(9H-Fluoren-9-yl)methyl (4-aminobutyl)carbamate hydrochloride
95%
- Product Code: 37153
CAS:
321660-77-9
| Molecular Weight: | 346.8511 g./mol | Molecular Formula: | C₁₉H₂₃ClN₂O₂ |
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| EC Number: | MDL Number: | MFCD01631652 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is widely used in peptide synthesis as a protecting group for amino acids. It helps to prevent unwanted reactions during the formation of peptide bonds, ensuring the synthesis proceeds efficiently. The fluorenylmethyloxycarbonyl (Fmoc) group, which is part of this compound, is particularly valued for its stability under basic conditions and its ease of removal under mild acidic conditions. This makes it a preferred choice in solid-phase peptide synthesis, where it allows for the stepwise construction of peptides with high precision. Additionally, it is employed in the production of pharmaceuticals and bioactive peptides, contributing to advancements in drug development and biochemical research. Its application is crucial in creating complex peptide structures with minimal side reactions.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,404.00 |
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(9H-Fluoren-9-yl)methyl (4-aminobutyl)carbamate hydrochloride
This compound is widely used in peptide synthesis as a protecting group for amino acids. It helps to prevent unwanted reactions during the formation of peptide bonds, ensuring the synthesis proceeds efficiently. The fluorenylmethyloxycarbonyl (Fmoc) group, which is part of this compound, is particularly valued for its stability under basic conditions and its ease of removal under mild acidic conditions. This makes it a preferred choice in solid-phase peptide synthesis, where it allows for the stepwise construction of peptides with high precision. Additionally, it is employed in the production of pharmaceuticals and bioactive peptides, contributing to advancements in drug development and biochemical research. Its application is crucial in creating complex peptide structures with minimal side reactions.
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