(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(2-methoxyphenyl)propanoic acid
98%
- Product Code: 38365
CAS:
501015-28-7
| Molecular Weight: | 417.4500 g./mol | Molecular Formula: | C₂₅H₂₃NO₅ |
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| EC Number: | MDL Number: | MFCD03427974 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used in the field of peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing peptides with specific sequences, particularly in solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amino functionality, ensuring selective reactions during peptide chain assembly. The methoxyphenyl moiety contributes to the structural diversity of the synthesized peptides, which can be tailored for research in drug development, biochemistry, and molecular biology. After synthesis, the Fmoc group can be easily removed under mild conditions, allowing for further modifications or deprotection steps. This compound is valuable in producing peptides with potential applications in therapeutic agents, enzyme studies, and biochemical probes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,231.00 |
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(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(2-methoxyphenyl)propanoic acid
This chemical is primarily used in the field of peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing peptides with specific sequences, particularly in solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amino functionality, ensuring selective reactions during peptide chain assembly. The methoxyphenyl moiety contributes to the structural diversity of the synthesized peptides, which can be tailored for research in drug development, biochemistry, and molecular biology. After synthesis, the Fmoc group can be easily removed under mild conditions, allowing for further modifications or deprotection steps. This compound is valuable in producing peptides with potential applications in therapeutic agents, enzyme studies, and biochemical probes.
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