(S)-Benzyl (1-amino-4-methyl-1-oxopentan-2-yl)carbamate
97%
- Product Code: 37820
CAS:
4801-79-0
| Molecular Weight: | 264.32 g./mol | Molecular Formula: | C₁₄H₂₀N₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00080252 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily utilized in the field of peptide synthesis, where it serves as a protective group for amino acids. It is particularly effective in safeguarding the amine functionality during the synthesis process, ensuring that reactions occur selectively at desired sites. Its stability under various reaction conditions makes it a valuable tool in the production of complex peptides and proteins. Additionally, it is employed in the development of pharmaceutical compounds, where precise control over molecular structure is crucial for achieving the desired therapeutic effects. Its application extends to research laboratories focused on organic chemistry and biochemistry, aiding in the study of peptide interactions and enzyme mechanisms.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | €112.78 |
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| 5.000 | 10-20 days | €225.80 |
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| 10.000 | 10-20 days | €322.68 |
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(S)-Benzyl (1-amino-4-methyl-1-oxopentan-2-yl)carbamate
This compound is primarily utilized in the field of peptide synthesis, where it serves as a protective group for amino acids. It is particularly effective in safeguarding the amine functionality during the synthesis process, ensuring that reactions occur selectively at desired sites. Its stability under various reaction conditions makes it a valuable tool in the production of complex peptides and proteins. Additionally, it is employed in the development of pharmaceutical compounds, where precise control over molecular structure is crucial for achieving the desired therapeutic effects. Its application extends to research laboratories focused on organic chemistry and biochemistry, aiding in the study of peptide interactions and enzyme mechanisms.
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