9H-fluoren-9-ylmethyl N-[(2S)-1-chloro-1-oxopropan-2-yl]carbamate
98%
- Product Code: 105462
CAS:
103321-50-2
| Molecular Weight: | 329.78 g./mol | Molecular Formula: | C₁₈H₁₆ClNO₃ |
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| EC Number: | MDL Number: | MFCD00235802 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily used in peptide synthesis as a protecting group for amino acids. It helps in selectively blocking reactive functional groups during the synthesis process, ensuring that reactions occur at the desired sites. The compound is particularly effective in solid-phase peptide synthesis, where it provides stability and prevents unwanted side reactions. Its cleavable nature allows for the easy removal of the protecting group once the synthesis is complete, facilitating the production of high-purity peptides. Additionally, it is utilized in the development of pharmaceuticals and bioactive compounds, where precise control over molecular structure is critical.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿2,880.00 |
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| 1.000 | 10-20 days | ฿7,200.00 |
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| 5.000 | 10-20 days | ฿25,092.00 |
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9H-fluoren-9-ylmethyl N-[(2S)-1-chloro-1-oxopropan-2-yl]carbamate
This chemical is primarily used in peptide synthesis as a protecting group for amino acids. It helps in selectively blocking reactive functional groups during the synthesis process, ensuring that reactions occur at the desired sites. The compound is particularly effective in solid-phase peptide synthesis, where it provides stability and prevents unwanted side reactions. Its cleavable nature allows for the easy removal of the protecting group once the synthesis is complete, facilitating the production of high-purity peptides. Additionally, it is utilized in the development of pharmaceuticals and bioactive compounds, where precise control over molecular structure is critical.
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