2872-64-2

Usage

Uses

Given the provided materials, the specific uses of 2,2-dimethyl-5-(2-thioxo-1,3-dioxolan-4-yl)tetrahydrofuro[2,3-d][1,3]dioxol-6-yl 4-methylbenzenesulfonate are not explicitly detailed. However, based on its chemical nature and the industries mentioned, we can infer potential applications:
Used in Pharmaceutical Industry:
2,2-dimethyl-5-(2-thioxo-1,3-dioxolan-4-yl)tetrahydrofuro[2,3-d][1,3]dioxol-6-yl 4-methylbenzenesulfonate (non-preferred name) could be used as an active pharmaceutical ingredient for [specific medical condition or treatment] due to its unique structural features that may offer novel therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 2,2-dimethyl-5-(2-thioxo-1,3-dioxolan-4-yl)tetrahydrofuro[2,3-d][1,3]dioxol-6-yl 4-methylbenzenesulfonate (non-preferred name) might serve as a key component in the development of new pesticides or herbicides, leveraging its chemical properties to target specific pests or weeds effectively.
Used in Materials Science:
2,2-dimethyl-5-(2-thioxo-1,3-dioxolan-4-yl)tetrahydrofuro[2,3-d][1,3]dioxol-6-yl 4-methylbenzenesulfonate (non-preferred name) could be utilized in materials science as a component in the synthesis of advanced materials with unique properties, such as high thermal stability or specific optical characteristics, for applications in various industries.

Upstream product

• 2816-87-7 1,2-di-O-isopropylidene-5,6-O-thiocarbonyl-α-D-glucofuranose 
• 98-59-9 p-toluenesulfonyl chloride 
• 18549-40-1 1,2-O-isopropylidene-α-D-glucofuranose 

Downstream Products

• 62102-11-8 5-deoxy-1,2-O-isopropylidene-3-O-p-tolylsulfonyl-α-D-xylo-hexofuranose 
• 32953-63-2 Toluene-4-sulfonic acid (3aR,5R,6S,6aR)-2,2-dimethyl-5-((S)-2-oxo-[1,3]oxathiolan-5-yl)-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl ester 
• 43138-33-6 5β-vinyl-4β-tosyl-2α,3α-O-isopropylidene tetrahydrofuran 
• 2818-57-7 5,6-O-carbonyl-1,2-O-isopropylidene-3-O-tosyl-α-D-glucofuranose 

Relevant academic research and scientific papers

Thio-sugars. I. Radical-promoted thione-thiol rearrangement of cyclic thionocarbonates: Synthesis of 5-thioglucose

The 5,6-O-thiocarbonyl-α-D-glucofuranose derivatives 2, when subjected to one of the following reactions, undergo a radical-promoted thione-thiol rearrangement to yield the 5-S-thiolcarbonates of gluco-configuration 8 as the major product. The reactions are, (A) thermolysis with a catalytic amount of tributyltin hydride and AIBN, (B) photolysis with hexabutyldistannane, and (C) thermolysis with dimethyl phosphonate and benzoyl peroxide. On the other hand, thermolysis of 2 with trialkylsilane (condition D) yielded olefins 13 as the major product. The 5-S-gluco product 8 was converted, in three steps, to 5-thioglucose (21) in 55% yield.