151435-01-7

Basic information

• Product Name: 4-Imidazolidinecarboxylicacid,4-hydroxy-2,5-dioxo-,(S)-(9CI)
• Synonyms: 4-Imidazolidinecarboxylicacid,4-hydroxy-2,5-dioxo-,(S)-(9CI)
• CAS NO: 151435-01-7
• Molecular Formula: C4H4N2O5
• Molecular Weight: 160.09
• Product Categories: CARBOXYLICACID;GLYCINESCAFFOLD
• Mol File: 151435-01-7.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-Imidazolidinecarboxylicacid,4-hydroxy-2,5-dioxo-,(S)-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Imidazolidinecarboxylicacid,4-hydroxy-2,5-dioxo-,(S)-(9CI)(151435-01-7)
• EPA Substance Registry System: 4-Imidazolidinecarboxylicacid,4-hydroxy-2,5-dioxo-,(S)-(9CI)(151435-01-7)

Safety Data

• Hazardous Substances Data: 151435-01-7(Hazardous Substances Data)

Upstream product

• 61066-33-9 pyrimidine-2,4,5,6(1H,3H)-tetraone 
• 69-93-2 uric Acid 
• 3237-50-1 5,5-dihydroxy-pyrimidine-2,4,6-trione 
• 34557-54-5 methane 
• 57-13-6 urea 
• 71886-22-1 4-Hydroxy-2,5-dioxo-4-imidazolidinecarboxyureide 

Relevant articles and documents

Absolute stereochemistry of alloxanic acid. A configurational relay for uricase reaction

Alloxanic acid (3) was resolved by means of brucine and converted into its enantiomorphic esters 8 and amides 9; ethyl (-)-alloxanate whose absolute (S)-configuration was established by X-ray analysis served as configurational standard for the correlation of (+)-(R)-(3) and its precursor (-)-(S)-5-hydroxyisourate (2), the key uricolytic intermediate.

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