32953-63-2 Usage
Uses
Used in Pharmaceutical Research:
2,2-dimethyl-5-(2-oxo-1,3-oxathiolan-5-yl)tetrahydrofuro[2,3-d][1,3]dioxol-6-yl 4-methylbenzenesulfonate (non-preferred name) is used as a research compound for its potential reactivity and unique structure in the development of new drugs and pharmaceuticals.
Used in Chemical Research:
2,2-dimethyl-5-(2-oxo-1,3-oxathiolan-5-yl)tetrahydrofuro[2,3-d][1,3]dioxol-6-yl 4-methylbenzenesulfonate (non-preferred name) is employed as a research chemical in chemical research, where its complex structure and potential reactivity are studied for various synthesis processes and to understand its properties and behavior.
Used in Organic Chemistry:
2,2-dimethyl-5-(2-oxo-1,3-oxathiolan-5-yl)tetrahydrofuro[2,3-d][1,3]dioxol-6-yl 4-methylbenzenesulfonate (non-preferred name) is used as a complex organic molecule in organic chemistry, where its structure and reactivity are explored for potential applications in the synthesis of other organic compounds.
Used in Material Science:
In material science, 2,2-dimethyl-5-(2-oxo-1,3-oxathiolan-5-yl)tetrahydrofuro[2,3-d][1,3]dioxol-6-yl 4-methylbenzenesulfonate (non-preferred name) is used as a component in the development of new materials, leveraging its complex structure and properties to create innovative materials with unique characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 32953-63-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,9,5 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 32953-63:
(7*3)+(6*2)+(5*9)+(4*5)+(3*3)+(2*6)+(1*3)=122
122 % 10 = 2
So 32953-63-2 is a valid CAS Registry Number.
32953-63-2Relevant academic research and scientific papers
Thio-sugars. I. Radical-promoted thione-thiol rearrangement of cyclic thionocarbonates: Synthesis of 5-thioglucose
Tsuda, Yoshisuke,Sato, Yoshiyuki,Kanemitsu, Kimihiro,Hosoi, Shinzo,Shibayama, Kenji,Nakao, Kayo,Ishikawa, Yuko
, p. 1465 - 1475 (2007/10/03)
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.
