24463-84-1 Usage
Description
(1,1-dioxidotetrahydrothiophen-2-yl)(phenyl)methanone is a chemical compound with the molecular formula C13H11NO3S. It features a tetrahydrothiophene ring, a ketone group, and a phenyl group attached to it. (1,1-dioxidotetrahydrothiophen-2-yl)(phenyl)methanone is known for its diverse reactivity and functional groups, as well as its aromatic nature and potential for hydrogen bonding, which may contribute to interesting biological and pharmacological properties.
Uses
Used in Pharmaceutical Industry:
(1,1-dioxidotetrahydrothiophen-2-yl)(phenyl)methanone is used as a pharmaceutical compound for its potential applications in drug development. Its diverse reactivity and functional groups make it a promising candidate for the creation of new medications.
Used in Agrochemical Industry:
In the agrochemical industry, (1,1-dioxidotetrahydrothiophen-2-yl)(phenyl)methanone is used as a component in the development of pesticides and other agricultural chemicals. Its unique structure and properties may contribute to the effectiveness of these products.
Used in Materials Science:
(1,1-dioxidotetrahydrothiophen-2-yl)(phenyl)methanone is utilized in materials science for the development of new materials with specific properties. Its aromatic nature and potential for hydrogen bonding may lead to the creation of innovative materials with unique characteristics.
However, it is important to note that further research and testing are required to fully understand the properties and potential uses of (1,1-dioxidotetrahydrothiophen-2-yl)(phenyl)methanone in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 24463-84-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,4,6 and 3 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 24463-84:
(7*2)+(6*4)+(5*4)+(4*6)+(3*3)+(2*8)+(1*4)=111
111 % 10 = 1
So 24463-84-1 is a valid CAS Registry Number.
24463-84-1Relevant articles and documents
Efficient conversion of sulfones into β-keto sulfones by N-acylbenzotriazoles
Katritzky, Alan R.,Abdel-Fattah, Ashraf A. A.,Wang, Mingyi
, p. 1443 - 1446 (2007/10/03)
Acyclic sulfones 4a-f and alicyclic sulfone 7 react with readily available N-acylbenzotriazoles 3a-g (derived from aliphatic, aromatic, and heteroaromatic carboxylic acids) to provide the corresponding β-keto sulfones 5a-n and 8a-c, respectively, in good