(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(2-(trifluoromethyl)phenyl)propanoic acid
95%
- Product Code: 104184
CAS:
352523-15-0
| Molecular Weight: | 455.43 g./mol | Molecular Formula: | C₂₅H₂₀F₃NO₄ |
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| EC Number: | MDL Number: | MFCD01863051 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily used in the field of peptide synthesis, where it serves as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amine functionality, ensuring selective reactions during peptide chain assembly. The trifluoromethylphenyl moiety enhances the compound's stability and can influence the overall properties of the synthesized peptides, such as their hydrophobicity and binding affinity. It is particularly valuable in the synthesis of complex peptides for pharmaceutical research, enabling the development of peptide-based drugs with specific biological activities.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,512.00 |
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| 1.000 | 10-20 days | ฿3,060.00 |
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| 5.000 | 10-20 days | ฿13,914.00 |
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(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(2-(trifluoromethyl)phenyl)propanoic acid
This compound is primarily used in the field of peptide synthesis, where it serves as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amine functionality, ensuring selective reactions during peptide chain assembly. The trifluoromethylphenyl moiety enhances the compound's stability and can influence the overall properties of the synthesized peptides, such as their hydrophobicity and binding affinity. It is particularly valuable in the synthesis of complex peptides for pharmaceutical research, enabling the development of peptide-based drugs with specific biological activities.
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