tert-Butyl 3,6,9,12,15,18,21-heptaoxatetracos-23-yn-1-ylcarbamate
95%
- Product Code: 107113
CAS:
2112737-90-1
| Molecular Weight: | 463.56 g./mol | Molecular Formula: | C₂₂H₄₁NO₉ |
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| EC Number: | MDL Number: | MFCD30828698 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This chemical is primarily utilized in the field of organic synthesis and material science. It serves as a functionalized building block for the creation of complex molecular architectures, particularly in the development of polymers and dendrimers. Its structure, featuring multiple ether linkages and a terminal alkyne, makes it suitable for click chemistry reactions, such as the copper-catalyzed azide-alkyne cycloaddition (CuAAC). This enables its use in the preparation of advanced materials, including hydrogels, coatings, and drug delivery systems. Additionally, it finds application in the synthesis of bioactive compounds, where its carbamate group can act as a protective group for amines during multi-step synthetic processes. Its unique properties also make it valuable in the design of surfactants and amphiphilic molecules for use in nanotechnology and self-assembly applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.250 | 10-20 days | £153.68 |
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| 1.000 | 10-20 days | £414.84 |
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| 5.000 | 10-20 days | £1,451.33 |
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tert-Butyl 3,6,9,12,15,18,21-heptaoxatetracos-23-yn-1-ylcarbamate
This chemical is primarily utilized in the field of organic synthesis and material science. It serves as a functionalized building block for the creation of complex molecular architectures, particularly in the development of polymers and dendrimers. Its structure, featuring multiple ether linkages and a terminal alkyne, makes it suitable for click chemistry reactions, such as the copper-catalyzed azide-alkyne cycloaddition (CuAAC). This enables its use in the preparation of advanced materials, including hydrogels, coatings, and drug delivery systems. Additionally, it finds application in the synthesis of bioactive compounds, where its carbamate group can act as a protective group for amines during multi-step synthetic processes. Its unique properties also make it valuable in the design of surfactants and amphiphilic molecules for use in nanotechnology and self-assembly applications.
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