406933-90-2

Upstream product

• 23974-79-0 1-benzylisoquinoline N-oxide 
• 844-25-7 2-benzoyl-1-cyano-1,2-dihydroisoquinoline 
• 210688-98-5 2-(hydroxymethyl)phenyl 4-methyl-1-benzenesulfonate 
• 90-02-8 salicylaldehyde 
• 6907-59-1 1-benzylisoquinoline 
• 406933-92-4 1-(2'-hydroxyfenilmethyl) isoquinoline N-oxide 

Downstream Products

• 406933-92-4 1-(2'-hydroxyfenilmethyl) isoquinoline N-oxide 

Relevant academic research and scientific papers

Regioselective hydroxylation of phenols by simultaneous photochemical generation of phenol cation-radical and hydroxyl radical

Substituted phenols having pendant isoquinoline N-oxide were synthesized and their photochemical and luminiscent properties studied. Photolysis in an acid medium was found to yield the related photohydroxylation products, in a regioselective process, in a

Covalently linked acceptor - Donor systems based on isoquinoline N-oxide acceptor: Photoinduced electron transfer produces dual-channel luminescent systems that evolve chemically to photohydroxylation of the aromatic donor

Acceptor-donor compounds containing the isoquinoline N-oxide acceptor and (methoxy)nbenzene (n = 0, 1, 2, 3) electron donors were studied. The two chromophores are connected by a CH2 bridging unit. All acceptor-donor compounds exhibi

Bis(isoquinoline N-oxide) pincers as a new type of metal cation dual channel fluorosensor.

[structure: see text] A new type of donor-spacer-acceptor podand system has been synthesized and proved as an efficient dual channel fluorosensor for Li+, Mg2+, and Ca2+. The known ability for the N-oxide function to bind Lewis acids is the key step in th