Methyl 2-(4-bromophenyl)-2-((tert-butoxycarbonyl)amino)acetate
≥95%
- Product Code: 41686
CAS:
709665-73-6
| Molecular Weight: | 344.20 g./mol | Molecular Formula: | C₁₄H₁₈BrNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD04115517 | |
| Melting Point: | Boiling Point: | 429.9°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in the preparation of complex molecules. It serves as a key intermediate in the production of pharmaceuticals, where its bromophenyl and tert-butoxycarbonyl (Boc) protected amino groups make it valuable for constructing peptide-like structures. The Boc group provides temporary protection for the amine during synthesis, allowing selective reactions to occur at other sites. Additionally, the bromophenyl moiety can participate in cross-coupling reactions, such as Suzuki or Heck reactions, enabling the formation of carbon-carbon bonds. This makes it a versatile building block for drug discovery and development, especially in the creation of bioactive compounds targeting specific biological pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft30,738.53 |
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| 0.250 | 10-20 days | Ft61,477.06 |
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Methyl 2-(4-bromophenyl)-2-((tert-butoxycarbonyl)amino)acetate
This compound is primarily utilized in organic synthesis, particularly in the preparation of complex molecules. It serves as a key intermediate in the production of pharmaceuticals, where its bromophenyl and tert-butoxycarbonyl (Boc) protected amino groups make it valuable for constructing peptide-like structures. The Boc group provides temporary protection for the amine during synthesis, allowing selective reactions to occur at other sites. Additionally, the bromophenyl moiety can participate in cross-coupling reactions, such as Suzuki or Heck reactions, enabling the formation of carbon-carbon bonds. This makes it a versatile building block for drug discovery and development, especially in the creation of bioactive compounds targeting specific biological pathways.
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