N-Carbobenzyloxy-L-valine: A Key Intermediate for Antiviral Drug Synthesis
Unlock advanced pharmaceutical synthesis with this high-purity chiral amino acid derivative, crucial for antiviral drug development.
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N-Carbobenzyloxy-L-valine
This compound is a vital chiral amino acid derivative, widely recognized for its critical role as an intermediate in the synthesis of essential pharmaceuticals. Its N-Carbobenzyloxy protection group facilitates controlled reactions, making it indispensable for constructing complex drug molecules.
- Leveraging the CAS 1149-26-4 number, we can ensure precise identification for your pharmaceutical intermediate needs.
- As a key component in peptide synthesis, its high purity (≥99.0%) ensures reliable outcomes in complex reaction sequences.
- The chiral nature of this amino acid derivative is fundamental for stereoselective synthesis of enantiomerically pure drug compounds.
- Discover the versatility of N-Carbobenzyloxy-L-valine as a building block for creating advanced antiviral drug candidates.
Key Advantages
Enhanced Bioavailability in Prodrugs
N-Carbobenzyloxy-L-valine is instrumental in creating prodrugs like Valaciclovir, significantly improving oral absorption and therapeutic efficacy.
Controlled Synthesis Pathways
The Cbz group offers robust protection, enabling precise control over chemical transformations in multi-step drug synthesis.
Stereochemical Integrity
Utilize this chiral amino acid derivative to maintain stereochemical purity, essential for enantiomerically specific drug actions.
Key Applications
Antiviral Drug Synthesis
A critical intermediate in the production of Valaciclovir and Valganciclovir, essential for treating viral infections.
Peptide Synthesis
Serves as a fundamental building block for creating complex peptides used in various therapeutic areas.
Pharmaceutical Intermediate Manufacturing
Its high purity and chemical stability make it ideal for large-scale production of Active Pharmaceutical Ingredients (APIs).
Drug Discovery Research
Used in the synthesis of novel compounds and libraries for screening potential drug candidates, contributing to new therapeutic developments.