N-Cbz-N-methyl-L-isoleucine: Your Key to Advanced Pharmaceutical Synthesis
A high-purity amino acid derivative essential for pharmaceutical intermediates and peptide synthesis.
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N-Cbz-N-methyl-L-isoleucine
N-Cbz-N-methyl-L-isoleucine is a critical amino acid derivative that serves as a vital building block in the complex world of pharmaceutical synthesis. With a high purity of u226598.0%, it is meticulously produced to meet the stringent demands of drug development and peptide synthesis.
- Discover the utility of this amino acid derivative synthesis for creating novel therapeutic compounds.
- Leverage N-Cbz-N-methyl-L-isoleucine as a versatile peptide synthesis building block in your research.
- Ensure reliable drug development compound sourcing with our high purity intermediates.
- Explore the wide range of chemical synthesis applications for this essential intermediate.
Advantages of Using N-Cbz-N-methyl-L-isoleucine
Exceptional Purity
Achieve consistent and reproducible results in your chemical synthesis applications with our N-Cbz-N-methyl-L-isoleucine, boasting u226598.0% assay.
Versatile Applications
This amino acid derivative is a cornerstone for peptide synthesis, offering a reliable peptide synthesis building block for complex molecules.
Enhanced Stability
Benefit from the inherent stability of this compound, ensuring its integrity throughout your drug development compound synthesis processes.
Key Applications
Pharmaceutical Intermediates
As a key pharmaceutical intermediate, N-Cbz-N-methyl-L-isoleucine is indispensable for synthesizing active pharmaceutical ingredients (APIs) and complex drug molecules.
Peptide Synthesis
Its role as a protected amino acid makes it a crucial component in solid-phase and solution-phase peptide synthesis, enabling the creation of therapeutic peptides.
Drug Development
Researchers utilize this compound in the early stages of drug discovery, leveraging its specific structure for creating novel drug candidates.
Chemical Synthesis
Beyond pharmaceuticals, it finds use in various organic synthesis pathways where a protected, chiral amino acid derivative is required.