Fmoc-Suberol
98%
- Product Code: 65741
Alias:
Fmoc-Cycloheptanol ; Fmoc-Cycloxanol
CAS:
212783-75-0
| Molecular Weight: | 505.56 g./mol | Molecular Formula: | C₃₂H₂₇NO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | 1.36 | Storage Condition: | room temperature |
Product Description:
Fmoc-Suberol is widely used in peptide synthesis as a protecting group for hydroxyl functionalities. Its primary application lies in solid-phase peptide synthesis (SPPS), where it helps to prevent unwanted reactions at hydroxyl sites during the assembly of peptide chains. The Fmoc group can be easily removed under mild basic conditions, making it highly suitable for stepwise peptide construction without disrupting other sensitive functional groups. Additionally, it is employed in the synthesis of complex organic molecules, particularly in the development of pharmaceuticals and bioactive compounds, where selective protection and deprotection of hydroxyl groups are critical. Its stability under acidic conditions further enhances its utility in multi-step synthetic processes.
Product Specification:
| Test | Specification |
|---|---|
| PurityGC | 98 100% |
| APPEARANCE | COLORLESS LIQUID |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿477.00 |
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| 5.000 | 10-20 days | ฿1,989.00 |
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Fmoc-Suberol
Fmoc-Suberol is widely used in peptide synthesis as a protecting group for hydroxyl functionalities. Its primary application lies in solid-phase peptide synthesis (SPPS), where it helps to prevent unwanted reactions at hydroxyl sites during the assembly of peptide chains. The Fmoc group can be easily removed under mild basic conditions, making it highly suitable for stepwise peptide construction without disrupting other sensitive functional groups. Additionally, it is employed in the synthesis of complex organic molecules, particularly in the development of pharmaceuticals and bioactive compounds, where selective protection and deprotection of hydroxyl groups are critical. Its stability under acidic conditions further enhances its utility in multi-step synthetic processes.
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