(R)-3-((tert-Butoxycarbonyl)amino)-4-(4-(trifluoromethyl)phenyl)butanoic acid
98%
- Product Code: 104257
CAS:
269726-77-4
| Molecular Weight: | 347.33 g./mol | Molecular Formula: | C₁₆H₂₀F₃NO₄ |
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| EC Number: | MDL Number: | MFCD01860972 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in the pharmaceutical and chemical research sectors as a key intermediate in the synthesis of more complex molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a trifluoromethylphenyl moiety, makes it valuable for developing peptides and small-molecule drugs. The Boc group is often employed to protect amines during multi-step synthetic processes, ensuring selective reactions. Additionally, the trifluoromethyl group enhances the biological activity and metabolic stability of the resulting compounds, making it useful in the design of potential therapeutic agents, particularly in areas like enzyme inhibition or receptor modulation. Its application is also seen in the preparation of chiral compounds, leveraging its stereocenter for asymmetric synthesis in drug development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿7,092.00 |
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| 0.250 | 10-20 days | ฿10,620.00 |
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(R)-3-((tert-Butoxycarbonyl)amino)-4-(4-(trifluoromethyl)phenyl)butanoic acid
This compound is primarily utilized in the pharmaceutical and chemical research sectors as a key intermediate in the synthesis of more complex molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a trifluoromethylphenyl moiety, makes it valuable for developing peptides and small-molecule drugs. The Boc group is often employed to protect amines during multi-step synthetic processes, ensuring selective reactions. Additionally, the trifluoromethyl group enhances the biological activity and metabolic stability of the resulting compounds, making it useful in the design of potential therapeutic agents, particularly in areas like enzyme inhibition or receptor modulation. Its application is also seen in the preparation of chiral compounds, leveraging its stereocenter for asymmetric synthesis in drug development.
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