Methyl 2-(4-bromobenzyl)-3-((tert-butoxycarbonyl)amino)propanoate
≥95%
- Product Code: 41684
CAS:
886366-46-7
| Molecular Weight: | 372.25 g./mol | Molecular Formula: | C₁₆H₂₂BrNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08061215 | |
| Melting Point: | Boiling Point: | 458.8±40.0°C at 760 mmHg | |
| Density: | 1.298g/cm3 | Storage Condition: | Room temperature, dry and sealed |
Product Description:
This compound is primarily utilized in organic synthesis as a key intermediate in the production of more complex molecules, particularly in pharmaceutical research. It serves as a building block for the development of peptide-based drugs, where the tert-butoxycarbonyl (Boc) group acts as a protective group for the amine functionality during synthesis. The presence of the bromobenzyl moiety allows for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical structures. Its application is significant in the design and synthesis of bioactive compounds, including potential therapeutic agents targeting specific biological pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | £131.50 |
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| 0.250 | 10-20 days | £263.19 |
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Methyl 2-(4-bromobenzyl)-3-((tert-butoxycarbonyl)amino)propanoate
This compound is primarily utilized in organic synthesis as a key intermediate in the production of more complex molecules, particularly in pharmaceutical research. It serves as a building block for the development of peptide-based drugs, where the tert-butoxycarbonyl (Boc) group acts as a protective group for the amine functionality during synthesis. The presence of the bromobenzyl moiety allows for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical structures. Its application is significant in the design and synthesis of bioactive compounds, including potential therapeutic agents targeting specific biological pathways.
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