(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-methyldodec-11-enoic acid
97%
- Product Code: 38020
CAS:
1640968-91-7
| Molecular Weight: | 449.58 g./mol | Molecular Formula: | C₂₈H₃₅NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD30471500 | |
| Melting Point: | Boiling Point: | 620.3±38.0°C at 760 mmHg | |
| Density: | Storage Condition: | -20°C, dry sealed |
Product Description:
This compound is primarily used in peptide synthesis as a protecting group for amino acids. The fluorenylmethoxycarbonyl (Fmoc) group shields the amino group during the synthesis process, preventing unwanted reactions. It is particularly valuable in solid-phase peptide synthesis (SPPS), where it allows for the stepwise assembly of peptides. The Fmoc group can be selectively removed under mild basic conditions, ensuring the integrity of the peptide chain. Additionally, the presence of the methyldodec-11-enoic acid moiety may contribute to the compound's solubility and stability in organic solvents, facilitating its use in complex peptide synthesis workflows. Its application is crucial in the development of pharmaceuticals, bioactive peptides, and research in biochemistry and molecular biology.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿6,174.00 |
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| 0.250 | 10-20 days | ฿12,357.00 |
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-methyldodec-11-enoic acid
This compound is primarily used in peptide synthesis as a protecting group for amino acids. The fluorenylmethoxycarbonyl (Fmoc) group shields the amino group during the synthesis process, preventing unwanted reactions. It is particularly valuable in solid-phase peptide synthesis (SPPS), where it allows for the stepwise assembly of peptides. The Fmoc group can be selectively removed under mild basic conditions, ensuring the integrity of the peptide chain. Additionally, the presence of the methyldodec-11-enoic acid moiety may contribute to the compound's solubility and stability in organic solvents, facilitating its use in complex peptide synthesis workflows. Its application is crucial in the development of pharmaceuticals, bioactive peptides, and research in biochemistry and molecular biology.
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