Product Overview

(5S)-N-(Methoxycarbonyl)-L-valyl-5-methyl-L-proline, as a key intermediate of velpatasvir, is widely used in the synthesis process of antiviral drugs. It is an important structural unit for constructing the molecular skeleton of nucleoside drugs and is suitable for drug development, small-scale preparation, pilot-scale amplification and commercial production stages. It has good reactivity and structural stability and can effectively improve the efficiency and controllability of subsequent synthetic routes.

Applications

• Synthesis of antiviral drug intermediates
• Structural modification of nucleoside drugs
• Medicinal chemistry research and development
• Process route optimization and validation
• Customized batch production support

Quality & Supply Capability

English Name: (5S)-N-(Methoxycarbonyl)-L-valyl-5-methyl-L-proline Properties: This product is an amino acid derivative containing a chiral center, possessing a stable cyclic structure and a specific functional group distribution. It exhibits good thermal and chemical stability and is suitable for multi-step organic synthesis reactions. Storage Recommendations: Store in a sealed, light-protected, and dry place, subject to the specific 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 a full-chain supply service from laboratory samples to industrial-scale production. We can conduct small-scale preparation, pilot-scale amplification, and customized batch production according to customer needs. We also support flexible adjustments to the supply plan based on customer requirements for purity, impurity control, packaging specifications, delivery cycle, and quality documentation. We provide complete process development and technology transfer support to help customers achieve efficient transformation from R&D to industrialization.

Why Choose Bioncan

Focused on pharmaceutical intermediates, with extensive experience in nucleoside analogue synthesis. Full-scale supply capability, covering all stages from laboratory to commercial production. Provides complete quality control documentation to ensure product compliance with pharmacopoeia and industry standards. Supports customized solutions to meet the specific process requirements of different clients. Provides comprehensive process optimization and scale-up technical support to improve clients' R&D efficiency and production conversion rates.

Online Consulting

For quotation, inventory, samples, COA, MSDS, or custom synthesis support for CAS 1335316-40-9, please submit your requirements. We will respond according to purity, quantity, delivery timeline, and documentation needs.