1346252-46-7

Basic information

• Product Name: 3,7-dimethyl-1-(5-oxohexyl)-8-(trifluoromethyl)-3,7-dihydro-1H-purine-2,6-dione
• Synonyms: 3,7-dimethyl-1-(5-oxohexyl)-8-(trifluoromethyl)-3,7-dihydro-1H-purine-2,6-dione
• CAS NO: 1346252-46-7
• Molecular Weight: 346.309
• Mol File: 1346252-46-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 3,7-dimethyl-1-(5-oxohexyl)-8-(trifluoromethyl)-3,7-dihydro-1H-purine-2,6-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 3,7-dimethyl-1-(5-oxohexyl)-8-(trifluoromethyl)-3,7-dihydro-1H-purine-2,6-dione(1346252-46-7)
• EPA Substance Registry System: 3,7-dimethyl-1-(5-oxohexyl)-8-(trifluoromethyl)-3,7-dihydro-1H-purine-2,6-dione(1346252-46-7)

Safety Data

• Hazardous Substances Data: 1346252-46-7(Hazardous Substances Data)

Upstream product

• 2926-29-6 Langlois reagent 
• 6493-05-6 pentoxyphylline 

Relevant articles and documents

Electrophotocatalytic Undirected C?H Trifluoromethylations of (Het)Arenes

Electrophotochemistry has enabled arene C?H trifluoromethylation with the Langlois reagent CF3SO2Na under mild reaction conditions. The merger of electrosynthesis and photoredox catalysis provided a chemical oxidant-free approach for the generation of the CF3 radical. The electrophotochemistry was carried out in an operationally simple manner, setting the stage for challenging C?H trifluoromethylations of unactivated arenes and heteroarenes. The robust nature of the electrophotochemical manifold was reflected by a wide scope, including electron-rich and electron-deficient benzenes, as well as naturally occurring heteroarenes. Electrophotochemical C?H trifluoromethylation was further achieved in flow with a modular electro-flow-cell equipped with an in-operando monitoring unit for on-line flow-NMR spectroscopy, providing support for the single electron transfer processes.