N-Cbz-DL-Tryptophan
≥98%
- Product Code: 105846
CAS:
13058-16-7
| Molecular Weight: | 338.36 g./mol | Molecular Formula: | C₁₉H₁₈N₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00069707 | |
| Melting Point: | 170 °C | Boiling Point: | 619.1ºC |
| Density: | 1.341g/cm3 | Storage Condition: | 2-8ºC |
Product Description:
N-Cbz-DL-Tryptophan is widely used in peptide synthesis as a protecting group for the amino acid tryptophan. The Cbz (carbobenzyloxy) group shields the amine functionality during the synthesis process, preventing unwanted reactions and ensuring the correct sequence of amino acids. This protection is crucial in the production of complex peptides and proteins, particularly in pharmaceutical research and development. After the peptide chain is assembled, the Cbz group can be selectively removed under mild conditions, revealing the free amine group for further modifications or final product formation. Its application is essential in the synthesis of bioactive peptides, hormones, and other therapeutic agents, contributing significantly to advancements in medicinal chemistry and drug discovery.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿315.00 |
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N-Cbz-DL-Tryptophan
N-Cbz-DL-Tryptophan is widely used in peptide synthesis as a protecting group for the amino acid tryptophan. The Cbz (carbobenzyloxy) group shields the amine functionality during the synthesis process, preventing unwanted reactions and ensuring the correct sequence of amino acids. This protection is crucial in the production of complex peptides and proteins, particularly in pharmaceutical research and development. After the peptide chain is assembled, the Cbz group can be selectively removed under mild conditions, revealing the free amine group for further modifications or final product formation. Its application is essential in the synthesis of bioactive peptides, hormones, and other therapeutic agents, contributing significantly to advancements in medicinal chemistry and drug discovery.
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