5-((3aS,4S,6aR)-2-Oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)-N-(prop-2-yn-1-yl)pentanamide
95%
- Product Code: 64553
CAS:
773888-45-2
| Molecular Weight: | 281.38 g./mol | Molecular Formula: | C₁₃H₁₉N₃O₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28385487 | |
| Melting Point: | 169-170 °C | Boiling Point: | 614.8±50.0 °C(Predicted) |
| Density: | 1.185±0.06 g/cm3(Predicted) | Storage Condition: | -20°C, dry, sealed |
Product Description:
This chemical is primarily utilized in biochemical research and pharmaceutical development due to its unique structure, which includes a biotin-like moiety and a propargyl group. The biotin-like component allows it to interact strongly with avidin or streptavidin proteins, making it valuable in bioconjugation and labeling techniques. The propargyl group enables click chemistry reactions, particularly copper-catalyzed azide-alkyne cycloaddition (CuAAC), which is widely used for attaching biomolecules or probes in a selective and efficient manner. Its applications include the development of targeted drug delivery systems, diagnostic imaging agents, and the study of protein interactions in cellular processes. Additionally, it serves as a building block in the synthesis of more complex molecules for therapeutic or diagnostic purposes.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Off-white Solid |
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,220.00 |
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| 0.250 | 10-20 days | ฿3,200.00 |
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| 1.000 | 10-20 days | ฿8,010.00 |
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5-((3aS,4S,6aR)-2-Oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)-N-(prop-2-yn-1-yl)pentanamide
This chemical is primarily utilized in biochemical research and pharmaceutical development due to its unique structure, which includes a biotin-like moiety and a propargyl group. The biotin-like component allows it to interact strongly with avidin or streptavidin proteins, making it valuable in bioconjugation and labeling techniques. The propargyl group enables click chemistry reactions, particularly copper-catalyzed azide-alkyne cycloaddition (CuAAC), which is widely used for attaching biomolecules or probes in a selective and efficient manner. Its applications include the development of targeted drug delivery systems, diagnostic imaging agents, and the study of protein interactions in cellular processes. Additionally, it serves as a building block in the synthesis of more complex molecules for therapeutic or diagnostic purposes.
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