76426-84-1

Basic information

• Product Name: 6-(4-Chloro-phenoxy)-3-methyl-1H-pyrimidine-2,4-dione
• Synonyms: 6-(4-Chloro-phenoxy)-3-methyl-1H-pyrimidine-2,4-dione
• CAS NO: 76426-84-1
• Molecular Weight: 252.657
• Mol File: 76426-84-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 6-(4-Chloro-phenoxy)-3-methyl-1H-pyrimidine-2,4-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 6-(4-Chloro-phenoxy)-3-methyl-1H-pyrimidine-2,4-dione(76426-84-1)
• EPA Substance Registry System: 6-(4-Chloro-phenoxy)-3-methyl-1H-pyrimidine-2,4-dione(76426-84-1)

Safety Data

• Hazardous Substances Data: 76426-84-1(Hazardous Substances Data)

Upstream product

• 106-48-9 4-chloro-phenol 
• 4318-56-3 3-methyl-6-chlorouracil 

Downstream Products

• 100-52-7 benzaldehyde 
• 76426-89-6 6-(4-Chloro-phenoxy)-3-methyl-2,4-dioxo-1,2,3,4-tetrahydro-pyrimidine-5-carbaldehyde 

Relevant articles and documents

Synthesis of 2H-Chromenopyrimidine-2,4(3H)-diones (10-Oxa-5-deazaflavins) and Their Use in the Oxidation of Benzyl Alcohol

Treatment of 6-phenoxyuracil derivatives with the Vilsmeier reagent (dimethylformamide-phosphorous oxychloride)gave the corresponding 5-formyl-6-phenoxyuracil derivatives or their equivalents (5-dimethylaminomethylene-6-phenoxyuracil derivatives).Dehydrative cyclization of the above 5-formyluracils or 5-dimethylaminomethyleneuracils with polyphosphoric acid gave the corresponding 2H-chromenopyrimidine-2,4(3H)diones (10-oxa-5-deazaflavins).These 10-oxa-5-deazaflavins showed strong oxidizing power in oxidizing benzyl alcohol even under neutral conditions (without base) to give benzaldehyde, while they were hydrogenated to 1,5-dihydro-10-oxa-5-deazaflavins.