Boc-Phe(4-NO2)-Oet
98%
- Product Code: 104841
CAS:
67630-00-6
| Molecular Weight: | 338.35568 g./mol | Molecular Formula: | C₁₆H₂₂N₂O₆ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 481.9±40.0℃ at 760 mmHg | |
| Density: | 1.198±0.06 g/cm3 | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used in peptide synthesis as a protected amino acid derivative. The Boc (tert-butyloxycarbonyl) group acts as a protective group for the amino function, while the ethyl ester (Oet) protects the carboxyl group. The 4-nitro (NO2) substituent on the phenylalanine side chain can influence the reactivity or serve as a handle for further chemical modifications. It is particularly useful in solid-phase peptide synthesis (SPPS) or solution-phase synthesis, where selective deprotection and coupling steps are required to build complex peptide sequences. Additionally, the nitro group can be reduced to an amine for further functionalization, making it versatile in designing peptides with specific properties or applications in drug development and biochemical research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 1.000 | 10-20 days | $8.10 |
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| 5.000 | 10-20 days | $26.73 |
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| 25.000 | 10-20 days | $95.59 |
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Boc-Phe(4-NO2)-Oet
This chemical is primarily used in peptide synthesis as a protected amino acid derivative. The Boc (tert-butyloxycarbonyl) group acts as a protective group for the amino function, while the ethyl ester (Oet) protects the carboxyl group. The 4-nitro (NO2) substituent on the phenylalanine side chain can influence the reactivity or serve as a handle for further chemical modifications. It is particularly useful in solid-phase peptide synthesis (SPPS) or solution-phase synthesis, where selective deprotection and coupling steps are required to build complex peptide sequences. Additionally, the nitro group can be reduced to an amine for further functionalization, making it versatile in designing peptides with specific properties or applications in drug development and biochemical research.
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