(S)-2-((tert-Butoxycarbonyl)amino)-3-(2,3,4-trifluorophenyl)propanoic acid
98%
- Product Code: 232637
CAS:
324028-24-2
| Molecular Weight: | 319.28 g./mol | Molecular Formula: | C₁₄H₁₆F₃NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD17214559 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, seal, dry |
Product Description:
Used as a chiral building block in the synthesis of biologically active compounds, particularly in pharmaceutical development. Its structure contains both a protected amine and a carboxylic acid group, making it suitable for peptide-like coupling reactions. The presence of the trifluorophenyl moiety enhances binding selectivity and metabolic stability in drug candidates. Commonly employed in the preparation of protease inhibitors and other therapeutic agents where stereochemistry plays a critical role in activity. The Boc-protected amine allows for controlled deprotection and further functionalization in multi-step syntheses.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿10,870.00 |
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| 0.250 | 10-20 days | ฿18,460.00 |
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| 1.000 | 10-20 days | ฿49,820.00 |
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(S)-2-((tert-Butoxycarbonyl)amino)-3-(2,3,4-trifluorophenyl)propanoic acid
Used as a chiral building block in the synthesis of biologically active compounds, particularly in pharmaceutical development. Its structure contains both a protected amine and a carboxylic acid group, making it suitable for peptide-like coupling reactions. The presence of the trifluorophenyl moiety enhances binding selectivity and metabolic stability in drug candidates. Commonly employed in the preparation of protease inhibitors and other therapeutic agents where stereochemistry plays a critical role in activity. The Boc-protected amine allows for controlled deprotection and further functionalization in multi-step syntheses.
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