(R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(furan-2-yl)propanoic acid
95%
- Product Code: 104243
CAS:
1217662-55-9
Molecular Weight: | 377.39 g./mol | Molecular Formula: | C₂₂H₁₉NO₅ |
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EC Number: | MDL Number: | MFCD04117844 | |
Melting Point: | Boiling Point: | 579.6±50.0 °C(Predicted) | |
Density: | 1.316±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily used in the field of peptide synthesis as a building block. It serves as a protected amino acid derivative, where the fluorenylmethoxycarbonyl (Fmoc) group acts as a protective group for the amine functionality. This allows for controlled and sequential addition of amino acids during solid-phase peptide synthesis, a key method in producing peptides for research and therapeutic applications. The furan moiety in its structure can also be utilized in further chemical modifications or as a handle for conjugation in bioconjugation chemistry. Its application is crucial in the development of peptides with potential use in pharmaceuticals, biochemical studies, and drug discovery.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿3,240.00 |
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0.250 | 10-20 days | ฿5,508.00 |
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1.000 | 10-20 days | ฿14,850.00 |
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(R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(furan-2-yl)propanoic acid
This compound is primarily used in the field of peptide synthesis as a building block. It serves as a protected amino acid derivative, where the fluorenylmethoxycarbonyl (Fmoc) group acts as a protective group for the amine functionality. This allows for controlled and sequential addition of amino acids during solid-phase peptide synthesis, a key method in producing peptides for research and therapeutic applications. The furan moiety in its structure can also be utilized in further chemical modifications or as a handle for conjugation in bioconjugation chemistry. Its application is crucial in the development of peptides with potential use in pharmaceuticals, biochemical studies, and drug discovery.
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