(9H-Fluoren-9-yl)methyl (2-aminoethyl)carbamate
95%
- Product Code: 37151
CAS:
166410-32-8
| Molecular Weight: | 282.34 g./mol | Molecular Formula: | C₁₇H₁₈N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01318872 | |
| Melting Point: | Boiling Point: | 487.1±28.0 °C at 760 mmHg | |
| Density: | 1.201±0.06 g/cm3 | Storage Condition: | 2-8℃, inert gas |
Product Description:
This chemical is widely used in peptide synthesis as a protecting group for amino acids. It is particularly effective in solid-phase peptide synthesis (SPPS) to protect the amino group, ensuring selective reactions during the assembly of peptide chains. Its stability under acidic and basic conditions makes it suitable for complex peptide synthesis processes. Additionally, it can be easily removed under mild conditions using piperidine, allowing for efficient deprotection without damaging the peptide structure. Its application extends to the synthesis of bioactive peptides, pharmaceuticals, and research compounds where precise control over amino acid reactivity is crucial.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | £148.59 |
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| 5.000 | 10-20 days | £412.81 |
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| 25.000 | 10-20 days | £1,376.43 |
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(9H-Fluoren-9-yl)methyl (2-aminoethyl)carbamate
This chemical is widely used in peptide synthesis as a protecting group for amino acids. It is particularly effective in solid-phase peptide synthesis (SPPS) to protect the amino group, ensuring selective reactions during the assembly of peptide chains. Its stability under acidic and basic conditions makes it suitable for complex peptide synthesis processes. Additionally, it can be easily removed under mild conditions using piperidine, allowing for efficient deprotection without damaging the peptide structure. Its application extends to the synthesis of bioactive peptides, pharmaceuticals, and research compounds where precise control over amino acid reactivity is crucial.
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