(S)-3-((tert-Butoxycarbonyl)amino)-3-(4-(trifluoromethyl)phenyl)propanoic acid
98%
- Product Code: 38377
CAS:
500770-79-6
| Molecular Weight: | 333.3000 g./mol | Molecular Formula: | C₁₅H₁₈F₃NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03427927 | |
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| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs) with potential therapeutic applications. Its structure, featuring a trifluoromethyl group and a Boc-protected amine, makes it a valuable building block in medicinal chemistry. It is often employed in the preparation of compounds targeting specific biological pathways, such as enzyme inhibition or receptor modulation. Additionally, it is used in peptide synthesis and drug discovery research, where its chiral center and functional groups enable the creation of enantiomerically pure molecules with enhanced biological activity. Its stability and reactivity also make it suitable for use in organic synthesis and combinatorial chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,384.00 |
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(S)-3-((tert-Butoxycarbonyl)amino)-3-(4-(trifluoromethyl)phenyl)propanoic acid
This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs) with potential therapeutic applications. Its structure, featuring a trifluoromethyl group and a Boc-protected amine, makes it a valuable building block in medicinal chemistry. It is often employed in the preparation of compounds targeting specific biological pathways, such as enzyme inhibition or receptor modulation. Additionally, it is used in peptide synthesis and drug discovery research, where its chiral center and functional groups enable the creation of enantiomerically pure molecules with enhanced biological activity. Its stability and reactivity also make it suitable for use in organic synthesis and combinatorial chemistry.
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