(R)-2-((tert-butoxycarbonyl)amino)-3-(perfluorophenyl)propanoic acid
95%
- Product Code: 104208
CAS:
136207-26-6
| Molecular Weight: | 355.26 g./mol | Molecular Formula: | C₁₄H₁₄F₅NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00151892 | |
| Melting Point: | Boiling Point: | 411.1±45.0 °C(Predicted) | |
| Density: | 1.422±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of complex molecules, particularly those involving peptide modifications. Its structure, featuring a perfluorophenyl group, makes it valuable for introducing fluorinated motifs into drug candidates, which can enhance metabolic stability and bioavailability. Additionally, the tert-butoxycarbonyl (Boc) protecting group allows for selective deprotection during multi-step synthetic processes, enabling the precise construction of target compounds. Its application is particularly relevant in the development of fluorinated amino acid derivatives, which are increasingly important in the design of therapeutic agents and imaging probes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿3,420.00 |
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| 1.000 | 10-20 days | ฿6,750.00 |
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| 5.000 | 10-20 days | ฿23,625.00 |
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(R)-2-((tert-butoxycarbonyl)amino)-3-(perfluorophenyl)propanoic acid
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of complex molecules, particularly those involving peptide modifications. Its structure, featuring a perfluorophenyl group, makes it valuable for introducing fluorinated motifs into drug candidates, which can enhance metabolic stability and bioavailability. Additionally, the tert-butoxycarbonyl (Boc) protecting group allows for selective deprotection during multi-step synthetic processes, enabling the precise construction of target compounds. Its application is particularly relevant in the development of fluorinated amino acid derivatives, which are increasingly important in the design of therapeutic agents and imaging probes.
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