(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-((1-(4,4-dimethyl-2,6-dioxocyclohexylidene)ethyl)amino)pentanoic acid
97%
- Product Code: 104200
CAS:
1419640-31-5
| Molecular Weight: | 518.6 g./mol | Molecular Formula: | C₃₀H₃₄N₂O₆ |
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| EC Number: | MDL Number: | MFCD02094127 | |
| 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), a method widely employed for constructing peptides and proteins. The fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amino functionality, ensuring selective reactions during the synthesis process. The 1-(4,4-dimethyl-2,6-dioxocyclohexylidene)ethyl (Dde) group protects the side chain amino group, allowing for orthogonal deprotection strategies. This dual protection enables precise control over the assembly of complex peptide sequences, making it a crucial tool in the development of pharmaceuticals, bioactive peptides, and research reagents. Its application is essential in producing peptides with high purity and specificity, which are critical for drug discovery and biochemical studies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,332.00 |
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| 0.250 | 10-20 days | ฿2,043.00 |
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| 1.000 | 10-20 days | ฿5,688.00 |
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| 5.000 | 10-20 days | ฿17,370.00 |
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(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-((1-(4,4-dimethyl-2,6-dioxocyclohexylidene)ethyl)amino)pentanoic 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), a method widely employed for constructing peptides and proteins. The fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amino functionality, ensuring selective reactions during the synthesis process. The 1-(4,4-dimethyl-2,6-dioxocyclohexylidene)ethyl (Dde) group protects the side chain amino group, allowing for orthogonal deprotection strategies. This dual protection enables precise control over the assembly of complex peptide sequences, making it a crucial tool in the development of pharmaceuticals, bioactive peptides, and research reagents. Its application is essential in producing peptides with high purity and specificity, which are critical for drug discovery and biochemical studies.
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