Fmoc-N-(tert-butyloxycarbonylmethyl)glycine
95%
- Product Code: 104444
CAS:
141743-16-0
Molecular Weight: | 411.45 g./mol | Molecular Formula: | C₂₃H₂₅NO₆ |
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EC Number: | MDL Number: | MFCD05663767 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amine functionality, while the tert-butyloxycarbonyl (Boc) group protects the carboxyl side chain. This dual protection allows for selective deprotection and coupling during the stepwise construction of peptides. Its application is crucial in the synthesis of complex peptides and proteins, enabling precise control over the sequence and structure. Additionally, it is employed in the development of peptide-based drugs, biomaterials, and research tools in biochemistry and molecular biology.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿900.00 |
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0.250 | 10-20 days | ฿1,710.00 |
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1.000 | 10-20 days | ฿5,742.00 |
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Fmoc-N-(tert-butyloxycarbonylmethyl)glycine
This compound is primarily utilized in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amine functionality, while the tert-butyloxycarbonyl (Boc) group protects the carboxyl side chain. This dual protection allows for selective deprotection and coupling during the stepwise construction of peptides. Its application is crucial in the synthesis of complex peptides and proteins, enabling precise control over the sequence and structure. Additionally, it is employed in the development of peptide-based drugs, biomaterials, and research tools in biochemistry and molecular biology.
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