393109-89-2

Basic information

• Product Name: 2-Phenyl-8-Methoxyquinoline
• Synonyms: 2-Phenyl-8-Methoxyquinoline;8-Methoxy-2-phenylquinoline
• CAS NO: 393109-89-2
• Molecular Formula: C₁₆H₁₃NO
• Molecular Weight: 235.28052
• Mol File: 393109-89-2.mol
• Article Data: 10

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2-Phenyl-8-Methoxyquinoline(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Phenyl-8-Methoxyquinoline(393109-89-2)
• EPA Substance Registry System: 2-Phenyl-8-Methoxyquinoline(393109-89-2)

Safety Data

• Hazardous Substances Data: 393109-89-2(Hazardous Substances Data)

Usage

General Description

2-Phenyl-8-Methoxyquinoline is a chemical compound with the molecular formula C17H13NO. It is a quinoline derivative with a phenyl group at the 2-position and a methoxy group at the 8-position. 2-Phenyl-8-Methoxyquinoline exhibits fluorescence properties and has been studied for its potential use in organic light-emitting diodes (OLEDs) and as a fluorescent probe for detecting DNA. Additionally, 2-Phenyl-8-Methoxyquinoline has shown potential as a therapeutic agent, with studies indicating its anticancer, antimicrobial, and antioxidant activities. Overall, this compound has garnered interest for its diverse range of potential applications in various fields, including materials science and medicinal chemistry.

Upstream product

• 872-36-6 vinylene carbonate 
• 90-04-0 2-methoxy-phenylamine 
• 100-52-7 benzaldehyde 
• 79-24-3 Nitroethane 
• 1636-34-6 2,3-diphenyl-2,3-butanediol 
• 53055-05-3 3-methoxy 2-nitrobenzaldehyde 
• 104-54-1 3-Phenylpropenol 
• 300-57-2 allylbenzene 
• 938-33-0 8-methoxyquinoline 
• 1078-58-6 diphenylzinc 
• 5395-00-6 N-(2-methoxyphenyl)benzamide 
• 5877-56-5 (E)-N-benzylidene-2-methoxybenzenamine 
• 109-92-2 ethyl vinyl ether 
• 70127-96-7 2-amino-3-methoxy-benzaldehyde 

Downstream Products

• 56162-63-1 6-phenyl-2-hydroxypyridine-3-carboxylic acid 

Relevant articles and documents

Rhodium-Catalyzed Dehydrogenative Annulation of N-Arylmethanimines with Vinylene Carbonate for Synthesizing Quinolines

Here we report a novel Rh-catalyzed C-H/C-H alkenylation of N-arylmethanimines with vinylene carbonate acting as a vinylene unit. Forty examples of C3,C4-nonsubstituted quinolines were achieved from commercially available starting materials. This identified process features an exceedingly simple system, a lower loading of catalyst, and the capacity for postfunctionalization with bioactive molecules.

Molybdenum-Catalyzed Sustainable Friedl?nder Synthesis of Quinolines

Polysubstituted quinolines have been efficiently synthesized from nitroarenes and glycols, as reducing agents, under dioxomolybdenum(VI)-catalysis. Interestingly, the waste reduction byproduct is incorporated into the final heterocycle. This method repres

An Unexpected Construction of 2-Arylquinolines from N-Cinnamylanilines through sp3 Ci-H Aerobic Oxidation Induced by a Catalytic Radical Cation Salt

An unexpected reaction of cinnamylanilines was achieved through the radical cation salt-induced aerobic oxidation of sp3 C-H bonds, providing a series of 2-arylquinolines. The mechanistic study shows that the cinnamylaniline was oxidized to an imine, which was attacked by the aniline generated through decomposition of the corresponding imine. After further intramolecular cyclization and aromatization, 2-arylquinolines were obtained. This reaction provides a new method to construct 2-arylquinolines from readily accessible starting materials.