Yamaguchi, Eiji published the artcileOlefin Bifunctionalization: A Visible-light Photoredox-catalyzed Aryl Alkoxylation of Olefins, Product Details of C7H6N2, the main research area is diarylethyl ether photochem preparation; ruthenium photoredox catalyst arylalkoxylation aryl alkene diazonium salt alc; photochem arylalkoxylation aryl alkene diazonium salt alc; alkoxylation; bifunctionalization; olefins; photoredox catalyst; visible light.
Aryl alkenes such as RCH:CH2 (R = Ph, 4-MeCOC6H4, 4-MeO2CC6H4, 4-BrC6H4, 4-ClC6H4, 4-MeC6H4, 3-MeC6H4, 2-MeC6H4, 4-MeC6H4, 1-naphthyl, 2-naphthyl) underwent photoredox arylalkoxylation under visible light with aryldiazonium tetrafluoroborates such as R1N2+BF4- (R1 = 4-O2NC6H4, 3-O2NC6H4, 4-MeCOC6H4, 4-MeO2CC6H4, 4-NCC6H4, 3-NCC6H4, 2-NCC6H4, 4-F3CC6H4, 3-BrC6H4, 2-BrC6H4, 4-ClC6H4, 4-FC6H4) and methanol, ethanol, or 1-propanol in acetonitrile/alc. mixtures in the presence of Ru(bpy)3Cl2 to yield diarylethyl ethers such as R1CH2CH(OMe)R (R = Ph, 4-MeCOC6H4, 4-MeO2CC6H4, 4-BrC6H4, 4-ClC6H4, 4-MeC6H4, 3-MeC6H4, 2-MeC6H4, 4-MeC6H4, 1-naphthyl, 2-naphthyl; R1 = 4-O2NC6H4, 3-O2NC6H4, 4-MeCOC6H4, 4-MeO2CC6H4, 4-NCC6H4, 3-NCC6H4, 2-NCC6H4, 4-F3CC6H4, 3-BrC6H4, 2-BrC6H4, 4-ClC6H4, 4-FC6H4).
Chemistry – An Asian Journal published new progress about Alcohols Role: RCT (Reactant), RACT (Reactant or Reagent). 1885-29-6 belongs to class nitriles-buliding-blocks, name is 2-Aminobenzonitrile(Flakes or Chunks), and the molecular formula is C7H6N2, Product Details of C7H6N2.
Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts