81067-98-3 Usage
General Description
5-methyl-5-phenyl-3-(phenylsulfanyl)imidazolidine-2,4-dione is a chemical compound with a complex structure and a unique combination of functional groups. It contains a five-membered ring system with a methyl group and a phenyl group attached to the carbon atoms at positions 5 and 3, respectively. Additionally, it has a phenylsulfanyl group connected to the nitrogen atom in the ring. 5-methyl-5-phenyl-3-(phenylsulfanyl)imidazolidine-2,4-dione belongs to the class of imidazolidine-2,4-dione derivatives, which have been studied for their potential pharmaceutical and biological activities. The specific properties and applications of 5-methyl-5-phenyl-3-(phenylsulfanyl)imidazolidine-2,4-dione may vary depending on its structural features and synthetic methods, and further research is needed to fully understand its potential uses.
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 articles and documents
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.
