(S)-(9H-Fluoren-9-yl)methyl (1-oxopropan-2-yl)carbamate
97%
- Product Code: 37847
CAS:
146803-41-0
| Molecular Weight: | 295.33 g./mol | Molecular Formula: | C₁₈H₁₇NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01318541 | |
| Melting Point: | Boiling Point: | 479.9±28.0°C at 760 mmHg | |
| Density: | Storage Condition: | -20°C, store under inert gas |
Product Description:
This chemical is primarily utilized in the field of peptide synthesis as a protecting group for amino acids. It is particularly effective in safeguarding the amino group during the synthesis process, preventing unwanted side reactions. The compound is often employed in solid-phase peptide synthesis (SPPS) due to its stability under various reaction conditions and its ability to be selectively removed without affecting other functional groups. Its application ensures the efficient and precise construction of complex peptide sequences, making it a valuable tool in biochemical research and pharmaceutical development. Additionally, it is used in the preparation of peptide-based drugs and bioactive compounds, contributing to advancements in medicinal chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿5,301.00 |
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| 1.000 | 10-20 days | ฿10,593.00 |
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(S)-(9H-Fluoren-9-yl)methyl (1-oxopropan-2-yl)carbamate
This chemical is primarily utilized in the field of peptide synthesis as a protecting group for amino acids. It is particularly effective in safeguarding the amino group during the synthesis process, preventing unwanted side reactions. The compound is often employed in solid-phase peptide synthesis (SPPS) due to its stability under various reaction conditions and its ability to be selectively removed without affecting other functional groups. Its application ensures the efficient and precise construction of complex peptide sequences, making it a valuable tool in biochemical research and pharmaceutical development. Additionally, it is used in the preparation of peptide-based drugs and bioactive compounds, contributing to advancements in medicinal chemistry.
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