(9H-Fluoren-9-yl)methyl 4-((tert-butoxycarbonyl)amino)piperidine-1-carboxylate
95%
- Product Code: 39741
CAS:
1935586-88-1
Molecular Weight: | 422.52 g./mol | Molecular Formula: | C₂₅H₃₀N₂O₄ |
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EC Number: | MDL Number: | MFCD29760298 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily utilized in peptide synthesis as a protecting group for amines. The fluorenylmethyloxycarbonyl (Fmoc) group safeguards the amine functionality during the synthesis process, preventing unwanted reactions. The tert-butoxycarbonyl (Boc) group, on the other hand, provides additional protection for the piperidine nitrogen, ensuring selective deprotection steps can be carried out. This dual protection strategy is crucial in the stepwise construction of complex peptides, particularly in solid-phase peptide synthesis (SPPS). The compound’s stability under basic conditions and its ability to be selectively removed make it a valuable tool in the production of pharmaceuticals, bioactive peptides, and other organic molecules requiring precise control over chemical reactions.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | $225.47 |
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1.000 | 10-20 days | $450.95 |
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(9H-Fluoren-9-yl)methyl 4-((tert-butoxycarbonyl)amino)piperidine-1-carboxylate
This compound is primarily utilized in peptide synthesis as a protecting group for amines. The fluorenylmethyloxycarbonyl (Fmoc) group safeguards the amine functionality during the synthesis process, preventing unwanted reactions. The tert-butoxycarbonyl (Boc) group, on the other hand, provides additional protection for the piperidine nitrogen, ensuring selective deprotection steps can be carried out. This dual protection strategy is crucial in the stepwise construction of complex peptides, particularly in solid-phase peptide synthesis (SPPS). The compound’s stability under basic conditions and its ability to be selectively removed make it a valuable tool in the production of pharmaceuticals, bioactive peptides, and other organic molecules requiring precise control over chemical reactions.
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