(S)-2-((tert-Butoxycarbonyl)amino)-5-(dimethylamino)-5-oxopentanoic acid
97%
- Product Code: 57136
CAS:
72449-42-4
| Molecular Weight: | 274.31 g./mol | Molecular Formula: | C₁₂H₂₂N₂O₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD29920880 | |
| Melting Point: | Boiling Point: | 460.4±40.0 °C(Predicted) | |
| Density: | 1.150±0.06 g/cm3(Predicted) | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This compound is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for creating complex peptides and proteins, particularly in research and pharmaceutical development. The tert-butoxycarbonyl (Boc) group acts as a protective group for the amino function, preventing unwanted reactions during the synthesis process. The dimethylamino group enhances solubility and can influence the reactivity of the compound. Its application is crucial in medicinal chemistry for designing peptide-based drugs, enzyme inhibitors, and other bioactive molecules. Additionally, it is utilized in the study of protein folding and structure-function relationships due to its ability to mimic natural amino acids while offering controlled reactivity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,572.00 |
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| 0.250 | 10-20 days | ฿7,623.00 |
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| 1.000 | 10-20 days | ฿20,574.00 |
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(S)-2-((tert-Butoxycarbonyl)amino)-5-(dimethylamino)-5-oxopentanoic acid
This compound is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for creating complex peptides and proteins, particularly in research and pharmaceutical development. The tert-butoxycarbonyl (Boc) group acts as a protective group for the amino function, preventing unwanted reactions during the synthesis process. The dimethylamino group enhances solubility and can influence the reactivity of the compound. Its application is crucial in medicinal chemistry for designing peptide-based drugs, enzyme inhibitors, and other bioactive molecules. Additionally, it is utilized in the study of protein folding and structure-function relationships due to its ability to mimic natural amino acids while offering controlled reactivity.
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