(S)-Benzyl 4-amino-2-((tert-butoxycarbonyl)amino)-4-oxobutanoate
97%
- Product Code: 50212
CAS:
13512-57-7
| Molecular Weight: | 322.36 g./mol | Molecular Formula: | C₁₆H₂₂N₂O₅ |
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| EC Number: | MDL Number: | MFCD00190784 | |
| Melting Point: | Boiling Point: | 538.6°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
Used in the synthesis of peptides and pharmaceutical intermediates, particularly in the production of chiral compounds. It serves as a key building block in the development of active pharmaceutical ingredients (APIs) due to its ability to introduce specific amino acid structures. Commonly employed in medicinal chemistry for designing drugs with targeted biological activities, such as enzyme inhibitors or receptor modulators. Its protective groups, like the tert-butoxycarbonyl (Boc) group, enable selective reactions during complex organic syntheses.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | €21.84 |
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| 0.250 | 10-20 days | €32.77 |
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| 1.000 | 10-20 days | €81.92 |
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| 5.000 | 10-20 days | €248.12 |
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(S)-Benzyl 4-amino-2-((tert-butoxycarbonyl)amino)-4-oxobutanoate
Used in the synthesis of peptides and pharmaceutical intermediates, particularly in the production of chiral compounds. It serves as a key building block in the development of active pharmaceutical ingredients (APIs) due to its ability to introduce specific amino acid structures. Commonly employed in medicinal chemistry for designing drugs with targeted biological activities, such as enzyme inhibitors or receptor modulators. Its protective groups, like the tert-butoxycarbonyl (Boc) group, enable selective reactions during complex organic syntheses.
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