(S)-2-((tert-Butoxycarbonyl)amino)-3-(2-nitrophenyl)propanoic acid
97%
- Product Code: 38087
CAS:
185146-84-3
| Molecular Weight: | 310.30 g./mol | Molecular Formula: | C₁₄H₁₈N₂O₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01317708 | |
| Melting Point: | Boiling Point: | 488°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily utilized in the synthesis of peptides and pharmaceuticals, where it serves as a protected amino acid derivative. The tert-butoxycarbonyl (Boc) group acts as a protective moiety for the amino group, ensuring selectivity during chemical reactions. Its nitrophenyl component can be involved in further functionalization or as a precursor for more complex molecules. It is often employed in organic and medicinal chemistry research for developing drug candidates, particularly in the creation of enzyme inhibitors or receptor-targeting agents. The compound’s structure allows for controlled deprotection and modification, making it valuable in multi-step synthetic processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,368.00 |
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| 1.000 | 10-20 days | ฿3,429.00 |
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| 5.000 | 10-20 days | ฿17,154.00 |
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| 10.000 | 10-20 days | ฿32,886.00 |
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(S)-2-((tert-Butoxycarbonyl)amino)-3-(2-nitrophenyl)propanoic acid
This compound is primarily utilized in the synthesis of peptides and pharmaceuticals, where it serves as a protected amino acid derivative. The tert-butoxycarbonyl (Boc) group acts as a protective moiety for the amino group, ensuring selectivity during chemical reactions. Its nitrophenyl component can be involved in further functionalization or as a precursor for more complex molecules. It is often employed in organic and medicinal chemistry research for developing drug candidates, particularly in the creation of enzyme inhibitors or receptor-targeting agents. The compound’s structure allows for controlled deprotection and modification, making it valuable in multi-step synthetic processes.
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