582-70-7

Usage

Chemical structure

1-[2-(4-fluorophenyl)-2-oxoethyl]pyridinium is a chemical compound with a pyridinium cation and a 2-(4-fluorophenyl)-2-oxoethyl group.

Position of substituents

The pyridinium cation has a substituent at the 1-position, and the 2-(4-fluorophenyl)-2-oxoethyl group is at the 2-position.

Potential applications

The compound has potential applications in the field of organic chemistry and chemical research.

Pharmaceutical applications

It may have pharmaceutical applications, as it can potentially act as a pharmacological agent by interacting with biological systems.

Unique structure

The compound's structure and properties make it an intriguing subject for further study and potential use in various applications.

Upstream product

• 110-86-1 pyridine 
• 403-42-9 1-(4-fluorophenyl)ethanone 

Downstream Products

• 1397062-99-5 6-(4-fluoro-phenyl)-4-thiophen-2-yl-[2,2′]bipyridine 
• 1258498-78-0 benzo[d]oxazol-2-yl(4-fluorophenyl)methanone 
• 1384987-38-5 diethyl 2-(4-fluorophenyl)-5H-chromeno[4,3-b]pyridin-4-ylphosphonate 
• 456-22-4 4-Fluorobenzoic acid 

Relevant academic research and scientific papers

Coupling of azomethine ylides with nitrilium derivatives of closo-decaborate clusters: A synthetic and theoretical study

The azomethine ylides p-R3C5H4N+CHCOC 6H4R2-p (3a: R3=H, R2=H, X=Br; 3b: R3=H, R2=Me, X=I; 3c: R3=H, R2=OMe, X=I; 3d: R3=H, R2=F, X=I; 3e: R3=Me, R2=Me, X=Br) react with the nitrile functio

Cyclization of Active Methylene Isocyanides with α-Oxodithioesters Induced by Base: An Expedient Synthesis of 4-Methylthio/Ethoxycarbonyl-5-acylthiazoles

Cyclization of tosylmethyl isocyanide with α-oxodithioesters in the presence of KOH is reported for the synthesis of 4-methylthio-5-acylthiazoles. Similarly, ethyl isocyanoacetate underwent cyclization with α-oxodithioesters to form 4-ethoxycarbonyl-5-acy

Stereoselective Synthesis of Atropisomeric Bipyridine N,N′-Dioxides by Oxidative Coupling

Bipyridine N,N′-dioxide is a structural fragment found in many bioactive compounds. Furthermore, chiral analogues secured their place as powerful Lewis base catalysts. The scope of the existing methods for the synthesis of atropisomeric bipyridine N,N′-di

Acid-Catalyzed Condensation of o-Phenylenediammines and o-Aminophenols with α-Oxodithioesters: A Divergent and Regio? selective Synthesis of 2-Methylthio-3-Aryl/Heteroarylquinoxalines and 2-Acylbenzoxazoles

o-Phenylenediammines and o-Aminophenols were reacted with α-oxodithioesters in a highly regioselective fashion to give 2-methylthio-3-Aryl/heteroarylquinoxalines and 2-Acylbenzoxazoles in 55-94percent and 45-86percent, respectively, in the presence of p-T