(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4,4-dimethylpentanoic acid
97%
- Product Code: 37427
CAS:
359766-58-8
| Molecular Weight: | 367.44 g./mol | Molecular Formula: | C₂₂H₂₅NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01861369 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
Used extensively in peptide synthesis as a protecting group for amino acids, particularly in solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group safeguards the amino group during the coupling process, allowing for selective deprotection without affecting other functional groups. Its steric bulk and stability under basic conditions make it ideal for constructing complex peptides. After synthesis, the Fmoc group is easily removed using piperidine, enabling the continuation of peptide chain elongation. This compound is crucial in the production of pharmaceuticals, bioactive peptides, and research-grade peptides for structural and functional studies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,924.00 |
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| 0.250 | 10-20 days | ฿7,839.00 |
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(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4,4-dimethylpentanoic acid
Used extensively in peptide synthesis as a protecting group for amino acids, particularly in solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group safeguards the amino group during the coupling process, allowing for selective deprotection without affecting other functional groups. Its steric bulk and stability under basic conditions make it ideal for constructing complex peptides. After synthesis, the Fmoc group is easily removed using piperidine, enabling the continuation of peptide chain elongation. This compound is crucial in the production of pharmaceuticals, bioactive peptides, and research-grade peptides for structural and functional studies.
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