Fmoc-3-Ala(3-benzothienyl)-OH
97%
- Product Code: 50396
CAS:
177966-60-8
| Molecular Weight: | 443.51 g./mol | Molecular Formula: | C₂₆H₂₁NO₄S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00672562 | |
| Melting Point: | Boiling Point: | 690.8°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This chemical is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amino group during the synthesis process. The 3-benzothienyl side chain introduces a unique aromatic structure, which can be beneficial in designing peptides with specific biological activities or binding properties. It is commonly employed in the development of peptide-based drugs, research peptides, and biochemical studies where the incorporation of non-natural amino acids is required to enhance stability, activity, or selectivity. Its application is crucial in the synthesis of complex peptides for pharmaceutical and biotechnology industries.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White to pale cream fused solid |
| Purity | 96.5-100 |
| Infrared Spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 250mg | 10-20 days | $69.44 |
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| 5g | 10-20 days | $1,117.00 |
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| 1g | 10-20 days | $248.22 |
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Fmoc-3-Ala(3-benzothienyl)-OH
This chemical is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amino group during the synthesis process. The 3-benzothienyl side chain introduces a unique aromatic structure, which can be beneficial in designing peptides with specific biological activities or binding properties. It is commonly employed in the development of peptide-based drugs, research peptides, and biochemical studies where the incorporation of non-natural amino acids is required to enhance stability, activity, or selectivity. Its application is crucial in the synthesis of complex peptides for pharmaceutical and biotechnology industries.
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