(2S)-2-[9H-Fluoren-9-ylmethoxycarbonyl(methyl)amino]-5-oxo-5-(tritylamino)pentanoic acid
97%
- Product Code: 86454
CAS:
1632075-13-8
Molecular Weight: | 624.72 g./mol | Molecular Formula: | C₄₀H₃₆N₂O₅ |
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EC Number: | MDL Number: | MFCD22200774 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This chemical is primarily used in the field of peptide synthesis, particularly as a protected amino acid derivative. It serves as a building block in the solid-phase peptide synthesis (SPPS) process, where the fluorenylmethoxycarbonyl (Fmoc) group acts as a temporary protecting group for the amine functionality. The trityl (Trt) group protects the side chain amino group, ensuring selective deprotection and coupling during the synthesis of complex peptides. Its application is crucial in the production of peptides for pharmaceutical research, drug development, and biochemical studies, enabling the precise assembly of peptide chains with high efficiency and minimal side reactions.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | Ft48,968.32 |
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0.250 | 10-20 days | Ft78,349.31 |
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1.000 | 10-20 days | Ft203,630.64 |
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(2S)-2-[9H-Fluoren-9-ylmethoxycarbonyl(methyl)amino]-5-oxo-5-(tritylamino)pentanoic acid
This chemical is primarily used in the field of peptide synthesis, particularly as a protected amino acid derivative. It serves as a building block in the solid-phase peptide synthesis (SPPS) process, where the fluorenylmethoxycarbonyl (Fmoc) group acts as a temporary protecting group for the amine functionality. The trityl (Trt) group protects the side chain amino group, ensuring selective deprotection and coupling during the synthesis of complex peptides. Its application is crucial in the production of peptides for pharmaceutical research, drug development, and biochemical studies, enabling the precise assembly of peptide chains with high efficiency and minimal side reactions.
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