78405-79-5

Basic information

• Product Name: Anthracene, 2-(2-phenylethenyl)-, (E)-
• CAS NO: 78405-79-5
• Molecular Formula: C22H16
• Molecular Weight: 280.369
• Mol File: 78405-79-5.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Anthracene, 2-(2-phenylethenyl)-, (E)-(CAS DataBase Reference)
• NIST Chemistry Reference: Anthracene, 2-(2-phenylethenyl)-, (E)-(78405-79-5)
• EPA Substance Registry System: Anthracene, 2-(2-phenylethenyl)-, (E)-(78405-79-5)

Safety Data

• Hazardous Substances Data: 78405-79-5(Hazardous Substances Data)

Upstream product

• 97643-53-3 cis-2-styrylanthracene 
• 88229-63-4 (2-Anthrylmethyl)triphenylphosphonium Bromide 
• 100-52-7 benzaldehyde 
• 7321-27-9 2-bromoanthracene 
• 83947-56-2 4,4,5,5-tetramethyl-2-((E)-styryl)-[1,3,2]dioxaborolane 
• 31124-71-7 2-(bromomethyl)anthracene 
• 613-12-7 2-methylanthracene 
• 538-51-2 benzylidene phenylamine 

Downstream Products

• 97643-53-3 cis-2-styrylanthracene 

Relevant articles and documents

Highly Efficient Conformer-Specifif Adiabatic Cis -> Trans Photoisomerization of cis-1-(2-Anthryl)-2-phenylethene in S1

Emission from cis-1-(2-anthryl)-2-phenylethene, c-APE, in toluene cosists primarily (up to 76percent) of fluorescence from adiabatically formed 1t-APEB*.In this respect, the behavior of c-APE is analogous to that of the na

Asymmetric organic semiconductors for high performance single crystalline field-effect transistors with low activation energy

Three anthracene derivatives with asymmetric structures, namely 2-phvA, 2-pheA and 2-phA, were synthesised and characterized. Single crystal OFETs of the three compounds were fabricated. 2-pheA and 2-phA showed a mobility of 0.79 cm2 V-1 s-1 and 0.66 cm2 V-1 s-1, while 2-phvA exhibited a high mobility of 10 cm2 V-1 s-1, which was one of the highest mobilities for asymmetric anthracene derivatives. Band-like charge transport with low activation energy was observed in 2-phvA single crystal FET devices at low temperature. These results demonstrated that asymmetry can serve as an alternative strategy to design high-performance organic semiconductors.

Features of the Quantum Chain Process in the Photochemical One-Way Isomerization of 2-Anthrylethylenes

Regarding 2-anthrylethylenes which undergo a photochemical cis-to-trans one-way isomerization, their preparative methods are presented.The isomerization of ArCH=CHPh and ArCH=CH(2-naphthyl) (Ar: 2-anthryl) proceeds through a quantum chain process slightly more efficiently than ArCH=CHtBu.The origin of the high efficiency in the quantum chain process of these ethylenes is discussed.