Boc-Orn(Fmoc)-OH
99%
- Product Code: 66127
CAS:
150828-96-9
| Molecular Weight: | 454.52 g./mol | Molecular Formula: | C₂₅H₃₀N₂O₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00080279 | |
| Melting Point: | 150-154 °C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
Boc-Orn(Fmoc)-OH is widely used in peptide synthesis as a building block for creating complex peptide structures. Its dual protection with Boc (tert-butyloxycarbonyl) and Fmoc (fluorenylmethyloxycarbonyl) groups allows for selective deprotection and sequential assembly of peptides. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), where it helps introduce ornithine residues into peptide chains with high precision. It is also employed in the development of peptide-based drugs, biomaterials, and research tools, enabling the study of peptide interactions and functions. The orthogonal protection strategy ensures efficient and controlled synthesis, making it a key reagent in both academic and industrial peptide chemistry.
Product Specification:
| Test | Specification |
|---|---|
| Melting point | 150-154 |
| PURITYHPLC | 99-100 |
| INFRARED SPECTROMETRY | Conforms to Structure |
| PROTON NMR SPECTRUM | Conforms to Structure |
| APPEARANCE | White to off-white solid |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿1,870.00 |
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| 5.000 | 10-20 days | ฿6,100.00 |
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Boc-Orn(Fmoc)-OH
Boc-Orn(Fmoc)-OH is widely used in peptide synthesis as a building block for creating complex peptide structures. Its dual protection with Boc (tert-butyloxycarbonyl) and Fmoc (fluorenylmethyloxycarbonyl) groups allows for selective deprotection and sequential assembly of peptides. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), where it helps introduce ornithine residues into peptide chains with high precision. It is also employed in the development of peptide-based drugs, biomaterials, and research tools, enabling the study of peptide interactions and functions. The orthogonal protection strategy ensures efficient and controlled synthesis, making it a key reagent in both academic and industrial peptide chemistry.
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