What is the (E)9-(2-phenylvinyl)anthracene?

(E)9-(2-phenylvinyl)anthracene is , while it's Molecular Formula is C22H16. Used in Organic Synthesis: (E)9-(2-phenylvinyl)anthracene is used as a key intermediate in the synthesis of various organic compounds due to its unique structure and reactivity. Used in Materials Science: (E)9-(2-phenylvinyl)anthracene is used as a building block for the development of novel materials with specific properties, such as high thermal stability and electrical conductivity. Used in Optoelectronics: (E)9-(2-phenylvinyl)anthracene is used as a component in optoelectronic devices, such as organic light-emitting diodes (OLEDs), due to its fluorescent properties. It contributes to the emission of light in these devices, enhancing their performance and efficiency. Used in Electronic Devices: (E)9-(2-phenylvinyl)anthracene is used in the development of electronic devices, such as sensors and transistors, due to its electronic properties and potential for integration with other materials. It is important to handle (E)9-(2-phenylvinyl)anthracene with caution, as it is classified as a hazardous chemical with potential health and environmental risks. Proper safety measures should be taken during its production, use, and disposal to minimize any adverse effects.

What is the CAS number for (E)9-(2-phenylvinyl)anthracene?

The CAS number of (E)9-(2-phenylvinyl)anthracene is 42196-97-4.

What is the (E)9-(2-phenylvinyl)anthracene?

(E)9-(2-phenylvinyl)anthracene is , while it's Molecular Formula is C22H16. Used in Organic Synthesis: (E)9-(2-phenylvinyl)anthracene is used as a key intermediate in the synthesis of various organic compounds due to its unique structure and reactivity. Used in Materials Science: (E)9-(2-phenylvinyl)anthracene is used as a building block for the development of novel materials with specific properties, such as high thermal stability and electrical conductivity. Used in Optoelectronics: (E)9-(2-phenylvinyl)anthracene is used as a component in optoelectronic devices, such as organic light-emitting diodes (OLEDs), due to its fluorescent properties. It contributes to the emission of light in these devices, enhancing their performance and efficiency. Used in Electronic Devices: (E)9-(2-phenylvinyl)anthracene is used in the development of electronic devices, such as sensors and transistors, due to its electronic properties and potential for integration with other materials. It is important to handle (E)9-(2-phenylvinyl)anthracene with caution, as it is classified as a hazardous chemical with potential health and environmental risks. Proper safety measures should be taken during its production, use, and disposal to minimize any adverse effects.

What is the CAS number for (E)9-(2-phenylvinyl)anthracene?

The CAS number of (E)9-(2-phenylvinyl)anthracene is 42196-97-4.

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(E)9-(2-phenylvinyl)anthracene

CasNo：42196-97-4
purity：99%

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Molecular Formula:C22H16
Molecular Weight:280.369
Vapor Pressure:8.8E-09mmHg at 25°C
Melting Point:132 °C
Boiling Point:476.4°Cat760mmHg
Flash Point:236.5°C
PSA：0.00000
Density:1.163g/cm³
LogP:6.16340

(E)9-(2-phenylvinyl)anthracene(Cas 42196-97-4) Usage

General Description

(E)9-(2-phenylvinyl)anthracene is a polycyclic aromatic hydrocarbon compound with a molecular formula of C24H18. It is a derivative of anthracene, consisting of a nine-carbon anthracene core with a vinyl group substituted at the 9 position and a phenyl group at the 2 position. (E)9-(2-phenylvinyl)anthracene is commonly used in organic synthesis and has been studied for its potential applications in materials science and optoelectronics. (E)9-(2-phenylvinyl)anthracene exhibits fluorescent properties and has been investigated for its use in organic light-emitting diodes (OLEDs) and other electronic devices. It is important to handle (E)9-(2-phenylvinyl)anthracene with caution, as it is classified as a hazardous chemical with potential health and environmental risks.

InChI:InChI=1/C22H16/c1-2-8-17(9-3-1)14-15-22-20-12-6-4-10-18(20)16-19-11-5-7-13-21(19)22/h1-16H

42196-97-4 Relevant articles

9-vinylanthracene based fluorogens: Synthesis, structure-property relationships and applications

Liu, Mengjie,Onchaiya, Sawaros,Tan, Lewis Yi Fong,Haghighatbin, Mohammad A.,Luu, Tracey,Owyong, Tze Cin,Hushiarian, Roozbeh,Hogan, Conor F.,Smith, Trevor A.,Hong, Yuning

, (2017)

Fluorescent dyes with aggregation-induce...

On the Relationship between Molecular Geometry and Excited-State Properties of 9-Anthrylalkenes

Becker, Hans-Dieter,Andersson, Kjell

, p. 4542 - 4549 (1983)

The excited-state properties of a series...

N-Heterocyclic carbene palladium (II)-pyridine (NHC-Pd (II)-Py) complex catalyzed heck reactions

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supporting information, p. 2041 - 2052 (2021/05/25)

A mild, efficient, and practical catalyt...

Two trans-1-(9-anthryl)-2-phenylethene derivatives as blue-green emitting materials for highly bright organic light-emitting diodes application

Zhou, Nonglin,Shao, Xiaona,Wang, Shirong,Xiao, Yin,Li, Xianggao

, p. 228 - 238 (2017/08/08)

1-(9-Anthryl)-2-phenylethene (t-APE) is ...

Synthesis and tyrosinase inhibition activity of trans-stilbene derivatives

Ismail, Tabasum,Shafi, Syed,Srinivas, Jada,Sarkar, Dhiman,Qurishi, Yasrib,Khazir, Jabeena,Alam, Mohammad Sarwar,Kumar, Halmuthur Mahabalarao Sampath

, p. 97 - 102 (2016/01/25)

Synthesis of a focussed library of trans...

42196-97-4 Process route

: 1100-88-5
benzyltriphenylphosphonium chloride

: 642-31-9
9-anthracene aldehyde

: 1895-98-3,42196-97-4,87337-00-6,139492-08-3,139492-10-7
9-styrylanthracene

Conditions

Conditions	Yield
In dichloromethane; at 20 ℃; for 0.0833333h;	67%

: 35984-40-8
Triphenyl-(9-anthracenylmethyl)phosphonium chloride

: 100-44-7
benzyl chloride

: 1895-98-3,42196-97-4,87337-00-6,139492-08-3,139492-10-7
9-styrylanthracene