CAS 892-02-4
:5-(3,4-dimethoxybenzyl)-5-methylimidazolidine-2,4-dione
Description:
5-(3,4-Dimethoxybenzyl)-5-methylimidazolidine-2,4-dione, with the CAS number 892-02-4, is a chemical compound that belongs to the class of imidazolidine derivatives. This substance features a five-membered ring structure containing two carbonyl groups, which contribute to its reactivity and potential biological activity. The presence of the 3,4-dimethoxybenzyl group enhances its lipophilicity, potentially influencing its solubility and interaction with biological membranes. The compound is known for its applications in medicinal chemistry, particularly as a scaffold for the development of pharmaceuticals. Its structural characteristics may impart antioxidant properties, making it of interest in studies related to oxidative stress and related diseases. Additionally, the compound's stability and reactivity can be influenced by the substituents on the imidazolidine ring, which may affect its pharmacokinetic and pharmacodynamic profiles. Overall, this compound represents a versatile structure with potential applications in drug development and therapeutic research.
Formula:C13H16N2O4
InChI:InChI=1/C13H16N2O4/c1-13(11(16)14-12(17)15-13)7-8-4-5-9(18-2)10(6-8)19-3/h4-6H,7H2,1-3H3,(H2,14,15,16,17)
SMILES:CC1(Cc2ccc(c(c2)OC)OC)C(=NC(=N1)O)O
Synonyms:- 2,4-Imidazolidinedione, 5-[(3,4-Dimethoxyphenyl)Methyl]-5-Methyl-
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5-[(3,4-Dimethoxyphenyl)methyl]-5-methyl-2,4-imidazolidinedione
CAS:Controlled Product<p>Applications Benzylhydantoins with anticovulsant potential.<br>References Mehta, N. et al.: J. Med. Chem. 24, 465 (1981).<br></p>Formula:C13H16N2O4Color and Shape:NeatMolecular weight:264.28
