2607-25-2

Upstream product

• 2216-69-5 1-Methoxynaphthalene 

Downstream Products

• 492-97-7 2,2'-Bithiophene 
• 105508-12-1 1-methoxy-4-(2-thienyl)naphthalene 
• 51010-48-1 1-methoxy-4-benzylnaphthalene 
• 34224-97-0 1-Cyclohexyl-4-methoxynaphthalin 
• 931120-69-3 5-isopropenyl-1-(4-methoxy-naphthalen-1-yl)-2-methyl-cyclohex-2-enol 
• 1380681-15-1 C₄₇H₄₄N₆O₇ 
• 5961-55-7 4-methoxy-1-naphthalenecarbonitrile 
• 1408053-84-8 2-(4-methoxynaphthalen-2-yl)benzaldehyde 
• 1408053-90-6 1-[2-(4-methoxynaphthalen-2-yl)phenyl]ethanone 
• 1408053-95-1 12-methoxy-6-methyl-6H-Benzo[d]naphtho[1,2-b]pyran 
• 1199939-51-9 1-methoxy-4-(2,3,5,6-tetrafluoro-4-methylphenyl)naphthalene 
• 934845-08-6 (4-methoxynaphthalen-1-yl)(4′-methoxyphenyl)sulfane 
• 109251-11-8 1-methoxy-4-(4'-methoxyphenyl)naphthalene 
• 721930-68-3 2-(4-methoxy-[1]naphthyl)-aniline 

Relevant academic research and scientific papers

Simple and regioselective oxyiodination of aromatic compounds with ammonium iodide and Oxone

Oxyiodination of aromatic compounds using NH4I and Oxone gives high yields and selectivity. A simple method for the iodination of aromatic compounds using NH4I as the iodine source and Oxone as the oxidant is described.

Effective and regioselective iodination of arenes using iron(III) nitrate in the presence of tungstophosphoric acid

An easy, cheap, and effective method for iodination of various aromatic compounds takes place with molecular iodine and iron nitrate nonahydrate as the oxidant in the presence of a catalytic amount of tungstophosphoric acid in dichloromethane, with good yield and high regioselectivity under very mild conditions.

Direct and regioselective iodination and bromination of benzene, naphthalene and other activated aromatic compounds using iodine and bromine

Direct and regioselective iodination and bromination of benzene, naphthalene and other activated aromatic compounds with iodine and bromine or their sodium salts proceed well in the presence of Fe(NO3) 3·1.5N2O4/charcoal in CH 2Cl2 at room temperature.

Regioselective oxyiodination of aromatic compounds using potassium iodide and oxone

A highly efficient, simple, mild and regioselective method for oxyiodination of aromatic compounds is reported. The electrophilic substitution of iodine generated in situ from KI as an iodine source and oxone as an oxidant for the first time.