(S)-Boc-3-methoxy-β-Phe-OH
98%
- Product Code: 60709
CAS:
499995-77-6
| Molecular Weight: | 295.33 g./mol | Molecular Formula: | C₁₅H₂₁NO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03427899 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is widely used in peptide synthesis as a building block for creating complex peptide structures. It is particularly valuable in the preparation of peptides with specific stereochemistry, thanks to its chiral center. The Boc (tert-butoxycarbonyl) group serves as a protective group for the amine functionality, allowing selective reactions at other sites during peptide chain assembly. The methoxy group on the phenyl ring can influence the peptide's interaction with biological targets, making it useful in drug discovery and development. Additionally, it is employed in the synthesis of modified amino acids, which are critical in studying protein structure and function. Its applications extend to medicinal chemistry, where it is used to design and optimize bioactive peptides and peptidomimetics.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,080.00 |
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| 0.250 | 10-20 days | ฿1,710.00 |
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| 1.000 | 10-20 days | ฿4,671.00 |
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(S)-Boc-3-methoxy-β-Phe-OH
This chemical is widely used in peptide synthesis as a building block for creating complex peptide structures. It is particularly valuable in the preparation of peptides with specific stereochemistry, thanks to its chiral center. The Boc (tert-butoxycarbonyl) group serves as a protective group for the amine functionality, allowing selective reactions at other sites during peptide chain assembly. The methoxy group on the phenyl ring can influence the peptide's interaction with biological targets, making it useful in drug discovery and development. Additionally, it is employed in the synthesis of modified amino acids, which are critical in studying protein structure and function. Its applications extend to medicinal chemistry, where it is used to design and optimize bioactive peptides and peptidomimetics.
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