91870-93-8 Usage
Uses
Used in Pharmaceutical Industry:
Ethanone, 1-(2-ethyl-2-methyl-1,3-benzoxathiol-5-yl)-, is utilized as a pharmaceutical intermediate due to its unique structure and properties. The presence of the benzoxathiol ring and the attached ethyl and methyl groups may contribute to its potential as a precursor in the synthesis of various medicinal compounds, particularly those that require sulfur-containing heterocycles for biological activity.
Used in Chemical Synthesis:
In the field of chemical synthesis, Ethanone, 1-(2-ethyl-2-methyl-1,3-benzoxathiol-5-yl)-, serves as a versatile building block for the creation of complex organic molecules. Its aromatic and aliphatic properties allow it to participate in a variety of reactions, making it a valuable component in the synthesis of specialty chemicals, agrochemicals, and other advanced materials.
Used in Material Science:
Ethanone, 1-(2-ethyl-2-methyl-1,3-benzoxathiol-5-yl)-, may also find applications in material science, where its unique chemical structure could be leveraged to develop new materials with specific properties. For instance, it could be incorporated into polymers to enhance their thermal stability, mechanical strength, or chemical resistance, depending on the desired application.
Check Digit Verification of cas no
The CAS Registry Mumber 91870-93-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,8,7 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 91870-93:
(7*9)+(6*1)+(5*8)+(4*7)+(3*0)+(2*9)+(1*3)=158
158 % 10 = 8
So 91870-93-8 is a valid CAS Registry Number.
91870-93-8Relevant academic research and scientific papers
On the Acylation of 1,3-Benzoxathiole Systems
Bernard, Angela Maria,Cocco, Maria Teresa,Congiu, Cenzo,Plumitallo, Antonio
, p. 591 - 593 (2007/10/02)
The acylation on 1,3-benzoxathiole systems, as well as the effect of the stoichiometry of the catalyst on the yields of ketones and of breaking products of the O-C-S bonds is here described.
