(R)-3-((tert-Butoxycarbonyl)amino)-3-(4-(trifluoromethyl)phenyl)propanoic acid
98%
- Product Code: 230633
CAS:
501015-19-6
| Molecular Weight: | 333.3 g./mol | Molecular Formula: | C₁₅H₁₈F₃NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03427965 | |
| Melting Point: | 157 - 159 ℃ | Boiling Point: | 432.7±45.0 ℃(Predicted) |
| Density: | 1.269±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C |
Product Description:
Used as a chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other biologically active molecules. Its structure supports the formation of peptide-like frameworks with enhanced metabolic stability due to the presence of the trifluoromethyl group. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies, especially in optimizing drug candidates targeting enzymes and receptors where stereochemistry plays a critical role in activity. The Boc-protected amine allows for selective deprotection and further coupling reactions in multi-step syntheses.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿5,260.00 |
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| 250mg | 10-20 days | ฿9,200.00 |
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| 1g | 10-20 days | ฿24,860.00 |
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| 10g | 10-20 days | ฿58,870.00 |
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| 5g | 10-20 days | ฿33,860.00 |
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(R)-3-((tert-Butoxycarbonyl)amino)-3-(4-(trifluoromethyl)phenyl)propanoic acid
Used as a chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other biologically active molecules. Its structure supports the formation of peptide-like frameworks with enhanced metabolic stability due to the presence of the trifluoromethyl group. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies, especially in optimizing drug candidates targeting enzymes and receptors where stereochemistry plays a critical role in activity. The Boc-protected amine allows for selective deprotection and further coupling reactions in multi-step syntheses.
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