110970-05-3

Basic information

• Product Name: 5-(4-hydroxy-phenyl)-5-methyl-imidazolidine-2,4-dione
• Synonyms: 5-(4-hydroxy-phenyl)-5-methyl-imidazolidine-2,4-dione
• CAS NO: 110970-05-3
• Molecular Weight: 206.201
• Mol File: 110970-05-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 5-(4-hydroxy-phenyl)-5-methyl-imidazolidine-2,4-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(4-hydroxy-phenyl)-5-methyl-imidazolidine-2,4-dione(110970-05-3)
• EPA Substance Registry System: 5-(4-hydroxy-phenyl)-5-methyl-imidazolidine-2,4-dione(110970-05-3)

Safety Data

• Hazardous Substances Data: 110970-05-3(Hazardous Substances Data)

Usage

Structure

Consists of a five-membered heterocyclic ring with a phenyl group and a methyl group attached, along with two oxygen atoms included in the ring.

Biological Interaction

Potential pharmaceutical and medical applications due to its ability to interact with biological systems, suggesting it may modulate processes in the body.

Research Interest

Likely of interest for drug development and medicinal chemistry research.

Organic Chemistry

Its structural features and reactivity make it an intriguing subject for further study in the field of organic chemistry.

Upstream product

• 506-87-6 ammonium carbonate 
• 99-93-4 4-Hydroxyacetophenone 
• 1066-33-7 ammonium bicarbonate 

Downstream Products

• 1186116-57-3 5-(4-hydroxyphenyl)-5-methyl-3-(4-(2-oxo-8-n-propyl-4-(trifluoromethyl)-2H-chromen-7-yloxy)butyl)imidazolidine-2,4-dione 

Relevant articles and documents

Solvent effects on the absorption spectra of potentially pharmacologically active 5-alkyl-5-arylhydantoins: A structure-property relationship study

To obtain insight into the interactions of potential anticonvulsant drugs with their surrounding, two series of 5-methyl-5-aryl- and 5-ethyl-5- -arylhydantoins were synthesized and their absorption spectra were recorded in the region from 200 to 400 nm in a set of selected solvents. The effects of solvent dipolarity/polarizability and solvent-solute hydrogen bonding interactions on the absorption maxima shifts were analyzed by means of the linear solvation energy relationship (LSER) concept of Kamlet and Taft. The ratio of the contributions of specific and non-specific solvent-solute interactions were correlated with the corresponding absorption, distribution, metabolism, and excretion (ADME) properties of the studied compounds. The correlation equations were combined with different physicochemical parameters to generate new equations, which demonstrate the reasonable relationships between the solvent- solute interactions and the structure-activity parameters. Copyright (C)2013 SCS.