3,6,9,12-Tetraoxapentadec-14-yn-1-yl 4-methylbenzenesulfonate

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Reagent Code: #107116
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CAS Number 875770-32-4

science Other reagents with same CAS 875770-32-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 386.46 g/mol
Formula C₁₈H₂₆O₇S
badge Registry Numbers
MDL Number MFCD28950765
inventory_2 Storage & Handling
Storage 2-8°C under inert gas

description 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.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,214.00
inventory 250mg
10-20 days ฿3,312.00
inventory 1g
10-20 days ฿8,280.00

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3,6,9,12-Tetraoxapentadec-14-yn-1-yl 4-methylbenzenesulfonate
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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 biomedi

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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