(R)-2-(1-(((9H-Fluoren-9-yl)methoxy)carbonyl)piperidin-2-yl)acetic acid
97%
- Product Code: 37275
CAS:
193693-63-9
| Molecular Weight: | 365.42 g./mol | Molecular Formula: | C₂₂H₂₃NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06656475 | |
| Melting Point: | Boiling Point: | 575.0±23.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is widely used in peptide synthesis as a protecting group for amines, particularly in solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group attached to the piperidine ring ensures selective protection of the amine during the synthesis process, preventing unwanted reactions. Its application allows for the stepwise construction of peptides with high precision. After the synthesis is complete, the Fmoc group can be easily removed under mild basic conditions, making it a versatile tool in the production of complex peptides and proteins for pharmaceutical and biochemical research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $84.24 |
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| 0.250 | 10-20 days | $168.12 |
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(R)-2-(1-(((9H-Fluoren-9-yl)methoxy)carbonyl)piperidin-2-yl)acetic acid
This compound is widely used in peptide synthesis as a protecting group for amines, particularly in solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group attached to the piperidine ring ensures selective protection of the amine during the synthesis process, preventing unwanted reactions. Its application allows for the stepwise construction of peptides with high precision. After the synthesis is complete, the Fmoc group can be easily removed under mild basic conditions, making it a versatile tool in the production of complex peptides and proteins for pharmaceutical and biochemical research.
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