4707-75-9

Basic information

• Product Name: 2-(2-Bromophenyl)-1,1-diphenylethene
• Synonyms: 2-(2-Bromophenyl)-1,1-diphenylethene
• CAS NO: 4707-75-9
• Molecular Formula: C₂₀H₁₅Br
• Molecular Weight: 0
• Mol File: 4707-75-9.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(2-Bromophenyl)-1,1-diphenylethene(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-Bromophenyl)-1,1-diphenylethene(4707-75-9)
• EPA Substance Registry System: 2-(2-Bromophenyl)-1,1-diphenylethene(4707-75-9)

Safety Data

• Hazardous Substances Data: 4707-75-9(Hazardous Substances Data)

Usage

General Description

2-(2-Bromophenyl)-1,1-diphenylethene is a chemical compound that belongs to the class of styrenes. It is also known as bromo stilbene and is a white solid at room temperature. 2-(2-Bromophenyl)-1,1-diphenylethene is used in the production of fluorescent optical brighteners and as a raw material in the synthesis of pharmaceuticals and agrochemicals. It possesses important optical and electronic properties, making it useful in the field of materials science for the design and development of new materials. Additionally, 2-(2-Bromophenyl)-1,1-diphenylethene has potential applications in organic electronics, such as in the fabrication of organic light-emitting diodes (OLEDs) and organic photovoltaic devices. Overall, this chemical compound has a range of industrial and scientific applications due to its unique properties and reactivity.

Upstream product

• 1072-85-1 o-fluorobromobenzene 
• 19997-66-1 1-iodo-2,2-diphenylethylene 
• 119-61-9 benzophenone 
• 56812-60-3 (2-bromobenzyl)magnesium bromide 
• 36901-75-4 (2-bromobenzyl)triphenylphosphonium bromide 
• 3433-80-5 1-Bromo-2-bromomethyl-benzene 
• 7333-65-5 (diphenylmethyl)triphenylphosphonium bromide 
• 6630-33-7 ortho-bromobenzaldehyde 
• 17507-57-2 (diphenylphosphinyl)phenyldiazomethane 

Downstream Products

• 844-20-2 9-phenylphenanthrene 
• 91388-36-2 1-formyl-2-(2,2-diphenylethenyl)benzene 
• 156360-95-1 2-(2,2-diphenylvinyl)benzoic acid 
• 91388-48-6 1-formyl-2-(2,2-diphenylethenyl)benzene tosylhydrazone 
• 96264-91-4 2-(2,2-Diphenyl-vinyl)-benzoesaeurechlorid 
• 1310800-16-8 C₂₄H₂₄OS 
• 130162-54-8 1-(4-methoxyphenyl)-2,3-diphenyl-1H-indole 
• 1227172-65-7 1-(diphenylmethylene)-2-phenyl-1H-indene 

Relevant articles and documents

Orbital symmetry governed reactions under high-intensity argon laser-jet conditions: The involvement of a [1,5S] sigmatropic shift in the photocyclization of an o-alkenylbenzaldehyde to a benzocyclobutenone

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A visible-light-mediated oxidative C-N bond formation/aromatization cascade: Photocatalytic preparation of N-arylindoles

Just add light and air: Structurally diverse N-arylindoles can be prepared from readily prepared o-styryl anilines through visible-light photocatalysis. The reaction, which is conducted open to air, is mediated by [Ru(bpz) 3](PF6)2 (bpz=2,2'-bipyrazine) and involves both C-N bond formation and aromatization (see scheme). Using suitably substituted substrates, a 1,2-carbon shift can be also incorporated into this cascade reaction. Copyright