(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(1H-tetrazol-5-yl)butanoic acid
97%
- Product Code: 38013
CAS:
954147-36-5
Molecular Weight: | 393.40 g./mol | Molecular Formula: | C₂₀H₁₉N₅O₄ |
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EC Number: | MDL Number: | MFCD26407302 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily utilized in peptide synthesis, particularly as a protected amino acid derivative. It serves as a building block for the introduction of tetrazole-containing amino acids into peptide chains. The fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amino functionality, ensuring selective reactions during peptide assembly. The tetrazole moiety is of interest due to its bioisosteric properties, often mimicking carboxylic acids or other functional groups in drug design, making it valuable in the development of pharmaceuticals. Its application is crucial in creating peptide-based drugs, enzyme inhibitors, and other bioactive molecules with enhanced stability and specificity.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | $306.02 |
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0.250 | 10-20 days | $612.46 |
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(1H-tetrazol-5-yl)butanoic acid
This compound is primarily utilized in peptide synthesis, particularly as a protected amino acid derivative. It serves as a building block for the introduction of tetrazole-containing amino acids into peptide chains. The fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amino functionality, ensuring selective reactions during peptide assembly. The tetrazole moiety is of interest due to its bioisosteric properties, often mimicking carboxylic acids or other functional groups in drug design, making it valuable in the development of pharmaceuticals. Its application is crucial in creating peptide-based drugs, enzyme inhibitors, and other bioactive molecules with enhanced stability and specificity.
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