197246-28-9

Usage

Uses

Used in Polymer and Resin Production:
1-(2',2',6',6'-tetramethyl-1'-piperidinyloxy)-tetrahydrofuran is used as a radical initiator for the production of polymers and resins. Its role is crucial in initiating the polymerization process, ensuring the formation of the desired polymer structure.
Used in Adhesive and Coating Formulation:
In the adhesive and coating industries, 1-(2',2',6',6'-tetramethyl-1'-piperidinyloxy)-tetrahydrofuran is used as a stabilizer. It helps maintain the stability of the formulations, preventing unwanted reactions that could compromise the product's performance.
Used as a Polymerization Inhibitor:
This chemical compound is also used as a polymerization inhibitor, efficiently preventing unwanted polymerization reactions during manufacturing processes. This ensures the quality and consistency of the final product.
Used for Extending Shelf Life:
Due to its antioxidant properties, 1-(2',2',6',6'-tetramethyl-1'-piperidinyloxy)-tetrahydrofuran is used to extend the shelf life of certain products. It helps protect against oxidation, which can lead to degradation and spoilage.
Used in Pharmaceutical and Nutraceutical Industries:
1-(2',2',6',6'-tetramethyl-1'-piperidinyloxy)-tetrahydrofuran has been studied for its potential use as a pharmaceutical and nutraceutical ingredient. Its antioxidant and free radical scavenging properties make it a promising candidate for various applications in these industries.

Upstream product

• 109-99-9 tetrahydrofuran 
• 2564-83-2 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical 
• 23277-04-5 2-benzylisoquinolin-2-ium bromide 
• 3340-78-1 2-phenyl-1,2,3,4-tetrahydroisoquinoline 

Downstream Products

• 59137-68-7 1-phenyl-2-(tetrahydrofuran-2-yl)ethan-1-one 
• 19426-60-9 tetrahydrofuran-2-yl 
• 2564-83-2 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical 

Relevant academic research and scientific papers

Construction of C(sp2)-X (X = Br, Cl) Bonds through a Copper-Catalyzed Atom-Transfer Radical Process: Application for the 1,4-Difunctionalization of Isoquinolinium Salts

A highly efficient Cu-catalyzed 1,4-difunctionalization of isoquinolinium salts was developed with ether and X- (X = Br, Cl) as the halogen source under mild conditions. This transformation involves the combination of oxidative coupling and copper-catalyzed halogen atom-transfer radical processes. This method not only provides an efficient way to prepare various substituted azaarenes but also achieves the selective construction of C(sp2)-X (X = Br, Cl) bonds from a halogen anion and nucleophilic carbon atom via a free-radical process.

Direct, Site-Selective and Redox-Neutral α-C?H Bond Functionalization of Tetrahydrofurans via Quantum Dots Photocatalysis

As one of the most ubiquitous bulk reagents available, the intrinsic chemical inertness of tetrahydrofuran (THF) makes direct and site-selective C(sp3)?H bond activation difficult, especially under redox neutral condition. Here, we demonstrate that semiconductor quantum dots (QDs) can activate α-C?H bond of THF via forming QDs/THF conjugates. Under visible light irradiation, the resultant alkoxyalkyl radical directly engages in radical cross-coupling with α-amino radical from amino C?H bonds or radical addition with alkene or phenylacetylene, respectively. In contrast to stoichiometric oxidant or hydrogen atom transfer reagents required in previous studies, the scalable benchtop approach can execute α-C?H bond activation of THF only by a QD photocatalyst under redox-neutral condition, thus providing a broad of value added chemicals starting from bulk THFs reagent.