18119-29-4

Basic information

• Product Name: 5-(3-oxo-1-phenylbutyl)pyrimidine-2,4,6(1H,3H,5H)-trione
• Synonyms: 5-(3-oxo-1-phenylbutyl)pyrimidine-2,4,6(1H,3H,5H)-trione
• CAS NO: 18119-29-4
• Molecular Weight: 274.276
• Mol File: 18119-29-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 5-(3-oxo-1-phenylbutyl)pyrimidine-2,4,6(1H,3H,5H)-trione(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(3-oxo-1-phenylbutyl)pyrimidine-2,4,6(1H,3H,5H)-trione(18119-29-4)
• EPA Substance Registry System: 5-(3-oxo-1-phenylbutyl)pyrimidine-2,4,6(1H,3H,5H)-trione(18119-29-4)

Safety Data

• Hazardous Substances Data: 18119-29-4(Hazardous Substances Data)

Upstream product

• 67-52-7 BARBITURIC ACID 
• 100-52-7 benzaldehyde 
• 67-64-1 acetone 
• 122-57-6 1-Phenylbut-1-en-3-one 
• 873-83-6 4-Amino-2,6-dihydroxypyrimidine 

Relevant articles and documents

Pot, atom and step economic (PASE) synthesis of 5-monoalkylbarbiturates through domino aldol-Michael reaction

A simple pot, atom and step economic (PASE) approach for the synthesis of 5-monoalkylbarbiturates by a one-pot reaction of barbituric acids, aldehydes, and ketones, involving a domino aldol-Michael reaction is described. The operational simplicity and cost effectiveness of this procedure makes it a sustainable strategy for the synthesis of 5-monoalkylbarbiturates.

Decarboxylation reactions. II. Reaction of conjugated unsaturated ketones and nitriles with carboxylic acids

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