2298-21-7

Basic information

• Product Name: 4-[2-(pyridin-4-yl)ethenyl]phenyl acetate
• CAS NO: 2298-21-7
• Molecular Formula: C₁₅H₁₃NO₂
• Molecular Weight: 239.2692
• Mol File: 2298-21-7.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 386.3°C at 760 mmHg
• Flash Point: 187.4°C
• Density: 1.175g/cm³
• Vapor Pressure: 3.59E-06mmHg at 25°C
• Refractive Index: 1.637
• CAS DataBase Reference: 4-[2-(pyridin-4-yl)ethenyl]phenyl acetate(CAS DataBase Reference)
• NIST Chemistry Reference: 4-[2-(pyridin-4-yl)ethenyl]phenyl acetate(2298-21-7)
• EPA Substance Registry System: 4-[2-(pyridin-4-yl)ethenyl]phenyl acetate(2298-21-7)

Safety Data

• Hazardous Substances Data: 2298-21-7(Hazardous Substances Data)

Usage

Type of compound

Acetate ester derivative

Structure

Substituted phenyl compound with a pyridine ring attached to the ethenyl group

Uses

Pharmaceutical research, drug development, synthesis of organic compounds

Properties

Potential ligand in metal complexation and catalysis, potential biological activity in drug discovery

Future potential

Further studies and research may reveal additional applications in various fields

Upstream product

• 108-89-4 picoline 
• 108-24-7 acetic anhydride 
• 123-08-0 4-hydroxy-benzaldehyde 
• 878-00-2 4-formylphenyl acetate 

Downstream Products

• 116223-44-0 trans-4-ethoxy-4'-stilbazole 
• 122408-78-0 trans-4-<(4-methoxybenzoyl)oxy>-4'-stilbazole 
• 67882-97-7 4-[(E)-2-(4-pyridinyl)ethenyl]phenol 

Relevant articles and documents

Use of intermolecular hydrogen bonding for the induction of liquid crystallinity in the side chain of polysiloxanes

A new type of liquid crystalline side chain polysiloxane has been built through self-assembly via intermolecular hydrogen bonding between H-bond donor and acceptor moieties. Poly(methylsiloxanes) and poly(methyl-co-dimethylsiloxanes) with side chains cont

Kinetics of Reaction of Phenacyl Bromide with 3- and 4-Substituted Pyridines and 4-Substituted 4-Styrylpyridines

The rates of reaction of phenacyl bromide with 3- and 4-substituted pyridines and 4'-substituted 4-styrylpyridines have been measured in aq. acetone (90percent, v/v) at 30 deg C, 35 deg C and 40 deg C and the activation parameters have been evaluated.Satisfactory Hammett correlations are obtained for both pyridine and styrylpyridine series.The effectiveness of transmission of substituent effect in styrylpyridine system relative to pyridine system in this reaction is calculated to be 0.104.From the Bronsted relationship the coefficient (βN) is found to be 0.48, indicating that the extent of bond formation in the transition state is moderate.