54833-61-3 Usage
Uses
Used in Pharmaceutical Industry:
2,4-Imidazolidinedione, 5-(4-methoxyphenyl)-3-methyl-5-phenylis used as an anticonvulsant for the treatment of seizures, providing a calming effect on the central nervous system by enhancing GABA activity. It is also used as a sedative for medical procedures such as surgeries, where its calming properties are beneficial in managing patient anxiety and ensuring a smooth procedure.
Used in Neurological Treatments:
In the field of neurology, 2,4-Imidazolidinedione, 5-(4-methoxyphenyl)-3-methyl-5-phenylis utilized for its anticonvulsant properties to manage conditions like epilepsy, where seizures can be debilitating and require effective control. Its ability to modulate GABA activity makes it a valuable asset in the management of seizure disorders.
Check Digit Verification of cas no
The CAS Registry Mumber 54833-61-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,8,3 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 54833-61:
(7*5)+(6*4)+(5*8)+(4*3)+(3*3)+(2*6)+(1*1)=133
133 % 10 = 3
So 54833-61-3 is a valid CAS Registry Number.
InChI:InChI=1/C17H16N2O3/c1-19-15(20)17(18-16(19)21,12-6-4-3-5-7-12)13-8-10-14(22-2)11-9-13/h3-11H,1-2H3,(H,18,21)
54833-61-3Relevant academic research and scientific papers
Concerning the reaction mechanism of the hydantoin synthesis according to Biltz, II: Influence of substituents on the direction of the rearrangement
Schwenker,Guo
, p. 45 - 50 (2007/10/02)
From 1-13C-labelled 4-monosubstituted benzils 1a-c and the ureas 3a-d the 5-aryl-5-phenylhydantoines 6a-c and the 3-substituted 5-aryl-5-phenylhydantoines 9a-i were obtaincd as mixtures of isotopomeres. The distribution of 13C-labelling of C-4 and C-5 was determined by mass- and 13C-nmr-spectroscopy. As in the case of benzilic acid rearrangement the a-methylphenyl- and 4-methoxyphenyl-increment, respectively, migrate less easily than does the unsubstituted phenyl group, which in turn migrates less easily than the 4-chlorophenylrest. In the latter case the differences are small and in one example cven slightly reversed. The characteristics of the rearrangement is explained by thermodynamic control of the reaction by preceding equilibria (Schemes 2 and 3).
