26031-63-0

Basic information

• Product Name: 1-(2-(4-fluorophenyl)-2-oxoethyl)pyridine-1-ium bromide
• Synonyms: 1-(2-(4-fluorophenyl)-2-oxoethyl)pyridine-1-ium bromide
• CAS NO: 26031-63-0
• Molecular Weight: 296.139
• Mol File: 26031-63-0.mol
• Article Data: 13

Chemical Properties

• CAS DataBase Reference: 1-(2-(4-fluorophenyl)-2-oxoethyl)pyridine-1-ium bromide(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2-(4-fluorophenyl)-2-oxoethyl)pyridine-1-ium bromide(26031-63-0)
• EPA Substance Registry System: 1-(2-(4-fluorophenyl)-2-oxoethyl)pyridine-1-ium bromide(26031-63-0)

Safety Data

• Hazardous Substances Data: 26031-63-0(Hazardous Substances Data)

Usage

General Description

1-(2-(4-fluorophenyl)-2-oxoethyl)pyridine-1-ium bromide is a chemical compound with a molecular formula C15H12BrFNO. It is a pyridinium salt, which is often used as an intermediate in the synthesis of pharmaceuticals and organic compounds. 1-(2-(4-fluorophenyl)-2-oxoethyl)pyridine-1-ium bromide contains a pyridine ring and a 4-fluorophenyl group, as well as a bromide ion. It is commonly used in organic synthesis as a reactant in various chemical reactions. Additionally, it may have potential applications in the development of new drugs and materials due to its unique chemical structure and properties.

Upstream product

• 110-86-1 pyridine 
• 403-29-2 2-bromo-4'-fluoroacetophenone 
• 403-42-9 1-(4-fluorophenyl)ethanone 

Downstream Products

• 129155-23-3 2-ethylthio-3-(4'-fluorophenacyl)-1,4-naphthoquinone 
• 76609-29-5 2-(4-fluorophenyl)-1H-benzo[g]indole 
• 76609-16-0 5-chloro-2-(4-fluorophenyl)-1H-indole 
• 76609-19-3 2-(4-fluorophenyl)-5-methoxy-1H-indole 
• 68290-37-9 2-(4-fluoro-phenyl)-5-nitro-indole 
• 782-17-2 2-(4-fluorophenyl)indole 
• 109358-56-7 2-(4-Fluoro-phenyl)-3H-benzo[e]indole 
• 85237-65-6 5-methyl-2-(4-fluorophenyl)-pyridine 
• 1233194-42-7 C₂₄H₁₅FN₂OS 
• 1233194-43-8 C₂₅H₁₇FN₂OS 
• 1233194-44-9 C₂₅H₁₇FN₂O₂S 
• 1240428-17-4 3-[6-(4-fluorphenyl)-4-(2,4-dimethoxyphenyl)pyridin-2-yl]-4-hydroxycoumarin 
• 1240428-16-3 3-[6-(4-fluorophenyl)-4-(4-methoxyphenyl)pyridin-2-yl]-4-hydroxycoumarin 
• 347-12-6 2-(4-fluorophenyl)imidazo[1,2-a]pyridine 

Relevant articles and documents

Anti-tubercular activity and molecular docking studies of indolizine derivatives targeting mycobacterial InhA enzyme

A series of 1,2,3-trisubstituted indolizines (2a–2f, 3a–3d, and 4a–4c) were screened for in?vitro whole-cell anti-tubercular activity against the susceptible H37Rv and multidrug-resistant (MDR) Mycobacterium tuberculosis (MTB) strains. Compounds 2b–2d, 3a

Base-mediated 1,3-dipolar cycloaddition of pyridinium bromides with bromoallyl sulfones: a facile access to indolizine scaffolds

An expedient and transition-metal-free synthetic strategy has been developed for the construction of substituted indolizines from a unique combination of pyridinium salts and 2-bromoallyl sulfones. This approach does not compromise with the diverse substitutions on both the pyridinium salts and 2-bromoallyl sulfones. Wide substrate scope, operational simplicity, milder reaction conditions and good to moderate yields are the merits associated with the current approach. Moreover, this method provides two products which are amenable for the generation of a library of key indolizine building blocks. This journal is

Greener synthesis of indolizine analogues using water as a base and solvent: study for larvicidal activity against Anopheles arabiensis

Greener synthesis of a series of novel indolizine analogues have been achieved by the cyclization of aromatic cycloimmonium ylides with electron-deficient alkynes in the presence of water as the base and solvent at 80?°C. Yield of the title compounds was