(S)-Methyl 4-amino-2-((tert-butoxycarbonyl)amino)-4-oxobutanoate
97%
- Product Code: 38519
CAS:
124842-28-0
| Molecular Weight: | 246.2603 g./mol | Molecular Formula: | C₁₀H₁₈N₂O₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08275816 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the synthesis of peptides and complex organic molecules, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of bioactive compounds and active pharmaceutical ingredients (APIs). Its structure, featuring both Boc-protected amino and ester functional groups, makes it valuable in controlled chemical reactions, ensuring selective modifications during multi-step synthesis. It is often employed in the development of drugs targeting neurological disorders, cancer, and metabolic diseases, where precise molecular design is critical. Additionally, it is used in research laboratories for studying enzymatic processes and protein interactions due to its stability and reactivity in biochemical environments.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,627.00 |
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(S)-Methyl 4-amino-2-((tert-butoxycarbonyl)amino)-4-oxobutanoate
This compound is primarily utilized in the synthesis of peptides and complex organic molecules, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of bioactive compounds and active pharmaceutical ingredients (APIs). Its structure, featuring both Boc-protected amino and ester functional groups, makes it valuable in controlled chemical reactions, ensuring selective modifications during multi-step synthesis. It is often employed in the development of drugs targeting neurological disorders, cancer, and metabolic diseases, where precise molecular design is critical. Additionally, it is used in research laboratories for studying enzymatic processes and protein interactions due to its stability and reactivity in biochemical environments.
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