(S)-a-(Fmoc-amino)-3,5-difluorobenzenebutanoic acid
95%
- Product Code: 38043
CAS:
1260591-27-2
| Molecular Weight: | 437.4354 g./mol | Molecular Formula: | C₂₅H₂₁F₂NO₄ |
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| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group safeguards the amino functionality during the synthesis process. The presence of difluoro substituents on the benzene ring can enhance the stability and reactivity of the molecule, making it valuable for constructing peptides with specific structural or functional properties. It is often employed in the development of pharmaceuticals, bioactive peptides, and research applications where precise control over peptide sequences is required. Additionally, its unique structure can be leveraged in the design of peptide-based probes or inhibitors for biochemical studies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | ฿9,090.00 |
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(S)-a-(Fmoc-amino)-3,5-difluorobenzenebutanoic acid
This compound is primarily utilized in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group safeguards the amino functionality during the synthesis process. The presence of difluoro substituents on the benzene ring can enhance the stability and reactivity of the molecule, making it valuable for constructing peptides with specific structural or functional properties. It is often employed in the development of pharmaceuticals, bioactive peptides, and research applications where precise control over peptide sequences is required. Additionally, its unique structure can be leveraged in the design of peptide-based probes or inhibitors for biochemical studies.
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