(S)-tert-Butyl 6-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-2-aminohexanoate hydrochloride
95%
- Product Code: 60744
CAS:
330795-57-8
| Molecular Weight: | 460.99 g./mol | Molecular Formula: | C₂₅H₃₃ClN₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD26131502 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in peptide synthesis, particularly as a protected amino acid derivative. It serves as a key intermediate in the construction of complex peptides, enabling the controlled addition of specific amino acids during solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amine functionality, ensuring selective reactivity during the synthesis process. The tert-butyl ester group protects the carboxyl group, allowing for deprotection under mild acidic conditions. This compound is especially valuable in the production of peptides for pharmaceutical research, drug development, and biochemical studies, where precise sequence control is critical. Its use facilitates the synthesis of peptides with high purity and efficiency, making it a crucial tool in modern peptide chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿900.00 |
+
-
|
| 5.000 | 10-20 days | ฿3,960.00 |
+
-
|
| 25.000 | 10-20 days | ฿12,402.00 |
+
-
|
(S)-tert-Butyl 6-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-2-aminohexanoate hydrochloride
This compound is primarily utilized in peptide synthesis, particularly as a protected amino acid derivative. It serves as a key intermediate in the construction of complex peptides, enabling the controlled addition of specific amino acids during solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amine functionality, ensuring selective reactivity during the synthesis process. The tert-butyl ester group protects the carboxyl group, allowing for deprotection under mild acidic conditions. This compound is especially valuable in the production of peptides for pharmaceutical research, drug development, and biochemical studies, where precise sequence control is critical. Its use facilitates the synthesis of peptides with high purity and efficiency, making it a crucial tool in modern peptide chemistry.
| Mechanism | - |
| Appearance | - |
| Longevity | - |
| Strength | - |
| Storage | - |
| Shelf Life | - |
| Allergen(s) | - |
| Dosage (Range) | - |
| Recommended Dosage | - |
| Dosage (Per Day) | - |
| Recommended Dosage (Per Day) | - |
| Mix Method | - |
| Heat Resistance | - |
| Stable in pH range | - |
| Solubility | - |
| Product Types | - |
| INCI | - |
Cart
No products
Subtotal:
฿0.00
฿0.00
Total :