4-(((9H-Fluoren-9-yl)methoxy)carbonyl)-1-(tert-butoxycarbonyl)piperazine-2-carboxylic acid
95%
- Product Code: 39854
CAS:
218278-58-1
Molecular Weight: | 452.5100 g./mol | Molecular Formula: | C₂₅H₂₈N₂O₆ |
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EC Number: | MDL Number: | MFCD01076217 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | -20°C |
Product Description:
This compound is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing complex peptide chains, where the fluorenylmethoxycarbonyl (Fmoc) and tert-butoxycarbonyl (Boc) groups act as protective groups for the amine and carboxylic acid functionalities, respectively. Its application is crucial in solid-phase peptide synthesis (SPPS), enabling the stepwise assembly of peptides with high precision. The Fmoc group can be selectively removed under mild basic conditions, while the Boc group requires acidic conditions, allowing for controlled deprotection during synthesis. This compound is particularly valuable in producing peptides for pharmaceutical research, drug development, and biochemical studies.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | ฿999.00 |
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4-(((9H-Fluoren-9-yl)methoxy)carbonyl)-1-(tert-butoxycarbonyl)piperazine-2-carboxylic acid
This compound is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing complex peptide chains, where the fluorenylmethoxycarbonyl (Fmoc) and tert-butoxycarbonyl (Boc) groups act as protective groups for the amine and carboxylic acid functionalities, respectively. Its application is crucial in solid-phase peptide synthesis (SPPS), enabling the stepwise assembly of peptides with high precision. The Fmoc group can be selectively removed under mild basic conditions, while the Boc group requires acidic conditions, allowing for controlled deprotection during synthesis. This compound is particularly valuable in producing peptides for pharmaceutical research, drug development, and biochemical studies.
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