16375-78-3

Basic information

• Product Name: Pyridine, 4-[(1E)-2-(1-naphthalenyl)ethenyl]-
• Synonyms: trans-1-(1-naphthyl)-2-(4-pyridyl)-ethylene;trans-1-(1-naphthyl)-2-(4-pyridyl)ethene;trans-1-(1-Naphthyl)-2-(4'-pyridyl)ethene;trans-4-[2-(1-naphthyl)vinyl]pyridine;trans-4-(β-naphthylvinyl)pyridine;(E)-4-[2-(1-naphthyl)vinyl]pyridine
• CAS NO: 16375-78-3
• Molecular Formula: C17H13N
• Molecular Weight: 231.297
• Mol File: 16375-78-3.mol

Chemical Properties

• Melting Point: 167-169 °C
• Boiling Point: 409.3±20.0 °C(Predicted)
• Density: 1.156±0.06 g/cm3(Predicted)
• CAS DataBase Reference: Pyridine, 4-[(1E)-2-(1-naphthalenyl)ethenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Pyridine, 4-[(1E)-2-(1-naphthalenyl)ethenyl]-(16375-78-3)
• EPA Substance Registry System: Pyridine, 4-[(1E)-2-(1-naphthalenyl)ethenyl]-(16375-78-3)

Safety Data

• Hazardous Substances Data: 16375-78-3(Hazardous Substances Data)

Downstream Products

• 89711-17-1 C₁₉H₁₉N₂⁽¹⁺⁾*BrH*Br^(1-) 
• 5426-19-7 1-(1-naphthyl)-2-(4-pyridyl)ethane 
• 16375-56-7 trans-1-(1-Naphthyl)-2-(4'-pyridyl)ethylene radical anion 
• 16375-56-7 trans-1-(1-Naphthyl)-2-(4'-pyridyl)ethylene radical cation 

Relevant articles and documents

Triplet and Radical Ion Properties of Styrylnaphthalenes and their Aza-derivatives: A Laser Flash Photolytic Study

Laser flash photolysis was used to produce and investigate the lowest excited triplet state (T1) and radical ions (DAE+ radical and DAE- radical) of some diarylethylenes (DAE).In particular, the two trans-styrylnaphthalene isomers (n-StN, where n = 1 or 2 on the naphthalene) and four trans-1-(n-naphthyl)-2-(n'-pyridyl)ethylenes (n,n'-NPE, with n,n' = 1,4'; 2,2'; 2,3' and 2,4') were studied.The transients were characterized in terms of their absorption spectra, decay kinetics, molar absorption coefficients (for DAE+ radical and DAE- radical) and formation quantum yields (for T1 and DAE+ radical).Except for 1-StN, under direct excitation in the absence of quenchers (λexc = 308 and 347 nm), T1 -> Tn absorption was undetectable and DAE+ radical was the only transient observed, even though it was produced in low yield (ΦPI 1 of the DAEs was characterized in n-hexane, in the presence of 4-bromo-N, N-dimethylaniline (BrDMA) which enhances the intersystem-crossing quantum yields, while DAE- radical was produced and studied in acetonitrile, by laser excitation at 347 nm, in the presence of diethylaniline (DEA) and BrDMA.