37463-85-7 Usage
Uses
Used in Organic Synthesis:
2,6-diethoxy-1,4-oxathiane 4,4-dioxide is utilized as a reagent in organic synthesis for the preparation of a variety of other organic compounds. Its unique ring structure and functional groups make it a valuable intermediate in the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 2,6-diethoxy-1,4-oxathiane 4,4-dioxide is employed as a precursor for the development of new pharmaceutical compounds. Its potential use in drug discovery is attributed to its ability to be modified and incorporated into diverse molecular frameworks, which can lead to the creation of novel therapeutic agents.
Used in Agricultural Industry:
2,6-diethoxy-1,4-oxathiane 4,4-dioxide has also been studied for its potential applications in the agricultural industry. It may serve as a starting material for the synthesis of agrochemicals, such as pesticides and herbicides, due to its reactivity and structural features.
Used in Material Science:
2,6-diethoxy-1,4-oxathiane 4,4-dioxide may have potential uses in the development of new materials, given its unique chemical properties. Researchers may explore its incorporation into polymers, coatings, or other materials to enhance their performance or introduce new functionalities.
Used as a Research Tool in Organic Chemistry:
2,6-diethoxy-1,4-oxathiane 4,4-dioxide also serves as an important research tool in the field of organic chemistry. It can be used to study reaction mechanisms, test synthetic methodologies, and explore the properties of novel chemical entities.
Check Digit Verification of cas no
The CAS Registry Mumber 37463-85-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,4,6 and 3 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 37463-85:
(7*3)+(6*7)+(5*4)+(4*6)+(3*3)+(2*8)+(1*5)=137
137 % 10 = 7
So 37463-85-7 is a valid CAS Registry Number.
37463-85-7Relevant academic research and scientific papers
ACETALS AND THIOACETALS FROM THIOGLYCOLALDEHYDE: SOME OXIDATION PRODUCTS
Aparicio, Lopez F. J.,Benitez, Zorilla F.,Gonzalez, Santoyo F.
, p. 195 - 206 (2007/10/02)
Thiodiglycolaldehyde (2,2'-thiobisacetaldehyde, 1a) reacted severally with methanol, ethanol, and 2-propanol to give mixtures variously of thiodiglycolaldehyde bis(dialkyl acetals) (3a,b), cis-2,6-dialkoxy-1,4-oxathianes (5b-d), and trans-2,6-dialkoxy-1,4-oxathianes (7a-c).Thiodiglycolaldehyde bis(di-isopropyl acetal) (3c) was not formed in the reaction of 1a and 2-propanol, but 3c was obtained after bromoacetaldehyde di-isopropyl acetal was treated with sodium sulfide.The stereoisomers corresponding to 2,6-dimethoxy-1,4-oxathiane (5b, 7a) were obtained from the acyclic dimethyl acetal 3a.The reaction between 1a and thiols in acid media have been studied.With ethanethiol, thiodiglycolaldehyde bis(diethyl dithioacetal) was the only product, but a mixture of thiodiglycolaldehyde bis(di-tert-butyl dithio-acetal), cis-2,6-bis(tert-butylthio)-1,4-dithiane, and trans-2,6-bis(tert-butylthio)-1,4-dithiane was obtained from 2-methyl-2-propanethiol.On oxidation to sulfones of the stereoisomers of 2,6-dialkoxy-1,4-oxathiane and 2,6-bis(alkylthio)-1,4-dioxane with hydrogen peroxide, the configurations were retained, but the stereoisomers of 2,6-bis(tert-butylthio)-1,4-dithiane were transformed into the same oxidation product.
