(S)-Boc-γ,γ-diphenyl-β-Homoala-OH
≥98%(HPLC)
- Product Code: 104645
CAS:
190190-50-2
| Molecular Weight: | 355.43 g./mol | Molecular Formula: | C₂₁H₂₅NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02094564 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily used in the synthesis of peptides and peptidomimetics, where it serves as a protected amino acid derivative. The Boc (tert-butoxycarbonyl) group provides stability during peptide bond formation, preventing unwanted side reactions. It is particularly valuable in the preparation of complex peptide structures, enabling the incorporation of diphenylalanine-like motifs. This compound is also employed in medicinal chemistry for designing drug candidates, especially those targeting protein-protein interactions, due to its unique structural features. Additionally, it finds application in the development of chiral catalysts and ligands for asymmetric synthesis.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿15,282.00 |
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| 0.500 | 10-20 days | ฿52,182.00 |
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(S)-Boc-γ,γ-diphenyl-β-Homoala-OH
This chemical is primarily used in the synthesis of peptides and peptidomimetics, where it serves as a protected amino acid derivative. The Boc (tert-butoxycarbonyl) group provides stability during peptide bond formation, preventing unwanted side reactions. It is particularly valuable in the preparation of complex peptide structures, enabling the incorporation of diphenylalanine-like motifs. This compound is also employed in medicinal chemistry for designing drug candidates, especially those targeting protein-protein interactions, due to its unique structural features. Additionally, it finds application in the development of chiral catalysts and ligands for asymmetric synthesis.
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