tert-Butyl 1-((2,4-dinitrophenyl)amino)-3,6,9,12-tetraoxapentadecan-15-oate
≥95%
- Product Code: 63033
CAS:
1817735-31-1
| Molecular Weight: | 487.5 g./mol | Molecular Formula: | C₂₁H₃₃N₃O₁₀ |
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| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, particularly as a specialized intermediate in the preparation of complex molecules. Its structure, featuring both a tert-butyl ester and a polyether chain, makes it suitable for constructing tailored compounds with specific solubility and reactivity profiles. It is often employed in the development of surfactants, polymers, or drug delivery systems, where the polyether segment can enhance water solubility and the tert-butyl group provides stability during synthesis. Additionally, the 2,4-dinitrophenyl moiety can serve as a protective group or a reactive site for further functionalization, enabling its use in peptide chemistry or other conjugation strategies. Its application is particularly valuable in research settings where precise control over molecular architecture is required.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $598.02 |
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tert-Butyl 1-((2,4-dinitrophenyl)amino)-3,6,9,12-tetraoxapentadecan-15-oate
This chemical is primarily utilized in the field of organic synthesis, particularly as a specialized intermediate in the preparation of complex molecules. Its structure, featuring both a tert-butyl ester and a polyether chain, makes it suitable for constructing tailored compounds with specific solubility and reactivity profiles. It is often employed in the development of surfactants, polymers, or drug delivery systems, where the polyether segment can enhance water solubility and the tert-butyl group provides stability during synthesis. Additionally, the 2,4-dinitrophenyl moiety can serve as a protective group or a reactive site for further functionalization, enabling its use in peptide chemistry or other conjugation strategies. Its application is particularly valuable in research settings where precise control over molecular architecture is required.
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