81067-98-3 Usage
Uses
Given the provided materials, there are no specific applications listed for 5-methyl-5-phenyl-3-(phenylsulfanyl)imidazolidine-2,4-dione. However, based on its classification as an imidazolidine-2,4-dione derivative, it can be inferred that 5-methyl-5-phenyl-3-(phenylsulfanyl)imidazolidine-2,4-dione may have potential uses in various fields, such as pharmaceuticals or materials science, pending further research and development. If future studies identify specific applications, they could be listed as follows:
Used in Pharmaceutical Industry:
5-methyl-5-phenyl-3-(phenylsulfanyl)imidazolidine-2,4-dione could be utilized as a pharmaceutical agent for [specific medical condition or treatment] due to its [particular property or mechanism of action].
Used in Materials Science:
In the field of materials science, 5-methyl-5-phenyl-3-(phenylsulfanyl)imidazolidine-2,4-dione might serve as a component in the development of [specific type of material or product], leveraging its [unique characteristic or property].
Check Digit Verification of cas no
The CAS Registry Mumber 81067-98-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,0,6 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 81067-98:
(7*8)+(6*1)+(5*0)+(4*6)+(3*7)+(2*9)+(1*8)=133
133 % 10 = 3
So 81067-98-3 is a valid CAS Registry Number.
81067-98-3Relevant academic research and scientific papers
In Search of New Sulfur Transfer Agents
Sosnovsky, George,Krogh, James A.
, p. 121 - 136 (2007/10/02)
The chemistry of various sulfur-transfer agents is studied.The reaction of aromatic sulfenyl chloride 5 in the presence of imidazole and/or triethylamine gives the aryl disulfides 7 in 14-85 percent yield, whereas in the case of the corresponding benzylsulfenyl chlorides 9 in the presence of triethylamine and/or caprolactam, both disulfide 10 and benzyl chlorides 11 are formed in 0-81 precent and 10-72 precent yield, respectively. - The transfer reactions of 3-sulfenylated hydantoins 18 with amines are useful for the preparation of the unsymmetric sulfenamides 20 in 31 -61 percent yield.Analogous transfer reactions of compounds 23 and 24 with piperidine give N,N'-thiodipiperidine (3, X = CH2) in 71-80 percent.
