112519-52-5 Usage
硫锉杂环化合物
2-(methylsulfonyl)-4H-thiochromen-4-one is a sulfur-containing heterocyclic compound, meaning it has a ring structure containing sulfur atoms.
噻吩酮骨架
The compound has a thiochromenone backbone, which is a structure consisting of a thiophene ring fused with a chromenone moiety.
潜在应用领域
2-(methylsulfonyl)-4H-thiochromen-4-one has potential applications in various fields, including pharmaceuticals, agrochemicals, and materials science.
独特的结构性质
The compound's unique structural properties arise from its thiochromenone backbone and the presence of the methylsulfonyl group.
潜在生物活性
2-(methylsulfonyl)-4H-thiochromen-4-one possesses potential biological activities, which may contribute to its applications in pharmaceuticals and agrochemicals.
甲基磺酰基团
The methylsulfonyl group on the thiochromenone backbone provides interesting opportunities for further functionalization and modification.
新衍生物的创造
The functionalization and modification of the methylsulfonyl group can lead to the creation of new derivatives with potentially enhanced properties.
有价值的构建模块
2-(methylsulfonyl)-4H-thiochromen-4-one represents an intriguing and valuable building block for the development of new chemical compounds and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 112519-52-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,5,1 and 9 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 112519-52:
(8*1)+(7*1)+(6*2)+(5*5)+(4*1)+(3*9)+(2*5)+(1*2)=95
95 % 10 = 5
So 112519-52-5 is a valid CAS Registry Number.
112519-52-5Relevant articles and documents
The Synthesis of 4-Hydroxydithiocoumarins: A Case of Unusual Tautomer Stability
Anderson-McKay, Janet E.,Liepa, Andris J.
, p. 1179 - 1190 (2007/10/02)
2'-Chloroacetophenones react with carbon disulfide in the presence of sodium hydride to form 4-hydroxydithiocoumarin anions.Kinetic protonation provides the 4-hydroxydithiocoumarins which can be tautomerized to 2-mercapto-1-thiochromones by treatment with
