product Overview

N-[(2R,3S)-2-(2,5-difluorophenyl)tetrahydro-5-oxo-2H-pyran-3-yl]carbamate, 1,1-dimethylethyl ester, is an important pharmaceutical intermediate widely used in the synthesis of innovative drugs such as antiviral and antitumor agents. This compound possesses a well-defined stereochemical structure and stable functional groups, making it suitable for key steps in drug molecule construction. It can support the entire process from laboratory research and development to pilot-scale amplification and commercial production, meeting the customized requirements of pharmaceutical companies for high-purity, high-quality intermediates.

Applications

• Antiviral drug synthesis
• Preparation of antitumor drug precursors
• Chemical modification and structural optimization studies
• Drug molecule skeleton construction
• Process route development and optimization

Quality & Supply Capability

English Name: tert-butyl [(2R,3S)-2-(2,5-difluorophenyl)-5-oxotetrahydro-2H-pvran-3yl]carbamate Properties: This product is a fluorinated heterocyclic carbamate compound with good thermal and chemical stability. Its core functional groups include a tetrahydropyran ring, difluorophenyl, and carbamate groups, making it suitable for various organic synthesis reactions. Storage Recommendations: Store in a sealed, light-protected, and dry place, subject to the COA/MSDS. Supply Capabilities: Samples, gram-level, kilogram-level, commercial batches. Packaging Specifications: Aluminum foil bags, fluorinated bottles, cardboard drums, customized packaging. Document Support: COA, MSDS, HPLC, NMR, etc. We provide sample supply, small-scale preparation, pilot-scale amplification, and customized batch production services. We can flexibly adjust the supply plan according to customer requirements for purity, impurity control, packaging specifications, delivery cycle, and quality documentation. Meanwhile, we have a professional technical support team that follows up on the entire process from laboratory research and development to large-scale production, helping customers advance process development, route optimization and project transformation, and ensuring efficient and compliant completion of the entire life cycle management of drug intermediates.

Why Choose Bioncan

Focused on pharmaceutical intermediates, possessing extensive synthesis experience and technological expertise. Full-scale supply capability, covering needs from laboratory to commercial production. Provides complete quality control documentation to ensure product compliance with GMP and industry standards. Supports customized requirements, adjusting purity, impurity control, and packaging specifications as needed. Supports process optimization technology to help customers improve synthesis efficiency and yield. Comprehensive project scale-up support services to ensure seamless transition from R&D to mass production.

Online Consulting

For quotation, inventory, samples, COA, MSDS, or custom synthesis support for CAS 951127-25-6, please submit your requirements. We will respond according to purity, quantity, delivery timeline, and documentation needs.