61259-55-0

Basic information

• Product Name: 2(1H)-Pyridinone, 1-(2-phenylethenyl)-, (E)-
• CAS NO: 61259-55-0
• Molecular Formula: C13H11NO
• Molecular Weight: 197.236
• Mol File: 61259-55-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2(1H)-Pyridinone, 1-(2-phenylethenyl)-, (E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2(1H)-Pyridinone, 1-(2-phenylethenyl)-, (E)-(61259-55-0)
• EPA Substance Registry System: 2(1H)-Pyridinone, 1-(2-phenylethenyl)-, (E)-(61259-55-0)

Safety Data

• Hazardous Substances Data: 61259-55-0(Hazardous Substances Data)

Usage

Structure

A pyridinone ring with a phenylethene group attached in the 1-position

Classification

Organic compound

Physical state

Colorless to yellow liquid at room temperature

Solubility

Insoluble in water, soluble in organic solvents

Uses

Manufacturing of pharmaceuticals, precursor for various organic compounds

Potential applications

Material science, reagent in organic synthesis

Upstream product

• 142-08-5 2-Pyridone 
• 536-74-3 phenylacetylene 
• 103-64-0 bromostyrene 
• 588-72-7 [(E)-2-bromoethenyl]benzene 

Downstream Products

• 69914-04-1 3-oxo-2-trans-styryl-2-aza-bicyclo[2.2.2]oct-7-ene-5exo,6exo-dicarboxylic acid anhydride 
• 89847-73-4 1,4-etheno-2-(2-trans-phenylvinyl)-3-oxo-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline 
• 102249-85-4 2,3-bis(benzyloxy)naphthalene 
• 102249-79-6 1,4-etheno-2-(2-trans-phenylvinyl)-6,7-dibenzyloxy-3-oxo-1,2,3,4-tetrahydroisoquinoline 
• 69914-02-9 1,4-etheno-2-(2-trans-phenylvinyl)-3-oxo-1,2,3,4-tetrahydroisoquinoline 
• 63828-82-0 1,4-ethano-2-(2-phenylethyl)-3-oxo-1,2,3,4-tetraisoquinoline 
• 63828-83-1 1,4-ethano-2-(2-phenylethyl)-1,2,3,4-tetrahydroisoquinoline 
• 89847-77-8 1,4-ethano-2-(2-phenylethyl)-3-oxo-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline 

Relevant articles and documents

Rhodium(III)-Catalyzed Annulation of Pyridinones with Alkynes via Double C-H Activation: A Route to Functionalized Quinolizinones

A Rh(III)-catalyzed oxidative annulation of pyridin-2(1H)-ones with alkynes via double C-H activation to produce highly functionalized 4H-quinolizin-4-ones is disclosed. This reaction features easily available starting materials, simple manipulation, a relatively wide substrate scope, and good functional group tolerance. The application of this protocol is demonstrated by the synthesis of a known fluorescent quinolizino[3,4,5,6-ija]quinolinium salt.

N-arylation of pyridin-2(1H)-ones with pentavalent organobismuth reagents under copper-free conditions

An efficient method for the N-arylation of pyridin-2(1H)-ones and the related heteroaromatic lactams has been established via ligand-coupling reactions using tri- or tetra-aryl organobismuth(V) reagents such as triarylbismuth dichlorides. Also, N-alkenylation of pyridin-2(1H)-one was achieved similarly by using alkenyltriarylbismuth(V) reagents.