5659-33-6

Basic information

• Product Name: 2-Phenylquinoline 1-oxide
• Synonyms: 2-Phenylquinoline 1-oxide
• CAS NO: 5659-33-6
• Molecular Formula: C₁₅H₁₁NO
• Molecular Weight: 221.25
• Mol File: 5659-33-6.mol
• Article Data: 27

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Phenylquinoline 1-oxide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Phenylquinoline 1-oxide(5659-33-6)
• EPA Substance Registry System: 2-Phenylquinoline 1-oxide(5659-33-6)

Safety Data

• Hazardous Substances Data: 5659-33-6(Hazardous Substances Data)

Upstream product

• 2311-91-3 monoperoxyphthalic acid 
• 612-96-4 2-Phenylquinoline 
• 1613-37-2 Quinoline N-oxide 
• 981-18-0 triphenyl(phenylazo)methane 
• 10285-99-1 2-methoxyquinoline N-oxide 
• 18457-79-9 2-cyanoquinoline N-oxide 
• 7473-93-0 (E)-3-(2-nitrophenyl)-1-phenylprop-2-en-1-one 
• 591-51-5 phenyllithium 
• 71-43-2 benzene 
• 108-86-1 bromobenzene 
• 53744-31-3 2-nitrochalcone 
• 634606-85-2 3-hydroxy-3-(2-nitrophenyl)-1-phenylpropane-1-one 
• 98-86-2 acetophenone 
• 552-89-6 2-nitro-benzaldehyde 

Downstream Products

• 4979-79-7 4-chloro-2-phenylquinoline 
• 14300-21-1 2-phenylbenzo[d][1,3]oxazepine 
• 87732-10-3 3H-3-methoxyallyl-3-methoxycarbonyl-2-phenyl-1-benzazepine 
• 612-96-4 2-Phenylquinoline 
• 25365-71-3 2-phenyl-1H-indol-3-carboxaldehyde 
• 116363-38-3 [Rh(C₈H₁₂)(C₉H₆N(O)C₆H₅)(P(C₆H₅)3)]⁽¹⁺⁾*ClO₄^(1-)=[Rh(C₈H₁₂)(C₉H₆N(O)C₆H₅)(P(C₆H₅)3)]ClO₄ 
• 1620101-21-4 8-(4-methylphenylsulfonamido)-2-phenylquinoline N-oxide 
• 1620100-81-3 8-iodo-2-phenylquinoline N-oxide 
• 5855-50-5 3-hydroxy-2-phenylquinoline 

Relevant articles and documents

N2H4-H2O Enabled Umpolung Cyclization of o-Nitro Chalcones for the Construction of Quinoline N-Oxides

Umpolung is a unique strategy which converts the property of an atom into the opposite one. An efficient and general method for the construction of quinoline N-oxides via umpolung of carbonyl groups was developed from ortho-nitro chalcones and hydrazine i

Visible-light-promoted c2 selective arylation of quinoline and pyridine n-oxides with diaryliodonium tetrafluoroborate

A protocol of visible-light-promoted C2 selective arylation of quinoline and pyridine N-oxides, with diaryliodonium tetrafluoroborate as an arylation reagent, using eosin Y as a photocatalyst for the construction of N-heterobiaryls was presented. This met

Co(III)-Catalyzed C-H Amidation of Nitrogen-Containing Heterocycles with Dioxazolones under Mild Conditions

A cobalt(III)-catalyzed C-8 selective C-H amidation of quinoline N-oxide using dioxazolone as an amidating reagent under mild conditions is disclosed. The reaction proceeds efficiently with excellent functional group compatibility. The utility of the current method is demonstrated by gram scale synthesis of C-8 amide quinoline N-oxide and by converting this amidated product into functionalized quinolines. Furthermore, the developed catalytic method is also applicable for C-7 amidation of N-pyrimidylindolines and ortho-amidation of benzamides.