N-(2-(2-Azidoethoxy)ethyl)-5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamide
98%
- Product Code: 214949
CAS:
1204085-48-2
| Molecular Weight: | 356.45 g./mol | Molecular Formula: | C₁₄H₂₄N₆O₃S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28386078 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C |
Product Description:
Used in bioconjugation and click chemistry applications due to the presence of the azide group. It enables selective ligation with alkynes via copper-catalyzed or strain-promoted azide-alkyne cycloaddition (CuAAC or SPAAC). Commonly employed in the modification of biomolecules such as peptides, proteins, and nucleic acids for labeling, immobilization, or drug delivery. The thienoimidazole moiety may contribute to binding or stability in specific biological systems, making it useful in the development of targeted therapeutics or probes. Its hydrophilic linker region enhances solubility and flexibility in aqueous environments, beneficial for assays and bioconjugate stability.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 250mg | 10-20 days | $768.64 |
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N-(2-(2-Azidoethoxy)ethyl)-5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamide
Used in bioconjugation and click chemistry applications due to the presence of the azide group. It enables selective ligation with alkynes via copper-catalyzed or strain-promoted azide-alkyne cycloaddition (CuAAC or SPAAC). Commonly employed in the modification of biomolecules such as peptides, proteins, and nucleic acids for labeling, immobilization, or drug delivery. The thienoimidazole moiety may contribute to binding or stability in specific biological systems, making it useful in the development of targeted therapeutics or probes. Its hydrophilic linker region enhances solubility and flexibility in aqueous environments, beneficial for assays and bioconjugate stability.
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