10129-71-2

Basic information

• Product Name: 2,6-bis(2-phenylvinyl)pyridine
• Synonyms: 2,6-bis(2-phenylvinyl)pyridine;2,6-Bis(2-phenylethenyl)pyridine
• CAS NO: 10129-71-2
• Molecular Formula: C₂₁H₁₇N
• Molecular Weight: 283.36638
• EINECS: 233-363-0
• Mol File: 10129-71-2.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 446.5°Cat760mmHg
• Flash Point: 196.1°C
• Appearance: /
• Density: 1.137g/cm³
• Vapor Pressure: 9.52E-08mmHg at 25°C
• Refractive Index: 1.727
• CAS DataBase Reference: 2,6-bis(2-phenylvinyl)pyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-bis(2-phenylvinyl)pyridine(10129-71-2)
• EPA Substance Registry System: 2,6-bis(2-phenylvinyl)pyridine(10129-71-2)

Safety Data

• Hazardous Substances Data: 10129-71-2(Hazardous Substances Data)

Usage

General Description

2,6-bis(2-phenylvinyl)pyridine, also known as DPVPP, is a chemical compound with the molecular formula C22H18N2. It is commonly used as a sensitizer in photochemical reactions and as a phosphorescent emitter in organic light-emitting diodes (OLEDs). DPVPP is a fluorescent compound with a high quantum yield, making it useful in various optoelectronic applications. Its unique chemical structure and photophysical properties make it a valuable material in the development of advanced technologies in the fields of electronics and photonics. Despite its potential applications, further research is needed to fully understand and exploit the capabilities of 2,6-bis(2-phenylvinyl)pyridine in various technological and scientific areas.

InChI:InChI=1/C21H17N/c1-3-8-18(9-4-1)14-16-20-12-7-13-21(22-20)17-15-19-10-5-2-6-11-19/h1-17H/b16-14+,17-15+

Upstream product

• 108-48-5 2,6-dimethylpyridine 
• 100-52-7 benzaldehyde 
• 5435-44-9 (E)-3-Ureido-but-2-enoic acid ethyl ester 
• 1195-59-1 2.6-bis(hydroxymethyl)pyridine 
• 140-29-4 phenylacetonitrile 
• 100-42-5 styrene 
• 626-05-1 2,6-Dibromopyridine 
• 109-06-8 α-picoline 

Downstream Products

• 5431-44-7 2,6-Pyridinedicarboxaldehyde 
• 2893-33-6 pyridine-2,6-dinitrile 
• 31250-16-5 [2-(2-chloro-2-oxoethoxy)phenoxy]acetyl chloride 
• 818377-18-3 Norlobelane 
• 856849-90-6 2,6-bis-(α,β-dibromo-phenethyl)-pyridine 
• 68031-94-7 2,6-bis (2-phenylethyl) pyridine 

Relevant articles and documents

Tandem Acceptorless Dehydrogenative Coupling-Decyanation under Nickel Catalysis

The development of new catalytic processes based on abundantly available starting materials by cheap metals is always a fascinating task and marks an important transition in the chemical industry. Herein, a nickel-catalyzed acceptorless dehydrogenative coupling of alcohols with nitriles followed by decyanation of nitriles to access diversely substituted olefins is reported. This unprecedented C=C bond-forming methodology takes place in a tandem manner with the formation of formamide as a sole byproduct. The significant advantages of this strategy are the low-cost nickel catalyst, good functional group compatibility (ether, thioether, halo, cyano, ester, amino, N/O/S heterocycles; 43 examples), synthetic convenience, and high reaction selectivity and efficiency.

Organostannoxane-supported Pd(0) nanoparticles as efficient catalysts for Heck-coupling reactions

A new functional organostannoxane cage, SnP, that contains phosphine ligands in its periphery has been structurally utilized as support palladium(0) nanoparticles SnPPd. The latter was shown to catalyze the Heck coupling reactions of wide variety of functionalities efficiently.