(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-6-(((4-Methoxyphenyl)diphenylmethyl)amino)hexanoic acid
95%
- Product Code: 76519
CAS:
159857-60-0
| Molecular Weight: | 640.79 g./mol | Molecular Formula: | C₄₁H₄₀N₂O₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00270542 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily used in the field of peptide synthesis, where it serves as a protected amino acid derivative. It is particularly valuable in solid-phase peptide synthesis (SPPS) due to its dual protection groups. The fluorenylmethoxycarbonyl (Fmoc) group protects the amino functionality, while the 4-methoxyphenyldiphenylmethyl (MMTr) group shields the side chain amino group. This allows for selective deprotection during the synthesis process, enabling the stepwise construction of complex peptides. Its application is crucial in the production of peptides for pharmaceutical research, drug development, and biochemical studies, where precise control over peptide sequences is essential. Additionally, it is employed in the synthesis of peptide-based therapeutics, including hormones, antibiotics, and enzyme inhibitors, contributing to advancements in medical treatments.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to off-white Solid |
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿960.00 |
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| 1.000 | 10-20 days | ฿2,460.00 |
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| 5.000 | 10-20 days | ฿12,150.00 |
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-6-(((4-Methoxyphenyl)diphenylmethyl)amino)hexanoic acid
This chemical is primarily used in the field of peptide synthesis, where it serves as a protected amino acid derivative. It is particularly valuable in solid-phase peptide synthesis (SPPS) due to its dual protection groups. The fluorenylmethoxycarbonyl (Fmoc) group protects the amino functionality, while the 4-methoxyphenyldiphenylmethyl (MMTr) group shields the side chain amino group. This allows for selective deprotection during the synthesis process, enabling the stepwise construction of complex peptides. Its application is crucial in the production of peptides for pharmaceutical research, drug development, and biochemical studies, where precise control over peptide sequences is essential. Additionally, it is employed in the synthesis of peptide-based therapeutics, including hormones, antibiotics, and enzyme inhibitors, contributing to advancements in medical treatments.
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