(S)-N-Boc-4-Bromophenylalanine
98%
- Product Code: 60753
Alias:
(S)-N-BOC-4-bromophenylalanine; Boc-L-4-bromophenylalanine, tert-butoxycarbonyl-4-bromo-L-phenylalanine
CAS:
62129-39-9
| Molecular Weight: | 344.2 g./mol | Molecular Formula: | C₁₄H₁₈BrNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00237571 | |
| Melting Point: | 118 °C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
Used primarily in peptide synthesis as a building block, it facilitates the creation of complex peptides with specific configurations. Its Boc group protects the amine functionality during synthesis, ensuring selective reactions. The bromine atom allows for further functionalization through cross-coupling reactions, making it valuable in medicinal chemistry for drug development. It is also employed in research to study enzyme interactions and protein folding due to its chiral nature.
Product Specification:
| Test | Specification |
|---|---|
| ENANTIOMERIC EXCESS | 97.5 100% |
| Melting point | 118 120? |
| PURITYHPLC | 98 100% |
| APPEARANCE | White or off-white powder |
| INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | Ft3,232.23 |
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| 5.000 | 10-20 days | Ft9,157.99 |
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| 25.000 | 10-20 days | Ft39,648.72 |
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(S)-N-Boc-4-Bromophenylalanine
Used primarily in peptide synthesis as a building block, it facilitates the creation of complex peptides with specific configurations. Its Boc group protects the amine functionality during synthesis, ensuring selective reactions. The bromine atom allows for further functionalization through cross-coupling reactions, making it valuable in medicinal chemistry for drug development. It is also employed in research to study enzyme interactions and protein folding due to its chiral nature.
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