40856-75-5 Usage
Description
(S)-5-(isobutyl)imidazolidine-2,4-dione is a heterocyclic chemical compound with the molecular formula C9H14N2O2. It features an imidazolidine ring and a carboxyl group, and is recognized for its potential pharmaceutical applications, particularly in the fields of neuroscience and mental health.
Uses
Used in Pharmaceutical Applications:
(S)-5-(isobutyl)imidazolidine-2,4-dione is used as a modulator of neurotransmitter systems, specifically the GABAergic system, which plays a crucial role in regulating anxiety and mood. Its potential applications in this area are currently under investigation.
Used in Neuroscience Research:
In the field of neuroscience, (S)-5-(isobutyl)imidazolidine-2,4-dione is used for its potential anticonvulsant and neuroprotective properties. These characteristics make it a compound of interest for further research into its therapeutic uses and mechanisms of action.
Used in Mental Health:
(S)-5-(isobutyl)imidazolidine-2,4-dione is also being explored for its potential to contribute to the treatment of mental health disorders, given its interaction with the GABAergic system, which is closely associated with mood regulation and anxiety management.
Note: The provided materials do not specify different applications in various industries, so the uses are listed under general categories related to the compound's potential pharmaceutical and research applications.
Check Digit Verification of cas no
The CAS Registry Mumber 40856-75-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,8,5 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 40856-75:
(7*4)+(6*0)+(5*8)+(4*5)+(3*6)+(2*7)+(1*5)=125
125 % 10 = 5
So 40856-75-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H12N2O2/c1-4(2)3-5-6(10)9-7(11)8-5/h4-5H,3H2,1-2H3,(H2,8,9,10,11)/t5-/m0/s1
40856-75-5Relevant articles and documents
3, 5-disubstituted hydantoin compound as well as preparation method and application thereof
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Paragraph 0041; 0053; 0054; 0065; 0066, (2018/10/19)
The invention provides a 3, 5-disubstituted hydantoin compound as well as a preparation method and an application thereof. The structure of the compound is shown in formula I in the description. The application of the 3, 5-disubstituted hydantoin compound shown in the formula I or solvates, hydrates or salts of the compound in preparation of medicines for treating Alzheimer's disease, vascular dementia and other dementia diseases with memory impairment also belongs to the protection scope. Animal experiments prove that the compound has the effect of saving memory of animal models, has high safety, does not have mutagenicity, can stay in blood for several hours after oral administration and intravenous injection, and can enter the brain.
Mechanochemical preparation of hydantoins from amino esters: Application to the synthesis of the antiepileptic drug phenytoin
Konnert, Laure,Reneaud, Benjamin,De Figueiredo, Renata Marcia,Campagne, Jean-Marc,Lamaty, Frdric,Martinez, Jean,Colacino, Evelina
, p. 10132 - 10142 (2015/02/19)
The eco-friendly preparation of 5- and 5,5-disubstituted hydantoins from various amino ester hydrochlorides and potassium cyanate in a planetary ball-mill is described. The one-pot/two-step protocol consisted in the formation of ureido ester intermediates, followed by a base-catalyzed cyclization to hydantoins. This easy-handling mechanochemical methodology was applied to a large variety of α- and β-amino esters, in smooth conditions, leading to hydantoins in good yields and with no need of purification steps. As an example, the methodology was applied to the "green" synthesis of the antiepileptic drug Phenytoin, with no use of any harmful organic solvent.
