3,6,9,12-Tetraoxapentadec-14-yn-1-yl 4-methylbenzenesulfonate
98%
- Product Code: 107116
CAS:
875770-32-4
| Molecular Weight: | 386.46 g./mol | Molecular Formula: | C₁₈H₂₆O₇S |
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| EC Number: | MDL Number: | MFCD28950765 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C under inert gas |
Product Description:
This chemical is primarily used as a reactive intermediate in organic synthesis, particularly in the preparation of specialized polymers and surfactants. Its structure, featuring both ether and alkyne groups, makes it suitable for click chemistry applications, where it can participate in copper-catalyzed azide-alkyne cycloaddition reactions to form triazole linkages. This property is valuable in creating functionalized materials, such as hydrogels or surface coatings, with tailored properties for biomedical or industrial use. Additionally, the tosylate group enhances its reactivity in nucleophilic substitution reactions, enabling the introduction of various functional groups into complex molecules. It is also explored in the development of advanced drug delivery systems, where its modular structure can be utilized to design targeted therapeutic agents.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | ฿2,214.00 |
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| 0.250 | 10-20 days | ฿3,312.00 |
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| 1.000 | 10-20 days | ฿8,280.00 |
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3,6,9,12-Tetraoxapentadec-14-yn-1-yl 4-methylbenzenesulfonate
This chemical is primarily used as a reactive intermediate in organic synthesis, particularly in the preparation of specialized polymers and surfactants. Its structure, featuring both ether and alkyne groups, makes it suitable for click chemistry applications, where it can participate in copper-catalyzed azide-alkyne cycloaddition reactions to form triazole linkages. This property is valuable in creating functionalized materials, such as hydrogels or surface coatings, with tailored properties for biomedical or industrial use. Additionally, the tosylate group enhances its reactivity in nucleophilic substitution reactions, enabling the introduction of various functional groups into complex molecules. It is also explored in the development of advanced drug delivery systems, where its modular structure can be utilized to design targeted therapeutic agents.
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